---
_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
license: https://creativecommons.org/licenses/by/4.0/
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'
...
---
_id: '7389'
abstract:
- lang: eng
text: "Recently Kloeckner described the structure of the isometry group of the quadratic
Wasserstein space W_2(R^n). It turned out that the case of the real line is exceptional
in the sense that there exists an exotic isometry flow. Following this line of
investigation, we compute Isom(W_p(R)), the isometry group of the Wasserstein
space\r\nW_p(R) for all p \\in [1,\\infty) \\setminus {2}. We show that W_2(R)
is also exceptional regarding the\r\nparameter p: W_p(R) is isometrically rigid
if and only if p is not equal to 2. Regarding the underlying\r\nspace, we prove
that the exceptionality of p = 2 disappears if we replace R by the compact\r\ninterval
[0,1]. Surprisingly, in that case, W_p([0,1]) is isometrically rigid if and only
if\r\np is not equal to 1. Moreover, W_1([0,1]) admits isometries that split mass,
and Isom(W_1([0,1]))\r\ncannot be embedded into Isom(W_1(R))."
article_processing_charge: No
article_type: original
author:
- first_name: Gyorgy Pal
full_name: Geher, Gyorgy Pal
last_name: Geher
- first_name: Tamas
full_name: Titkos, Tamas
last_name: Titkos
- first_name: Daniel
full_name: Virosztek, Daniel
id: 48DB45DA-F248-11E8-B48F-1D18A9856A87
last_name: Virosztek
orcid: 0000-0003-1109-5511
citation:
ama: Geher GP, Titkos T, Virosztek D. Isometric study of Wasserstein spaces - the
real line. Transactions of the American Mathematical Society. 2020;373(8):5855-5883.
doi:10.1090/tran/8113
apa: Geher, G. P., Titkos, T., & Virosztek, D. (2020). Isometric study of Wasserstein
spaces - the real line. Transactions of the American Mathematical Society.
American Mathematical Society. https://doi.org/10.1090/tran/8113
chicago: Geher, Gyorgy Pal, Tamas Titkos, and Daniel Virosztek. “Isometric Study
of Wasserstein Spaces - the Real Line.” Transactions of the American Mathematical
Society. American Mathematical Society, 2020. https://doi.org/10.1090/tran/8113.
ieee: G. P. Geher, T. Titkos, and D. Virosztek, “Isometric study of Wasserstein
spaces - the real line,” Transactions of the American Mathematical Society,
vol. 373, no. 8. American Mathematical Society, pp. 5855–5883, 2020.
ista: Geher GP, Titkos T, Virosztek D. 2020. Isometric study of Wasserstein spaces
- the real line. Transactions of the American Mathematical Society. 373(8), 5855–5883.
mla: Geher, Gyorgy Pal, et al. “Isometric Study of Wasserstein Spaces - the Real
Line.” Transactions of the American Mathematical Society, vol. 373, no.
8, American Mathematical Society, 2020, pp. 5855–83, doi:10.1090/tran/8113.
short: G.P. Geher, T. Titkos, D. Virosztek, Transactions of the American Mathematical
Society 373 (2020) 5855–5883.
date_created: 2020-01-29T10:20:46Z
date_published: 2020-08-01T00:00:00Z
date_updated: 2023-08-17T14:31:03Z
day: '01'
ddc:
- '515'
department:
- _id: LaEr
doi: 10.1090/tran/8113
ec_funded: 1
external_id:
arxiv:
- '2002.00859'
isi:
- '000551418100018'
intvolume: ' 373'
isi: 1
issue: '8'
keyword:
- Wasserstein space
- isometric embeddings
- isometric rigidity
- exotic isometry flow
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/2002.00859
month: '08'
oa: 1
oa_version: Preprint
page: 5855-5883
project:
- _id: 26A455A6-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '846294'
name: Geometric study of Wasserstein spaces and free probability
publication: Transactions of the American Mathematical Society
publication_identifier:
eissn:
- '10886850'
issn:
- '00029947'
publication_status: published
publisher: American Mathematical Society
quality_controlled: '1'
status: public
title: Isometric study of Wasserstein spaces - the real line
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 373
year: '2020'
...
---
_id: '7467'
abstract:
- lang: eng
text: Nanomaterials produced from the bottom-up assembly of nanocrystals may incorporate
∼1020–1021 cm–3 not fully coordinated surface atoms, i.e., ∼1020–1021 cm–3 potential
donor or acceptor states that can strongly affect transport properties. Therefore,
to exploit the full potential of nanocrystal building blocks to produce functional
nanomaterials and thin films, a proper control of their surface chemistry is required.
Here, we analyze how the ligand stripping procedure influences the charge and
heat transport properties of sintered PbSe nanomaterials produced from the bottom-up
assembly of colloidal PbSe nanocrystals. First, we show that the removal of the
native organic ligands by thermal decomposition in an inert atmosphere leaves
relatively large amounts of carbon at the crystal interfaces. This carbon blocks
crystal growth during consolidation and at the same time hampers charge and heat
transport through the final nanomaterial. Second, we demonstrate that, by stripping
ligands from the nanocrystal surface before consolidation, nanomaterials with
larger crystal domains, lower porosity, and higher charge carrier concentrations
are obtained, thus resulting in nanomaterials with higher electrical and thermal
conductivities. In addition, the ligand displacement leaves the nanocrystal surface
unprotected, facilitating oxidation and chalcogen evaporation. The influence of
the ligand displacement on the nanomaterial charge transport properties is rationalized
here using a two-band model based on the standard Boltzmann transport equation
with the relaxation time approximation. Finally, we present an application of
the produced functional nanomaterials by modeling, fabricating, and testing a
simple PbSe-based thermoelectric device with a ring geometry.
acknowledgement: This work was supported by the Spanish Ministerio de Economía y Competitividad
through the project SEHTOP (ENE2016-77798-C4-3-R) and the Generalitat de Catalunya
through the project 2017SGR1246. D.C. acknowledges support from Universidad Nacional
de Colombia. Y.L. acknowledges funding from the European Union’s Horizon 2020 research
and innovation programme under the Marie Sklodowska-Curie grant agreement no. 754411.
M.I. acknowledges financial support from IST Austria.
article_processing_charge: No
article_type: original
author:
- first_name: Doris
full_name: Cadavid, Doris
last_name: Cadavid
- first_name: Silvia
full_name: Ortega, Silvia
last_name: Ortega
- first_name: Sergio
full_name: Illera, Sergio
last_name: Illera
- first_name: Yu
full_name: Liu, Yu
id: 2A70014E-F248-11E8-B48F-1D18A9856A87
last_name: Liu
orcid: 0000-0001-7313-6740
- first_name: Maria
full_name: Ibáñez, Maria
id: 43C61214-F248-11E8-B48F-1D18A9856A87
last_name: Ibáñez
orcid: 0000-0001-5013-2843
- first_name: Alexey
full_name: Shavel, Alexey
last_name: Shavel
- first_name: Yu
full_name: Zhang, Yu
last_name: Zhang
- first_name: Mengyao
full_name: Li, Mengyao
last_name: Li
- first_name: Antonio M.
full_name: López, Antonio M.
last_name: López
- first_name: Germán
full_name: Noriega, Germán
last_name: Noriega
- first_name: Oscar Juan
full_name: Durá, Oscar Juan
last_name: Durá
- first_name: M. A.
full_name: López De La Torre, M. A.
last_name: López De La Torre
- first_name: Joan Daniel
full_name: Prades, Joan Daniel
last_name: Prades
- first_name: Andreu
full_name: Cabot, Andreu
last_name: Cabot
citation:
ama: Cadavid D, Ortega S, Illera S, et al. Influence of the ligand stripping on
the transport properties of nanoparticle-based PbSe nanomaterials. ACS Applied
Energy Materials. 2020;3(3):2120-2129. doi:10.1021/acsaem.9b02137
apa: Cadavid, D., Ortega, S., Illera, S., Liu, Y., Ibáñez, M., Shavel, A., … Cabot,
A. (2020). Influence of the ligand stripping on the transport properties of nanoparticle-based
PbSe nanomaterials. ACS Applied Energy Materials. American Chemical Society.
https://doi.org/10.1021/acsaem.9b02137
chicago: Cadavid, Doris, Silvia Ortega, Sergio Illera, Yu Liu, Maria Ibáñez, Alexey
Shavel, Yu Zhang, et al. “Influence of the Ligand Stripping on the Transport Properties
of Nanoparticle-Based PbSe Nanomaterials.” ACS Applied Energy Materials.
American Chemical Society, 2020. https://doi.org/10.1021/acsaem.9b02137.
ieee: D. Cadavid et al., “Influence of the ligand stripping on the transport
properties of nanoparticle-based PbSe nanomaterials,” ACS Applied Energy Materials,
vol. 3, no. 3. American Chemical Society, pp. 2120–2129, 2020.
ista: Cadavid D, Ortega S, Illera S, Liu Y, Ibáñez M, Shavel A, Zhang Y, Li M, López
AM, Noriega G, Durá OJ, López De La Torre MA, Prades JD, Cabot A. 2020. Influence
of the ligand stripping on the transport properties of nanoparticle-based PbSe
nanomaterials. ACS Applied Energy Materials. 3(3), 2120–2129.
mla: Cadavid, Doris, et al. “Influence of the Ligand Stripping on the Transport
Properties of Nanoparticle-Based PbSe Nanomaterials.” ACS Applied Energy Materials,
vol. 3, no. 3, American Chemical Society, 2020, pp. 2120–29, doi:10.1021/acsaem.9b02137.
short: D. Cadavid, S. Ortega, S. Illera, Y. Liu, M. Ibáñez, A. Shavel, Y. Zhang,
M. Li, A.M. López, G. Noriega, O.J. Durá, M.A. López De La Torre, J.D. Prades,
A. Cabot, ACS Applied Energy Materials 3 (2020) 2120–2129.
date_created: 2020-02-09T23:00:52Z
date_published: 2020-03-01T00:00:00Z
date_updated: 2023-08-17T14:36:16Z
day: '01'
ddc:
- '540'
department:
- _id: MaIb
doi: 10.1021/acsaem.9b02137
ec_funded: 1
external_id:
isi:
- '000526598300012'
file:
- access_level: open_access
checksum: f23be731a766a480c77c962c1380315c
content_type: application/pdf
creator: dernst
date_created: 2022-08-23T08:34:17Z
date_updated: 2022-08-23T08:34:17Z
file_id: '11942'
file_name: 2020_ACSAppliedEnergyMat_Cadavid.pdf
file_size: 6423548
relation: main_file
success: 1
file_date_updated: 2022-08-23T08:34:17Z
has_accepted_license: '1'
intvolume: ' 3'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Submitted Version
page: 2120-2129
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '754411'
name: ISTplus - Postdoctoral Fellowships
publication: ACS Applied Energy Materials
publication_identifier:
eissn:
- 2574-0962
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Influence of the ligand stripping on the transport properties of nanoparticle-based
PbSe nanomaterials
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 3
year: '2020'
...
---
_id: '7465'
abstract:
- lang: eng
text: The flexible development of plants is characterized by a high capacity for
post-embryonic organ formation and tissue regeneration, processes, which require
tightly regulated intercellular communication and coordinated tissue (re-)polarization.
The phytohormone auxin, the main driver for these processes, is able to establish
polarized auxin transport channels, which are characterized by the expression
and polar, subcellular localization of the PIN1 auxin transport proteins. These
channels are demarcating the position of future vascular strands necessary for
organ formation and tissue regeneration. Major progress has been made in the last
years to understand how PINs can change their polarity in different contexts and
thus guide auxin flow through the plant. However, it still remains elusive how
auxin mediates the establishment of auxin conducting channels and the formation
of vascular tissue and which cellular processes are involved. By the means of
sophisticated regeneration experiments combined with local auxin applications
in Arabidopsis thaliana inflorescence stems we show that (i) PIN subcellular dynamics,
(ii) PIN internalization by clathrin-mediated trafficking and (iii) an intact
actin cytoskeleton required for post-endocytic trafficking are indispensable for
auxin channel formation, de novo vascular formation and vascular regeneration
after wounding. These observations provide novel insights into cellular mechanism
of coordinated tissue polarization during auxin canalization.
article_number: '110414'
article_processing_charge: No
article_type: original
author:
- first_name: Ewa
full_name: Mazur, Ewa
last_name: Mazur
- 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: Maciek
full_name: Adamowski, Maciek
id: 45F536D2-F248-11E8-B48F-1D18A9856A87
last_name: Adamowski
orcid: 0000-0001-6463-5257
- first_name: Huibin
full_name: Han, Huibin
id: 31435098-F248-11E8-B48F-1D18A9856A87
last_name: Han
- first_name: Hélène S.
full_name: Robert, Hélène S.
last_name: Robert
- first_name: Jiří
full_name: Friml, Jiří
id: 4159519E-F248-11E8-B48F-1D18A9856A87
last_name: Friml
orcid: 0000-0002-8302-7596
citation:
ama: Mazur E, Gallei MC, Adamowski M, Han H, Robert HS, Friml J. Clathrin-mediated
trafficking and PIN trafficking are required for auxin canalization and vascular
tissue formation in Arabidopsis. Plant Science. 2020;293(4). doi:10.1016/j.plantsci.2020.110414
apa: Mazur, E., Gallei, M. C., Adamowski, M., Han, H., Robert, H. S., & Friml,
J. (2020). Clathrin-mediated trafficking and PIN trafficking are required for
auxin canalization and vascular tissue formation in Arabidopsis. Plant Science.
Elsevier. https://doi.org/10.1016/j.plantsci.2020.110414
chicago: Mazur, Ewa, Michelle C Gallei, Maciek Adamowski, Huibin Han, Hélène S.
Robert, and Jiří Friml. “Clathrin-Mediated Trafficking and PIN Trafficking Are
Required for Auxin Canalization and Vascular Tissue Formation in Arabidopsis.”
Plant Science. Elsevier, 2020. https://doi.org/10.1016/j.plantsci.2020.110414.
ieee: E. Mazur, M. C. Gallei, M. Adamowski, H. Han, H. S. Robert, and J. Friml,
“Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization
and vascular tissue formation in Arabidopsis,” Plant Science, vol. 293,
no. 4. Elsevier, 2020.
ista: Mazur E, Gallei MC, Adamowski M, Han H, Robert HS, Friml J. 2020. Clathrin-mediated
trafficking and PIN trafficking are required for auxin canalization and vascular
tissue formation in Arabidopsis. Plant Science. 293(4), 110414.
mla: Mazur, Ewa, et al. “Clathrin-Mediated Trafficking and PIN Trafficking Are Required
for Auxin Canalization and Vascular Tissue Formation in Arabidopsis.” Plant
Science, vol. 293, no. 4, 110414, Elsevier, 2020, doi:10.1016/j.plantsci.2020.110414.
short: E. Mazur, M.C. Gallei, M. Adamowski, H. Han, H.S. Robert, J. Friml, Plant
Science 293 (2020).
date_created: 2020-02-09T23:00:50Z
date_published: 2020-04-01T00:00:00Z
date_updated: 2023-08-17T14:37:32Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1016/j.plantsci.2020.110414
ec_funded: 1
external_id:
isi:
- '000520609800009'
file:
- access_level: open_access
checksum: f7f27c6a8fea985ceb9279be2204461c
content_type: application/pdf
creator: dernst
date_created: 2020-02-10T08:59:36Z
date_updated: 2020-07-14T12:47:59Z
file_id: '7471'
file_name: 2020_PlantScience_Mazur.pdf
file_size: 3499069
relation: main_file
file_date_updated: 2020-07-14T12:47:59Z
has_accepted_license: '1'
intvolume: ' 293'
isi: 1
issue: '4'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
project:
- _id: 261099A6-B435-11E9-9278-68D0E5697425
call_identifier: H2020
grant_number: '742985'
name: Tracing Evolution of Auxin Transport and Polarity in Plants
publication: Plant Science
publication_identifier:
eissn:
- '18732259'
issn:
- '01689452'
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
record:
- id: '11626'
relation: dissertation_contains
status: public
scopus_import: '1'
status: public
title: Clathrin-mediated trafficking and PIN trafficking are required for auxin canalization
and vascular tissue formation 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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 293
year: '2020'
...
---
_id: '7466'
abstract:
- lang: eng
text: Unpaired ligands are secreted signals that act via a GP130-like receptor,
domeless, to activate JAK/STAT signalling in Drosophila. Like many mammalian cytokines,
unpaireds can be activated by infection and other stresses and can promote insulin
resistance in target tissues. However, the importance of this effect in non-inflammatory
physiology is unknown. Here, we identify a requirement for unpaired-JAK signalling
as a metabolic regulator in healthy adult Drosophila muscle. Adult muscles show
basal JAK-STAT signalling activity in the absence of any immune challenge. Plasmatocytes
(Drosophila macrophages) are an important source of this tonic signal. Loss of
the dome receptor on adult muscles significantly reduces lifespan and causes local
and systemic metabolic pathology. These pathologies result from hyperactivation
of AKT and consequent deregulation of metabolism. Thus, we identify a cytokine
signal that must be received in muscle to control AKT activity and metabolic homeostasis.
article_number: e51595
article_processing_charge: No
article_type: original
author:
- first_name: Katrin
full_name: Kierdorf, Katrin
last_name: Kierdorf
- first_name: Fabian
full_name: Hersperger, Fabian
last_name: Hersperger
- first_name: Jessica
full_name: Sharrock, Jessica
last_name: Sharrock
- first_name: Crystal M.
full_name: Vincent, Crystal M.
last_name: Vincent
- first_name: Pinar
full_name: Ustaoglu, Pinar
last_name: Ustaoglu
- first_name: Jiawen
full_name: Dou, Jiawen
last_name: Dou
- first_name: Attila
full_name: György, Attila
id: 3BCEDBE0-F248-11E8-B48F-1D18A9856A87
last_name: György
orcid: 0000-0002-1819-198X
- first_name: Olaf
full_name: Groß, Olaf
last_name: Groß
- first_name: Daria E
full_name: Siekhaus, Daria E
id: 3D224B9E-F248-11E8-B48F-1D18A9856A87
last_name: Siekhaus
orcid: 0000-0001-8323-8353
- first_name: Marc S.
full_name: Dionne, Marc S.
last_name: Dionne
citation:
ama: Kierdorf K, Hersperger F, Sharrock J, et al. Muscle function and homeostasis
require cytokine inhibition of AKT activity in Drosophila. eLife. 2020;9.
doi:10.7554/eLife.51595
apa: Kierdorf, K., Hersperger, F., Sharrock, J., Vincent, C. M., Ustaoglu, P., Dou,
J., … Dionne, M. S. (2020). Muscle function and homeostasis require cytokine inhibition
of AKT activity in Drosophila. ELife. eLife Sciences Publications. https://doi.org/10.7554/eLife.51595
chicago: Kierdorf, Katrin, Fabian Hersperger, Jessica Sharrock, Crystal M. Vincent,
Pinar Ustaoglu, Jiawen Dou, Attila György, Olaf Groß, Daria E Siekhaus, and Marc
S. Dionne. “Muscle Function and Homeostasis Require Cytokine Inhibition of AKT
Activity in Drosophila.” ELife. eLife Sciences Publications, 2020. https://doi.org/10.7554/eLife.51595.
ieee: K. Kierdorf et al., “Muscle function and homeostasis require cytokine
inhibition of AKT activity in Drosophila,” eLife, vol. 9. eLife Sciences
Publications, 2020.
ista: Kierdorf K, Hersperger F, Sharrock J, Vincent CM, Ustaoglu P, Dou J, György
A, Groß O, Siekhaus DE, Dionne MS. 2020. Muscle function and homeostasis require
cytokine inhibition of AKT activity in Drosophila. eLife. 9, e51595.
mla: Kierdorf, Katrin, et al. “Muscle Function and Homeostasis Require Cytokine
Inhibition of AKT Activity in Drosophila.” ELife, vol. 9, e51595, eLife
Sciences Publications, 2020, doi:10.7554/eLife.51595.
short: K. Kierdorf, F. Hersperger, J. Sharrock, C.M. Vincent, P. Ustaoglu, J. Dou,
A. György, O. Groß, D.E. Siekhaus, M.S. Dionne, ELife 9 (2020).
date_created: 2020-02-09T23:00:51Z
date_published: 2020-01-20T00:00:00Z
date_updated: 2023-08-17T14:36:39Z
day: '20'
ddc:
- '570'
department:
- _id: DaSi
doi: 10.7554/eLife.51595
external_id:
isi:
- '000512304800001'
file:
- access_level: open_access
checksum: 3a072be843f416c7a7d532a51dc0addb
content_type: application/pdf
creator: dernst
date_created: 2020-02-10T08:53:16Z
date_updated: 2020-07-14T12:47:59Z
file_id: '7470'
file_name: 2020_eLife_Kierdorf.pdf
file_size: 4959933
relation: main_file
file_date_updated: 2020-07-14T12:47:59Z
has_accepted_license: '1'
intvolume: ' 9'
isi: 1
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: 253B6E48-B435-11E9-9278-68D0E5697425
call_identifier: FWF
grant_number: P29638
name: Drosophila TNFa´s Funktion in Immunzellen
publication: eLife
publication_identifier:
eissn:
- 2050084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
scopus_import: '1'
status: public
title: Muscle function and homeostasis require cytokine inhibition of AKT activity
in Drosophila
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: 9
year: '2020'
...
---
_id: '7472'
abstract:
- lang: eng
text: Temporally organized reactivation of experiences during awake immobility periods
is thought to underlie cognitive processes like planning and evaluation. While
replay of trajectories is well established for the hippocampus, it is unclear
whether the medial prefrontal cortex (mPFC) can reactivate sequential behavioral
experiences in the awake state to support task execution. We simultaneously recorded
from hippocampal and mPFC principal neurons in rats performing a mPFC-dependent
rule-switching task on a plus maze. We found that mPFC neuronal activity encoded
relative positions between the start and goal. During awake immobility periods,
the mPFC replayed temporally organized sequences of these generalized positions,
resembling entire spatial trajectories. The occurrence of mPFC trajectory replay
positively correlated with rule-switching performance. However, hippocampal and
mPFC trajectory replay occurred independently, indicating different functions.
These results demonstrate that the mPFC can replay ordered activity patterns representing
generalized locations and suggest that mPFC replay might have a role in flexible
behavior.
acknowledged_ssus:
- _id: M-Shop
acknowledgement: We thank Todor Asenov and Thomas Menner from the Machine Shop for
the drive design and production, Hugo Malagon-Vina for assistance in maze automatization,
Jago Wallenschus for taking the images of the histology, and Federico Stella and
Juan Felipe Ramirez-Villegas for comments on an earlier version of the manuscript.
This work was supported by the EU-FP7 MC-ITN IN-SENS (grant 607616 ).
article_processing_charge: No
article_type: original
author:
- first_name: Karola
full_name: Käfer, Karola
id: 2DAA49AA-F248-11E8-B48F-1D18A9856A87
last_name: Käfer
- first_name: Michele
full_name: Nardin, Michele
id: 30BD0376-F248-11E8-B48F-1D18A9856A87
last_name: Nardin
orcid: 0000-0001-8849-6570
- first_name: Karel
full_name: Blahna, Karel
id: 3EA859AE-F248-11E8-B48F-1D18A9856A87
last_name: Blahna
- first_name: Jozsef L
full_name: Csicsvari, Jozsef L
id: 3FA14672-F248-11E8-B48F-1D18A9856A87
last_name: Csicsvari
orcid: 0000-0002-5193-4036
citation:
ama: Käfer K, Nardin M, Blahna K, Csicsvari JL. Replay of behavioral sequences in
the medial prefrontal cortex during rule switching. Neuron. 2020;106(1):P154-165.e6.
doi:10.1016/j.neuron.2020.01.015
apa: Käfer, K., Nardin, M., Blahna, K., & Csicsvari, J. L. (2020). Replay of
behavioral sequences in the medial prefrontal cortex during rule switching. Neuron.
Elsevier. https://doi.org/10.1016/j.neuron.2020.01.015
chicago: Käfer, Karola, Michele Nardin, Karel Blahna, and Jozsef L Csicsvari. “Replay
of Behavioral Sequences in the Medial Prefrontal Cortex during Rule Switching.”
Neuron. Elsevier, 2020. https://doi.org/10.1016/j.neuron.2020.01.015.
ieee: K. Käfer, M. Nardin, K. Blahna, and J. L. Csicsvari, “Replay of behavioral
sequences in the medial prefrontal cortex during rule switching,” Neuron,
vol. 106, no. 1. Elsevier, p. P154–165.e6, 2020.
ista: Käfer K, Nardin M, Blahna K, Csicsvari JL. 2020. Replay of behavioral sequences
in the medial prefrontal cortex during rule switching. Neuron. 106(1), P154–165.e6.
mla: Käfer, Karola, et al. “Replay of Behavioral Sequences in the Medial Prefrontal
Cortex during Rule Switching.” Neuron, vol. 106, no. 1, Elsevier, 2020,
p. P154–165.e6, doi:10.1016/j.neuron.2020.01.015.
short: K. Käfer, M. Nardin, K. Blahna, J.L. Csicsvari, Neuron 106 (2020) P154–165.e6.
date_created: 2020-02-10T15:45:48Z
date_published: 2020-04-08T00:00:00Z
date_updated: 2023-08-17T14:38:02Z
day: '08'
department:
- _id: JoCs
doi: 10.1016/j.neuron.2020.01.015
ec_funded: 1
external_id:
isi:
- '000525319300016'
pmid:
- '32032512'
intvolume: ' 106'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/j.neuron.2020.01.015
month: '04'
oa: 1
oa_version: Published Version
page: P154-165.e6
pmid: 1
project:
- _id: 257BBB4C-B435-11E9-9278-68D0E5697425
call_identifier: FP7
grant_number: '607616'
name: Inter-and intracellular signalling in schizophrenia
publication: Neuron
publication_identifier:
issn:
- 0896-6273
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
link:
- description: News on IST Homepage
relation: press_release
url: https://ist.ac.at/en/news/this-brain-area-helps-us-decide/
scopus_import: '1'
status: public
title: Replay of behavioral sequences in the medial prefrontal cortex during rule
switching
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 106
year: '2020'
...
---
_id: '7388'
abstract:
- lang: eng
text: We give a Wong-Zakai type characterisation of the solutions of quasilinear
heat equations driven by space-time white noise in 1 + 1 dimensions. In order
to show that the renormalisation counterterms are local in the solution, a careful
arrangement of a few hundred terms is required. The main tool in this computation
is a general ‘integration by parts’ formula that provides a number of linear identities
for the renormalisation constants.
article_processing_charge: No
article_type: original
author:
- first_name: Mate
full_name: Gerencser, Mate
id: 44ECEDF2-F248-11E8-B48F-1D18A9856A87
last_name: Gerencser
citation:
ama: Gerencser M. Nondivergence form quasilinear heat equations driven by space-time
white noise. Annales de l’Institut Henri Poincaré C, Analyse non linéaire.
2020;37(3):663-682. doi:10.1016/j.anihpc.2020.01.003
apa: Gerencser, M. (2020). Nondivergence form quasilinear heat equations driven
by space-time white noise. Annales de l’Institut Henri Poincaré C, Analyse
Non Linéaire. Elsevier. https://doi.org/10.1016/j.anihpc.2020.01.003
chicago: Gerencser, Mate. “Nondivergence Form Quasilinear Heat Equations Driven
by Space-Time White Noise.” Annales de l’Institut Henri Poincaré C, Analyse
Non Linéaire. Elsevier, 2020. https://doi.org/10.1016/j.anihpc.2020.01.003.
ieee: M. Gerencser, “Nondivergence form quasilinear heat equations driven by space-time
white noise,” Annales de l’Institut Henri Poincaré C, Analyse non linéaire,
vol. 37, no. 3. Elsevier, pp. 663–682, 2020.
ista: Gerencser M. 2020. Nondivergence form quasilinear heat equations driven by
space-time white noise. Annales de l’Institut Henri Poincaré C, Analyse non linéaire.
37(3), 663–682.
mla: Gerencser, Mate. “Nondivergence Form Quasilinear Heat Equations Driven by Space-Time
White Noise.” Annales de l’Institut Henri Poincaré C, Analyse Non Linéaire,
vol. 37, no. 3, Elsevier, 2020, pp. 663–82, doi:10.1016/j.anihpc.2020.01.003.
short: M. Gerencser, Annales de l’Institut Henri Poincaré C, Analyse Non Linéaire
37 (2020) 663–682.
date_created: 2020-01-29T09:39:41Z
date_published: 2020-05-01T00:00:00Z
date_updated: 2023-08-17T14:35:46Z
day: '01'
department:
- _id: JaMa
doi: 10.1016/j.anihpc.2020.01.003
external_id:
arxiv:
- '1902.07635'
isi:
- '000531049800007'
intvolume: ' 37'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://arxiv.org/abs/1902.07635
month: '05'
oa: 1
oa_version: Preprint
page: 663-682
publication: Annales de l'Institut Henri Poincaré C, Analyse non linéaire
publication_identifier:
issn:
- 0294-1449
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Nondivergence form quasilinear heat equations driven by space-time white noise
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 37
year: '2020'
...
---
_id: '7487'
abstract:
- lang: eng
text: 'Glutaminase (GA) catalyzes the first step in mitochondrial glutaminolysis
playing a key role in cancer metabolic reprogramming. Humans express two types
of GA isoforms: GLS and GLS2. GLS isozymes have been consistently related to cell
proliferation, but the role of GLS2 in cancer remains poorly understood. GLS2
is repressed in many tumor cells and a better understanding of its function in
tumorigenesis may further the development of new therapeutic approaches. We analyzed
GLS2 expression in HCC, GBM and neuroblastoma cells, as well as in monkey COS-7
cells. We studied GLS2 expression after induction of differentiation with phorbol
ester (PMA) and transduction with the full-length cDNA of GLS2. In parallel, we
investigated cell cycle progression and levels of p53, p21 and c-Myc proteins.
Using the baculovirus system, human GLS2 protein was overexpressed, purified and
analyzed for posttranslational modifications employing a proteomics LC-MS/MS platform.
We have demonstrated a dual targeting of GLS2 in human cancer cells. Immunocytochemistry
and subcellular fractionation gave consistent results demonstrating nuclear and
mitochondrial locations, with the latter being predominant. Nuclear targeting
was confirmed in cancer cells overexpressing c-Myc- and GFP-tagged GLS2 proteins.
We assessed the subnuclear location finding a widespread distribution of GLS2
in the nucleoplasm without clear overlapping with specific nuclear substructures.
GLS2 expression and nuclear accrual notably increased by treatment of SH-SY5Y
cells with PMA and it correlated with cell cycle arrest at G2/M, upregulation
of tumor suppressor p53 and p21 protein. A similar response was obtained by overexpression
of GLS2 in T98G glioma cells, including downregulation of oncogene c-Myc. Furthermore,
human GLS2 was identified as being hypusinated by MS analysis, a posttranslational
modification which may be relevant for its nuclear targeting and/or function.
Our studies provide evidence for a tumor suppressor role of GLS2 in certain types
of cancer. The data imply that GLS2 can be regarded as a highly mobile and multilocalizing
protein translocated to both mitochondria and nuclei. Upregulation of GLS2 in
cancer cells induced an antiproliferative response with cell cycle arrest at the
G2/M phase.'
article_number: '2259'
article_processing_charge: No
article_type: original
author:
- first_name: Amada R.
full_name: López De La Oliva, Amada R.
last_name: López De La Oliva
- first_name: José A.
full_name: Campos-Sandoval, José A.
last_name: Campos-Sandoval
- first_name: María C.
full_name: Gómez-García, María C.
last_name: Gómez-García
- first_name: Carolina
full_name: Cardona, Carolina
last_name: Cardona
- first_name: Mercedes
full_name: Martín-Rufián, Mercedes
last_name: Martín-Rufián
- first_name: Fernando J.
full_name: Sialana, Fernando J.
last_name: Sialana
- first_name: Laura
full_name: Castilla, Laura
last_name: Castilla
- first_name: Narkhyun
full_name: Bae, Narkhyun
id: 3A5F7CD8-F248-11E8-B48F-1D18A9856A87
last_name: Bae
- first_name: Carolina
full_name: Lobo, Carolina
last_name: Lobo
- first_name: Ana
full_name: Peñalver, Ana
last_name: Peñalver
- first_name: Marina
full_name: García-Frutos, Marina
last_name: García-Frutos
- first_name: David
full_name: Carro, David
last_name: Carro
- first_name: Victoria
full_name: Enrique, Victoria
last_name: Enrique
- first_name: José C.
full_name: Paz, José C.
last_name: Paz
- first_name: Raghavendra G.
full_name: Mirmira, Raghavendra G.
last_name: Mirmira
- first_name: Antonia
full_name: Gutiérrez, Antonia
last_name: Gutiérrez
- first_name: Francisco J.
full_name: Alonso, Francisco J.
last_name: Alonso
- first_name: Juan A.
full_name: Segura, Juan A.
last_name: Segura
- first_name: José M.
full_name: Matés, José M.
last_name: Matés
- first_name: Gert
full_name: Lubec, Gert
last_name: Lubec
- first_name: Javier
full_name: Márquez, Javier
last_name: Márquez
citation:
ama: López De La Oliva AR, Campos-Sandoval JA, Gómez-García MC, et al. Nuclear translocation
of glutaminase GLS2 in human cancer cells associates with proliferation arrest
and differentiation. Scientific reports. 2020;10(1). doi:10.1038/s41598-020-58264-4
apa: López De La Oliva, A. R., Campos-Sandoval, J. A., Gómez-García, M. C., Cardona,
C., Martín-Rufián, M., Sialana, F. J., … Márquez, J. (2020). Nuclear translocation
of glutaminase GLS2 in human cancer cells associates with proliferation arrest
and differentiation. Scientific Reports. Springer Nature. https://doi.org/10.1038/s41598-020-58264-4
chicago: López De La Oliva, Amada R., José A. Campos-Sandoval, María C. Gómez-García,
Carolina Cardona, Mercedes Martín-Rufián, Fernando J. Sialana, Laura Castilla,
et al. “Nuclear Translocation of Glutaminase GLS2 in Human Cancer Cells Associates
with Proliferation Arrest and Differentiation.” Scientific Reports. Springer
Nature, 2020. https://doi.org/10.1038/s41598-020-58264-4.
ieee: A. R. López De La Oliva et al., “Nuclear translocation of glutaminase
GLS2 in human cancer cells associates with proliferation arrest and differentiation,”
Scientific reports, vol. 10, no. 1. Springer Nature, 2020.
ista: López De La Oliva AR, Campos-Sandoval JA, Gómez-García MC, Cardona C, Martín-Rufián
M, Sialana FJ, Castilla L, Bae N, Lobo C, Peñalver A, García-Frutos M, Carro D,
Enrique V, Paz JC, Mirmira RG, Gutiérrez A, Alonso FJ, Segura JA, Matés JM, Lubec
G, Márquez J. 2020. Nuclear translocation of glutaminase GLS2 in human cancer
cells associates with proliferation arrest and differentiation. Scientific reports.
10(1), 2259.
mla: López De La Oliva, Amada R., et al. “Nuclear Translocation of Glutaminase GLS2
in Human Cancer Cells Associates with Proliferation Arrest and Differentiation.”
Scientific Reports, vol. 10, no. 1, 2259, Springer Nature, 2020, doi:10.1038/s41598-020-58264-4.
short: A.R. López De La Oliva, J.A. Campos-Sandoval, M.C. Gómez-García, C. Cardona,
M. Martín-Rufián, F.J. Sialana, L. Castilla, N. Bae, C. Lobo, A. Peñalver, M.
García-Frutos, D. Carro, V. Enrique, J.C. Paz, R.G. Mirmira, A. Gutiérrez, F.J.
Alonso, J.A. Segura, J.M. Matés, G. Lubec, J. Márquez, Scientific Reports 10 (2020).
date_created: 2020-02-16T23:00:49Z
date_published: 2020-02-10T00:00:00Z
date_updated: 2023-08-18T06:35:13Z
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department:
- _id: CaBe
doi: 10.1038/s41598-020-58264-4
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title: Nuclear translocation of glutaminase GLS2 in human cancer cells associates
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