---
_id: '6952'
abstract:
- lang: eng
text: 'We present a unified framework tackling two problems: class-specific 3D reconstruction
from a single image, and generation of new 3D shape samples. These tasks have
received considerable attention recently; however, most existing approaches rely
on 3D supervision, annotation of 2D images with keypoints or poses, and/or training
with multiple views of each object instance. Our framework is very general: it
can be trained in similar settings to existing approaches, while also supporting
weaker supervision. Importantly, it can be trained purely from 2D images, without
pose annotations, and with only a single view per instance. We employ meshes as
an output representation, instead of voxels used in most prior work. This allows
us to reason over lighting parameters and exploit shading information during training,
which previous 2D-supervised methods cannot. Thus, our method can learn to generate
and reconstruct concave object classes. We evaluate our approach in various settings,
showing that: (i) it learns to disentangle shape from pose and lighting; (ii)
using shading in the loss improves performance compared to just silhouettes; (iii)
when using a standard single white light, our model outperforms state-of-the-art
2D-supervised methods, both with and without pose supervision, thanks to exploiting
shading cues; (iv) performance improves further when using multiple coloured lights,
even approaching that of state-of-the-art 3D-supervised methods; (v) shapes produced
by our model capture smooth surfaces and fine details better than voxel-based
approaches; and (vi) our approach supports concave classes such as bathtubs and
sofas, which methods based on silhouettes cannot learn.'
acknowledgement: Open access funding provided by Institute of Science and Technology
(IST Austria).
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Paul M
full_name: Henderson, Paul M
id: 13C09E74-18D9-11E9-8878-32CFE5697425
last_name: Henderson
orcid: 0000-0002-5198-7445
- first_name: Vittorio
full_name: Ferrari, Vittorio
last_name: Ferrari
citation:
ama: Henderson PM, Ferrari V. Learning single-image 3D reconstruction by generative
modelling of shape, pose and shading. International Journal of Computer Vision.
2020;128:835-854. doi:10.1007/s11263-019-01219-8
apa: Henderson, P. M., & Ferrari, V. (2020). Learning single-image 3D reconstruction
by generative modelling of shape, pose and shading. International Journal of
Computer Vision. Springer Nature. https://doi.org/10.1007/s11263-019-01219-8
chicago: Henderson, Paul M, and Vittorio Ferrari. “Learning Single-Image 3D Reconstruction
by Generative Modelling of Shape, Pose and Shading.” International Journal
of Computer Vision. Springer Nature, 2020. https://doi.org/10.1007/s11263-019-01219-8.
ieee: P. M. Henderson and V. Ferrari, “Learning single-image 3D reconstruction by
generative modelling of shape, pose and shading,” International Journal of
Computer Vision, vol. 128. Springer Nature, pp. 835–854, 2020.
ista: Henderson PM, Ferrari V. 2020. Learning single-image 3D reconstruction by
generative modelling of shape, pose and shading. International Journal of Computer
Vision. 128, 835–854.
mla: Henderson, Paul M., and Vittorio Ferrari. “Learning Single-Image 3D Reconstruction
by Generative Modelling of Shape, Pose and Shading.” International Journal
of Computer Vision, vol. 128, Springer Nature, 2020, pp. 835–54, doi:10.1007/s11263-019-01219-8.
short: P.M. Henderson, V. Ferrari, International Journal of Computer Vision 128
(2020) 835–854.
date_created: 2019-10-17T13:38:20Z
date_published: 2020-04-01T00:00:00Z
date_updated: 2023-08-17T14:01:16Z
day: '01'
ddc:
- '004'
department:
- _id: ChLa
doi: 10.1007/s11263-019-01219-8
external_id:
arxiv:
- '1901.06447'
isi:
- '000491042100002'
file:
- access_level: open_access
checksum: a0f05dd4f5f64e4f713d8d9d4b5b1e3f
content_type: application/pdf
creator: dernst
date_created: 2019-10-25T10:28:29Z
date_updated: 2020-07-14T12:47:46Z
file_id: '6973'
file_name: 2019_CompVision_Henderson.pdf
file_size: 2243134
relation: main_file
file_date_updated: 2020-07-14T12:47:46Z
has_accepted_license: '1'
intvolume: ' 128'
isi: 1
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '04'
oa: 1
oa_version: Published Version
page: 835-854
project:
- _id: B67AFEDC-15C9-11EA-A837-991A96BB2854
name: IST Austria Open Access Fund
publication: International Journal of Computer Vision
publication_identifier:
eissn:
- 1573-1405
issn:
- 0920-5691
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Learning single-image 3D reconstruction by generative modelling of shape, pose
and shading
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 128
year: '2020'
...
---
_id: '7148'
abstract:
- lang: eng
text: In the cerebellum, GluD2 is exclusively expressed in Purkinje cells, where
it regulates synapse formation and regeneration, synaptic plasticity, and motor
learning. Delayed cognitive development in humans with GluD2 gene mutations suggests
extracerebellar functions of GluD2. However, extracerebellar expression of GluD2
and its relationship with that of GluD1 are poorly understood. GluD2 mRNA and
protein were widely detected, with relatively high levels observed in the olfactory
glomerular layer, medial prefrontal cortex, cingulate cortex, retrosplenial granular
cortex, olfactory tubercle, subiculum, striatum, lateral septum, anterodorsal
thalamic nucleus, and arcuate hypothalamic nucleus. These regions were also enriched
for GluD1, and many individual neurons coexpressed the two GluDs. In the retrosplenial
granular cortex, GluD1 and GluD2 were selectively expressed at PSD‐95‐expressing
glutamatergic synapses, and their coexpression on the same synapses was shown
by SDS‐digested freeze‐fracture replica labeling. Biochemically, GluD1 and GluD2
formed coimmunoprecipitable complex formation in HEK293T cells and in the cerebral
cortex and hippocampus. We further estimated the relative protein amount by quantitative
immunoblotting using GluA2/GluD2 and GluA2/GluD1 chimeric proteins as standards
for titration of GluD1 and GluD2 antibodies. Intriguingly, the relative amount
of GluD2 was almost comparable to that of GluD1 in the postsynaptic density fraction
prepared from the cerebral cortex and hippocampus. In contrast, GluD2 was overwhelmingly
predominant in the cerebellum. Thus, we have determined the relative extracerebellar
expression of GluD1 and GluD2 at regional, neuronal, and synaptic levels. These
data provide a molecular–anatomical basis for possible competitive and cooperative
interactions of GluD family members at synapses in various brain regions.
acknowledgement: This study was supported by Grants-in-Aid for Scientific Research
to K.K. (18K06813), Y.M. (17K08503, 17H0631319), and K.S. (16H04650) and a grant
for Scientific Research on Innovative Areas to K.S (16H06276) from the Ministry
of Education, Culture, Sports, Science and Technology of Japan (MEXT). We thank
K. Akashi, I. Watanabe-Iida, Y. Suzuki, and H. Azechi for technical assistance and
advice, and H. Uchida for valuable discussions. We thank E. Kushiya,I. Yabe, C.
Ohori, Y. Mochizuki, Y. Ishikawa, and N. Ishimoto for technical assistance in generating
GluD1-KO mice.
article_processing_charge: No
article_type: original
author:
- first_name: Chihiro
full_name: Nakamoto, Chihiro
last_name: Nakamoto
- first_name: Kohtarou
full_name: Konno, Kohtarou
last_name: Konno
- first_name: Taisuke
full_name: Miyazaki, Taisuke
last_name: Miyazaki
- first_name: Ena
full_name: Nakatsukasa, Ena
last_name: Nakatsukasa
- first_name: Rie
full_name: Natsume, Rie
last_name: Natsume
- first_name: Manabu
full_name: Abe, Manabu
last_name: Abe
- first_name: Meiko
full_name: Kawamura, Meiko
last_name: Kawamura
- first_name: Yugo
full_name: Fukazawa, Yugo
last_name: Fukazawa
- first_name: Ryuichi
full_name: Shigemoto, Ryuichi
id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
last_name: Shigemoto
orcid: 0000-0001-8761-9444
- first_name: Miwako
full_name: Yamasaki, Miwako
last_name: Yamasaki
- first_name: Kenji
full_name: Sakimura, Kenji
last_name: Sakimura
- first_name: Masahiko
full_name: Watanabe, Masahiko
last_name: Watanabe
citation:
ama: Nakamoto C, Konno K, Miyazaki T, et al. Expression mapping, quantification,
and complex formation of GluD1 and GluD2 glutamate receptors in adult mouse brain.
Journal of Comparative Neurology. 2020;528(6):1003-1027. doi:10.1002/cne.24792
apa: Nakamoto, C., Konno, K., Miyazaki, T., Nakatsukasa, E., Natsume, R., Abe, M.,
… Watanabe, M. (2020). Expression mapping, quantification, and complex formation
of GluD1 and GluD2 glutamate receptors in adult mouse brain. Journal of Comparative
Neurology. Wiley. https://doi.org/10.1002/cne.24792
chicago: Nakamoto, Chihiro, Kohtarou Konno, Taisuke Miyazaki, Ena Nakatsukasa, Rie
Natsume, Manabu Abe, Meiko Kawamura, et al. “Expression Mapping, Quantification,
and Complex Formation of GluD1 and GluD2 Glutamate Receptors in Adult Mouse Brain.”
Journal of Comparative Neurology. Wiley, 2020. https://doi.org/10.1002/cne.24792.
ieee: C. Nakamoto et al., “Expression mapping, quantification, and complex
formation of GluD1 and GluD2 glutamate receptors in adult mouse brain,” Journal
of Comparative Neurology, vol. 528, no. 6. Wiley, pp. 1003–1027, 2020.
ista: Nakamoto C, Konno K, Miyazaki T, Nakatsukasa E, Natsume R, Abe M, Kawamura
M, Fukazawa Y, Shigemoto R, Yamasaki M, Sakimura K, Watanabe M. 2020. Expression
mapping, quantification, and complex formation of GluD1 and GluD2 glutamate receptors
in adult mouse brain. Journal of Comparative Neurology. 528(6), 1003–1027.
mla: Nakamoto, Chihiro, et al. “Expression Mapping, Quantification, and Complex
Formation of GluD1 and GluD2 Glutamate Receptors in Adult Mouse Brain.” Journal
of Comparative Neurology, vol. 528, no. 6, Wiley, 2020, pp. 1003–27, doi:10.1002/cne.24792.
short: C. Nakamoto, K. Konno, T. Miyazaki, E. Nakatsukasa, R. Natsume, M. Abe, M.
Kawamura, Y. Fukazawa, R. Shigemoto, M. Yamasaki, K. Sakimura, M. Watanabe, Journal
of Comparative Neurology 528 (2020) 1003–1027.
date_created: 2019-12-04T16:09:29Z
date_published: 2020-04-01T00:00:00Z
date_updated: 2023-08-17T14:06:50Z
day: '01'
ddc:
- '571'
- '599'
department:
- _id: RySh
doi: 10.1002/cne.24792
external_id:
isi:
- '000496410200001'
pmid:
- '31625608'
has_accepted_license: '1'
intvolume: ' 528'
isi: 1
issue: '6'
language:
- iso: eng
month: '04'
oa_version: None
page: 1003-1027
pmid: 1
publication: Journal of Comparative Neurology
publication_identifier:
eissn:
- 1096-9861
issn:
- 0021-9967
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Expression mapping, quantification, and complex formation of GluD1 and GluD2
glutamate receptors in adult mouse brain
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 528
year: '2020'
...
---
_id: '7033'
abstract:
- lang: eng
text: Removal of the Bax gene from mice completely protects the somas of retinal
ganglion cells (RGCs) from apoptosis following optic nerve injury. This makes
BAX a promising therapeutic target to prevent neurodegeneration. In this study,
Bax+/− mice were used to test the hypothesis that lowering the quantity of BAX
in RGCs would delay apoptosis following optic nerve injury. RGCs were damaged
by performing optic nerve crush (ONC) and then immunostaining for phospho-cJUN,
and quantitative PCR were used to monitor the status of the BAX activation mechanism
in the months following injury. The apoptotic susceptibility of injured cells
was directly tested by virally introducing GFP-BAX into Bax−/− RGCs after injury.
The competency of quiescent RGCs to reactivate their BAX activation mechanism
was tested by intravitreal injection of the JNK pathway agonist, anisomycin. Twenty-four
weeks after ONC, Bax+/− mice had significantly less cell loss in their RGC layer
than Bax+/+ mice 3 weeks after ONC. Bax+/− and Bax+/+ RGCs exhibited similar patterns
of nuclear phospho-cJUN accumulation immediately after ONC, which persisted in
Bax+/− RGCs for up to 7 weeks before abating. The transcriptional activation of
BAX-activating genes was similar in Bax+/− and Bax+/+ RGCs following ONC. Intriguingly,
cells deactivated their BAX activation mechanism between 7 and 12 weeks after
crush. Introduction of GFP-BAX into Bax−/− cells at 4 weeks after ONC showed that
these cells had a nearly normal capacity to activate this protein, but this capacity
was lost 8 weeks after crush. Collectively, these data suggest that 8–12 weeks
after crush, damaged cells no longer displayed increased susceptibility to BAX
activation relative to their naïve counterparts. In this same timeframe, retinal
glial activation and the signaling of the pro-apoptotic JNK pathway also abated.
Quiescent RGCs did not show a timely reactivation of their JNK pathway following
intravitreal injection with anisomycin. These findings demonstrate that lowering
the quantity of BAX in RGCs is neuroprotective after acute injury. Damaged RGCs
enter a quiescent state months after injury and are no longer responsive to an
apoptotic stimulus. Quiescent RGCs will require rejuvenation to reacquire functionality.
acknowledgement: This work was supported by National Eye Institute grants R01 EY012223
(RWN), R01 EY030123 (RWN), T32 EY027721 (Department of Ophthalmology and Visual
Sciences, University of Wisconsin-Madison), and a Vision Science Core grant P30
EY016665 (Department of Ophthalmology and Visual Sciences, University of Wisconsin-Madison),
an unrestricted funding grant from Research to Prevent Blindness (Department of
Ophthalmology and Visual Sciences, University of Wisconsin-Madison), the Frederick
A. Davis Endowment (RWN), and the Mr. and Mrs. George Taylor Foundation (RWN).
article_processing_charge: No
article_type: original
author:
- first_name: RJ
full_name: Donahue, RJ
last_name: Donahue
- first_name: Margaret E
full_name: Maes, Margaret E
id: 3838F452-F248-11E8-B48F-1D18A9856A87
last_name: Maes
orcid: 0000-0001-9642-1085
- first_name: JA
full_name: Grosser, JA
last_name: Grosser
- first_name: RW
full_name: Nickells, RW
last_name: Nickells
citation:
ama: Donahue R, Maes ME, Grosser J, Nickells R. BAX-depleted retinal ganglion cells
survive and become quiescent following optic nerve damage. Molecular Neurobiology.
2020;57(2):1070–1084. doi:10.1007/s12035-019-01783-7
apa: Donahue, R., Maes, M. E., Grosser, J., & Nickells, R. (2020). BAX-depleted
retinal ganglion cells survive and become quiescent following optic nerve damage.
Molecular Neurobiology. Springer Nature. https://doi.org/10.1007/s12035-019-01783-7
chicago: Donahue, RJ, Margaret E Maes, JA Grosser, and RW Nickells. “BAX-Depleted
Retinal Ganglion Cells Survive and Become Quiescent Following Optic Nerve Damage.”
Molecular Neurobiology. Springer Nature, 2020. https://doi.org/10.1007/s12035-019-01783-7.
ieee: R. Donahue, M. E. Maes, J. Grosser, and R. Nickells, “BAX-depleted retinal
ganglion cells survive and become quiescent following optic nerve damage,” Molecular
Neurobiology, vol. 57, no. 2. Springer Nature, pp. 1070–1084, 2020.
ista: Donahue R, Maes ME, Grosser J, Nickells R. 2020. BAX-depleted retinal ganglion
cells survive and become quiescent following optic nerve damage. Molecular Neurobiology.
57(2), 1070–1084.
mla: Donahue, RJ, et al. “BAX-Depleted Retinal Ganglion Cells Survive and Become
Quiescent Following Optic Nerve Damage.” Molecular Neurobiology, vol. 57,
no. 2, Springer Nature, 2020, pp. 1070–1084, doi:10.1007/s12035-019-01783-7.
short: R. Donahue, M.E. Maes, J. Grosser, R. Nickells, Molecular Neurobiology 57
(2020) 1070–1084.
date_created: 2019-11-18T14:18:39Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2023-08-17T14:05:48Z
day: '01'
department:
- _id: SaSi
doi: 10.1007/s12035-019-01783-7
external_id:
isi:
- '000493754200001'
pmid:
- '31673950'
intvolume: ' 57'
isi: 1
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035206/
month: '02'
oa: 1
oa_version: Submitted Version
page: 1070–1084
pmid: 1
publication: Molecular Neurobiology
publication_identifier:
eissn:
- 1559-1182
issn:
- 0893-7648
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: BAX-depleted retinal ganglion cells survive and become quiescent following
optic nerve damage
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 57
year: '2020'
...
---
_id: '6997'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Yuzhou
full_name: Zhang, Yuzhou
id: 3B6137F2-F248-11E8-B48F-1D18A9856A87
last_name: Zhang
orcid: 0000-0003-2627-6956
- first_name: Jiří
full_name: Friml, Jiří
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
citation:
ama: Zhang Y, Friml J. Auxin guides roots to avoid obstacles during gravitropic
growth. New Phytologist. 2020;225(3):1049-1052. doi:10.1111/nph.16203
apa: Zhang, Y., & Friml, J. (2020). Auxin guides roots to avoid obstacles during
gravitropic growth. New Phytologist. Wiley. https://doi.org/10.1111/nph.16203
chicago: Zhang, Yuzhou, and Jiří Friml. “Auxin Guides Roots to Avoid Obstacles during
Gravitropic Growth.” New Phytologist. Wiley, 2020. https://doi.org/10.1111/nph.16203.
ieee: Y. Zhang and J. Friml, “Auxin guides roots to avoid obstacles during gravitropic
growth,” New Phytologist, vol. 225, no. 3. Wiley, pp. 1049–1052, 2020.
ista: Zhang Y, Friml J. 2020. Auxin guides roots to avoid obstacles during gravitropic
growth. New Phytologist. 225(3), 1049–1052.
mla: Zhang, Yuzhou, and Jiří Friml. “Auxin Guides Roots to Avoid Obstacles during
Gravitropic Growth.” New Phytologist, vol. 225, no. 3, Wiley, 2020, pp.
1049–52, doi:10.1111/nph.16203.
short: Y. Zhang, J. Friml, New Phytologist 225 (2020) 1049–1052.
date_created: 2019-11-12T11:41:32Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2023-08-17T14:01:49Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1111/nph.16203
ec_funded: 1
external_id:
isi:
- '000489638800001'
pmid:
- '31603260'
file:
- access_level: open_access
checksum: cd42ffdb381fd52812b9583d4d407139
content_type: application/pdf
creator: dernst
date_created: 2020-11-18T16:42:48Z
date_updated: 2020-11-18T16:42:48Z
file_id: '8772'
file_name: 2020_NewPhytologist_Zhang.pdf
file_size: 717345
relation: main_file
success: 1
file_date_updated: 2020-11-18T16:42:48Z
has_accepted_license: '1'
intvolume: ' 225'
isi: 1
issue: '3'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 1049-1052
pmid: 1
project:
- _id: 261099A6-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '742985'
name: Tracing Evolution of Auxin Transport and Polarity in Plants
- _id: 26538374-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: I03630
name: Molecular mechanisms of endocytic cargo recognition in plants
- _id: 25681D80-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '291734'
name: International IST Postdoc Fellowship Programme
publication: New Phytologist
publication_identifier:
eissn:
- 1469-8137
issn:
- 0028-646x
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Auxin guides roots to avoid obstacles during gravitropic 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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 225
year: '2020'
...
---
_id: '7149'
abstract:
- lang: eng
text: In recent years, many genes have been associated with chromatinopathies classified
as “Cornelia de Lange Syndrome‐like.” It is known that the phenotype of these
patients becomes less recognizable, overlapping to features characteristic of
other syndromes caused by genetic variants affecting different regulators of chromatin
structure and function. Therefore, Cornelia de Lange syndrome diagnosis might
be arduous due to the seldom discordance between unexpected molecular diagnosis
and clinical evaluation. Here, we review the molecular features of Cornelia de
Lange syndrome, supporting the hypothesis that “CdLS‐like syndromes” are part
of a larger “rare disease family” sharing multiple clinical features and common
disrupted molecular pathways.
acknowledgement: ' Dipartimento DiSS, Università degli Studi di Milano, Grant/Award
Number: Linea 2; Fondazione Cariplo, Grant/Award Number: 2015-0783; German Federal
Ministry of Education and Research (BMBF), Grant/Award Number: CHROMATIN-Net; Medical
Faculty of the University of Lübeck, Grant/Award Number: J09-2017; Nickel & Co S.p.A.;
Università degli Studi di Milano, Grant/Award Numbers: Molecular & Translational
Medicine PhD Scholarship, Translational Medicine PhD Scholarship'
article_processing_charge: No
article_type: review
author:
- first_name: Laura
full_name: Avagliano, Laura
last_name: Avagliano
- first_name: Ilaria
full_name: Parenti, Ilaria
id: D93538B0-5B71-11E9-AC62-02EBE5697425
last_name: Parenti
- first_name: Paolo
full_name: Grazioli, Paolo
last_name: Grazioli
- first_name: Elisabetta
full_name: Di Fede, Elisabetta
last_name: Di Fede
- first_name: Chiara
full_name: Parodi, Chiara
last_name: Parodi
- first_name: Milena
full_name: Mariani, Milena
last_name: Mariani
- first_name: Frank J.
full_name: Kaiser, Frank J.
last_name: Kaiser
- first_name: Angelo
full_name: Selicorni, Angelo
last_name: Selicorni
- first_name: Cristina
full_name: Gervasini, Cristina
last_name: Gervasini
- first_name: Valentina
full_name: Massa, Valentina
last_name: Massa
citation:
ama: 'Avagliano L, Parenti I, Grazioli P, et al. Chromatinopathies: A focus on Cornelia
de Lange syndrome. Clinical Genetics. 2020;97(1):3-11. doi:10.1111/cge.13674'
apa: 'Avagliano, L., Parenti, I., Grazioli, P., Di Fede, E., Parodi, C., Mariani,
M., … Massa, V. (2020). Chromatinopathies: A focus on Cornelia de Lange syndrome.
Clinical Genetics. Wiley. https://doi.org/10.1111/cge.13674'
chicago: 'Avagliano, Laura, Ilaria Parenti, Paolo Grazioli, Elisabetta Di Fede,
Chiara Parodi, Milena Mariani, Frank J. Kaiser, Angelo Selicorni, Cristina Gervasini,
and Valentina Massa. “Chromatinopathies: A Focus on Cornelia de Lange Syndrome.”
Clinical Genetics. Wiley, 2020. https://doi.org/10.1111/cge.13674.'
ieee: 'L. Avagliano et al., “Chromatinopathies: A focus on Cornelia de Lange
syndrome,” Clinical Genetics, vol. 97, no. 1. Wiley, pp. 3–11, 2020.'
ista: 'Avagliano L, Parenti I, Grazioli P, Di Fede E, Parodi C, Mariani M, Kaiser
FJ, Selicorni A, Gervasini C, Massa V. 2020. Chromatinopathies: A focus on Cornelia
de Lange syndrome. Clinical Genetics. 97(1), 3–11.'
mla: 'Avagliano, Laura, et al. “Chromatinopathies: A Focus on Cornelia de Lange
Syndrome.” Clinical Genetics, vol. 97, no. 1, Wiley, 2020, pp. 3–11, doi:10.1111/cge.13674.'
short: L. Avagliano, I. Parenti, P. Grazioli, E. Di Fede, C. Parodi, M. Mariani,
F.J. Kaiser, A. Selicorni, C. Gervasini, V. Massa, Clinical Genetics 97 (2020)
3–11.
date_created: 2019-12-04T16:10:59Z
date_published: 2020-01-01T00:00:00Z
date_updated: 2023-08-17T14:06:20Z
day: '01'
department:
- _id: GaNo
doi: 10.1111/cge.13674
external_id:
isi:
- '000562561800001'
pmid:
- '31721174'
intvolume: ' 97'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 3-11
pmid: 1
publication: Clinical Genetics
publication_identifier:
eissn:
- 1399-0004
issn:
- 0009-9163
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Chromatinopathies: A focus on Cornelia de Lange syndrome'
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 97
year: '2020'
...
---
_id: '7004'
abstract:
- lang: eng
text: We define an action of the (double of) Cohomological Hall algebra of Kontsevich
and Soibelman on the cohomology of the moduli space of spiked instantons of Nekrasov.
We identify this action with the one of the affine Yangian of gl(1). Based on
that we derive the vertex algebra at the corner Wr1,r2,r3 of Gaiotto and Rapčák.
We conjecture that our approach works for a big class of Calabi–Yau categories,
including those associated with toric Calabi–Yau 3-folds.
article_processing_charge: No
article_type: original
author:
- first_name: Miroslav
full_name: Rapcak, Miroslav
last_name: Rapcak
- first_name: Yan
full_name: Soibelman, Yan
last_name: Soibelman
- first_name: Yaping
full_name: Yang, Yaping
last_name: Yang
- first_name: Gufang
full_name: Zhao, Gufang
id: 2BC2AC5E-F248-11E8-B48F-1D18A9856A87
last_name: Zhao
citation:
ama: Rapcak M, Soibelman Y, Yang Y, Zhao G. Cohomological Hall algebras, vertex
algebras and instantons. Communications in Mathematical Physics. 2020;376:1803-1873.
doi:10.1007/s00220-019-03575-5
apa: Rapcak, M., Soibelman, Y., Yang, Y., & Zhao, G. (2020). Cohomological Hall
algebras, vertex algebras and instantons. Communications in Mathematical Physics.
Springer Nature. https://doi.org/10.1007/s00220-019-03575-5
chicago: Rapcak, Miroslav, Yan Soibelman, Yaping Yang, and Gufang Zhao. “Cohomological
Hall Algebras, Vertex Algebras and Instantons.” Communications in Mathematical
Physics. Springer Nature, 2020. https://doi.org/10.1007/s00220-019-03575-5.
ieee: M. Rapcak, Y. Soibelman, Y. Yang, and G. Zhao, “Cohomological Hall algebras,
vertex algebras and instantons,” Communications in Mathematical Physics,
vol. 376. Springer Nature, pp. 1803–1873, 2020.
ista: Rapcak M, Soibelman Y, Yang Y, Zhao G. 2020. Cohomological Hall algebras,
vertex algebras and instantons. Communications in Mathematical Physics. 376, 1803–1873.
mla: Rapcak, Miroslav, et al. “Cohomological Hall Algebras, Vertex Algebras and
Instantons.” Communications in Mathematical Physics, vol. 376, Springer
Nature, 2020, pp. 1803–73, doi:10.1007/s00220-019-03575-5.
short: M. Rapcak, Y. Soibelman, Y. Yang, G. Zhao, Communications in Mathematical
Physics 376 (2020) 1803–1873.
date_created: 2019-11-12T14:01:27Z
date_published: 2020-06-01T00:00:00Z
date_updated: 2023-08-17T14:02:59Z
day: '01'
department:
- _id: TaHa
doi: 10.1007/s00220-019-03575-5
ec_funded: 1
external_id:
arxiv:
- '1810.10402'
isi:
- '000536255500004'
intvolume: ' 376'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1810.10402
month: '06'
oa: 1
oa_version: Preprint
page: 1803-1873
project:
- _id: 25E549F4-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '320593'
name: Arithmetic and physics of Higgs moduli spaces
publication: Communications in Mathematical Physics
publication_identifier:
eissn:
- 1432-0916
issn:
- 0010-3616
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Cohomological Hall algebras, vertex algebras and instantons
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 376
year: '2020'
...
---
_id: '7204'
abstract:
- lang: eng
text: Plant root architecture dynamically adapts to various environmental conditions,
such as salt‐containing soil. The phytohormone abscisic acid (ABA) is involved
among others also in these developmental adaptations, but the underlying molecular
mechanism remains elusive. Here, a novel branch of the ABA signaling pathway in
Arabidopsis involving PYR/PYL/RCAR (abbreviated as PYLs) receptor‐protein phosphatase
2A (PP2A) complex that acts in parallel to the canonical PYLs‐protein phosphatase
2C (PP2C) mechanism is identified. The PYLs‐PP2A signaling modulates root gravitropism
and lateral root formation through regulating phytohormone auxin transport. In
optimal conditions, PYLs ABA receptor interacts with the catalytic subunits of
PP2A, increasing their phosphatase activity and thus counteracting PINOID (PID)
kinase‐mediated phosphorylation of PIN‐FORMED (PIN) auxin transporters. By contrast,
in salt and osmotic stress conditions, ABA binds to PYLs, inhibiting the PP2A
activity, which leads to increased PIN phosphorylation and consequently modulated
directional auxin transport leading to adapted root architecture. This work reveals
an adaptive mechanism that may flexibly adjust plant root growth to withstand
saline and osmotic stresses. It occurs via the cross‐talk between the stress hormone
ABA and the versatile developmental regulator auxin.
article_number: '1901455'
article_processing_charge: No
article_type: original
author:
- first_name: Yang
full_name: Li, Yang
last_name: Li
- first_name: Yaping
full_name: Wang, Yaping
last_name: Wang
- first_name: Shutang
full_name: Tan, Shutang
id: 2DE75584-F248-11E8-B48F-1D18A9856A87
last_name: Tan
orcid: 0000-0002-0471-8285
- first_name: Zhen
full_name: Li, Zhen
last_name: Li
- first_name: Zhi
full_name: Yuan, Zhi
last_name: Yuan
- first_name: Matous
full_name: Glanc, Matous
id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2
last_name: Glanc
orcid: 0000-0003-0619-7783
- first_name: David
full_name: Domjan, David
id: C684CD7A-257E-11EA-9B6F-D8588B4F947F
last_name: Domjan
orcid: 0000-0003-2267-106X
- first_name: Kai
full_name: Wang, Kai
last_name: Wang
- first_name: Wei
full_name: Xuan, Wei
last_name: Xuan
- first_name: Yan
full_name: Guo, Yan
last_name: Guo
- first_name: Zhizhong
full_name: Gong, Zhizhong
last_name: Gong
- first_name: Jiří
full_name: Friml, Jiří
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
- first_name: Jing
full_name: Zhang, Jing
last_name: Zhang
citation:
ama: Li Y, Wang Y, Tan S, et al. Root growth adaptation is mediated by PYLs ABA
receptor-PP2A protein phosphatase complex. Advanced Science. 2020;7(3).
doi:10.1002/advs.201901455
apa: Li, Y., Wang, Y., Tan, S., Li, Z., Yuan, Z., Glanc, M., … Zhang, J. (2020).
Root growth adaptation is mediated by PYLs ABA receptor-PP2A protein phosphatase
complex. Advanced Science. Wiley. https://doi.org/10.1002/advs.201901455
chicago: Li, Yang, Yaping Wang, Shutang Tan, Zhen Li, Zhi Yuan, Matous Glanc, David
Domjan, et al. “Root Growth Adaptation Is Mediated by PYLs ABA Receptor-PP2A Protein
Phosphatase Complex.” Advanced Science. Wiley, 2020. https://doi.org/10.1002/advs.201901455.
ieee: Y. Li et al., “Root growth adaptation is mediated by PYLs ABA receptor-PP2A
protein phosphatase complex,” Advanced Science, vol. 7, no. 3. Wiley, 2020.
ista: Li Y, Wang Y, Tan S, Li Z, Yuan Z, Glanc M, Domjan D, Wang K, Xuan W, Guo
Y, Gong Z, Friml J, Zhang J. 2020. Root growth adaptation is mediated by PYLs
ABA receptor-PP2A protein phosphatase complex. Advanced Science. 7(3), 1901455.
mla: Li, Yang, et al. “Root Growth Adaptation Is Mediated by PYLs ABA Receptor-PP2A
Protein Phosphatase Complex.” Advanced Science, vol. 7, no. 3, 1901455,
Wiley, 2020, doi:10.1002/advs.201901455.
short: Y. Li, Y. Wang, S. Tan, Z. Li, Z. Yuan, M. Glanc, D. Domjan, K. Wang, W.
Xuan, Y. Guo, Z. Gong, J. Friml, J. Zhang, Advanced Science 7 (2020).
date_created: 2019-12-22T23:00:43Z
date_published: 2020-02-05T00:00:00Z
date_updated: 2023-08-17T14:13:17Z
day: '05'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1002/advs.201901455
external_id:
isi:
- '000501912800001'
pmid:
- '32042554'
file:
- access_level: open_access
checksum: 016eeab5860860af038e2da95ffe75c3
content_type: application/pdf
creator: dernst
date_created: 2020-02-24T14:29:54Z
date_updated: 2020-07-14T12:47:53Z
file_id: '7519'
file_name: 2020_AdvScience_Li.pdf
file_size: 3586924
relation: main_file
file_date_updated: 2020-07-14T12:47:53Z
has_accepted_license: '1'
intvolume: ' 7'
isi: 1
issue: '3'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
publication: Advanced Science
publication_identifier:
eissn:
- 2198-3844
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Root growth adaptation is mediated by PYLs ABA receptor-PP2A protein phosphatase
complex
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 7
year: '2020'
...
---
_id: '7220'
abstract:
- lang: eng
text: BACKGROUND:The introduction of image-guided methods to bypass surgery has
resulted in optimized preoperative identification of the recipients and excellent
patency rates. However, the recently presented methods have also been resource-consuming.
In the present study, we have reported a cost-efficient planning workflow for
extracranial-intracranial (EC-IC) revascularization combined with transdural indocyanine
green videoangiography (tICG-VA). METHODS:We performed a retrospective review
at a single tertiary referral center from 2011 to 2018. A novel software-derived
workflow was applied for 25 of 92 bypass procedures during the study period. The
precision and accuracy were assessed using tICG-VA identification of the cortical
recipients and a comparison of the virtual and actual data. The data from a control
group of 25 traditionally planned procedures were also matched. RESULTS:The intraoperative
transfer time of the calculated coordinates averaged 0.8 minute (range, 0.4-1.9
minutes). The definitive recipients matched the targeted branches in 80%, and
a neighboring branch was used in 16%. Our workflow led to a significant craniotomy
size reduction in the study group compared with that in the control group (P =
0.005). tICG-VA was successfully applied in 19 cases. An average of 2 potential
recipient arteries were identified transdurally, resulting in tailored durotomy
and 3 craniotomy adjustments. Follow-up patency results were available for 49
bypass surgeries, comprising 54 grafts. The overall patency rate was 91% at a
median follow-up period of 26 months. No significant difference was found in the
patency rate between the study and control groups (P = 0.317). CONCLUSIONS:Our
clinical results have validated the presented planning and surgical workflow and
support the routine implementation of tICG-VA for recipient identification before
durotomy.
article_processing_charge: No
article_type: original
author:
- first_name: Philippe
full_name: Dodier, Philippe
last_name: Dodier
- first_name: Thomas
full_name: Auzinger, Thomas
id: 4718F954-F248-11E8-B48F-1D18A9856A87
last_name: Auzinger
orcid: 0000-0002-1546-3265
- first_name: Gabriel
full_name: Mistelbauer, Gabriel
last_name: Mistelbauer
- first_name: Wei Te
full_name: Wang, Wei Te
last_name: Wang
- first_name: Heber
full_name: Ferraz-Leite, Heber
last_name: Ferraz-Leite
- first_name: Andreas
full_name: Gruber, Andreas
last_name: Gruber
- first_name: Wolfgang
full_name: Marik, Wolfgang
last_name: Marik
- first_name: Fabian
full_name: Winter, Fabian
last_name: Winter
- first_name: Gerrit
full_name: Fischer, Gerrit
last_name: Fischer
- first_name: Josa M.
full_name: Frischer, Josa M.
last_name: Frischer
- first_name: Gerhard
full_name: Bavinzski, Gerhard
last_name: Bavinzski
citation:
ama: Dodier P, Auzinger T, Mistelbauer G, et al. Novel software-derived workflow
in extracranial–intracranial bypass surgery validated by transdural indocyanine
green videoangiography. World Neurosurgery. 2020;134(2):e892-e902. doi:10.1016/j.wneu.2019.11.038
apa: Dodier, P., Auzinger, T., Mistelbauer, G., Wang, W. T., Ferraz-Leite, H., Gruber,
A., … Bavinzski, G. (2020). Novel software-derived workflow in extracranial–intracranial
bypass surgery validated by transdural indocyanine green videoangiography. World
Neurosurgery. Elsevier. https://doi.org/10.1016/j.wneu.2019.11.038
chicago: Dodier, Philippe, Thomas Auzinger, Gabriel Mistelbauer, Wei Te Wang, Heber
Ferraz-Leite, Andreas Gruber, Wolfgang Marik, et al. “Novel Software-Derived Workflow
in Extracranial–Intracranial Bypass Surgery Validated by Transdural Indocyanine
Green Videoangiography.” World Neurosurgery. Elsevier, 2020. https://doi.org/10.1016/j.wneu.2019.11.038.
ieee: P. Dodier et al., “Novel software-derived workflow in extracranial–intracranial
bypass surgery validated by transdural indocyanine green videoangiography,” World
Neurosurgery, vol. 134, no. 2. Elsevier, pp. e892–e902, 2020.
ista: Dodier P, Auzinger T, Mistelbauer G, Wang WT, Ferraz-Leite H, Gruber A, Marik
W, Winter F, Fischer G, Frischer JM, Bavinzski G. 2020. Novel software-derived
workflow in extracranial–intracranial bypass surgery validated by transdural indocyanine
green videoangiography. World Neurosurgery. 134(2), e892–e902.
mla: Dodier, Philippe, et al. “Novel Software-Derived Workflow in Extracranial–Intracranial
Bypass Surgery Validated by Transdural Indocyanine Green Videoangiography.” World
Neurosurgery, vol. 134, no. 2, Elsevier, 2020, pp. e892–902, doi:10.1016/j.wneu.2019.11.038.
short: P. Dodier, T. Auzinger, G. Mistelbauer, W.T. Wang, H. Ferraz-Leite, A. Gruber,
W. Marik, F. Winter, G. Fischer, J.M. Frischer, G. Bavinzski, World Neurosurgery
134 (2020) e892–e902.
date_created: 2019-12-29T23:00:48Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2023-08-17T14:14:23Z
day: '01'
department:
- _id: BeBi
doi: 10.1016/j.wneu.2019.11.038
external_id:
isi:
- '000512878200104'
pmid:
- '31733380'
intvolume: ' 134'
isi: 1
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
page: e892-e902
pmid: 1
publication: World Neurosurgery
publication_identifier:
eissn:
- 1878-8769
issn:
- 1878-8750
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Novel software-derived workflow in extracranial–intracranial bypass surgery
validated by transdural indocyanine green videoangiography
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 134
year: '2020'
...
---
_id: '7142'
abstract:
- lang: eng
text: The phytohormone auxin acts as an amazingly versatile coordinator of plant
growth and development. With its morphogen-like properties, auxin controls sites
and timing of differentiation and/or growth responses both, in quantitative and
qualitative terms. Specificity in the auxin response depends largely on distinct
modes of signal transmission, by which individual cells perceive and convert auxin
signals into a remarkable diversity of responses. The best understood, or so-called
canonical mechanism of auxin perception ultimately results in variable adjustments
of the cellular transcriptome, via a short, nuclear signal transduction pathway.
Additional findings that accumulated over decades implied that an additional,
presumably, cell surface-based auxin perception mechanism mediates very rapid
cellular responses and decisively contributes to the cell's overall hormonal response.
Recent investigations into both, nuclear and cell surface auxin signalling challenged
this assumed partition of roles for different auxin signalling pathways and revealed
an unexpected complexity in transcriptional and non-transcriptional cellular responses
mediated by auxin.
acknowledgement: Research in J.F. laboratory is funded by the European Union's Horizon
2020 program (ERC grant agreement n° 742985); C.L. is supported by the Austrian
Science Fund (FWF grant P 31493).
article_processing_charge: No
article_type: original
author:
- first_name: Michelle C
full_name: Gallei, Michelle C
id: 35A03822-F248-11E8-B48F-1D18A9856A87
last_name: Gallei
orcid: 0000-0003-1286-7368
- first_name: Christian
full_name: Luschnig, Christian
last_name: Luschnig
- first_name: Jiří
full_name: Friml, Jiří
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
citation:
ama: 'Gallei MC, Luschnig C, Friml J. Auxin signalling in growth: Schrödinger’s
cat out of the bag. Current Opinion in Plant Biology. 2020;53(2):43-49.
doi:10.1016/j.pbi.2019.10.003'
apa: 'Gallei, M. C., Luschnig, C., & Friml, J. (2020). Auxin signalling in growth:
Schrödinger’s cat out of the bag. Current Opinion in Plant Biology. Elsevier.
https://doi.org/10.1016/j.pbi.2019.10.003'
chicago: 'Gallei, Michelle C, Christian Luschnig, and Jiří Friml. “Auxin Signalling
in Growth: Schrödinger’s Cat out of the Bag.” Current Opinion in Plant Biology.
Elsevier, 2020. https://doi.org/10.1016/j.pbi.2019.10.003.'
ieee: 'M. C. Gallei, C. Luschnig, and J. Friml, “Auxin signalling in growth: Schrödinger’s
cat out of the bag,” Current Opinion in Plant Biology, vol. 53, no. 2.
Elsevier, pp. 43–49, 2020.'
ista: 'Gallei MC, Luschnig C, Friml J. 2020. Auxin signalling in growth: Schrödinger’s
cat out of the bag. Current Opinion in Plant Biology. 53(2), 43–49.'
mla: 'Gallei, Michelle C., et al. “Auxin Signalling in Growth: Schrödinger’s Cat
out of the Bag.” Current Opinion in Plant Biology, vol. 53, no. 2, Elsevier,
2020, pp. 43–49, doi:10.1016/j.pbi.2019.10.003.'
short: M.C. Gallei, C. Luschnig, J. Friml, Current Opinion in Plant Biology 53 (2020)
43–49.
date_created: 2019-12-02T12:05:26Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2023-08-17T14:07:22Z
day: '01'
department:
- _id: JiFr
doi: 10.1016/j.pbi.2019.10.003
ec_funded: 1
external_id:
isi:
- '000521120600007'
pmid:
- '31760231'
intvolume: ' 53'
isi: 1
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
page: 43-49
pmid: 1
project:
- _id: 261099A6-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '742985'
name: Tracing Evolution of Auxin Transport and Polarity in Plants
publication: Current Opinion in Plant Biology
publication_identifier:
eissn:
- 1879-0356
issn:
- 1369-5266
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
record:
- id: '11626'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: 'Auxin signalling in growth: Schrödinger''s cat out of the bag'
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 53
year: '2020'
...
---
_id: '7166'
abstract:
- lang: eng
text: In the living cell, we encounter a large variety of motile processes such
as organelle transport and cytoskeleton remodeling. These processes are driven
by motor proteins that generate force by transducing chemical free energy into
mechanical work. In many cases, the molecular motors work in teams to collectively
generate larger forces. Recent optical trapping experiments on small teams of
cytoskeletal motors indicated that the collectively generated force increases
with the size of the motor team but that this increase depends on the motor type
and on whether the motors are studied in vitro or in vivo. Here, we use the theory
of stochastic processes to describe the motion of N motors in a stationary optical
trap and to compute the N-dependence of the collectively generated forces. We
consider six distinct motor types, two kinesins, two dyneins, and two myosins.
We show that the force increases always linearly with N but with a prefactor that
depends on the performance of the single motor. Surprisingly, this prefactor increases
for weaker motors with a lower stall force. This counter-intuitive behavior reflects
the increased probability with which stronger motors detach from the filament
during strain generation. Our theoretical results are in quantitative agreement
with experimental data on small teams of kinesin-1 motors.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Mehmet C
full_name: Ucar, Mehmet C
id: 50B2A802-6007-11E9-A42B-EB23E6697425
last_name: Ucar
orcid: 0000-0003-0506-4217
- first_name: Reinhard
full_name: Lipowsky, Reinhard
last_name: Lipowsky
citation:
ama: Ucar MC, Lipowsky R. Collective force generation by molecular motors is determined
by strain-induced unbinding. Nano Letters. 2020;20(1):669-676. doi:10.1021/acs.nanolett.9b04445
apa: Ucar, M. C., & Lipowsky, R. (2020). Collective force generation by molecular
motors is determined by strain-induced unbinding. Nano Letters. American
Chemical Society. https://doi.org/10.1021/acs.nanolett.9b04445
chicago: Ucar, Mehmet C, and Reinhard Lipowsky. “Collective Force Generation by
Molecular Motors Is Determined by Strain-Induced Unbinding.” Nano Letters.
American Chemical Society, 2020. https://doi.org/10.1021/acs.nanolett.9b04445.
ieee: M. C. Ucar and R. Lipowsky, “Collective force generation by molecular motors
is determined by strain-induced unbinding,” Nano Letters, vol. 20, no.
1. American Chemical Society, pp. 669–676, 2020.
ista: Ucar MC, Lipowsky R. 2020. Collective force generation by molecular motors
is determined by strain-induced unbinding. Nano Letters. 20(1), 669–676.
mla: Ucar, Mehmet C., and Reinhard Lipowsky. “Collective Force Generation by Molecular
Motors Is Determined by Strain-Induced Unbinding.” Nano Letters, vol. 20,
no. 1, American Chemical Society, 2020, pp. 669–76, doi:10.1021/acs.nanolett.9b04445.
short: M.C. Ucar, R. Lipowsky, Nano Letters 20 (2020) 669–676.
date_created: 2019-12-10T15:36:05Z
date_published: 2020-01-08T00:00:00Z
date_updated: 2023-08-17T14:07:52Z
day: '08'
department:
- _id: EdHa
doi: 10.1021/acs.nanolett.9b04445
external_id:
isi:
- '000507151600087'
pmid:
- '31797672'
intvolume: ' 20'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1021/acs.nanolett.9b04445
month: '01'
oa: 1
oa_version: Published Version
page: 669-676
pmid: 1
publication: Nano Letters
publication_identifier:
eissn:
- 1530-6992
issn:
- 1530-6984
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
related_material:
record:
- id: '9726'
relation: research_data
status: public
- id: '9885'
relation: research_data
status: public
scopus_import: '1'
status: public
title: Collective force generation by molecular motors is determined by strain-induced
unbinding
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 20
year: '2020'
...
---
_id: '9885'
abstract:
- lang: eng
text: Data obtained from the fine-grained simulations used in Figures 2-5, data
obtained from the coarse-grained numerical calculations used in Figure 6, and
a sample script for the fine-grained simulation as a Jupyter notebook (ZIP)
article_processing_charge: No
author:
- first_name: Mehmet C
full_name: Ucar, Mehmet C
id: 50B2A802-6007-11E9-A42B-EB23E6697425
last_name: Ucar
orcid: 0000-0003-0506-4217
- first_name: Reinhard
full_name: Lipowsky, Reinhard
last_name: Lipowsky
citation:
ama: Ucar MC, Lipowsky R. MURL_Dataz. 2020. doi:10.1021/acs.nanolett.9b04445.s002
apa: Ucar, M. C., & Lipowsky, R. (2020). MURL_Dataz. American Chemical Society
. https://doi.org/10.1021/acs.nanolett.9b04445.s002
chicago: Ucar, Mehmet C, and Reinhard Lipowsky. “MURL_Dataz.” American Chemical
Society , 2020. https://doi.org/10.1021/acs.nanolett.9b04445.s002.
ieee: M. C. Ucar and R. Lipowsky, “MURL_Dataz.” American Chemical Society , 2020.
ista: Ucar MC, Lipowsky R. 2020. MURL_Dataz, American Chemical Society , 10.1021/acs.nanolett.9b04445.s002.
mla: Ucar, Mehmet C., and Reinhard Lipowsky. MURL_Dataz. American Chemical
Society , 2020, doi:10.1021/acs.nanolett.9b04445.s002.
short: M.C. Ucar, R. Lipowsky, (2020).
date_created: 2021-08-11T13:16:03Z
date_published: 2020-01-08T00:00:00Z
date_updated: 2023-08-17T14:07:52Z
day: '08'
department:
- _id: EdHa
doi: 10.1021/acs.nanolett.9b04445.s002
month: '01'
oa_version: Published Version
publisher: 'American Chemical Society '
related_material:
record:
- id: '7166'
relation: used_in_publication
status: public
status: public
title: MURL_Dataz
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2020'
...
---
_id: '7218'
abstract:
- lang: eng
text: The combined resection of skull-infiltrating tumours and immediate cranioplastic
reconstruction predominantly relies on freehand-moulded solutions. Techniques
that enable this procedure to be performed easily in routine clinical practice
would be useful. A cadaveric study was developed in which a new software tool
was used to perform single-stage reconstructions with prefabricated implants after
the resection of skull-infiltrating pathologies. A novel 3D visualization and
interaction framework was developed to create 10 virtual craniotomies in five
cadaveric specimens. Polyether ether ketone (PEEK) implants were manufactured
according to the bone defects. The image-guided craniotomy was reconstructed with
PEEK and compared to polymethyl methacrylate (PMMA). Navigational accuracy and
surgical precision were assessed. The PEEK workflow resulted in up to 10-fold
shorter reconstruction times than the standard technique. Surgical precision was
reflected by the mean 1.1 ± 0.29 mm distance between the virtual and real craniotomy,
with submillimetre precision in 50%. Assessment of the global offset between virtual
and actual craniotomy revealed an average shift of 4.5 ± 3.6 mm. The results validated
the ‘elective single-stage cranioplasty’ technique as a state-of-the-art virtual
planning method and surgical workflow. This patient-tailored workflow could significantly
reduce surgical times compared to the traditional, intraoperative acrylic moulding
method and may be an option for the reconstruction of bone defects in the craniofacial
region.
article_processing_charge: No
article_type: original
author:
- first_name: Philippe
full_name: Dodier, Philippe
last_name: Dodier
- first_name: Fabian
full_name: Winter, Fabian
last_name: Winter
- first_name: Thomas
full_name: Auzinger, Thomas
id: 4718F954-F248-11E8-B48F-1D18A9856A87
last_name: Auzinger
orcid: 0000-0002-1546-3265
- first_name: Gabriel
full_name: Mistelbauer, Gabriel
last_name: Mistelbauer
- first_name: Josa M.
full_name: Frischer, Josa M.
last_name: Frischer
- first_name: Wei Te
full_name: Wang, Wei Te
last_name: Wang
- first_name: Ammar
full_name: Mallouhi, Ammar
last_name: Mallouhi
- first_name: Wolfgang
full_name: Marik, Wolfgang
last_name: Marik
- first_name: Stefan
full_name: Wolfsberger, Stefan
last_name: Wolfsberger
- first_name: Lukas
full_name: Reissig, Lukas
last_name: Reissig
- first_name: Firas
full_name: Hammadi, Firas
last_name: Hammadi
- first_name: Christian
full_name: Matula, Christian
last_name: Matula
- first_name: Arnulf
full_name: Baumann, Arnulf
last_name: Baumann
- first_name: Gerhard
full_name: Bavinzski, Gerhard
last_name: Bavinzski
citation:
ama: 'Dodier P, Winter F, Auzinger T, et al. Single-stage bone resection and cranioplastic
reconstruction: Comparison of a novel software-derived PEEK workflow with the
standard reconstructive method. International Journal of Oral and Maxillofacial
Surgery. 2020;49(8):P1007-1015. doi:10.1016/j.ijom.2019.11.011'
apa: 'Dodier, P., Winter, F., Auzinger, T., Mistelbauer, G., Frischer, J. M., Wang,
W. T., … Bavinzski, G. (2020). Single-stage bone resection and cranioplastic reconstruction:
Comparison of a novel software-derived PEEK workflow with the standard reconstructive
method. International Journal of Oral and Maxillofacial Surgery. Elsevier.
https://doi.org/10.1016/j.ijom.2019.11.011'
chicago: 'Dodier, Philippe, Fabian Winter, Thomas Auzinger, Gabriel Mistelbauer,
Josa M. Frischer, Wei Te Wang, Ammar Mallouhi, et al. “Single-Stage Bone Resection
and Cranioplastic Reconstruction: Comparison of a Novel Software-Derived PEEK
Workflow with the Standard Reconstructive Method.” International Journal of
Oral and Maxillofacial Surgery. Elsevier, 2020. https://doi.org/10.1016/j.ijom.2019.11.011.'
ieee: 'P. Dodier et al., “Single-stage bone resection and cranioplastic reconstruction:
Comparison of a novel software-derived PEEK workflow with the standard reconstructive
method,” International Journal of Oral and Maxillofacial Surgery, vol.
49, no. 8. Elsevier, pp. P1007-1015, 2020.'
ista: 'Dodier P, Winter F, Auzinger T, Mistelbauer G, Frischer JM, Wang WT, Mallouhi
A, Marik W, Wolfsberger S, Reissig L, Hammadi F, Matula C, Baumann A, Bavinzski
G. 2020. Single-stage bone resection and cranioplastic reconstruction: Comparison
of a novel software-derived PEEK workflow with the standard reconstructive method.
International Journal of Oral and Maxillofacial Surgery. 49(8), P1007-1015.'
mla: 'Dodier, Philippe, et al. “Single-Stage Bone Resection and Cranioplastic Reconstruction:
Comparison of a Novel Software-Derived PEEK Workflow with the Standard Reconstructive
Method.” International Journal of Oral and Maxillofacial Surgery, vol.
49, no. 8, Elsevier, 2020, pp. P1007-1015, doi:10.1016/j.ijom.2019.11.011.'
short: P. Dodier, F. Winter, T. Auzinger, G. Mistelbauer, J.M. Frischer, W.T. Wang,
A. Mallouhi, W. Marik, S. Wolfsberger, L. Reissig, F. Hammadi, C. Matula, A. Baumann,
G. Bavinzski, International Journal of Oral and Maxillofacial Surgery 49 (2020)
P1007-1015.
date_created: 2019-12-29T23:00:47Z
date_published: 2020-08-01T00:00:00Z
date_updated: 2023-08-17T14:15:22Z
day: '01'
department:
- _id: BeBi
doi: 10.1016/j.ijom.2019.11.011
external_id:
isi:
- '000556819800005'
pmid:
- '31866145'
intvolume: ' 49'
isi: 1
issue: '8'
language:
- iso: eng
month: '08'
oa_version: None
page: P1007-1015
pmid: 1
publication: International Journal of Oral and Maxillofacial Surgery
publication_identifier:
eissn:
- 1399-0020
issn:
- 0901-5027
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Single-stage bone resection and cranioplastic reconstruction: Comparison of
a novel software-derived PEEK workflow with the standard reconstructive method'
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 49
year: '2020'
...
---
_id: '7219'
abstract:
- lang: eng
text: Root system architecture (RSA), governed by the phytohormone auxin, endows
plants with an adaptive advantage in particular environments. Using geographically
representative arabidopsis (Arabidopsis thaliana) accessions as a resource for
GWA mapping, Waidmann et al. and Ogura et al. recently identified two novel components
involved in modulating auxin-mediated RSA and conferring plant fitness in particular
habitats.
article_processing_charge: No
article_type: original
author:
- first_name: Guanghui
full_name: Xiao, Guanghui
last_name: Xiao
- first_name: Yuzhou
full_name: Zhang, Yuzhou
id: 3B6137F2-F248-11E8-B48F-1D18A9856A87
last_name: Zhang
orcid: 0000-0003-2627-6956
citation:
ama: 'Xiao G, Zhang Y. Adaptive growth: Shaping auxin-mediated root system architecture.
Trends in Plant Science. 2020;25(2):P121-123. doi:10.1016/j.tplants.2019.12.001'
apa: 'Xiao, G., & Zhang, Y. (2020). Adaptive growth: Shaping auxin-mediated
root system architecture. Trends in Plant Science. Elsevier. https://doi.org/10.1016/j.tplants.2019.12.001'
chicago: 'Xiao, Guanghui, and Yuzhou Zhang. “Adaptive Growth: Shaping Auxin-Mediated
Root System Architecture.” Trends in Plant Science. Elsevier, 2020. https://doi.org/10.1016/j.tplants.2019.12.001.'
ieee: 'G. Xiao and Y. Zhang, “Adaptive growth: Shaping auxin-mediated root system
architecture,” Trends in Plant Science, vol. 25, no. 2. Elsevier, pp. P121-123,
2020.'
ista: 'Xiao G, Zhang Y. 2020. Adaptive growth: Shaping auxin-mediated root system
architecture. Trends in Plant Science. 25(2), P121-123.'
mla: 'Xiao, Guanghui, and Yuzhou Zhang. “Adaptive Growth: Shaping Auxin-Mediated
Root System Architecture.” Trends in Plant Science, vol. 25, no. 2, Elsevier,
2020, pp. P121-123, doi:10.1016/j.tplants.2019.12.001.'
short: G. Xiao, Y. Zhang, Trends in Plant Science 25 (2020) P121-123.
date_created: 2019-12-29T23:00:48Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2023-08-17T14:14:50Z
day: '01'
department:
- _id: JiFr
doi: 10.1016/j.tplants.2019.12.001
external_id:
isi:
- '000508637500001'
pmid:
- '31843370'
intvolume: ' 25'
isi: 1
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
page: P121-123
pmid: 1
publication: Trends in Plant Science
publication_identifier:
issn:
- '13601385'
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Adaptive growth: Shaping auxin-mediated root system architecture'
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 25
year: '2020'
...
---
_id: '7234'
abstract:
- lang: eng
text: T lymphocytes utilize amoeboid migration to navigate effectively within complex
microenvironments. The precise rearrangement of the actin cytoskeleton required
for cellular forward propulsion is mediated by actin regulators, including the
actin‐related protein 2/3 (Arp2/3) complex, a macromolecular machine that nucleates
branched actin filaments at the leading edge. The consequences of modulating Arp2/3
activity on the biophysical properties of the actomyosin cortex and downstream
T cell function are incompletely understood. We report that even a moderate decrease
of Arp3 levels in T cells profoundly affects actin cortex integrity. Reduction
in total F‐actin content leads to reduced cortical tension and disrupted lamellipodia
formation. Instead, in Arp3‐knockdown cells, the motility mode is dominated by
blebbing migration characterized by transient, balloon‐like protrusions at the
leading edge. Although this migration mode seems to be compatible with interstitial
migration in three‐dimensional environments, diminished locomotion kinetics and
impaired cytotoxicity interfere with optimal T cell function. These findings define
the importance of finely tuned, Arp2/3‐dependent mechanophysical membrane integrity
in cytotoxic effector T lymphocyte activities.
article_processing_charge: No
article_type: original
author:
- first_name: Peyman
full_name: Obeidy, Peyman
last_name: Obeidy
- first_name: Lining A.
full_name: Ju, Lining A.
last_name: Ju
- first_name: Stefan H.
full_name: Oehlers, Stefan H.
last_name: Oehlers
- first_name: Nursafwana S.
full_name: Zulkhernain, Nursafwana S.
last_name: Zulkhernain
- first_name: Quintin
full_name: Lee, Quintin
last_name: Lee
- first_name: Jorge L.
full_name: Galeano Niño, Jorge L.
last_name: Galeano Niño
- first_name: Rain Y.Q.
full_name: Kwan, Rain Y.Q.
last_name: Kwan
- first_name: Shweta
full_name: Tikoo, Shweta
last_name: Tikoo
- first_name: Lois L.
full_name: Cavanagh, Lois L.
last_name: Cavanagh
- first_name: Paulus
full_name: Mrass, Paulus
last_name: Mrass
- first_name: Adam J.L.
full_name: Cook, Adam J.L.
last_name: Cook
- first_name: Shaun P.
full_name: Jackson, Shaun P.
last_name: Jackson
- first_name: Maté
full_name: Biro, Maté
last_name: Biro
- first_name: Ben
full_name: Roediger, Ben
last_name: Roediger
- 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: Wolfgang
full_name: Weninger, Wolfgang
last_name: Weninger
citation:
ama: Obeidy P, Ju LA, Oehlers SH, et al. Partial loss of actin nucleator actin-related
protein 2/3 activity triggers blebbing in primary T lymphocytes. Immunology
and Cell Biology. 2020;98(2):93-113. doi:10.1111/imcb.12304
apa: Obeidy, P., Ju, L. A., Oehlers, S. H., Zulkhernain, N. S., Lee, Q., Galeano
Niño, J. L., … Weninger, W. (2020). Partial loss of actin nucleator actin-related
protein 2/3 activity triggers blebbing in primary T lymphocytes. Immunology
and Cell Biology. Wiley. https://doi.org/10.1111/imcb.12304
chicago: Obeidy, Peyman, Lining A. Ju, Stefan H. Oehlers, Nursafwana S. Zulkhernain,
Quintin Lee, Jorge L. Galeano Niño, Rain Y.Q. Kwan, et al. “Partial Loss of Actin
Nucleator Actin-Related Protein 2/3 Activity Triggers Blebbing in Primary T Lymphocytes.”
Immunology and Cell Biology. Wiley, 2020. https://doi.org/10.1111/imcb.12304.
ieee: P. Obeidy et al., “Partial loss of actin nucleator actin-related protein
2/3 activity triggers blebbing in primary T lymphocytes,” Immunology and Cell
Biology, vol. 98, no. 2. Wiley, pp. 93–113, 2020.
ista: Obeidy P, Ju LA, Oehlers SH, Zulkhernain NS, Lee Q, Galeano Niño JL, Kwan
RYQ, Tikoo S, Cavanagh LL, Mrass P, Cook AJL, Jackson SP, Biro M, Roediger B,
Sixt MK, Weninger W. 2020. Partial loss of actin nucleator actin-related protein
2/3 activity triggers blebbing in primary T lymphocytes. Immunology and Cell Biology.
98(2), 93–113.
mla: Obeidy, Peyman, et al. “Partial Loss of Actin Nucleator Actin-Related Protein
2/3 Activity Triggers Blebbing in Primary T Lymphocytes.” Immunology and Cell
Biology, vol. 98, no. 2, Wiley, 2020, pp. 93–113, doi:10.1111/imcb.12304.
short: P. Obeidy, L.A. Ju, S.H. Oehlers, N.S. Zulkhernain, Q. Lee, J.L. Galeano
Niño, R.Y.Q. Kwan, S. Tikoo, L.L. Cavanagh, P. Mrass, A.J.L. Cook, S.P. Jackson,
M. Biro, B. Roediger, M.K. Sixt, W. Weninger, Immunology and Cell Biology 98 (2020)
93–113.
date_created: 2020-01-05T23:00:48Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2023-08-17T14:21:12Z
day: '01'
ddc:
- '570'
department:
- _id: MiSi
doi: 10.1111/imcb.12304
external_id:
isi:
- '000503885600001'
pmid:
- '31698518'
file:
- access_level: open_access
checksum: c389477b4b52172ef76afff8a06c6775
content_type: application/pdf
creator: dernst
date_created: 2020-11-19T11:22:33Z
date_updated: 2020-11-19T11:22:33Z
file_id: '8775'
file_name: 2020_ImmunologyCellBio_Obeidy.pdf
file_size: 8569945
relation: main_file
success: 1
file_date_updated: 2020-11-19T11:22:33Z
has_accepted_license: '1'
intvolume: ' 98'
isi: 1
issue: '2'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 93-113
pmid: 1
publication: Immunology and Cell Biology
publication_identifier:
eissn:
- '14401711'
issn:
- '08189641'
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Partial loss of actin nucleator actin-related protein 2/3 activity triggers
blebbing in primary T lymphocytes
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 98
year: '2020'
...
---
_id: '7253'
abstract:
- lang: eng
text: The cyclin-dependent kinase inhibitor p57KIP2 is encoded by the imprinted
Cdkn1c locus, exhibits maternal expression, and is essential for cerebral cortex
development. How Cdkn1c regulates corticogenesis is however not clear. To this
end we employ Mosaic Analysis with Double Markers (MADM) technology to genetically
dissect Cdkn1c gene function in corticogenesis at single cell resolution. We find
that the previously described growth-inhibitory Cdkn1c function is a non-cell-autonomous
one, acting on the whole organism. In contrast we reveal a growth-promoting cell-autonomous
Cdkn1c function which at the mechanistic level mediates radial glial progenitor
cell and nascent projection neuron survival. Strikingly, the growth-promoting
function of Cdkn1c is highly dosage sensitive but not subject to genomic imprinting.
Collectively, our results suggest that the Cdkn1c locus regulates cortical development
through distinct cell-autonomous and non-cell-autonomous mechanisms. More generally,
our study highlights the importance to probe the relative contributions of cell
intrinsic gene function and tissue-wide mechanisms to the overall phenotype.
acknowledged_ssus:
- _id: PreCl
article_number: '195'
article_processing_charge: No
article_type: original
author:
- first_name: Susanne
full_name: Laukoter, Susanne
id: 2D6B7A9A-F248-11E8-B48F-1D18A9856A87
last_name: Laukoter
orcid: 0000-0002-7903-3010
- first_name: Robert J
full_name: Beattie, Robert J
id: 2E26DF60-F248-11E8-B48F-1D18A9856A87
last_name: Beattie
orcid: 0000-0002-8483-8753
- first_name: Florian
full_name: Pauler, Florian
id: 48EA0138-F248-11E8-B48F-1D18A9856A87
last_name: Pauler
orcid: 0000-0002-7462-0048
- first_name: Nicole
full_name: Amberg, Nicole
id: 4CD6AAC6-F248-11E8-B48F-1D18A9856A87
last_name: Amberg
orcid: 0000-0002-3183-8207
- first_name: Keiichi I.
full_name: Nakayama, Keiichi I.
last_name: Nakayama
- first_name: Simon
full_name: Hippenmeyer, Simon
id: 37B36620-F248-11E8-B48F-1D18A9856A87
last_name: Hippenmeyer
orcid: 0000-0003-2279-1061
citation:
ama: Laukoter S, Beattie RJ, Pauler F, Amberg N, Nakayama KI, Hippenmeyer S. Imprinted
Cdkn1c genomic locus cell-autonomously promotes cell survival in cerebral cortex
development. Nature Communications. 2020;11. doi:10.1038/s41467-019-14077-2
apa: Laukoter, S., Beattie, R. J., Pauler, F., Amberg, N., Nakayama, K. I., &
Hippenmeyer, S. (2020). Imprinted Cdkn1c genomic locus cell-autonomously promotes
cell survival in cerebral cortex development. Nature Communications. Springer
Nature. https://doi.org/10.1038/s41467-019-14077-2
chicago: Laukoter, Susanne, Robert J Beattie, Florian Pauler, Nicole Amberg, Keiichi
I. Nakayama, and Simon Hippenmeyer. “Imprinted Cdkn1c Genomic Locus Cell-Autonomously
Promotes Cell Survival in Cerebral Cortex Development.” Nature Communications.
Springer Nature, 2020. https://doi.org/10.1038/s41467-019-14077-2.
ieee: S. Laukoter, R. J. Beattie, F. Pauler, N. Amberg, K. I. Nakayama, and S. Hippenmeyer,
“Imprinted Cdkn1c genomic locus cell-autonomously promotes cell survival in cerebral
cortex development,” Nature Communications, vol. 11. Springer Nature, 2020.
ista: Laukoter S, Beattie RJ, Pauler F, Amberg N, Nakayama KI, Hippenmeyer S. 2020.
Imprinted Cdkn1c genomic locus cell-autonomously promotes cell survival in cerebral
cortex development. Nature Communications. 11, 195.
mla: Laukoter, Susanne, et al. “Imprinted Cdkn1c Genomic Locus Cell-Autonomously
Promotes Cell Survival in Cerebral Cortex Development.” Nature Communications,
vol. 11, 195, Springer Nature, 2020, doi:10.1038/s41467-019-14077-2.
short: S. Laukoter, R.J. Beattie, F. Pauler, N. Amberg, K.I. Nakayama, S. Hippenmeyer,
Nature Communications 11 (2020).
date_created: 2020-01-11T10:42:48Z
date_published: 2020-01-10T00:00:00Z
date_updated: 2023-08-17T14:23:41Z
day: '10'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.1038/s41467-019-14077-2
ec_funded: 1
external_id:
isi:
- '000551459000005'
file:
- access_level: open_access
checksum: ebf1ed522f4e0be8d94c939c1806a709
content_type: application/pdf
creator: dernst
date_created: 2020-01-13T07:42:31Z
date_updated: 2020-07-14T12:47:54Z
file_id: '7261'
file_name: 2020_NatureComm_Laukoter.pdf
file_size: 8063333
relation: main_file
file_date_updated: 2020-07-14T12:47:54Z
has_accepted_license: '1'
intvolume: ' 11'
isi: 1
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: 268F8446-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: T0101031
name: Role of Eed in neural stem cell lineage progression
- _id: 264E56E2-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: M02416
name: Molecular Mechanisms Regulating Gliogenesis in the Cerebral Cortex
- _id: 260018B0-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '725780'
name: Principles of Neural Stem Cell Lineage Progression in Cerebral Cortex Development
- _id: 25D92700-B435-11E9-9278-68D0E5697425
grant_number: LS13-002
name: Mapping Cell-Type Specificity of the Genomic Imprintome in the Brain
publication: Nature Communications
publication_identifier:
issn:
- 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
link:
- description: News on IST Homepage
relation: press_release
url: https://ist.ac.at/en/news/new-function-for-potential-tumour-suppressor-in-brain-development/
scopus_import: '1'
status: public
title: Imprinted Cdkn1c genomic locus cell-autonomously promotes cell survival in
cerebral cortex development
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 11
year: '2020'
...
---
_id: '7339'
abstract:
- lang: eng
text: Cytoskeletal filaments such as microtubules (MTs) and filamentous actin (F-actin)
dynamically support cell structure and functions. In central presynaptic terminals,
F-actin is expressed along the release edge and reportedly plays diverse functional
roles, but whether axonal MTs extend deep into terminals and play any physiological
role remains controversial. At the calyx of Held in rats of either sex, confocal
and high-resolution microscopy revealed that MTs enter deep into presynaptic terminal
swellings and partially colocalize with a subset of synaptic vesicles (SVs). Electrophysiological
analysis demonstrated that depolymerization of MTs specifically prolonged the
slow-recovery time component of EPSCs from short-term depression induced by a
train of high-frequency stimulation, whereas depolymerization of F-actin specifically
prolonged the fast-recovery component. In simultaneous presynaptic and postsynaptic
action potential recordings, depolymerization of MTs or F-actin significantly
impaired the fidelity of high-frequency neurotransmission. We conclude that MTs
and F-actin differentially contribute to slow and fast SV replenishment, thereby
maintaining high-frequency neurotransmission.
article_processing_charge: No
article_type: original
author:
- first_name: Lashmi
full_name: Piriya Ananda Babu, Lashmi
last_name: Piriya Ananda Babu
- first_name: Han Ying
full_name: Wang, Han Ying
last_name: Wang
- first_name: Kohgaku
full_name: Eguchi, Kohgaku
id: 2B7846DC-F248-11E8-B48F-1D18A9856A87
last_name: Eguchi
orcid: 0000-0002-6170-2546
- first_name: Laurent
full_name: Guillaud, Laurent
last_name: Guillaud
- first_name: Tomoyuki
full_name: Takahashi, Tomoyuki
last_name: Takahashi
citation:
ama: Piriya Ananda Babu L, Wang HY, Eguchi K, Guillaud L, Takahashi T. Microtubule
and actin differentially regulate synaptic vesicle cycling to maintain high-frequency
neurotransmission. Journal of neuroscience. 2020;40(1):131-142. doi:10.1523/JNEUROSCI.1571-19.2019
apa: Piriya Ananda Babu, L., Wang, H. Y., Eguchi, K., Guillaud, L., & Takahashi,
T. (2020). Microtubule and actin differentially regulate synaptic vesicle cycling
to maintain high-frequency neurotransmission. Journal of Neuroscience.
Society for Neuroscience. https://doi.org/10.1523/JNEUROSCI.1571-19.2019
chicago: Piriya Ananda Babu, Lashmi, Han Ying Wang, Kohgaku Eguchi, Laurent Guillaud,
and Tomoyuki Takahashi. “Microtubule and Actin Differentially Regulate Synaptic
Vesicle Cycling to Maintain High-Frequency Neurotransmission.” Journal of Neuroscience.
Society for Neuroscience, 2020. https://doi.org/10.1523/JNEUROSCI.1571-19.2019.
ieee: L. Piriya Ananda Babu, H. Y. Wang, K. Eguchi, L. Guillaud, and T. Takahashi,
“Microtubule and actin differentially regulate synaptic vesicle cycling to maintain
high-frequency neurotransmission,” Journal of neuroscience, vol. 40, no.
1. Society for Neuroscience, pp. 131–142, 2020.
ista: Piriya Ananda Babu L, Wang HY, Eguchi K, Guillaud L, Takahashi T. 2020. Microtubule
and actin differentially regulate synaptic vesicle cycling to maintain high-frequency
neurotransmission. Journal of neuroscience. 40(1), 131–142.
mla: Piriya Ananda Babu, Lashmi, et al. “Microtubule and Actin Differentially Regulate
Synaptic Vesicle Cycling to Maintain High-Frequency Neurotransmission.” Journal
of Neuroscience, vol. 40, no. 1, Society for Neuroscience, 2020, pp. 131–42,
doi:10.1523/JNEUROSCI.1571-19.2019.
short: L. Piriya Ananda Babu, H.Y. Wang, K. Eguchi, L. Guillaud, T. Takahashi, Journal
of Neuroscience 40 (2020) 131–142.
date_created: 2020-01-19T23:00:38Z
date_published: 2020-01-02T00:00:00Z
date_updated: 2023-08-17T14:25:23Z
day: '02'
ddc:
- '570'
department:
- _id: RySh
doi: 10.1523/JNEUROSCI.1571-19.2019
external_id:
isi:
- '000505167600013'
pmid:
- '31767677'
file:
- access_level: open_access
checksum: 92f5e8a47f454fc131fb94cd7f106e60
content_type: application/pdf
creator: dernst
date_created: 2020-01-20T14:44:10Z
date_updated: 2020-07-14T12:47:56Z
file_id: '7345'
file_name: 2020_JourNeuroscience_Piriya.pdf
file_size: 4460781
relation: main_file
file_date_updated: 2020-07-14T12:47:56Z
has_accepted_license: '1'
intvolume: ' 40'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 131-142
pmid: 1
publication: Journal of neuroscience
publication_identifier:
eissn:
- '15292401'
publication_status: published
publisher: Society for Neuroscience
quality_controlled: '1'
scopus_import: '1'
status: public
title: Microtubule and actin differentially regulate synaptic vesicle cycling to maintain
high-frequency neurotransmission
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 40
year: '2020'
...
---
_id: '7350'
abstract:
- lang: eng
text: The ability to sense environmental temperature and to coordinate growth and
development accordingly, is critical to the reproductive success of plants. Flowering
time is regulated at the level of gene expression by a complex network of factors
that integrate environmental and developmental cues. One of the main players,
involved in modulating flowering time in response to changes in ambient temperature
is FLOWERING LOCUS M (FLM). FLM transcripts can undergo extensive alternative
splicing producing multiple variants, of which FLM-β and FLM-δ are the most representative.
While FLM-β codes for the flowering repressor FLM protein, translation of FLM-δ
has the opposite effect on flowering. Here we show that the cyclin-dependent kinase
G2 (CDKG2), together with its cognate cyclin, CYCLYN L1 (CYCL1) affects the alternative
splicing of FLM, balancing the levels of FLM-β and FLM-δ across the ambient temperature
range. In the absence of the CDKG2/CYCL1 complex, FLM-β expression is reduced
while FLM-δ is increased in a temperature dependent manner and these changes are
associated with an early flowering phenotype in the cdkg2 mutant lines. In addition,
we found that transcript variants retaining the full FLM intron 1 are sequestered
in the cell nucleus. Strikingly, FLM intron 1 splicing is also regulated by CDKG2/CYCL1.
Our results provide evidence that temperature and CDKs regulate the alternative
splicing of FLM, contributing to flowering time definition.
article_number: '1680'
article_processing_charge: No
article_type: original
author:
- first_name: Candida
full_name: Nibau, Candida
last_name: Nibau
- first_name: Marçal
full_name: Gallemi, Marçal
id: 460C6802-F248-11E8-B48F-1D18A9856A87
last_name: Gallemi
orcid: 0000-0003-4675-6893
- first_name: Despoina
full_name: Dadarou, Despoina
last_name: Dadarou
- first_name: John H.
full_name: Doonan, John H.
last_name: Doonan
- first_name: Nicola
full_name: Cavallari, Nicola
id: 457160E6-F248-11E8-B48F-1D18A9856A87
last_name: Cavallari
citation:
ama: Nibau C, Gallemi M, Dadarou D, Doonan JH, Cavallari N. Thermo-sensitive alternative
splicing of FLOWERING LOCUS M is modulated by cyclin-dependent kinase G2. Frontiers
in Plant Science. 2020;10. doi:10.3389/fpls.2019.01680
apa: Nibau, C., Gallemi, M., Dadarou, D., Doonan, J. H., & Cavallari, N. (2020).
Thermo-sensitive alternative splicing of FLOWERING LOCUS M is modulated by cyclin-dependent
kinase G2. Frontiers in Plant Science. Frontiers Media. https://doi.org/10.3389/fpls.2019.01680
chicago: Nibau, Candida, Marçal Gallemi, Despoina Dadarou, John H. Doonan, and Nicola
Cavallari. “Thermo-Sensitive Alternative Splicing of FLOWERING LOCUS M Is Modulated
by Cyclin-Dependent Kinase G2.” Frontiers in Plant Science. Frontiers Media,
2020. https://doi.org/10.3389/fpls.2019.01680.
ieee: C. Nibau, M. Gallemi, D. Dadarou, J. H. Doonan, and N. Cavallari, “Thermo-sensitive
alternative splicing of FLOWERING LOCUS M is modulated by cyclin-dependent kinase
G2,” Frontiers in Plant Science, vol. 10. Frontiers Media, 2020.
ista: Nibau C, Gallemi M, Dadarou D, Doonan JH, Cavallari N. 2020. Thermo-sensitive
alternative splicing of FLOWERING LOCUS M is modulated by cyclin-dependent kinase
G2. Frontiers in Plant Science. 10, 1680.
mla: Nibau, Candida, et al. “Thermo-Sensitive Alternative Splicing of FLOWERING
LOCUS M Is Modulated by Cyclin-Dependent Kinase G2.” Frontiers in Plant Science,
vol. 10, 1680, Frontiers Media, 2020, doi:10.3389/fpls.2019.01680.
short: C. Nibau, M. Gallemi, D. Dadarou, J.H. Doonan, N. Cavallari, Frontiers in
Plant Science 10 (2020).
date_created: 2020-01-22T15:23:57Z
date_published: 2020-01-22T00:00:00Z
date_updated: 2023-08-17T14:21:45Z
day: '22'
ddc:
- '580'
department:
- _id: EvBe
doi: 10.3389/fpls.2019.01680
external_id:
isi:
- '000511376000001'
file:
- access_level: open_access
checksum: d1f92e60a713fbd15097ce895e5c7ccb
content_type: application/pdf
creator: dernst
date_created: 2020-01-27T09:07:02Z
date_updated: 2020-07-14T12:47:56Z
file_id: '7366'
file_name: 2020_FrontiersPlantScience_Nibau.pdf
file_size: 1951438
relation: main_file
file_date_updated: 2020-07-14T12:47:56Z
has_accepted_license: '1'
intvolume: ' 10'
isi: 1
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
publication: Frontiers in Plant Science
publication_identifier:
issn:
- 1664-462X
publication_status: published
publisher: Frontiers Media
quality_controlled: '1'
scopus_import: '1'
status: public
title: Thermo-sensitive alternative splicing of FLOWERING LOCUS M is modulated by
cyclin-dependent kinase G2
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 10
year: '2020'
...
---
_id: '7369'
abstract:
- lang: eng
text: Neuronal responses to complex stimuli and tasks can encompass a wide range
of time scales. Understanding these responses requires measures that characterize
how the information on these response patterns are represented across multiple
temporal resolutions. In this paper we propose a metric – which we call multiscale
relevance (MSR) – to capture the dynamical variability of the activity of single
neurons across different time scales. The MSR is a non-parametric, fully featureless
indicator in that it uses only the time stamps of the firing activity without
resorting to any a priori covariate or invoking any specific structure in the
tuning curve for neural activity. When applied to neural data from the mEC and
from the ADn and PoS regions of freely-behaving rodents, we found that neurons
having low MSR tend to have low mutual information and low firing sparsity across
the correlates that are believed to be encoded by the region of the brain where
the recordings were made. In addition, neurons with high MSR contain significant
information on spatial navigation and allow to decode spatial position or head
direction as efficiently as those neurons whose firing activity has high mutual
information with the covariate to be decoded and significantly better than the
set of neurons with high local variations in their interspike intervals. Given
these results, we propose that the MSR can be used as a measure to rank and select
neurons for their information content without the need to appeal to any a priori
covariate.
acknowledgement: This research was supported by the Kavli Foundation and the Centre
of Excellence scheme of the Research Council of Norway (Centre for Neural Computation).
RJC is currently receiving funding from the European Union’s Horizon 2020 research
and innovation programme under the Marie Skłodowska-Curie Grant Agreement No. 754411.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Ryan J
full_name: Cubero, Ryan J
id: 850B2E12-9CD4-11E9-837F-E719E6697425
last_name: Cubero
orcid: 0000-0003-0002-1867
- first_name: Matteo
full_name: Marsili, Matteo
last_name: Marsili
- first_name: Yasser
full_name: Roudi, Yasser
last_name: Roudi
citation:
ama: Cubero RJ, Marsili M, Roudi Y. Multiscale relevance and informative encoding
in neuronal spike trains. Journal of Computational Neuroscience. 2020;48:85-102.
doi:10.1007/s10827-020-00740-x
apa: Cubero, R. J., Marsili, M., & Roudi, Y. (2020). Multiscale relevance and
informative encoding in neuronal spike trains. Journal of Computational Neuroscience.
Springer Nature. https://doi.org/10.1007/s10827-020-00740-x
chicago: Cubero, Ryan J, Matteo Marsili, and Yasser Roudi. “Multiscale Relevance
and Informative Encoding in Neuronal Spike Trains.” Journal of Computational
Neuroscience. Springer Nature, 2020. https://doi.org/10.1007/s10827-020-00740-x.
ieee: R. J. Cubero, M. Marsili, and Y. Roudi, “Multiscale relevance and informative
encoding in neuronal spike trains,” Journal of Computational Neuroscience,
vol. 48. Springer Nature, pp. 85–102, 2020.
ista: Cubero RJ, Marsili M, Roudi Y. 2020. Multiscale relevance and informative
encoding in neuronal spike trains. Journal of Computational Neuroscience. 48,
85–102.
mla: Cubero, Ryan J., et al. “Multiscale Relevance and Informative Encoding in Neuronal
Spike Trains.” Journal of Computational Neuroscience, vol. 48, Springer
Nature, 2020, pp. 85–102, doi:10.1007/s10827-020-00740-x.
short: R.J. Cubero, M. Marsili, Y. Roudi, Journal of Computational Neuroscience
48 (2020) 85–102.
date_created: 2020-01-28T10:34:00Z
date_published: 2020-02-01T00:00:00Z
date_updated: 2023-08-17T14:35:22Z
day: '01'
ddc:
- '004'
- '519'
- '570'
department:
- _id: SaSi
doi: 10.1007/s10827-020-00740-x
ec_funded: 1
external_id:
isi:
- '000515321800006'
file:
- access_level: open_access
checksum: 036e9451d6cd0c190ad25791bf82393b
content_type: application/pdf
creator: rcubero
date_created: 2020-01-28T09:31:09Z
date_updated: 2020-07-14T12:47:56Z
file_id: '7380'
file_name: 10827_2020_740_MOESM1_ESM.pdf
file_size: 1941355
relation: supplementary_material
- access_level: open_access
checksum: 4dd8b1fd4b54486f79d82ac7b2a412b2
content_type: application/pdf
creator: rcubero
date_created: 2020-01-28T09:31:09Z
date_updated: 2020-07-14T12:47:56Z
file_id: '7381'
file_name: Cubero2020_Article_MultiscaleRelevanceAndInformat.pdf
file_size: 3257880
relation: main_file
file_date_updated: 2020-07-14T12:47:56Z
has_accepted_license: '1'
intvolume: ' 48'
isi: 1
keyword:
- Time series analysis
- Multiple time scale analysis
- Spike train data
- Information theory
- Bayesian decoding
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 85-102
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
publication: Journal of Computational Neuroscience
publication_identifier:
eissn:
- 1573-6873
issn:
- 0929-5313
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Multiscale relevance and informative encoding in neuronal spike trains
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 48
year: '2020'
...
---
_id: '7364'
abstract:
- lang: eng
text: We present nsCouette, a highly scalable software tool to solve the Navier–Stokes
equations for incompressible fluid flow between differentially heated and independently
rotating, concentric cylinders. It is based on a pseudospectral spatial discretization
and dynamic time-stepping. It is implemented in modern Fortran with a hybrid MPI-OpenMP
parallelization scheme and thus designed to compute turbulent flows at high Reynolds
and Rayleigh numbers. An additional GPU implementation (C-CUDA) for intermediate
problem sizes and a version for pipe flow (nsPipe) are also provided.
article_number: '100395'
article_processing_charge: No
article_type: original
author:
- first_name: Jose M
full_name: Lopez Alonso, Jose M
id: 40770848-F248-11E8-B48F-1D18A9856A87
last_name: Lopez Alonso
orcid: 0000-0002-0384-2022
- first_name: Daniel
full_name: Feldmann, Daniel
last_name: Feldmann
- first_name: Markus
full_name: Rampp, Markus
last_name: Rampp
- first_name: Alberto
full_name: Vela-Martín, Alberto
last_name: Vela-Martín
- first_name: Liang
full_name: Shi, Liang
id: 374A3F1A-F248-11E8-B48F-1D18A9856A87
last_name: Shi
- first_name: Marc
full_name: Avila, Marc
last_name: Avila
citation:
ama: Lopez Alonso JM, Feldmann D, Rampp M, Vela-Martín A, Shi L, Avila M. nsCouette
– A high-performance code for direct numerical simulations of turbulent Taylor–Couette
flow. SoftwareX. 2020;11. doi:10.1016/j.softx.2019.100395
apa: Lopez Alonso, J. M., Feldmann, D., Rampp, M., Vela-Martín, A., Shi, L., &
Avila, M. (2020). nsCouette – A high-performance code for direct numerical simulations
of turbulent Taylor–Couette flow. SoftwareX. Elsevier. https://doi.org/10.1016/j.softx.2019.100395
chicago: Lopez Alonso, Jose M, Daniel Feldmann, Markus Rampp, Alberto Vela-Martín,
Liang Shi, and Marc Avila. “NsCouette – A High-Performance Code for Direct Numerical
Simulations of Turbulent Taylor–Couette Flow.” SoftwareX. Elsevier, 2020.
https://doi.org/10.1016/j.softx.2019.100395.
ieee: J. M. Lopez Alonso, D. Feldmann, M. Rampp, A. Vela-Martín, L. Shi, and M.
Avila, “nsCouette – A high-performance code for direct numerical simulations of
turbulent Taylor–Couette flow,” SoftwareX, vol. 11. Elsevier, 2020.
ista: Lopez Alonso JM, Feldmann D, Rampp M, Vela-Martín A, Shi L, Avila M. 2020.
nsCouette – A high-performance code for direct numerical simulations of turbulent
Taylor–Couette flow. SoftwareX. 11, 100395.
mla: Lopez Alonso, Jose M., et al. “NsCouette – A High-Performance Code for Direct
Numerical Simulations of Turbulent Taylor–Couette Flow.” SoftwareX, vol.
11, 100395, Elsevier, 2020, doi:10.1016/j.softx.2019.100395.
short: J.M. Lopez Alonso, D. Feldmann, M. Rampp, A. Vela-Martín, L. Shi, M. Avila,
SoftwareX 11 (2020).
date_created: 2020-01-26T23:00:35Z
date_published: 2020-01-17T00:00:00Z
date_updated: 2023-08-17T14:29:59Z
day: '17'
ddc:
- '000'
department:
- _id: BjHo
doi: 10.1016/j.softx.2019.100395
external_id:
arxiv:
- '1908.00587'
isi:
- '000552271200011'
file:
- access_level: open_access
checksum: 2af1a1a3cc33557b345145276f221668
content_type: application/pdf
creator: dernst
date_created: 2020-01-27T07:32:46Z
date_updated: 2020-07-14T12:47:56Z
file_id: '7365'
file_name: 2020_SoftwareX_Lopez.pdf
file_size: 679707
relation: main_file
file_date_updated: 2020-07-14T12:47:56Z
has_accepted_license: '1'
intvolume: ' 11'
isi: 1
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '01'
oa: 1
oa_version: Published Version
publication: SoftwareX
publication_identifier:
eissn:
- '23527110'
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: nsCouette – A high-performance code for direct numerical simulations of turbulent
Taylor–Couette flow
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: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 11
year: '2020'
...
---
_id: '7431'
abstract:
- lang: eng
text: 'In many real-world systems, information can be transmitted in two qualitatively
different ways: by copying or by transformation. Copying occurs when messages
are transmitted without modification, e.g. when an offspring receives an unaltered
copy of a gene from its parent. Transformation occurs when messages are modified
systematically during transmission, e.g. when mutational biases occur during genetic
replication. Standard information-theoretic measures do not distinguish these
two modes of information transfer, although they may reflect different mechanisms
and have different functional consequences. Starting from a few simple axioms,
we derive a decomposition of mutual information into the information transmitted
by copying versus the information transmitted by transformation. We begin with
a decomposition that applies when the source and destination of the channel have
the same set of messages and a notion of message identity exists. We then generalize
our decomposition to other kinds of channels, which can involve different source
and destination sets and broader notions of similarity. In addition, we show that
copy information can be interpreted as the minimal work needed by a physical copying
process, which is relevant for understanding the physics of replication. We use
the proposed decomposition to explore a model of amino acid substitution rates.
Our results apply to any system in which the fidelity of copying, rather than
simple predictability, is of critical relevance.'
acknowledgement: "AK was supported by Grant No. FQXi-RFP-1622 from the FQXi foundation,
and Grant No. CHE-1648973 from the U.S.\r\nNational Science Foundation. AK would
like to thank the Santa Fe Institute for supporting this research. The authors\r\nthank
Jordi Fortuny, Rudolf Hanel, Joshua Garland, and Blai Vidiella for helpful discussions,
as well as the anonymous\r\nreviewers for their insightful suggestions. "
article_number: '0623'
article_processing_charge: No
article_type: original
author:
- first_name: Artemy
full_name: Kolchinsky, Artemy
last_name: Kolchinsky
- first_name: Bernat
full_name: Corominas-Murtra, Bernat
id: 43BE2298-F248-11E8-B48F-1D18A9856A87
last_name: Corominas-Murtra
orcid: 0000-0001-9806-5643
citation:
ama: Kolchinsky A, Corominas-Murtra B. Decomposing information into copying versus
transformation. Journal of the Royal Society Interface. 2020;17(162). doi:10.1098/rsif.2019.0623
apa: Kolchinsky, A., & Corominas-Murtra, B. (2020). Decomposing information
into copying versus transformation. Journal of the Royal Society Interface.
The Royal Society. https://doi.org/10.1098/rsif.2019.0623
chicago: Kolchinsky, Artemy, and Bernat Corominas-Murtra. “Decomposing Information
into Copying versus Transformation.” Journal of the Royal Society Interface.
The Royal Society, 2020. https://doi.org/10.1098/rsif.2019.0623.
ieee: A. Kolchinsky and B. Corominas-Murtra, “Decomposing information into copying
versus transformation,” Journal of the Royal Society Interface, vol. 17,
no. 162. The Royal Society, 2020.
ista: Kolchinsky A, Corominas-Murtra B. 2020. Decomposing information into copying
versus transformation. Journal of the Royal Society Interface. 17(162), 0623.
mla: Kolchinsky, Artemy, and Bernat Corominas-Murtra. “Decomposing Information into
Copying versus Transformation.” Journal of the Royal Society Interface,
vol. 17, no. 162, 0623, The Royal Society, 2020, doi:10.1098/rsif.2019.0623.
short: A. Kolchinsky, B. Corominas-Murtra, Journal of the Royal Society Interface
17 (2020).
date_created: 2020-02-02T23:01:03Z
date_published: 2020-01-29T00:00:00Z
date_updated: 2023-08-17T14:31:28Z
day: '29'
department:
- _id: EdHa
doi: 10.1098/rsif.2019.0623
external_id:
arxiv:
- '1903.10693'
isi:
- '000538369800002'
pmid:
- '31964273'
intvolume: ' 17'
isi: 1
issue: '162'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1903.10693
month: '01'
oa: 1
oa_version: Preprint
pmid: 1
publication: Journal of the Royal Society Interface
publication_identifier:
eissn:
- '17425662'
publication_status: published
publisher: The Royal Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Decomposing information into copying versus transformation
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 17
year: '2020'
...