---
_id: '5581'
abstract:
- lang: ger
text: Data on Austrian open access publication output at Springer from 2013-2016
including data analysis.
article_processing_charge: No
author:
- first_name: Márton
full_name: Villányi, Márton
id: 3FFCCD3A-F248-11E8-B48F-1D18A9856A87
last_name: Villányi
orcid: 0000-0001-8126-0426
citation:
ama: Villányi M. Springer Austrian Publications 2013-2016. 2018. doi:10.15479/AT:ISTA:93
apa: Villányi, M. (2018). Springer Austrian Publications 2013-2016. Institute of
Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:93
chicago: Villányi, Márton. “Springer Austrian Publications 2013-2016.” Institute
of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:93.
ieee: M. Villányi, “Springer Austrian Publications 2013-2016.” Institute of Science
and Technology Austria, 2018.
ista: Villányi M. 2018. Springer Austrian Publications 2013-2016, Institute of Science
and Technology Austria, 10.15479/AT:ISTA:93.
mla: Villányi, Márton. Springer Austrian Publications 2013-2016. Institute
of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:93.
short: M. Villányi, (2018).
datarep_id: '93'
date_created: 2018-12-12T12:31:39Z
date_published: 2018-01-16T00:00:00Z
date_updated: 2024-02-21T13:43:53Z
day: '16'
ddc:
- '020'
department:
- _id: E-Lib
doi: 10.15479/AT:ISTA:93
file:
- access_level: open_access
checksum: 7cc8274975162a99ea4681dc344b927d
content_type: application/zip
creator: system
date_created: 2018-12-12T13:05:20Z
date_updated: 2020-07-14T12:47:06Z
file_id: '5646'
file_name: IST-2018-93-v1+1_Springer_Austrian_Publications_2013-2016.zip
file_size: 304018
relation: main_file
file_date_updated: 2020-07-14T12:47:06Z
has_accepted_license: '1'
keyword:
- Publication analysis
- Bibliography
- Open Access
license: https://creativecommons.org/publicdomain/zero/1.0/
month: '01'
oa: 1
oa_version: Submitted Version
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '278'
relation: part_of_dissertation
status: public
status: public
title: Springer Austrian Publications 2013-2016
tmp:
image: /images/cc_0.png
legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
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short: CC0 (1.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '5580'
abstract:
- lang: ger
text: Data on Austrian open access publication output at SAGE from 2013-2017 including
data analysis.
article_processing_charge: No
author:
- first_name: Márton
full_name: Villányi, Márton
id: 3FFCCD3A-F248-11E8-B48F-1D18A9856A87
last_name: Villányi
orcid: 0000-0001-8126-0426
citation:
ama: Villányi M. SAGE Austrian Publications 2013-2017. 2018. doi:10.15479/AT:ISTA:92
apa: Villányi, M. (2018). SAGE Austrian Publications 2013-2017. Institute of Science
and Technology Austria. https://doi.org/10.15479/AT:ISTA:92
chicago: Villányi, Márton. “SAGE Austrian Publications 2013-2017.” Institute of
Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:92.
ieee: M. Villányi, “SAGE Austrian Publications 2013-2017.” Institute of Science
and Technology Austria, 2018.
ista: Villányi M. 2018. SAGE Austrian Publications 2013-2017, Institute of Science
and Technology Austria, 10.15479/AT:ISTA:92.
mla: Villányi, Márton. SAGE Austrian Publications 2013-2017. Institute of
Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:92.
short: M. Villányi, (2018).
datarep_id: '92'
date_created: 2018-12-12T12:31:38Z
date_published: 2018-01-16T00:00:00Z
date_updated: 2024-02-21T13:44:07Z
day: '16'
ddc:
- '020'
department:
- _id: E-Lib
doi: 10.15479/AT:ISTA:92
file:
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checksum: 1ed83efc33aab2fc5dbe5ffe95de5c2b
content_type: application/zip
creator: system
date_created: 2018-12-12T13:03:01Z
date_updated: 2020-07-14T12:47:06Z
file_id: '5619'
file_name: IST-2018-92-v1+1_SAGE_Austrian_Publications_2013-2017.zip
file_size: 724017
relation: main_file
file_date_updated: 2020-07-14T12:47:06Z
has_accepted_license: '1'
keyword:
- Publication analysis
- Bibliography
- Open Access
month: '01'
oa: 1
oa_version: Submitted Version
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '278'
relation: part_of_dissertation
status: public
status: public
title: SAGE Austrian Publications 2013-2017
tmp:
image: /images/cc_0.png
legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
name: Creative Commons Public Domain Dedication (CC0 1.0)
short: CC0 (1.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '5579'
abstract:
- lang: eng
text: Data on Austrian open access publication output at RSC from 2013-2017 including
data analysis.
article_processing_charge: No
author:
- first_name: Márton
full_name: Villányi, Márton
id: 3FFCCD3A-F248-11E8-B48F-1D18A9856A87
last_name: Villányi
orcid: 0000-0001-8126-0426
citation:
ama: Villányi M. RSC Austrian Publications 2013-2017. 2018. doi:10.15479/AT:ISTA:91
apa: Villányi, M. (2018). RSC Austrian Publications 2013-2017. Institute of Science
and Technology Austria. https://doi.org/10.15479/AT:ISTA:91
chicago: Villányi, Márton. “RSC Austrian Publications 2013-2017.” Institute of Science
and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:91.
ieee: M. Villányi, “RSC Austrian Publications 2013-2017.” Institute of Science and
Technology Austria, 2018.
ista: Villányi M. 2018. RSC Austrian Publications 2013-2017, Institute of Science
and Technology Austria, 10.15479/AT:ISTA:91.
mla: Villányi, Márton. RSC Austrian Publications 2013-2017. Institute of
Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:91.
short: M. Villányi, (2018).
datarep_id: '91'
date_created: 2018-12-12T12:31:38Z
date_published: 2018-01-16T00:00:00Z
date_updated: 2024-02-21T13:42:53Z
day: '16'
ddc:
- '020'
department:
- _id: E-Lib
doi: 10.15479/AT:ISTA:91
file:
- access_level: open_access
checksum: 2a73efc5f94f8deb00e2b08c3dff8547
content_type: application/zip
creator: system
date_created: 2018-12-12T13:02:40Z
date_updated: 2020-07-14T12:47:06Z
file_id: '5605'
file_name: IST-2018-91-v1+1_RSC_Austrian__Publications_2013-2017.zip
file_size: 791408
relation: main_file
file_date_updated: 2020-07-14T12:47:06Z
has_accepted_license: '1'
keyword:
- Publication analysis
- Bibliography
- Open Access
month: '01'
oa: 1
oa_version: Submitted Version
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '278'
relation: part_of_dissertation
status: public
status: public
title: RSC Austrian Publications 2013-2017
tmp:
image: /images/cc_0.png
legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
name: Creative Commons Public Domain Dedication (CC0 1.0)
short: CC0 (1.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '5576'
abstract:
- lang: ger
text: Comparison of Scopus' and FWF's data on Austrian publication output at T&F.
article_processing_charge: No
author:
- first_name: Márton
full_name: Villányi, Márton
id: 3FFCCD3A-F248-11E8-B48F-1D18A9856A87
last_name: Villányi
orcid: 0000-0001-8126-0426
citation:
ama: Villányi M. Data Check T&F Scopus vs. FWF. 2018. doi:10.15479/AT:ISTA:88
apa: Villányi, M. (2018). Data Check T&F Scopus vs. FWF. Institute of Science
and Technology Austria. https://doi.org/10.15479/AT:ISTA:88
chicago: Villányi, Márton. “Data Check T&F Scopus vs. FWF.” Institute of Science
and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:88.
ieee: M. Villányi, “Data Check T&F Scopus vs. FWF.” Institute of Science and
Technology Austria, 2018.
ista: Villányi M. 2018. Data Check T&F Scopus vs. FWF, Institute of Science
and Technology Austria, 10.15479/AT:ISTA:88.
mla: Villányi, Márton. Data Check T&F Scopus vs. FWF. Institute of Science
and Technology Austria, 2018, doi:10.15479/AT:ISTA:88.
short: M. Villányi, (2018).
datarep_id: '88'
date_created: 2018-12-12T12:31:37Z
date_published: 2018-01-16T00:00:00Z
date_updated: 2024-02-21T13:43:10Z
day: '16'
ddc:
- '020'
department:
- _id: E-Lib
doi: 10.15479/AT:ISTA:88
file:
- access_level: open_access
checksum: a887246c2b41b98df90ccbc1d62b4487
content_type: application/zip
creator: system
date_created: 2018-12-12T13:02:32Z
date_updated: 2020-07-14T12:47:05Z
file_id: '5598'
file_name: IST-2018-88-v1+1_Data_Check_T_F_Scopus_vs._FWF.zip
file_size: 741195
relation: main_file
file_date_updated: 2020-07-14T12:47:05Z
has_accepted_license: '1'
keyword:
- Publication analysis
- Bibliography
- Open Access
month: '01'
oa: 1
oa_version: Submitted Version
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '278'
relation: part_of_dissertation
status: public
status: public
title: Data Check T&F Scopus vs. FWF
tmp:
image: /images/cc_0.png
legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
name: Creative Commons Public Domain Dedication (CC0 1.0)
short: CC0 (1.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '5575'
abstract:
- lang: ger
text: 'Comparison of Scopus'' and FWF''s data on Austrian publication output at
RSC. '
article_processing_charge: No
author:
- first_name: Márton
full_name: Villányi, Márton
id: 3FFCCD3A-F248-11E8-B48F-1D18A9856A87
last_name: Villányi
orcid: 0000-0001-8126-0426
citation:
ama: Villányi M. Data Check RSC Scopus vs. FWF. 2018. doi:10.15479/AT:ISTA:87
apa: Villányi, M. (2018). Data Check RSC Scopus vs. FWF. Institute of Science and
Technology Austria. https://doi.org/10.15479/AT:ISTA:87
chicago: Villányi, Márton. “Data Check RSC Scopus vs. FWF.” Institute of Science
and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:87.
ieee: M. Villányi, “Data Check RSC Scopus vs. FWF.” Institute of Science and Technology
Austria, 2018.
ista: Villányi M. 2018. Data Check RSC Scopus vs. FWF, Institute of Science and
Technology Austria, 10.15479/AT:ISTA:87.
mla: Villányi, Márton. Data Check RSC Scopus vs. FWF. Institute of Science
and Technology Austria, 2018, doi:10.15479/AT:ISTA:87.
short: M. Villányi, (2018).
datarep_id: '87'
date_created: 2018-12-12T12:31:37Z
date_published: 2018-01-16T00:00:00Z
date_updated: 2024-02-21T13:43:25Z
day: '16'
ddc:
- '020'
department:
- _id: E-Lib
doi: 10.15479/AT:ISTA:87
file:
- access_level: open_access
checksum: 563cc5266c0bac354007873c92be777b
content_type: application/zip
creator: system
date_created: 2018-12-12T13:02:44Z
date_updated: 2020-07-14T12:47:05Z
file_id: '5610'
file_name: IST-2018-87-v1+1_Data_Check_RSC_Scopus_vs._FWF.zip
file_size: 277078
relation: main_file
file_date_updated: 2020-07-14T12:47:05Z
has_accepted_license: '1'
keyword:
- Publication analysis
- Bibliography
- Open Access
month: '01'
oa: 1
oa_version: Submitted Version
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '278'
relation: part_of_dissertation
status: public
status: public
title: Data Check RSC Scopus vs. FWF
tmp:
image: /images/cc_0.png
legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
name: Creative Commons Public Domain Dedication (CC0 1.0)
short: CC0 (1.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '292'
abstract:
- lang: eng
text: 'Retina is a paradigmatic system for studying sensory encoding: the transformation
of light into spiking activity of ganglion cells. The inverse problem, where stimulus
is reconstructed from spikes, has received less attention, especially for complex
stimuli that should be reconstructed “pixel-by-pixel”. We recorded around a hundred
neurons from a dense patch in a rat retina and decoded movies of multiple small
randomly-moving discs. We constructed nonlinear (kernelized and neural network)
decoders that improved significantly over linear results. An important contribution
to this was the ability of nonlinear decoders to reliably separate between neural
responses driven by locally fluctuating light signals, and responses at locally
constant light driven by spontaneous-like activity. This improvement crucially
depended on the precise, non-Poisson temporal structure of individual spike trains,
which originated in the spike-history dependence of neural responses. We propose
a general principle by which downstream circuitry could discriminate between spontaneous
and stimulus-driven activity based solely on higher-order statistical structure
in the incoming spike trains.'
article_number: e1006057
article_processing_charge: Yes
article_type: original
author:
- first_name: Vicent
full_name: Botella Soler, Vicent
id: 421234E8-F248-11E8-B48F-1D18A9856A87
last_name: Botella Soler
orcid: 0000-0002-8790-1914
- first_name: Stephane
full_name: Deny, Stephane
last_name: Deny
- first_name: Georg S
full_name: Martius, Georg S
last_name: Martius
- first_name: Olivier
full_name: Marre, Olivier
last_name: Marre
- first_name: Gasper
full_name: Tkacik, Gasper
id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
last_name: Tkacik
orcid: 0000-0002-6699-1455
citation:
ama: Botella Soler V, Deny S, Martius GS, Marre O, Tkačik G. Nonlinear decoding
of a complex movie from the mammalian retina. PLoS Computational Biology.
2018;14(5). doi:10.1371/journal.pcbi.1006057
apa: Botella Soler, V., Deny, S., Martius, G. S., Marre, O., & Tkačik, G. (2018).
Nonlinear decoding of a complex movie from the mammalian retina. PLoS Computational
Biology. Public Library of Science. https://doi.org/10.1371/journal.pcbi.1006057
chicago: Botella Soler, Vicente, Stephane Deny, Georg S Martius, Olivier Marre,
and Gašper Tkačik. “Nonlinear Decoding of a Complex Movie from the Mammalian Retina.”
PLoS Computational Biology. Public Library of Science, 2018. https://doi.org/10.1371/journal.pcbi.1006057.
ieee: V. Botella Soler, S. Deny, G. S. Martius, O. Marre, and G. Tkačik, “Nonlinear
decoding of a complex movie from the mammalian retina,” PLoS Computational
Biology, vol. 14, no. 5. Public Library of Science, 2018.
ista: Botella Soler V, Deny S, Martius GS, Marre O, Tkačik G. 2018. Nonlinear decoding
of a complex movie from the mammalian retina. PLoS Computational Biology. 14(5),
e1006057.
mla: Botella Soler, Vicente, et al. “Nonlinear Decoding of a Complex Movie from
the Mammalian Retina.” PLoS Computational Biology, vol. 14, no. 5, e1006057,
Public Library of Science, 2018, doi:10.1371/journal.pcbi.1006057.
short: V. Botella Soler, S. Deny, G.S. Martius, O. Marre, G. Tkačik, PLoS Computational
Biology 14 (2018).
date_created: 2018-12-11T11:45:39Z
date_published: 2018-05-10T00:00:00Z
date_updated: 2024-02-21T13:45:25Z
day: '10'
ddc:
- '570'
department:
- _id: GaTk
doi: 10.1371/journal.pcbi.1006057
ec_funded: 1
external_id:
isi:
- '000434012100002'
file:
- access_level: open_access
checksum: 3026f94d235219e15514505fdbadf34e
content_type: application/pdf
creator: dernst
date_created: 2019-02-13T11:07:15Z
date_updated: 2020-07-14T12:45:53Z
file_id: '5974'
file_name: 2018_Plos_Botella_Soler.pdf
file_size: 3460786
relation: main_file
file_date_updated: 2020-07-14T12:45:53Z
has_accepted_license: '1'
intvolume: ' 14'
isi: 1
issue: '5'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
project:
- _id: 25CBA828-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '720270'
name: Human Brain Project Specific Grant Agreement 1 (HBP SGA 1)
- _id: 254D1A94-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P 25651-N26
name: Sensitivity to higher-order statistics in natural scenes
publication: PLoS Computational Biology
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
related_material:
link:
- description: News on IST Homepage
relation: press_release
url: https://ist.ac.at/en/news/video-of-moving-discs-reconstructed-from-rat-retinal-neuron-signals/
record:
- id: '5584'
relation: research_data
status: public
scopus_import: '1'
status: public
title: Nonlinear decoding of a complex movie from the mammalian retina
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 14
year: '2018'
...
---
_id: '438'
abstract:
- lang: eng
text: The MazF toxin sequence-specifically cleaves single-stranded RNA upon various
stressful conditions, and it is activated as a part of the mazEF toxin–antitoxin
module in Escherichia coli. Although autoregulation of mazEF expression through
the MazE antitoxin-dependent transcriptional repression has been biochemically
characterized, less is known about post-transcriptional autoregulation, as well
as how both of these autoregulatory features affect growth of single cells during
conditions that promote MazF production. Here, we demonstrate post-transcriptional
autoregulation of mazF expression dynamics by MazF cleaving its own transcript.
Single-cell analyses of bacterial populations during ectopic MazF production indicated
that two-level autoregulation of mazEF expression influences cell-to-cell growth
rate heterogeneity. The increase in growth rate heterogeneity is governed by the
MazE antitoxin, and tuned by the MazF-dependent mazF mRNA cleavage. Also, both
autoregulatory features grant rapid exit from the stress caused by mazF overexpression.
Time-lapse microscopy revealed that MazF-mediated cleavage of mazF mRNA leads
to increased temporal variability in length of individual cells during ectopic
mazF overexpression, as explained by a stochastic model indicating that mazEF
mRNA cleavage underlies temporal fluctuations in MazF levels during stress.
article_processing_charge: Yes (in subscription journal)
author:
- first_name: Nela
full_name: Nikolic, Nela
id: 42D9CABC-F248-11E8-B48F-1D18A9856A87
last_name: Nikolic
orcid: 0000-0001-9068-6090
- first_name: Tobias
full_name: Bergmiller, Tobias
id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
last_name: Bergmiller
orcid: 0000-0001-5396-4346
- first_name: Alexandra
full_name: Vandervelde, Alexandra
last_name: Vandervelde
- first_name: Tanino
full_name: Albanese, Tanino
last_name: Albanese
- first_name: Lendert
full_name: Gelens, Lendert
last_name: Gelens
- first_name: Isabella
full_name: Moll, Isabella
last_name: Moll
citation:
ama: Nikolic N, Bergmiller T, Vandervelde A, Albanese T, Gelens L, Moll I. Autoregulation
of mazEF expression underlies growth heterogeneity in bacterial populations. Nucleic
Acids Research. 2018;46(6):2918-2931. doi:10.1093/nar/gky079
apa: Nikolic, N., Bergmiller, T., Vandervelde, A., Albanese, T., Gelens, L., &
Moll, I. (2018). Autoregulation of mazEF expression underlies growth heterogeneity
in bacterial populations. Nucleic Acids Research. Oxford University Press.
https://doi.org/10.1093/nar/gky079
chicago: Nikolic, Nela, Tobias Bergmiller, Alexandra Vandervelde, Tanino Albanese,
Lendert Gelens, and Isabella Moll. “Autoregulation of MazEF Expression Underlies
Growth Heterogeneity in Bacterial Populations.” Nucleic Acids Research.
Oxford University Press, 2018. https://doi.org/10.1093/nar/gky079.
ieee: N. Nikolic, T. Bergmiller, A. Vandervelde, T. Albanese, L. Gelens, and I.
Moll, “Autoregulation of mazEF expression underlies growth heterogeneity in bacterial
populations,” Nucleic Acids Research, vol. 46, no. 6. Oxford University
Press, pp. 2918–2931, 2018.
ista: Nikolic N, Bergmiller T, Vandervelde A, Albanese T, Gelens L, Moll I. 2018.
Autoregulation of mazEF expression underlies growth heterogeneity in bacterial
populations. Nucleic Acids Research. 46(6), 2918–2931.
mla: Nikolic, Nela, et al. “Autoregulation of MazEF Expression Underlies Growth
Heterogeneity in Bacterial Populations.” Nucleic Acids Research, vol. 46,
no. 6, Oxford University Press, 2018, pp. 2918–31, doi:10.1093/nar/gky079.
short: N. Nikolic, T. Bergmiller, A. Vandervelde, T. Albanese, L. Gelens, I. Moll,
Nucleic Acids Research 46 (2018) 2918–2931.
date_created: 2018-12-11T11:46:29Z
date_published: 2018-04-06T00:00:00Z
date_updated: 2024-02-21T13:44:45Z
day: '06'
ddc:
- '576'
department:
- _id: CaGu
doi: 10.1093/nar/gky079
external_id:
isi:
- '000429009500021'
file:
- access_level: open_access
checksum: 3ff4f545c27e11a4cd20ccb30778793e
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:15:30Z
date_updated: 2020-07-14T12:46:27Z
file_id: '5151'
file_name: IST-2018-971-v1+1_2018_Nikoloc_Autoregulation_of.pdf
file_size: 5027978
relation: main_file
file_date_updated: 2020-07-14T12:46:27Z
has_accepted_license: '1'
intvolume: ' 46'
isi: 1
issue: '6'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 2918-2931
project:
- _id: 3AC91DDA-15DF-11EA-824D-93A3E7B544D1
call_identifier: FWF
name: FWF Open Access Fund
publication: Nucleic Acids Research
publication_status: published
publisher: Oxford University Press
pubrep_id: '971'
quality_controlled: '1'
related_material:
record:
- id: '5569'
relation: popular_science
status: public
scopus_import: '1'
status: public
title: Autoregulation of mazEF expression underlies growth heterogeneity in bacterial
populations
tmp:
image: /images/cc_by.png
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name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 46
year: '2018'
...
---
_id: '131'
abstract:
- lang: eng
text: 'XY systems usually show chromosome-wide compensation of X-linked genes, while
in many ZW systems, compensation is restricted to a minority of dosage-sensitive
genes. Why such differences arose is still unclear. Here, we combine comparative
genomics, transcriptomics and proteomics to obtain a complete overview of the
evolution of gene dosage on the Z-chromosome of Schistosoma parasites. We compare
the Z-chromosome gene content of African (Schistosoma mansoni and S. haematobium)
and Asian (S. japonicum) schistosomes and describe lineage-specific evolutionary
strata. We use these to assess gene expression evolution following sex-linkage.
The resulting patterns suggest a reduction in expression of Z-linked genes in
females, combined with upregulation of the Z in both sexes, in line with the first
step of Ohno’s classic model of dosage compensation evolution. Quantitative proteomics
suggest that post-transcriptional mechanisms do not play a major role in balancing
the expression of Z-linked genes. '
acknowledgement: We are grateful to Lu Dabing (Soochow University, Suzhou, China)
for providing Schistosoma japonicum samples, to Ariana Macon (IST Austria) and Georgette
Stovall (JLU Giessen) for technical assistance, to IT support at IST Austria for
providing optimal environment to bioinformatic analyses, and to the Vicoso lab for
comments on the manuscript.
article_number: e35684
article_processing_charge: No
article_type: original
author:
- first_name: Marion A
full_name: Picard, Marion A
id: 2C921A7A-F248-11E8-B48F-1D18A9856A87
last_name: Picard
orcid: 0000-0002-8101-2518
- first_name: Celine
full_name: Cosseau, Celine
last_name: Cosseau
- first_name: Sabrina
full_name: Ferré, Sabrina
last_name: Ferré
- first_name: Thomas
full_name: Quack, Thomas
last_name: Quack
- first_name: Christoph
full_name: Grevelding, Christoph
last_name: Grevelding
- first_name: Yohann
full_name: Couté, Yohann
last_name: Couté
- first_name: Beatriz
full_name: Vicoso, Beatriz
id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
last_name: Vicoso
orcid: 0000-0002-4579-8306
citation:
ama: Picard MAL, Cosseau C, Ferré S, et al. Evolution of gene dosage on the Z-chromosome
of schistosome parasites. eLife. 2018;7. doi:10.7554/eLife.35684
apa: Picard, M. A. L., Cosseau, C., Ferré, S., Quack, T., Grevelding, C., Couté,
Y., & Vicoso, B. (2018). Evolution of gene dosage on the Z-chromosome of schistosome
parasites. ELife. eLife Sciences Publications. https://doi.org/10.7554/eLife.35684
chicago: Picard, Marion A L, Celine Cosseau, Sabrina Ferré, Thomas Quack, Christoph
Grevelding, Yohann Couté, and Beatriz Vicoso. “Evolution of Gene Dosage on the
Z-Chromosome of Schistosome Parasites.” ELife. eLife Sciences Publications,
2018. https://doi.org/10.7554/eLife.35684.
ieee: M. A. L. Picard et al., “Evolution of gene dosage on the Z-chromosome
of schistosome parasites,” eLife, vol. 7. eLife Sciences Publications,
2018.
ista: Picard MAL, Cosseau C, Ferré S, Quack T, Grevelding C, Couté Y, Vicoso B.
2018. Evolution of gene dosage on the Z-chromosome of schistosome parasites. eLife.
7, e35684.
mla: Picard, Marion A. L., et al. “Evolution of Gene Dosage on the Z-Chromosome
of Schistosome Parasites.” ELife, vol. 7, e35684, eLife Sciences Publications,
2018, doi:10.7554/eLife.35684.
short: M.A.L. Picard, C. Cosseau, S. Ferré, T. Quack, C. Grevelding, Y. Couté, B.
Vicoso, ELife 7 (2018).
date_created: 2018-12-11T11:44:47Z
date_published: 2018-08-13T00:00:00Z
date_updated: 2024-02-21T13:45:12Z
day: '13'
ddc:
- '570'
department:
- _id: BeVi
doi: 10.7554/eLife.35684
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name: Sex chromosome evolution under male- and female- heterogamety
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publication_status: published
publisher: eLife Sciences Publications
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title: Evolution of gene dosage on the Z-chromosome of schistosome parasites
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abstract:
- lang: eng
text: "This package contains data for the publication \"Nonlinear decoding of a
complex movie from the mammalian retina\" by Deny S. et al, PLOS Comput Biol (2018).
\r\n\r\nThe data consists of\r\n(i) 91 spike sorted, isolated rat retinal ganglion
cells that pass stability and quality criteria, recorded on the multi-electrode
array, in response to the presentation of the complex movie with many randomly
moving dark discs. The responses are represented as 648000 x 91 binary matrix,
where the first index indicates the timebin of duration 12.5 ms, and the second
index the neural identity. The matrix entry is 0/1 if the neuron didn't/did spike
in the particular time bin.\r\n(ii) README file and a graphical illustration of
the structure of the experiment, specifying how the 648000 timebins are split
into epochs where 1, 2, 4, or 10 discs were displayed, and which stimulus segments
are exact repeats or unique ball trajectories.\r\n(iii) a 648000 x 400 matrix
of luminance traces for each of the 20 x 20 positions (\"sites\") in the movie
frame, with time that is locked to the recorded raster. The luminance traces are
produced as described in the manuscript by filtering the raw disc movie with a
small gaussian spatial kernel. "
article_processing_charge: No
author:
- first_name: Stephane
full_name: Deny, Stephane
last_name: Deny
- first_name: Olivier
full_name: Marre, Olivier
last_name: Marre
- first_name: Vicente
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- first_name: Georg S
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id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
last_name: Tkacik
orcid: 0000-0002-6699-1455
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of a complex movie from the mammalian retina. 2018. doi:10.15479/AT:ISTA:98
apa: Deny, S., Marre, O., Botella-Soler, V., Martius, G. S., & Tkačik, G. (2018).
Nonlinear decoding of a complex movie from the mammalian retina. Institute of
Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:98
chicago: Deny, Stephane, Olivier Marre, Vicente Botella-Soler, Georg S Martius,
and Gašper Tkačik. “Nonlinear Decoding of a Complex Movie from the Mammalian Retina.”
Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:98.
ieee: S. Deny, O. Marre, V. Botella-Soler, G. S. Martius, and G. Tkačik, “Nonlinear
decoding of a complex movie from the mammalian retina.” Institute of Science and
Technology Austria, 2018.
ista: Deny S, Marre O, Botella-Soler V, Martius GS, Tkačik G. 2018. Nonlinear decoding
of a complex movie from the mammalian retina, Institute of Science and Technology
Austria, 10.15479/AT:ISTA:98.
mla: Deny, Stephane, et al. Nonlinear Decoding of a Complex Movie from the Mammalian
Retina. Institute of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:98.
short: S. Deny, O. Marre, V. Botella-Soler, G.S. Martius, G. Tkačik, (2018).
datarep_id: '98'
date_created: 2018-12-12T12:31:39Z
date_published: 2018-03-29T00:00:00Z
date_updated: 2024-02-21T13:45:26Z
day: '29'
ddc:
- '570'
department:
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- _id: GaTk
doi: 10.15479/AT:ISTA:98
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keyword:
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month: '03'
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title: Nonlinear decoding of a complex movie from the mammalian retina
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...
---
_id: '5586'
abstract:
- lang: eng
text: Input files and scripts from "Evolution of gene dosage on the Z-chromosome
of schistosome parasites" by Picard M.A.L., et al (2018).
article_processing_charge: No
author:
- first_name: Beatriz
full_name: Vicoso, Beatriz
id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
last_name: Vicoso
orcid: 0000-0002-4579-8306
citation:
ama: Vicoso B. Input files and scripts from “Evolution of gene dosage on the Z-chromosome
of schistosome parasites” by Picard M.A.L., et al (2018). 2018. doi:10.15479/AT:ISTA:109
apa: Vicoso, B. (2018). Input files and scripts from “Evolution of gene dosage on
the Z-chromosome of schistosome parasites” by Picard M.A.L., et al (2018). Institute
of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:109
chicago: Vicoso, Beatriz. “Input Files and Scripts from ‘Evolution of Gene Dosage
on the Z-Chromosome of Schistosome Parasites’ by Picard M.A.L., et Al (2018).”
Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:109.
ieee: B. Vicoso, “Input files and scripts from ‘Evolution of gene dosage on the
Z-chromosome of schistosome parasites’ by Picard M.A.L., et al (2018).” Institute
of Science and Technology Austria, 2018.
ista: Vicoso B. 2018. Input files and scripts from ‘Evolution of gene dosage on
the Z-chromosome of schistosome parasites’ by Picard M.A.L., et al (2018), Institute
of Science and Technology Austria, 10.15479/AT:ISTA:109.
mla: Vicoso, Beatriz. Input Files and Scripts from “Evolution of Gene Dosage
on the Z-Chromosome of Schistosome Parasites” by Picard M.A.L., et Al (2018).
Institute of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:109.
short: B. Vicoso, (2018).
contributor:
- first_name: Marion A
id: 2C921A7A-F248-11E8-B48F-1D18A9856A87
last_name: Picard
orcid: 0000-0002-8101-2518
datarep_id: '109'
date_created: 2018-12-12T12:31:40Z
date_published: 2018-07-24T00:00:00Z
date_updated: 2024-02-21T13:45:12Z
day: '24'
ddc:
- '570'
department:
- _id: BeVi
doi: 10.15479/AT:ISTA:109
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checksum: e60b484bd6f55c08eb66a189cb72c923
content_type: application/zip
creator: system
date_created: 2018-12-12T13:02:35Z
date_updated: 2020-07-14T12:47:08Z
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file_name: IST-2018-109-v1+1_SupplementaryMethods.zip
file_size: 11918144
relation: main_file
file_date_updated: 2020-07-14T12:47:08Z
has_accepted_license: '1'
keyword:
- schistosoma
- Z-chromosome
- gene expression
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 250ED89C-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P28842-B22
name: Sex chromosome evolution under male- and female- heterogamety
publisher: Institute of Science and Technology Austria
related_material:
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- id: '131'
relation: research_paper
status: public
status: public
title: Input files and scripts from "Evolution of gene dosage on the Z-chromosome
of schistosome parasites" by Picard M.A.L., et al (2018)
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...
---
_id: '5583'
abstract:
- lang: eng
text: "Data and scripts are provided in support of the manuscript \"Efficient inference
of paternity and sibship inference given known maternity via hierarchical clustering\",
and the associated Python package FAPS, available from www.github.com/ellisztamas/faps.\r\n\r\nSimulation
scripts cover:\r\n1. Performance under different mating scenarios.\r\n2. Comparison
with Colony2.\r\n3. Effect of changing the number of Monte Carlo draws\r\n\r\nThe
final script covers the analysis of half-sib arrays from wild-pollinated seed
in an Antirrhinum majus hybrid zone."
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full_name: Ellis, Thomas
id: 3153D6D4-F248-11E8-B48F-1D18A9856A87
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citation:
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apa: Ellis, T. (2018). Data and Python scripts supporting Python package FAPS. Institute
of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:95
chicago: Ellis, Thomas. “Data and Python Scripts Supporting Python Package FAPS.”
Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:95.
ieee: T. Ellis, “Data and Python scripts supporting Python package FAPS.” Institute
of Science and Technology Austria, 2018.
ista: Ellis T. 2018. Data and Python scripts supporting Python package FAPS, Institute
of Science and Technology Austria, 10.15479/AT:ISTA:95.
mla: Ellis, Thomas. Data and Python Scripts Supporting Python Package FAPS.
Institute of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:95.
short: T. Ellis, (2018).
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last_name: Field
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last_name: Barton
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date_created: 2018-12-12T12:31:39Z
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oa: 1
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...
---
_id: '5569'
abstract:
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text: "Nela Nikolic, Tobias Bergmiller, Alexandra Vandervelde, Tanino G. Albanese,
Lendert Gelens, and Isabella Moll (2018)\r\n“Autoregulation of mazEF expression
underlies growth heterogeneity in bacterial populations” Nucleic Acids Research,
doi: 10.15479/AT:ISTA:74;\r\nmicroscopy experiments by Tobias Bergmiller; image
and data analysis by Nela Nikolic."
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full_name: Bergmiller, Tobias
id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
last_name: Bergmiller
orcid: 0000-0001-5396-4346
- first_name: Nela
full_name: Nikolic, Nela
id: 42D9CABC-F248-11E8-B48F-1D18A9856A87
last_name: Nikolic
orcid: 0000-0001-9068-6090
citation:
ama: Bergmiller T, Nikolic N. Time-lapse microscopy data. 2018. doi:10.15479/AT:ISTA:74
apa: Bergmiller, T., & Nikolic, N. (2018). Time-lapse microscopy data. Institute
of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:74
chicago: Bergmiller, Tobias, and Nela Nikolic. “Time-Lapse Microscopy Data.” Institute
of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:74.
ieee: T. Bergmiller and N. Nikolic, “Time-lapse microscopy data.” Institute of Science
and Technology Austria, 2018.
ista: Bergmiller T, Nikolic N. 2018. Time-lapse microscopy data, Institute of Science
and Technology Austria, 10.15479/AT:ISTA:74.
mla: Bergmiller, Tobias, and Nela Nikolic. Time-Lapse Microscopy Data. Institute
of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:74.
short: T. Bergmiller, N. Nikolic, (2018).
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date_published: 2018-02-07T00:00:00Z
date_updated: 2024-02-21T13:44:45Z
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doi: 10.15479/AT:ISTA:74
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has_accepted_license: '1'
keyword:
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- microfluidics
month: '02'
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publisher: Institute of Science and Technology Austria
publist_id: '7385'
related_material:
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title: Time-lapse microscopy data
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...
---
_id: '161'
abstract:
- lang: eng
text: 'Which properties of metabolic networks can be derived solely from stoichiometry?
Predictive results have been obtained by flux balance analysis (FBA), by postulating
that cells set metabolic fluxes to maximize growth rate. Here we consider a generalization
of FBA to single-cell level using maximum entropy modeling, which we extend and
test experimentally. Specifically, we define for Escherichia coli metabolism a
flux distribution that yields the experimental growth rate: the model, containing
FBA as a limit, provides a better match to measured fluxes and it makes a wide
range of predictions: on flux variability, regulation, and correlations; on the
relative importance of stoichiometry vs. optimization; on scaling relations for
growth rate distributions. We validate the latter here with single-cell data at
different sub-inhibitory antibiotic concentrations. The model quantifies growth
optimization as emerging from the interplay of competitive dynamics in the population
and regulation of metabolism at the level of single cells.'
article_number: '2988'
article_processing_charge: No
author:
- first_name: Daniele
full_name: De Martino, Daniele
id: 3FF5848A-F248-11E8-B48F-1D18A9856A87
last_name: De Martino
orcid: 0000-0002-5214-4706
- first_name: Andersson Anna
full_name: Mc, Andersson Anna
last_name: Mc
- first_name: Tobias
full_name: Bergmiller, Tobias
id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
last_name: Bergmiller
orcid: 0000-0001-5396-4346
- first_name: Calin C
full_name: Guet, Calin C
id: 47F8433E-F248-11E8-B48F-1D18A9856A87
last_name: Guet
orcid: 0000-0001-6220-2052
- first_name: Gasper
full_name: Tkacik, Gasper
id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
last_name: Tkacik
orcid: 0000-0002-6699-1455
citation:
ama: De Martino D, Mc AA, Bergmiller T, Guet CC, Tkačik G. Statistical mechanics
for metabolic networks during steady state growth. Nature Communications.
2018;9(1). doi:10.1038/s41467-018-05417-9
apa: De Martino, D., Mc, A. A., Bergmiller, T., Guet, C. C., & Tkačik, G. (2018).
Statistical mechanics for metabolic networks during steady state growth. Nature
Communications. Springer Nature. https://doi.org/10.1038/s41467-018-05417-9
chicago: De Martino, Daniele, Andersson Anna Mc, Tobias Bergmiller, Calin C Guet,
and Gašper Tkačik. “Statistical Mechanics for Metabolic Networks during Steady
State Growth.” Nature Communications. Springer Nature, 2018. https://doi.org/10.1038/s41467-018-05417-9.
ieee: D. De Martino, A. A. Mc, T. Bergmiller, C. C. Guet, and G. Tkačik, “Statistical
mechanics for metabolic networks during steady state growth,” Nature Communications,
vol. 9, no. 1. Springer Nature, 2018.
ista: De Martino D, Mc AA, Bergmiller T, Guet CC, Tkačik G. 2018. Statistical mechanics
for metabolic networks during steady state growth. Nature Communications. 9(1),
2988.
mla: De Martino, Daniele, et al. “Statistical Mechanics for Metabolic Networks during
Steady State Growth.” Nature Communications, vol. 9, no. 1, 2988, Springer
Nature, 2018, doi:10.1038/s41467-018-05417-9.
short: D. De Martino, A.A. Mc, T. Bergmiller, C.C. Guet, G. Tkačik, Nature Communications
9 (2018).
date_created: 2018-12-11T11:44:57Z
date_published: 2018-07-30T00:00:00Z
date_updated: 2024-02-21T13:45:39Z
day: '30'
ddc:
- '570'
department:
- _id: GaTk
- _id: CaGu
doi: 10.1038/s41467-018-05417-9
ec_funded: 1
external_id:
isi:
- '000440149300021'
file:
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checksum: 3ba7ab27b27723c7dcf633e8fc1f8f18
content_type: application/pdf
creator: dernst
date_created: 2018-12-17T16:44:28Z
date_updated: 2020-07-14T12:45:06Z
file_id: '5728'
file_name: 2018_NatureComm_DeMartino.pdf
file_size: 1043205
relation: main_file
file_date_updated: 2020-07-14T12:45:06Z
has_accepted_license: '1'
intvolume: ' 9'
isi: 1
issue: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
project:
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call_identifier: FWF
grant_number: P28844-B27
name: Biophysics of information processing in gene regulation
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
publication: Nature Communications
publication_status: published
publisher: Springer Nature
publist_id: '7760'
quality_controlled: '1'
related_material:
record:
- id: '5587'
relation: popular_science
status: public
scopus_import: '1'
status: public
title: Statistical mechanics for metabolic networks during steady state growth
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 9
year: '2018'
...
---
_id: '5587'
abstract:
- lang: eng
text: "Supporting material to the article \r\nSTATISTICAL MECHANICS FOR METABOLIC
NETWORKS IN STEADY-STATE GROWTH\r\n\r\nboundscoli.dat\r\nFlux Bounds of the E.
coli catabolic core model iAF1260 in a glucose limited minimal medium. \r\n\r\npolcoli.dat\r\nMatrix
enconding the polytope of the E. coli catabolic core model iAF1260 in a glucose
limited minimal medium, \r\nobtained from the soichiometric matrix by standard
linear algebra (reduced row echelon form).\r\n\r\nellis.dat\r\nApproximate Lowner-John
ellipsoid rounding the polytope of the E. coli catabolic core model iAF1260 in
a glucose limited minimal medium\r\nobtained with the Lovasz method.\r\n\r\npoint0.dat\r\nCenter
of the approximate Lowner-John ellipsoid rounding the polytope of the E. coli
catabolic core model iAF1260 in a glucose limited minimal medium\r\nobtained with
the Lovasz method.\r\n\r\nlovasz.cpp \r\nThis c++ code file receives in input
the polytope of the feasible steady states of a metabolic network, \r\n(matrix
and bounds), and it gives in output an approximate Lowner-John ellipsoid rounding
the polytope\r\nwith the Lovasz method \r\nNB inputs are referred by defaults
to the catabolic core of the E.Coli network iAF1260. \r\nFor further details we
refer to PLoS ONE 10.4 e0122670 (2015).\r\n\r\nsampleHRnew.cpp \r\nThis c++
code file receives in input the polytope of the feasible steady states of a metabolic
network, \r\n(matrix and bounds), the ellipsoid rounding the polytope, a point
inside and \r\nit gives in output a max entropy sampling at fixed average growth
rate \r\nof the steady states by performing an Hit-and-Run Monte Carlo Markov
chain.\r\nNB inputs are referred by defaults to the catabolic core of the E.Coli
network iAF1260. \r\nFor further details we refer to PLoS ONE 10.4 e0122670 (2015)."
article_processing_charge: No
author:
- first_name: Daniele
full_name: De Martino, Daniele
id: 3FF5848A-F248-11E8-B48F-1D18A9856A87
last_name: De Martino
orcid: 0000-0002-5214-4706
- first_name: Gasper
full_name: Tkacik, Gasper
id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
last_name: Tkacik
orcid: 0000-0002-6699-1455
citation:
ama: De Martino D, Tkačik G. Supporting materials “STATISTICAL MECHANICS FOR METABOLIC
NETWORKS IN STEADY-STATE GROWTH.” 2018. doi:10.15479/AT:ISTA:62
apa: De Martino, D., & Tkačik, G. (2018). Supporting materials “STATISTICAL
MECHANICS FOR METABOLIC NETWORKS IN STEADY-STATE GROWTH.” Institute of Science
and Technology Austria. https://doi.org/10.15479/AT:ISTA:62
chicago: De Martino, Daniele, and Gašper Tkačik. “Supporting Materials ‘STATISTICAL
MECHANICS FOR METABOLIC NETWORKS IN STEADY-STATE GROWTH.’” Institute of Science
and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:62.
ieee: D. De Martino and G. Tkačik, “Supporting materials ‘STATISTICAL MECHANICS
FOR METABOLIC NETWORKS IN STEADY-STATE GROWTH.’” Institute of Science and Technology
Austria, 2018.
ista: De Martino D, Tkačik G. 2018. Supporting materials ‘STATISTICAL MECHANICS
FOR METABOLIC NETWORKS IN STEADY-STATE GROWTH’, Institute of Science and Technology
Austria, 10.15479/AT:ISTA:62.
mla: De Martino, Daniele, and Gašper Tkačik. Supporting Materials “STATISTICAL
MECHANICS FOR METABOLIC NETWORKS IN STEADY-STATE GROWTH.” Institute of Science
and Technology Austria, 2018, doi:10.15479/AT:ISTA:62.
short: D. De Martino, G. Tkačik, (2018).
datarep_id: '111'
date_created: 2018-12-12T12:31:41Z
date_published: 2018-09-21T00:00:00Z
date_updated: 2024-02-21T13:45:39Z
day: '21'
ddc:
- '530'
department:
- _id: GaTk
doi: 10.15479/AT:ISTA:62
ec_funded: 1
file:
- access_level: open_access
checksum: 97992e3e8cf8544ec985a48971708726
content_type: application/zip
creator: system
date_created: 2018-12-12T13:05:13Z
date_updated: 2020-07-14T12:47:08Z
file_id: '5641'
file_name: IST-2018-111-v1+1_CODES.zip
file_size: 14376
relation: main_file
file_date_updated: 2020-07-14T12:47:08Z
has_accepted_license: '1'
keyword:
- metabolic networks
- e.coli core
- maximum entropy
- monte carlo markov chain sampling
- ellipsoidal rounding
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
- _id: 254E9036-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P28844-B27
name: Biophysics of information processing in gene regulation
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '161'
relation: research_paper
status: public
status: public
title: Supporting materials "STATISTICAL MECHANICS FOR METABOLIC NETWORKS IN STEADY-STATE
GROWTH"
tmp:
image: /images/cc_0.png
legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
name: Creative Commons Public Domain Dedication (CC0 1.0)
short: CC0 (1.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '542'
abstract:
- lang: eng
text: The t-haplotype, a mouse meiotic driver found on chromosome 17, has been a
model for autosomal segregation distortion for close to a century, but several
questions remain regarding its biology and evolutionary history. A recently published
set of population genomics resources for wild mice includes several individuals
heterozygous for the t-haplotype, which we use to characterize this selfish element
at the genomic and transcriptomic level. Our results show that large sections
of the t-haplotype have been replaced by standard homologous sequences, possibly
due to occasional events of recombination, and that this complicates the inference
of its history. As expected for a long genomic segment of very low recombination,
the t-haplotype carries an excess of fixed nonsynonymous mutations compared to
the standard chromosome. This excess is stronger for regions that have not undergone
recent recombination, suggesting that occasional gene flow between the t and the
standard chromosome may provide a mechanism to regenerate coding sequences that
have accumulated deleterious mutations. Finally, we find that t-complex genes
with altered expression largely overlap with deleted or amplified regions, and
that carrying a t-haplotype alters the testis expression of genes outside of the
t-complex, providing new leads into the pathways involved in the biology of this
segregation distorter.
article_processing_charge: No
article_type: original
author:
- first_name: Réka K
full_name: Kelemen, Réka K
id: 48D3F8DE-F248-11E8-B48F-1D18A9856A87
last_name: Kelemen
orcid: 0000-0002-8489-9281
- first_name: Beatriz
full_name: Vicoso, Beatriz
id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
last_name: Vicoso
orcid: 0000-0002-4579-8306
citation:
ama: Kelemen RK, Vicoso B. Complex history and differentiation patterns of the t-haplotype,
a mouse meiotic driver. Genetics. 2018;208(1):365-375. doi:10.1534/genetics.117.300513
apa: Kelemen, R. K., & Vicoso, B. (2018). Complex history and differentiation
patterns of the t-haplotype, a mouse meiotic driver. Genetics. Genetics
Society of America. https://doi.org/10.1534/genetics.117.300513
chicago: Kelemen, Réka K, and Beatriz Vicoso. “Complex History and Differentiation
Patterns of the T-Haplotype, a Mouse Meiotic Driver.” Genetics. Genetics
Society of America, 2018. https://doi.org/10.1534/genetics.117.300513.
ieee: R. K. Kelemen and B. Vicoso, “Complex history and differentiation patterns
of the t-haplotype, a mouse meiotic driver,” Genetics, vol. 208, no. 1.
Genetics Society of America, pp. 365–375, 2018.
ista: Kelemen RK, Vicoso B. 2018. Complex history and differentiation patterns of
the t-haplotype, a mouse meiotic driver. Genetics. 208(1), 365–375.
mla: Kelemen, Réka K., and Beatriz Vicoso. “Complex History and Differentiation
Patterns of the T-Haplotype, a Mouse Meiotic Driver.” Genetics, vol. 208,
no. 1, Genetics Society of America, 2018, pp. 365–75, doi:10.1534/genetics.117.300513.
short: R.K. Kelemen, B. Vicoso, Genetics 208 (2018) 365–375.
date_created: 2018-12-11T11:47:04Z
date_published: 2018-01-01T00:00:00Z
date_updated: 2024-02-21T13:48:27Z
day: '01'
ddc:
- '576'
department:
- _id: BeVi
doi: 10.1534/genetics.117.300513
ec_funded: 1
external_id:
isi:
- '000419356300024'
file:
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checksum: 2123845e7031a0cf043905be160f9e69
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:15:14Z
date_updated: 2020-07-14T12:46:50Z
file_id: '5132'
file_name: IST-2018-1058-v1+1_365.full__1_.pdf
file_size: 1311661
relation: main_file
file_date_updated: 2020-07-14T12:46:50Z
has_accepted_license: '1'
intvolume: ' 208'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 365 - 375
project:
- _id: 250BDE62-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '715257'
name: Prevalence and Influence of Sexual Antagonism on Genome Evolution
publication: Genetics
publication_status: published
publisher: Genetics Society of America
publist_id: '7274'
pubrep_id: '1058'
quality_controlled: '1'
related_material:
record:
- id: '5571'
relation: popular_science
status: public
- id: '5572'
relation: popular_science
status: public
scopus_import: '1'
status: public
title: Complex history and differentiation patterns of the t-haplotype, a mouse meiotic
driver
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 208
year: '2018'
...
---
_id: '5751'
abstract:
- lang: eng
text: 'Because of the intrinsic randomness of the evolutionary process, a mutant
with a fitness advantage has some chance to be selected but no certainty. Any
experiment that searches for advantageous mutants will lose many of them due to
random drift. It is therefore of great interest to find population structures
that improve the odds of advantageous mutants. Such structures are called amplifiers
of natural selection: they increase the probability that advantageous mutants
are selected. Arbitrarily strong amplifiers guarantee the selection of advantageous
mutants, even for very small fitness advantage. Despite intensive research over
the past decade, arbitrarily strong amplifiers have remained rare. Here we show
how to construct a large variety of them. Our amplifiers are so simple that they
could be useful in biotechnology, when optimizing biological molecules, or as
a diagnostic tool, when searching for faster dividing cells or viruses. They could
also occur in natural population structures.'
article_number: '71'
article_processing_charge: No
author:
- first_name: Andreas
full_name: Pavlogiannis, Andreas
id: 49704004-F248-11E8-B48F-1D18A9856A87
last_name: Pavlogiannis
orcid: 0000-0002-8943-0722
- first_name: Josef
full_name: Tkadlec, Josef
id: 3F24CCC8-F248-11E8-B48F-1D18A9856A87
last_name: Tkadlec
orcid: 0000-0002-1097-9684
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Martin A.
full_name: Nowak, Martin A.
last_name: Nowak
citation:
ama: Pavlogiannis A, Tkadlec J, Chatterjee K, Nowak MA. Construction of arbitrarily
strong amplifiers of natural selection using evolutionary graph theory. Communications
Biology. 2018;1(1). doi:10.1038/s42003-018-0078-7
apa: Pavlogiannis, A., Tkadlec, J., Chatterjee, K., & Nowak, M. A. (2018). Construction
of arbitrarily strong amplifiers of natural selection using evolutionary graph
theory. Communications Biology. Springer Nature. https://doi.org/10.1038/s42003-018-0078-7
chicago: Pavlogiannis, Andreas, Josef Tkadlec, Krishnendu Chatterjee, and Martin
A. Nowak. “Construction of Arbitrarily Strong Amplifiers of Natural Selection
Using Evolutionary Graph Theory.” Communications Biology. Springer Nature,
2018. https://doi.org/10.1038/s42003-018-0078-7.
ieee: A. Pavlogiannis, J. Tkadlec, K. Chatterjee, and M. A. Nowak, “Construction
of arbitrarily strong amplifiers of natural selection using evolutionary graph
theory,” Communications Biology, vol. 1, no. 1. Springer Nature, 2018.
ista: Pavlogiannis A, Tkadlec J, Chatterjee K, Nowak MA. 2018. Construction of arbitrarily
strong amplifiers of natural selection using evolutionary graph theory. Communications
Biology. 1(1), 71.
mla: Pavlogiannis, Andreas, et al. “Construction of Arbitrarily Strong Amplifiers
of Natural Selection Using Evolutionary Graph Theory.” Communications Biology,
vol. 1, no. 1, 71, Springer Nature, 2018, doi:10.1038/s42003-018-0078-7.
short: A. Pavlogiannis, J. Tkadlec, K. Chatterjee, M.A. Nowak, Communications Biology
1 (2018).
date_created: 2018-12-18T13:22:58Z
date_published: 2018-06-14T00:00:00Z
date_updated: 2024-02-21T13:48:42Z
day: '14'
ddc:
- '004'
- '519'
- '576'
department:
- _id: KrCh
doi: 10.1038/s42003-018-0078-7
ec_funded: 1
external_id:
isi:
- '000461126500071'
file:
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checksum: a9db825fa3b64a51ff3de035ec973b3e
content_type: application/pdf
creator: dernst
date_created: 2018-12-18T13:37:04Z
date_updated: 2020-07-14T12:47:10Z
file_id: '5752'
file_name: 2018_CommBiology_Pavlogiannis.pdf
file_size: 1804194
relation: main_file
file_date_updated: 2020-07-14T12:47:10Z
has_accepted_license: '1'
intvolume: ' 1'
isi: 1
issue: '1'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
project:
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '279307'
name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2584A770-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P 23499-N23
name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
publication: Communications Biology
publication_identifier:
issn:
- 2399-3642
publication_status: published
publisher: Springer Nature
pubrep_id: '1045'
quality_controlled: '1'
related_material:
record:
- id: '7196'
relation: part_of_dissertation
status: public
- id: '5559'
relation: popular_science
status: public
scopus_import: '1'
status: public
title: Construction of arbitrarily strong amplifiers of natural selection using evolutionary
graph theory
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 1
year: '2018'
...
---
_id: '5757'
abstract:
- lang: eng
text: "File S1. Variant Calling Format file of the ingroup: 197 haploid sequences
of D. melanogaster from Zambia (Africa) aligned to the D. melanogaster 5.57 reference
genome.\r\n\r\nFile S2. Variant Calling Format file of the outgroup: 1 haploid
sequence of D. simulans aligned to the D. melanogaster 5.57 reference genome.\r\n\r\nFile
S3. Annotations of each transcript in coding regions with SNPeff: Ps (# of synonymous
polymorphic sites); Pn (# of non-synonymous polymorphic sites); Ds (# of synonymous
divergent sites); Dn (# of non-synonymous divergent sites); DoS; ⍺ MK . All variants
were included.\r\n\r\nFile S4. Annotations of each transcript in non-coding regions
with SNPeff: Ps (# of synonymous polymorphic sites); Pu (# of UTR polymorphic
sites); Ds (# of synonymous divergent sites); Du (# of UTR divergent sites); DoS;
⍺ MK . All variants were included.\r\n\r\nFile S5. Annotations of each transcript
in coding regions with SNPGenie: Ps (# of synonymous polymorphic sites); πs (synonymous
diversity); Ss_p (total # of synonymous sites in the polymorphism data); Pn (#
of non-synonymous polymorphic sites); πn (non-synonymous diversity); Sn_p (total
# of non-synonymous sites in the polymorphism data); Ds (# of synonymous divergent
sites); ks (synonymous evolutionary rate); Ss_d (total # of synonymous sites in
the divergence data); Dn (# of non-synonymous divergent sites); kn (non-synonymous
evolutionary rate); Sn_d (total # of non-\r\nsynonymous sites in the divergence
data); DoS; ⍺ MK . All variants were included.\r\n\r\nFile S6. Gene expression
values (RPKM summed over all transcripts) for each sample. Values were quantile-normalized
across all samples.\r\n\r\nFile S7. Final dataset with all covariates, ⍺ MK ,
ωA MK and DoS for coding sites, excluding variants below 5% frequency.\r\n\r\nFile
S8. Final dataset with all covariates, ⍺ MK , ωA MK and DoS for non-coding sites,
excluding variants below 5%\r\nfrequency.\r\n\r\nFile S9. Final dataset with all
covariates, ⍺ EWK , ωA EWK and deleterious SFS for coding sites obtained with
the Eyre-Walker and Keightley method on binned data and using all variants."
article_processing_charge: No
author:
- first_name: Christelle
full_name: Fraisse, Christelle
id: 32DF5794-F248-11E8-B48F-1D18A9856A87
last_name: Fraisse
orcid: 0000-0001-8441-5075
citation:
ama: Fraisse C. Supplementary Files for “Pleiotropy modulates the efficacy of selection
in Drosophila melanogaster.” 2018. doi:10.15479/at:ista:/5757
apa: Fraisse, C. (2018). Supplementary Files for “Pleiotropy modulates the efficacy
of selection in Drosophila melanogaster.” Institute of Science and Technology
Austria. https://doi.org/10.15479/at:ista:/5757
chicago: Fraisse, Christelle. “Supplementary Files for ‘Pleiotropy Modulates the
Efficacy of Selection in Drosophila Melanogaster.’” Institute of Science and Technology
Austria, 2018. https://doi.org/10.15479/at:ista:/5757.
ieee: C. Fraisse, “Supplementary Files for ‘Pleiotropy modulates the efficacy of
selection in Drosophila melanogaster.’” Institute of Science and Technology Austria,
2018.
ista: Fraisse C. 2018. Supplementary Files for ‘Pleiotropy modulates the efficacy
of selection in Drosophila melanogaster’, Institute of Science and Technology
Austria, 10.15479/at:ista:/5757.
mla: Fraisse, Christelle. Supplementary Files for “Pleiotropy Modulates the Efficacy
of Selection in Drosophila Melanogaster.” Institute of Science and Technology
Austria, 2018, doi:10.15479/at:ista:/5757.
short: C. Fraisse, (2018).
contributor:
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last_name: Fraisse
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last_name: Puixeu Sala
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last_name: Vicoso
orcid: 0000-0002-4579-8306
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has_accepted_license: '1'
keyword:
- (mal)adaptation
- pleiotropy
- selective constraint
- evo-devo
- gene expression
- Drosophila melanogaster
month: '12'
oa: 1
oa_version: Published Version
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '6089'
relation: research_paper
status: public
status: public
title: Supplementary Files for "Pleiotropy modulates the efficacy of selection in
Drosophila melanogaster"
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '149'
abstract:
- lang: eng
text: The eigenvalue density of many large random matrices is well approximated
by a deterministic measure, the self-consistent density of states. In the present
work, we show this behaviour for several classes of random matrices. In fact,
we establish that, in each of these classes, the self-consistent density of states
approximates the eigenvalue density of the random matrix on all scales slightly
above the typical eigenvalue spacing. For large classes of random matrices, the
self-consistent density of states exhibits several universal features. We prove
that, under suitable assumptions, random Gram matrices and Hermitian random matrices
with decaying correlations have a 1/3-Hölder continuous self-consistent density
of states ρ on R, which is analytic, where it is positive, and has either a square
root edge or a cubic root cusp, where it vanishes. We, thus, extend the validity
of the corresponding result for Wigner-type matrices from [4, 5, 7]. We show that
ρ is determined as the inverse Stieltjes transform of the normalized trace of
the unique solution m(z) to the Dyson equation −m(z) −1 = z − a + S[m(z)] on C
N×N with the constraint Im m(z) ≥ 0. Here, z lies in the complex upper half-plane,
a is a self-adjoint element of C N×N and S is a positivity-preserving operator
on C N×N encoding the first two moments of the random matrix. In order to analyze
a possible limit of ρ for N → ∞ and address some applications in free probability
theory, we also consider the Dyson equation on infinite dimensional von Neumann
algebras. We present two applications to random matrices. We first establish that,
under certain assumptions, large random matrices with independent entries have
a rotationally symmetric self-consistent density of states which is supported
on a centered disk in C. Moreover, it is infinitely often differentiable apart
from a jump on the boundary of this disk. Second, we show edge universality at
all regular (not necessarily extreme) spectral edges for Hermitian random matrices
with decaying correlations.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Johannes
full_name: Alt, Johannes
id: 36D3D8B6-F248-11E8-B48F-1D18A9856A87
last_name: Alt
citation:
ama: Alt J. Dyson equation and eigenvalue statistics of random matrices. 2018. doi:10.15479/AT:ISTA:TH_1040
apa: Alt, J. (2018). Dyson equation and eigenvalue statistics of random matrices.
Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:TH_1040
chicago: Alt, Johannes. “Dyson Equation and Eigenvalue Statistics of Random Matrices.”
Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:TH_1040.
ieee: J. Alt, “Dyson equation and eigenvalue statistics of random matrices,” Institute
of Science and Technology Austria, 2018.
ista: Alt J. 2018. Dyson equation and eigenvalue statistics of random matrices.
Institute of Science and Technology Austria.
mla: Alt, Johannes. Dyson Equation and Eigenvalue Statistics of Random Matrices.
Institute of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:TH_1040.
short: J. Alt, Dyson Equation and Eigenvalue Statistics of Random Matrices, Institute
of Science and Technology Austria, 2018.
date_created: 2018-12-11T11:44:53Z
date_published: 2018-07-12T00:00:00Z
date_updated: 2024-02-22T14:34:33Z
day: '12'
ddc:
- '515'
- '519'
degree_awarded: PhD
department:
- _id: LaEr
doi: 10.15479/AT:ISTA:TH_1040
ec_funded: 1
file:
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creator: dernst
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file_name: 2018_thesis_Alt_source.zip
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relation: source_file
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language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: '456'
project:
- _id: 258DCDE6-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '338804'
name: Random matrices, universality and disordered quantum systems
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '7772'
pubrep_id: '1040'
related_material:
record:
- id: '1677'
relation: part_of_dissertation
status: public
- id: '550'
relation: part_of_dissertation
status: public
- id: '6183'
relation: part_of_dissertation
status: public
- id: '566'
relation: part_of_dissertation
status: public
- id: '1010'
relation: part_of_dissertation
status: public
- id: '6240'
relation: part_of_dissertation
status: public
- id: '6184'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: László
full_name: Erdös, László
id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
last_name: Erdös
orcid: 0000-0001-5366-9603
title: Dyson equation and eigenvalue statistics of random matrices
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '415'
abstract:
- lang: eng
text: Recently it was shown that a molecule rotating in a quantum solvent can be
described in terms of the “angulon” quasiparticle [M. Lemeshko, Phys. Rev. Lett.
118, 095301 (2017)]. Here we extend the angulon theory to the case of molecules
possessing an additional spin-1/2 degree of freedom and study the behavior of
the system in the presence of a static magnetic field. We show that exchange of
angular momentum between the molecule and the solvent can be altered by the field,
even though the solvent itself is non-magnetic. In particular, we demonstrate
a possibility to control resonant emission of phonons with a given angular momentum
using a magnetic field.
acknowledgement: "We acknowledge insightful discussions with Giacomo Bighin, Igor
Cherepanov, Johan Mentink, and Enderalp Yakaboylu. This work was supported by the
Austrian Science Fund (FWF), Project No. P29902-N27. W.R. was supported by the Polish
Ministry of Science and Higher Education Grant No. MNISW/2016/DIR/285/NN and by
the European Union’s Horizon 2020 research and innovation programme under the Marie
Skłodowska-Curie Grant Agreement No. 665385.\r\n"
article_number: '104307'
article_processing_charge: No
article_type: original
author:
- first_name: Wojciech
full_name: Rzadkowski, Wojciech
id: 48C55298-F248-11E8-B48F-1D18A9856A87
last_name: Rzadkowski
orcid: 0000-0002-1106-4419
- first_name: Mikhail
full_name: Lemeshko, Mikhail
id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
last_name: Lemeshko
orcid: 0000-0002-6990-7802
citation:
ama: Rzadkowski W, Lemeshko M. Effect of a magnetic field on molecule–solvent angular
momentum transfer. The Journal of Chemical Physics. 2018;148(10). doi:10.1063/1.5017591
apa: Rzadkowski, W., & Lemeshko, M. (2018). Effect of a magnetic field on molecule–solvent
angular momentum transfer. The Journal of Chemical Physics. AIP Publishing.
https://doi.org/10.1063/1.5017591
chicago: Rzadkowski, Wojciech, and Mikhail Lemeshko. “Effect of a Magnetic Field
on Molecule–Solvent Angular Momentum Transfer.” The Journal of Chemical Physics.
AIP Publishing, 2018. https://doi.org/10.1063/1.5017591.
ieee: W. Rzadkowski and M. Lemeshko, “Effect of a magnetic field on molecule–solvent
angular momentum transfer,” The Journal of Chemical Physics, vol. 148,
no. 10. AIP Publishing, 2018.
ista: Rzadkowski W, Lemeshko M. 2018. Effect of a magnetic field on molecule–solvent
angular momentum transfer. The Journal of Chemical Physics. 148(10), 104307.
mla: Rzadkowski, Wojciech, and Mikhail Lemeshko. “Effect of a Magnetic Field on
Molecule–Solvent Angular Momentum Transfer.” The Journal of Chemical Physics,
vol. 148, no. 10, 104307, AIP Publishing, 2018, doi:10.1063/1.5017591.
short: W. Rzadkowski, M. Lemeshko, The Journal of Chemical Physics 148 (2018).
date_created: 2018-12-11T11:46:21Z
date_published: 2018-03-14T00:00:00Z
date_updated: 2024-02-28T13:01:59Z
day: '14'
department:
- _id: MiLe
doi: 10.1063/1.5017591
ec_funded: 1
external_id:
arxiv:
- '1711.09904'
isi:
- '000427517200065'
intvolume: ' 148'
isi: 1
issue: '10'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1711.09904
month: '03'
oa: 1
oa_version: Preprint
project:
- _id: 26031614-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P29902
name: Quantum rotations in the presence of a many-body environment
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '665385'
name: International IST Doctoral Program
publication: The Journal of Chemical Physics
publication_status: published
publisher: AIP Publishing
publist_id: '7408'
quality_controlled: '1'
related_material:
record:
- id: '10759'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Effect of a magnetic field on molecule–solvent angular momentum transfer
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 148
year: '2018'
...
---
_id: '134'
abstract:
- lang: eng
text: "The current state of the art in real-time two-dimensional water wave simulation
requires developers to choose between efficient Fourier-based methods, which lack
interactions with moving obstacles, and finite-difference or finite element methods,
which handle environmental interactions but are significantly more expensive.
This paper attempts to bridge this long-standing gap between complexity and performance,
by proposing a new wave simulation method that can faithfully simulate wave interactions
with moving obstacles in real time while simultaneously preserving minute details
and accommodating very large simulation domains.\r\n\r\nPrevious methods for simulating
2D water waves directly compute the change in height of the water surface, a strategy
which imposes limitations based on the CFL condition (fast moving waves require
small time steps) and Nyquist's limit (small wave details require closely-spaced
simulation variables). This paper proposes a novel wavelet transformation that
discretizes the liquid motion in terms of amplitude-like functions that vary over
space, frequency, and direction, effectively generalizing Fourier-based methods
to handle local interactions. Because these new variables change much more slowly
over space than the original water height function, our change of variables drastically
reduces the limitations of the CFL condition and Nyquist limit, allowing us to
simulate highly detailed water waves at very large visual resolutions. Our discretization
is amenable to fast summation and easy to parallelize. We also present basic extensions
like pre-computed wave paths and two-way solid fluid coupling. Finally, we argue
that our discretization provides a convenient set of variables for artistic manipulation,
which we illustrate with a novel wave-painting interface."
acknowledged_ssus:
- _id: ScienComp
alternative_title:
- SIGGRAPH
article_number: '94'
article_processing_charge: No
author:
- first_name: Stefan
full_name: Jeschke, Stefan
id: 44D6411A-F248-11E8-B48F-1D18A9856A87
last_name: Jeschke
- first_name: Tomas
full_name: Skrivan, Tomas
id: 486A5A46-F248-11E8-B48F-1D18A9856A87
last_name: Skrivan
- first_name: Matthias
full_name: Mueller Fischer, Matthias
last_name: Mueller Fischer
- first_name: Nuttapong
full_name: Chentanez, Nuttapong
last_name: Chentanez
- first_name: Miles
full_name: Macklin, Miles
last_name: Macklin
- first_name: Christopher J
full_name: Wojtan, Christopher J
id: 3C61F1D2-F248-11E8-B48F-1D18A9856A87
last_name: Wojtan
orcid: 0000-0001-6646-5546
citation:
ama: Jeschke S, Skrivan T, Mueller Fischer M, Chentanez N, Macklin M, Wojtan C.
Water surface wavelets. ACM Transactions on Graphics. 2018;37(4). doi:10.1145/3197517.3201336
apa: Jeschke, S., Skrivan, T., Mueller Fischer, M., Chentanez, N., Macklin, M.,
& Wojtan, C. (2018). Water surface wavelets. ACM Transactions on Graphics.
ACM. https://doi.org/10.1145/3197517.3201336
chicago: Jeschke, Stefan, Tomas Skrivan, Matthias Mueller Fischer, Nuttapong Chentanez,
Miles Macklin, and Chris Wojtan. “Water Surface Wavelets.” ACM Transactions
on Graphics. ACM, 2018. https://doi.org/10.1145/3197517.3201336.
ieee: S. Jeschke, T. Skrivan, M. Mueller Fischer, N. Chentanez, M. Macklin, and
C. Wojtan, “Water surface wavelets,” ACM Transactions on Graphics, vol.
37, no. 4. ACM, 2018.
ista: Jeschke S, Skrivan T, Mueller Fischer M, Chentanez N, Macklin M, Wojtan C.
2018. Water surface wavelets. ACM Transactions on Graphics. 37(4), 94.
mla: Jeschke, Stefan, et al. “Water Surface Wavelets.” ACM Transactions on Graphics,
vol. 37, no. 4, 94, ACM, 2018, doi:10.1145/3197517.3201336.
short: S. Jeschke, T. Skrivan, M. Mueller Fischer, N. Chentanez, M. Macklin, C.
Wojtan, ACM Transactions on Graphics 37 (2018).
date_created: 2018-12-11T11:44:48Z
date_published: 2018-07-30T00:00:00Z
date_updated: 2024-02-28T13:58:51Z
day: '30'
ddc:
- '000'
department:
- _id: ChWo
doi: 10.1145/3197517.3201336
ec_funded: 1
external_id:
isi:
- '000448185000055'
file:
- access_level: open_access
checksum: db75ebabe2ec432bf41389e614d6ef62
content_type: application/pdf
creator: dernst
date_created: 2018-12-18T09:59:23Z
date_updated: 2020-07-14T12:44:45Z
file_id: '5744'
file_name: 2018_ACM_Jeschke.pdf
file_size: 22185016
relation: main_file
file_date_updated: 2020-07-14T12:44:45Z
has_accepted_license: '1'
intvolume: ' 37'
isi: 1
issue: '4'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-sa/4.0/
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 2533E772-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '638176'
name: Efficient Simulation of Natural Phenomena at Extremely Large Scales
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '665385'
name: International IST Doctoral Program
publication: ACM Transactions on Graphics
publication_status: published
publisher: ACM
publist_id: '7789'
quality_controlled: '1'
related_material:
link:
- description: News on IST Homepage
relation: press_release
url: https://ist.ac.at/en/news/new-water-simulation-captures-small-details-even-in-large-scenes/
scopus_import: '1'
status: public
title: Water surface wavelets
tmp:
image: /images/cc_by_nc_sa.png
legal_code_url: https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode
name: Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC
BY-NC-SA 4.0)
short: CC BY-NC-SA (4.0)
type: journal_article
user_id: 2EBD1598-F248-11E8-B48F-1D18A9856A87
volume: 37
year: '2018'
...
---
_id: '6339'
abstract:
- lang: eng
text: We introduce a diagrammatic Monte Carlo approach to angular momentum properties
of quantum many-particle systems possessing a macroscopic number of degrees of
freedom. The treatment is based on a diagrammatic expansion that merges the usual
Feynman diagrams with the angular momentum diagrams known from atomic and nuclear
structure theory, thereby incorporating the non-Abelian algebra inherent to quantum
rotations. Our approach is applicable at arbitrary coupling, is free of systematic
errors and of finite-size effects, and naturally provides access to the impurity
Green function. We exemplify the technique by obtaining an all-coupling solution
of the angulon model; however, the method is quite general and can be applied
to a broad variety of systems in which particles exchange quantum angular momentum
with their many-body environment.
article_number: '165301'
article_processing_charge: No
author:
- first_name: Giacomo
full_name: Bighin, Giacomo
id: 4CA96FD4-F248-11E8-B48F-1D18A9856A87
last_name: Bighin
orcid: 0000-0001-8823-9777
- first_name: Timur
full_name: Tscherbul, Timur
last_name: Tscherbul
- first_name: Mikhail
full_name: Lemeshko, Mikhail
id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
last_name: Lemeshko
orcid: 0000-0002-6990-7802
citation:
ama: Bighin G, Tscherbul T, Lemeshko M. Diagrammatic Monte Carlo approach to angular
momentum in quantum many-particle systems. Physical Review Letters. 2018;121(16).
doi:10.1103/physrevlett.121.165301
apa: Bighin, G., Tscherbul, T., & Lemeshko, M. (2018). Diagrammatic Monte Carlo
approach to angular momentum in quantum many-particle systems. Physical Review
Letters. American Physical Society. https://doi.org/10.1103/physrevlett.121.165301
chicago: Bighin, Giacomo, Timur Tscherbul, and Mikhail Lemeshko. “Diagrammatic Monte Carlo
Approach to Angular Momentum in Quantum Many-Particle Systems.” Physical Review
Letters. American Physical Society, 2018. https://doi.org/10.1103/physrevlett.121.165301.
ieee: G. Bighin, T. Tscherbul, and M. Lemeshko, “Diagrammatic Monte Carlo approach
to angular momentum in quantum many-particle systems,” Physical Review Letters,
vol. 121, no. 16. American Physical Society, 2018.
ista: Bighin G, Tscherbul T, Lemeshko M. 2018. Diagrammatic Monte Carlo approach
to angular momentum in quantum many-particle systems. Physical Review Letters.
121(16), 165301.
mla: Bighin, Giacomo, et al. “Diagrammatic Monte Carlo Approach to Angular Momentum
in Quantum Many-Particle Systems.” Physical Review Letters, vol. 121, no.
16, 165301, American Physical Society, 2018, doi:10.1103/physrevlett.121.165301.
short: G. Bighin, T. Tscherbul, M. Lemeshko, Physical Review Letters 121 (2018).
date_created: 2019-04-17T10:53:38Z
date_published: 2018-10-16T00:00:00Z
date_updated: 2024-02-28T13:15:09Z
day: '16'
department:
- _id: MiLe
doi: 10.1103/physrevlett.121.165301
external_id:
arxiv:
- '1803.07990'
isi:
- '000447468400008'
intvolume: ' 121'
isi: 1
issue: '16'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1803.07990
month: '10'
oa: 1
oa_version: Preprint
project:
- _id: 26031614-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P29902
name: Quantum rotations in the presence of a many-body environment
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
related_material:
link:
- description: News on IST Homepage
relation: press_release
url: https://ist.ac.at/en/news/description-of-rotating-molecules-made-easy/
scopus_import: '1'
status: public
title: Diagrammatic Monte Carlo approach to angular momentum in quantum many-particle
systems
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 121
year: '2018'
...
---
_id: '417'
abstract:
- lang: eng
text: 'We introduce a Diagrammatic Monte Carlo (DiagMC) approach to complex molecular
impurities with rotational degrees of freedom interacting with a many-particle
environment. The treatment is based on the diagrammatic expansion that merges
the usual Feynman diagrams with the angular momentum diagrams known from atomic
and nuclear structure theory, thereby incorporating the non-Abelian algebra inherent
to quantum rotations. Our approach works at arbitrary coupling, is free of systematic
errors and of finite size effects, and naturally provides access to the impurity
Green function. We exemplify the technique by obtaining an all-coupling solution
of the angulon model, however, the method is quite general and can be applied
to a broad variety of quantum impurities possessing angular momentum degrees of
freedom. '
article_number: '165301'
article_processing_charge: No
author:
- first_name: Giacomo
full_name: Bighin, Giacomo
id: 4CA96FD4-F248-11E8-B48F-1D18A9856A87
last_name: Bighin
orcid: 0000-0001-8823-9777
- first_name: Timur
full_name: Tscherbul, Timur
last_name: Tscherbul
- first_name: Mikhail
full_name: Lemeshko, Mikhail
id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
last_name: Lemeshko
orcid: 0000-0002-6990-7802
citation:
ama: Bighin G, Tscherbul T, Lemeshko M. Diagrammatic Monte Carlo approach to rotating
molecular impurities. Physical Review Letters. 2018;121(16). doi:10.1103/PhysRevLett.121.165301
apa: Bighin, G., Tscherbul, T., & Lemeshko, M. (2018). Diagrammatic Monte Carlo
approach to rotating molecular impurities. Physical Review Letters. American
Physical Society. https://doi.org/10.1103/PhysRevLett.121.165301
chicago: Bighin, Giacomo, Timur Tscherbul, and Mikhail Lemeshko. “Diagrammatic Monte
Carlo Approach to Rotating Molecular Impurities.” Physical Review Letters.
American Physical Society, 2018. https://doi.org/10.1103/PhysRevLett.121.165301.
ieee: G. Bighin, T. Tscherbul, and M. Lemeshko, “Diagrammatic Monte Carlo approach
to rotating molecular impurities,” Physical Review Letters, vol. 121, no.
16. American Physical Society, 2018.
ista: Bighin G, Tscherbul T, Lemeshko M. 2018. Diagrammatic Monte Carlo approach
to rotating molecular impurities. Physical Review Letters. 121(16), 165301.
mla: Bighin, Giacomo, et al. “Diagrammatic Monte Carlo Approach to Rotating Molecular
Impurities.” Physical Review Letters, vol. 121, no. 16, 165301, American
Physical Society, 2018, doi:10.1103/PhysRevLett.121.165301.
short: G. Bighin, T. Tscherbul, M. Lemeshko, Physical Review Letters 121 (2018).
date_created: 2018-12-11T11:46:22Z
date_published: 2018-10-16T00:00:00Z
date_updated: 2024-02-28T13:14:53Z
day: '16'
department:
- _id: MiLe
doi: 10.1103/PhysRevLett.121.165301
external_id:
arxiv:
- '1803.07990'
intvolume: ' 121'
issue: '16'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1803.07990
month: '10'
oa: 1
oa_version: Preprint
project:
- _id: 26031614-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P29902
name: Quantum rotations in the presence of a many-body environment
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '8025'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Diagrammatic Monte Carlo approach to rotating molecular impurities
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 121
year: '2018'
...
---
_id: '6665'
abstract:
- lang: eng
text: We prove that, at least for the binary erasure channel, the polar-coding paradigm
gives rise to codes that not only approach the Shannon limit but, in fact, do
so under the best possible scaling of their block length as a function of the
gap to capacity. This result exhibits the first known family of binary codes that
attain both optimal scaling and quasi-linear complexity of encoding and decoding.
Specifically, for any fixed δ > 0, we exhibit binary linear codes that ensure
reliable communication at rates within ε > 0 of capacity with block length n =
O(1/ε 2+δ ), construction complexity Θ(n), and encoding/decoding complexity Θ(n
log n).
author:
- first_name: Arman
full_name: Fazeli, Arman
last_name: Fazeli
- first_name: Hamed
full_name: Hassani, Hamed
last_name: Hassani
- first_name: Marco
full_name: Mondelli, Marco
id: 27EB676C-8706-11E9-9510-7717E6697425
last_name: Mondelli
orcid: 0000-0002-3242-7020
- first_name: Alexander
full_name: Vardy, Alexander
last_name: Vardy
citation:
ama: 'Fazeli A, Hassani H, Mondelli M, Vardy A. Binary linear codes with optimal
scaling: Polar codes with large kernels. In: 2018 IEEE Information Theory Workshop.
IEEE; 2018:1-5. doi:10.1109/itw.2018.8613428'
apa: 'Fazeli, A., Hassani, H., Mondelli, M., & Vardy, A. (2018). Binary linear
codes with optimal scaling: Polar codes with large kernels. In 2018 IEEE Information
Theory Workshop (pp. 1–5). Guangzhou, China: IEEE. https://doi.org/10.1109/itw.2018.8613428'
chicago: 'Fazeli, Arman, Hamed Hassani, Marco Mondelli, and Alexander Vardy. “Binary
Linear Codes with Optimal Scaling: Polar Codes with Large Kernels.” In 2018
IEEE Information Theory Workshop, 1–5. IEEE, 2018. https://doi.org/10.1109/itw.2018.8613428.'
ieee: 'A. Fazeli, H. Hassani, M. Mondelli, and A. Vardy, “Binary linear codes with
optimal scaling: Polar codes with large kernels,” in 2018 IEEE Information
Theory Workshop, Guangzhou, China, 2018, pp. 1–5.'
ista: 'Fazeli A, Hassani H, Mondelli M, Vardy A. 2018. Binary linear codes with
optimal scaling: Polar codes with large kernels. 2018 IEEE Information Theory
Workshop. ITW: Information Theory Workshop, 1–5.'
mla: 'Fazeli, Arman, et al. “Binary Linear Codes with Optimal Scaling: Polar Codes
with Large Kernels.” 2018 IEEE Information Theory Workshop, IEEE, 2018,
pp. 1–5, doi:10.1109/itw.2018.8613428.'
short: A. Fazeli, H. Hassani, M. Mondelli, A. Vardy, in:, 2018 IEEE Information
Theory Workshop, IEEE, 2018, pp. 1–5.
conference:
end_date: 2018-11-29
location: Guangzhou, China
name: 'ITW: Information Theory Workshop'
start_date: 2018-11-25
date_created: 2019-07-23T11:01:42Z
date_published: 2018-11-01T00:00:00Z
date_updated: 2024-03-07T12:18:50Z
day: '01'
doi: 10.1109/itw.2018.8613428
extern: '1'
external_id:
arxiv:
- '1711.01339'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1711.01339
month: '11'
oa: 1
oa_version: Preprint
page: 1-5
publication: 2018 IEEE Information Theory Workshop
publication_status: published
publisher: IEEE
quality_controlled: '1'
related_material:
record:
- id: '9002'
relation: later_version
status: public
status: public
title: 'Binary linear codes with optimal scaling: Polar codes with large kernels'
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '15143'
abstract:
- lang: eng
text: To maintain genome integrity, segmented double-stranded RNA viruses of the
Reoviridae family must accurately select and package a complete set of up to a
dozen distinct genomic RNAs. It is thought that the high fidelity segmented genome
assembly involves multiple sequence-specific RNA–RNA interactions between single-stranded
RNA segment precursors. These are mediated by virus-encoded non-structural proteins
with RNA chaperone-like activities, such as rotavirus (RV) NSP2 and avian reovirus
σNS. Here, we compared the abilities of NSP2 and σNS to mediate sequence-specific
interactions between RV genomic segment precursors. Despite their similar activities,
NSP2 successfully promotes inter-segment association, while σNS fails to do so.
To understand the mechanisms underlying such selectivity in promoting inter-molecular
duplex formation, we compared RNA-binding and helix-unwinding activities of both
proteins. We demonstrate that octameric NSP2 binds structured RNAs with high affinity,
resulting in efficient intramolecular RNA helix disruption. Hexameric σNS oligomerizes
into an octamer that binds two RNAs, yet it exhibits only limited RNA-unwinding
activity compared to NSP2. Thus, the formation of intersegment RNA–RNA interactions
is governed by both helix-unwinding capacity of the chaperones and stability of
RNA structure. We propose that this protein-mediated RNA selection mechanism may
underpin the high fidelity assembly of multi-segmented RNA genomes in Reoviridae.
article_processing_charge: Yes
article_type: original
author:
- first_name: Jack Peter Kelly
full_name: Bravo, Jack Peter Kelly
id: 96aecfa5-8931-11ee-af30-aa6a5d6eee0e
last_name: Bravo
orcid: 0000-0003-0456-0753
- first_name: Alexander
full_name: Borodavka, Alexander
last_name: Borodavka
- first_name: Anders
full_name: Barth, Anders
last_name: Barth
- first_name: Antonio N
full_name: Calabrese, Antonio N
last_name: Calabrese
- first_name: Peter
full_name: Mojzes, Peter
last_name: Mojzes
- first_name: Joseph J B
full_name: Cockburn, Joseph J B
last_name: Cockburn
- first_name: Don C
full_name: Lamb, Don C
last_name: Lamb
- first_name: Roman
full_name: Tuma, Roman
last_name: Tuma
citation:
ama: Bravo JPK, Borodavka A, Barth A, et al. Stability of local secondary structure
determines selectivity of viral RNA chaperones. Nucleic Acids Research.
2018;46(15):7924-7937. doi:10.1093/nar/gky394
apa: Bravo, J. P. K., Borodavka, A., Barth, A., Calabrese, A. N., Mojzes, P., Cockburn,
J. J. B., … Tuma, R. (2018). Stability of local secondary structure determines
selectivity of viral RNA chaperones. Nucleic Acids Research. Oxford University
Press. https://doi.org/10.1093/nar/gky394
chicago: Bravo, Jack Peter Kelly, Alexander Borodavka, Anders Barth, Antonio N Calabrese,
Peter Mojzes, Joseph J B Cockburn, Don C Lamb, and Roman Tuma. “Stability of Local
Secondary Structure Determines Selectivity of Viral RNA Chaperones.” Nucleic
Acids Research. Oxford University Press, 2018. https://doi.org/10.1093/nar/gky394.
ieee: J. P. K. Bravo et al., “Stability of local secondary structure determines
selectivity of viral RNA chaperones,” Nucleic Acids Research, vol. 46,
no. 15. Oxford University Press, pp. 7924–7937, 2018.
ista: Bravo JPK, Borodavka A, Barth A, Calabrese AN, Mojzes P, Cockburn JJB, Lamb
DC, Tuma R. 2018. Stability of local secondary structure determines selectivity
of viral RNA chaperones. Nucleic Acids Research. 46(15), 7924–7937.
mla: Bravo, Jack Peter Kelly, et al. “Stability of Local Secondary Structure Determines
Selectivity of Viral RNA Chaperones.” Nucleic Acids Research, vol. 46,
no. 15, Oxford University Press, 2018, pp. 7924–37, doi:10.1093/nar/gky394.
short: J.P.K. Bravo, A. Borodavka, A. Barth, A.N. Calabrese, P. Mojzes, J.J.B. Cockburn,
D.C. Lamb, R. Tuma, Nucleic Acids Research 46 (2018) 7924–7937.
date_created: 2024-03-20T10:43:13Z
date_published: 2018-09-06T00:00:00Z
date_updated: 2024-03-20T11:10:56Z
day: '06'
doi: 10.1093/nar/gky394
extern: '1'
external_id:
pmid:
- '29796667'
intvolume: ' 46'
issue: '15'
keyword:
- Genetics
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1093/nar/gky394
month: '09'
oa: 1
oa_version: Published Version
page: 7924-7937
pmid: 1
publication: Nucleic Acids Research
publication_identifier:
eissn:
- 1362-4962
issn:
- 0305-1048
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Stability of local secondary structure determines selectivity of viral RNA
chaperones
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 46
year: '2018'
...
---
_id: '412'
abstract:
- lang: eng
text: Clathrin-mediated endocytosis (CME) is a cellular trafficking process in which
cargoes and lipids are internalized from the plasma membrane into vesicles coated
with clathrin and adaptor proteins. CME is essential for many developmental and
physiological processes in plants, but its underlying mechanism is not well characterised
compared to that in yeast and animal systems. Here, we searched for new factors
involved in CME in Arabidopsis thaliana by performing Tandem Affinity Purification
of proteins that interact with clathrin light chain, a principal component of
the clathrin coat. Among the confirmed interactors, we found two putative homologues
of the clathrin-coat uncoating factor auxilin previously described in non-plant
systems. Overexpression of AUXILIN-LIKE1 and AUXILIN-LIKE2 in A. thaliana caused
an arrest of seedling growth and development. This was concomitant with inhibited
endocytosis due to blocking of clathrin recruitment after the initial step of
adaptor protein binding to the plasma membrane. By contrast, auxilin-like(1/2)
loss-of-function lines did not present endocytosis-related developmental or cellular
phenotypes under normal growth conditions. This work contributes to the on-going
characterization of the endocytotic machinery in plants and provides a robust
tool for conditionally and specifically interfering with CME in A. thaliana.
acknowledgement: We thank James Matthew Watson, Monika Borowska, and Peggy Stolt-Bergner
at ProTech Facility of the Vienna Biocenter Core Facilities for the CRISPR/CAS9
construct; Anna Müller for assistance with molecular cloning; Sebastian Bednarek,
Liwen Jiang, and Daniël Van Damme for sharing published material; Matyáš Fendrych,
Daniël Van Damme, and Lindy Abas for valuable discussions; and Martine De Cock for
help with correcting the manuscript. This work was supported by the European Research
Council under the European Union Seventh Framework Programme (FP7/2007-2013)/ERC
Grant 282300 and by the Ministry of Education of the Czech Republic/MŠMT project
NPUI-LO1417.
article_processing_charge: No
article_type: original
author:
- first_name: Maciek
full_name: Adamowski, Maciek
id: 45F536D2-F248-11E8-B48F-1D18A9856A87
last_name: Adamowski
orcid: 0000-0001-6463-5257
- first_name: Madhumitha
full_name: Narasimhan, Madhumitha
id: 44BF24D0-F248-11E8-B48F-1D18A9856A87
last_name: Narasimhan
orcid: 0000-0002-8600-0671
- first_name: Urszula
full_name: Kania, Urszula
id: 4AE5C486-F248-11E8-B48F-1D18A9856A87
last_name: Kania
- first_name: Matous
full_name: Glanc, Matous
id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2
last_name: Glanc
orcid: 0000-0003-0619-7783
- first_name: Geert
full_name: De Jaeger, Geert
last_name: De Jaeger
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
citation:
ama: Adamowski M, Narasimhan M, Kania U, Glanc M, De Jaeger G, Friml J. A functional
study of AUXILIN LIKE1 and 2 two putative clathrin uncoating factors in Arabidopsis.
The Plant Cell. 2018;30(3):700-716. doi:10.1105/tpc.17.00785
apa: Adamowski, M., Narasimhan, M., Kania, U., Glanc, M., De Jaeger, G., & Friml,
J. (2018). A functional study of AUXILIN LIKE1 and 2 two putative clathrin uncoating
factors in Arabidopsis. The Plant Cell. American Society of Plant Biologists.
https://doi.org/10.1105/tpc.17.00785
chicago: Adamowski, Maciek, Madhumitha Narasimhan, Urszula Kania, Matous Glanc,
Geert De Jaeger, and Jiří Friml. “A Functional Study of AUXILIN LIKE1 and 2 Two
Putative Clathrin Uncoating Factors in Arabidopsis.” The Plant Cell. American
Society of Plant Biologists, 2018. https://doi.org/10.1105/tpc.17.00785.
ieee: M. Adamowski, M. Narasimhan, U. Kania, M. Glanc, G. De Jaeger, and J. Friml,
“A functional study of AUXILIN LIKE1 and 2 two putative clathrin uncoating factors
in Arabidopsis,” The Plant Cell, vol. 30, no. 3. American Society of Plant
Biologists, pp. 700–716, 2018.
ista: Adamowski M, Narasimhan M, Kania U, Glanc M, De Jaeger G, Friml J. 2018. A
functional study of AUXILIN LIKE1 and 2 two putative clathrin uncoating factors
in Arabidopsis. The Plant Cell. 30(3), 700–716.
mla: Adamowski, Maciek, et al. “A Functional Study of AUXILIN LIKE1 and 2 Two Putative
Clathrin Uncoating Factors in Arabidopsis.” The Plant Cell, vol. 30, no.
3, American Society of Plant Biologists, 2018, pp. 700–16, doi:10.1105/tpc.17.00785.
short: M. Adamowski, M. Narasimhan, U. Kania, M. Glanc, G. De Jaeger, J. Friml,
The Plant Cell 30 (2018) 700–716.
date_created: 2018-12-11T11:46:20Z
date_published: 2018-04-09T00:00:00Z
date_updated: 2024-03-28T23:30:06Z
day: '09'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1105/tpc.17.00785
ec_funded: 1
external_id:
isi:
- '000429441400018'
pmid:
- '29511054'
file:
- access_level: open_access
checksum: 4e165e653b67d3f0684697f21aace5a1
content_type: application/pdf
creator: dernst
date_created: 2022-05-23T09:12:38Z
date_updated: 2022-05-23T09:12:38Z
file_id: '11406'
file_name: 2018_PlantCell_Adamowski.pdf
file_size: 4407538
relation: main_file
success: 1
file_date_updated: 2022-05-23T09:12:38Z
has_accepted_license: '1'
intvolume: ' 30'
isi: 1
issue: '3'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 700 - 716
pmid: 1
project:
- _id: 25716A02-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '282300'
name: Polarity and subcellular dynamics in plants
publication: The Plant Cell
publication_identifier:
eissn:
- 1532-298X
issn:
- 1040-4651
publication_status: published
publisher: American Society of Plant Biologists
publist_id: '7417'
quality_controlled: '1'
related_material:
record:
- id: '6269'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: A functional study of AUXILIN LIKE1 and 2 two putative clathrin uncoating factors
in Arabidopsis
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 30
year: '2018'
...
---
_id: '5914'
abstract:
- lang: eng
text: With the advent of optogenetics, it became possible to change the activity
of a targeted population of neurons in a temporally controlled manner. To combine
the advantages of 60-channel in vivo tetrode recording and laser-based optogenetics,
we have developed a closed-loop recording system that allows for the actual electrophysiological
signal to be used as a trigger for the laser light mediating the optogenetic intervention.
We have optimized the weight, size, and shape of the corresponding implant to
make it compatible with the size, force, and movements of a behaving mouse, and
we have shown that the system can efficiently block sharp wave ripple (SWR) events
using those events themselves as a trigger. To demonstrate the full potential
of the optogenetic recording system we present a pilot study addressing the contribution
of SWR events to learning in a complex behavioral task.
article_number: e0087
article_processing_charge: No
author:
- first_name: Dámaris K
full_name: Rangel Guerrero, Dámaris K
id: 4871BCE6-F248-11E8-B48F-1D18A9856A87
last_name: Rangel Guerrero
orcid: 0000-0002-8602-4374
- first_name: James G.
full_name: Donnett, James G.
last_name: Donnett
- first_name: Jozsef L
full_name: Csicsvari, Jozsef L
id: 3FA14672-F248-11E8-B48F-1D18A9856A87
last_name: Csicsvari
orcid: 0000-0002-5193-4036
- first_name: Krisztián
full_name: Kovács, Krisztián
id: 2AB5821E-F248-11E8-B48F-1D18A9856A87
last_name: Kovács
orcid: 0000-0001-6251-1007
citation:
ama: 'Rangel Guerrero DK, Donnett JG, Csicsvari JL, Kovács K. Tetrode recording
from the hippocampus of behaving mice coupled with four-point-irradiation closed-loop
optogenetics: A technique to study the contribution of Hippocampal SWR events
to learning. eNeuro. 2018;5(4). doi:10.1523/ENEURO.0087-18.2018'
apa: 'Rangel Guerrero, D. K., Donnett, J. G., Csicsvari, J. L., & Kovács, K.
(2018). Tetrode recording from the hippocampus of behaving mice coupled with four-point-irradiation
closed-loop optogenetics: A technique to study the contribution of Hippocampal
SWR events to learning. ENeuro. Society of Neuroscience. https://doi.org/10.1523/ENEURO.0087-18.2018'
chicago: 'Rangel Guerrero, Dámaris K, James G. Donnett, Jozsef L Csicsvari, and
Krisztián Kovács. “Tetrode Recording from the Hippocampus of Behaving Mice Coupled
with Four-Point-Irradiation Closed-Loop Optogenetics: A Technique to Study the
Contribution of Hippocampal SWR Events to Learning.” ENeuro. Society of
Neuroscience, 2018. https://doi.org/10.1523/ENEURO.0087-18.2018.'
ieee: 'D. K. Rangel Guerrero, J. G. Donnett, J. L. Csicsvari, and K. Kovács, “Tetrode
recording from the hippocampus of behaving mice coupled with four-point-irradiation
closed-loop optogenetics: A technique to study the contribution of Hippocampal
SWR events to learning,” eNeuro, vol. 5, no. 4. Society of Neuroscience,
2018.'
ista: 'Rangel Guerrero DK, Donnett JG, Csicsvari JL, Kovács K. 2018. Tetrode recording
from the hippocampus of behaving mice coupled with four-point-irradiation closed-loop
optogenetics: A technique to study the contribution of Hippocampal SWR events
to learning. eNeuro. 5(4), e0087.'
mla: 'Rangel Guerrero, Dámaris K., et al. “Tetrode Recording from the Hippocampus
of Behaving Mice Coupled with Four-Point-Irradiation Closed-Loop Optogenetics:
A Technique to Study the Contribution of Hippocampal SWR Events to Learning.”
ENeuro, vol. 5, no. 4, e0087, Society of Neuroscience, 2018, doi:10.1523/ENEURO.0087-18.2018.'
short: D.K. Rangel Guerrero, J.G. Donnett, J.L. Csicsvari, K. Kovács, ENeuro 5 (2018).
date_created: 2019-02-03T22:59:16Z
date_published: 2018-07-27T00:00:00Z
date_updated: 2024-03-28T23:30:10Z
day: '27'
ddc:
- '570'
department:
- _id: JoCs
doi: 10.1523/ENEURO.0087-18.2018
ec_funded: 1
external_id:
isi:
- '000443994700007'
file:
- access_level: open_access
checksum: f4915d45fc7ad4648b7b7a13fdecca01
content_type: application/pdf
creator: dernst
date_created: 2019-02-05T12:48:36Z
date_updated: 2020-07-14T12:47:13Z
file_id: '5921'
file_name: 2018_ENeuro_Guerrero.pdf
file_size: 3746884
relation: main_file
file_date_updated: 2020-07-14T12:47:13Z
has_accepted_license: '1'
intvolume: ' 5'
isi: 1
issue: '4'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
- _id: 257D4372-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: I2072-B27
name: Interneuron plasticity during spatial learning
publication: eNeuro
publication_status: published
publisher: Society of Neuroscience
quality_controlled: '1'
related_material:
record:
- id: '6849'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: 'Tetrode recording from the hippocampus of behaving mice coupled with four-point-irradiation
closed-loop optogenetics: A technique to study the contribution of Hippocampal SWR
events to learning'
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 5
year: '2018'
...
---
_id: '402'
abstract:
- lang: eng
text: During metastasis, malignant cells escape the primary tumor, intravasate lymphatic
vessels, and reach draining sentinel lymph nodes before they colonize distant
organs via the blood circulation. Although lymph node metastasis in cancer patients
correlates with poor prognosis, evidence is lacking as to whether and how tumor
cells enter the bloodstream via lymph nodes. To investigate this question, we
delivered carcinoma cells into the lymph nodes of mice by microinfusing the cells
into afferent lymphatic vessels. We found that tumor cells rapidly infiltrated
the lymph node parenchyma, invaded blood vessels, and seeded lung metastases without
involvement of the thoracic duct. These results suggest that the lymph node blood
vessels can serve as an exit route for systemic dissemination of cancer cells
in experimental mouse models. Whether this form of tumor cell spreading occurs
in cancer patients remains to be determined.
acknowledged_ssus:
- _id: Bio
acknowledgement: "M.B. was supported by the Cell Communication in Health and Disease
graduate study program of the Austrian Science Fund (FWF) and the Medical University
of Vienna. M.S. was supported by the European Research Council (grant ERC GA 281556)
and an FWF START award.\r\nWe thank C. Moussion for establishing the intralymphatic
injection at IST Austria and for providing anti-PNAd hybridoma supernatant, R. Förster
and A. Braun for sharing the intralymphatic injection technology, K. Vaahtomeri
for the lentiviral constructs, M. Hons for establishing in vivo multiphoton imaging,
the Sixt lab for intellectual input, M. Schunn for help with the design of the in
vivo experiments, F. Langer for technical assistance with the in vivo experiments,
the bioimaging facility of IST Austria for support, and R. Efferl for providing
the CT26 cell line."
article_processing_charge: No
article_type: original
author:
- first_name: Markus
full_name: Brown, Markus
id: 3DAB9AFC-F248-11E8-B48F-1D18A9856A87
last_name: Brown
- first_name: Frank P
full_name: Assen, Frank P
id: 3A8E7F24-F248-11E8-B48F-1D18A9856A87
last_name: Assen
orcid: 0000-0003-3470-6119
- first_name: Alexander F
full_name: Leithner, Alexander F
id: 3B1B77E4-F248-11E8-B48F-1D18A9856A87
last_name: Leithner
orcid: 0000-0002-1073-744X
- first_name: Jun
full_name: Abe, Jun
last_name: Abe
- first_name: Helga
full_name: Schachner, Helga
last_name: Schachner
- first_name: Gabriele
full_name: Asfour, Gabriele
last_name: Asfour
- first_name: Zsuzsanna
full_name: Bagó Horváth, Zsuzsanna
last_name: Bagó Horváth
- first_name: Jens
full_name: Stein, Jens
last_name: Stein
- first_name: Pavel
full_name: Uhrin, Pavel
last_name: Uhrin
- first_name: Michael K
full_name: Sixt, Michael K
id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
last_name: Sixt
orcid: 0000-0002-6620-9179
- first_name: Dontscho
full_name: Kerjaschki, Dontscho
last_name: Kerjaschki
citation:
ama: Brown M, Assen FP, Leithner AF, et al. Lymph node blood vessels provide exit
routes for metastatic tumor cell dissemination in mice. Science. 2018;359(6382):1408-1411.
doi:10.1126/science.aal3662
apa: Brown, M., Assen, F. P., Leithner, A. F., Abe, J., Schachner, H., Asfour, G.,
… Kerjaschki, D. (2018). Lymph node blood vessels provide exit routes for metastatic
tumor cell dissemination in mice. Science. American Association for the
Advancement of Science. https://doi.org/10.1126/science.aal3662
chicago: Brown, Markus, Frank P Assen, Alexander F Leithner, Jun Abe, Helga Schachner,
Gabriele Asfour, Zsuzsanna Bagó Horváth, et al. “Lymph Node Blood Vessels Provide
Exit Routes for Metastatic Tumor Cell Dissemination in Mice.” Science.
American Association for the Advancement of Science, 2018. https://doi.org/10.1126/science.aal3662.
ieee: M. Brown et al., “Lymph node blood vessels provide exit routes for
metastatic tumor cell dissemination in mice,” Science, vol. 359, no. 6382.
American Association for the Advancement of Science, pp. 1408–1411, 2018.
ista: Brown M, Assen FP, Leithner AF, Abe J, Schachner H, Asfour G, Bagó Horváth
Z, Stein J, Uhrin P, Sixt MK, Kerjaschki D. 2018. Lymph node blood vessels provide
exit routes for metastatic tumor cell dissemination in mice. Science. 359(6382),
1408–1411.
mla: Brown, Markus, et al. “Lymph Node Blood Vessels Provide Exit Routes for Metastatic
Tumor Cell Dissemination in Mice.” Science, vol. 359, no. 6382, American
Association for the Advancement of Science, 2018, pp. 1408–11, doi:10.1126/science.aal3662.
short: M. Brown, F.P. Assen, A.F. Leithner, J. Abe, H. Schachner, G. Asfour, Z.
Bagó Horváth, J. Stein, P. Uhrin, M.K. Sixt, D. Kerjaschki, Science 359 (2018)
1408–1411.
date_created: 2018-12-11T11:46:16Z
date_published: 2018-03-23T00:00:00Z
date_updated: 2024-03-28T23:30:09Z
day: '23'
department:
- _id: MiSi
doi: 10.1126/science.aal3662
ec_funded: 1
external_id:
isi:
- '000428043600047'
pmid:
- '29567714'
intvolume: ' 359'
isi: 1
issue: '6382'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1126/science.aal3662
month: '03'
oa: 1
oa_version: Published Version
page: 1408 - 1411
pmid: 1
project:
- _id: 25A8E5EA-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: Y 564-B12
name: Cytoskeletal force generation and transduction of leukocytes (FWF)
- _id: 25A603A2-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '281556'
name: Cytoskeletal force generation and force transduction of migrating leukocytes
(EU)
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '7428'
quality_controlled: '1'
related_material:
record:
- id: '6947'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Lymph node blood vessels provide exit routes for metastatic tumor cell dissemination
in mice
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 359
year: '2018'
...
---
_id: '395'
abstract:
- lang: eng
text: 'Autism spectrum disorders (ASD) are a group of genetic disorders often overlapping
with other neurological conditions. Despite the remarkable number of scientific
breakthroughs of the last 100 years, the treatment of neurodevelopmental disorders
(e.g. autism spectrum disorder, intellectual disability, epilepsy) remains a great
challenge. Recent advancements in geno mics, like whole-exome or whole-genome
sequencing, have enabled scientists to identify numerous mutations underlying
neurodevelopmental disorders. Given the few hundred risk genes that were discovered,
the etiological variability and the heterogeneous phenotypic outcomes, the need
for genotype -along with phenotype- based diagnosis of individual patients becomes
a requisite. Driven by this rationale, in a previous study our group described
mutations, identified via whole - exome sequencing, in the gene BCKDK – encoding
for a key regulator of branched chain amin o acid (BCAA) catabolism - as a cause
of ASD. Following up on the role of BCAAs, in the study described here we show
that the solute carrier transporter 7a5 (SLC7A5), a large neutral amino acid transporter
localized mainly at the blood brain barrier (BBB), has an essential role in maintaining
normal levels of brain BCAAs. In mice, deletion of Slc7a5 from the endothelial
cells of the BBB leads to atypical brain amino acid profile, abnormal mRNA translation
and severe neurolo gical abnormalities. Additionally, deletion of Slc7a5 from
the neural progenitor cell population leads to microcephaly. Interestingly, we
demonstrate that BCAA intracerebroventricular administration ameliorates abnormal
behaviors in adult mutant mice. Furthermore, whole - exome sequencing of patients
diagnosed with neurological dis o r ders helped us identify several patients with
autistic traits, microcephaly and motor delay carrying deleterious homozygous
mutations in the SLC7A5 gene. In conclusion, our data elucidate a neurological
syndrome defined by SLC7A5 mutations and support an essential role for t he BCAA
s in human bra in function. Together with r ecent studies (described in chapter
two) that have successfully made the transition into clinical practice, our findings
on the role of B CAAs might have a crucial impact on the development of novel
individualized therapeutic strategies for ASD. '
acknowledged_ssus:
- _id: PreCl
- _id: EM-Fac
- _id: Bio
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Dora-Clara
full_name: Tarlungeanu, Dora-Clara
id: 2ABCE612-F248-11E8-B48F-1D18A9856A87
last_name: Tarlungeanu
citation:
ama: Tarlungeanu D-C. The branched chain amino acids in autism spectrum disorders
. 2018. doi:10.15479/AT:ISTA:th_992
apa: Tarlungeanu, D.-C. (2018). The branched chain amino acids in autism spectrum
disorders . Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:th_992
chicago: Tarlungeanu, Dora-Clara. “The Branched Chain Amino Acids in Autism Spectrum
Disorders .” Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:th_992.
ieee: D.-C. Tarlungeanu, “The branched chain amino acids in autism spectrum disorders
,” Institute of Science and Technology Austria, 2018.
ista: Tarlungeanu D-C. 2018. The branched chain amino acids in autism spectrum disorders
. Institute of Science and Technology Austria.
mla: Tarlungeanu, Dora-Clara. The Branched Chain Amino Acids in Autism Spectrum
Disorders . Institute of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:th_992.
short: D.-C. Tarlungeanu, The Branched Chain Amino Acids in Autism Spectrum Disorders
, Institute of Science and Technology Austria, 2018.
date_created: 2018-12-11T11:46:14Z
date_published: 2018-03-01T00:00:00Z
date_updated: 2023-09-07T12:38:59Z
day: '01'
ddc:
- '570'
- '616'
degree_awarded: PhD
department:
- _id: GaNo
doi: 10.15479/AT:ISTA:th_992
file:
- access_level: closed
checksum: 9f5231c96e0ad945040841a8630232da
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-04-05T09:19:17Z
date_updated: 2021-02-11T23:30:15Z
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file_name: 2018_Thesis_Tarlungeanu_source.docx
file_size: 43684035
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checksum: 0c33c370aa2010df5c552db57a6d01e9
content_type: application/pdf
creator: dernst
date_created: 2019-04-05T09:19:17Z
date_updated: 2021-02-11T11:17:16Z
embargo: 2018-03-15
file_id: '6218'
file_name: 2018_Thesis_Tarlungeanu.pdf
file_size: 30511532
relation: main_file
file_date_updated: 2021-02-11T23:30:15Z
has_accepted_license: '1'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: '88'
project:
- _id: 25473368-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: F03523
name: Transmembrane Transporters in Health and Disease
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '7434'
pubrep_id: '992'
related_material:
record:
- id: '1183'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Gaia
full_name: Novarino, Gaia
id: 3E57A680-F248-11E8-B48F-1D18A9856A87
last_name: Novarino
orcid: 0000-0002-7673-7178
title: 'The branched chain amino acids in autism spectrum disorders '
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '51'
abstract:
- lang: eng
text: Asymmetries have long been known about in the central nervous system. From
gross anatomical differences, such as the presence of the parapineal organ in
only one hemisphere of the developing zebrafish, to more subtle differences in
activity between both hemispheres, as seen in freely roaming animals or human
participants under PET and fMRI imaging analysis. The presence of asymmetries
has been demonstrated to have huge behavioural implications, with their disruption
often leading to the generation of neurological disorders, memory problems, changes
in personality, and in an organism's health and well-being. For my Ph.D. work
I aimed to tackle two important avenues of research. The first being the process
of input-side dependency in the hippocampus, with the goal of finding a key gene
responsible for its development (Gene X). The second project was to do with experience-induced
laterality formation in the hippocampus. Specifically, how laterality in the synapse
density of the CA1 stratum radiatum (s.r.) could be induced purely through environmental
enrichment. Through unilateral tracer injections into the CA3, I was able to selectively
measure the properties of synapses within the CA1 and investigate how they differed
based upon which hemisphere the presynaptic neurone originated. Having found the
existence of a previously unreported reversed (left-isomerism) i.v. mutant, through
morpholocal examination of labelled terminals in the CA1 s.r., I aimed to elucidate
a key gene responsible for the process of left or right determination of inputs
to the CA1 s.r.. This work relates to the previous finding of input-side dependent
asymmetry in the wild-type rodent, where the origin of the projecting neurone
to the CA1 will determine the morphology of a synapse, to a greater degree than
the hemisphere in which the projection terminates. Using left- and right-isomerism
i.v. mice, in combination with whole genome sequence analysis, I highlight Ena/VASP-like
(Evl) as a potential target for Gene X. In relation to this topic, I also highlight
my work in the recently published paper of how knockout of PirB can lead to a
lack of input-side dependency in the murine hippocampus. For the second question,
I show that the environmental enrichment paradigm will lead to an asymmetry in
the synapse densities in the hippocampus of mice. I also highlight that the nature
of the enrichment is of less consequence than the process of enrichment itself.
I demonstrate that the CA3 region will dramatically alter its projection targets,
in relation to environmental stimulation, with the asymmetry in synaptic density,
caused by enrichment, relying heavily on commissural fibres. I also highlight
the vital importance of input-side dependent asymmetry, as a necessary component
of experience-dependent laterality formation in the CA1 s.r.. However, my results
suggest that it isn't the only cause, as there appears to be a CA1 dependent mechanism
also at play. Upon further investigation, I highlight the significant, and highly
important, finding that the changes seen in the CA1 s.r. were predominantly caused
through projections from the left-CA3, with the right-CA3 having less involvement
in this mechanism.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Matthew J
full_name: Case, Matthew J
id: 44B7CA5A-F248-11E8-B48F-1D18A9856A87
last_name: Case
citation:
ama: 'Case MJ. From the left to the right: A tale of asymmetries, environments,
and hippocampal development. 2018. doi:10.15479/AT:ISTA:th_1032'
apa: 'Case, M. J. (2018). From the left to the right: A tale of asymmetries,
environments, and hippocampal development. Institute of Science and Technology
Austria. https://doi.org/10.15479/AT:ISTA:th_1032'
chicago: 'Case, Matthew J. “From the Left to the Right: A Tale of Asymmetries, Environments,
and Hippocampal Development.” Institute of Science and Technology Austria, 2018.
https://doi.org/10.15479/AT:ISTA:th_1032.'
ieee: 'M. J. Case, “From the left to the right: A tale of asymmetries, environments,
and hippocampal development,” Institute of Science and Technology Austria, 2018.'
ista: 'Case MJ. 2018. From the left to the right: A tale of asymmetries, environments,
and hippocampal development. Institute of Science and Technology Austria.'
mla: 'Case, Matthew J. From the Left to the Right: A Tale of Asymmetries, Environments,
and Hippocampal Development. Institute of Science and Technology Austria,
2018, doi:10.15479/AT:ISTA:th_1032.'
short: 'M.J. Case, From the Left to the Right: A Tale of Asymmetries, Environments,
and Hippocampal Development, Institute of Science and Technology Austria, 2018.'
date_created: 2018-12-11T11:44:22Z
date_published: 2018-06-27T00:00:00Z
date_updated: 2023-09-07T12:39:22Z
day: '27'
ddc:
- '571'
- '576'
degree_awarded: PhD
department:
- _id: RySh
doi: 10.15479/AT:ISTA:th_1032
file:
- access_level: closed
checksum: dcc7b55619d8509dd62b8e99d6cdee44
content_type: application/msword
creator: dernst
date_created: 2019-04-09T07:16:26Z
date_updated: 2021-02-11T23:30:13Z
embargo_to: open_access
file_id: '6251'
file_name: 2018_Thesis_Case_Source.doc
file_size: 141270528
relation: source_file
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checksum: f69fdd5c8709c4e618aa8c1a1221153d
content_type: application/pdf
creator: dernst
date_created: 2019-04-09T07:16:23Z
date_updated: 2021-02-11T11:17:14Z
embargo: 2019-07-05
file_id: '6252'
file_name: 2018_Thesis_Case.pdf
file_size: 15193621
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file_date_updated: 2021-02-11T23:30:13Z
has_accepted_license: '1'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
page: '186'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '8003'
pubrep_id: '1032'
related_material:
record:
- id: '682'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Ryuichi
full_name: Shigemoto, Ryuichi
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
title: 'From the left to the right: A tale of asymmetries, environments, and hippocampal
development'
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '10'
abstract:
- lang: eng
text: Genomic imprinting is an epigenetic process that leads to parent of origin-specific
gene expression in a subset of genes. Imprinted genes are essential for brain
development, and deregulation of imprinting is associated with neurodevelopmental
diseases and the pathogenesis of psychiatric disorders. However, the cell-type
specificity of imprinting at single cell resolution, and how imprinting and thus
gene dosage regulates neuronal circuit assembly is still largely unknown. Here,
MADM (Mosaic Analysis with Double Markers) technology was employed to assess genomic
imprinting at single cell level. By visualizing MADM-induced uniparental disomies
(UPDs) in distinct colors at single cell level in genetic mosaic animals, this
experimental paradigm provides a unique quantitative platform to systematically
assay the UPD-mediated imbalances in imprinted gene expression at unprecedented
resolution. An experimental pipeline based on FACS, RNA-seq and bioinformatics
analysis was established and applied to systematically map cell-type-specific
‘imprintomes’ in the mouse brain. The results revealed that parental-specific
expression of imprinted genes per se is rarely cell-type-specific even at the
individual cell level. Conversely, when we extended the comparison to downstream
responses resulting from imbalanced imprinted gene expression, we discovered an
unexpectedly high degree of cell-type specificity. Furthermore, we determined
a novel function of genomic imprinting in cortical astrocyte production and in
olfactory bulb (OB) granule cell generation. These results suggest important functional
implication of genomic imprinting for generating cell-type diversity in the brain.
In addition, MADM provides a powerful tool to study candidate genes by concomitant
genetic manipulation and fluorescent labelling of single cells. MADM-based candidate
gene approach was utilized to identify potential imprinted genes involved in the
generation of cortical astrocytes and OB granule cells. We investigated p57Kip2,
a maternally expressed gene and known cell cycle regulator. Although we found
that p57Kip2 does not play a role in these processes, we detected an unexpected
function of the paternal allele previously thought to be silent. Finally, we took
advantage of a key property of MADM which is to allow unambiguous investigation
of environmental impact on single cells. The experimental pipeline based on FACS
and RNA-seq analysis of MADM-labeled cells was established to probe the functional
differences of single cell loss of gene function compared to global loss of function
on a transcriptional level. With this method, both common and distinct responses
were isolated due to cell-autonomous and non-autonomous effects acting on genotypically
identical cells. As a result, transcriptional changes were identified which result
solely from the surrounding environment. Using the MADM technology to study genomic
imprinting at single cell resolution, we have identified cell-type-specific gene
expression, novel gene function and the impact of environment on single cell transcriptomes.
Together, these provide important insights to the understanding of mechanisms
regulating cell-type specificity and thus diversity in the brain.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Susanne
full_name: Laukoter, Susanne
id: 2D6B7A9A-F248-11E8-B48F-1D18A9856A87
last_name: Laukoter
orcid: 0000-0002-7903-3010
citation:
ama: Laukoter S. Role of genomic imprinting in cerebral cortex development. 2018:1-139.
doi:10.15479/AT:ISTA:th1057
apa: Laukoter, S. (2018). Role of genomic imprinting in cerebral cortex development.
Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:th1057
chicago: Laukoter, Susanne. “Role of Genomic Imprinting in Cerebral Cortex Development.”
Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:th1057.
ieee: S. Laukoter, “Role of genomic imprinting in cerebral cortex development,”
Institute of Science and Technology Austria, 2018.
ista: Laukoter S. 2018. Role of genomic imprinting in cerebral cortex development.
Institute of Science and Technology Austria.
mla: Laukoter, Susanne. Role of Genomic Imprinting in Cerebral Cortex Development.
Institute of Science and Technology Austria, 2018, pp. 1–139, doi:10.15479/AT:ISTA:th1057.
short: S. Laukoter, Role of Genomic Imprinting in Cerebral Cortex Development, Institute
of Science and Technology Austria, 2018.
date_created: 2018-12-11T11:44:08Z
date_published: 2018-11-21T00:00:00Z
date_updated: 2023-09-07T12:40:44Z
day: '21'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: SiHi
doi: 10.15479/AT:ISTA:th1057
file:
- access_level: closed
checksum: 41fdbf5fdce312802935d88a8ad9932c
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-05-10T07:47:04Z
date_updated: 2019-11-23T23:30:03Z
embargo_to: open_access
file_id: '6396'
file_name: Thesis_LaukoterSusanne_FINAL.docx
file_size: 17949175
relation: source_file
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content_type: application/pdf
creator: dernst
date_created: 2019-05-10T07:47:04Z
date_updated: 2021-02-11T11:17:16Z
embargo: 2019-11-21
file_id: '6397'
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file_size: 21187245
relation: main_file
file_date_updated: 2021-02-11T11:17:16Z
has_accepted_license: '1'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: 1 - 139
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '8046'
pubrep_id: '1057'
status: public
supervisor:
- first_name: Beatriz
full_name: Vicoso, Beatriz
id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
last_name: Vicoso
orcid: 0000-0002-4579-8306
title: Role of genomic imprinting in cerebral cortex development
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '323'
abstract:
- lang: eng
text: 'In the here presented thesis, we explore the role of branched actin networks
in cell migration and antigen presentation, the two most relevant processes in
dendritic cell biology. Branched actin networks construct lamellipodial protrusions
at the leading edge of migrating cells. These are typically seen as adhesive structures,
which mediate force transduction to the extracellular matrix that leads to forward
locomotion. We ablated Arp2/3 nucleation promoting factor WAVE in DCs and found
that the resulting cells lack lamellipodial protrusions. Instead, depending on
the maturation state, one or multiple filopodia were formed. By challenging these
cells in a variety of migration assays we found that lamellipodial protrusions
are dispensable for the locomotion of leukocytes and actually dampen the speed
of migration. However, lamellipodia are critically required to negotiate complex
environments that DCs experience while they travel to the next draining lymph
node. Taken together our results suggest that leukocyte lamellipodia have rather
a sensory- than a force transducing function. Furthermore, we show for the first
time structure and dynamics of dendritic cell F-actin at the immunological synapse
with naïve T cells. Dendritic cell F-actin appears as dynamic foci that are nucleated
by the Arp2/3 complex. WAVE ablated dendritic cells show increased membrane tension,
leading to an altered ultrastructure of the immunological synapse and severe T
cell priming defects. These results point towards a previously unappreciated role
of the cellular mechanics of dendritic cells in T cell activation. Additionally,
we present a novel cell culture based system for the differentiation of dendritic
cells from conditionally immortalized hematopoietic precursors. These precursor
cells are genetically tractable via the CRISPR/Cas9 system while they retain their
ability to differentiate into highly migratory dendritic cells and other immune
cells. This will foster the study of all aspects of dendritic cell biology and
beyond. '
acknowledged_ssus:
- _id: NanoFab
- _id: Bio
- _id: PreCl
- _id: EM-Fac
acknowledgement: "First of all I would like to thank Michael Sixt for giving me the
opportunity to work in \r\nhis group and for his support throughout the years. He
is a truly inspiring person and \r\nthe best boss one can imagine. I would
\ also like to thank all current and past \r\nmembers of the Sixt group for
their help and the great working atmosphere in the lab. \r\nIt is a true privilege
to work with such a bright, funny and friendly group of people and \r\nI’m proud
\ that I could be part of it. Furthermore, I would like to say ‘thank
\ you’ to Daria Siekhaus for all the meetings and discussion we had throughout
the years \r\nand to Federica Benvenuti for being part of my committee.
\ I am also grateful to Jack \r\nMerrin in the nanofabrication facility
\ and all the people working in the bioimaging-\r\n, the electron microscopy-
and the preclinical facilities."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Alexander F
full_name: Leithner, Alexander F
id: 3B1B77E4-F248-11E8-B48F-1D18A9856A87
last_name: Leithner
orcid: 0000-0002-1073-744X
citation:
ama: Leithner AF. Branched actin networks in dendritic cell biology. 2018. doi:10.15479/AT:ISTA:th_998
apa: Leithner, A. F. (2018). Branched actin networks in dendritic cell biology.
Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:th_998
chicago: Leithner, Alexander F. “Branched Actin Networks in Dendritic Cell Biology.”
Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:th_998.
ieee: A. F. Leithner, “Branched actin networks in dendritic cell biology,” Institute
of Science and Technology Austria, 2018.
ista: Leithner AF. 2018. Branched actin networks in dendritic cell biology. Institute
of Science and Technology Austria.
mla: Leithner, Alexander F. Branched Actin Networks in Dendritic Cell Biology.
Institute of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:th_998.
short: A.F. Leithner, Branched Actin Networks in Dendritic Cell Biology, Institute
of Science and Technology Austria, 2018.
date_created: 2018-12-11T11:45:49Z
date_published: 2018-04-12T00:00:00Z
date_updated: 2023-09-07T12:39:44Z
day: '12'
ddc:
- '571'
- '599'
- '610'
degree_awarded: PhD
department:
- _id: MiSi
doi: 10.15479/AT:ISTA:th_998
file:
- access_level: closed
checksum: d5e3edbac548c26c1fa43a4b37a54a4c
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-04-05T09:23:11Z
date_updated: 2021-02-11T23:30:17Z
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file_id: '6219'
file_name: PhD_thesis_AlexLeithner_final_version.docx
file_size: 29027671
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checksum: 071f7476db29e41146824ebd0697cb10
content_type: application/pdf
creator: dernst
date_created: 2019-04-05T09:23:11Z
date_updated: 2021-02-11T11:17:16Z
embargo: 2019-04-15
file_id: '6220'
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file_size: 66045341
relation: main_file
file_date_updated: 2021-02-11T23:30:17Z
has_accepted_license: '1'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: '99'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '7542'
pubrep_id: '998'
related_material:
record:
- id: '1321'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Michael K
full_name: Sixt, Michael K
id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
last_name: Sixt
orcid: 0000-0002-6620-9179
title: Branched actin networks in dendritic cell biology
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '539'
abstract:
- lang: eng
text: The whole life cycle of plants as well as their responses to environmental
stimuli is governed by a complex network of hormonal regulations. A number of
studies have demonstrated an essential role of both auxin and cytokinin in the
regulation of many aspects of plant growth and development including embryogenesis,
postembryonic organogenic processes such as root, and shoot branching, root and
shoot apical meristem activity and phyllotaxis. Over the last decades essential
knowledge on the key molecular factors and pathways that spatio-temporally define
auxin and cytokinin activities in the plant body has accumulated. However, how
both hormonal pathways are interconnected by a complex network of interactions
and feedback circuits that determines the final outcome of the individual hormone
actions is still largely unknown. Root system architecture establishment and in
particular formation of lateral organs is prime example of developmental process
at whose regulation both auxin and cytokinin pathways converge. To dissect convergence
points and pathways that tightly balance auxin - cytokinin antagonistic activities
that determine the root branching pattern transcriptome profiling was applied.
Genome wide expression analyses of the xylem pole pericycle, a tissue giving rise
to lateral roots, led to identification of genes that are highly responsive to
combinatorial auxin and cytokinin treatments and play an essential function in
the auxin-cytokinin regulated root branching. SYNERGISTIC AUXIN CYTOKININ 1 (SYAC1)
gene, which encodes for a protein of unknown function, was detected among the
top candidate genes of which expression was synergistically up-regulated by simultaneous
hormonal treatment. Plants with modulated SYAC1 activity exhibit severe defects
in the root system establishment and attenuate developmental responses to both
auxin and cytokinin. To explore the biological function of the SYAC1, we employed
different strategies including expression pattern analysis, subcellular localization
and phenotypic analyses of the syac1 loss-of-function and gain-of-function transgenic
lines along with the identification of the SYAC1 interaction partners. Detailed
functional characterization revealed that SYAC1 acts as a developmentally specific
regulator of the secretory pathway to control deposition of cell wall components
and thereby rapidly fine tune elongation growth.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Andrej
full_name: Hurny, Andrej
id: 4DC4AF46-F248-11E8-B48F-1D18A9856A87
last_name: Hurny
orcid: 0000-0003-3638-1426
citation:
ama: Hurny A. Identification and characterization of novel auxin-cytokinin cross-talk
components. 2018. doi:10.15479/AT:ISTA:th_930
apa: Hurny, A. (2018). Identification and characterization of novel auxin-cytokinin
cross-talk components. Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:th_930
chicago: Hurny, Andrej. “Identification and Characterization of Novel Auxin-Cytokinin
Cross-Talk Components.” Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:th_930.
ieee: A. Hurny, “Identification and characterization of novel auxin-cytokinin cross-talk
components,” Institute of Science and Technology Austria, 2018.
ista: Hurny A. 2018. Identification and characterization of novel auxin-cytokinin
cross-talk components. Institute of Science and Technology Austria.
mla: Hurny, Andrej. Identification and Characterization of Novel Auxin-Cytokinin
Cross-Talk Components. Institute of Science and Technology Austria, 2018,
doi:10.15479/AT:ISTA:th_930.
short: A. Hurny, Identification and Characterization of Novel Auxin-Cytokinin Cross-Talk
Components, Institute of Science and Technology Austria, 2018.
date_created: 2018-12-11T11:47:03Z
date_published: 2018-01-01T00:00:00Z
date_updated: 2023-09-07T12:41:06Z
day: '01'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: EvBe
doi: 10.15479/AT:ISTA:th_930
file:
- access_level: closed
checksum: 0c9d6d1c80d9857e6e545213467bbcb2
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-04-05T09:37:56Z
date_updated: 2020-12-02T23:30:08Z
embargo_to: open_access
file_id: '6226'
file_name: 2018_Hurny_thesis_source.docx
file_size: 28112114
relation: source_file
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checksum: ecbe481a1413d270bd501b872c7ed54f
content_type: application/pdf
creator: dernst
date_created: 2019-04-05T09:37:55Z
date_updated: 2020-12-02T09:52:16Z
embargo: 2019-07-10
file_id: '6227'
file_name: 2018_Hurny_thesis.pdf
file_size: 12524427
relation: main_file
file_date_updated: 2020-12-02T23:30:08Z
has_accepted_license: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: '147'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '7277'
pubrep_id: '930'
related_material:
record:
- id: '1024'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Eva
full_name: Benková, Eva
id: 38F4F166-F248-11E8-B48F-1D18A9856A87
last_name: Benková
orcid: 0000-0002-8510-9739
title: Identification and characterization of novel auxin-cytokinin cross-talk components
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '48'
abstract:
- lang: eng
text: 'The hippocampus is a key brain region for spatial memory and navigation and
is needed at all stages of memory, including encoding, consolidation, and recall.
Hippocampal place cells selectively discharge at specific locations of the environment
to form a cognitive map of the space. During the rest period and sleep following
spatial navigation and/or learning, the waking activity of the place cells is
reactivated within high synchrony events. This reactivation is thought to be important
for memory consolidation and stabilization of the spatial representations. The
aim of my thesis was to directly test whether the reactivation content encoded
in firing patterns of place cells is important for consolidation of spatial memories.
In particular, I aimed to test whether, in cases when multiple spatial memory
traces are acquired during learning, the specific disruption of the reactivation
of a subset of these memories leads to the selective disruption of the corresponding
memory traces or through memory interference the other learned memories are disrupted
as well. In this thesis, using a modified cheeseboard paradigm and a closed-loop
recording setup with feedback optogenetic stimulation, I examined how the disruption
of the reactivation of specific spiking patterns affects consolidation of the
corresponding memory traces. To obtain multiple distinctive memories, animals
had to perform a spatial task in two distinct cheeseboard environments and the
reactivation of spiking patterns associated with one of the environments (target)
was disrupted after learning during four hours rest period using a real-time decoding
method. This real-time decoding method was capable of selectively affecting the
firing rates and cofiring correlations of the target environment-encoding cells.
The selective disruption led to behavioural impairment in the memory tests after
the rest periods in the target environment but not in the other undisrupted control
environment. In addition, the map of the target environment was less stable in
the impaired memory tests compared to the learning session before than the map
of the control environment. However, when the animal relearned the task, the same
map recurred in the target environment that was present during learning before
the disruption. Altogether my work demonstrated that the reactivation content
is important: assembly-related disruption of reactivation can lead to a selective
memory impairment and deficiency in map stability. These findings indeed suggest
that reactivated assembly patterns reflect processes associated with the consolidation
of memory traces. '
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Igor
full_name: Gridchyn, Igor
id: 4B60654C-F248-11E8-B48F-1D18A9856A87
last_name: Gridchyn
orcid: 0000-0002-1807-1929
citation:
ama: Gridchyn I. Reactivation content is important for consolidation of spatial
memory. 2018. doi:10.15479/AT:ISTA:th_1042
apa: Gridchyn, I. (2018). Reactivation content is important for consolidation
of spatial memory. Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:th_1042
chicago: Gridchyn, Igor. “Reactivation Content Is Important for Consolidation of
Spatial Memory.” Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:th_1042.
ieee: I. Gridchyn, “Reactivation content is important for consolidation of spatial
memory,” Institute of Science and Technology Austria, 2018.
ista: Gridchyn I. 2018. Reactivation content is important for consolidation of spatial
memory. Institute of Science and Technology Austria.
mla: Gridchyn, Igor. Reactivation Content Is Important for Consolidation of Spatial
Memory. Institute of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:th_1042.
short: I. Gridchyn, Reactivation Content Is Important for Consolidation of Spatial
Memory, Institute of Science and Technology Austria, 2018.
date_created: 2018-12-11T11:44:21Z
date_published: 2018-08-27T00:00:00Z
date_updated: 2023-09-07T12:42:44Z
day: '27'
ddc:
- '573'
degree_awarded: PhD
department:
- _id: JoCs
doi: 10.15479/AT:ISTA:th_1042
file:
- access_level: closed
checksum: 7db4415e435590fa33542c7b0a0321d7
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-04-08T13:36:01Z
date_updated: 2021-02-11T23:30:22Z
embargo_to: open_access
file_id: '6236'
file_name: 2018_Thesis_Gridchyn_source.docx
file_size: 7666687
relation: source_file
- access_level: open_access
checksum: f96f3fe8979f7b1e6db6acaca962b10c
content_type: application/pdf
creator: dernst
date_created: 2019-04-08T13:36:01Z
date_updated: 2021-02-11T11:17:18Z
embargo: 2019-08-29
file_id: '6237'
file_name: 2018_Thesis_Gridchyn.pdf
file_size: 6034153
relation: main_file
file_date_updated: 2021-02-11T23:30:22Z
has_accepted_license: '1'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: '104'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '8006'
pubrep_id: '1042'
status: public
supervisor:
- first_name: Jozsef L
full_name: Csicsvari, Jozsef L
id: 3FA14672-F248-11E8-B48F-1D18A9856A87
last_name: Csicsvari
orcid: 0000-0002-5193-4036
title: Reactivation content is important for consolidation of spatial memory
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '9'
abstract:
- lang: eng
text: 'Immune cells migrating to the sites of infection navigate through diverse
tissue architectures and switch their migratory mechanisms upon demand. However,
little is known about systemic regulators that could allow the acquisition of
these mechanisms. We performed a genetic screen in Drosophila melanogaster to
identify regulators of germband invasion by embryonic macrophages into the confined
space between the ectoderm and mesoderm. We have found that bZIP circadian transcription
factors (TFs) Kayak (dFos) and Vrille (dNFIL3) have opposite effects on macrophage
germband infiltration: Kayak facilitated and Vrille inhibited it. These TFs are
enriched in the macrophages during migration and genetically interact to control
it. Kayak sets a less coordinated mode of migration of the macrophage group and
increases the probability and length of Levy walks. Intriguingly, the motility
of kayak mutant macrophages was also strongly affected during initial germband
invasion but not along another less confined route. Inhibiting Rho1 signaling
within the tail ectoderm partially rescued the Kayak mutant phenotype, strongly
suggesting that migrating macrophages have to overcome a barrier imposed by the
stiffness of the ectoderm. Also, Kayak appeared to be important for the maintenance
of the round cell shape and the rear edge translocation of the macrophages invading
the germband. Complementary to this, the cortical actin cytoskeleton of Kayak-
deficient macrophages was strongly affected. RNA sequencing revealed the filamin
Cheerio and tetraspanin TM4SF to be downstream of Kayak. Chromatin immunoprecipitation
and immunostaining revealed that the formin Diaphanous is another downstream target
of Kayak. Immunostaining revealed that the formin Diaphanous is another downstream
target of Kayak. Indeed, Cheerio, TM4SF and Diaphanous are required within macrophages
for germband invasion, and expression of constitutively active Diaphanous in macrophages
was able to rescue the kayak mutant phenotype. Moreover, Cher and Diaphanous are
also reduced in the macrophages overexpressing Vrille. We hypothesize that Kayak,
through its targets, increases actin polymerization and cortical tension in macrophages
and thus allows extra force generation necessary for macrophage dissemination
and migration through confined stiff tissues, while Vrille counterbalances it.'
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Vera
full_name: Belyaeva, Vera
id: 47F080FE-F248-11E8-B48F-1D18A9856A87
last_name: Belyaeva
citation:
ama: Belyaeva V. Transcriptional regulation of macrophage migration in the Drosophila
melanogaster embryo . 2018. doi:10.15479/AT:ISTA:th1064
apa: Belyaeva, V. (2018). Transcriptional regulation of macrophage migration
in the Drosophila melanogaster embryo . Institute of Science and Technology
Austria. https://doi.org/10.15479/AT:ISTA:th1064
chicago: Belyaeva, Vera. “Transcriptional Regulation of Macrophage Migration in
the Drosophila Melanogaster Embryo .” Institute of Science and Technology Austria,
2018. https://doi.org/10.15479/AT:ISTA:th1064.
ieee: V. Belyaeva, “Transcriptional regulation of macrophage migration in the Drosophila
melanogaster embryo ,” Institute of Science and Technology Austria, 2018.
ista: Belyaeva V. 2018. Transcriptional regulation of macrophage migration in the
Drosophila melanogaster embryo . Institute of Science and Technology Austria.
mla: Belyaeva, Vera. Transcriptional Regulation of Macrophage Migration in the
Drosophila Melanogaster Embryo . Institute of Science and Technology Austria,
2018, doi:10.15479/AT:ISTA:th1064.
short: V. Belyaeva, Transcriptional Regulation of Macrophage Migration in the Drosophila
Melanogaster Embryo , Institute of Science and Technology Austria, 2018.
date_created: 2018-12-11T11:44:08Z
date_published: 2018-07-01T00:00:00Z
date_updated: 2023-09-07T12:43:10Z
day: '01'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: DaSi
doi: 10.15479/AT:ISTA:th1064
file:
- access_level: closed
checksum: d27b2465cb70d0c9678a0381b9b6ced1
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-04-08T14:13:12Z
date_updated: 2020-07-14T12:48:14Z
embargo_to: open_access
file_id: '6243'
file_name: 2018_Thesis_Belyaeva_source.docx
file_size: 102737483
relation: source_file
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checksum: a2939b61bde2de7b8ced77bbae0eaaed
content_type: application/pdf
creator: dernst
date_created: 2019-04-08T14:14:08Z
date_updated: 2021-02-11T11:17:16Z
embargo: 2019-11-19
file_id: '6244'
file_name: 2018_Thesis_Belyaeva.pdf
file_size: 88077843
relation: main_file
file_date_updated: 2021-02-11T11:17:16Z
has_accepted_license: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: '96'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '8047'
pubrep_id: '1064'
status: public
supervisor:
- first_name: Daria E
full_name: Siekhaus, Daria E
id: 3D224B9E-F248-11E8-B48F-1D18A9856A87
last_name: Siekhaus
orcid: 0000-0001-8323-8353
title: 'Transcriptional regulation of macrophage migration in the Drosophila melanogaster
embryo '
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '6266'
abstract:
- lang: eng
text: 'A major challenge in neuroscience research is to dissect the circuits that
orchestrate behavior in health and disease. Proteins from a wide range of non-mammalian
species, such as microbial opsins, have been successfully transplanted to specific
neuronal targets to override their natural communication patterns. The goal of
our work is to manipulate synaptic communication in a manner that closely incorporates
the functional intricacies of synapses by preserving temporal encoding (i.e. the
firing pattern of the presynaptic neuron) and connectivity (i.e. target specific
synapses rather than specific neurons). Our strategy to achieve this goal builds
on the use of non-mammalian transplants to create a synthetic synapse. The mode
of modulation comes from pre-synaptic uptake of a synthetic neurotransmitter (SN)
into synaptic vesicles by means of a genetically targeted transporter selective
for the SN. Upon natural vesicular release, exposure of the SN to the synaptic
cleft will modify the post-synaptic potential through an orthogonal ligand gated
ion channel. To achieve this goal we have functionally characterized a mixed cationic
methionine-gated ion channel from Arabidopsis thaliana, designed a method to functionally
characterize a synthetic transporter in isolated synaptic vesicles without the
need for transgenic animals, identified and extracted multiple prokaryotic uptake
systems that are substrate specific for methionine (Met), and established a primary/cell
line co-culture system that would allow future combinatorial testing of this orthogonal
transmitter-transporter-channel trifecta. Synthetic synapses will provide a unique
opportunity to manipulate synaptic communication while maintaining the electrophysiological
integrity of the pre-synaptic cell. In this way, information may be preserved
that was generated in upstream circuits and that could be essential for concerted
function and information processing. '
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Catherine
full_name: Mckenzie, Catherine
id: 3EEDE19A-F248-11E8-B48F-1D18A9856A87
last_name: Mckenzie
citation:
ama: Mckenzie C. Design and characterization of methods and biological components
to realize synthetic neurotransmission . 2018. doi:10.15479/at:ista:th_1055
apa: Mckenzie, C. (2018). Design and characterization of methods and biological
components to realize synthetic neurotransmission . Institute of Science and
Technology Austria. https://doi.org/10.15479/at:ista:th_1055
chicago: Mckenzie, Catherine. “Design and Characterization of Methods and Biological
Components to Realize Synthetic Neurotransmission .” Institute of Science and
Technology Austria, 2018. https://doi.org/10.15479/at:ista:th_1055.
ieee: C. Mckenzie, “Design and characterization of methods and biological components
to realize synthetic neurotransmission ,” Institute of Science and Technology
Austria, 2018.
ista: Mckenzie C. 2018. Design and characterization of methods and biological components
to realize synthetic neurotransmission . Institute of Science and Technology Austria.
mla: Mckenzie, Catherine. Design and Characterization of Methods and Biological
Components to Realize Synthetic Neurotransmission . Institute of Science and
Technology Austria, 2018, doi:10.15479/at:ista:th_1055.
short: C. Mckenzie, Design and Characterization of Methods and Biological Components
to Realize Synthetic Neurotransmission , Institute of Science and Technology Austria,
2018.
date_created: 2019-04-09T14:13:39Z
date_published: 2018-10-31T00:00:00Z
date_updated: 2023-09-07T13:02:37Z
day: '31'
ddc:
- '571'
- '573'
degree_awarded: PhD
department:
- _id: HaJa
doi: 10.15479/at:ista:th_1055
file:
- access_level: open_access
checksum: 9d2c2dca04b00e485470c28b262af59a
content_type: application/pdf
creator: dernst
date_created: 2019-04-09T14:12:40Z
date_updated: 2021-02-11T11:17:16Z
embargo: 2019-11-24
file_id: '6267'
file_name: 2018_Thesis_McKenzie.pdf
file_size: 4906420
relation: main_file
- access_level: closed
checksum: 50b58c272899601bc6fd9642c4dc97f1
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-04-09T14:12:40Z
date_updated: 2020-07-14T12:47:25Z
embargo_to: open_access
file_id: '6268'
file_name: 2018_Thesis_McKenzie_source.docx
file_size: 5053545
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file_date_updated: 2021-02-11T11:17:16Z
has_accepted_license: '1'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: '95'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
pubrep_id: '1055'
related_material:
record:
- id: '7132'
relation: new_edition
status: public
status: public
supervisor:
- first_name: Harald L
full_name: Janovjak, Harald L
id: 33BA6C30-F248-11E8-B48F-1D18A9856A87
last_name: Janovjak
orcid: 0000-0002-8023-9315
title: 'Design and characterization of methods and biological components to realize
synthetic neurotransmission '
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '50'
abstract:
- lang: eng
text: The Wnt/planar cell polarity (Wnt/PCP) pathway determines planar polarity
of epithelial cells in both vertebrates and invertebrates. The role that Wnt/PCP
signaling plays in mesenchymal contexts, however, is only poorly understood. While
previous studies have demonstrated the capacity of Wnt/PCP signaling to polarize
and guide directed migration of mesenchymal cells, it remains unclear whether
endogenous Wnt/PCP signaling performs these functions instructively, as it does
in epithelial cells. Here we developed a light-switchable version of the Wnt/PCP
receptor Frizzled 7 (Fz7) to unambiguously distinguish between an instructive
and a permissive role of Wnt/PCP signaling for the directional collective migration
of mesendoderm progenitor cells during zebrafish gastrulation. We show that prechordal
plate (ppl) cell migration is defective in maternal-zygotic fz7a and fz7b (MZ
fz7a,b) double mutant embryos, and that Fz7 functions cell-autonomously in this
process by promoting ppl cell protrusion formation and directed migration. We
further show that local activation of Fz7 can direct ppl cell migration both in
vitro and in vivo. Surprisingly, however, uniform Fz7 activation is sufficient
to fully rescue the ppl cell migration defect in MZ fz7a,b mutant embryos, indicating
that Wnt/PCP signaling functions permissively rather than instructively in directed
mesendoderm cell migration during zebrafish gastrulation.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Daniel
full_name: Capek, Daniel
id: 31C42484-F248-11E8-B48F-1D18A9856A87
last_name: Capek
orcid: 0000-0001-5199-9940
citation:
ama: Capek D. Optogenetic Frizzled 7 reveals a permissive function of Wnt/PCP signaling
in directed mesenchymal cell migration. 2018. doi:10.15479/AT:ISTA:TH_1031
apa: Capek, D. (2018). Optogenetic Frizzled 7 reveals a permissive function of
Wnt/PCP signaling in directed mesenchymal cell migration. Institute of Science
and Technology Austria. https://doi.org/10.15479/AT:ISTA:TH_1031
chicago: Capek, Daniel. “Optogenetic Frizzled 7 Reveals a Permissive Function of
Wnt/PCP Signaling in Directed Mesenchymal Cell Migration.” Institute of Science
and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:TH_1031.
ieee: D. Capek, “Optogenetic Frizzled 7 reveals a permissive function of Wnt/PCP
signaling in directed mesenchymal cell migration,” Institute of Science and Technology
Austria, 2018.
ista: Capek D. 2018. Optogenetic Frizzled 7 reveals a permissive function of Wnt/PCP
signaling in directed mesenchymal cell migration. Institute of Science and Technology
Austria.
mla: Capek, Daniel. Optogenetic Frizzled 7 Reveals a Permissive Function of Wnt/PCP
Signaling in Directed Mesenchymal Cell Migration. Institute of Science and
Technology Austria, 2018, doi:10.15479/AT:ISTA:TH_1031.
short: D. Capek, Optogenetic Frizzled 7 Reveals a Permissive Function of Wnt/PCP
Signaling in Directed Mesenchymal Cell Migration, Institute of Science and Technology
Austria, 2018.
date_created: 2018-12-11T11:44:21Z
date_published: 2018-06-22T00:00:00Z
date_updated: 2023-09-07T12:48:16Z
day: '22'
ddc:
- '570'
- '591'
- '596'
degree_awarded: PhD
department:
- _id: CaHe
doi: 10.15479/AT:ISTA:TH_1031
file:
- access_level: open_access
checksum: d3eca3dcacb67bffdde6e6609c31cdd0
content_type: application/pdf
creator: dernst
date_created: 2019-04-08T13:42:26Z
date_updated: 2021-02-11T11:17:17Z
embargo: 2019-06-25
file_id: '6238'
file_name: 2018_Thesis_Capek.pdf
file_size: 31576521
relation: main_file
- access_level: closed
checksum: 876deb14067e638aba65d209668bd821
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-04-08T13:42:27Z
date_updated: 2021-02-11T23:30:21Z
embargo_to: open_access
file_id: '6239'
file_name: 2018_Thesis_Capek_source.docx
file_size: 38992956
relation: source_file
file_date_updated: 2021-02-11T23:30:21Z
has_accepted_license: '1'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
page: '95'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '8004'
pubrep_id: '1031'
related_material:
record:
- id: '1100'
relation: part_of_dissertation
status: public
- id: '661'
relation: part_of_dissertation
status: public
- id: '676'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Carl-Philipp J
full_name: Heisenberg, Carl-Philipp J
id: 39427864-F248-11E8-B48F-1D18A9856A87
last_name: Heisenberg
orcid: 0000-0002-0912-4566
title: Optogenetic Frizzled 7 reveals a permissive function of Wnt/PCP signaling in
directed mesenchymal cell migration
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '26'
abstract:
- lang: eng
text: Expression of genes is a fundamental molecular phenotype that is subject to
evolution by different types of mutations. Both the rate and the effect of mutations
may depend on the DNA sequence context of a particular gene or a particular promoter
sequence. In this thesis I investigate the nature of this dependence using simple
genetic systems in Escherichia coli. With these systems I explore the evolution
of constitutive gene expression from random starting sequences at different loci
on the chromosome and at different locations in sequence space. First, I dissect
chromosomal neighborhood effects that underlie locus-dependent differences in
the potential of a gene under selection to become more highly expressed. Next,
I find that the effects of point mutations in promoter sequences are dependent
on sequence context, and that an existing energy matrix model performs poorly
in predicting relative expression of unrelated sequences. Finally, I show that
a substantial fraction of random sequences contain functional promoters and I
present an extended thermodynamic model that predicts promoter strength in full
sequence space. Taken together, these results provide new insights and guides
on how to integrate information on sequence context to improve our qualitative
and quantitative understanding of bacterial gene expression, with implications
for rapid evolution of drug resistance, de novo evolution of genes, and horizontal
gene transfer.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Magdalena
full_name: Steinrück, Magdalena
id: 2C023F40-F248-11E8-B48F-1D18A9856A87
last_name: Steinrück
orcid: 0000-0003-1229-9719
citation:
ama: Steinrück M. The influence of sequence context on the evolution of bacterial
gene expression. 2018. doi:10.15479/AT:ISTA:th1059
apa: Steinrück, M. (2018). The influence of sequence context on the evolution
of bacterial gene expression. Institute of Science and Technology Austria.
https://doi.org/10.15479/AT:ISTA:th1059
chicago: Steinrück, Magdalena. “The Influence of Sequence Context on the Evolution
of Bacterial Gene Expression.” Institute of Science and Technology Austria, 2018.
https://doi.org/10.15479/AT:ISTA:th1059.
ieee: M. Steinrück, “The influence of sequence context on the evolution of bacterial
gene expression,” Institute of Science and Technology Austria, 2018.
ista: Steinrück M. 2018. The influence of sequence context on the evolution of bacterial
gene expression. Institute of Science and Technology Austria.
mla: Steinrück, Magdalena. The Influence of Sequence Context on the Evolution
of Bacterial Gene Expression. Institute of Science and Technology Austria,
2018, doi:10.15479/AT:ISTA:th1059.
short: M. Steinrück, The Influence of Sequence Context on the Evolution of Bacterial
Gene Expression, Institute of Science and Technology Austria, 2018.
date_created: 2018-12-11T11:44:14Z
date_published: 2018-10-30T00:00:00Z
date_updated: 2023-09-07T12:48:43Z
day: '30'
ddc:
- '576'
- '579'
degree_awarded: PhD
department:
- _id: CaGu
doi: 10.15479/AT:ISTA:th1059
file:
- access_level: closed
checksum: 413cbce1cd1debeae3abe2a25dbc70d1
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-02-08T10:51:22Z
date_updated: 2020-07-14T12:45:43Z
embargo_to: open_access
file_id: '5941'
file_name: Thesis_Steinrueck_final.docx
file_size: 9190845
relation: source_file
- access_level: open_access
checksum: 3def8b7854c8b42d643597ce0215efac
content_type: application/pdf
creator: dernst
date_created: 2019-02-08T10:51:22Z
date_updated: 2021-02-11T11:17:14Z
embargo: 2019-11-02
file_id: '5942'
file_name: Thesis_Steinrueck_final.pdf
file_size: 7521973
relation: main_file
file_date_updated: 2021-02-11T11:17:14Z
has_accepted_license: '1'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: '109'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '8029'
pubrep_id: '1059'
related_material:
record:
- id: '704'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Calin C
full_name: Guet, Calin C
id: 47F8433E-F248-11E8-B48F-1D18A9856A87
last_name: Guet
orcid: 0000-0001-6220-2052
title: The influence of sequence context on the evolution of bacterial gene expression
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '5816'
abstract:
- lang: eng
text: Solid-state qubit manipulation and read-out fidelities are reaching fault-tolerance,
but quantum error correction requires millions of physical qubits and therefore
a scalable quantum computer architecture. To solve signal-line bandwidth and fan-out
problems, microwave sources required for qubit manipulation might be embedded
close to the qubit chip, typically operating at temperatures below 4 K. Here,
we perform the first low temperature measurements of a 130 nm BiCMOS based SiGe
voltage controlled oscillator at cryogenic temperature. We determined the frequency
and output power dependence on temperature and magnetic field up to 5 T and measured
the temperature influence on its noise performance. The device maintains its full
functionality from 300 K to 4 K. The carrier frequency at 4 K increases by 3%
with respect to the carrier frequency at 300 K, and the output power at 4 K increases
by 10 dB relative to the output power at 300 K. The frequency tuning range of
approximately 20% remains unchanged between 300 K and 4 K. In an in-plane magnetic
field of 5 T, the carrier frequency shifts by only 0.02% compared to the frequency
at zero magnetic field.
article_number: '114701'
article_processing_charge: No
author:
- first_name: Arne
full_name: Hollmann, Arne
last_name: Hollmann
- first_name: Daniel
full_name: Jirovec, Daniel
id: 4C473F58-F248-11E8-B48F-1D18A9856A87
last_name: Jirovec
orcid: 0000-0002-7197-4801
- first_name: Maciej
full_name: Kucharski, Maciej
last_name: Kucharski
- first_name: Dietmar
full_name: Kissinger, Dietmar
last_name: Kissinger
- first_name: Gunter
full_name: Fischer, Gunter
last_name: Fischer
- first_name: Lars R.
full_name: Schreiber, Lars R.
last_name: Schreiber
citation:
ama: Hollmann A, Jirovec D, Kucharski M, Kissinger D, Fischer G, Schreiber LR. 30
GHz-voltage controlled oscillator operating at 4 K. Review of Scientific Instruments.
2018;89(11). doi:10.1063/1.5038258
apa: Hollmann, A., Jirovec, D., Kucharski, M., Kissinger, D., Fischer, G., &
Schreiber, L. R. (2018). 30 GHz-voltage controlled oscillator operating at 4 K.
Review of Scientific Instruments. AIP Publishing. https://doi.org/10.1063/1.5038258
chicago: Hollmann, Arne, Daniel Jirovec, Maciej Kucharski, Dietmar Kissinger, Gunter
Fischer, and Lars R. Schreiber. “30 GHz-Voltage Controlled Oscillator Operating
at 4 K.” Review of Scientific Instruments. AIP Publishing, 2018. https://doi.org/10.1063/1.5038258.
ieee: A. Hollmann, D. Jirovec, M. Kucharski, D. Kissinger, G. Fischer, and L. R.
Schreiber, “30 GHz-voltage controlled oscillator operating at 4 K,” Review
of Scientific Instruments, vol. 89, no. 11. AIP Publishing, 2018.
ista: Hollmann A, Jirovec D, Kucharski M, Kissinger D, Fischer G, Schreiber LR.
2018. 30 GHz-voltage controlled oscillator operating at 4 K. Review of Scientific
Instruments. 89(11), 114701.
mla: Hollmann, Arne, et al. “30 GHz-Voltage Controlled Oscillator Operating at 4
K.” Review of Scientific Instruments, vol. 89, no. 11, 114701, AIP Publishing,
2018, doi:10.1063/1.5038258.
short: A. Hollmann, D. Jirovec, M. Kucharski, D. Kissinger, G. Fischer, L.R. Schreiber,
Review of Scientific Instruments 89 (2018).
date_created: 2019-01-10T14:22:23Z
date_published: 2018-11-01T00:00:00Z
date_updated: 2024-03-28T23:30:27Z
day: '01'
department:
- _id: GeKa
doi: 10.1063/1.5038258
external_id:
arxiv:
- '1804.09522'
isi:
- '000451735700054'
intvolume: ' 89'
isi: 1
issue: '11'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1804.09522
month: '11'
oa: 1
oa_version: Preprint
publication: Review of Scientific Instruments
publication_identifier:
issn:
- '00346748'
publication_status: published
publisher: AIP Publishing
quality_controlled: '1'
related_material:
record:
- id: '10058'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: 30 GHz-voltage controlled oscillator operating at 4 K
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 89
year: '2018'
...
---
_id: '6263'
abstract:
- lang: eng
text: 'Antibiotic resistance can emerge spontaneously through genomic mutation and render
treatment ineffective. To counteract this process, in addition to the discovery and
description of resistance mechanisms,a deeper understanding of resistanceevolvabilityand
its determinantsis needed. To address this challenge, this thesisuncoversnew genetic
determinants of resistance evolvability using a customized robotic setup,
exploressystematic ways in which resistance evolution is perturbed due to
dose-responsecharacteristics of drugs and mutation rate differences,and mathematically investigates
the evolutionary fate of one specific type of evolvability modifier -a stress-induced
mutagenesis allele.We find severalgenes which strongly inhibit or potentiate resistance evolution. In order
to identify them, we first developedan automated high-throughput feedback-controlled
protocol whichkeeps the population size and selection pressure approximately constant
for hundreds of cultures by dynamically re-diluting the cultures and adjusting the antibiotic
concentration. We implementedthis protocol on a customized liquid handling robot and
propagated 100 different gene deletion strains of Escherichia coliin triplicate for over 100
generations in tetracycline and in chloramphenicol, and comparedtheir adaptation rates.We find a diminishing returns pattern, where initially sensitive strains adapted more
compared to less sensitive ones. Our data uncover that deletions of certain genes
which do not affect mutation rate,including efflux pump components, a chaperone and
severalstructural and regulatory genes can strongly and reproducibly alterresistance evolution.
Sequencing analysis of evolved populations indicates that epistasis with resistance
mutations is the most likelyexplanation. This work could inspire treatment strategies in
which targeted inhibitors of evolvability mechanisms will be given alongside antibiotics to
slow down resistance evolution and extend theefficacy of antibiotics.We implemented astochasticpopulation genetics model,
toverifyways in which general properties, namely, dose-response characteristics of drugs and mutation rates, influence
evolutionary dynamics. In particular, under the exposure to antibiotics with shallow dose-response curves,bacteria have narrower distributions of fitness effects of new mutations.
We show that in silicothis also leads to slower resistance evolution. We
see and confirm with experiments that increased mutation rates, apart from speeding
up evolution, also leadto high reproducibility of phenotypic adaptation in a context
of continually strong selection pressure.Knowledge of these patterns can aid in predicting the dynamics of antibiotic
resistance evolutionand adapting treatment schemes accordingly.Focusing on a previously described type of evolvability modifier
–a stress-induced mutagenesis allele –we find conditions under which it can persist in a population under
periodic selectionakin to clinical treatment. We set up a deterministic
infinite populationcontinuous time model tracking the frequencies of a mutator and resistance allele and
evaluate various treatment schemes in how well they maintain a stress-induced
mutator allele. In particular,a high diversity of stresses is crucial for the persistence
of the mutator allele. This leads to a general trade-off where exactly those
diversifying treatment schemes which are likely to decrease levels of resistance could lead to stronger selection of highly
evolvable genotypes.In the long run, this work will lead to a deeper understanding of the genetic and cellular
mechanisms involved in antibiotic resistance evolution and could inspire new strategies
for slowing down its rate. '
acknowledged_ssus:
- _id: M-Shop
- _id: LifeSc
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Marta
full_name: Lukacisinova, Marta
id: 4342E402-F248-11E8-B48F-1D18A9856A87
last_name: Lukacisinova
orcid: 0000-0002-2519-8004
citation:
ama: Lukacisinova M. Genetic determinants of antibiotic resistance evolution. 2018.
doi:10.15479/AT:ISTA:th1072
apa: Lukacisinova, M. (2018). Genetic determinants of antibiotic resistance evolution.
Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:th1072
chicago: Lukacisinova, Marta. “Genetic Determinants of Antibiotic Resistance Evolution.”
Institute of Science and Technology Austria, 2018. https://doi.org/10.15479/AT:ISTA:th1072.
ieee: M. Lukacisinova, “Genetic determinants of antibiotic resistance evolution,”
Institute of Science and Technology Austria, 2018.
ista: Lukacisinova M. 2018. Genetic determinants of antibiotic resistance evolution.
Institute of Science and Technology Austria.
mla: Lukacisinova, Marta. Genetic Determinants of Antibiotic Resistance Evolution.
Institute of Science and Technology Austria, 2018, doi:10.15479/AT:ISTA:th1072.
short: M. Lukacisinova, Genetic Determinants of Antibiotic Resistance Evolution,
Institute of Science and Technology Austria, 2018.
date_created: 2019-04-09T13:57:15Z
date_published: 2018-12-28T00:00:00Z
date_updated: 2023-09-22T09:20:37Z
day: '28'
ddc:
- '570'
- '576'
- '579'
degree_awarded: PhD
department:
- _id: ToBo
doi: 10.15479/AT:ISTA:th1072
file:
- access_level: open_access
checksum: fc60585c9eaad868ac007004ef130908
content_type: application/pdf
creator: dernst
date_created: 2019-04-09T13:49:24Z
date_updated: 2021-02-11T11:17:17Z
embargo: 2020-01-25
file_id: '6264'
file_name: 2018_Thesis_Lukacisinova.pdf
file_size: 5656866
relation: main_file
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checksum: 264057ec0a92ab348cc83b41f021ba92
content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
creator: dernst
date_created: 2019-04-09T13:49:23Z
date_updated: 2020-07-14T12:47:25Z
embargo_to: open_access
file_id: '6265'
file_name: 2018_Thesis_Lukacisinova_source.docx
file_size: 5168054
relation: source_file
file_date_updated: 2021-02-11T11:17:17Z
has_accepted_license: '1'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: '91'
publication_identifier:
issn:
- 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '1619'
relation: part_of_dissertation
status: public
- id: '696'
relation: part_of_dissertation
status: public
- id: '1027'
relation: part_of_dissertation
status: public
status: public
supervisor:
- first_name: Tobias
full_name: Bollenbach, Tobias
id: 3E6DB97A-F248-11E8-B48F-1D18A9856A87
last_name: Bollenbach
orcid: 0000-0003-4398-476X
title: Genetic determinants of antibiotic resistance evolution
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '544'
abstract:
- lang: eng
text: Drosophila melanogaster plasmatocytes, the phagocytic cells among hemocytes,
are essential for immune responses, but also play key roles from early development
to death through their interactions with other cell types. They regulate homeostasis
and signaling during development, stem cell proliferation, metabolism, cancer,
wound responses and aging, displaying intriguing molecular and functional conservation
with vertebrate macrophages. Given the relative ease of genetics in Drosophila
compared to vertebrates, tools permitting visualization and genetic manipulation
of plasmatocytes and surrounding tissues independently at all stages would greatly
aid in fully understanding these processes, but are lacking. Here we describe
a comprehensive set of transgenic lines that allow this. These include extremely
brightly fluorescing mCherry-based lines that allow GAL4-independent visualization
of plasmatocyte nuclei, cytoplasm or actin cytoskeleton from embryonic Stage 8
through adulthood in both live and fixed samples even as heterozygotes, greatly
facilitating screening. These lines allow live visualization and tracking of embryonic
plasmatocytes, as well as larval plasmatocytes residing at the body wall or flowing
with the surrounding hemolymph. With confocal imaging, interactions of plasmatocytes
and inner tissues can be seen in live or fixed embryos, larvae and adults. They
permit efficient GAL4-independent FACS analysis/sorting of plasmatocytes throughout
life. To facilitate genetic analysis of reciprocal signaling, we have also made
a plasmatocyte-expressing QF2 line that in combination with extant GAL4 drivers
allows independent genetic manipulation of both plasmatocytes and surrounding
tissues, and a GAL80 line that blocks GAL4 drivers from affecting plasmatocytes,
both of which function from the early embryo to the adult.
acknowledged_ssus:
- _id: LifeSc
acknowledgement: ' A. Ratheesh also by Marie Curie IIF GA-2012-32950BB:DICJI, Marko
Roblek by the provincial government of Lower Austria, K. Valoskova and S. Wachner
by DOC Fellowships from the Austrian Academy of Sciences, '
article_processing_charge: No
author:
- first_name: Attila
full_name: György, Attila
id: 3BCEDBE0-F248-11E8-B48F-1D18A9856A87
last_name: György
orcid: 0000-0002-1819-198X
- first_name: Marko
full_name: Roblek, Marko
id: 3047D808-F248-11E8-B48F-1D18A9856A87
last_name: Roblek
orcid: 0000-0001-9588-1389
- first_name: Aparna
full_name: Ratheesh, Aparna
id: 2F064CFE-F248-11E8-B48F-1D18A9856A87
last_name: Ratheesh
orcid: 0000-0001-7190-0776
- first_name: Katarina
full_name: Valosková, Katarina
id: 46F146FC-F248-11E8-B48F-1D18A9856A87
last_name: Valosková
- first_name: Vera
full_name: Belyaeva, Vera
id: 47F080FE-F248-11E8-B48F-1D18A9856A87
last_name: Belyaeva
- first_name: Stephanie
full_name: Wachner, Stephanie
id: 2A95E7B0-F248-11E8-B48F-1D18A9856A87
last_name: Wachner
- first_name: Yutaka
full_name: Matsubayashi, Yutaka
last_name: Matsubayashi
- first_name: Besaiz
full_name: Sanchez Sanchez, Besaiz
last_name: Sanchez Sanchez
- first_name: Brian
full_name: Stramer, Brian
last_name: Stramer
- first_name: Daria E
full_name: Siekhaus, Daria E
id: 3D224B9E-F248-11E8-B48F-1D18A9856A87
last_name: Siekhaus
orcid: 0000-0001-8323-8353
citation:
ama: 'György A, Roblek M, Ratheesh A, et al. Tools allowing independent visualization
and genetic manipulation of Drosophila melanogaster macrophages and surrounding
tissues. G3: Genes, Genomes, Genetics. 2018;8(3):845-857. doi:10.1534/g3.117.300452'
apa: 'György, A., Roblek, M., Ratheesh, A., Valosková, K., Belyaeva, V., Wachner,
S., … Siekhaus, D. E. (2018). Tools allowing independent visualization and genetic
manipulation of Drosophila melanogaster macrophages and surrounding tissues. G3:
Genes, Genomes, Genetics. Genetics Society of America. https://doi.org/10.1534/g3.117.300452'
chicago: 'György, Attila, Marko Roblek, Aparna Ratheesh, Katarina Valosková, Vera
Belyaeva, Stephanie Wachner, Yutaka Matsubayashi, Besaiz Sanchez Sanchez, Brian
Stramer, and Daria E Siekhaus. “Tools Allowing Independent Visualization and Genetic
Manipulation of Drosophila Melanogaster Macrophages and Surrounding Tissues.”
G3: Genes, Genomes, Genetics. Genetics Society of America, 2018. https://doi.org/10.1534/g3.117.300452.'
ieee: 'A. György et al., “Tools allowing independent visualization and genetic
manipulation of Drosophila melanogaster macrophages and surrounding tissues,”
G3: Genes, Genomes, Genetics, vol. 8, no. 3. Genetics Society of America,
pp. 845–857, 2018.'
ista: 'György A, Roblek M, Ratheesh A, Valosková K, Belyaeva V, Wachner S, Matsubayashi
Y, Sanchez Sanchez B, Stramer B, Siekhaus DE. 2018. Tools allowing independent
visualization and genetic manipulation of Drosophila melanogaster macrophages
and surrounding tissues. G3: Genes, Genomes, Genetics. 8(3), 845–857.'
mla: 'György, Attila, et al. “Tools Allowing Independent Visualization and Genetic
Manipulation of Drosophila Melanogaster Macrophages and Surrounding Tissues.”
G3: Genes, Genomes, Genetics, vol. 8, no. 3, Genetics Society of America,
2018, pp. 845–57, doi:10.1534/g3.117.300452.'
short: 'A. György, M. Roblek, A. Ratheesh, K. Valosková, V. Belyaeva, S. Wachner,
Y. Matsubayashi, B. Sanchez Sanchez, B. Stramer, D.E. Siekhaus, G3: Genes, Genomes,
Genetics 8 (2018) 845–857.'
date_created: 2018-12-11T11:47:05Z
date_published: 2018-03-01T00:00:00Z
date_updated: 2024-03-28T23:30:30Z
day: '01'
ddc:
- '570'
department:
- _id: DaSi
doi: 10.1534/g3.117.300452
ec_funded: 1
external_id:
isi:
- '000426693300011'
file:
- access_level: open_access
checksum: 7d9d28b915159078a4ca7add568010e8
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:11:48Z
date_updated: 2020-07-14T12:46:56Z
file_id: '4905'
file_name: IST-2018-990-v1+1_2018_Gyoergy_Tools_allowing.pdf
file_size: 2251222
relation: main_file
file_date_updated: 2020-07-14T12:46:56Z
has_accepted_license: '1'
intvolume: ' 8'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 845 - 857
project:
- _id: 253B6E48-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P29638
name: Drosophila TNFa´s Funktion in Immunzellen
- _id: 253B6E48-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P29638
name: The role of Drosophila TNF alpha in immune cell invasion
- _id: 2637E9C0-B435-11E9-9278-68D0E5697425
grant_number: 'LSC16-021 '
name: Investigating the role of the novel major superfamily facilitator transporter
family member MFSD1 in metastasis
- _id: 2536F660-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '334077'
name: Investigating the role of transporters in invasive migration through junctions
publication: 'G3: Genes, Genomes, Genetics'
publication_status: published
publisher: Genetics Society of America
publist_id: '7271'
pubrep_id: '990'
quality_controlled: '1'
related_material:
record:
- id: '6530'
relation: research_paper
- id: '6543'
relation: research_paper
- id: '11193'
relation: dissertation_contains
status: public
- id: '6546'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Tools allowing independent visualization and genetic manipulation of Drosophila
melanogaster macrophages and surrounding tissues
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 8
year: '2018'
...
---
_id: '612'
abstract:
- lang: eng
text: Metabotropic GABAB receptors mediate slow inhibitory effects presynaptically
and postsynaptically through the modulation of different effector signalling pathways.
Here, we analysed the distribution of GABAB receptors using highly sensitive SDS-digested
freeze-fracture replica labelling in mouse cerebellar Purkinje cells. Immunoreactivity
for GABAB1 was observed on presynaptic and, more abundantly, on postsynaptic compartments,
showing both scattered and clustered distribution patterns. Quantitative analysis
of immunoparticles revealed a somato-dendritic gradient, with the density of immunoparticles
increasing 26-fold from somata to dendritic spines. To understand the spatial
relationship of GABAB receptors with two key effector ion channels, the G protein-gated
inwardly rectifying K+ (GIRK/Kir3) channel and the voltage-dependent Ca2+ channel,
biochemical and immunohistochemical approaches were performed. Co-immunoprecipitation
analysis demonstrated that GABAB receptors co-assembled with GIRK and CaV2.1 channels
in the cerebellum. Using double-labelling immunoelectron microscopic techniques,
co-clustering between GABAB1 and GIRK2 was detected in dendritic spines, whereas
they were mainly segregated in the dendritic shafts. In contrast, co-clustering
of GABAB1 and CaV2.1 was detected in dendritic shafts but not spines. Presynaptically,
although no significant co-clustering of GABAB1 and GIRK2 or CaV2.1 channels was
detected, inter-cluster distance for GABAB1 and GIRK2 was significantly smaller
in the active zone than in the dendritic shafts, and that for GABAB1 and CaV2.1
was significantly smaller in the active zone than in the dendritic shafts and
spines. Thus, GABAB receptors are associated with GIRK and CaV2.1 channels in
different subcellular compartments. These data provide a better framework for
understanding the different roles played by GABAB receptors and their effector
ion channels in the cerebellar network.
article_processing_charge: No
article_type: original
author:
- first_name: Rafael
full_name: Luján, Rafael
last_name: Luján
- first_name: Carolina
full_name: Aguado, Carolina
last_name: Aguado
- first_name: Francisco
full_name: Ciruela, Francisco
last_name: Ciruela
- first_name: Javier
full_name: Cózar, Javier
last_name: Cózar
- first_name: David
full_name: Kleindienst, David
id: 42E121A4-F248-11E8-B48F-1D18A9856A87
last_name: Kleindienst
- first_name: Luis
full_name: De La Ossa, Luis
last_name: De La Ossa
- first_name: Bernhard
full_name: Bettler, Bernhard
last_name: Bettler
- first_name: Kevin
full_name: Wickman, Kevin
last_name: Wickman
- first_name: Masahiko
full_name: Watanabe, Masahiko
last_name: Watanabe
- first_name: Ryuichi
full_name: Shigemoto, Ryuichi
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Yugo
full_name: Fukazawa, Yugo
last_name: Fukazawa
citation:
ama: Luján R, Aguado C, Ciruela F, et al. Differential association of GABAB receptors
with their effector ion channels in Purkinje cells. Brain Structure and Function.
2018;223(3):1565-1587. doi:10.1007/s00429-017-1568-y
apa: Luján, R., Aguado, C., Ciruela, F., Cózar, J., Kleindienst, D., De La Ossa,
L., … Fukazawa, Y. (2018). Differential association of GABAB receptors with their
effector ion channels in Purkinje cells. Brain Structure and Function.
Springer. https://doi.org/10.1007/s00429-017-1568-y
chicago: Luján, Rafael, Carolina Aguado, Francisco Ciruela, Javier Cózar, David
Kleindienst, Luis De La Ossa, Bernhard Bettler, et al. “Differential Association
of GABAB Receptors with Their Effector Ion Channels in Purkinje Cells.” Brain
Structure and Function. Springer, 2018. https://doi.org/10.1007/s00429-017-1568-y.
ieee: R. Luján et al., “Differential association of GABAB receptors with
their effector ion channels in Purkinje cells,” Brain Structure and Function,
vol. 223, no. 3. Springer, pp. 1565–1587, 2018.
ista: Luján R, Aguado C, Ciruela F, Cózar J, Kleindienst D, De La Ossa L, Bettler
B, Wickman K, Watanabe M, Shigemoto R, Fukazawa Y. 2018. Differential association
of GABAB receptors with their effector ion channels in Purkinje cells. Brain Structure
and Function. 223(3), 1565–1587.
mla: Luján, Rafael, et al. “Differential Association of GABAB Receptors with Their
Effector Ion Channels in Purkinje Cells.” Brain Structure and Function,
vol. 223, no. 3, Springer, 2018, pp. 1565–87, doi:10.1007/s00429-017-1568-y.
short: R. Luján, C. Aguado, F. Ciruela, J. Cózar, D. Kleindienst, L. De La Ossa,
B. Bettler, K. Wickman, M. Watanabe, R. Shigemoto, Y. Fukazawa, Brain Structure
and Function 223 (2018) 1565–1587.
date_created: 2018-12-11T11:47:29Z
date_published: 2018-04-01T00:00:00Z
date_updated: 2024-03-28T23:30:31Z
day: '01'
ddc:
- '571'
department:
- _id: RySh
doi: 10.1007/s00429-017-1568-y
ec_funded: 1
external_id:
isi:
- '000428419500030'
file:
- access_level: open_access
checksum: a55b3103476ecb5f4f983d8801807e8b
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:15:36Z
date_updated: 2020-07-14T12:47:20Z
file_id: '5157'
file_name: IST-2018-1013-v1+1_2018_Kleindienst_Differential.pdf
file_size: 5542926
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has_accepted_license: '1'
intvolume: ' 223'
isi: 1
issue: '3'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 1565 - 1587
project:
- _id: 25CBA828-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '720270'
name: Human Brain Project Specific Grant Agreement 1 (HBP SGA 1)
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
publication: Brain Structure and Function
publication_status: published
publisher: Springer
publist_id: '7192'
pubrep_id: '1013'
quality_controlled: '1'
related_material:
record:
- id: '9562'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Differential association of GABAB receptors with their effector ion channels
in Purkinje cells
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 223
year: '2018'
...
---
_id: '21'
abstract:
- lang: eng
text: Parvalbumin-positive (PV+) GABAergic interneurons in hippocampal microcircuits
are thought to play a key role in several higher network functions, such as feedforward
and feedback inhibition, network oscillations, and pattern separation. Fast lateral
inhibition mediated by GABAergic interneurons may implement a winner-takes-all
mechanism in the hippocampal input layer. However, it is not clear whether the
functional connectivity rules of granule cells (GCs) and interneurons in the dentate
gyrus are consistent with such a mechanism. Using simultaneous patch-clamp recordings
from up to seven GCs and up to four PV+ interneurons in the dentate gyrus, we
find that connectivity is structured in space, synapse-specific, and enriched
in specific disynaptic motifs. In contrast to the neocortex, lateral inhibition
in the dentate gyrus (in which a GC inhibits neighboring GCs via a PV+ interneuron)
is ~ 10-times more abundant than recurrent inhibition (in which a GC inhibits
itself). Thus, unique connectivity rules may enable the dentate gyrus to perform
specific higher-order computations
acknowledgement: This project received funding from the European Research Council
(ERC) under the European Union’s Horizon 2020 research and innovation programme
(grant agreement No 692692) and the Fond zur Förderung der Wissenschaftlichen Forschung
(Z 312-B27, Wittgenstein award), both to P.J..
article_number: '4605'
article_processing_charge: No
article_type: original
author:
- first_name: 'Claudia '
full_name: 'Espinoza Martinez, Claudia '
id: 31FFEE2E-F248-11E8-B48F-1D18A9856A87
last_name: Espinoza Martinez
orcid: 0000-0003-4710-2082
- first_name: José
full_name: Guzmán, José
id: 30CC5506-F248-11E8-B48F-1D18A9856A87
last_name: Guzmán
orcid: 0000-0003-2209-5242
- first_name: Xiaomin
full_name: Zhang, Xiaomin
id: 423EC9C2-F248-11E8-B48F-1D18A9856A87
last_name: Zhang
- first_name: Peter M
full_name: Jonas, Peter M
id: 353C1B58-F248-11E8-B48F-1D18A9856A87
last_name: Jonas
orcid: 0000-0001-5001-4804
citation:
ama: Espinoza Martinez C, Guzmán J, Zhang X, Jonas PM. Parvalbumin+ interneurons
obey unique connectivity rules and establish a powerful lateral-inhibition microcircuit
in dentate gyrus. Nature Communications. 2018;9(1). doi:10.1038/s41467-018-06899-3
apa: Espinoza Martinez, C., Guzmán, J., Zhang, X., & Jonas, P. M. (2018). Parvalbumin+
interneurons obey unique connectivity rules and establish a powerful lateral-inhibition
microcircuit in dentate gyrus. Nature Communications. Nature Publishing
Group. https://doi.org/10.1038/s41467-018-06899-3
chicago: Espinoza Martinez, Claudia , José Guzmán, Xiaomin Zhang, and Peter M Jonas.
“Parvalbumin+ Interneurons Obey Unique Connectivity Rules and Establish a Powerful
Lateral-Inhibition Microcircuit in Dentate Gyrus.” Nature Communications.
Nature Publishing Group, 2018. https://doi.org/10.1038/s41467-018-06899-3.
ieee: C. Espinoza Martinez, J. Guzmán, X. Zhang, and P. M. Jonas, “Parvalbumin+
interneurons obey unique connectivity rules and establish a powerful lateral-inhibition
microcircuit in dentate gyrus,” Nature Communications, vol. 9, no. 1. Nature
Publishing Group, 2018.
ista: Espinoza Martinez C, Guzmán J, Zhang X, Jonas PM. 2018. Parvalbumin+ interneurons
obey unique connectivity rules and establish a powerful lateral-inhibition microcircuit
in dentate gyrus. Nature Communications. 9(1), 4605.
mla: Espinoza Martinez, Claudia, et al. “Parvalbumin+ Interneurons Obey Unique Connectivity
Rules and Establish a Powerful Lateral-Inhibition Microcircuit in Dentate Gyrus.”
Nature Communications, vol. 9, no. 1, 4605, Nature Publishing Group, 2018,
doi:10.1038/s41467-018-06899-3.
short: C. Espinoza Martinez, J. Guzmán, X. Zhang, P.M. Jonas, Nature Communications
9 (2018).
date_created: 2018-12-11T11:44:12Z
date_published: 2018-11-02T00:00:00Z
date_updated: 2024-03-28T23:30:31Z
day: '02'
ddc:
- '570'
department:
- _id: PeJo
doi: 10.1038/s41467-018-06899-3
ec_funded: 1
external_id:
isi:
- '000449069700009'
file:
- access_level: open_access
checksum: 9fe2a63bd95a5067d896c087d07998f3
content_type: application/pdf
creator: dernst
date_created: 2018-12-17T15:41:57Z
date_updated: 2020-07-14T12:45:28Z
file_id: '5715'
file_name: 2018_NatureComm_Espinoza.pdf
file_size: 4651930
relation: main_file
file_date_updated: 2020-07-14T12:45:28Z
has_accepted_license: '1'
intvolume: ' 9'
isi: 1
issue: '1'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
project:
- _id: 25B7EB9E-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '692692'
name: Biophysics and circuit function of a giant cortical glumatergic synapse
- _id: 25C5A090-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: Z00312
name: The Wittgenstein Prize
publication: Nature Communications
publication_status: published
publisher: Nature Publishing Group
publist_id: '8034'
quality_controlled: '1'
related_material:
link:
- description: News on IST Homepage
relation: press_release
url: https://ist.ac.at/en/news/lateral-inhibition-keeps-similar-memories-apart/
record:
- id: '6363'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Parvalbumin+ interneurons obey unique connectivity rules and establish a powerful
lateral-inhibition microcircuit in dentate gyrus
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 9
year: '2018'
...
---
_id: '66'
abstract:
- lang: eng
text: 'Crypto-currencies are digital assets designed to work as a medium of exchange,
e.g., Bitcoin, but they are susceptible to attacks (dishonest behavior of participants).
A framework for the analysis of attacks in crypto-currencies requires (a) modeling
of game-theoretic aspects to analyze incentives for deviation from honest behavior;
(b) concurrent interactions between participants; and (c) analysis of long-term
monetary gains. Traditional game-theoretic approaches for the analysis of security
protocols consider either qualitative temporal properties such as safety and termination,
or the very special class of one-shot (stateless) games. However, to analyze general
attacks on protocols for crypto-currencies, both stateful analysis and quantitative
objectives are necessary. In this work our main contributions are as follows:
(a) we show how a class of concurrent mean-payo games, namely ergodic games, can
model various attacks that arise naturally in crypto-currencies; (b) we present
the first practical implementation of algorithms for ergodic games that scales
to model realistic problems for crypto-currencies; and (c) we present experimental
results showing that our framework can handle games with thousands of states and
millions of transitions.'
alternative_title:
- LIPIcs
article_number: '11'
article_processing_charge: No
author:
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Amir
full_name: Goharshady, Amir
id: 391365CE-F248-11E8-B48F-1D18A9856A87
last_name: Goharshady
orcid: 0000-0003-1702-6584
- first_name: Rasmus
full_name: Ibsen-Jensen, Rasmus
id: 3B699956-F248-11E8-B48F-1D18A9856A87
last_name: Ibsen-Jensen
orcid: 0000-0003-4783-0389
- first_name: Yaron
full_name: Velner, Yaron
last_name: Velner
citation:
ama: 'Chatterjee K, Goharshady AK, Ibsen-Jensen R, Velner Y. Ergodic mean-payoff
games for the analysis of attacks in crypto-currencies. In: Vol 118. Schloss Dagstuhl
- Leibniz-Zentrum für Informatik; 2018. doi:10.4230/LIPIcs.CONCUR.2018.11'
apa: 'Chatterjee, K., Goharshady, A. K., Ibsen-Jensen, R., & Velner, Y. (2018).
Ergodic mean-payoff games for the analysis of attacks in crypto-currencies (Vol.
118). Presented at the CONCUR: Conference on Concurrency Theory, Beijing, China:
Schloss Dagstuhl - Leibniz-Zentrum für Informatik. https://doi.org/10.4230/LIPIcs.CONCUR.2018.11'
chicago: Chatterjee, Krishnendu, Amir Kafshdar Goharshady, Rasmus Ibsen-Jensen,
and Yaron Velner. “Ergodic Mean-Payoff Games for the Analysis of Attacks in Crypto-Currencies,”
Vol. 118. Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2018. https://doi.org/10.4230/LIPIcs.CONCUR.2018.11.
ieee: 'K. Chatterjee, A. K. Goharshady, R. Ibsen-Jensen, and Y. Velner, “Ergodic
mean-payoff games for the analysis of attacks in crypto-currencies,” presented
at the CONCUR: Conference on Concurrency Theory, Beijing, China, 2018, vol. 118.'
ista: 'Chatterjee K, Goharshady AK, Ibsen-Jensen R, Velner Y. 2018. Ergodic mean-payoff
games for the analysis of attacks in crypto-currencies. CONCUR: Conference on
Concurrency Theory, LIPIcs, vol. 118, 11.'
mla: Chatterjee, Krishnendu, et al. Ergodic Mean-Payoff Games for the Analysis
of Attacks in Crypto-Currencies. Vol. 118, 11, Schloss Dagstuhl - Leibniz-Zentrum
für Informatik, 2018, doi:10.4230/LIPIcs.CONCUR.2018.11.
short: K. Chatterjee, A.K. Goharshady, R. Ibsen-Jensen, Y. Velner, in:, Schloss
Dagstuhl - Leibniz-Zentrum für Informatik, 2018.
conference:
end_date: 2018-09-07
location: Beijing, China
name: 'CONCUR: Conference on Concurrency Theory'
start_date: 2018-09-04
date_created: 2018-12-11T11:44:27Z
date_published: 2018-09-01T00:00:00Z
date_updated: 2024-03-28T23:30:34Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.4230/LIPIcs.CONCUR.2018.11
ec_funded: 1
external_id:
arxiv:
- '1806.03108'
file:
- access_level: open_access
checksum: 68a055b1aaa241cc38375083cf832a7d
content_type: application/pdf
creator: dernst
date_created: 2018-12-17T12:08:00Z
date_updated: 2020-07-14T12:47:34Z
file_id: '5696'
file_name: 2018_CONCUR_Chatterjee.pdf
file_size: 1078309
relation: main_file
file_date_updated: 2020-07-14T12:47:34Z
has_accepted_license: '1'
intvolume: ' 118'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 25892FC0-B435-11E9-9278-68D0E5697425
grant_number: ICT15-003
name: Efficient Algorithms for Computer Aided Verification
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '279307'
name: 'Quantitative Graph Games: Theory and Applications'
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
- _id: 266EEEC0-B435-11E9-9278-68D0E5697425
name: Quantitative Game-theoretic Analysis of Blockchain Applications and Smart
Contracts
publication_identifier:
isbn:
- 978-3-95977-087-3
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
publist_id: '7988'
quality_controlled: '1'
related_material:
record:
- id: '8934'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Ergodic mean-payoff games for the analysis of attacks in crypto-currencies
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 118
year: '2018'
...
---
_id: '311'
abstract:
- lang: eng
text: 'Smart contracts are computer programs that are executed by a network of mutually
distrusting agents, without the need of an external trusted authority. Smart contracts
handle and transfer assets of considerable value (in the form of crypto-currency
like Bitcoin). Hence, it is crucial that their implementation is bug-free. We
identify the utility (or expected payoff) of interacting with such smart contracts
as the basic and canonical quantitative property for such contracts. We present
a framework for such quantitative analysis of smart contracts. Such a formal framework
poses new and novel research challenges in programming languages, as it requires
modeling of game-theoretic aspects to analyze incentives for deviation from honest
behavior and modeling utilities which are not specified as standard temporal properties
such as safety and termination. While game-theoretic incentives have been analyzed
in the security community, their analysis has been restricted to the very special
case of stateless games. However, to analyze smart contracts, stateful analysis
is required as it must account for the different program states of the protocol.
Our main contributions are as follows: we present (i)~a simplified programming
language for smart contracts; (ii)~an automatic translation of the programs to
state-based games; (iii)~an abstraction-refinement approach to solve such games;
and (iv)~experimental results on real-world-inspired smart contracts.'
acknowledgement: 'The research was partially supported by Vienna Science and Technology
Fund (WWTF) Project ICT15-003, Austrian Science Fund (FWF) NFN Grant No S11407-N23
(RiSE/SHiNE), and ERC Starting grant (279307: Graph Games).'
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Amir
full_name: Goharshady, Amir
id: 391365CE-F248-11E8-B48F-1D18A9856A87
last_name: Goharshady
orcid: 0000-0003-1702-6584
- first_name: Yaron
full_name: Velner, Yaron
last_name: Velner
citation:
ama: 'Chatterjee K, Goharshady AK, Velner Y. Quantitative analysis of smart contracts.
In: Vol 10801. Springer; 2018:739-767. doi:10.1007/978-3-319-89884-1_26'
apa: 'Chatterjee, K., Goharshady, A. K., & Velner, Y. (2018). Quantitative analysis
of smart contracts (Vol. 10801, pp. 739–767). Presented at the ESOP: European
Symposium on Programming, Thessaloniki, Greece: Springer. https://doi.org/10.1007/978-3-319-89884-1_26'
chicago: Chatterjee, Krishnendu, Amir Kafshdar Goharshady, and Yaron Velner. “Quantitative
Analysis of Smart Contracts,” 10801:739–67. Springer, 2018. https://doi.org/10.1007/978-3-319-89884-1_26.
ieee: 'K. Chatterjee, A. K. Goharshady, and Y. Velner, “Quantitative analysis of
smart contracts,” presented at the ESOP: European Symposium on Programming, Thessaloniki,
Greece, 2018, vol. 10801, pp. 739–767.'
ista: 'Chatterjee K, Goharshady AK, Velner Y. 2018. Quantitative analysis of smart
contracts. ESOP: European Symposium on Programming, LNCS, vol. 10801, 739–767.'
mla: Chatterjee, Krishnendu, et al. Quantitative Analysis of Smart Contracts.
Vol. 10801, Springer, 2018, pp. 739–67, doi:10.1007/978-3-319-89884-1_26.
short: K. Chatterjee, A.K. Goharshady, Y. Velner, in:, Springer, 2018, pp. 739–767.
conference:
end_date: 2018-04-19
location: Thessaloniki, Greece
name: 'ESOP: European Symposium on Programming'
start_date: 2018-04-16
date_created: 2018-12-11T11:45:45Z
date_published: 2018-04-01T00:00:00Z
date_updated: 2024-03-28T23:30:33Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1007/978-3-319-89884-1_26
ec_funded: 1
file:
- access_level: open_access
checksum: 9c8a8338c571903b599b6ca93abd2cce
content_type: application/pdf
creator: dernst
date_created: 2018-12-17T15:45:49Z
date_updated: 2020-07-14T12:46:00Z
file_id: '5716'
file_name: 2018_ESOP_Chatterjee.pdf
file_size: 1394993
relation: main_file
file_date_updated: 2020-07-14T12:46:00Z
has_accepted_license: '1'
intvolume: ' 10801'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 739 - 767
project:
- _id: 25892FC0-B435-11E9-9278-68D0E5697425
grant_number: ICT15-003
name: Efficient Algorithms for Computer Aided Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '279307'
name: 'Quantitative Graph Games: Theory and Applications'
publication_status: published
publisher: Springer
publist_id: '7554'
quality_controlled: '1'
related_material:
record:
- id: '8934'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Quantitative analysis of smart contracts
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 10801
year: '2018'
...
---
_id: '6340'
abstract:
- lang: eng
text: We present a secure approach for maintaining andreporting credit history records on the Blockchain. Our ap-proach removes third-parties such as credit reporting agen-cies from the lending process and replaces them with smartcontracts. This allows customers to interact directly with thelenders or banks while ensuring the integrity, unmalleabilityand privacy of their credit data. Additionally, each customerhas full control over complete or selective disclosure of hercredit
records, eliminating the risk of privacy violations or databreaches. Moreover,
our approach provides strong guaranteesfor the lenders as well. A lender can check
both correctness andcompleteness of the credit data disclosed to her. This is
the firstapproach that can perform all credit reporting tasks withouta central authority or changing the financial mechanisms*.
article_processing_charge: No
author:
- first_name: Amir Kafshdar
full_name: Goharshady, Amir Kafshdar
id: 391365CE-F248-11E8-B48F-1D18A9856A87
last_name: Goharshady
orcid: 0000-0003-1702-6584
- first_name: Ali
full_name: Behrouz, Ali
last_name: Behrouz
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
citation:
ama: 'Goharshady AK, Behrouz A, Chatterjee K. Secure Credit Reporting on the Blockchain.
In: Proceedings of the IEEE International Conference on Blockchain. IEEE;
2018:1343-1348. doi:10.1109/Cybermatics_2018.2018.00231'
apa: 'Goharshady, A. K., Behrouz, A., & Chatterjee, K. (2018). Secure Credit
Reporting on the Blockchain. In Proceedings of the IEEE International Conference
on Blockchain (pp. 1343–1348). Halifax, Canada: IEEE. https://doi.org/10.1109/Cybermatics_2018.2018.00231'
chicago: Goharshady, Amir Kafshdar, Ali Behrouz, and Krishnendu Chatterjee. “Secure
Credit Reporting on the Blockchain.” In Proceedings of the IEEE International
Conference on Blockchain, 1343–48. IEEE, 2018. https://doi.org/10.1109/Cybermatics_2018.2018.00231.
ieee: A. K. Goharshady, A. Behrouz, and K. Chatterjee, “Secure Credit Reporting
on the Blockchain,” in Proceedings of the IEEE International Conference on
Blockchain, Halifax, Canada, 2018, pp. 1343–1348.
ista: Goharshady AK, Behrouz A, Chatterjee K. 2018. Secure Credit Reporting on the
Blockchain. Proceedings of the IEEE International Conference on Blockchain. IEEE
International Conference on Blockchain, 1343–1348.
mla: Goharshady, Amir Kafshdar, et al. “Secure Credit Reporting on the Blockchain.”
Proceedings of the IEEE International Conference on Blockchain, IEEE, 2018,
pp. 1343–48, doi:10.1109/Cybermatics_2018.2018.00231.
short: A.K. Goharshady, A. Behrouz, K. Chatterjee, in:, Proceedings of the IEEE
International Conference on Blockchain, IEEE, 2018, pp. 1343–1348.
conference:
end_date: 2018-08-03
location: Halifax, Canada
name: IEEE International Conference on Blockchain
start_date: 2018-07-30
date_created: 2019-04-18T10:37:35Z
date_published: 2018-09-01T00:00:00Z
date_updated: 2024-03-28T23:30:34Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1109/Cybermatics_2018.2018.00231
ec_funded: 1
external_id:
arxiv:
- '1805.09104'
isi:
- '000481634500196'
file:
- access_level: open_access
checksum: b25c9bb7cf6e7e6634e692d26d41ead8
content_type: application/pdf
creator: akafshda
date_created: 2019-04-18T10:36:39Z
date_updated: 2020-07-14T12:47:27Z
file_id: '6341'
file_name: blockchain2018.pdf
file_size: 624338
relation: main_file
file_date_updated: 2020-07-14T12:47:27Z
has_accepted_license: '1'
isi: 1
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '09'
oa: 1
oa_version: Submitted Version
page: 1343-1348
project:
- _id: 25892FC0-B435-11E9-9278-68D0E5697425
grant_number: ICT15-003
name: Efficient Algorithms for Computer Aided Verification
- _id: 266EEEC0-B435-11E9-9278-68D0E5697425
name: Quantitative Game-theoretic Analysis of Blockchain Applications and Smart
Contracts
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '279307'
name: 'Quantitative Graph Games: Theory and Applications'
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
publication: Proceedings of the IEEE International Conference on Blockchain
publication_identifier:
isbn:
- '978-1-5386-7975-3 '
publication_status: published
publisher: IEEE
quality_controlled: '1'
related_material:
record:
- id: '8934'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Secure Credit Reporting on the Blockchain
tmp:
image: /images/cc_by_nc_nd.png
legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
(CC BY-NC-ND 4.0)
short: CC BY-NC-ND (4.0)
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '6009'
abstract:
- lang: eng
text: "We study algorithmic questions wrt algebraic path properties in concurrent
systems, where the transitions of the system are labeled from a complete, closed
semiring. The algebraic path properties can model dataflow analysis problems,
the shortest path problem, and many other natural problems that arise in program
analysis. We consider that each component of the concurrent system is a graph
with constant treewidth, a property satisfied by the controlflow graphs of most
programs. We allow for multiple possible queries, which arise naturally in demand
driven dataflow analysis. The study of multiple queries allows us to consider
the tradeoff between the resource usage of the one-time preprocessing and for
each individual query. The traditional approach constructs the product graph of
all components and applies the best-known graph algorithm on the product. In this
approach, even the answer to a single query requires the transitive closure (i.e.,
the results of all possible queries), which provides no room for tradeoff between
preprocessing and query time.\r\nOur main contributions are algorithms that significantly
improve the worst-case running time of the traditional approach, and provide various
tradeoffs depending on the number of queries. For example, in a concurrent system
of two components, the traditional approach requires hexic time in the worst case
for answering one query as well as computing the transitive closure, whereas we
show that with one-time preprocessing in almost cubic time, each subsequent query
can be answered in at most linear time, and even the transitive closure can be
computed in almost quartic time. Furthermore, we establish conditional optimality
results showing that the worst-case running time of our algorithms cannot be improved
without achieving major breakthroughs in graph algorithms (i.e., improving the
worst-case bound for the shortest path problem in general graphs). Preliminary
experimental results show that our algorithms perform favorably on several benchmarks.\r\n"
article_number: '9'
article_processing_charge: No
author:
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Rasmus
full_name: Ibsen-Jensen, Rasmus
id: 3B699956-F248-11E8-B48F-1D18A9856A87
last_name: Ibsen-Jensen
orcid: 0000-0003-4783-0389
- first_name: Amir Kafshdar
full_name: Goharshady, Amir Kafshdar
id: 391365CE-F248-11E8-B48F-1D18A9856A87
last_name: Goharshady
orcid: 0000-0003-1702-6584
- first_name: Andreas
full_name: Pavlogiannis, Andreas
id: 49704004-F248-11E8-B48F-1D18A9856A87
last_name: Pavlogiannis
orcid: 0000-0002-8943-0722
citation:
ama: Chatterjee K, Ibsen-Jensen R, Goharshady AK, Pavlogiannis A. Algorithms for
algebraic path properties in concurrent systems of constant treewidth components.
ACM Transactions on Programming Languages and Systems. 2018;40(3). doi:10.1145/3210257
apa: Chatterjee, K., Ibsen-Jensen, R., Goharshady, A. K., & Pavlogiannis, A.
(2018). Algorithms for algebraic path properties in concurrent systems of constant
treewidth components. ACM Transactions on Programming Languages and Systems.
Association for Computing Machinery (ACM). https://doi.org/10.1145/3210257
chicago: Chatterjee, Krishnendu, Rasmus Ibsen-Jensen, Amir Kafshdar Goharshady,
and Andreas Pavlogiannis. “Algorithms for Algebraic Path Properties in Concurrent
Systems of Constant Treewidth Components.” ACM Transactions on Programming
Languages and Systems. Association for Computing Machinery (ACM), 2018. https://doi.org/10.1145/3210257.
ieee: K. Chatterjee, R. Ibsen-Jensen, A. K. Goharshady, and A. Pavlogiannis, “Algorithms
for algebraic path properties in concurrent systems of constant treewidth components,”
ACM Transactions on Programming Languages and Systems, vol. 40, no. 3.
Association for Computing Machinery (ACM), 2018.
ista: Chatterjee K, Ibsen-Jensen R, Goharshady AK, Pavlogiannis A. 2018. Algorithms
for algebraic path properties in concurrent systems of constant treewidth components.
ACM Transactions on Programming Languages and Systems. 40(3), 9.
mla: Chatterjee, Krishnendu, et al. “Algorithms for Algebraic Path Properties in
Concurrent Systems of Constant Treewidth Components.” ACM Transactions on Programming
Languages and Systems, vol. 40, no. 3, 9, Association for Computing Machinery
(ACM), 2018, doi:10.1145/3210257.
short: K. Chatterjee, R. Ibsen-Jensen, A.K. Goharshady, A. Pavlogiannis, ACM Transactions
on Programming Languages and Systems 40 (2018).
date_created: 2019-02-14T14:31:52Z
date_published: 2018-08-01T00:00:00Z
date_updated: 2024-03-28T23:30:34Z
day: '01'
department:
- _id: KrCh
doi: 10.1145/3210257
ec_funded: 1
external_id:
arxiv:
- '1510.07565'
isi:
- '000444694800001'
intvolume: ' 40'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1510.07565
month: '08'
oa: 1
oa_version: Preprint
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P 23499-N23
name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '279307'
name: 'Quantitative Graph Games: Theory and Applications'
publication: ACM Transactions on Programming Languages and Systems
publication_identifier:
issn:
- 0164-0925
publication_status: published
publisher: Association for Computing Machinery (ACM)
quality_controlled: '1'
related_material:
record:
- id: '1437'
relation: earlier_version
status: public
- id: '5441'
relation: earlier_version
status: public
- id: '5442'
relation: earlier_version
status: public
- id: '8934'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Algorithms for algebraic path properties in concurrent systems of constant
treewidth components
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 40
year: '2018'
...
---
_id: '5977'
abstract:
- lang: eng
text: 'We consider the stochastic shortest path (SSP)problem for succinct Markov
decision processes(MDPs), where the MDP consists of a set of vari-ables, and a
set of nondeterministic rules that up-date the variables. First, we show that
several ex-amples from the AI literature can be modeled assuccinct MDPs. Then
we present computationalapproaches for upper and lower bounds for theSSP problem:
(a) for computing upper bounds, ourmethod is polynomial-time in the implicit descrip-tion
of the MDP; (b) for lower bounds, we present apolynomial-time (in the size of
the implicit descrip-tion) reduction to quadratic programming. Our ap-proach is
applicable even to infinite-state MDPs.Finally, we present experimental results
to demon-strate the effectiveness of our approach on severalclassical examples
from the AI literature.'
article_processing_charge: No
author:
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Hongfei
full_name: Fu, Hongfei
id: 3AAD03D6-F248-11E8-B48F-1D18A9856A87
last_name: Fu
- first_name: Amir
full_name: Goharshady, Amir
id: 391365CE-F248-11E8-B48F-1D18A9856A87
last_name: Goharshady
orcid: 0000-0003-1702-6584
- first_name: Nastaran
full_name: Okati, Nastaran
last_name: Okati
citation:
ama: 'Chatterjee K, Fu H, Goharshady AK, Okati N. Computational approaches for stochastic
shortest path on succinct MDPs. In: Proceedings of the Twenty-Seventh International
Joint Conference on Artificial Intelligence. Vol 2018. IJCAI; 2018:4700-4707.
doi:10.24963/ijcai.2018/653'
apa: 'Chatterjee, K., Fu, H., Goharshady, A. K., & Okati, N. (2018). Computational
approaches for stochastic shortest path on succinct MDPs. In Proceedings of
the Twenty-Seventh International Joint Conference on Artificial Intelligence
(Vol. 2018, pp. 4700–4707). Stockholm, Sweden: IJCAI. https://doi.org/10.24963/ijcai.2018/653'
chicago: Chatterjee, Krishnendu, Hongfei Fu, Amir Kafshdar Goharshady, and Nastaran
Okati. “Computational Approaches for Stochastic Shortest Path on Succinct MDPs.”
In Proceedings of the Twenty-Seventh International Joint Conference on Artificial
Intelligence, 2018:4700–4707. IJCAI, 2018. https://doi.org/10.24963/ijcai.2018/653.
ieee: K. Chatterjee, H. Fu, A. K. Goharshady, and N. Okati, “Computational approaches
for stochastic shortest path on succinct MDPs,” in Proceedings of the Twenty-Seventh
International Joint Conference on Artificial Intelligence, Stockholm, Sweden,
2018, vol. 2018, pp. 4700–4707.
ista: 'Chatterjee K, Fu H, Goharshady AK, Okati N. 2018. Computational approaches
for stochastic shortest path on succinct MDPs. Proceedings of the Twenty-Seventh
International Joint Conference on Artificial Intelligence. IJCAI: International
Joint Conference on Artificial Intelligence vol. 2018, 4700–4707.'
mla: Chatterjee, Krishnendu, et al. “Computational Approaches for Stochastic Shortest
Path on Succinct MDPs.” Proceedings of the Twenty-Seventh International Joint
Conference on Artificial Intelligence, vol. 2018, IJCAI, 2018, pp. 4700–07,
doi:10.24963/ijcai.2018/653.
short: K. Chatterjee, H. Fu, A.K. Goharshady, N. Okati, in:, Proceedings of the
Twenty-Seventh International Joint Conference on Artificial Intelligence, IJCAI,
2018, pp. 4700–4707.
conference:
end_date: 2018-07-19
location: Stockholm, Sweden
name: 'IJCAI: International Joint Conference on Artificial Intelligence'
start_date: 2018-07-13
date_created: 2019-02-13T13:26:27Z
date_published: 2018-07-17T00:00:00Z
date_updated: 2024-03-28T23:30:34Z
day: '17'
department:
- _id: KrCh
doi: 10.24963/ijcai.2018/653
ec_funded: 1
external_id:
arxiv:
- '1804.08984'
isi:
- '000764175404118'
intvolume: ' 2018'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1804.08984
month: '07'
oa: 1
oa_version: Preprint
page: 4700-4707
project:
- _id: 25892FC0-B435-11E9-9278-68D0E5697425
grant_number: ICT15-003
name: Efficient Algorithms for Computer Aided Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '279307'
name: 'Quantitative Graph Games: Theory and Applications'
publication: Proceedings of the Twenty-Seventh International Joint Conference on Artificial
Intelligence
publication_identifier:
isbn:
- 978-099924112-7
issn:
- '10450823'
publication_status: published
publisher: IJCAI
quality_controlled: '1'
related_material:
record:
- id: '8934'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Computational approaches for stochastic shortest path on succinct MDPs
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 2018
year: '2018'
...
---
_id: '422'
abstract:
- lang: eng
text: We show that a rather simple, steady modification of the streamwise velocity
profile in a pipe can lead to a complete collapse of turbulence and the flow fully
relaminarizes. Two different devices, a stationary obstacle (inset) and a device
which injects fluid through an annular gap close to the wall, are used to control
the flow. Both devices modify the streamwise velocity profile such that the flow
in the center of the pipe is decelerated and the flow in the near wall region
is accelerated. We present measurements with stereoscopic particle image velocimetry
to investigate and capture the development of the relaminarizing flow downstream
these devices and the specific circumstances responsible for relaminarization.
We find total relaminarization up to Reynolds numbers of 6000, where the skin
friction in the far downstream distance is reduced by a factor of 3.4 due to relaminarization.
In a smooth straight pipe the flow remains completely laminar downstream of the
control. Furthermore, we show that transient (temporary) relaminarization in a
spatially confined region right downstream the devices occurs also at much higher
Reynolds numbers, accompanied by a significant local skin friction drag reduction.
The underlying physical mechanism of relaminarization is attributed to a weakening
of the near-wall turbulence production cycle.
article_processing_charge: Yes (via OA deal)
author:
- first_name: Jakob
full_name: Kühnen, Jakob
id: 3A47AE32-F248-11E8-B48F-1D18A9856A87
last_name: Kühnen
orcid: 0000-0003-4312-0179
- first_name: Davide
full_name: Scarselli, Davide
id: 40315C30-F248-11E8-B48F-1D18A9856A87
last_name: Scarselli
orcid: 0000-0001-5227-4271
- first_name: Markus
full_name: Schaner, Markus
id: 316CE034-F248-11E8-B48F-1D18A9856A87
last_name: Schaner
- first_name: Björn
full_name: Hof, Björn
id: 3A374330-F248-11E8-B48F-1D18A9856A87
last_name: Hof
orcid: 0000-0003-2057-2754
citation:
ama: Kühnen J, Scarselli D, Schaner M, Hof B. Relaminarization by steady modification
of the streamwise velocity profile in a pipe. Flow Turbulence and Combustion.
2018;100(4):919-942. doi:10.1007/s10494-018-9896-4
apa: Kühnen, J., Scarselli, D., Schaner, M., & Hof, B. (2018). Relaminarization
by steady modification of the streamwise velocity profile in a pipe. Flow Turbulence
and Combustion. Springer. https://doi.org/10.1007/s10494-018-9896-4
chicago: Kühnen, Jakob, Davide Scarselli, Markus Schaner, and Björn Hof. “Relaminarization
by Steady Modification of the Streamwise Velocity Profile in a Pipe.” Flow
Turbulence and Combustion. Springer, 2018. https://doi.org/10.1007/s10494-018-9896-4.
ieee: J. Kühnen, D. Scarselli, M. Schaner, and B. Hof, “Relaminarization by steady
modification of the streamwise velocity profile in a pipe,” Flow Turbulence
and Combustion, vol. 100, no. 4. Springer, pp. 919–942, 2018.
ista: Kühnen J, Scarselli D, Schaner M, Hof B. 2018. Relaminarization by steady
modification of the streamwise velocity profile in a pipe. Flow Turbulence and
Combustion. 100(4), 919–942.
mla: Kühnen, Jakob, et al. “Relaminarization by Steady Modification of the Streamwise
Velocity Profile in a Pipe.” Flow Turbulence and Combustion, vol. 100,
no. 4, Springer, 2018, pp. 919–42, doi:10.1007/s10494-018-9896-4.
short: J. Kühnen, D. Scarselli, M. Schaner, B. Hof, Flow Turbulence and Combustion
100 (2018) 919–942.
date_created: 2018-12-11T11:46:23Z
date_published: 2018-01-01T00:00:00Z
date_updated: 2024-03-28T23:30:36Z
day: '01'
ddc:
- '530'
department:
- _id: BjHo
doi: 10.1007/s10494-018-9896-4
ec_funded: 1
external_id:
isi:
- '000433113900004'
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checksum: d7c0bade150faabca150b0a9986e60ca
content_type: application/pdf
creator: dernst
date_created: 2018-12-17T15:52:37Z
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file_id: '5717'
file_name: 2018_FlowTurbulenceCombust_Kuehnen.pdf
file_size: 2210020
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intvolume: ' 100'
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language:
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month: '01'
oa: 1
oa_version: Published Version
page: 919 - 942
project:
- _id: 25152F3A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '306589'
name: Decoding the complexity of turbulence at its origin
publication: Flow Turbulence and Combustion
publication_status: published
publisher: Springer
publist_id: '7401'
quality_controlled: '1'
related_material:
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- id: '7258'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Relaminarization by steady modification of the streamwise velocity profile
in a pipe
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 100
year: '2018'
...
---
_id: '461'
abstract:
- lang: eng
text: Turbulence is the major cause of friction losses in transport processes and
it is responsible for a drastic drag increase in flows over bounding surfaces.
While much effort is invested into developing ways to control and reduce turbulence
intensities, so far no methods exist to altogether eliminate turbulence if velocities
are sufficiently large. We demonstrate for pipe flow that appropriate distortions
to the velocity profile lead to a complete collapse of turbulence and subsequently
friction losses are reduced by as much as 90%. Counterintuitively, the return
to laminar motion is accomplished by initially increasing turbulence intensities
or by transiently amplifying wall shear. Since neither the Reynolds number nor
the shear stresses decrease (the latter often increase), these measures are not
indicative of turbulence collapse. Instead, an amplification mechanism measuring
the interaction between eddies and the mean shear is found to set a threshold
below which turbulence is suppressed beyond recovery.
acknowledgement: We acknowledge the European Research Council under the European Union’s
Seventh Framework Programme (FP/2007-2013)/ERC Grant Agreement 306589, the European
Research Council (ERC) under the European Union’s Horizon 2020 research and innovation
programme (grant agreement no. 737549) and the Deutsche Forschungsgemeinschaft (Project
No. FOR 1182) for financial support. We thank our technician P. Maier for providing
highly valuable ideas and greatly supporting us in all technical aspects. We thank
M. Schaner for technical drawings, construction and design. We thank M. Schwegel
for a Matlab code to post-process experimental data.
article_processing_charge: No
author:
- first_name: Jakob
full_name: Kühnen, Jakob
id: 3A47AE32-F248-11E8-B48F-1D18A9856A87
last_name: Kühnen
orcid: 0000-0003-4312-0179
- first_name: Baofang
full_name: Song, Baofang
last_name: Song
- first_name: Davide
full_name: Scarselli, Davide
id: 40315C30-F248-11E8-B48F-1D18A9856A87
last_name: Scarselli
orcid: 0000-0001-5227-4271
- first_name: Nazmi B
full_name: Budanur, Nazmi B
id: 3EA1010E-F248-11E8-B48F-1D18A9856A87
last_name: Budanur
orcid: 0000-0003-0423-5010
- first_name: Michael
full_name: Riedl, Michael
id: 3BE60946-F248-11E8-B48F-1D18A9856A87
last_name: Riedl
orcid: 0000-0003-4844-6311
- first_name: Ashley
full_name: Willis, Ashley
last_name: Willis
- first_name: Marc
full_name: Avila, Marc
last_name: Avila
- first_name: Björn
full_name: Hof, Björn
id: 3A374330-F248-11E8-B48F-1D18A9856A87
last_name: Hof
orcid: 0000-0003-2057-2754
citation:
ama: Kühnen J, Song B, Scarselli D, et al. Destabilizing turbulence in pipe flow.
Nature Physics. 2018;14:386-390. doi:10.1038/s41567-017-0018-3
apa: Kühnen, J., Song, B., Scarselli, D., Budanur, N. B., Riedl, M., Willis, A.,
… Hof, B. (2018). Destabilizing turbulence in pipe flow. Nature Physics.
Nature Publishing Group. https://doi.org/10.1038/s41567-017-0018-3
chicago: Kühnen, Jakob, Baofang Song, Davide Scarselli, Nazmi B Budanur, Michael
Riedl, Ashley Willis, Marc Avila, and Björn Hof. “Destabilizing Turbulence in
Pipe Flow.” Nature Physics. Nature Publishing Group, 2018. https://doi.org/10.1038/s41567-017-0018-3.
ieee: J. Kühnen et al., “Destabilizing turbulence in pipe flow,” Nature
Physics, vol. 14. Nature Publishing Group, pp. 386–390, 2018.
ista: Kühnen J, Song B, Scarselli D, Budanur NB, Riedl M, Willis A, Avila M, Hof
B. 2018. Destabilizing turbulence in pipe flow. Nature Physics. 14, 386–390.
mla: Kühnen, Jakob, et al. “Destabilizing Turbulence in Pipe Flow.” Nature Physics,
vol. 14, Nature Publishing Group, 2018, pp. 386–90, doi:10.1038/s41567-017-0018-3.
short: J. Kühnen, B. Song, D. Scarselli, N.B. Budanur, M. Riedl, A. Willis, M. Avila,
B. Hof, Nature Physics 14 (2018) 386–390.
date_created: 2018-12-11T11:46:36Z
date_published: 2018-01-08T00:00:00Z
date_updated: 2024-03-28T23:30:36Z
day: '08'
department:
- _id: BjHo
doi: 10.1038/s41567-017-0018-3
ec_funded: 1
external_id:
isi:
- '000429434100020'
intvolume: ' 14'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1711.06543
month: '01'
oa: 1
oa_version: Preprint
page: 386-390
project:
- _id: 25152F3A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '306589'
name: Decoding the complexity of turbulence at its origin
- _id: 25104D44-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '737549'
name: Eliminating turbulence in oil pipelines
publication: Nature Physics
publication_status: published
publisher: Nature Publishing Group
publist_id: '7360'
quality_controlled: '1'
related_material:
record:
- id: '12726'
relation: dissertation_contains
status: public
- id: '14530'
relation: dissertation_contains
status: public
- id: '7258'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Destabilizing turbulence in pipe flow
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 14
year: '2018'
...
---
_id: '449'
abstract:
- lang: eng
text: Auxin is unique among plant hormones due to its directional transport that
is mediated by the polarly distributed PIN auxin transporters at the plasma membrane.
The canalization hypothesis proposes that the auxin feedback on its polar flow
is a crucial, plant-specific mechanism mediating multiple self-organizing developmental
processes. Here, we used the auxin effect on the PIN polar localization in Arabidopsis
thaliana roots as a proxy for the auxin feedback on the PIN polarity during canalization.
We performed microarray experiments to find regulators of this process that act
downstream of auxin. We identified genes that were transcriptionally regulated
by auxin in an AXR3/IAA17- and ARF7/ARF19-dependent manner. Besides the known
components of the PIN polarity, such as PID and PIP5K kinases, a number of potential
new regulators were detected, among which the WRKY23 transcription factor, which
was characterized in more detail. Gain- and loss-of-function mutants confirmed
a role for WRKY23 in mediating the auxin effect on the PIN polarity. Accordingly,
processes requiring auxin-mediated PIN polarity rearrangements, such as vascular
tissue development during leaf venation, showed a higher WRKY23 expression and
required the WRKY23 activity. Our results provide initial insights into the auxin
transcriptional network acting upstream of PIN polarization and, potentially,
canalization-mediated plant development.
article_processing_charge: Yes
author:
- first_name: Tomas
full_name: Prat, Tomas
id: 3DA3BFEE-F248-11E8-B48F-1D18A9856A87
last_name: Prat
- first_name: Jakub
full_name: Hajny, Jakub
id: 4800CC20-F248-11E8-B48F-1D18A9856A87
last_name: Hajny
orcid: 0000-0003-2140-7195
- first_name: Wim
full_name: Grunewald, Wim
last_name: Grunewald
- first_name: Mina K
full_name: Vasileva, Mina K
id: 3407EB18-F248-11E8-B48F-1D18A9856A87
last_name: Vasileva
- first_name: Gergely
full_name: Molnar, Gergely
id: 34F1AF46-F248-11E8-B48F-1D18A9856A87
last_name: Molnar
- first_name: Ricardo
full_name: Tejos, Ricardo
last_name: Tejos
- first_name: Markus
full_name: Schmid, Markus
last_name: Schmid
- first_name: Michael
full_name: Sauer, Michael
last_name: Sauer
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
citation:
ama: Prat T, Hajny J, Grunewald W, et al. WRKY23 is a component of the transcriptional
network mediating auxin feedback on PIN polarity. PLoS Genetics. 2018;14(1).
doi:10.1371/journal.pgen.1007177
apa: Prat, T., Hajny, J., Grunewald, W., Vasileva, M. K., Molnar, G., Tejos, R.,
… Friml, J. (2018). WRKY23 is a component of the transcriptional network mediating
auxin feedback on PIN polarity. PLoS Genetics. Public Library of Science.
https://doi.org/10.1371/journal.pgen.1007177
chicago: Prat, Tomas, Jakub Hajny, Wim Grunewald, Mina K Vasileva, Gergely Molnar,
Ricardo Tejos, Markus Schmid, Michael Sauer, and Jiří Friml. “WRKY23 Is a Component
of the Transcriptional Network Mediating Auxin Feedback on PIN Polarity.” PLoS
Genetics. Public Library of Science, 2018. https://doi.org/10.1371/journal.pgen.1007177.
ieee: T. Prat et al., “WRKY23 is a component of the transcriptional network
mediating auxin feedback on PIN polarity,” PLoS Genetics, vol. 14, no.
1. Public Library of Science, 2018.
ista: Prat T, Hajny J, Grunewald W, Vasileva MK, Molnar G, Tejos R, Schmid M, Sauer
M, Friml J. 2018. WRKY23 is a component of the transcriptional network mediating
auxin feedback on PIN polarity. PLoS Genetics. 14(1).
mla: Prat, Tomas, et al. “WRKY23 Is a Component of the Transcriptional Network Mediating
Auxin Feedback on PIN Polarity.” PLoS Genetics, vol. 14, no. 1, Public
Library of Science, 2018, doi:10.1371/journal.pgen.1007177.
short: T. Prat, J. Hajny, W. Grunewald, M.K. Vasileva, G. Molnar, R. Tejos, M. Schmid,
M. Sauer, J. Friml, PLoS Genetics 14 (2018).
date_created: 2018-12-11T11:46:32Z
date_published: 2018-01-29T00:00:00Z
date_updated: 2024-03-28T23:30:38Z
day: '29'
ddc:
- '581'
department:
- _id: JiFr
doi: 10.1371/journal.pgen.1007177
ec_funded: 1
external_id:
isi:
- '000423718600034'
file:
- access_level: open_access
checksum: 0276d66788ec076f4924164a39e6a712
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:10:52Z
date_updated: 2020-07-14T12:46:30Z
file_id: '4843'
file_name: IST-2018-967-v1+1_journal.pgen.1007177.pdf
file_size: 24709062
relation: main_file
file_date_updated: 2020-07-14T12:46:30Z
has_accepted_license: '1'
intvolume: ' 14'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: 25716A02-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '282300'
name: Polarity and subcellular dynamics in plants
publication: PLoS Genetics
publication_status: published
publisher: Public Library of Science
publist_id: '7373'
pubrep_id: '967'
quality_controlled: '1'
related_material:
record:
- id: '1127'
relation: dissertation_contains
status: public
- id: '7172'
relation: dissertation_contains
status: public
- id: '8822'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: WRKY23 is a component of the transcriptional network mediating auxin feedback
on PIN polarity
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 14
year: '2018'
...
---
_id: '191'
abstract:
- lang: eng
text: Intercellular distribution of the plant hormone auxin largely depends on the
polar subcellular distribution of the plasma membrane PIN-FORMED (PIN) auxin transporters.
PIN polarity switches in response to different developmental and environmental
signals have been shown to redirect auxin fluxes mediating certain developmental
responses. PIN phosphorylation at different sites and by different kinases is
crucial for PIN function. Here we investigate the role of PIN phosphorylation
during gravitropic response. Loss- and gain-of-function mutants in PINOID and
related kinases but not in D6PK kinase as well as mutations mimicking constitutive
dephosphorylated or phosphorylated status of two clusters of predicted phosphorylation
sites partially disrupted PIN3 phosphorylation and caused defects in gravitropic
bending in roots and hypocotyls. In particular, they impacted PIN3 polarity rearrangements
in response to gravity and during feed-back regulation by auxin itself. Thus PIN
phosphorylation, besides regulating transport activity and apical-basal targeting,
is also important for the rapid polarity switches in response to environmental
and endogenous signals.
article_number: '10279'
article_processing_charge: No
author:
- first_name: Peter
full_name: Grones, Peter
id: 399876EC-F248-11E8-B48F-1D18A9856A87
last_name: Grones
- first_name: Melinda F
full_name: Abas, Melinda F
id: 3CFB3B1C-F248-11E8-B48F-1D18A9856A87
last_name: Abas
- first_name: Jakub
full_name: Hajny, Jakub
id: 4800CC20-F248-11E8-B48F-1D18A9856A87
last_name: Hajny
orcid: 0000-0003-2140-7195
- first_name: Angharad
full_name: Jones, Angharad
last_name: Jones
- first_name: Sascha
full_name: Waidmann, Sascha
last_name: Waidmann
- first_name: Jürgen
full_name: Kleine Vehn, Jürgen
last_name: Kleine Vehn
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
citation:
ama: Grones P, Abas MF, Hajny J, et al. PID/WAG-mediated phosphorylation of the
Arabidopsis PIN3 auxin transporter mediates polarity switches during gravitropism.
Scientific Reports. 2018;8(1). doi:10.1038/s41598-018-28188-1
apa: Grones, P., Abas, M. F., Hajny, J., Jones, A., Waidmann, S., Kleine Vehn, J.,
& Friml, J. (2018). PID/WAG-mediated phosphorylation of the Arabidopsis PIN3
auxin transporter mediates polarity switches during gravitropism. Scientific
Reports. Springer. https://doi.org/10.1038/s41598-018-28188-1
chicago: Grones, Peter, Melinda F Abas, Jakub Hajny, Angharad Jones, Sascha Waidmann,
Jürgen Kleine Vehn, and Jiří Friml. “PID/WAG-Mediated Phosphorylation of the Arabidopsis
PIN3 Auxin Transporter Mediates Polarity Switches during Gravitropism.” Scientific
Reports. Springer, 2018. https://doi.org/10.1038/s41598-018-28188-1.
ieee: P. Grones et al., “PID/WAG-mediated phosphorylation of the Arabidopsis
PIN3 auxin transporter mediates polarity switches during gravitropism,” Scientific
Reports, vol. 8, no. 1. Springer, 2018.
ista: Grones P, Abas MF, Hajny J, Jones A, Waidmann S, Kleine Vehn J, Friml J. 2018.
PID/WAG-mediated phosphorylation of the Arabidopsis PIN3 auxin transporter mediates
polarity switches during gravitropism. Scientific Reports. 8(1), 10279.
mla: Grones, Peter, et al. “PID/WAG-Mediated Phosphorylation of the Arabidopsis
PIN3 Auxin Transporter Mediates Polarity Switches during Gravitropism.” Scientific
Reports, vol. 8, no. 1, 10279, Springer, 2018, doi:10.1038/s41598-018-28188-1.
short: P. Grones, M.F. Abas, J. Hajny, A. Jones, S. Waidmann, J. Kleine Vehn, J.
Friml, Scientific Reports 8 (2018).
date_created: 2018-12-11T11:45:06Z
date_published: 2018-07-06T00:00:00Z
date_updated: 2024-03-28T23:30:38Z
day: '06'
ddc:
- '581'
department:
- _id: JiFr
- _id: EvBe
doi: 10.1038/s41598-018-28188-1
ec_funded: 1
external_id:
isi:
- '000437673200053'
file:
- access_level: open_access
checksum: 266b03f4fb8198e83141617aaa99dcab
content_type: application/pdf
creator: dernst
date_created: 2018-12-17T15:38:56Z
date_updated: 2020-07-14T12:45:20Z
file_id: '5714'
file_name: 2018_ScientificReports_Grones.pdf
file_size: 2413876
relation: main_file
file_date_updated: 2020-07-14T12:45:20Z
has_accepted_license: '1'
intvolume: ' 8'
isi: 1
issue: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 25716A02-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '282300'
name: Polarity and subcellular dynamics in plants
- _id: 261099A6-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '742985'
name: Tracing Evolution of Auxin Transport and Polarity in Plants
publication: Scientific Reports
publication_status: published
publisher: Springer
publist_id: '7729'
quality_controlled: '1'
related_material:
record:
- id: '8822'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: PID/WAG-mediated phosphorylation of the Arabidopsis PIN3 auxin transporter
mediates polarity switches during gravitropism
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 8
year: '2018'
...
---
_id: '15'
abstract:
- lang: eng
text: Although much is known about the physiological framework of T cell motility,
and numerous rate-limiting molecules have been identified through loss-of-function
approaches, an integrated functional concept of T cell motility is lacking. Here,
we used in vivo precision morphometry together with analysis of cytoskeletal dynamics
in vitro to deconstruct the basic mechanisms of T cell migration within lymphatic
organs. We show that the contributions of the integrin LFA-1 and the chemokine
receptor CCR7 are complementary rather than positioned in a linear pathway, as
they are during leukocyte extravasation from the blood vasculature. Our data demonstrate
that CCR7 controls cortical actin flows, whereas integrins mediate substrate friction
that is sufficient to drive locomotion in the absence of considerable surface
adhesions and plasma membrane flux.
acknowledged_ssus:
- _id: SSU
acknowledgement: This work was funded by grants from the European Research Council
(ERC StG 281556 and CoG 724373) and the Austrian Science Foundation (FWF) to M.S.
and by Swiss National Foundation (SNF) project grants 31003A_135649, 31003A_153457
and CR23I3_156234 to J.V.S. F.G. received funding from the European Union’s Horizon
2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement
no. 747687, and J.R. was funded by an EMBO long-term fellowship (ALTF 1396-2014).
article_processing_charge: No
author:
- first_name: Miroslav
full_name: Hons, Miroslav
id: 4167FE56-F248-11E8-B48F-1D18A9856A87
last_name: Hons
orcid: 0000-0002-6625-3348
- first_name: Aglaja
full_name: Kopf, Aglaja
id: 31DAC7B6-F248-11E8-B48F-1D18A9856A87
last_name: Kopf
orcid: 0000-0002-2187-6656
- first_name: Robert
full_name: Hauschild, Robert
id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87
last_name: Hauschild
orcid: 0000-0001-9843-3522
- first_name: Alexander F
full_name: Leithner, Alexander F
id: 3B1B77E4-F248-11E8-B48F-1D18A9856A87
last_name: Leithner
orcid: 0000-0002-1073-744X
- first_name: Florian R
full_name: Gärtner, Florian R
id: 397A88EE-F248-11E8-B48F-1D18A9856A87
last_name: Gärtner
orcid: 0000-0001-6120-3723
- first_name: Jun
full_name: Abe, Jun
last_name: Abe
- first_name: Jörg
full_name: Renkawitz, Jörg
id: 3F0587C8-F248-11E8-B48F-1D18A9856A87
last_name: Renkawitz
orcid: 0000-0003-2856-3369
- first_name: Jens
full_name: Stein, Jens
last_name: Stein
- first_name: Michael K
full_name: Sixt, Michael K
id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
last_name: Sixt
orcid: 0000-0002-6620-9179
citation:
ama: Hons M, Kopf A, Hauschild R, et al. Chemokines and integrins independently
tune actin flow and substrate friction during intranodal migration of T cells.
Nature Immunology. 2018;19(6):606-616. doi:10.1038/s41590-018-0109-z
apa: Hons, M., Kopf, A., Hauschild, R., Leithner, A. F., Gärtner, F. R., Abe, J.,
… Sixt, M. K. (2018). Chemokines and integrins independently tune actin flow and
substrate friction during intranodal migration of T cells. Nature Immunology.
Nature Publishing Group. https://doi.org/10.1038/s41590-018-0109-z
chicago: Hons, Miroslav, Aglaja Kopf, Robert Hauschild, Alexander F Leithner, Florian
R Gärtner, Jun Abe, Jörg Renkawitz, Jens Stein, and Michael K Sixt. “Chemokines
and Integrins Independently Tune Actin Flow and Substrate Friction during Intranodal
Migration of T Cells.” Nature Immunology. Nature Publishing Group, 2018.
https://doi.org/10.1038/s41590-018-0109-z.
ieee: M. Hons et al., “Chemokines and integrins independently tune actin
flow and substrate friction during intranodal migration of T cells,” Nature
Immunology, vol. 19, no. 6. Nature Publishing Group, pp. 606–616, 2018.
ista: Hons M, Kopf A, Hauschild R, Leithner AF, Gärtner FR, Abe J, Renkawitz J,
Stein J, Sixt MK. 2018. Chemokines and integrins independently tune actin flow
and substrate friction during intranodal migration of T cells. Nature Immunology.
19(6), 606–616.
mla: Hons, Miroslav, et al. “Chemokines and Integrins Independently Tune Actin Flow
and Substrate Friction during Intranodal Migration of T Cells.” Nature Immunology,
vol. 19, no. 6, Nature Publishing Group, 2018, pp. 606–16, doi:10.1038/s41590-018-0109-z.
short: M. Hons, A. Kopf, R. Hauschild, A.F. Leithner, F.R. Gärtner, J. Abe, J. Renkawitz,
J. Stein, M.K. Sixt, Nature Immunology 19 (2018) 606–616.
date_created: 2018-12-11T11:44:10Z
date_published: 2018-05-18T00:00:00Z
date_updated: 2024-03-28T23:30:40Z
day: '18'
department:
- _id: MiSi
- _id: Bio
doi: 10.1038/s41590-018-0109-z
ec_funded: 1
external_id:
isi:
- '000433041500026'
pmid:
- '29777221'
intvolume: ' 19'
isi: 1
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.ncbi.nlm.nih.gov/pubmed/29777221
month: '05'
oa: 1
oa_version: Published Version
page: 606 - 616
pmid: 1
project:
- _id: 25FE9508-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '724373'
name: Cellular navigation along spatial gradients
- _id: 260AA4E2-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '747687'
name: Mechanical Adaptation of Lamellipodial Actin Networks in Migrating Cells
- _id: 25A48D24-B435-11E9-9278-68D0E5697425
grant_number: ALTF 1396-2014
name: Molecular and system level view of immune cell migration
- _id: 25A603A2-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '281556'
name: Cytoskeletal force generation and force transduction of migrating leukocytes
(EU)
publication: Nature Immunology
publication_status: published
publisher: Nature Publishing Group
publist_id: '8040'
quality_controlled: '1'
related_material:
record:
- id: '6891'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Chemokines and integrins independently tune actin flow and substrate friction
during intranodal migration of T cells
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 19
year: '2018'
...
---
_id: '442'
abstract:
- lang: eng
text: The rapid auxin-triggered growth of the Arabidopsis hypocotyls involves the
nuclear TIR1/AFB-Aux/IAA signaling and is accompanied by acidification of the
apoplast and cell walls (Fendrych et al., 2016). Here, we describe in detail the
method for analysis of the elongation and the TIR1/AFB-Aux/IAA-dependent auxin
response in hypocotyl segments as well as the determination of relative values
of the cell wall pH.
acknowledgement: 'This protocol was adapted from Fendrych et al., 2016. This project
has received funding from the European Union’s Horizon 2020 research and innovation
programme under the Marie Skłodowska-Curie Grant Agreement No. 665385, and Austrian
Science Fund (FWF) [M 2128-B21]. '
article_processing_charge: No
article_type: original
author:
- first_name: Lanxin
full_name: Li, Lanxin
id: 367EF8FA-F248-11E8-B48F-1D18A9856A87
last_name: Li
orcid: 0000-0002-5607-272X
- first_name: Gabriel
full_name: Krens, Gabriel
id: 2B819732-F248-11E8-B48F-1D18A9856A87
last_name: Krens
orcid: 0000-0003-4761-5996
- first_name: Matyas
full_name: Fendrych, Matyas
id: 43905548-F248-11E8-B48F-1D18A9856A87
last_name: Fendrych
orcid: 0000-0002-9767-8699
- first_name: Jirí
full_name: Friml, Jirí
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
citation:
ama: Li L, Krens G, Fendrych M, Friml J. Real-time analysis of auxin response, cell
wall pH and elongation in Arabidopsis thaliana Hypocotyls. Bio-protocol.
2018;8(1). doi:10.21769/BioProtoc.2685
apa: Li, L., Krens, G., Fendrych, M., & Friml, J. (2018). Real-time analysis
of auxin response, cell wall pH and elongation in Arabidopsis thaliana Hypocotyls.
Bio-Protocol. Bio-protocol. https://doi.org/10.21769/BioProtoc.2685
chicago: Li, Lanxin, Gabriel Krens, Matyas Fendrych, and Jiří Friml. “Real-Time
Analysis of Auxin Response, Cell Wall PH and Elongation in Arabidopsis Thaliana
Hypocotyls.” Bio-Protocol. Bio-protocol, 2018. https://doi.org/10.21769/BioProtoc.2685.
ieee: L. Li, G. Krens, M. Fendrych, and J. Friml, “Real-time analysis of auxin response,
cell wall pH and elongation in Arabidopsis thaliana Hypocotyls,” Bio-protocol,
vol. 8, no. 1. Bio-protocol, 2018.
ista: Li L, Krens G, Fendrych M, Friml J. 2018. Real-time analysis of auxin response,
cell wall pH and elongation in Arabidopsis thaliana Hypocotyls. Bio-protocol.
8(1).
mla: Li, Lanxin, et al. “Real-Time Analysis of Auxin Response, Cell Wall PH and
Elongation in Arabidopsis Thaliana Hypocotyls.” Bio-Protocol, vol. 8, no.
1, Bio-protocol, 2018, doi:10.21769/BioProtoc.2685.
short: L. Li, G. Krens, M. Fendrych, J. Friml, Bio-Protocol 8 (2018).
date_created: 2018-12-11T11:46:30Z
date_published: 2018-01-05T00:00:00Z
date_updated: 2024-03-28T23:30:43Z
day: '05'
ddc:
- '576'
- '581'
department:
- _id: JiFr
- _id: Bio
doi: 10.21769/BioProtoc.2685
ec_funded: 1
file:
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checksum: 6644ba698206eda32b0abf09128e63e3
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:17:43Z
date_updated: 2020-07-14T12:46:29Z
file_id: '5299'
file_name: IST-2018-970-v1+1_2018_Lanxin_Real-time_analysis.pdf
file_size: 11352389
relation: main_file
file_date_updated: 2020-07-14T12:46:29Z
has_accepted_license: '1'
intvolume: ' 8'
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '665385'
name: International IST Doctoral Program
publication: Bio-protocol
publication_identifier:
eissn:
- 2331-8325
publication_status: published
publisher: Bio-protocol
publist_id: '7381'
pubrep_id: '970'
quality_controlled: '1'
related_material:
record:
- id: '10083'
relation: dissertation_contains
status: public
status: public
title: Real-time analysis of auxin response, cell wall pH and elongation in Arabidopsis
thaliana Hypocotyls
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2018'
...
---
_id: '3'
abstract:
- lang: eng
text: SETD5 gene mutations have been identified as a frequent cause of idiopathic
intellectual disability. Here we show that Setd5-haploinsufficient mice present
developmental defects such as abnormal brain-to-body weight ratios and neural
crest defect-associated phenotypes. Furthermore, Setd5-mutant mice show impairments
in cognitive tasks, enhanced long-term potentiation, delayed ontogenetic profile
of ultrasonic vocalization, and behavioral inflexibility. Behavioral issues are
accompanied by abnormal expression of postsynaptic density proteins previously
associated with cognition. Our data additionally indicate that Setd5 regulates
RNA polymerase II dynamics and gene transcription via its interaction with the
Hdac3 and Paf1 complexes, findings potentially explaining the gene expression
defects observed in Setd5-haploinsufficient mice. Our results emphasize the decisive
role of Setd5 in a biological pathway found to be disrupted in humans with intellectual
disability and autism spectrum disorder.
acknowledged_ssus:
- _id: M-Shop
- _id: PreCl
acknowledgement: This work was supported by the Simons Foundation Autism Research
Initiative (grant 401299) to G.N. and the DFG (SPP1738 grant NO 1249) to K.-M.N.
article_processing_charge: No
article_type: original
author:
- first_name: Elena
full_name: Deliu, Elena
id: 37A40D7E-F248-11E8-B48F-1D18A9856A87
last_name: Deliu
orcid: 0000-0002-7370-5293
- first_name: Niccoló
full_name: Arecco, Niccoló
last_name: Arecco
- first_name: Jasmin
full_name: Morandell, Jasmin
id: 4739D480-F248-11E8-B48F-1D18A9856A87
last_name: Morandell
- first_name: Christoph
full_name: Dotter, Christoph
id: 4C66542E-F248-11E8-B48F-1D18A9856A87
last_name: Dotter
orcid: 0000-0002-9033-9096
- first_name: Ximena
full_name: Contreras, Ximena
id: 475990FE-F248-11E8-B48F-1D18A9856A87
last_name: Contreras
- first_name: Charles
full_name: Girardot, Charles
last_name: Girardot
- first_name: Eva
full_name: Käsper, Eva
last_name: Käsper
- first_name: Alena
full_name: Kozlova, Alena
id: C50A9596-02D0-11E9-976E-E38CFE5CBC1D
last_name: Kozlova
- first_name: Kasumi
full_name: Kishi, Kasumi
id: 3065DFC4-F248-11E8-B48F-1D18A9856A87
last_name: Kishi
- first_name: Ilaria
full_name: Chiaradia, Ilaria
id: B6467F20-02D0-11E9-BDA5-E960C241894A
last_name: Chiaradia
orcid: 0000-0002-9529-4464
- first_name: Kyung
full_name: Noh, Kyung
last_name: Noh
- first_name: Gaia
full_name: Novarino, Gaia
id: 3E57A680-F248-11E8-B48F-1D18A9856A87
last_name: Novarino
orcid: 0000-0002-7673-7178
citation:
ama: Deliu E, Arecco N, Morandell J, et al. Haploinsufficiency of the intellectual
disability gene SETD5 disturbs developmental gene expression and cognition. Nature
Neuroscience. 2018;21(12):1717-1727. doi:10.1038/s41593-018-0266-2
apa: Deliu, E., Arecco, N., Morandell, J., Dotter, C., Contreras, X., Girardot,
C., … Novarino, G. (2018). Haploinsufficiency of the intellectual disability gene
SETD5 disturbs developmental gene expression and cognition. Nature Neuroscience.
Nature Publishing Group. https://doi.org/10.1038/s41593-018-0266-2
chicago: Deliu, Elena, Niccoló Arecco, Jasmin Morandell, Christoph Dotter, Ximena
Contreras, Charles Girardot, Eva Käsper, et al. “Haploinsufficiency of the Intellectual
Disability Gene SETD5 Disturbs Developmental Gene Expression and Cognition.” Nature
Neuroscience. Nature Publishing Group, 2018. https://doi.org/10.1038/s41593-018-0266-2.
ieee: E. Deliu et al., “Haploinsufficiency of the intellectual disability
gene SETD5 disturbs developmental gene expression and cognition,” Nature Neuroscience,
vol. 21, no. 12. Nature Publishing Group, pp. 1717–1727, 2018.
ista: Deliu E, Arecco N, Morandell J, Dotter C, Contreras X, Girardot C, Käsper
E, Kozlova A, Kishi K, Chiaradia I, Noh K, Novarino G. 2018. Haploinsufficiency
of the intellectual disability gene SETD5 disturbs developmental gene expression
and cognition. Nature Neuroscience. 21(12), 1717–1727.
mla: Deliu, Elena, et al. “Haploinsufficiency of the Intellectual Disability Gene
SETD5 Disturbs Developmental Gene Expression and Cognition.” Nature Neuroscience,
vol. 21, no. 12, Nature Publishing Group, 2018, pp. 1717–27, doi:10.1038/s41593-018-0266-2.
short: E. Deliu, N. Arecco, J. Morandell, C. Dotter, X. Contreras, C. Girardot,
E. Käsper, A. Kozlova, K. Kishi, I. Chiaradia, K. Noh, G. Novarino, Nature Neuroscience
21 (2018) 1717–1727.
date_created: 2018-12-11T11:44:05Z
date_published: 2018-11-19T00:00:00Z
date_updated: 2024-03-28T23:30:45Z
day: '19'
ddc:
- '570'
department:
- _id: GaNo
- _id: EdHa
doi: 10.1038/s41593-018-0266-2
external_id:
isi:
- '000451324700010'
file:
- access_level: open_access
checksum: 60abd0f05b7cdc08a6b0ec460884084f
content_type: application/pdf
creator: dernst
date_created: 2019-04-09T07:41:57Z
date_updated: 2020-07-14T12:45:58Z
file_id: '6255'
file_name: 2017_NatureNeuroscience_Deliu.pdf
file_size: 8167169
relation: main_file
file_date_updated: 2020-07-14T12:45:58Z
has_accepted_license: '1'
intvolume: ' 21'
isi: 1
issue: '12'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Submitted Version
page: 1717 - 1727
project:
- _id: 254BA948-B435-11E9-9278-68D0E5697425
grant_number: '401299'
name: Probing development and reversibility of autism spectrum disorders
publication: Nature Neuroscience
publication_status: published
publisher: Nature Publishing Group
publist_id: '8054'
pubrep_id: '1071'
quality_controlled: '1'
related_material:
link:
- description: News on IST Homepage
relation: press_release
url: https://ist.ac.at/en/news/mutation-that-causes-autism-and-intellectual-disability-makes-brain-less-flexible/
record:
- id: '6074'
relation: popular_science
status: public
- id: '12364'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental
gene expression and cognition
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 21
year: '2018'
...
---
_id: '2'
abstract:
- lang: eng
text: Indirect reciprocity explores how humans act when their reputation is at stake,
and which social norms they use to assess the actions of others. A crucial question
in indirect reciprocity is which social norms can maintain stable cooperation
in a society. Past research has highlighted eight such norms, called “leading-eight”
strategies. This past research, however, is based on the assumption that all relevant
information about other population members is publicly available and that everyone
agrees on who is good or bad. Instead, here we explore the reputation dynamics
when information is private and noisy. We show that under these conditions, most
leading-eight strategies fail to evolve. Those leading-eight strategies that do
evolve are unable to sustain full cooperation.Indirect reciprocity is a mechanism
for cooperation based on shared moral systems and individual reputations. It assumes
that members of a community routinely observe and assess each other and that they
use this information to decide who is good or bad, and who deserves cooperation.
When information is transmitted publicly, such that all community members agree
on each other’s reputation, previous research has highlighted eight crucial moral
systems. These “leading-eight” strategies can maintain cooperation and resist
invasion by defectors. However, in real populations individuals often hold their
own private views of others. Once two individuals disagree about their opinion
of some third party, they may also see its subsequent actions in a different light.
Their opinions may further diverge over time. Herein, we explore indirect reciprocity
when information transmission is private and noisy. We find that in the presence
of perception errors, most leading-eight strategies cease to be stable. Even if
a leading-eight strategy evolves, cooperation rates may drop considerably when
errors are common. Our research highlights the role of reliable information and
synchronized reputations to maintain stable moral systems.
article_processing_charge: No
author:
- first_name: Christian
full_name: Hilbe, Christian
id: 2FDF8F3C-F248-11E8-B48F-1D18A9856A87
last_name: Hilbe
orcid: 0000-0001-5116-955X
- first_name: Laura
full_name: Schmid, Laura
id: 38B437DE-F248-11E8-B48F-1D18A9856A87
last_name: Schmid
orcid: 0000-0002-6978-7329
- first_name: Josef
full_name: Tkadlec, Josef
id: 3F24CCC8-F248-11E8-B48F-1D18A9856A87
last_name: Tkadlec
orcid: 0000-0002-1097-9684
- first_name: Krishnendu
full_name: Chatterjee, Krishnendu
id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
last_name: Chatterjee
orcid: 0000-0002-4561-241X
- first_name: Martin
full_name: Nowak, Martin
last_name: Nowak
citation:
ama: Hilbe C, Schmid L, Tkadlec J, Chatterjee K, Nowak M. Indirect reciprocity with
private, noisy, and incomplete information. PNAS. 2018;115(48):12241-12246.
doi:10.1073/pnas.1810565115
apa: Hilbe, C., Schmid, L., Tkadlec, J., Chatterjee, K., & Nowak, M. (2018).
Indirect reciprocity with private, noisy, and incomplete information. PNAS.
National Academy of Sciences. https://doi.org/10.1073/pnas.1810565115
chicago: Hilbe, Christian, Laura Schmid, Josef Tkadlec, Krishnendu Chatterjee, and
Martin Nowak. “Indirect Reciprocity with Private, Noisy, and Incomplete Information.”
PNAS. National Academy of Sciences, 2018. https://doi.org/10.1073/pnas.1810565115.
ieee: C. Hilbe, L. Schmid, J. Tkadlec, K. Chatterjee, and M. Nowak, “Indirect reciprocity
with private, noisy, and incomplete information,” PNAS, vol. 115, no. 48.
National Academy of Sciences, pp. 12241–12246, 2018.
ista: Hilbe C, Schmid L, Tkadlec J, Chatterjee K, Nowak M. 2018. Indirect reciprocity
with private, noisy, and incomplete information. PNAS. 115(48), 12241–12246.
mla: Hilbe, Christian, et al. “Indirect Reciprocity with Private, Noisy, and Incomplete
Information.” PNAS, vol. 115, no. 48, National Academy of Sciences, 2018,
pp. 12241–46, doi:10.1073/pnas.1810565115.
short: C. Hilbe, L. Schmid, J. Tkadlec, K. Chatterjee, M. Nowak, PNAS 115 (2018)
12241–12246.
date_created: 2018-12-11T11:44:05Z
date_published: 2018-11-27T00:00:00Z
date_updated: 2024-03-28T23:30:45Z
day: '27'
department:
- _id: KrCh
doi: 10.1073/pnas.1810565115
ec_funded: 1
external_id:
isi:
- '000451351000063'
pmid:
- '30429320'
intvolume: ' 115'
isi: 1
issue: '48'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.ncbi.nlm.nih.gov/pubmed/30429320
month: '11'
oa: 1
oa_version: Submitted Version
page: 12241-12246
pmid: 1
project:
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '279307'
name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2584A770-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P 23499-N23
name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: S 11407_N23
name: Rigorous Systems Engineering
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
related_material:
link:
- description: News on IST Homepage
relation: press_release
url: https://ist.ac.at/en/news/no-cooperation-without-open-communication/
record:
- id: '10293'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Indirect reciprocity with private, noisy, and incomplete information
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 115
year: '2018'
...
---
_id: '67'
abstract:
- lang: eng
text: 'Gene regulatory networks evolve through rewiring of individual components—that
is, through changes in regulatory connections. However, the mechanistic basis
of regulatory rewiring is poorly understood. Using a canonical gene regulatory
system, we quantify the properties of transcription factors that determine the
evolutionary potential for rewiring of regulatory connections: robustness, tunability
and evolvability. In vivo repression measurements of two repressors at mutated
operator sites reveal their contrasting evolutionary potential: while robustness
and evolvability were positively correlated, both were in trade-off with tunability.
Epistatic interactions between adjacent operators alleviated this trade-off. A
thermodynamic model explains how the differences in robustness, tunability and
evolvability arise from biophysical characteristics of repressor–DNA binding.
The model also uncovers that the energy matrix, which describes how mutations
affect repressor–DNA binding, encodes crucial information about the evolutionary
potential of a repressor. The biophysical determinants of evolutionary potential
for regulatory rewiring constitute a mechanistic framework for understanding network
evolution.'
article_processing_charge: No
article_type: original
author:
- first_name: Claudia
full_name: Igler, Claudia
id: 46613666-F248-11E8-B48F-1D18A9856A87
last_name: Igler
- first_name: Mato
full_name: Lagator, Mato
id: 345D25EC-F248-11E8-B48F-1D18A9856A87
last_name: Lagator
- first_name: Gasper
full_name: Tkacik, Gasper
id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
last_name: Tkacik
orcid: 0000-0002-6699-1455
- first_name: Jonathan P
full_name: Bollback, Jonathan P
id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
last_name: Bollback
orcid: 0000-0002-4624-4612
- first_name: Calin C
full_name: Guet, Calin C
id: 47F8433E-F248-11E8-B48F-1D18A9856A87
last_name: Guet
orcid: 0000-0001-6220-2052
citation:
ama: Igler C, Lagator M, Tkačik G, Bollback JP, Guet CC. Evolutionary potential
of transcription factors for gene regulatory rewiring. Nature Ecology and Evolution.
2018;2(10):1633-1643. doi:10.1038/s41559-018-0651-y
apa: Igler, C., Lagator, M., Tkačik, G., Bollback, J. P., & Guet, C. C. (2018).
Evolutionary potential of transcription factors for gene regulatory rewiring.
Nature Ecology and Evolution. Nature Publishing Group. https://doi.org/10.1038/s41559-018-0651-y
chicago: Igler, Claudia, Mato Lagator, Gašper Tkačik, Jonathan P Bollback, and Calin
C Guet. “Evolutionary Potential of Transcription Factors for Gene Regulatory Rewiring.”
Nature Ecology and Evolution. Nature Publishing Group, 2018. https://doi.org/10.1038/s41559-018-0651-y.
ieee: C. Igler, M. Lagator, G. Tkačik, J. P. Bollback, and C. C. Guet, “Evolutionary
potential of transcription factors for gene regulatory rewiring,” Nature Ecology
and Evolution, vol. 2, no. 10. Nature Publishing Group, pp. 1633–1643, 2018.
ista: Igler C, Lagator M, Tkačik G, Bollback JP, Guet CC. 2018. Evolutionary potential
of transcription factors for gene regulatory rewiring. Nature Ecology and Evolution.
2(10), 1633–1643.
mla: Igler, Claudia, et al. “Evolutionary Potential of Transcription Factors for
Gene Regulatory Rewiring.” Nature Ecology and Evolution, vol. 2, no. 10,
Nature Publishing Group, 2018, pp. 1633–43, doi:10.1038/s41559-018-0651-y.
short: C. Igler, M. Lagator, G. Tkačik, J.P. Bollback, C.C. Guet, Nature Ecology
and Evolution 2 (2018) 1633–1643.
date_created: 2018-12-11T11:44:27Z
date_published: 2018-09-10T00:00:00Z
date_updated: 2024-03-28T23:30:49Z
day: '10'
ddc:
- '570'
department:
- _id: CaGu
- _id: GaTk
- _id: JoBo
doi: 10.1038/s41559-018-0651-y
ec_funded: 1
external_id:
isi:
- '000447947600021'
file:
- access_level: open_access
checksum: 383a2e2c944a856e2e821ec8e7bf71b6
content_type: application/pdf
creator: dernst
date_created: 2020-05-14T11:28:52Z
date_updated: 2020-07-14T12:47:37Z
file_id: '7830'
file_name: 2018_NatureEcology_Igler.pdf
file_size: 1135973
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has_accepted_license: '1'
intvolume: ' 2'
isi: 1
issue: '10'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Submitted Version
page: 1633 - 1643
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
- _id: 2578D616-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '648440'
name: Selective Barriers to Horizontal Gene Transfer
- _id: 251EE76E-B435-11E9-9278-68D0E5697425
grant_number: '24573'
name: Design principles underlying genetic switch architecture (DOC Fellowship)
publication: Nature Ecology and Evolution
publication_status: published
publisher: Nature Publishing Group
publist_id: '7987'
quality_controlled: '1'
related_material:
record:
- id: '5585'
relation: popular_science
status: public
- id: '6371'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Evolutionary potential of transcription factors for gene regulatory rewiring
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 2
year: '2018'
...
---
_id: '5585'
abstract:
- lang: eng
text: Mean repression values and standard error of the mean are given for all operator
mutant libraries.
article_processing_charge: No
author:
- first_name: Claudia
full_name: Igler, Claudia
id: 46613666-F248-11E8-B48F-1D18A9856A87
last_name: Igler
- first_name: Mato
full_name: Lagator, Mato
id: 345D25EC-F248-11E8-B48F-1D18A9856A87
last_name: Lagator
- first_name: Gasper
full_name: Tkacik, Gasper
id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
last_name: Tkacik
orcid: 0000-0002-6699-1455
- first_name: Jonathan P
full_name: Bollback, Jonathan P
id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
last_name: Bollback
orcid: 0000-0002-4624-4612
- first_name: Calin C
full_name: Guet, Calin C
id: 47F8433E-F248-11E8-B48F-1D18A9856A87
last_name: Guet
orcid: 0000-0001-6220-2052
citation:
ama: Igler C, Lagator M, Tkačik G, Bollback JP, Guet CC. Data for the paper Evolutionary
potential of transcription factors for gene regulatory rewiring. 2018. doi:10.15479/AT:ISTA:108
apa: Igler, C., Lagator, M., Tkačik, G., Bollback, J. P., & Guet, C. C. (2018).
Data for the paper Evolutionary potential of transcription factors for gene regulatory
rewiring. Institute of Science and Technology Austria. https://doi.org/10.15479/AT:ISTA:108
chicago: Igler, Claudia, Mato Lagator, Gašper Tkačik, Jonathan P Bollback, and Calin
C Guet. “Data for the Paper Evolutionary Potential of Transcription Factors for
Gene Regulatory Rewiring.” Institute of Science and Technology Austria, 2018.
https://doi.org/10.15479/AT:ISTA:108.
ieee: C. Igler, M. Lagator, G. Tkačik, J. P. Bollback, and C. C. Guet, “Data for
the paper Evolutionary potential of transcription factors for gene regulatory
rewiring.” Institute of Science and Technology Austria, 2018.
ista: Igler C, Lagator M, Tkačik G, Bollback JP, Guet CC. 2018. Data for the paper
Evolutionary potential of transcription factors for gene regulatory rewiring,
Institute of Science and Technology Austria, 10.15479/AT:ISTA:108.
mla: Igler, Claudia, et al. Data for the Paper Evolutionary Potential of Transcription
Factors for Gene Regulatory Rewiring. Institute of Science and Technology
Austria, 2018, doi:10.15479/AT:ISTA:108.
short: C. Igler, M. Lagator, G. Tkačik, J.P. Bollback, C.C. Guet, (2018).
datarep_id: '108'
date_created: 2018-12-12T12:31:40Z
date_published: 2018-07-20T00:00:00Z
date_updated: 2024-03-28T23:30:49Z
day: '20'
ddc:
- '576'
department:
- _id: CaGu
- _id: GaTk
doi: 10.15479/AT:ISTA:108
ec_funded: 1
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creator: system
date_created: 2018-12-12T13:02:45Z
date_updated: 2020-07-14T12:47:07Z
file_id: '5611'
file_name: IST-2018-108-v1+1_data_figures.xlsx
file_size: 16507
relation: main_file
file_date_updated: 2020-07-14T12:47:07Z
has_accepted_license: '1'
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
- _id: 2578D616-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '648440'
name: Selective Barriers to Horizontal Gene Transfer
- _id: 251EE76E-B435-11E9-9278-68D0E5697425
grant_number: '24573'
name: Design principles underlying genetic switch architecture (DOC Fellowship)
publisher: Institute of Science and Technology Austria
related_material:
record:
- id: '67'
relation: research_paper
status: public
- id: '6371'
relation: research_paper
status: public
status: public
title: Data for the paper Evolutionary potential of transcription factors for gene
regulatory rewiring
tmp:
image: /images/cc_0.png
legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
name: Creative Commons Public Domain Dedication (CC0 1.0)
short: CC0 (1.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '1013'
abstract:
- lang: eng
text: From microwave ovens to satellite television to the GPS and data services
on our mobile phones, microwave technology is everywhere today. But one technology
that has so far failed to prove its worth in this wavelength regime is quantum
communication that uses the states of single photons as information carriers.
This is because single microwave photons, as opposed to classical microwave signals,
are extremely vulnerable to noise from thermal excitations in the channels through
which they travel. Two new independent studies, one by Ze-Liang Xiang at Technische
Universität Wien (Vienna), Austria, and colleagues [1] and another by Benoît Vermersch
at the University of Innsbruck, also in Austria, and colleagues [2] now describe
a theoretical protocol for microwave quantum communication that is resilient to
thermal and other types of noise. Their approach could become a powerful technique
to establish fast links between superconducting data processors in a future all-microwave
quantum network.
article_processing_charge: No
article_type: review
author:
- first_name: Johannes M
full_name: Fink, Johannes M
id: 4B591CBA-F248-11E8-B48F-1D18A9856A87
last_name: Fink
orcid: 0000-0001-8112-028X
citation:
ama: 'Fink JM. Viewpoint: Microwave quantum states beat the heat. Physics.
2017;10(32). doi:10.1103/Physics.10.32'
apa: 'Fink, J. M. (2017). Viewpoint: Microwave quantum states beat the heat. Physics.
American Physical Society. https://doi.org/10.1103/Physics.10.32'
chicago: 'Fink, Johannes M. “Viewpoint: Microwave Quantum States Beat the Heat.”
Physics. American Physical Society, 2017. https://doi.org/10.1103/Physics.10.32.'
ieee: 'J. M. Fink, “Viewpoint: Microwave quantum states beat the heat,” Physics,
vol. 10, no. 32. American Physical Society, 2017.'
ista: 'Fink JM. 2017. Viewpoint: Microwave quantum states beat the heat. Physics.
10(32).'
mla: 'Fink, Johannes M. “Viewpoint: Microwave Quantum States Beat the Heat.” Physics,
vol. 10, no. 32, American Physical Society, 2017, doi:10.1103/Physics.10.32.'
short: J.M. Fink, Physics 10 (2017).
date_created: 2018-12-11T11:49:41Z
date_published: 2017-03-27T00:00:00Z
date_updated: 2022-06-07T10:58:31Z
day: '27'
ddc:
- '530'
department:
- _id: JoFi
doi: 10.1103/Physics.10.32
file:
- access_level: open_access
content_type: application/pdf
creator: dernst
date_created: 2019-10-24T11:38:14Z
date_updated: 2019-10-24T11:38:14Z
file_id: '6968'
file_name: 2017_Physics_Fink.pdf
file_size: 193622
relation: main_file
success: 1
file_date_updated: 2019-10-24T11:38:14Z
has_accepted_license: '1'
intvolume: ' 10'
issue: '32'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
publication: Physics
publication_status: published
publisher: American Physical Society
publist_id: '6382'
quality_controlled: '1'
status: public
title: 'Viewpoint: Microwave quantum states beat the heat'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 10
year: '2017'
...
---
_id: '10126'
article_number: 391a
article_processing_charge: No
article_type: letter_note
author:
- first_name: Afshin
full_name: Vahid Belarghou, Afshin
last_name: Vahid Belarghou
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: Timon
full_name: Idema, Timon
last_name: Idema
citation:
ama: Vahid Belarghou A, Šarić A, Idema T. Curvature mediated interactions in highly
curved membranes. Biophysical Journal. 2017;112(3). doi:10.1016/j.bpj.2016.11.2123
apa: Vahid Belarghou, A., Šarić, A., & Idema, T. (2017). Curvature mediated
interactions in highly curved membranes. Biophysical Journal. Elsevier
. https://doi.org/10.1016/j.bpj.2016.11.2123
chicago: Vahid Belarghou, Afshin, Anđela Šarić, and Timon Idema. “Curvature Mediated
Interactions in Highly Curved Membranes.” Biophysical Journal. Elsevier
, 2017. https://doi.org/10.1016/j.bpj.2016.11.2123.
ieee: A. Vahid Belarghou, A. Šarić, and T. Idema, “Curvature mediated interactions
in highly curved membranes,” Biophysical Journal, vol. 112, no. 3. Elsevier
, 2017.
ista: Vahid Belarghou A, Šarić A, Idema T. 2017. Curvature mediated interactions
in highly curved membranes. Biophysical Journal. 112(3), 391a.
mla: Vahid Belarghou, Afshin, et al. “Curvature Mediated Interactions in Highly
Curved Membranes.” Biophysical Journal, vol. 112, no. 3, 391a, Elsevier
, 2017, doi:10.1016/j.bpj.2016.11.2123.
short: A. Vahid Belarghou, A. Šarić, T. Idema, Biophysical Journal 112 (2017).
date_created: 2021-10-12T07:47:55Z
date_published: 2017-02-03T00:00:00Z
date_updated: 2021-11-03T10:02:45Z
day: '03'
doi: 10.1016/j.bpj.2016.11.2123
extern: '1'
intvolume: ' 112'
issue: '3'
keyword:
- biophysics
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.cell.com/biophysj/fulltext/S0006-3495(16)33153-8
month: '02'
oa: 1
oa_version: Published Version
publication: Biophysical Journal
publication_identifier:
issn:
- 0006-3495
publication_status: published
publisher: 'Elsevier '
quality_controlled: '1'
status: public
title: Curvature mediated interactions in highly curved membranes
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 112
year: '2017'
...
---
_id: '10175'
abstract:
- lang: eng
text: We study periodic homogenization by Γ-convergence of integral functionals
with integrands W(x,ξ) having no polynomial growth and which are both not necessarily
continuous with respect to the space variable and not necessarily convex with
respect to the matrix variable. This allows to deal with homogenization of composite
hyperelastic materials consisting of two or more periodic components whose the
energy densities tend to infinity as the volume of matter tends to zero, i.e.,
W(x,ξ)=∑j∈J1Vj(x)Hj(ξ) where {Vj}j∈J is a finite family of open disjoint subsets
of RN, with |∂Vj|=0 for all j∈J and ∣∣RN∖⋃j∈JVj|=0, and, for each j∈J, Hj(ξ)→∞
as detξ→0. In fact, our results apply to integrands of type W(x,ξ)=a(x)H(ξ) when
H(ξ)→∞ as detξ→0 and a∈L∞(RN;[0,∞[) is 1-periodic and is either continuous almost
everywhere or not continuous. When a is not continuous, we obtain a density homogenization
formula which is a priori different from the classical one by Braides–Müller.
Although applications to hyperelasticity are limited due to the fact that our
framework is not consistent with the constraint of noninterpenetration of the
matter, our results can be of technical interest to analysis of homogenization
of integral functionals.
article_processing_charge: No
article_type: original
author:
- first_name: Omar
full_name: Anza Hafsa, Omar
last_name: Anza Hafsa
- first_name: Nicolas
full_name: Clozeau, Nicolas
id: fea1b376-906f-11eb-847d-b2c0cf46455b
last_name: Clozeau
- first_name: Jean-Philippe
full_name: Mandallena, Jean-Philippe
last_name: Mandallena
citation:
ama: Anza Hafsa O, Clozeau N, Mandallena J-P. Homogenization of nonconvex unbounded
singular integrals. Annales mathématiques Blaise Pascal. 2017;24(2):135-193.
doi:10.5802/ambp.367
apa: Anza Hafsa, O., Clozeau, N., & Mandallena, J.-P. (2017). Homogenization
of nonconvex unbounded singular integrals. Annales Mathématiques Blaise Pascal.
Université Clermont Auvergne. https://doi.org/10.5802/ambp.367
chicago: Anza Hafsa, Omar, Nicolas Clozeau, and Jean-Philippe Mandallena. “Homogenization
of Nonconvex Unbounded Singular Integrals.” Annales Mathématiques Blaise Pascal.
Université Clermont Auvergne, 2017. https://doi.org/10.5802/ambp.367.
ieee: O. Anza Hafsa, N. Clozeau, and J.-P. Mandallena, “Homogenization of nonconvex
unbounded singular integrals,” Annales mathématiques Blaise Pascal, vol.
24, no. 2. Université Clermont Auvergne, pp. 135–193, 2017.
ista: Anza Hafsa O, Clozeau N, Mandallena J-P. 2017. Homogenization of nonconvex
unbounded singular integrals. Annales mathématiques Blaise Pascal. 24(2), 135–193.
mla: Anza Hafsa, Omar, et al. “Homogenization of Nonconvex Unbounded Singular Integrals.”
Annales Mathématiques Blaise Pascal, vol. 24, no. 2, Université Clermont
Auvergne, 2017, pp. 135–93, doi:10.5802/ambp.367.
short: O. Anza Hafsa, N. Clozeau, J.-P. Mandallena, Annales Mathématiques Blaise
Pascal 24 (2017) 135–193.
date_created: 2021-10-23T10:54:23Z
date_published: 2017-11-20T00:00:00Z
date_updated: 2021-10-28T15:16:25Z
day: '20'
ddc:
- '510'
doi: 10.5802/ambp.367
extern: '1'
file:
- access_level: open_access
checksum: 18f40d13dc5d1e24438260b1875b886f
content_type: application/pdf
creator: cziletti
date_created: 2021-10-28T15:02:56Z
date_updated: 2021-10-28T15:02:56Z
file_id: '10194'
file_name: 2017_AMBP_AnzaHafsa.pdf
file_size: 850726
relation: main_file
success: 1
file_date_updated: 2021-10-28T15:02:56Z
has_accepted_license: '1'
intvolume: ' 24'
issue: '2'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nd/3.0/
month: '11'
oa: 1
oa_version: Published Version
page: 135-193
publication: Annales mathématiques Blaise Pascal
publication_identifier:
eissn:
- 2118-7436
issn:
- 1259-1734
publication_status: published
publisher: Université Clermont Auvergne
quality_controlled: '1'
status: public
title: Homogenization of nonconvex unbounded singular integrals
tmp:
image: /images/cc_by_nd.png
legal_code_url: https://creativecommons.org/licenses/by-nd/3.0/legalcode
name: Creative Commons Attribution-NoDerivs 3.0 Unported (CC BY-ND 3.0)
short: CC BY-ND (3.0)
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 24
year: '2017'
...
---
_id: '103'
abstract:
- lang: eng
text: We investigate effects of quasiparticle poisoning in a Majorana island with
strong tunnel coupling to normal-metal leads. In addition to the main Coulomb
blockade diamonds, "shadow" diamonds appear, shifted by 1e in gate voltage,
consistent with transport through an excited (poisoned) state of the island. Comparison
to a simple model yields an estimate of parity lifetime for the strongly coupled
island (∼1 μs) and sets a bound for a weakly coupled island (>10 μs). Fluctuations
in the gate-voltage spacing of Coulomb peaks at high field, reflecting Majorana
hybridization, are enhanced by the reduced lever arm at strong coupling. When
converted from gate voltage to energy units, fluctuations are consistent with
previous measurements.
acknowledgement: Research supported by Microsoft, the Danish National Research Foundation,
the Lundbeck Foundation, Carlsberg Foundation, Villum Foundation, and the European
Commission.
article_number: '137701'
author:
- first_name: S M
full_name: Albrecht, S M
last_name: Albrecht
- first_name: Esben
full_name: Hansen, Esben
last_name: Hansen
- first_name: Andrew P
full_name: Higginbotham, Andrew P
id: 4AD6785A-F248-11E8-B48F-1D18A9856A87
last_name: Higginbotham
orcid: 0000-0003-2607-2363
- first_name: Ferdinand
full_name: Kuemmeth, Ferdinand
last_name: Kuemmeth
- first_name: Thomas
full_name: Jespersen, Thomas
last_name: Jespersen
- first_name: Jesper
full_name: Nygård, Jesper
last_name: Nygård
- first_name: Peter
full_name: Krogstrup, Peter
last_name: Krogstrup
- first_name: Jeroen
full_name: Danon, Jeroen
last_name: Danon
- first_name: Karsten
full_name: Flensberg, Karsten
last_name: Flensberg
- first_name: Charles
full_name: Marcus, Charles
last_name: Marcus
citation:
ama: Albrecht SM, Hansen E, Higginbotham AP, et al. Transport signatures of quasiparticle
poisoning in a majorana island. APS Physics, Physical Review Letters. 2017;118(13).
doi:10.1103/PhysRevLett.118.137701
apa: Albrecht, S. M., Hansen, E., Higginbotham, A. P., Kuemmeth, F., Jespersen,
T., Nygård, J., … Marcus, C. (2017). Transport signatures of quasiparticle poisoning
in a majorana island. APS Physics, Physical Review Letters. American Physical
Society. https://doi.org/10.1103/PhysRevLett.118.137701
chicago: Albrecht, S M, Esben Hansen, Andrew P Higginbotham, Ferdinand Kuemmeth,
Thomas Jespersen, Jesper Nygård, Peter Krogstrup, Jeroen Danon, Karsten Flensberg,
and Charles Marcus. “Transport Signatures of Quasiparticle Poisoning in a Majorana
Island.” APS Physics, Physical Review Letters. American Physical Society,
2017. https://doi.org/10.1103/PhysRevLett.118.137701.
ieee: S. M. Albrecht et al., “Transport signatures of quasiparticle poisoning
in a majorana island,” APS Physics, Physical Review Letters, vol. 118,
no. 13. American Physical Society, 2017.
ista: Albrecht SM, Hansen E, Higginbotham AP, Kuemmeth F, Jespersen T, Nygård J,
Krogstrup P, Danon J, Flensberg K, Marcus C. 2017. Transport signatures of quasiparticle
poisoning in a majorana island. APS Physics, Physical Review Letters. 118(13),
137701.
mla: Albrecht, S. M., et al. “Transport Signatures of Quasiparticle Poisoning in
a Majorana Island.” APS Physics, Physical Review Letters, vol. 118, no.
13, 137701, American Physical Society, 2017, doi:10.1103/PhysRevLett.118.137701.
short: S.M. Albrecht, E. Hansen, A.P. Higginbotham, F. Kuemmeth, T. Jespersen, J.
Nygård, P. Krogstrup, J. Danon, K. Flensberg, C. Marcus, APS Physics, Physical
Review Letters 118 (2017).
date_created: 2018-12-11T11:44:39Z
date_published: 2017-03-31T00:00:00Z
date_updated: 2021-01-12T06:47:47Z
day: '31'
doi: 10.1103/PhysRevLett.118.137701
extern: '1'
external_id:
arxiv:
- '1612.05748'
intvolume: ' 118'
issue: '13'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1612.05748
month: '03'
oa: 1
oa_version: Preprint
publication: APS Physics, Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '7951'
quality_controlled: '1'
status: public
title: Transport signatures of quasiparticle poisoning in a majorana island
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 118
year: '2017'
...
---
_id: '10370'
abstract:
- lang: eng
text: Eukaryotic cells are densely packed with macromolecular complexes and intertwining
organelles, continually transported and reshaped. Intriguingly, organelles avoid
clashing and entangling with each other in such limited space. Mitochondria form
extensive networks constantly remodeled by fission and fusion. Here, we show that
mitochondrial fission is triggered by mechanical forces. Mechano-stimulation of
mitochondria – via encounter with motile intracellular pathogens, via external
pressure applied by an atomic force microscope, or via cell migration across uneven
microsurfaces – results in the recruitment of the mitochondrial fission machinery,
and subsequent division. We propose that MFF, owing to affinity for narrow mitochondria,
acts as a membrane-bound force sensor to recruit the fission machinery to mechanically
strained sites. Thus, mitochondria adapt to the environment by sensing and responding
to biomechanical cues. Our findings that mechanical triggers can be coupled to
biochemical responses in membrane dynamics may explain how organelles orderly
cohabit in the crowded cytoplasm.
article_number: e30292
article_processing_charge: No
article_type: original
author:
- first_name: Sebastian Carsten Johannes
full_name: Helle, Sebastian Carsten Johannes
last_name: Helle
- first_name: Qian
full_name: Feng, Qian
last_name: Feng
- first_name: Mathias J
full_name: Aebersold, Mathias J
last_name: Aebersold
- first_name: Luca
full_name: Hirt, Luca
last_name: Hirt
- first_name: Raphael R
full_name: Grüter, Raphael R
last_name: Grüter
- first_name: Afshin
full_name: Vahid, Afshin
last_name: Vahid
- first_name: Andrea
full_name: Sirianni, Andrea
last_name: Sirianni
- first_name: Serge
full_name: Mostowy, Serge
last_name: Mostowy
- first_name: Jess G
full_name: Snedeker, Jess G
last_name: Snedeker
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: Timon
full_name: Idema, Timon
last_name: Idema
- first_name: Tomaso
full_name: Zambelli, Tomaso
last_name: Zambelli
- first_name: Benoît
full_name: Kornmann, Benoît
last_name: Kornmann
citation:
ama: Helle SCJ, Feng Q, Aebersold MJ, et al. Mechanical force induces mitochondrial
fission. eLife. 2017;6. doi:10.7554/elife.30292
apa: Helle, S. C. J., Feng, Q., Aebersold, M. J., Hirt, L., Grüter, R. R., Vahid,
A., … Kornmann, B. (2017). Mechanical force induces mitochondrial fission. ELife.
eLife Sciences Publications. https://doi.org/10.7554/elife.30292
chicago: Helle, Sebastian Carsten Johannes, Qian Feng, Mathias J Aebersold, Luca
Hirt, Raphael R Grüter, Afshin Vahid, Andrea Sirianni, et al. “Mechanical Force
Induces Mitochondrial Fission.” ELife. eLife Sciences Publications, 2017.
https://doi.org/10.7554/elife.30292.
ieee: S. C. J. Helle et al., “Mechanical force induces mitochondrial fission,”
eLife, vol. 6. eLife Sciences Publications, 2017.
ista: Helle SCJ, Feng Q, Aebersold MJ, Hirt L, Grüter RR, Vahid A, Sirianni A, Mostowy
S, Snedeker JG, Šarić A, Idema T, Zambelli T, Kornmann B. 2017. Mechanical force
induces mitochondrial fission. eLife. 6, e30292.
mla: Helle, Sebastian Carsten Johannes, et al. “Mechanical Force Induces Mitochondrial
Fission.” ELife, vol. 6, e30292, eLife Sciences Publications, 2017, doi:10.7554/elife.30292.
short: S.C.J. Helle, Q. Feng, M.J. Aebersold, L. Hirt, R.R. Grüter, A. Vahid, A.
Sirianni, S. Mostowy, J.G. Snedeker, A. Šarić, T. Idema, T. Zambelli, B. Kornmann,
ELife 6 (2017).
date_created: 2021-11-29T08:51:38Z
date_published: 2017-11-09T00:00:00Z
date_updated: 2021-11-29T09:28:14Z
day: '09'
ddc:
- '572'
doi: 10.7554/elife.30292
extern: '1'
external_id:
pmid:
- '29119945'
file:
- access_level: open_access
checksum: c35f42dcfb007f6d6c761a27e24c26d3
content_type: application/pdf
creator: cchlebak
date_created: 2021-11-29T09:07:41Z
date_updated: 2021-11-29T09:07:41Z
file_id: '10372'
file_name: 2017_eLife_Helle.pdf
file_size: 6120157
relation: main_file
success: 1
file_date_updated: 2021-11-29T09:07:41Z
has_accepted_license: '1'
intvolume: ' 6'
keyword:
- general immunology and microbiology
- general biochemistry
- genetics and molecular biology
- general medicine
- general neuroscience
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://elifesciences.org/articles/30292
month: '11'
oa: 1
oa_version: Published Version
pmid: 1
publication: eLife
publication_identifier:
issn:
- 2050-084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mechanical force induces mitochondrial fission
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 6
year: '2017'
...
---
_id: '10369'
abstract:
- lang: eng
text: Biological membranes have a central role in mediating the organization of
membrane-curving proteins, a dynamic process that has proven to be challenging
to probe experimentally. Using atomic force microscopy, we capture the hierarchically
organized assemblies of Bin/amphiphysin/Rvs (BAR) proteins on supported lipid
membranes. Their structure reveals distinct long linear aggregates of proteins,
regularly spaced by up to 300 nm. Employing accurate free-energy calculations
from large-scale coarse-grained computer simulations, we found that the membrane
mediates the interaction among protein filaments as a combination of short- and
long-ranged interactions. The long-ranged component acts at strikingly long distances,
giving rise to a variety of micron-sized ordered patterns. This mechanism may
contribute to the long-ranged spatiotemporal control of membrane remodeling by
proteins in the cell.
acknowledgement: M.S. and G.A.V. acknowledge their research reported in this publication
as being supported by the National Institute of General Medical Sciences of the
National Institutes of Health under Award Number R01-GM063796. Computational resources
were provided to M.S. and G.A.V. by the National Science Foundation through XSEDE
(Grant TG-MCA94P017, supercomputers Stampede and Gordon), and also by the Blue Waters
computing project at the National Center for Supercomputing Applications (University
of Illinois at Urbana–Champaign, NSF Awards OCI-0725070 and ACI-1238993). A.Š. acknowledges
support from the Human Frontier Science Program and Royal Society. J.M.H. and K.Y.C.L.
acknowledge the support from the National Science Foundation (Grant MCB-1413613)
and the NSF-supported MRSEC program at the University of Chicago (Grant DMR-1420709).
We are grateful to Carsten Mim and Vinzenz Unger of Northwestern University for
generously providing us with the protein. We thank all the members of the Voth group
for fruitful discussions, especially John M. A. Grime.
article_processing_charge: No
article_type: original
author:
- first_name: Mijo
full_name: Simunovic, Mijo
last_name: Simunovic
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: J. Michael
full_name: Henderson, J. Michael
last_name: Henderson
- first_name: Ka Yee C.
full_name: Lee, Ka Yee C.
last_name: Lee
- first_name: Gregory A.
full_name: Voth, Gregory A.
last_name: Voth
citation:
ama: Simunovic M, Šarić A, Henderson JM, Lee KYC, Voth GA. Long-range organization
of membrane-curving proteins. ACS Central Science. 2017;3(12):1246-1253.
doi:10.1021/acscentsci.7b00392
apa: Simunovic, M., Šarić, A., Henderson, J. M., Lee, K. Y. C., & Voth, G. A.
(2017). Long-range organization of membrane-curving proteins. ACS Central Science.
American Chemical Society. https://doi.org/10.1021/acscentsci.7b00392
chicago: Simunovic, Mijo, Anđela Šarić, J. Michael Henderson, Ka Yee C. Lee, and
Gregory A. Voth. “Long-Range Organization of Membrane-Curving Proteins.” ACS
Central Science. American Chemical Society, 2017. https://doi.org/10.1021/acscentsci.7b00392.
ieee: M. Simunovic, A. Šarić, J. M. Henderson, K. Y. C. Lee, and G. A. Voth, “Long-range
organization of membrane-curving proteins,” ACS Central Science, vol. 3,
no. 12. American Chemical Society, pp. 1246–1253, 2017.
ista: Simunovic M, Šarić A, Henderson JM, Lee KYC, Voth GA. 2017. Long-range organization
of membrane-curving proteins. ACS Central Science. 3(12), 1246–1253.
mla: Simunovic, Mijo, et al. “Long-Range Organization of Membrane-Curving Proteins.”
ACS Central Science, vol. 3, no. 12, American Chemical Society, 2017, pp.
1246–53, doi:10.1021/acscentsci.7b00392.
short: M. Simunovic, A. Šarić, J.M. Henderson, K.Y.C. Lee, G.A. Voth, ACS Central
Science 3 (2017) 1246–1253.
date_created: 2021-11-29T08:49:50Z
date_published: 2017-11-21T00:00:00Z
date_updated: 2021-11-29T09:28:06Z
day: '21'
ddc:
- '540'
doi: 10.1021/acscentsci.7b00392
extern: '1'
external_id:
pmid:
- '29296664'
file:
- access_level: open_access
checksum: 1cf3e5e5342f2d728f47560acc3ec560
content_type: application/pdf
creator: cchlebak
date_created: 2021-11-29T09:00:40Z
date_updated: 2021-11-29T09:00:40Z
file_id: '10371'
file_name: 2017_ACSCentSci_Simunovic.pdf
file_size: 2635263
relation: main_file
success: 1
file_date_updated: 2021-11-29T09:00:40Z
has_accepted_license: '1'
intvolume: ' 3'
issue: '12'
keyword:
- general chemical engineering
- general chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://pubs.acs.org/doi/10.1021/acscentsci.7b00392
month: '11'
oa: 1
oa_version: Published Version
page: 1246-1253
pmid: 1
publication: ACS Central Science
publication_identifier:
eissn:
- 2374-7951
issn:
- 2374-7943
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Long-range organization of membrane-curving proteins
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 3
year: '2017'
...
---
_id: '10373'
abstract:
- lang: eng
text: 'Electric charges are conserved. The same would be expected to hold for magnetic
charges, yet magnetic monopoles have never been observed. It is therefore surprising
that the laws of nonequilibrium thermodynamics, combined with Maxwell’s equations,
suggest that colloidal particles heated or cooled in certain polar or paramagnetic
solvents may behave as if they carry an electric/magnetic charge. Here, we present
numerical simulations that show that the field distribution around a pair of such
heated/cooled colloidal particles agrees quantitatively with the theoretical predictions
for a pair of oppositely charged electric or magnetic monopoles. However, in other
respects, the nonequilibrium colloidal particles do not behave as monopoles: They
cannot be moved by a homogeneous applied field. The numerical evidence for the
monopole-like fields around heated/cooled colloidal particles is crucial because
the experimental and numerical determination of forces between such colloidal
particles would be complicated by the presence of other effects, such as thermophoresis.'
acknowledgement: P.W. acknowledges many invaluable discussions with Martin Neumann,
Chao Zhang, Michiel Sprik, Aleks Reinhardt, Carl Pölking, and Tine Curk. We acknowledge
financial support from the Austrian Academy of Sciences through a doctoral (DOC)
fellowship (to P.W.), the Austrian Science Fund (FWF) within the Spezialforschungsbereich
Vienna Computational Materials Laboratory (Project F41) (C.D.), and the European
Union Early Training Network NANOTRANS (Grant 674979 to D. Frenkel). The results
presented here have been achieved in part using the Vienna Scientific Cluster.
article_processing_charge: No
article_type: original
author:
- first_name: Peter
full_name: Wirnsberger, Peter
last_name: Wirnsberger
- first_name: Domagoj
full_name: Fijan, Domagoj
last_name: Fijan
- first_name: Roger A.
full_name: Lightwood, Roger A.
last_name: Lightwood
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: Christoph
full_name: Dellago, Christoph
last_name: Dellago
- first_name: Daan
full_name: Frenkel, Daan
last_name: Frenkel
citation:
ama: Wirnsberger P, Fijan D, Lightwood RA, Šarić A, Dellago C, Frenkel D. Numerical
evidence for thermally induced monopoles. Proceedings of the National Academy
of Sciences. 2017;114(19):4911-4914. doi:10.1073/pnas.1621494114
apa: Wirnsberger, P., Fijan, D., Lightwood, R. A., Šarić, A., Dellago, C., &
Frenkel, D. (2017). Numerical evidence for thermally induced monopoles. Proceedings
of the National Academy of Sciences. National Academy of Sciences. https://doi.org/10.1073/pnas.1621494114
chicago: Wirnsberger, Peter, Domagoj Fijan, Roger A. Lightwood, Anđela Šarić, Christoph
Dellago, and Daan Frenkel. “Numerical Evidence for Thermally Induced Monopoles.”
Proceedings of the National Academy of Sciences. National Academy of Sciences,
2017. https://doi.org/10.1073/pnas.1621494114.
ieee: P. Wirnsberger, D. Fijan, R. A. Lightwood, A. Šarić, C. Dellago, and D. Frenkel,
“Numerical evidence for thermally induced monopoles,” Proceedings of the National
Academy of Sciences, vol. 114, no. 19. National Academy of Sciences, pp. 4911–4914,
2017.
ista: Wirnsberger P, Fijan D, Lightwood RA, Šarić A, Dellago C, Frenkel D. 2017.
Numerical evidence for thermally induced monopoles. Proceedings of the National
Academy of Sciences. 114(19), 4911–4914.
mla: Wirnsberger, Peter, et al. “Numerical Evidence for Thermally Induced Monopoles.”
Proceedings of the National Academy of Sciences, vol. 114, no. 19, National
Academy of Sciences, 2017, pp. 4911–14, doi:10.1073/pnas.1621494114.
short: P. Wirnsberger, D. Fijan, R.A. Lightwood, A. Šarić, C. Dellago, D. Frenkel,
Proceedings of the National Academy of Sciences 114 (2017) 4911–4914.
date_created: 2021-11-29T09:28:24Z
date_published: 2017-04-24T00:00:00Z
date_updated: 2021-11-29T09:59:12Z
day: '24'
doi: 10.1073/pnas.1621494114
extern: '1'
external_id:
arxiv:
- '1610.06840'
pmid:
- '28439003'
intvolume: ' 114'
issue: '19'
keyword:
- multidisciplinary
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.pnas.org/content/114/19/4911
month: '04'
oa: 1
oa_version: Published Version
page: 4911-4914
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
eissn:
- 1091-6490
issn:
- 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: Numerical evidence for thermally induced monopoles
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 114
year: '2017'
...
---
_id: '10374'
abstract:
- lang: eng
text: The formation of filaments from naturally occurring protein molecules is a
process at the core of a range of functional and aberrant biological phenomena,
such as the assembly of the cytoskeleton or the appearance of aggregates in Alzheimer's
disease. The macroscopic behaviour associated with such processes is remarkably
diverse, ranging from simple nucleated growth to highly cooperative processes
with a well-defined lagtime. Thus, conventionally, different molecular mechanisms
have been used to explain the self-assembly of different proteins. Here we show
that this range of behaviour can be quantitatively captured by a single unifying
Petri net that describes filamentous growth in terms of aggregate number and aggregate
mass concentrations. By considering general features associated with a particular
network connectivity, we are able to establish directly the rate-determining steps
of the overall aggregation reaction from the system's scaling behaviour. We illustrate
the power of this framework on a range of different experimental and simulated
aggregating systems. The approach is general and will be applicable to any future
extensions of the reaction network of filamentous self-assembly.
acknowledgement: The research leading to these results has received funding from the
European Research Council under the European Union's Seventh Framework Programme
(FP7/2007-2013) through the ERC grant PhysProt (agreement no. 337969) (SL, TPJK),
Sidney Sussex College Cambridge (GM), the Frances and Augusta Newman Foundation
(TPJK), the Biotechnology and Biological Science Research Council (TPJK), the Swedish
Research Council (SL), the Academy of Medical Sciences (AŠ), Wellcome Trust (AŠ),
and the Cambridge Centre for Misfolding Diseases (CMD, TPJK, MV).
article_processing_charge: No
article_type: original
author:
- first_name: Georg
full_name: Meisl, Georg
last_name: Meisl
- first_name: Luke
full_name: Rajah, Luke
last_name: Rajah
- first_name: Samuel A. I.
full_name: Cohen, Samuel A. I.
last_name: Cohen
- first_name: Manuela
full_name: Pfammatter, Manuela
last_name: Pfammatter
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: Erik
full_name: Hellstrand, Erik
last_name: Hellstrand
- first_name: Alexander K.
full_name: Buell, Alexander K.
last_name: Buell
- first_name: Adriano
full_name: Aguzzi, Adriano
last_name: Aguzzi
- first_name: Sara
full_name: Linse, Sara
last_name: Linse
- first_name: Michele
full_name: Vendruscolo, Michele
last_name: Vendruscolo
- first_name: Christopher M.
full_name: Dobson, Christopher M.
last_name: Dobson
- first_name: Tuomas P. J.
full_name: Knowles, Tuomas P. J.
last_name: Knowles
citation:
ama: Meisl G, Rajah L, Cohen SAI, et al. Scaling behaviour and rate-determining
steps in filamentous self-assembly. Chemical Science. 2017;8(10):7087-7097.
doi:10.1039/c7sc01965c
apa: Meisl, G., Rajah, L., Cohen, S. A. I., Pfammatter, M., Šarić, A., Hellstrand,
E., … Knowles, T. P. J. (2017). Scaling behaviour and rate-determining steps in
filamentous self-assembly. Chemical Science. Royal Society of Chemistry.
https://doi.org/10.1039/c7sc01965c
chicago: Meisl, Georg, Luke Rajah, Samuel A. I. Cohen, Manuela Pfammatter, Anđela
Šarić, Erik Hellstrand, Alexander K. Buell, et al. “Scaling Behaviour and Rate-Determining
Steps in Filamentous Self-Assembly.” Chemical Science. Royal Society of
Chemistry, 2017. https://doi.org/10.1039/c7sc01965c.
ieee: G. Meisl et al., “Scaling behaviour and rate-determining steps in filamentous
self-assembly,” Chemical Science, vol. 8, no. 10. Royal Society of Chemistry,
pp. 7087–7097, 2017.
ista: Meisl G, Rajah L, Cohen SAI, Pfammatter M, Šarić A, Hellstrand E, Buell AK,
Aguzzi A, Linse S, Vendruscolo M, Dobson CM, Knowles TPJ. 2017. Scaling behaviour
and rate-determining steps in filamentous self-assembly. Chemical Science. 8(10),
7087–7097.
mla: Meisl, Georg, et al. “Scaling Behaviour and Rate-Determining Steps in Filamentous
Self-Assembly.” Chemical Science, vol. 8, no. 10, Royal Society of Chemistry,
2017, pp. 7087–97, doi:10.1039/c7sc01965c.
short: G. Meisl, L. Rajah, S.A.I. Cohen, M. Pfammatter, A. Šarić, E. Hellstrand,
A.K. Buell, A. Aguzzi, S. Linse, M. Vendruscolo, C.M. Dobson, T.P.J. Knowles,
Chemical Science 8 (2017) 7087–7097.
date_created: 2021-11-29T09:29:31Z
date_published: 2017-08-31T00:00:00Z
date_updated: 2021-11-29T10:00:00Z
day: '31'
ddc:
- '540'
doi: 10.1039/c7sc01965c
extern: '1'
external_id:
pmid:
- '29147538'
intvolume: ' 8'
issue: '10'
keyword:
- general chemistry
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc/3.0/
main_file_link:
- open_access: '1'
url: https://pubs.rsc.org/en/content/articlelanding/2017/SC/C7SC01965C
month: '08'
oa: 1
oa_version: Published Version
page: 7087-7097
pmid: 1
publication: Chemical Science
publication_identifier:
eissn:
- 2041-6539
issn:
- 2041-6520
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Scaling behaviour and rate-determining steps in filamentous self-assembly
tmp:
image: /images/cc_by_nc.png
legal_code_url: https://creativecommons.org/licenses/by-nc/3.0/legalcode
name: Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)
short: CC BY-NC (3.0)
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 8
year: '2017'
...
---
_id: '10375'
abstract:
- lang: eng
text: 'Cellular membranes exhibit a large variety of shapes, strongly coupled to
their function. Many biological processes involve dynamic reshaping of membranes,
usually mediated by proteins. This interaction works both ways: while proteins
influence the membrane shape, the membrane shape affects the interactions between
the proteins. To study these membrane-mediated interactions on closed and anisotropically
curved membranes, we use colloids adhered to ellipsoidal membrane vesicles as
a model system. We find that two particles on a closed system always attract each
other, and tend to align with the direction of largest curvature. Multiple particles
form arcs, or, at large enough numbers, a complete ring surrounding the vesicle
in its equatorial plane. The resulting vesicle shape resembles a snowman. Our
results indicate that these physical interactions on membranes with anisotropic
shapes can be exploited by cells to drive macromolecules to preferred regions
of cellular or intracellular membranes, and utilized to initiate dynamic processes
such as cell division. The same principle could be used to find the midplane of
an artificial vesicle, as a first step towards dividing it into two equal parts.'
acknowledgement: This work was supported by the Netherlands Organisation for Scientific
Research (NWO/OCW), as part of the Frontiers of Nanoscience program.
article_processing_charge: No
article_type: original
author:
- first_name: Afshin
full_name: Vahid, Afshin
last_name: Vahid
- first_name: Anđela
full_name: Šarić, Anđela
id: bf63d406-f056-11eb-b41d-f263a6566d8b
last_name: Šarić
orcid: 0000-0002-7854-2139
- first_name: Timon
full_name: Idema, Timon
last_name: Idema
citation:
ama: Vahid A, Šarić A, Idema T. Curvature variation controls particle aggregation
on fluid vesicles. Soft Matter. 2017;13(28):4924-4930. doi:10.1039/c7sm00433h
apa: Vahid, A., Šarić, A., & Idema, T. (2017). Curvature variation controls
particle aggregation on fluid vesicles. Soft Matter. Royal Society of Chemistry.
https://doi.org/10.1039/c7sm00433h
chicago: Vahid, Afshin, Anđela Šarić, and Timon Idema. “Curvature Variation Controls
Particle Aggregation on Fluid Vesicles.” Soft Matter. Royal Society of
Chemistry, 2017. https://doi.org/10.1039/c7sm00433h.
ieee: A. Vahid, A. Šarić, and T. Idema, “Curvature variation controls particle aggregation
on fluid vesicles,” Soft Matter, vol. 13, no. 28. Royal Society of Chemistry,
pp. 4924–4930, 2017.
ista: Vahid A, Šarić A, Idema T. 2017. Curvature variation controls particle aggregation
on fluid vesicles. Soft Matter. 13(28), 4924–4930.
mla: Vahid, Afshin, et al. “Curvature Variation Controls Particle Aggregation on
Fluid Vesicles.” Soft Matter, vol. 13, no. 28, Royal Society of Chemistry,
2017, pp. 4924–30, doi:10.1039/c7sm00433h.
short: A. Vahid, A. Šarić, T. Idema, Soft Matter 13 (2017) 4924–4930.
date_created: 2021-11-29T10:00:39Z
date_published: 2017-06-15T00:00:00Z
date_updated: 2021-11-29T10:33:36Z
day: '15'
doi: 10.1039/c7sm00433h
extern: '1'
external_id:
arxiv:
- '1703.00776'
pmid:
- '28677712'
intvolume: ' 13'
issue: '28'
keyword:
- condensed matter physics
- general chemistry
language:
- iso: eng
license: https://creativecommons.org/licenses/by/3.0/
main_file_link:
- open_access: '1'
url: https://pubs.rsc.org/en/content/articlelanding/2017/SM/C7SM00433H
month: '06'
oa: 1
oa_version: Published Version
page: 4924-4930
pmid: 1
publication: Soft Matter
publication_identifier:
eissn:
- 1744-6848
issn:
- 1744-683X
publication_status: published
publisher: Royal Society of Chemistry
quality_controlled: '1'
scopus_import: '1'
status: public
title: Curvature variation controls particle aggregation on fluid vesicles
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/3.0/legalcode
name: Creative Commons Attribution 3.0 Unported (CC BY 3.0)
short: CC BY (3.0)
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 13
year: '2017'
...
---
_id: '10418'
abstract:
- lang: eng
text: We present a new proof rule for proving almost-sure termination of probabilistic
programs, including those that contain demonic non-determinism. An important question
for a probabilistic program is whether the probability mass of all its diverging
runs is zero, that is that it terminates "almost surely". Proving that can be
hard, and this paper presents a new method for doing so. It applies directly to
the program's source code, even if the program contains demonic choice. Like others,
we use variant functions (a.k.a. "super-martingales") that are real-valued and
decrease randomly on each loop iteration; but our key innovation is that the amount
as well as the probability of the decrease are parametric. We prove the soundness
of the new rule, indicate where its applicability goes beyond existing rules,
and explain its connection to classical results on denumerable (non-demonic) Markov
chains.
acknowledgement: "McIver and Morgan are grateful to David Basin and the Information
Security Group at ETH Zürich for hosting a six-month stay in Switzerland, during
part of which this work began. And thanks particularly to Andreas Lochbihler, who
shared with us the probabilistic termination problem that led to it. They acknowledge
the support of ARC grant DP140101119. Part of this work was carried out during the
Workshop on Probabilistic Programming Semantics\r\nat McGill University’s Bellairs
Research Institute on Barbados organised by Alexandra Silva and\r\nPrakash Panangaden.
Kaminski and Katoen are grateful to Sebastian Junges for spotting a flaw in §5.4."
article_number: '33'
article_processing_charge: No
article_type: original
author:
- first_name: Annabelle
full_name: Mciver, Annabelle
last_name: Mciver
- first_name: Carroll
full_name: Morgan, Carroll
last_name: Morgan
- first_name: Benjamin Lucien
full_name: Kaminski, Benjamin Lucien
last_name: Kaminski
- first_name: Joost P
full_name: Katoen, Joost P
id: 4524F760-F248-11E8-B48F-1D18A9856A87
last_name: Katoen
citation:
ama: Mciver A, Morgan C, Kaminski BL, Katoen JP. A new proof rule for almost-sure
termination. Proceedings of the ACM on Programming Languages. 2017;2(POPL).
doi:10.1145/3158121
apa: 'Mciver, A., Morgan, C., Kaminski, B. L., & Katoen, J. P. (2017). A new
proof rule for almost-sure termination. Proceedings of the ACM on Programming
Languages. Los Angeles, CA, United States: Association for Computing Machinery.
https://doi.org/10.1145/3158121'
chicago: Mciver, Annabelle, Carroll Morgan, Benjamin Lucien Kaminski, and Joost
P Katoen. “A New Proof Rule for Almost-Sure Termination.” Proceedings of the
ACM on Programming Languages. Association for Computing Machinery, 2017. https://doi.org/10.1145/3158121.
ieee: A. Mciver, C. Morgan, B. L. Kaminski, and J. P. Katoen, “A new proof rule
for almost-sure termination,” Proceedings of the ACM on Programming Languages,
vol. 2, no. POPL. Association for Computing Machinery, 2017.
ista: Mciver A, Morgan C, Kaminski BL, Katoen JP. 2017. A new proof rule for almost-sure
termination. Proceedings of the ACM on Programming Languages. 2(POPL), 33.
mla: Mciver, Annabelle, et al. “A New Proof Rule for Almost-Sure Termination.” Proceedings
of the ACM on Programming Languages, vol. 2, no. POPL, 33, Association for
Computing Machinery, 2017, doi:10.1145/3158121.
short: A. Mciver, C. Morgan, B.L. Kaminski, J.P. Katoen, Proceedings of the ACM
on Programming Languages 2 (2017).
conference:
end_date: 2018-01-13
location: Los Angeles, CA, United States
name: 'POPL: Programming Languages'
start_date: 2018-01-07
date_created: 2021-12-05T23:01:49Z
date_published: 2017-12-07T00:00:00Z
date_updated: 2021-12-07T08:04:14Z
day: '07'
department:
- _id: KrCh
- _id: ToHe
doi: 10.1145/3158121
external_id:
arxiv:
- '1711.03588'
intvolume: ' 2'
issue: POPL
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://dl.acm.org/doi/10.1145/3158121
month: '12'
oa: 1
oa_version: Published Version
publication: Proceedings of the ACM on Programming Languages
publication_identifier:
eissn:
- 2475-1421
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
scopus_import: '1'
status: public
title: A new proof rule for almost-sure termination
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 2
year: '2017'
...
---
_id: '10663'
abstract:
- lang: eng
text: 'The superconducting state of matter enables one to observe quantum effects
on the macroscopic scale and hosts many fascinating phenomena. Topological defects
of the superconducting order parameter, such as vortices and fluxoid states in
multiply connected structures, are often the key ingredients of these phenomena.
This dissertation describes a new mode of magnetic force microscopy (Φ0-MFM) for
investigating vortex and fluxoid sates in mesoscopic superconducting (SC) structures.
The technique relies on the magneto-mechanical coupling of a MFM cantilever to
the motion of fluxons. The novelty of the technique is that a magnetic particle
attached to the cantilever is used not only to sense the state of a SC structure,
but also as a primary source of the inhomogeneous magnetic field which induces
that state. Φ0-MFM enables us to map the transitions between tip-induced states
during a scan: at the positions of the tip, where the two lowest energy states
become degenerate, small oscillations of the tip drive the transitions between
these states, which causes a significant shift in the resonant frequency and dissipation
of the cantilever. For narrow-wall aluminum rings, the mapped fluxoid transitions
form concentric contours on a scan. We show that the changes in the cantilever
resonant frequency and dissipation are well-described by a stochastic resonance
(SR) of cantilever-driven thermally activated phase slips (TAPS). The SR model
allows us to experimentally determine the rate of TAPS and compare it to the Langer-Ambegaokar-McCumber-Halperin
(LAMH) theory for TAPS in 1D superconducting structures. Further, we use the SR
model to qualitatively study the effects of a locally applied magnetic field on
the phase slip rate in rings containing constrictions. The states with multiple
vortices or winding numbers could be useful for the development of novel superconducting
devices, or the study of vortex interactions and interference effects. Using Φ0-MFM
allows us to induce, probe and control fluxoid states in thin wall structures
comprised of multiple loops. We show that Φ0-MFM images of the fluxoid transitions
allow us to identify the underlying states and to investigate their energetics
and dynamics even in complicated structures.'
alternative_title:
- Graduate Dissertations and Theses at Illinois
article_processing_charge: No
author:
- first_name: Hryhoriy
full_name: Polshyn, Hryhoriy
id: edfc7cb1-526e-11ec-b05a-e6ecc27e4e48
last_name: Polshyn
orcid: 0000-0001-8223-8896
citation:
ama: Polshyn H. Magnetic force microscopy studies of mesoscopic superconducting
structures. 2017.
apa: Polshyn, H. (2017). Magnetic force microscopy studies of mesoscopic superconducting
structures. University of Illinois at Urbana-Champaign.
chicago: Polshyn, Hryhoriy. “Magnetic Force Microscopy Studies of Mesoscopic Superconducting
Structures.” University of Illinois at Urbana-Champaign, 2017.
ieee: H. Polshyn, “Magnetic force microscopy studies of mesoscopic superconducting
structures,” University of Illinois at Urbana-Champaign, 2017.
ista: Polshyn H. 2017. Magnetic force microscopy studies of mesoscopic superconducting
structures. University of Illinois at Urbana-Champaign.
mla: Polshyn, Hryhoriy. Magnetic Force Microscopy Studies of Mesoscopic Superconducting
Structures. University of Illinois at Urbana-Champaign, 2017.
short: H. Polshyn, Magnetic Force Microscopy Studies of Mesoscopic Superconducting
Structures, University of Illinois at Urbana-Champaign, 2017.
date_created: 2022-01-25T14:54:14Z
date_published: 2017-09-18T00:00:00Z
date_updated: 2022-01-25T15:00:26Z
day: '18'
degree_awarded: PhD
extern: '1'
keyword:
- physics
- superconductivity
- magnetic force microscopy
- phase slips
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://hdl.handle.net/2142/99178
month: '09'
oa: 1
oa_version: Published Version
page: '103'
publication_status: published
publisher: University of Illinois at Urbana-Champaign
status: public
supervisor:
- first_name: Raffi
full_name: Budakian, Raffi
last_name: Budakian
title: Magnetic force microscopy studies of mesoscopic superconducting structures
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2017'
...
---
_id: '10745'
abstract:
- lang: eng
text: New ways to investigate and manipulate fluxoid and vortex states of mesoscopic
superconducting structures are of great interest. The states with multiple vortices
or winding numbers could be useful for the study of vortex interactions and interference
effects, the braiding of Majorana bound states by winding vortices, and the development
of novel superconducting devices. We demonstrate a methodology based on magnetic
force microscopy that allows us to induce, probe and control fluxoid states in
thin wall structures comprised of multiple loops. By using micro-magnet as a source
of inhomogeneous magnetic field, we can efficiently explore the configuration
space of fluxoid states. Scanning over the structure reveals the energy crossing
points of the lowest laying fluxoid states. This is due the strong interaction
of cantilever with thermally activated fluxoid transitions at points of degeneracy.
We show that measured patterns of fluxoid transitions allow to identify the states,
investigate their energetics, and manipulate them. Further, we show that the dynamics
of driven fluxoid transitions can be described by stochastic resonance model,
which provides a unique way of measuring fluxoid transition rate and related energy
barrier for chosen transitions even in complicated structures
alternative_title:
- Bulletin of the American Physical Society
article_number: P39.00011
article_processing_charge: No
author:
- first_name: Hryhoriy
full_name: Polshyn, Hryhoriy
id: edfc7cb1-526e-11ec-b05a-e6ecc27e4e48
last_name: Polshyn
orcid: 0000-0001-8223-8896
- first_name: Tyler
full_name: Naibert, Tyler
last_name: Naibert
- first_name: Raffi
full_name: Budakian, Raffi
last_name: Budakian
citation:
ama: 'Polshyn H, Naibert T, Budakian R. Probing and controlling fluxoid states
in multiply-connected mesoscopic superconducting structures. In: APS March
Meeting 2017. Vol 62. American Physical Society; 2017.'
apa: 'Polshyn, H., Naibert, T., & Budakian, R. (2017). Probing and controlling
fluxoid states in multiply-connected mesoscopic superconducting structures. In
APS March Meeting 2017 (Vol. 62). New Orleans, LA, United States: American
Physical Society.'
chicago: Polshyn, Hryhoriy, Tyler Naibert, and Raffi Budakian. “ Probing and Controlling
Fluxoid States in Multiply-Connected Mesoscopic Superconducting Structures.” In
APS March Meeting 2017, Vol. 62. American Physical Society, 2017.
ieee: H. Polshyn, T. Naibert, and R. Budakian, “ Probing and controlling fluxoid
states in multiply-connected mesoscopic superconducting structures,” in APS
March Meeting 2017, New Orleans, LA, United States, 2017, vol. 62, no. 4.
ista: 'Polshyn H, Naibert T, Budakian R. 2017. Probing and controlling fluxoid
states in multiply-connected mesoscopic superconducting structures. APS March
Meeting 2017. APS: American Physical Society, Bulletin of the American Physical
Society, vol. 62, P39.00011.'
mla: Polshyn, Hryhoriy, et al. “ Probing and Controlling Fluxoid States in Multiply-Connected
Mesoscopic Superconducting Structures.” APS March Meeting 2017, vol. 62,
no. 4, P39.00011, American Physical Society, 2017.
short: H. Polshyn, T. Naibert, R. Budakian, in:, APS March Meeting 2017, American
Physical Society, 2017.
conference:
end_date: 2017-03-17
location: New Orleans, LA, United States
name: 'APS: American Physical Society'
start_date: 2017-03-13
date_created: 2022-02-08T09:49:17Z
date_published: 2017-03-01T00:00:00Z
date_updated: 2022-02-08T10:44:35Z
day: '01'
extern: '1'
intvolume: ' 62'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://meetings.aps.org/Meeting/MAR17/Session/P39.11
month: '03'
oa: 1
oa_version: Published Version
publication: APS March Meeting 2017
publication_identifier:
issn:
- 0003-0503
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
status: public
title: ' Probing and controlling fluxoid states in multiply-connected mesoscopic superconducting
structures'
type: conference
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 62
year: '2017'
...
---
_id: '1075'
alternative_title:
- American Studies in Austria
author:
- first_name: Bernhard
full_name: Wenzl, Bernhard
id: 479E9046-F248-11E8-B48F-1D18A9856A87
last_name: Wenzl
citation:
ama: 'Wenzl B. An American in Allied-occupied Austria: John Dos Passos Reports on
"The Vienna Frontier" In: Parker J, Poole R, eds. Austria
and America: 20th-Century Cross-Cultural Encounters. Vol 15. LIT Verlag Berlin-Münster-Wien-Zürich-London;
2017:73-80.'
apa: 'Wenzl, B. (2017). An American in Allied-occupied Austria: John Dos Passos
Reports on "The Vienna Frontier" In J. Parker & R. Poole
(Eds.), Austria and America: 20th-Century Cross-Cultural Encounters (Vol.
15, pp. 73–80). LIT Verlag Berlin-Münster-Wien-Zürich-London.'
chicago: 'Wenzl, Bernhard. “An American in Allied-Occupied Austria: John Dos Passos
Reports on "The Vienna Frontier"” In Austria and America:
20th-Century Cross-Cultural Encounters, edited by Joshua Parker and Ralph
Poole, 15:73–80. LIT Verlag Berlin-Münster-Wien-Zürich-London, 2017.'
ieee: 'B. Wenzl, “An American in Allied-occupied Austria: John Dos Passos Reports
on "The Vienna Frontier",” in Austria and America: 20th-Century
Cross-Cultural Encounters, vol. 15, J. Parker and R. Poole, Eds. LIT Verlag
Berlin-Münster-Wien-Zürich-London, 2017, pp. 73–80.'
ista: 'Wenzl B. 2017.An American in Allied-occupied Austria: John Dos Passos Reports
on "The Vienna Frontier" In: Austria and America: 20th-Century
Cross-Cultural Encounters. American Studies in Austria, vol. 15, 73–80.'
mla: 'Wenzl, Bernhard. “An American in Allied-Occupied Austria: John Dos Passos
Reports on "The Vienna Frontier"” Austria and America: 20th-Century
Cross-Cultural Encounters, edited by Joshua Parker and Ralph Poole, vol. 15,
LIT Verlag Berlin-Münster-Wien-Zürich-London, 2017, pp. 73–80.'
short: 'B. Wenzl, in:, J. Parker, R. Poole (Eds.), Austria and America: 20th-Century
Cross-Cultural Encounters, LIT Verlag Berlin-Münster-Wien-Zürich-London, 2017,
pp. 73–80.'
date_created: 2018-12-11T11:50:00Z
date_published: 2017-02-01T00:00:00Z
date_updated: 2021-01-12T06:48:06Z
day: '01'
ddc:
- '001'
editor:
- first_name: Joshua
full_name: Parker, Joshua
last_name: Parker
- first_name: Ralph
full_name: Poole, Ralph
last_name: Poole
extern: '1'
file:
- access_level: open_access
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:08:06Z
date_updated: 2018-12-12T10:08:06Z
file_id: '4666'
file_name: IST-2017-732-v1+1_Austria_and_America_Cross-Cultural_Encounters.pdf
file_size: 380624
relation: main_file
file_date_updated: 2018-12-12T10:08:06Z
has_accepted_license: '1'
intvolume: ' 15'
language:
- iso: eng
month: '02'
oa: 1
oa_version: None
page: 73 - 80
publication: 'Austria and America: 20th-Century Cross-Cultural Encounters'
publication_identifier:
isbn:
- 978-3643908124
publication_status: published
publisher: LIT Verlag Berlin-Münster-Wien-Zürich-London
publist_id: '6306'
status: public
title: 'An American in Allied-occupied Austria: John Dos Passos Reports on "The
Vienna Frontier"'
type: book_chapter
user_id: 2EBD1598-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2017'
...
---
_id: '11066'
abstract:
- lang: eng
text: Recent studies have shown that a subset of nucleoporins (Nups) can detach
from the nuclear pore complex and move into the nuclear interior to regulate transcription.
One such dynamic Nup, called Nup98, has been implicated in gene activation in
healthy cells and has been shown to drive leukemogenesis when mutated in patients
with acute myeloid leukemia (AML). Here we show that in hematopoietic cells, Nup98
binds predominantly to transcription start sites to recruit the Wdr82–Set1A/COMPASS
(complex of proteins associated with Set1) complex, which is required for deposition
of the histone 3 Lys4 trimethyl (H3K4me3)-activating mark. Depletion of Nup98
or Wdr82 abolishes Set1A recruitment to chromatin and subsequently ablates H3K4me3
at adjacent promoters. Furthermore, expression of a Nup98 fusion protein implicated
in aggressive AML causes mislocalization of H3K4me3 at abnormal regions and up-regulation
of associated genes. Our findings establish a function of Nup98 in hematopoietic
gene activation and provide mechanistic insight into which Nup98 leukemic fusion
proteins promote AML.
article_processing_charge: No
article_type: original
author:
- first_name: Tobias M.
full_name: Franks, Tobias M.
last_name: Franks
- first_name: Asako
full_name: McCloskey, Asako
last_name: McCloskey
- first_name: Maxim Nikolaievich
full_name: Shokhirev, Maxim Nikolaievich
last_name: Shokhirev
- first_name: Chris
full_name: Benner, Chris
last_name: Benner
- first_name: Annie
full_name: Rathore, Annie
last_name: Rathore
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Franks TM, McCloskey A, Shokhirev MN, Benner C, Rathore A, Hetzer M. Nup98
recruits the Wdr82–Set1A/COMPASS complex to promoters to regulate H3K4 trimethylation
in hematopoietic progenitor cells. Genes & Development. 2017;31(22):2222-2234.
doi:10.1101/gad.306753.117
apa: Franks, T. M., McCloskey, A., Shokhirev, M. N., Benner, C., Rathore, A., &
Hetzer, M. (2017). Nup98 recruits the Wdr82–Set1A/COMPASS complex to promoters
to regulate H3K4 trimethylation in hematopoietic progenitor cells. Genes &
Development. Cold Spring Harbor Laboratory. https://doi.org/10.1101/gad.306753.117
chicago: Franks, Tobias M., Asako McCloskey, Maxim Nikolaievich Shokhirev, Chris
Benner, Annie Rathore, and Martin Hetzer. “Nup98 Recruits the Wdr82–Set1A/COMPASS
Complex to Promoters to Regulate H3K4 Trimethylation in Hematopoietic Progenitor
Cells.” Genes & Development. Cold Spring Harbor Laboratory, 2017. https://doi.org/10.1101/gad.306753.117.
ieee: T. M. Franks, A. McCloskey, M. N. Shokhirev, C. Benner, A. Rathore, and M.
Hetzer, “Nup98 recruits the Wdr82–Set1A/COMPASS complex to promoters to regulate
H3K4 trimethylation in hematopoietic progenitor cells,” Genes & Development,
vol. 31, no. 22. Cold Spring Harbor Laboratory, pp. 2222–2234, 2017.
ista: Franks TM, McCloskey A, Shokhirev MN, Benner C, Rathore A, Hetzer M. 2017.
Nup98 recruits the Wdr82–Set1A/COMPASS complex to promoters to regulate H3K4 trimethylation
in hematopoietic progenitor cells. Genes & Development. 31(22), 2222–2234.
mla: Franks, Tobias M., et al. “Nup98 Recruits the Wdr82–Set1A/COMPASS Complex to
Promoters to Regulate H3K4 Trimethylation in Hematopoietic Progenitor Cells.”
Genes & Development, vol. 31, no. 22, Cold Spring Harbor Laboratory,
2017, pp. 2222–34, doi:10.1101/gad.306753.117.
short: T.M. Franks, A. McCloskey, M.N. Shokhirev, C. Benner, A. Rathore, M. Hetzer,
Genes & Development 31 (2017) 2222–2234.
date_created: 2022-04-07T07:45:59Z
date_published: 2017-12-21T00:00:00Z
date_updated: 2022-07-18T08:33:05Z
day: '21'
doi: 10.1101/gad.306753.117
extern: '1'
external_id:
pmid:
- '29269482'
intvolume: ' 31'
issue: '22'
keyword:
- Developmental Biology
- Genetics
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1101/gad.306753.117
month: '12'
oa: 1
oa_version: Published Version
page: 2222-2234
pmid: 1
publication: Genes & Development
publication_identifier:
issn:
- 0890-9369
- 1549-5477
publication_status: published
publisher: Cold Spring Harbor Laboratory
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nup98 recruits the Wdr82–Set1A/COMPASS complex to promoters to regulate H3K4
trimethylation in hematopoietic progenitor cells
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 31
year: '2017'
...
---
_id: '11067'
abstract:
- lang: eng
text: Neural progenitor cells (NeuPCs) possess a unique nuclear architecture that
changes during differentiation. Nucleoporins are linked with cell-type-specific
gene regulation, coupling physical changes in nuclear structure to transcriptional
output; but, whether and how they coordinate with key fate-determining transcription
factors is unclear. Here we show that the nucleoporin Nup153 interacts with Sox2
in adult NeuPCs, where it is indispensable for their maintenance and controls
neuronal differentiation. Genome-wide analyses show that Nup153 and Sox2 bind
and co-regulate hundreds of genes. Binding of Nup153 to gene promoters or transcriptional
end sites correlates with increased or decreased gene expression, respectively,
and inhibiting Nup153 expression alters open chromatin configurations at its target
genes, disrupts genomic localization of Sox2, and promotes differentiation in
vitro and a gliogenic fate switch in vivo. Together, these findings reveal that
nuclear structural proteins may exert bimodal transcriptional effects to control
cell fate.
article_processing_charge: No
article_type: original
author:
- first_name: Tomohisa
full_name: Toda, Tomohisa
last_name: Toda
- first_name: Jonathan Y.
full_name: Hsu, Jonathan Y.
last_name: Hsu
- first_name: Sara B.
full_name: Linker, Sara B.
last_name: Linker
- first_name: Lauren
full_name: Hu, Lauren
last_name: Hu
- first_name: Simon T.
full_name: Schafer, Simon T.
last_name: Schafer
- first_name: Jerome
full_name: Mertens, Jerome
last_name: Mertens
- first_name: Filipe V.
full_name: Jacinto, Filipe V.
last_name: Jacinto
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
- first_name: Fred H.
full_name: Gage, Fred H.
last_name: Gage
citation:
ama: Toda T, Hsu JY, Linker SB, et al. Nup153 interacts with Sox2 to enable bimodal
gene regulation and maintenance of neural progenitor cells. Cell Stem Cell.
2017;21(5):618-634.e7. doi:10.1016/j.stem.2017.08.012
apa: Toda, T., Hsu, J. Y., Linker, S. B., Hu, L., Schafer, S. T., Mertens, J., …
Gage, F. H. (2017). Nup153 interacts with Sox2 to enable bimodal gene regulation
and maintenance of neural progenitor cells. Cell Stem Cell. Elsevier. https://doi.org/10.1016/j.stem.2017.08.012
chicago: Toda, Tomohisa, Jonathan Y. Hsu, Sara B. Linker, Lauren Hu, Simon T. Schafer,
Jerome Mertens, Filipe V. Jacinto, Martin Hetzer, and Fred H. Gage. “Nup153 Interacts
with Sox2 to Enable Bimodal Gene Regulation and Maintenance of Neural Progenitor
Cells.” Cell Stem Cell. Elsevier, 2017. https://doi.org/10.1016/j.stem.2017.08.012.
ieee: T. Toda et al., “Nup153 interacts with Sox2 to enable bimodal gene
regulation and maintenance of neural progenitor cells,” Cell Stem Cell,
vol. 21, no. 5. Elsevier, p. 618–634.e7, 2017.
ista: Toda T, Hsu JY, Linker SB, Hu L, Schafer ST, Mertens J, Jacinto FV, Hetzer
M, Gage FH. 2017. Nup153 interacts with Sox2 to enable bimodal gene regulation
and maintenance of neural progenitor cells. Cell Stem Cell. 21(5), 618–634.e7.
mla: Toda, Tomohisa, et al. “Nup153 Interacts with Sox2 to Enable Bimodal Gene Regulation
and Maintenance of Neural Progenitor Cells.” Cell Stem Cell, vol. 21, no.
5, Elsevier, 2017, p. 618–634.e7, doi:10.1016/j.stem.2017.08.012.
short: T. Toda, J.Y. Hsu, S.B. Linker, L. Hu, S.T. Schafer, J. Mertens, F.V. Jacinto,
M. Hetzer, F.H. Gage, Cell Stem Cell 21 (2017) 618–634.e7.
date_created: 2022-04-07T07:46:12Z
date_published: 2017-11-02T00:00:00Z
date_updated: 2022-07-18T08:33:07Z
day: '02'
doi: 10.1016/j.stem.2017.08.012
extern: '1'
external_id:
pmid:
- '28919367'
intvolume: ' 21'
issue: '5'
keyword:
- Cell Biology
- Genetics
- Molecular Medicine
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.stem.2017.08.012
month: '11'
oa: 1
oa_version: Published Version
page: 618-634.e7
pmid: 1
publication: Cell Stem Cell
publication_identifier:
issn:
- 1934-5909
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nup153 interacts with Sox2 to enable bimodal gene regulation and maintenance
of neural progenitor cells
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 21
year: '2017'
...
---
_id: '11065'
abstract:
- lang: eng
text: Premature aging disorders provide an opportunity to study the mechanisms that
drive aging. In Hutchinson-Gilford progeria syndrome (HGPS), a mutant form of
the nuclear scaffold protein lamin A distorts nuclei and sequesters nuclear proteins.
We sought to investigate protein homeostasis in this disease. Here, we report
a widespread increase in protein turnover in HGPS-derived cells compared to normal
cells. We determine that global protein synthesis is elevated as a consequence
of activated nucleoli and enhanced ribosome biogenesis in HGPS-derived fibroblasts.
Depleting normal lamin A or inducing mutant lamin A expression are each sufficient
to drive nucleolar expansion. We further show that nucleolar size correlates with
donor age in primary fibroblasts derived from healthy individuals and that ribosomal
RNA production increases with age, indicating that nucleolar size and activity
can serve as aging biomarkers. While limiting ribosome biogenesis extends lifespan
in several systems, we show that increased ribosome biogenesis and activity are
a hallmark of premature aging.
article_number: '328'
article_processing_charge: No
article_type: original
author:
- first_name: Abigail
full_name: Buchwalter, Abigail
last_name: Buchwalter
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
citation:
ama: Buchwalter A, Hetzer M. Nucleolar expansion and elevated protein translation
in premature aging. Nature Communications. 2017;8. doi:10.1038/s41467-017-00322-z
apa: Buchwalter, A., & Hetzer, M. (2017). Nucleolar expansion and elevated protein
translation in premature aging. Nature Communications. Springer Nature.
https://doi.org/10.1038/s41467-017-00322-z
chicago: Buchwalter, Abigail, and Martin Hetzer. “Nucleolar Expansion and Elevated
Protein Translation in Premature Aging.” Nature Communications. Springer
Nature, 2017. https://doi.org/10.1038/s41467-017-00322-z.
ieee: A. Buchwalter and M. Hetzer, “Nucleolar expansion and elevated protein translation
in premature aging,” Nature Communications, vol. 8. Springer Nature, 2017.
ista: Buchwalter A, Hetzer M. 2017. Nucleolar expansion and elevated protein translation
in premature aging. Nature Communications. 8, 328.
mla: Buchwalter, Abigail, and Martin Hetzer. “Nucleolar Expansion and Elevated Protein
Translation in Premature Aging.” Nature Communications, vol. 8, 328, Springer
Nature, 2017, doi:10.1038/s41467-017-00322-z.
short: A. Buchwalter, M. Hetzer, Nature Communications 8 (2017).
date_created: 2022-04-07T07:45:50Z
date_published: 2017-08-30T00:00:00Z
date_updated: 2022-07-18T08:33:03Z
day: '30'
doi: 10.1038/s41467-017-00322-z
extern: '1'
external_id:
pmid:
- '28855503'
intvolume: ' 8'
keyword:
- General Physics and Astronomy
- General Biochemistry
- Genetics and Molecular Biology
- General Chemistry
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1038/s41467-017-00322-z
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
issn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nucleolar expansion and elevated protein translation in premature aging
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 8
year: '2017'
...
---
_id: '11518'
abstract:
- lang: eng
text: "We present spectroscopic follow-up observations of CR7 with ALMA, targeted
at constraining the infrared (IR) continuum and [C II]158 mm line-emission at
high spatial resolution matched to the HST/WFC3 imaging. CR7 is a luminous Lyα
emitting galaxy at z = 6.6 that consists of three separated UV-continuum components.
Our observations reveal several well-separated components of [C II] emission.
The two most luminous components in [C II] coincide with the brightest UV components
(A and B), blueshifted by »150 km s−1 with respect to the\r\npeak of Lyα emission.
Other [C II] components are observed close to UV clumps B and C and are blueshifted
by »300 and ≈80 km s−1 with respect to the systemic redshift. We do not detect
FIR continuum emission due to dust with a 3σ limiting luminosity LIR T L d 35
K 3.1 10 = <´ 10 ( ) . This allows us to mitigate uncertainties in the dust-corrected
SFR and derive SFRs for the three UV clumps A, B, and C of 28, 5, and 7 M yr−1.
All clumps have [C II] luminosities consistent within the scatter observed in
the local relation between SFR and L[ ] C II , implying that strong Lyα emission
does not necessarily anti-correlate with [C II] luminosity. Combining\r\nour measurements
with the literature, we show that galaxies with blue UV slopes have weaker [C
II] emission at fixed SFR, potentially due to their lower metallicities and/or
higher photoionization. Comparison with hydrodynamical simulations suggests that
CR7ʼs clumps have metallicities of 0.1 Z Z 0.2 < < . The observed ISM structure
of CR7 indicates that we are likely witnessing the build up of a central galaxy
in the early universe through complex accretion of satellites."
acknowledgement: 'We thank the referee for their constructive comments, which have
helped improve the quality and clarity of this work. We thank Raffaella Schneider
for comments on an earlier version of this paper. We thank Leindert Boogaard, Steven
Bos, Rychard Bouwens, and Renske Smit for discussions. J.M. acknowledges the support
of a Huygens PhD fellowship from Leiden University. D.S. acknowledges financial
support from the Netherlands Organisation for Scientific research (NWO) through
a Veni fellowship and from Lancaster University through an Early Career Internal
Grant A100679. A.F. acknowledges support from the ERC Advanced Grant INTERSTELLAR
H2020/740120. B.D. acknowledges financial support from NASA through the Astrophysics
Data Analysis Program (ADAP), grant number NNX12AE20G. Based on observations made
with ESO Telescopes at the La Silla Paranal Observatory under programme ID 294.A-5018.
This paper makes use of the following ALMA data: ADS/JAO.ALMA#2015.1.00122.S. ALMA
is a partnership of ESO (representing its member states), NSF (USA), and NINS (Japan),
together with NRC (Canada) and NSC and ASIAA (Taiwan), and KASI (Republic of Korea),
in cooperation with the Republic of Chile. The Joint ALMA Observatory is operated
by ESO, AUI/NRAO, and NAOJ.'
article_number: '145'
article_processing_charge: No
article_type: original
author:
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: D.
full_name: Sobral, D.
last_name: Sobral
- first_name: F.
full_name: Boone, F.
last_name: Boone
- first_name: H.
full_name: Röttgering, H.
last_name: Röttgering
- first_name: D.
full_name: Schaerer, D.
last_name: Schaerer
- first_name: M.
full_name: Girard, M.
last_name: Girard
- first_name: A.
full_name: Pallottini, A.
last_name: Pallottini
- first_name: L.
full_name: Vallini, L.
last_name: Vallini
- first_name: A.
full_name: Ferrara, A.
last_name: Ferrara
- first_name: B.
full_name: Darvish, B.
last_name: Darvish
- first_name: B.
full_name: Mobasher, B.
last_name: Mobasher
citation:
ama: Matthee JJ, Sobral D, Boone F, et al. ALMA reveals metals yet no dust within
multiple components in CR7. The Astrophysical Journal. 2017;851(2). doi:10.3847/1538-4357/aa9931
apa: Matthee, J. J., Sobral, D., Boone, F., Röttgering, H., Schaerer, D., Girard,
M., … Mobasher, B. (2017). ALMA reveals metals yet no dust within multiple components
in CR7. The Astrophysical Journal. IOP Publishing. https://doi.org/10.3847/1538-4357/aa9931
chicago: Matthee, Jorryt J, D. Sobral, F. Boone, H. Röttgering, D. Schaerer, M.
Girard, A. Pallottini, et al. “ALMA Reveals Metals yet No Dust within Multiple
Components in CR7.” The Astrophysical Journal. IOP Publishing, 2017. https://doi.org/10.3847/1538-4357/aa9931.
ieee: J. J. Matthee et al., “ALMA reveals metals yet no dust within multiple
components in CR7,” The Astrophysical Journal, vol. 851, no. 2. IOP Publishing,
2017.
ista: Matthee JJ, Sobral D, Boone F, Röttgering H, Schaerer D, Girard M, Pallottini
A, Vallini L, Ferrara A, Darvish B, Mobasher B. 2017. ALMA reveals metals yet
no dust within multiple components in CR7. The Astrophysical Journal. 851(2),
145.
mla: Matthee, Jorryt J., et al. “ALMA Reveals Metals yet No Dust within Multiple
Components in CR7.” The Astrophysical Journal, vol. 851, no. 2, 145, IOP
Publishing, 2017, doi:10.3847/1538-4357/aa9931.
short: J.J. Matthee, D. Sobral, F. Boone, H. Röttgering, D. Schaerer, M. Girard,
A. Pallottini, L. Vallini, A. Ferrara, B. Darvish, B. Mobasher, The Astrophysical
Journal 851 (2017).
date_created: 2022-07-07T08:48:04Z
date_published: 2017-12-21T00:00:00Z
date_updated: 2022-08-18T10:23:35Z
day: '21'
doi: 10.3847/1538-4357/aa9931
extern: '1'
external_id:
arxiv:
- '1709.06569'
intvolume: ' 851'
issue: '2'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- dark ages
- reionization
- 'first stars – galaxies: formation – galaxies: high-redshift – galaxies: ISM – galaxies:
kinematics and dynamics'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1709.06569
month: '12'
oa: 1
oa_version: Preprint
publication: The Astrophysical Journal
publication_identifier:
eissn:
- 1538-4357
issn:
- 0004-637X
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: ALMA reveals metals yet no dust within multiple components in CR7
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 851
year: '2017'
...
---
_id: '11562'
abstract:
- lang: eng
text: We present the CAlibrating LYMan-α with Hα (CALYMHA) pilot survey and new
results on Lyman α (Lyα) selected galaxies at z ∼ 2. We use a custom-built Lyα
narrow-band filter at the Isaac Newton Telescope, designed to provide a matched
volume coverage to the z = 2.23 Hα HiZELS survey. Here, we present the first results
for the COSMOS and UDS fields. Our survey currently reaches a 3σ line flux limit
of ∼4 × 10−17 erg s−1 cm−2, and a Lyα luminosity limit of ∼1042.3 erg s−1. We
find 188 Lyα emitters over 7.3 × 105 Mpc3, but also find significant numbers of
other line-emitting sources corresponding to He II, C III] and C IV emission lines.
These sources are important contaminants, and we carefully remove them, unlike
most previous studies. We find that the Lyα luminosity function at z = 2.23 is
very well described by a Schechter function up to LLy α ≈ 1043 erg s−1 with L∗=1042.59+0.16−0.08
erg s−1, ϕ∗=10−3.09+0.14−0.34 Mpc−3 and α = −1.75 ± 0.25. Above LLy α ≈ 1043 erg
s−1, the Lyα luminosity function becomes power-law like, driven by X-ray AGN.
We find that Lyα-selected emitters have a high escape fraction of 37 ± 7 per cent,
anticorrelated with Lyα luminosity and correlated with Lyα equivalent width. Lyα
emitters have ubiquitous large (≈40 kpc) Lyα haloes, ∼2 times larger than their
Hα extents. By directly comparing our Lyα and Hα luminosity functions, we find
that the global/overall escape fraction of Lyα photons (within a 13 kpc radius)
from the full population of star-forming galaxies is 5.1 ± 0.2 per cent at the
peak of the star formation history. An extra 3.3 ± 0.3 per cent of Lyα photons
likely still escape, but at larger radii.
acknowledgement: 'We thank the reviewer for his/her helpful comments and suggestions
that have greatly improved this work. DS and JM acknowledge financial support from
the Netherlands Organisation for Scientific research (NWO) through a Veni fellowship.
DS also acknowledges funding from FCT through an FCT Investigator Starting Grant
and Start-up Grant (IF/01154/2012/CP0189/CT0010). PNB is grateful for support from
the UK STFC via grant ST/M001229/1. IRS acknowledges support from STFC (ST/L00075X/1),
the ERC Advanced Investigator programme DUSTYGAL 321334 and a Royal Society/Wolfson
merit award. We thank Matthew Hayes, Ryan Trainor, Kimihiko Nakajima and Anne Verhamme
for many helpful discussions and Ana Sobral, Carolina Duarte and Miguel Domingos
for taking part in observations with the NB392 filter. We also thank Sergio Santos
for helpful comments. This research is based on observations obtained on the Isaac
Newton Telescope (INT), programs: I13AN002, I14AN002, 088-INT7/14A, I14BN006, 118-INT13/14B
& I15AN008. The authors acknowledge the award of time from programmes: I13AN002,
I14AN002, 088-INT7/14A, I14BN006, 118-INT13/14B, I15AN008 on the INT. INT is operated
on the island of La Palma by the Isaac Newton Group in the Spanish Observatorio
del Roque de los Muchachos of the Instituto de Astrofisica de Canarias. Based on
observations made with ESO Telescopes at the La Silla Paranal Observatory under
programme ID 098.A 0819. We have benefited greatly from the publicly available programming
language PYTHON, including the NUMPY, MATPLOTLIB, PYFITS, SCIPY and ASTROPY packages,
the astronomical imaging tools SEXTRACTOR, SWARP (Bertin & Arnouts 1996; Bertin
2010), SCAMP (Bertin 2006) and TOPCAT (Taylor 2005). Dedicated to the memory of
M. L. Nicolau and M. C. Serrano.'
article_processing_charge: No
article_type: original
author:
- first_name: David
full_name: Sobral, David
last_name: Sobral
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: Philip
full_name: Best, Philip
last_name: Best
- first_name: Andra
full_name: Stroe, Andra
last_name: Stroe
- first_name: Huub
full_name: Röttgering, Huub
last_name: Röttgering
- first_name: Iván
full_name: Oteo, Iván
last_name: Oteo
- first_name: Ian
full_name: Smail, Ian
last_name: Smail
- first_name: Leah
full_name: Morabito, Leah
last_name: Morabito
- first_name: Ana
full_name: Paulino-Afonso, Ana
last_name: Paulino-Afonso
citation:
ama: 'Sobral D, Matthee JJ, Best P, et al. The CALYMHA survey: Lyα luminosity function
and global escape fraction of Lyα photons at z = 2.23. Monthly Notices of the
Royal Astronomical Society. 2017;466(1):1242-1258. doi:10.1093/mnras/stw3090'
apa: 'Sobral, D., Matthee, J. J., Best, P., Stroe, A., Röttgering, H., Oteo, I.,
… Paulino-Afonso, A. (2017). The CALYMHA survey: Lyα luminosity function and global
escape fraction of Lyα photons at z = 2.23. Monthly Notices of the Royal Astronomical
Society. Oxford University Press. https://doi.org/10.1093/mnras/stw3090'
chicago: 'Sobral, David, Jorryt J Matthee, Philip Best, Andra Stroe, Huub Röttgering,
Iván Oteo, Ian Smail, Leah Morabito, and Ana Paulino-Afonso. “The CALYMHA Survey:
Lyα Luminosity Function and Global Escape Fraction of Lyα Photons at z = 2.23.”
Monthly Notices of the Royal Astronomical Society. Oxford University Press,
2017. https://doi.org/10.1093/mnras/stw3090.'
ieee: 'D. Sobral et al., “The CALYMHA survey: Lyα luminosity function and
global escape fraction of Lyα photons at z = 2.23,” Monthly Notices of the
Royal Astronomical Society, vol. 466, no. 1. Oxford University Press, pp.
1242–1258, 2017.'
ista: 'Sobral D, Matthee JJ, Best P, Stroe A, Röttgering H, Oteo I, Smail I, Morabito
L, Paulino-Afonso A. 2017. The CALYMHA survey: Lyα luminosity function and global
escape fraction of Lyα photons at z = 2.23. Monthly Notices of the Royal Astronomical
Society. 466(1), 1242–1258.'
mla: 'Sobral, David, et al. “The CALYMHA Survey: Lyα Luminosity Function and Global
Escape Fraction of Lyα Photons at z = 2.23.” Monthly Notices of the Royal Astronomical
Society, vol. 466, no. 1, Oxford University Press, 2017, pp. 1242–58, doi:10.1093/mnras/stw3090.'
short: D. Sobral, J.J. Matthee, P. Best, A. Stroe, H. Röttgering, I. Oteo, I. Smail,
L. Morabito, A. Paulino-Afonso, Monthly Notices of the Royal Astronomical Society
466 (2017) 1242–1258.
date_created: 2022-07-12T12:04:16Z
date_published: 2017-04-01T00:00:00Z
date_updated: 2022-08-19T07:18:20Z
day: '01'
doi: 10.1093/mnras/stw3090
extern: '1'
external_id:
arxiv:
- '1609.05897'
intvolume: ' 466'
issue: '1'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'galaxies: evolution'
- 'galaxies: haloes'
- 'galaxies: high-redshift'
- 'galaxies: luminosity function'
- mass function
- 'galaxies: statistics'
- 'cosmology: observations'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1609.05897
month: '04'
oa: 1
oa_version: Preprint
page: 1242-1258
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
eissn:
- 1365-2966
issn:
- 0035-8711
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'The CALYMHA survey: Lyα luminosity function and global escape fraction of
Lyα photons at z = 2.23'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 466
year: '2017'
...
---
_id: '11566'
abstract:
- lang: eng
text: While traditionally associated with active galactic nuclei (AGN), the properties
of the C II] (λ = 2326 Å), C III] (λ, λ = 1907, 1909 Å) and C IV (λ, λ = 1549,
1551 Å) emission lines are still uncertain as large, unbiased samples of sources
are scarce. We present the first blind, statistical study of C II], C III] and
C IV emitters at z ∼ 0.68, 1.05, 1.53, respectively, uniformly selected down to
a flux limit of ∼4 × 10−17 erg s−1 cm−1 through a narrow-band survey covering
an area of ∼1.4 deg2 over COSMOS and UDS. We detect 16 C II], 35 C III] and 17
C IV emitters, whose nature we investigate using optical colours as well as Hubble
Space Telescope (HST), X-ray, radio and far-infrared data. We find that z ∼ 0.7
C II] emitters are consistent with a mixture of blue (UV slope β = −2.0 ± 0.4)
star-forming (SF) galaxies with discy HST structure and AGN with Seyfert-like
morphologies. Bright C II] emitters have individual X-ray detections as well as
high average black hole accretion rates (BHARs) of ∼0.1 M⊙ yr−1. C III] emitters
at z ∼ 1.05 trace a general population of SF galaxies, with β = −0.8 ± 1.1, a
variety of optical morphologies, including isolated and interacting galaxies and
low BHAR (<0.02 M⊙ yr−1). Our C IV emitters at z ∼ 1.5 are consistent with young,
blue quasars (β ∼ −1.9) with point-like optical morphologies, bright X-ray counterparts
and large BHAR (0.8 M⊙ yr−1). We also find some surprising C II], C III] and
C IV emitters with rest-frame equivalent widths (EWs) that could be as large as
50–100 Å. AGN or spatial offsets between the UV continuum stellar disc and the
line-emitting regions may explain the large EW. These bright C II], C III] and
C IV emitters are ideal candidates for spectroscopic follow-up to fully unveil
their nature.
acknowledgement: 'We would like to thank the anonymous referee for her/his valuable
input that helped improve the clarity and interpretation of our results. DS acknowledges
financial support from the Netherlands Organisation for Scientific research (NWO),
through a Veni fellowship. IO acknowledges support from the European Research Council
in the form of the Advanced Investigator Programme, 321302, COSMICISM. CALYMHA data
are based on observations made with the Isaac Newton Telescope (proposals 13AN002,
I14AN002, 088-INT7/14A, I14BN006, 118-INT13/14B, I15AN008) operated on the island
of La Palma by the Isaac Newton Group in the Spanish Observatorio del Roque de los
Muchachos of the Instituto de Astrofísica de Canarias. Also based on data products
from observations made with ESO Telescopes at the La Silla Paranal Observatory under
ESO programme IDs 098.A-0819 and 179.A-2005. We are grateful to E. L. Wright and
J. Schombert for their cosmology calculator. We would like to thank the authors
of NUMPY (van der Walt et al. 2011), SCIPY (Jones et al. 2001), MATPLOTLIB (Hunter
2007) and ASTROPY (Astropy Collaboration et al. 2013) for making these packages
publicly available. This research has made use of the NASA/IPAC Extragalactic Database
(NED), which is '
article_processing_charge: No
article_type: original
author:
- first_name: Andra
full_name: Stroe, Andra
last_name: Stroe
- first_name: David
full_name: Sobral, David
last_name: Sobral
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: João
full_name: Calhau, João
last_name: Calhau
- first_name: Ivan
full_name: Oteo, Ivan
last_name: Oteo
citation:
ama: Stroe A, Sobral D, Matthee JJ, Calhau J, Oteo I. A 1.4 deg2 blind survey for
C II], C III] and C IV at z ∼ 0.7–1.5 – I. Nature, morphologies and equivalent
widths . Monthly Notices of the Royal Astronomical Society. 2017;471(3):2558-2574.
doi:10.1093/mnras/stx1712
apa: Stroe, A., Sobral, D., Matthee, J. J., Calhau, J., & Oteo, I. (2017). A
1.4 deg2 blind survey for C II], C III] and C IV at z ∼ 0.7–1.5 – I. Nature, morphologies
and equivalent widths . Monthly Notices of the Royal Astronomical Society.
Oxford University Press. https://doi.org/10.1093/mnras/stx1712
chicago: Stroe, Andra, David Sobral, Jorryt J Matthee, João Calhau, and Ivan Oteo.
“A 1.4 Deg2 Blind Survey for C II], C III] and C IV at z ∼ 0.7–1.5 – I. Nature,
Morphologies and Equivalent Widths .” Monthly Notices of the Royal Astronomical
Society. Oxford University Press, 2017. https://doi.org/10.1093/mnras/stx1712.
ieee: A. Stroe, D. Sobral, J. J. Matthee, J. Calhau, and I. Oteo, “A 1.4 deg2 blind
survey for C II], C III] and C IV at z ∼ 0.7–1.5 – I. Nature, morphologies and
equivalent widths ,” Monthly Notices of the Royal Astronomical Society,
vol. 471, no. 3. Oxford University Press, pp. 2558–2574, 2017.
ista: Stroe A, Sobral D, Matthee JJ, Calhau J, Oteo I. 2017. A 1.4 deg2 blind survey
for C II], C III] and C IV at z ∼ 0.7–1.5 – I. Nature, morphologies and equivalent
widths . Monthly Notices of the Royal Astronomical Society. 471(3), 2558–2574.
mla: Stroe, Andra, et al. “A 1.4 Deg2 Blind Survey for C II], C III] and C IV at
z ∼ 0.7–1.5 – I. Nature, Morphologies and Equivalent Widths .” Monthly Notices
of the Royal Astronomical Society, vol. 471, no. 3, Oxford University Press,
2017, pp. 2558–74, doi:10.1093/mnras/stx1712.
short: A. Stroe, D. Sobral, J.J. Matthee, J. Calhau, I. Oteo, Monthly Notices of
the Royal Astronomical Society 471 (2017) 2558–2574.
date_created: 2022-07-12T12:33:16Z
date_published: 2017-11-01T00:00:00Z
date_updated: 2022-08-19T07:59:57Z
day: '01'
doi: 10.1093/mnras/stx1712
extern: '1'
external_id:
arxiv:
- '1703.10169'
intvolume: ' 471'
issue: '3'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'galaxies: active'
- 'galaxies: high-redshift'
- 'quasars: emission lines'
- 'galaxies: star formation'
- 'cosmology: observations'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1703.10169
month: '11'
oa: 1
oa_version: Preprint
page: 2558-2574
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
eissn:
- 1365-2966
issn:
- 0035-8711
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'A 1.4 deg2 blind survey for C II], C III] and C IV at z ∼ 0.7–1.5 – I. Nature,
morphologies and equivalent widths '
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 471
year: '2017'
...
---
_id: '11564'
abstract:
- lang: eng
text: We study the production rate of ionizing photons of a sample of 588 Hα emitters
(HAEs) and 160 Lyman-α emitters (LAEs) at z = 2.2 in the COSMOS field in order
to assess the implied emissivity from galaxies, based on their ultraviolet (UV)
luminosity. By exploring the rest-frame Lyman Continuum (LyC) with GALEX/NUV data,
we find fesc < 2.8 (6.4) per cent through median (mean) stacking. By combining
the Hα luminosity density with intergalactic medium emissivity measurements from
absorption studies, we find a globally averaged 〈fesc〉 of 5.9+14.5−4.2 per cent
at z = 2.2 if we assume HAEs are the only source of ionizing photons. We find
similarly low values of the global 〈fesc〉 at z ≈ 3–5, also ruling out a high 〈fesc〉
at z < 5. These low escape fractions allow us to measure ξion, the number of produced
ionizing photons per unit UV luminosity, and investigate how this depends on galaxy
properties. We find a typical ξion ≈ 1024.77 ± 0.04 Hz erg−1 for HAEs and ξion
≈ 1025.14 ± 0.09 Hz erg−1 for LAEs. LAEs and low-mass HAEs at z = 2.2 show similar
values of ξion as typically assumed in the reionization era, while the typical
HAE is three times less ionizing. Due to an increasing ξion with increasing EW(Hα),
ξion likely increases with redshift. This evolution alone is fully in line with
the observed evolution of ξion between z ≈ 2 and 5, indicating a typical value
of ξion ≈ 1025.4 Hz erg−1 in the reionization era.
acknowledgement: "We thank the referee for the many helpful and constructive comments
which have significantly improved this paper. JM acknowledges the support of a Huygens
PhD fellowship from Leiden University. DS acknowledges financial support from the
Netherlands Organization for Scientific research (NWO) through a Veni fellowship
and from FCT through an FCT Investigator Starting Grant and Start-up Grant (IF/01154/2012/CP0189/CT0010).
PNB is grateful for support from the UK STFC via grant ST/M001229/1. IO acknowledges
support from the European Research Council in the form of the Advanced Investigator
Programme, 321302, COSMICISM. The authors thank Andreas Faisst, Michael Rutkowski
and Andreas Sandberg for answering questions related to this work and Daniel Schaerer
and Mark Dijkstra for discussions. We acknowledge the work that has been done by
both the COSMOS team in assembling such large, state-of-the-art multi-wavelength
data set, as this has been crucial for the results presented in this paper. We have
benefited greatly from the public available programming language PYTHON, including
the NUMPY, MATPLOTLIB, PYFITS, SCIPY (Jones et al. 2001; Hunter 2007; Van Der Walt,
Colbert & Varoquaux 2011) and ASTROPY (Astropy Collaboration et al. 2013) packages,
the astronomical imaging tools SEXTRACTOR and SWARP (Bertin & Arnouts 1996;\r\nBertin
2010) and the TOPCAT analysis program (Taylor 2013)."
article_processing_charge: No
article_type: original
author:
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: David
full_name: Sobral, David
last_name: Sobral
- first_name: Philip
full_name: Best, Philip
last_name: Best
- first_name: Ali Ahmad
full_name: Khostovan, Ali Ahmad
last_name: Khostovan
- first_name: Iván
full_name: Oteo, Iván
last_name: Oteo
- first_name: Rychard
full_name: Bouwens, Rychard
last_name: Bouwens
- first_name: Huub
full_name: Röttgering, Huub
last_name: Röttgering
citation:
ama: Matthee JJ, Sobral D, Best P, et al. The production and escape of Lyman-Continuum
radiation from star-forming galaxies at z ∼ 2 and their redshift evolution. Monthly
Notices of the Royal Astronomical Society. 2017;465(3):3637-3655. doi:10.1093/mnras/stw2973
apa: Matthee, J. J., Sobral, D., Best, P., Khostovan, A. A., Oteo, I., Bouwens,
R., & Röttgering, H. (2017). The production and escape of Lyman-Continuum
radiation from star-forming galaxies at z ∼ 2 and their redshift evolution. Monthly
Notices of the Royal Astronomical Society. Oxford University Press. https://doi.org/10.1093/mnras/stw2973
chicago: Matthee, Jorryt J, David Sobral, Philip Best, Ali Ahmad Khostovan, Iván
Oteo, Rychard Bouwens, and Huub Röttgering. “The Production and Escape of Lyman-Continuum
Radiation from Star-Forming Galaxies at z ∼ 2 and Their Redshift Evolution.” Monthly
Notices of the Royal Astronomical Society. Oxford University Press, 2017.
https://doi.org/10.1093/mnras/stw2973.
ieee: J. J. Matthee et al., “The production and escape of Lyman-Continuum
radiation from star-forming galaxies at z ∼ 2 and their redshift evolution,” Monthly
Notices of the Royal Astronomical Society, vol. 465, no. 3. Oxford University
Press, pp. 3637–3655, 2017.
ista: Matthee JJ, Sobral D, Best P, Khostovan AA, Oteo I, Bouwens R, Röttgering
H. 2017. The production and escape of Lyman-Continuum radiation from star-forming
galaxies at z ∼ 2 and their redshift evolution. Monthly Notices of the Royal Astronomical
Society. 465(3), 3637–3655.
mla: Matthee, Jorryt J., et al. “The Production and Escape of Lyman-Continuum Radiation
from Star-Forming Galaxies at z ∼ 2 and Their Redshift Evolution.” Monthly
Notices of the Royal Astronomical Society, vol. 465, no. 3, Oxford University
Press, 2017, pp. 3637–55, doi:10.1093/mnras/stw2973.
short: J.J. Matthee, D. Sobral, P. Best, A.A. Khostovan, I. Oteo, R. Bouwens, H.
Röttgering, Monthly Notices of the Royal Astronomical Society 465 (2017) 3637–3655.
date_created: 2022-07-12T12:12:14Z
date_published: 2017-03-01T00:00:00Z
date_updated: 2022-08-19T07:53:04Z
day: '01'
doi: 10.1093/mnras/stw2973
extern: '1'
external_id:
arxiv:
- '1605.08782'
intvolume: ' 465'
issue: '3'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'galaxies: evolution'
- 'galaxies: high-redshift'
- 'cosmology: observations'
- dark ages
- reionization
- first stars
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1605.08782
month: '03'
oa: 1
oa_version: Preprint
page: 3637-3655
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
eissn:
- 1365-2966
issn:
- 0035-8711
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: The production and escape of Lyman-Continuum radiation from star-forming galaxies
at z ∼ 2 and their redshift evolution
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 465
year: '2017'
...
---
_id: '11567'
abstract:
- lang: eng
text: Recently, the C III] and C IV emission lines have been observed in galaxies
in the early Universe (z > 5), providing new ways to measure their redshift and
study their stellar populations and active galactic nuclei (AGN). We explore the
first blind C II], C III] and C IV survey (z ∼ 0.68, 1.05, 1.53, respectively)
presented in Stroe et al. (2017). We derive luminosity functions (LF) and study
properties of C II], C III] and C IV line emitters through comparisons to the
LFs of H α and Ly α emitters, UV selected star-forming (SF) galaxies and quasars
at similar redshifts. The C II] LF at z ∼ 0.68 is equally well described by a
Schechter or a power-law LF, characteristic of a mixture of SF and AGN activity.
The C III] LF (z ∼ 1.05) is consistent to a scaled down version of the Schechter
H α and Ly α LF at their redshift, indicating a SF origin. In stark contrast,
the C IV LF at z ∼ 1.53 is well fit by a power-law, quasar-like LF. We find that
the brightest UV sources (MUV < −22) will universally have C III] and C IV emission.
However, on average, C III] and C IV are not as abundant as H α or Ly α emitters
at the same redshift, with cosmic average ratios of ∼0.02–0.06 to H α and ∼0.01–0.1
to intrinsic Ly α. We predict that the C III] and C IV lines can only be truly
competitive in confirming high-redshift candidates when the hosts are intrinsically
bright and the effective Ly α escape fraction is below 1 per cent. While C III]
and C IV were proposed as good tracers of young, relatively low-metallicity galaxies
typical of the early Universe, we find that, at least at z ∼ 1.5, C IV is exclusively
hosted by AGN/quasars, especially at large line equivalent widths.
article_processing_charge: No
article_type: original
author:
- first_name: Andra
full_name: Stroe, Andra
last_name: Stroe
- first_name: David
full_name: Sobral, David
last_name: Sobral
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: João
full_name: Calhau, João
last_name: Calhau
- first_name: Ivan
full_name: Oteo, Ivan
last_name: Oteo
citation:
ama: Stroe A, Sobral D, Matthee JJ, Calhau J, Oteo I. A 1.4 deg2 blind survey for
C II], C III] and C IV at z ∼ 0.7–1.5 – II. Luminosity functions and cosmic average
line ratios. Monthly Notices of the Royal Astronomical Society. 2017;471(3):2575-2586.
doi:10.1093/mnras/stx1713
apa: Stroe, A., Sobral, D., Matthee, J. J., Calhau, J., & Oteo, I. (2017). A
1.4 deg2 blind survey for C II], C III] and C IV at z ∼ 0.7–1.5 – II. Luminosity
functions and cosmic average line ratios. Monthly Notices of the Royal Astronomical
Society. Oxford University Press. https://doi.org/10.1093/mnras/stx1713
chicago: Stroe, Andra, David Sobral, Jorryt J Matthee, João Calhau, and Ivan Oteo.
“A 1.4 Deg2 Blind Survey for C II], C III] and C IV at z ∼ 0.7–1.5 – II. Luminosity
Functions and Cosmic Average Line Ratios.” Monthly Notices of the Royal Astronomical
Society. Oxford University Press, 2017. https://doi.org/10.1093/mnras/stx1713.
ieee: A. Stroe, D. Sobral, J. J. Matthee, J. Calhau, and I. Oteo, “A 1.4 deg2 blind
survey for C II], C III] and C IV at z ∼ 0.7–1.5 – II. Luminosity functions and
cosmic average line ratios,” Monthly Notices of the Royal Astronomical Society,
vol. 471, no. 3. Oxford University Press, pp. 2575–2586, 2017.
ista: Stroe A, Sobral D, Matthee JJ, Calhau J, Oteo I. 2017. A 1.4 deg2 blind survey
for C II], C III] and C IV at z ∼ 0.7–1.5 – II. Luminosity functions and cosmic
average line ratios. Monthly Notices of the Royal Astronomical Society. 471(3),
2575–2586.
mla: Stroe, Andra, et al. “A 1.4 Deg2 Blind Survey for C II], C III] and C IV at
z ∼ 0.7–1.5 – II. Luminosity Functions and Cosmic Average Line Ratios.” Monthly
Notices of the Royal Astronomical Society, vol. 471, no. 3, Oxford University
Press, 2017, pp. 2575–86, doi:10.1093/mnras/stx1713.
short: A. Stroe, D. Sobral, J.J. Matthee, J. Calhau, I. Oteo, Monthly Notices of
the Royal Astronomical Society 471 (2017) 2575–2586.
date_created: 2022-07-12T12:54:57Z
date_published: 2017-11-01T00:00:00Z
date_updated: 2022-08-19T08:02:04Z
day: '01'
doi: 10.1093/mnras/stx1713
extern: '1'
external_id:
arxiv:
- '1703.10169'
intvolume: ' 471'
issue: '3'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'galaxies: active'
- 'galaxies: high redshift'
- 'galaxies: luminosity function'
- mass function
- 'quasars: emission lines'
- star formation
- 'cosmology: observations'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1703.10169
month: '11'
oa: 1
oa_version: Preprint
page: 2575-2586
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
eissn:
- 1365-2966
issn:
- 0035-8711
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: A 1.4 deg2 blind survey for C II], C III] and C IV at z ∼ 0.7–1.5 – II. Luminosity
functions and cosmic average line ratios
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 471
year: '2017'
...
---
_id: '11565'
abstract:
- lang: eng
text: We use the hydrodynamical EAGLE simulation to study the magnitude and origin
of the scatter in the stellar mass–halo mass relation for central galaxies. We
separate cause and effect by correlating stellar masses in the baryonic simulation
with halo properties in a matched dark matter only (DMO) simulation. The scatter
in stellar mass increases with redshift and decreases with halo mass. At z = 0.1,
it declines from 0.25 dex at M200, DMO ≈ 1011 M⊙ to 0.12 dex at M200, DMO ≈ 1013
M⊙, but the trend is weak above 1012 M⊙. For M200, DMO < 1012.5 M⊙ up to 0.04
dex of the scatter is due to scatter in the halo concentration. At fixed halo
mass, a larger stellar mass corresponds to a more concentrated halo. This is likely
because higher concentrations imply earlier formation times and hence more time
for accretion and star formation, and/or because feedback is less efficient in
haloes with higher binding energies. The maximum circular velocity, Vmax, DMO,
and binding energy are therefore more fundamental properties than halo mass, meaning
that they are more accurate predictors of stellar mass, and we provide fitting
formulae for their relations with stellar mass. However, concentration alone cannot
explain the total scatter in the Mstar−M200,DMO relation, and it does not explain
the scatter in Mstar–Vmax, DMO. Halo spin, sphericity, triaxiality, substructure
and environment are also not responsible for the remaining scatter, which thus
could be due to more complex halo properties or non-linear/stochastic baryonic
effects.
acknowledgement: We thank the anonymous referee for their comments. JM acknowledges
the support of a Huygens PhD fellowship from Leiden University. JM thanks David
Sobral for useful discussions and help with fitting routines and Jonas Chavez Montero
and Ying Zu for providing data. We thank PRACE for the access to the Curie facility
in France. We have used the DiRAC system which is a part of National E-Infrastructure
at Durham University, operated by the Institute for Computational Cosmology on behalf
of the STFC DiRAC HPC Facility (www.dirac.ac.uk); the equipment was funded by BIS
National E-infrastructure capital grant ST/K00042X/1, STFC capital grant ST/H008519/1,
STFC DiRAC Operations grant ST/K003267/1 and Durham University. The study was sponsored
by the Dutch National Computing Facilities Foundation (NCF) for the use of supercomputer
facilities, with financial support from the Netherlands Organisation for Scientific
Research (NWO), through VICI grant 639.043.409, and the European Research Council
under the European Union’s Seventh Framework Programme (FP7/2007-2013)/ERC Grant
agreement 278594- GasAroundGalaxies, and from the Belgian Science Policy Office
([AP P7/08 CHARM]). We have benefited greatly from the public available programming
language PYTHON, including the NUMPY, MATPLOTLIB, PYFITS, SCIPY, H5PY and RPY2 packages,
and the TOPCAT analysis program (Taylor 2005).
article_processing_charge: No
article_type: original
author:
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: Joop
full_name: Schaye, Joop
last_name: Schaye
- first_name: Robert A.
full_name: Crain, Robert A.
last_name: Crain
- first_name: Matthieu
full_name: Schaller, Matthieu
last_name: Schaller
- first_name: Richard
full_name: Bower, Richard
last_name: Bower
- first_name: Tom
full_name: Theuns, Tom
last_name: Theuns
citation:
ama: Matthee JJ, Schaye J, Crain RA, Schaller M, Bower R, Theuns T. The origin of
scatter in the stellar mass–halo mass relation of central galaxies in the EAGLE
simulation. Monthly Notices of the Royal Astronomical Society. 2017;465(2):2381-2396.
doi:10.1093/mnras/stw2884
apa: Matthee, J. J., Schaye, J., Crain, R. A., Schaller, M., Bower, R., & Theuns,
T. (2017). The origin of scatter in the stellar mass–halo mass relation of central
galaxies in the EAGLE simulation. Monthly Notices of the Royal Astronomical
Society. Oxford University Press. https://doi.org/10.1093/mnras/stw2884
chicago: Matthee, Jorryt J, Joop Schaye, Robert A. Crain, Matthieu Schaller, Richard
Bower, and Tom Theuns. “The Origin of Scatter in the Stellar Mass–Halo Mass Relation
of Central Galaxies in the EAGLE Simulation.” Monthly Notices of the Royal
Astronomical Society. Oxford University Press, 2017. https://doi.org/10.1093/mnras/stw2884.
ieee: J. J. Matthee, J. Schaye, R. A. Crain, M. Schaller, R. Bower, and T. Theuns,
“The origin of scatter in the stellar mass–halo mass relation of central galaxies
in the EAGLE simulation,” Monthly Notices of the Royal Astronomical Society,
vol. 465, no. 2. Oxford University Press, pp. 2381–2396, 2017.
ista: Matthee JJ, Schaye J, Crain RA, Schaller M, Bower R, Theuns T. 2017. The origin
of scatter in the stellar mass–halo mass relation of central galaxies in the EAGLE
simulation. Monthly Notices of the Royal Astronomical Society. 465(2), 2381–2396.
mla: Matthee, Jorryt J., et al. “The Origin of Scatter in the Stellar Mass–Halo
Mass Relation of Central Galaxies in the EAGLE Simulation.” Monthly Notices
of the Royal Astronomical Society, vol. 465, no. 2, Oxford University Press,
2017, pp. 2381–96, doi:10.1093/mnras/stw2884.
short: J.J. Matthee, J. Schaye, R.A. Crain, M. Schaller, R. Bower, T. Theuns, Monthly
Notices of the Royal Astronomical Society 465 (2017) 2381–2396.
date_created: 2022-07-12T12:25:08Z
date_published: 2017-02-01T00:00:00Z
date_updated: 2022-08-19T07:56:07Z
day: '01'
doi: 10.1093/mnras/stw2884
extern: '1'
external_id:
arxiv:
- '1608.08218'
intvolume: ' 465'
issue: '2'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'galaxies: evolution'
- 'galaxies: formation'
- 'galaxies: haloes'
- 'cosmology: theory'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1608.08218
month: '02'
oa: 1
oa_version: Preprint
page: 2381-2396
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
eissn:
- 1365-2966
issn:
- 0035-8711
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: The origin of scatter in the stellar mass–halo mass relation of central galaxies
in the EAGLE simulation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 465
year: '2017'
...
---
_id: '11561'
abstract:
- lang: eng
text: We present a sample of ∼1000 emission-line galaxies at z = 0.4–4.7 from the
∼0.7deg2 High-z Emission-Line Survey in the Boötes field identified with a suite
of six narrow-band filters at ≈0.4–2.1 μm. These galaxies have been selected on
their Ly α (73), [O II] (285), H β/[O III] (387) or H α (362) emission line, and
have been classified with optical to near-infrared colours. A subsample of 98
sources have reliable redshifts from multiple narrow-band (e.g. [O II]–H α) detections
and/or spectroscopy. In this survey paper, we present the observations, selection
and catalogues of emitters. We measure number densities of Ly α, [O II], H β/[O III]
and H α and confirm strong luminosity evolution in star-forming galaxies from
z ∼ 0.4 to ∼5, in agreement with previous results. To demonstrate the usefulness
of dual-line emitters, we use the sample of dual [O II]–H α emitters to measure
the observed [O II]/H α ratio at z = 1.47. The observed [O II]/H α ratio increases
significantly from 0.40 ± 0.01 at z = 0.1 to 0.52 ± 0.05 at z = 1.47, which we
attribute to either decreasing dust attenuation with redshift, or due to a bias
in the (typically) fibre measurements in the local Universe that only measure
the central kpc regions. At the bright end, we find that both the H α and Ly α
number densities at z ≈ 2.2 deviate significantly from a Schechter form, following
a power law. We show that this is driven entirely by an increasing X-ray/active
galactic nucleus fraction with line luminosity, which reaches ≈100 per cent at
line luminosities L ≳ 3 × 1044 erg s−1.
article_processing_charge: No
article_type: original
author:
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: David
full_name: Sobral, David
last_name: Sobral
- first_name: Philip
full_name: Best, Philip
last_name: Best
- first_name: Ian
full_name: Smail, Ian
last_name: Smail
- first_name: Fuyan
full_name: Bian, Fuyan
last_name: Bian
- first_name: Behnam
full_name: Darvish, Behnam
last_name: Darvish
- first_name: Huub
full_name: Röttgering, Huub
last_name: Röttgering
- first_name: Xiaohui
full_name: Fan, Xiaohui
last_name: Fan
citation:
ama: 'Matthee JJ, Sobral D, Best P, et al. Boötes-HiZELS: An optical to near-infrared
survey of emission-line galaxies at z = 0.4–4.7. Monthly Notices of the Royal
Astronomical Society. 2017;471(1):629-649. doi:10.1093/mnras/stx1569'
apa: 'Matthee, J. J., Sobral, D., Best, P., Smail, I., Bian, F., Darvish, B., …
Fan, X. (2017). Boötes-HiZELS: An optical to near-infrared survey of emission-line
galaxies at z = 0.4–4.7. Monthly Notices of the Royal Astronomical Society.
Oxford University Press. https://doi.org/10.1093/mnras/stx1569'
chicago: 'Matthee, Jorryt J, David Sobral, Philip Best, Ian Smail, Fuyan Bian, Behnam
Darvish, Huub Röttgering, and Xiaohui Fan. “Boötes-HiZELS: An Optical to near-Infrared
Survey of Emission-Line Galaxies at z = 0.4–4.7.” Monthly Notices of the Royal
Astronomical Society. Oxford University Press, 2017. https://doi.org/10.1093/mnras/stx1569.'
ieee: 'J. J. Matthee et al., “Boötes-HiZELS: An optical to near-infrared
survey of emission-line galaxies at z = 0.4–4.7,” Monthly Notices of the Royal
Astronomical Society, vol. 471, no. 1. Oxford University Press, pp. 629–649,
2017.'
ista: 'Matthee JJ, Sobral D, Best P, Smail I, Bian F, Darvish B, Röttgering H, Fan
X. 2017. Boötes-HiZELS: An optical to near-infrared survey of emission-line galaxies
at z = 0.4–4.7. Monthly Notices of the Royal Astronomical Society. 471(1), 629–649.'
mla: 'Matthee, Jorryt J., et al. “Boötes-HiZELS: An Optical to near-Infrared Survey
of Emission-Line Galaxies at z = 0.4–4.7.” Monthly Notices of the Royal Astronomical
Society, vol. 471, no. 1, Oxford University Press, 2017, pp. 629–49, doi:10.1093/mnras/stx1569.'
short: J.J. Matthee, D. Sobral, P. Best, I. Smail, F. Bian, B. Darvish, H. Röttgering,
X. Fan, Monthly Notices of the Royal Astronomical Society 471 (2017) 629–649.
date_created: 2022-07-12T11:01:35Z
date_published: 2017-10-01T00:00:00Z
date_updated: 2022-08-19T07:15:14Z
day: '01'
doi: 10.1093/mnras/stx1569
extern: '1'
external_id:
arxiv:
- '1702.04721'
intvolume: ' 471'
issue: '1'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics galaxies
- active
- galaxies
- evolution
- galaxies
- high-redshift
- galaxies
- luminosity function
- mass function
- 'galaxies: star formation'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1702.04721
month: '10'
oa: 1
oa_version: Preprint
page: 629-649
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
issn:
- 0035-8711
- 1365-2966
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Boötes-HiZELS: An optical to near-infrared survey of emission-line galaxies
at z = 0.4–4.7'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 471
year: '2017'
...
---
_id: '11572'
abstract:
- lang: eng
text: We present spectroscopic follow-up of candidate luminous Ly α emitters (LAEs)
at z = 5.7–6.6 in the SA22 field with VLT/X-SHOOTER. We confirm two new luminous
LAEs at z = 5.676 (SR6) and z = 6.532 (VR7), and also present HST follow-up of
both sources. These sources have luminosities LLy α ≈ 3 × 1043 erg s−1, very high
rest-frame equivalent widths of EW0 ≳ 200 Å and narrow Ly α lines (200–340 km s−1).
VR7 is the most UV-luminous LAE at z > 6.5, with M1500 = −22.5, even brighter
in the UV than CR7. Besides Ly α, we do not detect any other rest-frame UV lines
in the spectra of SR6 and VR7, and argue that rest-frame UV lines are easier to
observe in bright galaxies with low Ly α equivalent widths. We confirm that Ly α
line widths increase with Ly α luminosity at z = 5.7, while there are indications
that Ly α lines of faint LAEs become broader at z = 6.6, potentially due to reionization.
We find a large spread of up to 3 dex in UV luminosity for >L⋆ LAEs, but find
that the Ly α luminosity of the brightest LAEs is strongly related to UV luminosity
at z = 6.6. Under basic assumptions, we find that several LAEs at z ≈ 6–7 have
Ly α escape fractions ≳ 100 per cent, indicating bursty star formation histories,
alternative Ly α production mechanisms, or dust attenuating Ly α emission differently
than UV emission. Finally, we present a method to compute ξion, the production
efficiency of ionizing photons, and find that LAEs at z ≈ 6–7 have high values
of log10(ξion/Hz erg−1) ≈ 25.51 ± 0.09 that may alleviate the need for high Lyman-Continuum
escape fractions required for reionization.
acknowledgement: 'We thank the referee for a constructive report that has improved
the quality and clarity of this work. The authors thank Grecco Oyarzún for discussions.
JM acknowledges the support of a Huygens PhD fellowship from Leiden University.
DS acknowledges financial support from the Netherlands Organisation for Scientific
research (NWO) through a Veni fellowship and from Lancaster University through an
Early Career Internal Grant A100679. BD acknowledges financial support from NASA
through the Astrophysics Data Analysis Program (ADAP), grant number NNX12AE20G.
We thank Kasper Schmidt for providing measurements. Based on observations with the
W.M. Keck Observatory through programme C267D. The W.M. Keck Observatory is operated
as a scientific partnership amongst the California Institute of Technology, the
University of California and the National Aeronautics and Space Administration.
Based on observations made with ESO Telescopes at the La Silla Paranal Observatory
under programme IDs 097.A-0943, 294.A 5018 and 098.A-0819 and on data products produced
by TERAPIX and the Cambridge Astronomy Survey Unit on behalf of the UltraVISTA consortium.
The authors acknowledge the award of observing time (W16AN004) and of service time
(SW2014b20) on the William Herschel Telescope (WHT). WHT and its service programme
are operated on the island of La Palma by the Isaac Newton Group in the Spanish
Observatorio del Roque de los Muchachos of the Instituto de Astrofisica de Canarias.
Based on observations made with the NASA/ESA HST, obtained (from the Data Archive)
at the Space Telescope Science Institute, which is operated by the Association of
Universities for Research in Astronomy, Inc., under NASA contract NAS 5-26555. These
observations are associated with programme #14699. We are grateful for the excellent
data sets from the COSMOS, UltraVISTA, SXDS, UDS and CFHTLS survey teams; without
these legacy surveys, this research would have been impossible. We have benefited
from the public available programming language PYTHON, including the NUMPY, MATPLOTLIB,
PYFITS, SCIPY and ASTROPY packages, the astronomical imaging tools SEXTRACTOR, SWARP
and SCAMP and the TOPCAT analysis tool (Taylor 2013).'
article_processing_charge: No
article_type: original
author:
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: David
full_name: Sobral, David
last_name: Sobral
- first_name: Behnam
full_name: Darvish, Behnam
last_name: Darvish
- first_name: Sérgio
full_name: Santos, Sérgio
last_name: Santos
- first_name: Bahram
full_name: Mobasher, Bahram
last_name: Mobasher
- first_name: Ana
full_name: Paulino-Afonso, Ana
last_name: Paulino-Afonso
- first_name: Huub
full_name: Röttgering, Huub
last_name: Röttgering
- first_name: Lara
full_name: Alegre, Lara
last_name: Alegre
citation:
ama: Matthee JJ, Sobral D, Darvish B, et al. Spectroscopic properties of luminous
Ly α emitters at z ≈ 6–7 and comparison to the Lyman-break population. Monthly
Notices of the Royal Astronomical Society. 2017;472(1):772-787. doi:10.1093/mnras/stx2061
apa: Matthee, J. J., Sobral, D., Darvish, B., Santos, S., Mobasher, B., Paulino-Afonso,
A., … Alegre, L. (2017). Spectroscopic properties of luminous Ly α emitters at
z ≈ 6–7 and comparison to the Lyman-break population. Monthly Notices of the
Royal Astronomical Society. Oxford University Press. https://doi.org/10.1093/mnras/stx2061
chicago: Matthee, Jorryt J, David Sobral, Behnam Darvish, Sérgio Santos, Bahram
Mobasher, Ana Paulino-Afonso, Huub Röttgering, and Lara Alegre. “Spectroscopic
Properties of Luminous Ly α Emitters at z ≈ 6–7 and Comparison to the Lyman-Break
Population.” Monthly Notices of the Royal Astronomical Society. Oxford
University Press, 2017. https://doi.org/10.1093/mnras/stx2061.
ieee: J. J. Matthee et al., “Spectroscopic properties of luminous Ly α emitters
at z ≈ 6–7 and comparison to the Lyman-break population,” Monthly Notices of
the Royal Astronomical Society, vol. 472, no. 1. Oxford University Press,
pp. 772–787, 2017.
ista: Matthee JJ, Sobral D, Darvish B, Santos S, Mobasher B, Paulino-Afonso A, Röttgering
H, Alegre L. 2017. Spectroscopic properties of luminous Ly α emitters at z ≈ 6–7
and comparison to the Lyman-break population. Monthly Notices of the Royal Astronomical
Society. 472(1), 772–787.
mla: Matthee, Jorryt J., et al. “Spectroscopic Properties of Luminous Ly α Emitters
at z ≈ 6–7 and Comparison to the Lyman-Break Population.” Monthly Notices of
the Royal Astronomical Society, vol. 472, no. 1, Oxford University Press,
2017, pp. 772–87, doi:10.1093/mnras/stx2061.
short: J.J. Matthee, D. Sobral, B. Darvish, S. Santos, B. Mobasher, A. Paulino-Afonso,
H. Röttgering, L. Alegre, Monthly Notices of the Royal Astronomical Society 472
(2017) 772–787.
date_created: 2022-07-13T09:47:39Z
date_published: 2017-11-01T00:00:00Z
date_updated: 2022-08-19T08:05:37Z
day: '01'
doi: 10.1093/mnras/stx2061
extern: '1'
external_id:
arxiv:
- '1706.06591'
intvolume: ' 472'
issue: '1'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'galaxies: evolution – galaxies: high-redshift'
- dark ages
- reionization
- first stars
- 'cosmology: observations'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1706.06591
month: '11'
oa: 1
oa_version: Preprint
page: 772-787
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
eissn:
- 1365-2966
issn:
- 0035-8711
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Spectroscopic properties of luminous Ly α emitters at z ≈ 6–7 and comparison
to the Lyman-break population
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 472
year: '2017'
...
---
_id: '11573'
abstract:
- lang: eng
text: We present dynamical measurements from the KMOS (K-band multi-object spectrograph)
Deep Survey (KDS), which comprises 77 typical star-forming galaxies at z ≃ 3.5
in the mass range 9.0 < log (M⋆/M⊙) < 10.5. These measurements constrain the internal
dynamics, the intrinsic velocity dispersions (σint) and rotation velocities (VC)
of galaxies in the high-redshift Universe. The mean velocity dispersion of the
galaxies in our sample is σint=70.8+3.3−3.1kms−1, revealing that the increasing
average σint with increasing redshift, reported for z ≲ 2, continues out to z
≃ 3.5. Only 36 ± 8 per cent of our galaxies are rotation-dominated (VC/σint >
1), with the sample average VC/σint value much smaller than at lower redshift.
After carefully selecting comparable star-forming samples at multiple epochs,
we find that the rotation-dominated fraction evolves with redshift with a z−0.2
dependence. The rotation-dominated KDS galaxies show no clear offset from the
local rotation velocity–stellar mass (i.e. VC–M⋆) relation, although a smaller
fraction of the galaxies are on the relation due to the increase in the dispersion-dominated
fraction. These observations are consistent with a simple equilibrium model picture,
in which random motions are boosted in high-redshift galaxies by a combination
of the increasing gas fractions, accretion efficiency, specific star formation
rate and stellar feedback and which may provide significant pressure support against
gravity on the galactic disc scale.
acknowledgement: 'We wish to thank the anonymous referee for their comments, which
have improved the quality and clarity of this work. OJT acknowledges the financial
support of the Science and Technology Facilities Council through a studentship award.
MC and OJT acknowledge the KMOS team and all the personnel of the European Southern
Observatory Very Large Telescope for outstanding support during the KMOS GTO observations.
CMH, AMS and RMS acknowledge the Science and Technology Facilities Council through
grant code ST/L00075X/1. RJM acknowledges the support of the European Research Council
via the award of a Consolidator Grant (PI: McLure). JSD acknowledges the support
of the European Research Council via the award of an Advanced Grant (PI J. Dunlop),
and the contribution of the EC FP7 SPACE project ASTRODEEP (Ref.No: 312725). AMS
acknowledges the Leverhulme Foundation. JM acknowledges the support of a Huygens
PhD fellowship from Leiden University. DS acknowledges financial support from the
Netherlands Organization for Scientific research (NWO) through a Veni fellowship
and from FCT through an FCT Investigator Starting Grant and Start-up Grant (IF/01154/2012/CP0189/CT0010).
This work is based on observations taken by the CANDELS Multi-Cycle Treasury Program
with the NASA/ESA HST, which is operated by the Association of Universities for
Research in Astronomy, Inc., under NASA contract NAS5-26555. This work is based
on observations taken by the 3D HST Treasury Program (GO 12177 and 12328) with the
NASA/ESA HST, which is operated by the Association of Universities for Research
in Astronomy, Inc., under NASA contract NAS5-26555. Based on data obtained with
the European Southern Observatory Very Large Telescope, Paranal, Chile, under Large
Program 185.A-0791, and made available by the VUDS team at the CESAM data centre,
Laboratoire d’Astrophysique de Marseille, France. Based on observations obtained
at the Very Large Telescope of the European Southern Observatory. Programme IDs:
092.A 0399(A), 093.A-0122(A,B), 094.A-0214(A,B),095.A0680(A,B),096.A-0315(A,B,C).'
article_processing_charge: No
article_type: original
author:
- first_name: O. J.
full_name: Turner, O. J.
last_name: Turner
- first_name: M.
full_name: Cirasuolo, M.
last_name: Cirasuolo
- first_name: C. M.
full_name: Harrison, C. M.
last_name: Harrison
- first_name: R. J.
full_name: McLure, R. J.
last_name: McLure
- first_name: J. S.
full_name: Dunlop, J. S.
last_name: Dunlop
- first_name: A. M.
full_name: Swinbank, A. M.
last_name: Swinbank
- first_name: H. L.
full_name: Johnson, H. L.
last_name: Johnson
- first_name: D.
full_name: Sobral, D.
last_name: Sobral
- first_name: Jorryt J
full_name: Matthee, Jorryt J
id: 7439a258-f3c0-11ec-9501-9df22fe06720
last_name: Matthee
orcid: 0000-0003-2871-127X
- first_name: R. M.
full_name: Sharples, R. M.
last_name: Sharples
citation:
ama: Turner OJ, Cirasuolo M, Harrison CM, et al. The KMOS Deep Survey (KDS) – I.
Dynamical measurements of typical star-forming galaxies at z ≃ 3.5. Monthly
Notices of the Royal Astronomical Society. 2017;471(2):1280-1320. doi:10.1093/mnras/stx1366
apa: Turner, O. J., Cirasuolo, M., Harrison, C. M., McLure, R. J., Dunlop, J. S.,
Swinbank, A. M., … Sharples, R. M. (2017). The KMOS Deep Survey (KDS) – I. Dynamical
measurements of typical star-forming galaxies at z ≃ 3.5. Monthly Notices of
the Royal Astronomical Society. Oxford University Press. https://doi.org/10.1093/mnras/stx1366
chicago: Turner, O. J., M. Cirasuolo, C. M. Harrison, R. J. McLure, J. S. Dunlop,
A. M. Swinbank, H. L. Johnson, D. Sobral, Jorryt J Matthee, and R. M. Sharples.
“The KMOS Deep Survey (KDS) – I. Dynamical Measurements of Typical Star-Forming
Galaxies at z ≃ 3.5.” Monthly Notices of the Royal Astronomical Society.
Oxford University Press, 2017. https://doi.org/10.1093/mnras/stx1366.
ieee: O. J. Turner et al., “The KMOS Deep Survey (KDS) – I. Dynamical measurements
of typical star-forming galaxies at z ≃ 3.5,” Monthly Notices of the Royal
Astronomical Society, vol. 471, no. 2. Oxford University Press, pp. 1280–1320,
2017.
ista: Turner OJ, Cirasuolo M, Harrison CM, McLure RJ, Dunlop JS, Swinbank AM, Johnson
HL, Sobral D, Matthee JJ, Sharples RM. 2017. The KMOS Deep Survey (KDS) – I. Dynamical
measurements of typical star-forming galaxies at z ≃ 3.5. Monthly Notices of the
Royal Astronomical Society. 471(2), 1280–1320.
mla: Turner, O. J., et al. “The KMOS Deep Survey (KDS) – I. Dynamical Measurements
of Typical Star-Forming Galaxies at z ≃ 3.5.” Monthly Notices of the Royal
Astronomical Society, vol. 471, no. 2, Oxford University Press, 2017, pp.
1280–320, doi:10.1093/mnras/stx1366.
short: O.J. Turner, M. Cirasuolo, C.M. Harrison, R.J. McLure, J.S. Dunlop, A.M.
Swinbank, H.L. Johnson, D. Sobral, J.J. Matthee, R.M. Sharples, Monthly Notices
of the Royal Astronomical Society 471 (2017) 1280–1320.
date_created: 2022-07-13T10:03:01Z
date_published: 2017-10-01T00:00:00Z
date_updated: 2022-08-19T08:07:31Z
day: '01'
doi: 10.1093/mnras/stx1366
extern: '1'
external_id:
arxiv:
- '1704.06263'
intvolume: ' 471'
issue: '2'
keyword:
- Space and Planetary Science
- Astronomy and Astrophysics
- 'galaxies: evolution'
- 'galaxies: high-redshift'
- 'galaxies: kinematics and dynamics'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1704.06263
month: '10'
oa: 1
oa_version: Preprint
page: 1280-1320
publication: Monthly Notices of the Royal Astronomical Society
publication_identifier:
eissn:
- 1365-2966
issn:
- 0035-8711
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: The KMOS Deep Survey (KDS) – I. Dynamical measurements of typical star-forming
galaxies at z ≃ 3.5
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 471
year: '2017'
...
---
_id: '11633'
abstract:
- lang: eng
text: Our understanding of stars through asteroseismic data analysis is limited
by our ability to take advantage of the huge amount of observed stars provided
by space missions such as CoRoT, Kepler , K2, and soon TESS and PLATO. Global
seismic pipelines provide global stellar parameters such as mass and radius using
the mean seismic parameters, as well as the effective temperature. These pipelines
are commonly used automatically on thousands of stars observed by K2 for 3 months
(and soon TESS for at least ∼ 1 month). However, pipelines are not immune from
misidentifying noise peaks and stellar oscillations. Therefore, new validation
techniques are required to assess the quality of these results. We present a new
metric called FliPer (Flicker in Power), which takes into account the average
variability at all measured time scales. The proper calibration of FliPer enables
us to obtain good estimations of global stellar parameters such as surface gravity
that are robust against the influence of noise peaks and hence are an excellent
way to find faults in asteroseismic pipelines.
article_number: '1711.02890'
article_processing_charge: No
author:
- first_name: Lisa Annabelle
full_name: Bugnet, Lisa Annabelle
id: d9edb345-f866-11ec-9b37-d119b5234501
last_name: Bugnet
orcid: 0000-0003-0142-4000
- first_name: R. A.
full_name: Garcia, R. A.
last_name: Garcia
- first_name: G. R.
full_name: Davies, G. R.
last_name: Davies
- first_name: S.
full_name: Mathur, S.
last_name: Mathur
- first_name: E.
full_name: Corsaro, E.
last_name: Corsaro
citation:
ama: 'Bugnet LA, Garcia RA, Davies GR, Mathur S, Corsaro E. FliPer: Checking the
reliability of global seismic parameters from automatic pipelines. arXiv.
doi:10.48550/arXiv.1711.02890'
apa: 'Bugnet, L. A., Garcia, R. A., Davies, G. R., Mathur, S., & Corsaro, E.
(n.d.). FliPer: Checking the reliability of global seismic parameters from automatic
pipelines. arXiv. https://doi.org/10.48550/arXiv.1711.02890'
chicago: 'Bugnet, Lisa Annabelle, R. A. Garcia, G. R. Davies, S. Mathur, and E.
Corsaro. “FliPer: Checking the Reliability of Global Seismic Parameters from Automatic
Pipelines.” ArXiv, n.d. https://doi.org/10.48550/arXiv.1711.02890.'
ieee: 'L. A. Bugnet, R. A. Garcia, G. R. Davies, S. Mathur, and E. Corsaro, “FliPer:
Checking the reliability of global seismic parameters from automatic pipelines,”
arXiv. .'
ista: 'Bugnet LA, Garcia RA, Davies GR, Mathur S, Corsaro E. FliPer: Checking the
reliability of global seismic parameters from automatic pipelines. arXiv, 1711.02890.'
mla: 'Bugnet, Lisa Annabelle, et al. “FliPer: Checking the Reliability of Global
Seismic Parameters from Automatic Pipelines.” ArXiv, 1711.02890, doi:10.48550/arXiv.1711.02890.'
short: L.A. Bugnet, R.A. Garcia, G.R. Davies, S. Mathur, E. Corsaro, ArXiv (n.d.).
date_created: 2022-07-21T07:13:13Z
date_published: 2017-11-08T00:00:00Z
date_updated: 2022-08-22T08:45:42Z
day: '08'
doi: 10.48550/arXiv.1711.02890
extern: '1'
external_id:
arxiv:
- '1711.02890'
keyword:
- asteroseismology - methods
- data analysis - stars
- oscillations
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.48550/arXiv.1711.02890
month: '11'
oa: 1
oa_version: Preprint
publication: arXiv
publication_status: submitted
status: public
title: 'FliPer: Checking the reliability of global seismic parameters from automatic
pipelines'
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2017'
...
---
_id: '11651'
abstract:
- lang: eng
text: Diffusions and related random walk procedures are of central importance in
many areas of machine learning, data analysis, and applied mathematics. Because
they spread mass agnostically at each step in an iterative manner, they can sometimes
spread mass “too aggressively,” thereby failing to find the “right” clusters.
We introduce a novel Capacity Releasing Diffusion (CRD) Process, which is both
faster and stays more local than the classical spectral diffusion process. As
an application, we use our CRD Process to develop an improved local algorithm
for graph clustering. Our local graph clustering method can find local clusters
in a model of clustering where one begins the CRD Process in a cluster whose vertices
are connected better internally than externally by an O(log2n) factor, where n
is the number of nodes in the cluster. Thus, our CRD Process is the first local
graph clustering algorithm that is not subject to the well-known quadratic Cheeger
barrier. Our result requires a certain smoothness condition, which we expect to
be an artifact of our analysis. Our empirical evaluation demonstrates improved
results, in particular for realistic social graphs where there are moderately
good—but not very good—clusters.
alternative_title:
- PMLR
article_processing_charge: No
author:
- first_name: Di
full_name: Wang, Di
last_name: Wang
- first_name: Kimon
full_name: Fountoulakis, Kimon
last_name: Fountoulakis
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Michael W.
full_name: Mahoney, Michael W.
last_name: Mahoney
- first_name: ' Satish'
full_name: Rao , Satish
last_name: 'Rao '
citation:
ama: 'Wang D, Fountoulakis K, Henzinger MH, Mahoney MW, Rao Satish. Capacity releasing
diffusion for speed and locality. In: Proceedings of the 34th International
Conference on Machine Learning. Vol 70. ML Research Press; 2017:3598-3607.'
apa: 'Wang, D., Fountoulakis, K., Henzinger, M. H., Mahoney, M. W., & Rao , Satish.
(2017). Capacity releasing diffusion for speed and locality. In Proceedings
of the 34th International Conference on Machine Learning (Vol. 70, pp. 3598–3607).
Sydney, Australia: ML Research Press.'
chicago: Wang, Di, Kimon Fountoulakis, Monika H Henzinger, Michael W. Mahoney, and Satish
Rao . “Capacity Releasing Diffusion for Speed and Locality.” In Proceedings
of the 34th International Conference on Machine Learning, 70:3598–3607. ML
Research Press, 2017.
ieee: D. Wang, K. Fountoulakis, M. H. Henzinger, M. W. Mahoney, and Satish Rao
, “Capacity releasing diffusion for speed and locality,” in Proceedings of
the 34th International Conference on Machine Learning, Sydney, Australia,
2017, vol. 70, pp. 3598–3607.
ista: Wang D, Fountoulakis K, Henzinger MH, Mahoney MW, Rao Satish. 2017. Capacity
releasing diffusion for speed and locality. Proceedings of the 34th International
Conference on Machine Learning. International Conference on Machine Learning,
PMLR, vol. 70, 3598–3607.
mla: Wang, Di, et al. “Capacity Releasing Diffusion for Speed and Locality.” Proceedings
of the 34th International Conference on Machine Learning, vol. 70, ML Research
Press, 2017, pp. 3598–607.
short: D. Wang, K. Fountoulakis, M.H. Henzinger, M.W. Mahoney, Satish Rao , in:,
Proceedings of the 34th International Conference on Machine Learning, ML Research
Press, 2017, pp. 3598–3607.
conference:
end_date: 2017-08-11
location: Sydney, Australia
name: International Conference on Machine Learning
start_date: 2017-08-06
date_created: 2022-07-25T13:59:21Z
date_published: 2017-09-01T00:00:00Z
date_updated: 2023-02-09T09:15:31Z
day: '01'
extern: '1'
external_id:
arxiv:
- '1706.05826'
intvolume: ' 70'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: http://proceedings.mlr.press/v70/wang17b/wang17b.pdf
month: '09'
oa: 1
oa_version: Published Version
page: 3598-3607
publication: Proceedings of the 34th International Conference on Machine Learning
publication_identifier:
eissn:
- 2640-3498
publication_status: published
publisher: ML Research Press
quality_controlled: '1'
status: public
title: Capacity releasing diffusion for speed and locality
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 70
year: '2017'
...
---
_id: '11665'
abstract:
- lang: eng
text: "We study the problem of maintaining a breadth-first spanning tree (BFS tree)
in partially dynamic distributed networks modeling a sequence of either failures
or additions of communication links (but not both). We present deterministic (1+ϵ)-approximation
algorithms whose amortized time (over some number of link changes) is sublinear
in D, the maximum diameter of the network.\r\n\r\nOur technique also leads to
a deterministic (1+ϵ)-approximate incremental algorithm for single-source shortest
paths in the sequential (usual RAM) model. Prior to our work, the state of the
art was the classic exact algorithm of Even and Shiloach (1981), which is optimal
under some assumptions (Roditty and Zwick 2011; Henzinger et al. 2015). Our result
is the first to show that, in the incremental setting, this bound can be beaten
in certain cases if some approximation is allowed."
acknowledgement: "We thank the reviewers of ICALP 2013 for pointing to related articles
and to an error in an example\r\ngiven in a previous version of this article. We
also thank one of the reviewers of Transactions on\r\nAlgorithms for very detailed
comments."
article_number: '51'
article_processing_charge: No
article_type: original
author:
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Sebastian
full_name: Krinninger, Sebastian
last_name: Krinninger
- first_name: Danupon
full_name: Nanongkai, Danupon
last_name: Nanongkai
citation:
ama: Henzinger MH, Krinninger S, Nanongkai D. Sublinear-time maintenance of breadth-first
spanning trees in partially dynamic networks. ACM Transactions on Algorithms.
2017;13(4). doi:10.1145/3146550
apa: Henzinger, M. H., Krinninger, S., & Nanongkai, D. (2017). Sublinear-time
maintenance of breadth-first spanning trees in partially dynamic networks. ACM
Transactions on Algorithms. Association for Computing Machinery. https://doi.org/10.1145/3146550
chicago: Henzinger, Monika H, Sebastian Krinninger, and Danupon Nanongkai. “Sublinear-Time
Maintenance of Breadth-First Spanning Trees in Partially Dynamic Networks.” ACM
Transactions on Algorithms. Association for Computing Machinery, 2017. https://doi.org/10.1145/3146550.
ieee: M. H. Henzinger, S. Krinninger, and D. Nanongkai, “Sublinear-time maintenance
of breadth-first spanning trees in partially dynamic networks,” ACM Transactions
on Algorithms, vol. 13, no. 4. Association for Computing Machinery, 2017.
ista: Henzinger MH, Krinninger S, Nanongkai D. 2017. Sublinear-time maintenance
of breadth-first spanning trees in partially dynamic networks. ACM Transactions
on Algorithms. 13(4), 51.
mla: Henzinger, Monika H., et al. “Sublinear-Time Maintenance of Breadth-First Spanning
Trees in Partially Dynamic Networks.” ACM Transactions on Algorithms, vol.
13, no. 4, 51, Association for Computing Machinery, 2017, doi:10.1145/3146550.
short: M.H. Henzinger, S. Krinninger, D. Nanongkai, ACM Transactions on Algorithms
13 (2017).
date_created: 2022-07-27T11:37:23Z
date_published: 2017-10-01T00:00:00Z
date_updated: 2022-09-09T11:57:42Z
day: '01'
doi: 10.1145/3146550
extern: '1'
external_id:
arxiv:
- '1512.08147'
intvolume: ' 13'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1512.08147
month: '10'
oa: 1
oa_version: Preprint
publication: ACM Transactions on Algorithms
publication_identifier:
eissn:
- 1549-6333
issn:
- 1549-6325
publication_status: published
publisher: Association for Computing Machinery
quality_controlled: '1'
scopus_import: '1'
status: public
title: Sublinear-time maintenance of breadth-first spanning trees in partially dynamic
networks
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 13
year: '2017'
...
---
_id: '11676'
abstract:
- lang: eng
text: We study the problem of maximizing a monotone submodular function with viability
constraints. This problem originates from computational biology, where we are
given a phylogenetic tree over a set of species and a directed graph, the so-called
food web, encoding viability constraints between these species. These food webs
usually have constant depth. The goal is to select a subset of k species that
satisfies the viability constraints and has maximal phylogenetic diversity. As
this problem is known to be NP-hard, we investigate approximation algorithms.
We present the first constant factor approximation algorithm if the depth is constant.
Its approximation ratio is (1−1e√). This algorithm not only applies to phylogenetic
trees with viability constraints but for arbitrary monotone submodular set functions
with viability constraints. Second, we show that there is no (1−1/e+ϵ)-approximation
algorithm for our problem setting (even for additive functions) and that there
is no approximation algorithm for a slight extension of this setting.
acknowledgement: "The research leading to these results has received funding from
the European Research\r\nCouncil under the European Union’s Seventh Framework Programme
(FP/2007-2013)/ERC Grant Agreement No. 340506."
article_processing_charge: No
article_type: original
author:
- first_name: Wolfgang
full_name: Dvořák, Wolfgang
last_name: Dvořák
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: David P.
full_name: Williamson, David P.
last_name: Williamson
citation:
ama: Dvořák W, Henzinger MH, Williamson DP. Maximizing a submodular function with
viability constraints. Algorithmica. 2017;77(1):152-172. doi:10.1007/s00453-015-0066-y
apa: Dvořák, W., Henzinger, M. H., & Williamson, D. P. (2017). Maximizing a
submodular function with viability constraints. Algorithmica. Springer
Nature. https://doi.org/10.1007/s00453-015-0066-y
chicago: Dvořák, Wolfgang, Monika H Henzinger, and David P. Williamson. “Maximizing
a Submodular Function with Viability Constraints.” Algorithmica. Springer
Nature, 2017. https://doi.org/10.1007/s00453-015-0066-y.
ieee: W. Dvořák, M. H. Henzinger, and D. P. Williamson, “Maximizing a submodular
function with viability constraints,” Algorithmica, vol. 77, no. 1. Springer
Nature, pp. 152–172, 2017.
ista: Dvořák W, Henzinger MH, Williamson DP. 2017. Maximizing a submodular function
with viability constraints. Algorithmica. 77(1), 152–172.
mla: Dvořák, Wolfgang, et al. “Maximizing a Submodular Function with Viability Constraints.”
Algorithmica, vol. 77, no. 1, Springer Nature, 2017, pp. 152–72, doi:10.1007/s00453-015-0066-y.
short: W. Dvořák, M.H. Henzinger, D.P. Williamson, Algorithmica 77 (2017) 152–172.
date_created: 2022-07-27T14:37:24Z
date_published: 2017-01-01T00:00:00Z
date_updated: 2022-09-12T08:58:16Z
day: '01'
doi: 10.1007/s00453-015-0066-y
extern: '1'
external_id:
arxiv:
- '1611.05753'
intvolume: ' 77'
issue: '1'
keyword:
- Approximation algorithms
- Submodular functions
- Phylogenetic diversity
- Viability constraints
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1611.05753
month: '01'
oa: 1
oa_version: Preprint
page: 152-172
publication: Algorithmica
publication_identifier:
eissn:
- 1432-0541
issn:
- 0178-4617
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Maximizing a submodular function with viability constraints
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 77
year: '2017'
...
---
_id: '1175'
abstract:
- lang: eng
text: We study space complexity and time-space trade-offs with a focus not on peak
memory usage but on overall memory consumption throughout the computation. Such
a cumulative space measure was introduced for the computational model of parallel
black pebbling by [Alwen and Serbinenko ’15] as a tool for obtaining results in
cryptography. We consider instead the non- deterministic black-white pebble game
and prove optimal cumulative space lower bounds and trade-offs, where in order
to minimize pebbling time the space has to remain large during a significant fraction
of the pebbling. We also initiate the study of cumulative space in proof complexity,
an area where other space complexity measures have been extensively studied during
the last 10–15 years. Using and extending the connection between proof complexity
and pebble games in [Ben-Sasson and Nordström ’08, ’11] we obtain several strong
cumulative space results for (even parallel versions of) the resolution proof
system, and outline some possible future directions of study of this, in our opinion,
natural and interesting space measure.
alternative_title:
- LIPIcs
author:
- first_name: Joel F
full_name: Alwen, Joel F
id: 2A8DFA8C-F248-11E8-B48F-1D18A9856A87
last_name: Alwen
- first_name: Susanna
full_name: De Rezende, Susanna
last_name: De Rezende
- first_name: Jakob
full_name: Nordstrom, Jakob
last_name: Nordstrom
- first_name: Marc
full_name: Vinyals, Marc
last_name: Vinyals
citation:
ama: 'Alwen JF, De Rezende S, Nordstrom J, Vinyals M. Cumulative space in black-white
pebbling and resolution. In: Papadimitriou C, ed. Vol 67. Schloss Dagstuhl - Leibniz-Zentrum
für Informatik; 2017:38:1-38-21. doi:10.4230/LIPIcs.ITCS.2017.38'
apa: 'Alwen, J. F., De Rezende, S., Nordstrom, J., & Vinyals, M. (2017). Cumulative
space in black-white pebbling and resolution. In C. Papadimitriou (Ed.) (Vol.
67, p. 38:1-38-21). Presented at the ITCS: Innovations in Theoretical Computer
Science, Berkeley, CA, United States: Schloss Dagstuhl - Leibniz-Zentrum für Informatik.
https://doi.org/10.4230/LIPIcs.ITCS.2017.38'
chicago: Alwen, Joel F, Susanna De Rezende, Jakob Nordstrom, and Marc Vinyals. “Cumulative
Space in Black-White Pebbling and Resolution.” edited by Christos Papadimitriou,
67:38:1-38-21. Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017. https://doi.org/10.4230/LIPIcs.ITCS.2017.38.
ieee: 'J. F. Alwen, S. De Rezende, J. Nordstrom, and M. Vinyals, “Cumulative space
in black-white pebbling and resolution,” presented at the ITCS: Innovations in
Theoretical Computer Science, Berkeley, CA, United States, 2017, vol. 67, p. 38:1-38-21.'
ista: 'Alwen JF, De Rezende S, Nordstrom J, Vinyals M. 2017. Cumulative space in
black-white pebbling and resolution. ITCS: Innovations in Theoretical Computer
Science, LIPIcs, vol. 67, 38:1-38-21.'
mla: Alwen, Joel F., et al. Cumulative Space in Black-White Pebbling and Resolution.
Edited by Christos Papadimitriou, vol. 67, Schloss Dagstuhl - Leibniz-Zentrum
für Informatik, 2017, p. 38:1-38-21, doi:10.4230/LIPIcs.ITCS.2017.38.
short: J.F. Alwen, S. De Rezende, J. Nordstrom, M. Vinyals, in:, C. Papadimitriou
(Ed.), Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017, p. 38:1-38-21.
conference:
end_date: 2017-01-11
location: Berkeley, CA, United States
name: 'ITCS: Innovations in Theoretical Computer Science'
start_date: 2017-01-09
date_created: 2018-12-11T11:50:33Z
date_published: 2017-01-01T00:00:00Z
date_updated: 2021-01-12T06:48:51Z
day: '01'
ddc:
- '005'
- '600'
department:
- _id: KrPi
doi: 10.4230/LIPIcs.ITCS.2017.38
editor:
- first_name: Christos
full_name: Papadimitriou, Christos
last_name: Papadimitriou
file:
- access_level: open_access
checksum: dbc94810be07c2fb1945d5c2a6130e6c
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:17:11Z
date_updated: 2020-07-14T12:44:37Z
file_id: '5263'
file_name: IST-2018-927-v1+1_LIPIcs-ITCS-2017-38.pdf
file_size: 557769
relation: main_file
file_date_updated: 2020-07-14T12:44:37Z
has_accepted_license: '1'
intvolume: ' 67'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 38:1-38-21
publication_identifier:
issn:
- '18688969'
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
publist_id: '6179'
pubrep_id: '927'
quality_controlled: '1'
scopus_import: 1
status: public
title: Cumulative space in black-white pebbling and resolution
tmp:
image: /images/cc_by.png
legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
short: CC BY (4.0)
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 67
year: '2017'
...
---
_id: '11829'
abstract:
- lang: eng
text: "In recent years it has become popular to study dynamic problems in a sensitivity
setting: Instead of allowing for an arbitrary sequence of updates, the sensitivity
model only allows to apply batch updates of small size to the original input data.
The sensitivity model is particularly appealing since recent strong conditional
lower bounds ruled out fast algorithms for many dynamic problems, such as shortest
paths, reachability, or subgraph connectivity.\r\n\r\nIn this paper we prove conditional
lower bounds for these and additional problems in a sensitivity setting. For example,
we show that under the Boolean Matrix Multiplication (BMM) conjecture combinatorial
algorithms cannot compute the (4/3-\\varepsilon)-approximate diameter of an undirected
unweighted dense graph with truly subcubic preprocessing time and truly subquadratic
update/query time. This result is surprising since in the static setting it is
not clear whether a reduction from BMM to diameter is possible. We further show
under the BMM conjecture that many problems, such as reachability or approximate
shortest paths, cannot be solved faster than by recomputation from scratch even
after only one or two edge insertions. We extend our reduction from BMM to Diameter
to give a reduction from All Pairs Shortest Paths to Diameter under one deletion
in weighted graphs. This is intriguing, as in the static setting it is a big open
problem whether Diameter is as hard as APSP. We further get a nearly tight lower
bound for shortest paths after two edge deletions based on the APSP conjecture.
We give more lower bounds under the Strong Exponential Time Hypothesis. Many of
our lower bounds also hold for static oracle data structures where no sensitivity
is required.\r\n\r\nFinally, we give the first algorithm for the (1+\\varepsilon)-approximate
radius, diameter, and eccentricity problems in directed or undirected unweighted
graphs in case of single edges failures. The algorithm has a truly subcubic running
time for graphs with a truly subquadratic number of edges; it is tight w.r.t.
the conditional lower bounds we obtain."
alternative_title:
- LIPIcs
article_number: '26'
article_processing_charge: No
author:
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Andrea
full_name: Lincoln, Andrea
last_name: Lincoln
- first_name: Stefan
full_name: Neumann, Stefan
last_name: Neumann
- first_name: Virginia
full_name: Vassilevska Williams, Virginia
last_name: Vassilevska Williams
citation:
ama: 'Henzinger MH, Lincoln A, Neumann S, Vassilevska Williams V. Conditional hardness
for sensitivity problems. In: 8th Innovations in Theoretical Computer Science
Conference. Vol 67. Schloss Dagstuhl - Leibniz-Zentrum für Informatik; 2017.
doi:10.4230/LIPICS.ITCS.2017.26'
apa: 'Henzinger, M. H., Lincoln, A., Neumann, S., & Vassilevska Williams, V.
(2017). Conditional hardness for sensitivity problems. In 8th Innovations in
Theoretical Computer Science Conference (Vol. 67). Berkley, CA, United States:
Schloss Dagstuhl - Leibniz-Zentrum für Informatik. https://doi.org/10.4230/LIPICS.ITCS.2017.26'
chicago: Henzinger, Monika H, Andrea Lincoln, Stefan Neumann, and Virginia Vassilevska
Williams. “Conditional Hardness for Sensitivity Problems.” In 8th Innovations
in Theoretical Computer Science Conference, Vol. 67. Schloss Dagstuhl - Leibniz-Zentrum
für Informatik, 2017. https://doi.org/10.4230/LIPICS.ITCS.2017.26.
ieee: M. H. Henzinger, A. Lincoln, S. Neumann, and V. Vassilevska Williams, “Conditional
hardness for sensitivity problems,” in 8th Innovations in Theoretical Computer
Science Conference, Berkley, CA, United States, 2017, vol. 67.
ista: 'Henzinger MH, Lincoln A, Neumann S, Vassilevska Williams V. 2017. Conditional
hardness for sensitivity problems. 8th Innovations in Theoretical Computer Science
Conference. ITCS: Innovations in Theoretical Computer Science Conference, LIPIcs,
vol. 67, 26.'
mla: Henzinger, Monika H., et al. “Conditional Hardness for Sensitivity Problems.”
8th Innovations in Theoretical Computer Science Conference, vol. 67, 26,
Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017, doi:10.4230/LIPICS.ITCS.2017.26.
short: M.H. Henzinger, A. Lincoln, S. Neumann, V. Vassilevska Williams, in:, 8th
Innovations in Theoretical Computer Science Conference, Schloss Dagstuhl - Leibniz-Zentrum
für Informatik, 2017.
conference:
end_date: 2017-01-11
location: Berkley, CA, United States
name: 'ITCS: Innovations in Theoretical Computer Science Conference'
start_date: 2017-01-09
date_created: 2022-08-12T08:55:33Z
date_published: 2017-11-28T00:00:00Z
date_updated: 2023-02-16T11:49:15Z
day: '28'
doi: 10.4230/LIPICS.ITCS.2017.26
extern: '1'
external_id:
arxiv:
- '1703.01638'
intvolume: ' 67'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.4230/LIPICS.ITCS.2017.26
month: '11'
oa: 1
oa_version: Published Version
publication: 8th Innovations in Theoretical Computer Science Conference
publication_identifier:
isbn:
- '9783959770293'
issn:
- 1868-8969
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
quality_controlled: '1'
scopus_import: '1'
status: public
title: Conditional hardness for sensitivity problems
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 67
year: '2017'
...
---
_id: '11833'
abstract:
- lang: eng
text: "We introduce a new algorithmic framework for designing dynamic graph algorithms
in minor-free graphs, by exploiting the structure of such graphs and a tool called
vertex sparsification, which is a way to compress large graphs into small ones
that well preserve relevant properties among a subset of vertices and has previously
mainly been used in the design of approximation algorithms.\r\n\r\nUsing this
framework, we obtain a Monte Carlo randomized fully dynamic algorithm for (1 +
epsilon)-approximating the energy of electrical flows in n-vertex planar graphs
with tilde{O}(r epsilon^{-2}) worst-case update time and tilde{O}((r + n / sqrt{r})
epsilon^{-2}) worst-case query time, for any r larger than some constant. For
r=n^{2/3}, this gives tilde{O}(n^{2/3} epsilon^{-2}) update time and tilde{O}(n^{2/3}
epsilon^{-2}) query time. We also extend this algorithm to work for minor-free
graphs with similar approximation and running time guarantees. Furthermore, we
illustrate our framework on the all-pairs max flow and shortest path problems
by giving corresponding dynamic algorithms in minor-free graphs with both sublinear
update and query times. To the best of our knowledge, our results are the first
to systematically establish such a connection between dynamic graph algorithms
and vertex sparsification.\r\n\r\nWe also present both upper bound and lower bound
for maintaining the energy of electrical flows in the incremental subgraph model,
where updates consist of only vertex activations, which might be of independent
interest."
alternative_title:
- LIPIcs
article_number: '45'
article_processing_charge: No
author:
- first_name: Gramoz
full_name: Goranci, Gramoz
last_name: Goranci
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Pan
full_name: Peng, Pan
last_name: Peng
citation:
ama: 'Goranci G, Henzinger MH, Peng P. The power of vertex sparsifiers in dynamic
graph algorithms. In: 25th Annual European Symposium on Algorithms. Vol
87. Schloss Dagstuhl - Leibniz-Zentrum für Informatik; 2017. doi:10.4230/LIPICS.ESA.2017.45'
apa: 'Goranci, G., Henzinger, M. H., & Peng, P. (2017). The power of vertex
sparsifiers in dynamic graph algorithms. In 25th Annual European Symposium
on Algorithms (Vol. 87). Vienna, Austria: Schloss Dagstuhl - Leibniz-Zentrum
für Informatik. https://doi.org/10.4230/LIPICS.ESA.2017.45'
chicago: Goranci, Gramoz, Monika H Henzinger, and Pan Peng. “The Power of Vertex
Sparsifiers in Dynamic Graph Algorithms.” In 25th Annual European Symposium
on Algorithms, Vol. 87. Schloss Dagstuhl - Leibniz-Zentrum für Informatik,
2017. https://doi.org/10.4230/LIPICS.ESA.2017.45.
ieee: G. Goranci, M. H. Henzinger, and P. Peng, “The power of vertex sparsifiers
in dynamic graph algorithms,” in 25th Annual European Symposium on Algorithms,
Vienna, Austria, 2017, vol. 87.
ista: 'Goranci G, Henzinger MH, Peng P. 2017. The power of vertex sparsifiers in
dynamic graph algorithms. 25th Annual European Symposium on Algorithms. ESA: Annual
European Symposium on Algorithms, LIPIcs, vol. 87, 45.'
mla: Goranci, Gramoz, et al. “The Power of Vertex Sparsifiers in Dynamic Graph Algorithms.”
25th Annual European Symposium on Algorithms, vol. 87, 45, Schloss Dagstuhl
- Leibniz-Zentrum für Informatik, 2017, doi:10.4230/LIPICS.ESA.2017.45.
short: G. Goranci, M.H. Henzinger, P. Peng, in:, 25th Annual European Symposium
on Algorithms, Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017.
conference:
end_date: 2017-09-06
location: Vienna, Austria
name: 'ESA: Annual European Symposium on Algorithms'
start_date: 2017-09-04
date_created: 2022-08-12T10:46:26Z
date_published: 2017-09-01T00:00:00Z
date_updated: 2023-02-16T11:56:37Z
day: '01'
doi: 10.4230/LIPICS.ESA.2017.45
extern: '1'
external_id:
arxiv:
- '1712.06473'
intvolume: ' 87'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.4230/LIPIcs.ESA.2017.45
month: '09'
oa: 1
oa_version: Published Version
publication: 25th Annual European Symposium on Algorithms
publication_identifier:
isbn:
- 978-3-95977-049-1
issn:
- 1868-8969
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
quality_controlled: '1'
scopus_import: '1'
status: public
title: The power of vertex sparsifiers in dynamic graph algorithms
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 87
year: '2017'
...
---
_id: '11832'
abstract:
- lang: eng
text: "In this paper, we study the problem of opening centers to cluster a set of
clients in a metric space so as to minimize the sum of the costs of the centers
and of the cluster radii, in a dynamic environment where clients arrive and depart,
and the solution must be updated efficiently while remaining competitive with
respect to the current optimal solution. We call this dynamic sum-of-radii clustering
problem.\r\n\r\nWe present a data structure that maintains a solution whose cost
is within a constant factor of the cost of an optimal solution in metric spaces
with bounded doubling dimension and whose worst-case update time is logarithmic
in the parameters of the problem."
alternative_title:
- LIPIcs
article_number: '48'
article_processing_charge: No
author:
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Dariusz
full_name: Leniowski, Dariusz
last_name: Leniowski
- first_name: Claire
full_name: Mathieu, Claire
last_name: Mathieu
citation:
ama: 'Henzinger MH, Leniowski D, Mathieu C. Dynamic clustering to minimize the sum
of radii. In: 25th Annual European Symposium on Algorithms. Vol 87. Schloss
Dagstuhl - Leibniz-Zentrum für Informatik; 2017. doi:10.4230/LIPICS.ESA.2017.48'
apa: 'Henzinger, M. H., Leniowski, D., & Mathieu, C. (2017). Dynamic clustering
to minimize the sum of radii. In 25th Annual European Symposium on Algorithms
(Vol. 87). Vienna, Austria: Schloss Dagstuhl - Leibniz-Zentrum für Informatik.
https://doi.org/10.4230/LIPICS.ESA.2017.48'
chicago: Henzinger, Monika H, Dariusz Leniowski, and Claire Mathieu. “Dynamic Clustering
to Minimize the Sum of Radii.” In 25th Annual European Symposium on Algorithms,
Vol. 87. Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017. https://doi.org/10.4230/LIPICS.ESA.2017.48.
ieee: M. H. Henzinger, D. Leniowski, and C. Mathieu, “Dynamic clustering to minimize
the sum of radii,” in 25th Annual European Symposium on Algorithms, Vienna,
Austria, 2017, vol. 87.
ista: 'Henzinger MH, Leniowski D, Mathieu C. 2017. Dynamic clustering to minimize
the sum of radii. 25th Annual European Symposium on Algorithms. ESA: Annual European
Symposium on Algorithms, LIPIcs, vol. 87, 48.'
mla: Henzinger, Monika H., et al. “Dynamic Clustering to Minimize the Sum of Radii.”
25th Annual European Symposium on Algorithms, vol. 87, 48, Schloss Dagstuhl
- Leibniz-Zentrum für Informatik, 2017, doi:10.4230/LIPICS.ESA.2017.48.
short: M.H. Henzinger, D. Leniowski, C. Mathieu, in:, 25th Annual European Symposium
on Algorithms, Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017.
conference:
end_date: 2017-09-06
location: Vienna, Austria
name: 'ESA: Annual European Symposium on Algorithms'
start_date: 2017-09-04
date_created: 2022-08-12T09:58:46Z
date_published: 2017-09-01T00:00:00Z
date_updated: 2023-02-16T11:54:12Z
day: '01'
doi: 10.4230/LIPICS.ESA.2017.48
extern: '1'
external_id:
arxiv:
- '1707.02577'
intvolume: ' 87'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.4230/LIPICS.ESA.2017.48
month: '09'
oa: 1
oa_version: Published Version
publication: 25th Annual European Symposium on Algorithms
publication_identifier:
isbn:
- 978-3-95977-049-1
issn:
- 1868-8969
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
quality_controlled: '1'
scopus_import: '1'
status: public
title: Dynamic clustering to minimize the sum of radii
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 87
year: '2017'
...
---
_id: '11874'
abstract:
- lang: eng
text: "We consider the problem of maintaining an approximately maximum (fractional)
matching and an approximately minimum vertex cover in a dynamic graph. Starting
with the seminal paper by Onak and Rubinfeld [STOC 2010], this problem has received
significant attention in recent years. There remains, however, a polynomial gap
between the best known worst case update time and the best known amortised update
time for this problem, even after allowing for randomisation. Specifically, Bernstein
and Stein [ICALP 2015, SODA 2016] have the best known worst case update time.
They present a deterministic data structure with approximation ratio (3/2 + ∊)
and worst case update time O(m1/4/ ∊2), where m is the number of edges in the
graph. In recent past, Gupta and Peng [FOCS 2013] gave a deterministic data structure
with approximation ratio (1+ ∊) and worst case update time No known randomised
data structure beats the worst case update times of these two results. In contrast,
the paper by Onak and Rubinfeld [STOC 2010] gave a randomised data structure with
approximation ratio O(1) and amortised update time O(log2 n), where n is the number
of nodes in the graph. This was later improved by Baswana, Gupta and Sen [FOCS
2011] and Solomon [FOCS 2016], leading to a randomised date structure with approximation
ratio 2 and amortised update time O(1).\r\n\r\nWe bridge the polynomial gap between
the worst case and amortised update times for this problem, without using any
randomisation. We present a deterministic data structure with approximation ratio
(2 + ∊) and worst case update time O(log3 n), for all sufficiently small constants
∊."
article_processing_charge: No
author:
- first_name: Sayan
full_name: Bhattacharya, Sayan
last_name: Bhattacharya
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Danupon
full_name: Nanongkai, Danupon
last_name: Nanongkai
citation:
ama: 'Bhattacharya S, Henzinger MH, Nanongkai D. Fully dynamic approximate maximum
matching and minimum vertex cover in o(log3 n) worst case update time. In: 28th
Annual ACM-SIAM Symposium on Discrete Algorithms. Vol 0. Society for Industrial
and Applied Mathematics; 2017:470-489. doi:10.1137/1.9781611974782.30'
apa: 'Bhattacharya, S., Henzinger, M. H., & Nanongkai, D. (2017). Fully dynamic
approximate maximum matching and minimum vertex cover in o(log3 n) worst case
update time. In 28th Annual ACM-SIAM Symposium on Discrete Algorithms (Vol.
0, pp. 470–489). Barcelona, Spain: Society for Industrial and Applied Mathematics.
https://doi.org/10.1137/1.9781611974782.30'
chicago: Bhattacharya, Sayan, Monika H Henzinger, and Danupon Nanongkai. “Fully
Dynamic Approximate Maximum Matching and Minimum Vertex Cover in o(Log3 n) Worst
Case Update Time.” In 28th Annual ACM-SIAM Symposium on Discrete Algorithms,
0:470–89. Society for Industrial and Applied Mathematics, 2017. https://doi.org/10.1137/1.9781611974782.30.
ieee: S. Bhattacharya, M. H. Henzinger, and D. Nanongkai, “Fully dynamic approximate
maximum matching and minimum vertex cover in o(log3 n) worst case update time,”
in 28th Annual ACM-SIAM Symposium on Discrete Algorithms, Barcelona, Spain,
2017, vol. 0, pp. 470–489.
ista: 'Bhattacharya S, Henzinger MH, Nanongkai D. 2017. Fully dynamic approximate
maximum matching and minimum vertex cover in o(log3 n) worst case update time.
28th Annual ACM-SIAM Symposium on Discrete Algorithms. SODA: Symposium on Discrete
Algorithms vol. 0, 470–489.'
mla: Bhattacharya, Sayan, et al. “Fully Dynamic Approximate Maximum Matching and
Minimum Vertex Cover in o(Log3 n) Worst Case Update Time.” 28th Annual ACM-SIAM
Symposium on Discrete Algorithms, vol. 0, Society for Industrial and Applied
Mathematics, 2017, pp. 470–89, doi:10.1137/1.9781611974782.30.
short: S. Bhattacharya, M.H. Henzinger, D. Nanongkai, in:, 28th Annual ACM-SIAM
Symposium on Discrete Algorithms, Society for Industrial and Applied Mathematics,
2017, pp. 470–489.
conference:
end_date: 2017-01-19
location: Barcelona, Spain
name: 'SODA: Symposium on Discrete Algorithms'
start_date: 2017-01-16
date_created: 2022-08-16T12:28:27Z
date_published: 2017-01-01T00:00:00Z
date_updated: 2023-02-17T11:54:22Z
day: '01'
doi: 10.1137/1.9781611974782.30
extern: '1'
external_id:
arxiv:
- '1704.02844'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1704.02844
month: '01'
oa: 1
oa_version: Preprint
page: 470 - 489
publication: 28th Annual ACM-SIAM Symposium on Discrete Algorithms
publication_identifier:
eisbn:
- 978-161197478-2
publication_status: published
publisher: Society for Industrial and Applied Mathematics
quality_controlled: '1'
scopus_import: '1'
status: public
title: Fully dynamic approximate maximum matching and minimum vertex cover in o(log3
n) worst case update time
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: '0'
year: '2017'
...
---
_id: '11873'
abstract:
- lang: eng
text: "We study the problem of computing a minimum cut in a simple, undirected graph
and give a deterministic O(m log2 n log log2 n) time algorithm. This improves
both on the best previously known deterministic running time of O(m log12 n) (Kawarabayashi
and Thorup [12]) and the best previously known randomized running time of O(mlog3n)
(Karger [11]) for this problem, though Karger's algorithm can be further applied
to weighted graphs.\r\n\r\nOur approach is using the Kawarabayashi and Tho- rup
graph compression technique, which repeatedly finds low-conductance cuts. To find
these cuts they use a diffusion-based local algorithm. We use instead a flow-
based local algorithm and suitably adjust their framework to work with our flow-based
subroutine. Both flow and diffusion based methods have a long history of being
applied to finding low conductance cuts. Diffusion algorithms have several variants
that are naturally local while it is more complicated to make flow methods local.
Some prior work has proven nice properties for local flow based algorithms with
respect to improving or cleaning up low conductance cuts. Our flow subroutine,
however, is the first that is both local and produces low conductance cuts. Thus,
it may be of independent interest."
article_processing_charge: No
author:
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Satish
full_name: Rao, Satish
last_name: Rao
- first_name: Di
full_name: Wang, Di
last_name: Wang
citation:
ama: 'Henzinger MH, Rao S, Wang D. Local flow partitioning for faster edge connectivity.
In: 28th Annual ACM-SIAM Symposium on Discrete Algorithms. Society for
Industrial and Applied Mathematics; 2017:1919-1938. doi:10.1137/1.9781611974782.125'
apa: 'Henzinger, M. H., Rao, S., & Wang, D. (2017). Local flow partitioning
for faster edge connectivity. In 28th Annual ACM-SIAM Symposium on Discrete
Algorithms (pp. 1919–1938). Barcelona, Spain: Society for Industrial and Applied
Mathematics. https://doi.org/10.1137/1.9781611974782.125'
chicago: Henzinger, Monika H, Satish Rao, and Di Wang. “Local Flow Partitioning
for Faster Edge Connectivity.” In 28th Annual ACM-SIAM Symposium on Discrete
Algorithms, 1919–38. Society for Industrial and Applied Mathematics, 2017.
https://doi.org/10.1137/1.9781611974782.125.
ieee: M. H. Henzinger, S. Rao, and D. Wang, “Local flow partitioning for faster
edge connectivity,” in 28th Annual ACM-SIAM Symposium on Discrete Algorithms,
Barcelona, Spain, 2017, pp. 1919–1938.
ista: 'Henzinger MH, Rao S, Wang D. 2017. Local flow partitioning for faster edge
connectivity. 28th Annual ACM-SIAM Symposium on Discrete Algorithms. SODA: Symposium
on Discrete Algorithms, 1919–1938.'
mla: Henzinger, Monika H., et al. “Local Flow Partitioning for Faster Edge Connectivity.”
28th Annual ACM-SIAM Symposium on Discrete Algorithms, Society for Industrial
and Applied Mathematics, 2017, pp. 1919–38, doi:10.1137/1.9781611974782.125.
short: M.H. Henzinger, S. Rao, D. Wang, in:, 28th Annual ACM-SIAM Symposium on Discrete
Algorithms, Society for Industrial and Applied Mathematics, 2017, pp. 1919–1938.
conference:
end_date: 2017-01-19
location: Barcelona, Spain
name: 'SODA: Symposium on Discrete Algorithms'
start_date: 2017-01-16
date_created: 2022-08-16T12:20:59Z
date_published: 2017-01-01T00:00:00Z
date_updated: 2023-02-21T16:32:01Z
day: '01'
doi: 10.1137/1.9781611974782.125
extern: '1'
external_id:
arxiv:
- '1704.01254'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1704.01254
month: '01'
oa: 1
oa_version: Preprint
page: 1919-1938
publication: 28th Annual ACM-SIAM Symposium on Discrete Algorithms
publication_identifier:
eisbn:
- 978-161197478-2
publication_status: published
publisher: Society for Industrial and Applied Mathematics
quality_controlled: '1'
related_material:
record:
- id: '11889'
relation: earlier_version
status: public
scopus_import: '1'
status: public
title: Local flow partitioning for faster edge connectivity
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2017'
...
---
_id: '11831'
abstract:
- lang: eng
text: "Graph Sparsification aims at compressing large graphs into smaller ones while
(approximately) preserving important characteristics of the input graph. In this
work we study Vertex Sparsifiers, i.e., sparsifiers whose goal is to reduce the
number of vertices. Given a weighted graph G=(V,E), and a terminal set K with
|K|=k, a quality-q vertex cut sparsifier of G is a graph H with K contained in
V_H that preserves the value of minimum cuts separating any bipartition of K,
up to a factor of q. We show that planar graphs with all the k terminals lying
on the same face admit quality-1 vertex cut sparsifier of size O(k^2) that are
also planar. Our result extends to vertex flow and distance sparsifiers. It improves
the previous best known bound of O(k^2 2^(2k)) for cut and flow sparsifiers by
an exponential factor, and matches an Omega(k^2) lower-bound for this class of
graphs.\r\n\r\nWe also study vertex reachability sparsifiers for directed graphs.
Given a digraph G=(V,E) and a terminal set K, a vertex reachability sparsifier
of G is a digraph H=(V_H,E_H), K contained in V_H that preserves all reachability
information among terminal pairs. We introduce the notion of reachability-preserving
minors, i.e., we require H to be a minor of G. Among others, for general planar
digraphs, we construct reachability-preserving minors of size O(k^2 log^2 k).
We complement our upper-bound by showing that there exists an infinite family
of acyclic planar digraphs such that any reachability-preserving minor must have
Omega(k^2) vertices."
alternative_title:
- LIPIcs
article_number: '44'
article_processing_charge: No
author:
- first_name: Gramoz
full_name: Goranci, Gramoz
last_name: Goranci
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Pan
full_name: Peng, Pan
last_name: Peng
citation:
ama: 'Goranci G, Henzinger MH, Peng P. Improved guarantees for vertex sparsification
in planar graphs. In: 25th Annual European Symposium on Algorithms. Vol
87. Schloss Dagstuhl - Leibniz-Zentrum für Informatik; 2017. doi:10.4230/LIPICS.ESA.2017.44'
apa: 'Goranci, G., Henzinger, M. H., & Peng, P. (2017). Improved guarantees
for vertex sparsification in planar graphs. In 25th Annual European Symposium
on Algorithms (Vol. 87). Vienna, Austria: Schloss Dagstuhl - Leibniz-Zentrum
für Informatik. https://doi.org/10.4230/LIPICS.ESA.2017.44'
chicago: Goranci, Gramoz, Monika H Henzinger, and Pan Peng. “Improved Guarantees
for Vertex Sparsification in Planar Graphs.” In 25th Annual European Symposium
on Algorithms, Vol. 87. Schloss Dagstuhl - Leibniz-Zentrum für Informatik,
2017. https://doi.org/10.4230/LIPICS.ESA.2017.44.
ieee: G. Goranci, M. H. Henzinger, and P. Peng, “Improved guarantees for vertex
sparsification in planar graphs,” in 25th Annual European Symposium on Algorithms,
Vienna, Austria, 2017, vol. 87.
ista: 'Goranci G, Henzinger MH, Peng P. 2017. Improved guarantees for vertex sparsification
in planar graphs. 25th Annual European Symposium on Algorithms. ESA: Annual European
Symposium on Algorithms, LIPIcs, vol. 87, 44.'
mla: Goranci, Gramoz, et al. “Improved Guarantees for Vertex Sparsification in Planar
Graphs.” 25th Annual European Symposium on Algorithms, vol. 87, 44, Schloss
Dagstuhl - Leibniz-Zentrum für Informatik, 2017, doi:10.4230/LIPICS.ESA.2017.44.
short: G. Goranci, M.H. Henzinger, P. Peng, in:, 25th Annual European Symposium
on Algorithms, Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017.
conference:
end_date: 2017-09-06
location: Vienna, Austria
name: 'ESA: Annual European Symposium on Algorithms'
start_date: 2017-09-04
date_created: 2022-08-12T09:27:11Z
date_published: 2017-09-01T00:00:00Z
date_updated: 2023-02-21T16:32:16Z
day: '01'
doi: 10.4230/LIPICS.ESA.2017.44
extern: '1'
external_id:
arxiv:
- '1702.01136'
intvolume: ' 87'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.4230/LIPIcs.ESA.2017.44
month: '09'
oa: 1
oa_version: Published Version
publication: 25th Annual European Symposium on Algorithms
publication_identifier:
isbn:
- 978-3-95977-049-1
issn:
- 1868-8969
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
quality_controlled: '1'
related_material:
record:
- id: '11894'
relation: later_version
status: public
scopus_import: '1'
status: public
title: Improved guarantees for vertex sparsification in planar graphs
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 87
year: '2017'
...
---
_id: '11903'
abstract:
- lang: eng
text: "Online social networks allow the collection of large amounts of data about
the influence between users connected by a friendship-like relationship. When
distributing items among agents forming a social network, this information allows
us to exploit network externalities that each agent receives from his neighbors
that get the same item. In this paper we consider Friends-of-Friends (2-hop) network
externalities, i.e., externalities that not only depend on the neighbors that
get the same item but also on neighbors of neighbors. For these externalities
we study a setting where multiple different items are assigned to unit-demand
agents. Specifically, we study the problem of welfare maximization under different
types of externality functions. Let n be the number of agents and m be the number
of items. Our contributions are the following: (1) We show that welfare maximization
is APX-hard; we show that even for step functions with 2-hop (and also with 1-hop)
externalities it is NP-hard to approximate social welfare better than (1−1/e).
(2) On the positive side we present (i) an \U0001D442(\U0001D45B√)-approximation
algorithm for general concave externality functions, (ii) an O(log m)-approximation
algorithm for linear externality functions, and (iii) a 518(1−1/\U0001D452)-approximation
algorithm for 2-hop step function externalities. We also improve the result from
[7] for 1-hop step function externalities by giving a 12(1−1/\U0001D452)-approximation
algorithm."
article_processing_charge: No
article_type: original
author:
- first_name: Sayan
full_name: Bhattacharya, Sayan
last_name: Bhattacharya
- first_name: Wolfgang
full_name: Dvořák, Wolfgang
last_name: Dvořák
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: Martin
full_name: Starnberger, Martin
last_name: Starnberger
citation:
ama: Bhattacharya S, Dvořák W, Henzinger MH, Starnberger M. Welfare maximization
with friends-of-friends network externalities. Theory of Computing Systems.
2017;61(4):948-986. doi:10.1007/s00224-017-9759-8
apa: Bhattacharya, S., Dvořák, W., Henzinger, M. H., & Starnberger, M. (2017).
Welfare maximization with friends-of-friends network externalities. Theory
of Computing Systems. Springer Nature. https://doi.org/10.1007/s00224-017-9759-8
chicago: Bhattacharya, Sayan, Wolfgang Dvořák, Monika H Henzinger, and Martin Starnberger.
“Welfare Maximization with Friends-of-Friends Network Externalities.” Theory
of Computing Systems. Springer Nature, 2017. https://doi.org/10.1007/s00224-017-9759-8.
ieee: S. Bhattacharya, W. Dvořák, M. H. Henzinger, and M. Starnberger, “Welfare
maximization with friends-of-friends network externalities,” Theory of Computing
Systems, vol. 61, no. 4. Springer Nature, pp. 948–986, 2017.
ista: Bhattacharya S, Dvořák W, Henzinger MH, Starnberger M. 2017. Welfare maximization
with friends-of-friends network externalities. Theory of Computing Systems. 61(4),
948–986.
mla: Bhattacharya, Sayan, et al. “Welfare Maximization with Friends-of-Friends Network
Externalities.” Theory of Computing Systems, vol. 61, no. 4, Springer Nature,
2017, pp. 948–86, doi:10.1007/s00224-017-9759-8.
short: S. Bhattacharya, W. Dvořák, M.H. Henzinger, M. Starnberger, Theory of Computing
Systems 61 (2017) 948–986.
date_created: 2022-08-17T11:14:12Z
date_published: 2017-11-01T00:00:00Z
date_updated: 2023-02-21T16:29:58Z
day: '01'
doi: 10.1007/s00224-017-9759-8
extern: '1'
intvolume: ' 61'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1007/s00224-017-9759-8
month: '11'
oa: 1
oa_version: Published Version
page: 948-986
publication: Theory of Computing Systems
publication_identifier:
eissn:
- 1433-0490
issn:
- 1432-4350
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
record:
- id: '11837'
relation: earlier_version
status: public
scopus_import: '1'
status: public
title: Welfare maximization with friends-of-friends network externalities
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 61
year: '2017'
...
---
_id: '1191'
abstract:
- lang: eng
text: Variation in genotypes may be responsible for differences in dispersal rates,
directional biases, and growth rates of individuals. These traits may favor certain
genotypes and enhance their spatiotemporal spreading into areas occupied by the
less advantageous genotypes. We study how these factors influence the speed of
spreading in the case of two competing genotypes under the assumption that spatial
variation of the total population is small compared to the spatial variation of
the frequencies of the genotypes in the population. In that case, the dynamics
of the frequency of one of the genotypes is approximately described by a generalized
Fisher–Kolmogorov–Petrovskii–Piskunov (F–KPP) equation. This generalized F–KPP
equation with (nonlinear) frequency-dependent diffusion and advection terms admits
traveling wave solutions that characterize the invasion of the dominant genotype.
Our existence results generalize the classical theory for traveling waves for
the F–KPP with constant coefficients. Moreover, in the particular case of the
quadratic (monostable) nonlinear growth–decay rate in the generalized F–KPP we
study in detail the influence of the variance in diffusion and mean displacement
rates of the two genotypes on the minimal wave propagation speed.
acknowledgement: "We thank Nick Barton, Katarína Bod’ová, and Sr\r\n-\r\ndan Sarikas
for constructive feed-\r\nback and support. Furthermore, we would like to express
our deep gratitude to the anonymous referees (one\r\nof whom, Jimmy Garnier, agreed
to reveal his identity) and the editor Max Souza, for very helpful and\r\ndetailed
comments and suggestions that significantly helped us to improve the manuscript.
This project has\r\nreceived funding from the European Union’s Seventh Framework
Programme for research, technological\r\ndevelopment and demonstration under Grant
Agreement 618091 Speed of Adaptation in Population Genet-\r\nics and Evolutionary
Computation (SAGE) and the European Research Council (ERC) Grant No. 250152\r\n(SN),
from the Scientific Grant Agency of the Slovak Republic under the Grant 1/0459/13
and by the Slovak\r\nResearch and Development Agency under the Contract No. APVV-14-0378
(RK). RK would also like to\r\nthank IST Austria for its hospitality during the
work on this project."
author:
- first_name: Richard
full_name: Kollár, Richard
last_name: Kollár
- first_name: Sebastian
full_name: Novak, Sebastian
id: 461468AE-F248-11E8-B48F-1D18A9856A87
last_name: Novak
citation:
ama: Kollár R, Novak S. Existence of traveling waves for the generalized F–KPP equation.
Bulletin of Mathematical Biology. 2017;79(3):525-559. doi:10.1007/s11538-016-0244-3
apa: Kollár, R., & Novak, S. (2017). Existence of traveling waves for the generalized
F–KPP equation. Bulletin of Mathematical Biology. Springer. https://doi.org/10.1007/s11538-016-0244-3
chicago: Kollár, Richard, and Sebastian Novak. “Existence of Traveling Waves for
the Generalized F–KPP Equation.” Bulletin of Mathematical Biology. Springer,
2017. https://doi.org/10.1007/s11538-016-0244-3.
ieee: R. Kollár and S. Novak, “Existence of traveling waves for the generalized
F–KPP equation,” Bulletin of Mathematical Biology, vol. 79, no. 3. Springer,
pp. 525–559, 2017.
ista: Kollár R, Novak S. 2017. Existence of traveling waves for the generalized
F–KPP equation. Bulletin of Mathematical Biology. 79(3), 525–559.
mla: Kollár, Richard, and Sebastian Novak. “Existence of Traveling Waves for the
Generalized F–KPP Equation.” Bulletin of Mathematical Biology, vol. 79,
no. 3, Springer, 2017, pp. 525–59, doi:10.1007/s11538-016-0244-3.
short: R. Kollár, S. Novak, Bulletin of Mathematical Biology 79 (2017) 525–559.
date_created: 2018-12-11T11:50:38Z
date_published: 2017-03-01T00:00:00Z
date_updated: 2021-01-12T06:48:58Z
day: '01'
department:
- _id: NiBa
doi: 10.1007/s11538-016-0244-3
ec_funded: 1
intvolume: ' 79'
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1607.00944
month: '03'
oa: 1
oa_version: Preprint
page: 525-559
project:
- _id: 25B1EC9E-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '618091'
name: Speed of Adaptation in Population Genetics and Evolutionary Computation
- _id: 25B07788-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '250152'
name: Limits to selection in biology and in evolutionary computation
publication: Bulletin of Mathematical Biology
publication_status: published
publisher: Springer
publist_id: '6160'
quality_controlled: '1'
scopus_import: 1
status: public
title: Existence of traveling waves for the generalized F–KPP equation
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 79
year: '2017'
...
---
_id: '11976'
abstract:
- lang: eng
text: The way organic multistep synthesis is performed is changing due to the adoption
of flow chemical techniques, which has enabled the development of improved methods
to make complex molecules. The modular nature of the technique provides not only
access to target molecules via linear flow approaches but also for the targeting
of structural cores with single systems. This perspective article summarizes the
state of the art of continuous multistep synthesis and discusses the main challenges
and opportunities in this area.
article_processing_charge: No
article_type: original
author:
- first_name: Bartholomäus
full_name: Pieber, Bartholomäus
id: 93e5e5b2-0da6-11ed-8a41-af589a024726
last_name: Pieber
orcid: 0000-0001-8689-388X
- first_name: Kerry
full_name: Gilmore, Kerry
last_name: Gilmore
- first_name: Peter H.
full_name: Seeberger, Peter H.
last_name: Seeberger
citation:
ama: Pieber B, Gilmore K, Seeberger PH. Integrated flow processing - challenges
in continuous multistep synthesis. Journal of Flow Chemistry. 2017;7(3-4):129-136.
doi:10.1556/1846.2017.00016
apa: Pieber, B., Gilmore, K., & Seeberger, P. H. (2017). Integrated flow processing
- challenges in continuous multistep synthesis. Journal of Flow Chemistry.
AKJournals. https://doi.org/10.1556/1846.2017.00016
chicago: Pieber, Bartholomäus, Kerry Gilmore, and Peter H. Seeberger. “Integrated
Flow Processing - Challenges in Continuous Multistep Synthesis.” Journal of
Flow Chemistry. AKJournals, 2017. https://doi.org/10.1556/1846.2017.00016.
ieee: B. Pieber, K. Gilmore, and P. H. Seeberger, “Integrated flow processing -
challenges in continuous multistep synthesis,” Journal of Flow Chemistry,
vol. 7, no. 3–4. AKJournals, pp. 129–136, 2017.
ista: Pieber B, Gilmore K, Seeberger PH. 2017. Integrated flow processing - challenges
in continuous multistep synthesis. Journal of Flow Chemistry. 7(3–4), 129–136.
mla: Pieber, Bartholomäus, et al. “Integrated Flow Processing - Challenges in Continuous
Multistep Synthesis.” Journal of Flow Chemistry, vol. 7, no. 3–4, AKJournals,
2017, pp. 129–36, doi:10.1556/1846.2017.00016.
short: B. Pieber, K. Gilmore, P.H. Seeberger, Journal of Flow Chemistry 7 (2017)
129–136.
date_created: 2022-08-25T10:47:51Z
date_published: 2017-09-01T00:00:00Z
date_updated: 2023-02-21T10:10:02Z
day: '01'
doi: 10.1556/1846.2017.00016
extern: '1'
intvolume: ' 7'
issue: 3-4
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1556/1846.2017.00016
month: '09'
oa: 1
oa_version: Published Version
page: 129-136
publication: Journal of Flow Chemistry
publication_identifier:
eissn:
- 2063-0212
issn:
- 2062-249X
publication_status: published
publisher: AKJournals
quality_controlled: '1'
scopus_import: '1'
status: public
title: Integrated flow processing - challenges in continuous multistep synthesis
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2017'
...
---
_id: '1211'
abstract:
- lang: eng
text: Systems such as fluid flows in channels and pipes or the complex Ginzburg–Landau
system, defined over periodic domains, exhibit both continuous symmetries, translational
and rotational, as well as discrete symmetries under spatial reflections or complex
conjugation. The simplest, and very common symmetry of this type is the equivariance
of the defining equations under the orthogonal group O(2). We formulate a novel
symmetry reduction scheme for such systems by combining the method of slices with
invariant polynomial methods, and show how it works by applying it to the Kuramoto–Sivashinsky
system in one spatial dimension. As an example, we track a relative periodic orbit
through a sequence of bifurcations to the onset of chaos. Within the symmetry-reduced
state space we are able to compute and visualize the unstable manifolds of relative
periodic orbits, their torus bifurcations, a transition to chaos via torus breakdown,
and heteroclinic connections between various relative periodic orbits. It would
be very hard to carry through such analysis in the full state space, without a
symmetry reduction such as the one we present here.
acknowledgement: 'This work was supported by the family of late G. Robinson, Jr. and
NSF Grant DMS-1211827. '
author:
- first_name: Nazmi B
full_name: Budanur, Nazmi B
id: 3EA1010E-F248-11E8-B48F-1D18A9856A87
last_name: Budanur
orcid: 0000-0003-0423-5010
- first_name: Predrag
full_name: Cvitanović, Predrag
last_name: Cvitanović
citation:
ama: Budanur NB, Cvitanović P. Unstable manifolds of relative periodic orbits in
the symmetry reduced state space of the Kuramoto–Sivashinsky system. Journal
of Statistical Physics. 2017;167(3-4):636-655. doi:10.1007/s10955-016-1672-z
apa: Budanur, N. B., & Cvitanović, P. (2017). Unstable manifolds of relative
periodic orbits in the symmetry reduced state space of the Kuramoto–Sivashinsky
system. Journal of Statistical Physics. Springer. https://doi.org/10.1007/s10955-016-1672-z
chicago: Budanur, Nazmi B, and Predrag Cvitanović. “Unstable Manifolds of Relative
Periodic Orbits in the Symmetry Reduced State Space of the Kuramoto–Sivashinsky
System.” Journal of Statistical Physics. Springer, 2017. https://doi.org/10.1007/s10955-016-1672-z.
ieee: N. B. Budanur and P. Cvitanović, “Unstable manifolds of relative periodic
orbits in the symmetry reduced state space of the Kuramoto–Sivashinsky system,”
Journal of Statistical Physics, vol. 167, no. 3–4. Springer, pp. 636–655,
2017.
ista: Budanur NB, Cvitanović P. 2017. Unstable manifolds of relative periodic orbits
in the symmetry reduced state space of the Kuramoto–Sivashinsky system. Journal
of Statistical Physics. 167(3–4), 636–655.
mla: Budanur, Nazmi B., and Predrag Cvitanović. “Unstable Manifolds of Relative
Periodic Orbits in the Symmetry Reduced State Space of the Kuramoto–Sivashinsky
System.” Journal of Statistical Physics, vol. 167, no. 3–4, Springer, 2017,
pp. 636–55, doi:10.1007/s10955-016-1672-z.
short: N.B. Budanur, P. Cvitanović, Journal of Statistical Physics 167 (2017) 636–655.
date_created: 2018-12-11T11:50:44Z
date_published: 2017-05-01T00:00:00Z
date_updated: 2021-01-12T06:49:07Z
day: '01'
ddc:
- '530'
department:
- _id: BjHo
doi: 10.1007/s10955-016-1672-z
file:
- access_level: open_access
checksum: 3e971d09eb167761aa0888ed415b0056
content_type: application/pdf
creator: system
date_created: 2018-12-12T10:18:01Z
date_updated: 2020-07-14T12:44:39Z
file_id: '5319'
file_name: IST-2017-782-v1+1_BudCvi15.pdf
file_size: 2820207
relation: main_file
file_date_updated: 2020-07-14T12:44:39Z
has_accepted_license: '1'
intvolume: ' 167'
issue: 3-4
language:
- iso: eng
month: '05'
oa: 1
oa_version: Submitted Version
page: 636-655
publication: Journal of Statistical Physics
publication_status: published
publisher: Springer
publist_id: '6136'
pubrep_id: '782'
quality_controlled: '1'
scopus_import: 1
status: public
title: Unstable manifolds of relative periodic orbits in the symmetry reduced state
space of the Kuramoto–Sivashinsky system
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 167
year: '2017'
...
---
_id: '123'
abstract:
- lang: eng
text: The Leidenfrost effect occurs when an object near a hot surface vaporizes
rapidly enough to lift itself up and hover. Although well understood for liquids
and stiff sublimable solids, nothing is known about the effect with materials
whose stiffness lies between these extremes. Here we introduce a new phenomenon
that occurs with vaporizable soft solids - the elastic Leidenfrost effect. By
dropping hydrogel spheres onto hot surfaces we find that, rather than hovering,
they energetically bounce several times their diameter for minutes at a time.
With high-speed video during a single impact, we uncover high-frequency microscopic
gap dynamics at the sphere/substrate interface. We show how these otherwise-hidden
agitations constitute work cycles that harvest mechanical energy from the vapour
and sustain the bouncing. Our findings suggest a new strategy for injecting mechanical
energy into a widely used class of soft materials, with potential relevance to
fields such as active matter, soft robotics and microfluidics.
acknowledgement: A.S. acknowledges funding from the Delta Institute for Theoretical
Physics and the hospitality of the IBS Center for Theoretical Physics of Complex
Systems, Daejeon, South Korea. We acknowledge funding from the Netherlands Organisation
for Scientific Research through grants VICI No. NWO-680-47-609 (M.v.H. and S.R.W.),
VENI No. NWO-680-47-445 (C.C.) and VENI No. NWO-680-47-453 (S.R.W.).
author:
- first_name: Scott R
full_name: Waitukaitis, Scott R
id: 3A1FFC16-F248-11E8-B48F-1D18A9856A87
last_name: Waitukaitis
orcid: 0000-0002-2299-3176
- first_name: Antal
full_name: Zuiderwijk, Antal
last_name: Zuiderwijk
- first_name: Anton
full_name: Souslov, Anton
last_name: Souslov
- first_name: Corentin
full_name: Coulais, Corentin
last_name: Coulais
- first_name: Martin
full_name: Van Hecke, Martin
last_name: Van Hecke
citation:
ama: Waitukaitis SR, Zuiderwijk A, Souslov A, Coulais C, Van Hecke M. Coupling the
Leidenfrost effect and elastic deformations to power sustained bouncing. Nature
Physics. 2017;13(11):1095-1099. doi:10.1038/nphys4194
apa: Waitukaitis, S. R., Zuiderwijk, A., Souslov, A., Coulais, C., & Van Hecke,
M. (2017). Coupling the Leidenfrost effect and elastic deformations to power sustained
bouncing. Nature Physics. Nature Publishing Group. https://doi.org/10.1038/nphys4194
chicago: Waitukaitis, Scott R, Antal Zuiderwijk, Anton Souslov, Corentin Coulais,
and Martin Van Hecke. “Coupling the Leidenfrost Effect and Elastic Deformations
to Power Sustained Bouncing.” Nature Physics. Nature Publishing Group,
2017. https://doi.org/10.1038/nphys4194.
ieee: S. R. Waitukaitis, A. Zuiderwijk, A. Souslov, C. Coulais, and M. Van Hecke,
“Coupling the Leidenfrost effect and elastic deformations to power sustained bouncing,”
Nature Physics, vol. 13, no. 11. Nature Publishing Group, pp. 1095–1099,
2017.
ista: Waitukaitis SR, Zuiderwijk A, Souslov A, Coulais C, Van Hecke M. 2017. Coupling
the Leidenfrost effect and elastic deformations to power sustained bouncing. Nature
Physics. 13(11), 1095–1099.
mla: Waitukaitis, Scott R., et al. “Coupling the Leidenfrost Effect and Elastic
Deformations to Power Sustained Bouncing.” Nature Physics, vol. 13, no.
11, Nature Publishing Group, 2017, pp. 1095–99, doi:10.1038/nphys4194.
short: S.R. Waitukaitis, A. Zuiderwijk, A. Souslov, C. Coulais, M. Van Hecke, Nature
Physics 13 (2017) 1095–1099.
date_created: 2018-12-11T11:44:45Z
date_published: 2017-07-24T00:00:00Z
date_updated: 2021-01-12T06:49:14Z
day: '24'
doi: 10.1038/nphys4194
extern: '1'
external_id:
arxiv:
- '1705.03530'
intvolume: ' 13'
issue: '11'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1705.03530
month: '07'
oa: 1
oa_version: Preprint
page: 1095 - 1099
publication: Nature Physics
publication_status: published
publisher: Nature Publishing Group
publist_id: '7931'
quality_controlled: '1'
status: public
title: Coupling the Leidenfrost effect and elastic deformations to power sustained
bouncing
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 13
year: '2017'
...
---
_id: '12571'
abstract:
- lang: eng
text: We consider the problems of maintaining approximate maximum matching and minimum
vertex cover in a dynamic graph. Starting with the seminal work of Onak and Rubinfeld
[STOC 2010], this problem has received significant attention in recent years.
Very recently, extending the framework of Baswana, Gupta and Sen [FOCS 2011],
Solomon [FOCS 2016] gave a randomized 2-approximation dynamic algorithm for this
problem that has amortized update time of O(1) with high probability. We consider
the natural open question of derandomizing this result. We present a new deterministic
fully dynamic algorithm that maintains a O(1)-approximate minimum vertex cover
and maximum fractional matching, with an amortized update time of O(1). Previously,
the best deterministic algorithm for this problem was due to Bhattacharya, Henzinger
and Italiano [SODA 2015]; it had an approximation ratio of (2+ϵ) and an amortized
update time of O(logn/ϵ2). Our result can be generalized to give a fully dynamic
O(f3)-approximation algorithm with O(f2) amortized update time for the hypergraph
vertex cover and fractional matching problems, where every hyperedge has at most
f vertices.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Sayan
full_name: Bhattacharya, Sayan
last_name: Bhattacharya
- first_name: Deeparnab
full_name: Chakrabarty, Deeparnab
last_name: Chakrabarty
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
citation:
ama: 'Bhattacharya S, Chakrabarty D, Henzinger MH. Deterministic fully dynamic approximate
vertex cover and fractional matching in O(1) amortized update time. In: 19th
International Conference on Integer Programming and Combinatorial Optimization.
Vol 10328. Springer Nature; 2017:86-98. doi:10.1007/978-3-319-59250-3_8'
apa: 'Bhattacharya, S., Chakrabarty, D., & Henzinger, M. H. (2017). Deterministic
fully dynamic approximate vertex cover and fractional matching in O(1) amortized
update time. In 19th International Conference on Integer Programming and Combinatorial
Optimization (Vol. 10328, pp. 86–98). Waterloo, ON, Canada: Springer Nature.
https://doi.org/10.1007/978-3-319-59250-3_8'
chicago: Bhattacharya, Sayan, Deeparnab Chakrabarty, and Monika H Henzinger. “Deterministic
Fully Dynamic Approximate Vertex Cover and Fractional Matching in O(1) Amortized
Update Time.” In 19th International Conference on Integer Programming and Combinatorial
Optimization, 10328:86–98. Springer Nature, 2017. https://doi.org/10.1007/978-3-319-59250-3_8.
ieee: S. Bhattacharya, D. Chakrabarty, and M. H. Henzinger, “Deterministic fully
dynamic approximate vertex cover and fractional matching in O(1) amortized update
time,” in 19th International Conference on Integer Programming and Combinatorial
Optimization, Waterloo, ON, Canada, 2017, vol. 10328, pp. 86–98.
ista: 'Bhattacharya S, Chakrabarty D, Henzinger MH. 2017. Deterministic fully dynamic
approximate vertex cover and fractional matching in O(1) amortized update time.
19th International Conference on Integer Programming and Combinatorial Optimization.
IPCO: Integer Programming and Combinatorial Optimization, LNCS, vol. 10328, 86–98.'
mla: Bhattacharya, Sayan, et al. “Deterministic Fully Dynamic Approximate Vertex
Cover and Fractional Matching in O(1) Amortized Update Time.” 19th International
Conference on Integer Programming and Combinatorial Optimization, vol. 10328,
Springer Nature, 2017, pp. 86–98, doi:10.1007/978-3-319-59250-3_8.
short: S. Bhattacharya, D. Chakrabarty, M.H. Henzinger, in:, 19th International
Conference on Integer Programming and Combinatorial Optimization, Springer Nature,
2017, pp. 86–98.
conference:
end_date: 2017-06-28
location: Waterloo, ON, Canada
name: 'IPCO: Integer Programming and Combinatorial Optimization'
start_date: 2017-06-26
date_created: 2023-02-20T07:52:31Z
date_published: 2017-05-24T00:00:00Z
date_updated: 2023-02-20T07:57:24Z
day: '24'
doi: 10.1007/978-3-319-59250-3_8
extern: '1'
external_id:
arxiv:
- '1611.00198'
intvolume: ' 10328'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1611.00198
month: '05'
oa: 1
oa_version: Preprint
page: 86-98
publication: 19th International Conference on Integer Programming and Combinatorial
Optimization
publication_identifier:
eisbn:
- '9783319592503'
isbn:
- '9783319592497'
issn:
- 0302-9743
- 1611-3349
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Deterministic fully dynamic approximate vertex cover and fractional matching
in O(1) amortized update time
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 10328
year: '2017'
...
---
_id: '1113'
abstract:
- lang: eng
text: 'A drawing of a graph G is radial if the vertices of G are placed on concentric
circles C 1 , . . . , C k with common center c , and edges are drawn radially
: every edge intersects every circle centered at c at most once. G is radial planar
if it has a radial embedding, that is, a crossing-free radial drawing. If the
vertices of G are ordered or partitioned into ordered levels (as they are for
leveled graphs), we require that the assignment of vertices to circles corresponds
to the given ordering or leveling. We show that a graph G is radial planar if
G has a radial drawing in which every two edges cross an even number of times;
the radial embedding has the same leveling as the radial drawing. In other words,
we establish the weak variant of the Hanani-Tutte theorem for radial planarity.
This generalizes a result by Pach and Toth.'
article_processing_charge: No
article_type: original
author:
- first_name: Radoslav
full_name: Fulek, Radoslav
id: 39F3FFE4-F248-11E8-B48F-1D18A9856A87
last_name: Fulek
orcid: 0000-0001-8485-1774
- first_name: Michael
full_name: Pelsmajer, Michael
last_name: Pelsmajer
- first_name: Marcus
full_name: Schaefer, Marcus
last_name: Schaefer
citation:
ama: Fulek R, Pelsmajer M, Schaefer M. Hanani-Tutte for radial planarity. Journal
of Graph Algorithms and Applications. 2017;21(1):135-154. doi:10.7155/jgaa.00408
apa: Fulek, R., Pelsmajer, M., & Schaefer, M. (2017). Hanani-Tutte for radial
planarity. Journal of Graph Algorithms and Applications. Brown University.
https://doi.org/10.7155/jgaa.00408
chicago: Fulek, Radoslav, Michael Pelsmajer, and Marcus Schaefer. “Hanani-Tutte
for Radial Planarity.” Journal of Graph Algorithms and Applications. Brown
University, 2017. https://doi.org/10.7155/jgaa.00408.
ieee: R. Fulek, M. Pelsmajer, and M. Schaefer, “Hanani-Tutte for radial planarity,”
Journal of Graph Algorithms and Applications, vol. 21, no. 1. Brown University,
pp. 135–154, 2017.
ista: Fulek R, Pelsmajer M, Schaefer M. 2017. Hanani-Tutte for radial planarity.
Journal of Graph Algorithms and Applications. 21(1), 135–154.
mla: Fulek, Radoslav, et al. “Hanani-Tutte for Radial Planarity.” Journal of
Graph Algorithms and Applications, vol. 21, no. 1, Brown University, 2017,
pp. 135–54, doi:10.7155/jgaa.00408.
short: R. Fulek, M. Pelsmajer, M. Schaefer, Journal of Graph Algorithms and Applications
21 (2017) 135–154.
date_created: 2018-12-11T11:50:13Z
date_published: 2017-01-01T00:00:00Z
date_updated: 2023-02-23T10:05:57Z
day: '01'
ddc:
- '510'
department:
- _id: UlWa
doi: 10.7155/jgaa.00408
ec_funded: 1
external_id:
arxiv:
- '1608.08662'
file:
- access_level: open_access
content_type: application/pdf
creator: dernst
date_created: 2019-10-24T10:54:37Z
date_updated: 2019-10-24T10:54:37Z
file_id: '6967'
file_name: 2017_JournalGraphAlgorithms_Fulek.pdf
file_size: 573623
relation: main_file
success: 1
file_date_updated: 2019-10-24T10:54:37Z
has_accepted_license: '1'
intvolume: ' 21'
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 135 - 154
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
publication: Journal of Graph Algorithms and Applications
publication_status: published
publisher: Brown University
publist_id: '6254'
quality_controlled: '1'
related_material:
record:
- id: '1164'
relation: earlier_version
status: public
- id: '1595'
relation: earlier_version
status: public
scopus_import: 1
status: public
title: Hanani-Tutte for radial planarity
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 21
year: '2017'
...