---
_id: '2837'
abstract:
- lang: eng
  text: We consider a general class of N × N random matrices whose entries hij are
    independent up to a symmetry constraint, but not necessarily identically distributed.
    Our main result is a local semicircle law which improves previous results [17]
    both in the bulk and at the edge. The error bounds are given in terms of the basic
    small parameter of the model, maxi,j E|hij|2. As a consequence, we prove the universality
    of the local n-point correlation functions in the bulk spectrum for a class of
    matrices whose entries do not have comparable variances, including random band
    matrices with band width W ≫N1-εn with some εn &gt; 0 and with a negligible mean-field
    component. In addition, we provide a coherent and pedagogical proof of the local
    semicircle law, streamlining and strengthening previous arguments from [17, 19,
    6].
article_processing_charge: No
author:
- first_name: László
  full_name: Erdös, László
  id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
  last_name: Erdös
  orcid: 0000-0001-5366-9603
- first_name: Antti
  full_name: Knowles, Antti
  last_name: Knowles
- first_name: Horng
  full_name: Yau, Horng
  last_name: Yau
- first_name: Jun
  full_name: Yin, Jun
  last_name: Yin
citation:
  ama: Erdös L, Knowles A, Yau H, Yin J. The local semicircle law for a general class
    of random matrices. <i>Electronic Journal of Probability</i>. 2013;18(59):1-58.
    doi:<a href="https://doi.org/10.1214/EJP.v18-2473">10.1214/EJP.v18-2473</a>
  apa: Erdös, L., Knowles, A., Yau, H., &#38; Yin, J. (2013). The local semicircle
    law for a general class of random matrices. <i>Electronic Journal of Probability</i>.
    Institute of Mathematical Statistics. <a href="https://doi.org/10.1214/EJP.v18-2473">https://doi.org/10.1214/EJP.v18-2473</a>
  chicago: Erdös, László, Antti Knowles, Horng Yau, and Jun Yin. “The Local Semicircle
    Law for a General Class of Random Matrices.” <i>Electronic Journal of Probability</i>.
    Institute of Mathematical Statistics, 2013. <a href="https://doi.org/10.1214/EJP.v18-2473">https://doi.org/10.1214/EJP.v18-2473</a>.
  ieee: L. Erdös, A. Knowles, H. Yau, and J. Yin, “The local semicircle law for a
    general class of random matrices,” <i>Electronic Journal of Probability</i>, vol.
    18, no. 59. Institute of Mathematical Statistics, pp. 1–58, 2013.
  ista: Erdös L, Knowles A, Yau H, Yin J. 2013. The local semicircle law for a general
    class of random matrices. Electronic Journal of Probability. 18(59), 1–58.
  mla: Erdös, László, et al. “The Local Semicircle Law for a General Class of Random
    Matrices.” <i>Electronic Journal of Probability</i>, vol. 18, no. 59, Institute
    of Mathematical Statistics, 2013, pp. 1–58, doi:<a href="https://doi.org/10.1214/EJP.v18-2473">10.1214/EJP.v18-2473</a>.
  short: L. Erdös, A. Knowles, H. Yau, J. Yin, Electronic Journal of Probability 18
    (2013) 1–58.
date_created: 2018-12-11T11:59:51Z
date_published: 2013-05-29T00:00:00Z
date_updated: 2025-09-29T13:46:52Z
day: '29'
ddc:
- '530'
department:
- _id: LaEr
doi: 10.1214/EJP.v18-2473
external_id:
  isi:
  - '000319561600001'
file:
- access_level: open_access
  checksum: aac9e52a00cb2f5149dc9e362b5ccf44
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:15:46Z
  date_updated: 2020-07-14T12:45:50Z
  file_id: '5169'
  file_name: IST-2016-406-v1+1_2473-13759-1-PB.pdf
  file_size: 651497
  relation: main_file
file_date_updated: 2020-07-14T12:45:50Z
has_accepted_license: '1'
intvolume: '        18'
isi: 1
issue: '59'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: 1-58
publication: Electronic Journal of Probability
publication_status: published
publisher: Institute of Mathematical Statistics
publist_id: '3962'
pubrep_id: '406'
quality_controlled: '1'
scopus_import: '1'
status: public
title: The local semicircle law for a general class of random matrices
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 18
year: '2013'
...
---
_id: '2838'
abstract:
- lang: eng
  text: Individuals with Down syndrome (DS) present important motor deficits that
    derive from altered motor development of infants and young children. DYRK1A, a
    candidate gene for DS abnormalities has been implicated in motor function due
    to its expression in motor nuclei in the adult brain, and its overexpression in
    DS mouse models leads to hyperactivity and altered motor learning. However, its
    precise role in the adult motor system, or its possible involvement in postnatal
    locomotor development has not yet been clarified. During the postnatal period
    we observed time-specific expression of Dyrk1A in discrete subsets of brainstem
    nuclei and spinal cord motor neurons. Interestingly, we describe for the first
    time the presence of Dyrk1A in the presynaptic terminal of the neuromuscular junctions
    and its axonal transport from the facial nucleus, suggesting a function for Dyrk1A
    in these structures. Relevant to DS, Dyrk1A overexpression in transgenic mice
    (TgDyrk1A) produces motor developmental alterations possibly contributing to DS
    motor phenotypes and modifies the numbers of motor cholinergic neurons, suggesting
    that the kinase may have a role in the development of the brainstem and spinal
    cord motor system.
article_number: e54285
article_processing_charge: No
author:
- first_name: Gloria
  full_name: Arquè Fuste, Gloria
  id: 3CF33908-F248-11E8-B48F-1D18A9856A87
  last_name: Arquè Fuste
- first_name: Anna
  full_name: Casanovas, Anna
  last_name: Casanovas
- first_name: Mara
  full_name: Dierssen, Mara
  last_name: Dierssen
citation:
  ama: 'Arquè Fuste G, Casanovas A, Dierssen M. Dyrk1A is dynamically expressed on
    subsets of motor neurons and in the neuromuscular junction: Possible role in Down
    syndrome. <i>PLoS One</i>. 2013;8(1). doi:<a href="https://doi.org/10.1371/journal.pone.0054285">10.1371/journal.pone.0054285</a>'
  apa: 'Arquè Fuste, G., Casanovas, A., &#38; Dierssen, M. (2013). Dyrk1A is dynamically
    expressed on subsets of motor neurons and in the neuromuscular junction: Possible
    role in Down syndrome. <i>PLoS One</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pone.0054285">https://doi.org/10.1371/journal.pone.0054285</a>'
  chicago: 'Arquè Fuste, Gloria, Anna Casanovas, and Mara Dierssen. “Dyrk1A Is Dynamically
    Expressed on Subsets of Motor Neurons and in the Neuromuscular Junction: Possible
    Role in Down Syndrome.” <i>PLoS One</i>. Public Library of Science, 2013. <a href="https://doi.org/10.1371/journal.pone.0054285">https://doi.org/10.1371/journal.pone.0054285</a>.'
  ieee: 'G. Arquè Fuste, A. Casanovas, and M. Dierssen, “Dyrk1A is dynamically expressed
    on subsets of motor neurons and in the neuromuscular junction: Possible role in
    Down syndrome,” <i>PLoS One</i>, vol. 8, no. 1. Public Library of Science, 2013.'
  ista: 'Arquè Fuste G, Casanovas A, Dierssen M. 2013. Dyrk1A is dynamically expressed
    on subsets of motor neurons and in the neuromuscular junction: Possible role in
    Down syndrome. PLoS One. 8(1), e54285.'
  mla: 'Arquè Fuste, Gloria, et al. “Dyrk1A Is Dynamically Expressed on Subsets of
    Motor Neurons and in the Neuromuscular Junction: Possible Role in Down Syndrome.”
    <i>PLoS One</i>, vol. 8, no. 1, e54285, Public Library of Science, 2013, doi:<a
    href="https://doi.org/10.1371/journal.pone.0054285">10.1371/journal.pone.0054285</a>.'
  short: G. Arquè Fuste, A. Casanovas, M. Dierssen, PLoS One 8 (2013).
date_created: 2018-12-11T11:59:52Z
date_published: 2013-01-16T00:00:00Z
date_updated: 2025-09-29T13:46:22Z
day: '16'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.1371/journal.pone.0054285
external_id:
  isi:
  - '000313682700103'
file:
- access_level: open_access
  checksum: 512733b21419574a45f10cabef3d7f81
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:15:38Z
  date_updated: 2020-07-14T12:45:50Z
  file_id: '5160'
  file_name: IST-2016-407-v1+1_journal.pone.0054285.pdf
  file_size: 4795977
  relation: main_file
file_date_updated: 2020-07-14T12:45:50Z
has_accepted_license: '1'
intvolume: '         8'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
publication: PLoS One
publication_status: published
publisher: Public Library of Science
publist_id: '3960'
pubrep_id: '407'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Dyrk1A is dynamically expressed on subsets of motor neurons and in the neuromuscular
  junction: Possible role in Down syndrome'
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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 8
year: '2013'
...
---
_id: '2839'
abstract:
- lang: eng
  text: Directional guidance of cells via gradients of chemokines is considered crucial
    for embryonic development, cancer dissemination, and immune responses. Nevertheless,
    the concept still lacks direct experimental confirmation in vivo. Here, we identify
    endogenous gradients of the chemokine CCL21 within mouse skin and show that they
    guide dendritic cells toward lymphatic vessels. Quantitative imaging reveals depots
    of CCL21 within lymphatic endothelial cells and steeply decaying gradients within
    the perilymphatic interstitium. These gradients match the migratory patterns of
    the dendritic cells, which directionally approach vessels from a distance of up
    to 90-micrometers. Interstitial CCL21 is immobilized to heparan sulfates, and
    its experimental delocalization or swamping the endogenous gradients abolishes
    directed migration. These findings functionally establish the concept of haptotaxis,
    directed migration along immobilized gradients, in tissues.
acknowledgement: We thank M. Frank for technical assistance and S. Cremer, P. Schmalhorst,
  and E. Kiermaier for critical reading of the manuscript. This work was supported
  by a Humboldt Foundation postdoctoral fellowship (to M.W.), the German Research
  Foundation (Si1323 1,2 to M.S.), the Human Frontier Science Program (HFSP RGP0058/2011
  to M.S.), the European Research Council (ERC StG 281556 to M.S.), and the Swiss
  National Science Foundation (31003A 127474 to D.F.L., 130488 to S.A.L.).
article_processing_charge: No
article_type: original
author:
- first_name: Michele
  full_name: Weber, Michele
  id: 3A3FC708-F248-11E8-B48F-1D18A9856A87
  last_name: Weber
- first_name: Robert
  full_name: Hauschild, Robert
  id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87
  last_name: Hauschild
  orcid: 0000-0001-9843-3522
- first_name: Jan
  full_name: Schwarz, Jan
  id: 346C1EC6-F248-11E8-B48F-1D18A9856A87
  last_name: Schwarz
- first_name: Christine
  full_name: Moussion, Christine
  id: 3356F664-F248-11E8-B48F-1D18A9856A87
  last_name: Moussion
- first_name: Ingrid
  full_name: De Vries, Ingrid
  id: 4C7D837E-F248-11E8-B48F-1D18A9856A87
  last_name: De Vries
- first_name: Daniel
  full_name: Legler, Daniel
  last_name: Legler
- first_name: Sanjiv
  full_name: Luther, Sanjiv
  last_name: Luther
- first_name: Mark Tobias
  full_name: Bollenbach, Mark Tobias
  id: 3E6DB97A-F248-11E8-B48F-1D18A9856A87
  last_name: Bollenbach
  orcid: 0000-0003-4398-476X
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
citation:
  ama: Weber M, Hauschild R, Schwarz J, et al. Interstitial dendritic cell guidance
    by haptotactic chemokine gradients. <i>Science</i>. 2013;339(6117):328-332. doi:<a
    href="https://doi.org/10.1126/science.1228456">10.1126/science.1228456</a>
  apa: Weber, M., Hauschild, R., Schwarz, J., Moussion, C., de Vries, I., Legler,
    D., … Sixt, M. K. (2013). Interstitial dendritic cell guidance by haptotactic
    chemokine gradients. <i>Science</i>. American Association for the Advancement
    of Science. <a href="https://doi.org/10.1126/science.1228456">https://doi.org/10.1126/science.1228456</a>
  chicago: Weber, Michele, Robert Hauschild, Jan Schwarz, Christine Moussion, Ingrid
    de Vries, Daniel Legler, Sanjiv Luther, Mark Tobias Bollenbach, and Michael K
    Sixt. “Interstitial Dendritic Cell Guidance by Haptotactic Chemokine Gradients.”
    <i>Science</i>. American Association for the Advancement of Science, 2013. <a
    href="https://doi.org/10.1126/science.1228456">https://doi.org/10.1126/science.1228456</a>.
  ieee: M. Weber <i>et al.</i>, “Interstitial dendritic cell guidance by haptotactic
    chemokine gradients,” <i>Science</i>, vol. 339, no. 6117. American Association
    for the Advancement of Science, pp. 328–332, 2013.
  ista: Weber M, Hauschild R, Schwarz J, Moussion C, de Vries I, Legler D, Luther
    S, Bollenbach MT, Sixt MK. 2013. Interstitial dendritic cell guidance by haptotactic
    chemokine gradients. Science. 339(6117), 328–332.
  mla: Weber, Michele, et al. “Interstitial Dendritic Cell Guidance by Haptotactic
    Chemokine Gradients.” <i>Science</i>, vol. 339, no. 6117, American Association
    for the Advancement of Science, 2013, pp. 328–32, doi:<a href="https://doi.org/10.1126/science.1228456">10.1126/science.1228456</a>.
  short: M. Weber, R. Hauschild, J. Schwarz, C. Moussion, I. de Vries, D. Legler,
    S. Luther, M.T. Bollenbach, M.K. Sixt, Science 339 (2013) 328–332.
corr_author: '1'
date_created: 2018-12-11T11:59:52Z
date_published: 2013-01-18T00:00:00Z
date_updated: 2025-09-29T13:45:52Z
day: '18'
department:
- _id: MiSi
- _id: Bio
doi: 10.1126/science.1228456
ec_funded: 1
external_id:
  isi:
  - '000313622000047'
intvolume: '       339'
isi: 1
issue: '6117'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://kops.uni-konstanz.de/bitstream/123456789/26341/2/Weber_263418.pdf
month: '01'
oa: 1
oa_version: Published Version
page: 328 - 332
project:
- _id: 25A603A2-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '281556'
  name: Cytoskeletal force generation and force transduction of migrating leukocytes
- _id: 25ABD200-B435-11E9-9278-68D0E5697425
  grant_number: RGP0058/2011
  name: 'Cell migration in complex environments: from in vivo experiments to theoretical
    models'
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '3959'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Interstitial dendritic cell guidance by haptotactic chemokine gradients
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 339
year: '2013'
...
---
_id: '2840'
abstract:
- lang: eng
  text: It is known that the entorhinal cortex plays a crucial role in spatial cognition
    in rodents. Neuroanatomical and electrophysiological data suggest that there is
    a functional distinction between 2 subregions within the entorhinal cortex, the
    medial entorhinal cortex (MEC), and the lateral entorhinal cortex (LEC). Rats
    with MEC or LEC lesions were trained in 2 navigation tasks requiring allothetic
    (water maze task) or idiothetic (path integration) information processing and
    2-object exploration tasks allowing testing of spatial and nonspatial processing
    of intramaze objects. MEC lesions mildly affected place navigation in the water
    maze and produced a path integration deficit. They also altered the processing
    of spatial information in both exploration tasks while sparing the processing
    of nonspatial information. LEC lesions did not affect navigation abilities in
    both the water maze and the path integration tasks. They altered spatial and nonspatial
    processing in the object exploration task but not in the one-trial recognition
    task. Overall, these results indicate that the MEC is important for spatial processing
    and path integration. The LEC has some influence on both spatial and nonspatial
    processes, suggesting that the 2 kinds of information interact at the level of
    the EC.
article_processing_charge: No
author:
- first_name: Tiffany
  full_name: Van Cauter, Tiffany
  last_name: Van Cauter
- first_name: Jeremy
  full_name: Camon, Jeremy
  last_name: Camon
- first_name: Alice
  full_name: Alvernhe, Alice
  id: 467FB3D4-F248-11E8-B48F-1D18A9856A87
  last_name: Alvernhe
- first_name: Coralie
  full_name: Elduayen, Coralie
  last_name: Elduayen
- first_name: Francesca
  full_name: Sargolini, Francesca
  last_name: Sargolini
- first_name: Étienne
  full_name: Save, Étienne
  last_name: Save
citation:
  ama: Van Cauter T, Camon J, Alvernhe A, Elduayen C, Sargolini F, Save É. Distinct
    roles of medial and lateral entorhinal cortex in spatial cognition. <i>Cerebral
    Cortex</i>. 2013;23(2):451-459. doi:<a href="https://doi.org/10.1093/cercor/bhs033">10.1093/cercor/bhs033</a>
  apa: Van Cauter, T., Camon, J., Alvernhe, A., Elduayen, C., Sargolini, F., &#38;
    Save, É. (2013). Distinct roles of medial and lateral entorhinal cortex in spatial
    cognition. <i>Cerebral Cortex</i>. Oxford University Press. <a href="https://doi.org/10.1093/cercor/bhs033">https://doi.org/10.1093/cercor/bhs033</a>
  chicago: Van Cauter, Tiffany, Jeremy Camon, Alice Alvernhe, Coralie Elduayen, Francesca
    Sargolini, and Étienne Save. “Distinct Roles of Medial and Lateral Entorhinal
    Cortex in Spatial Cognition.” <i>Cerebral Cortex</i>. Oxford University Press,
    2013. <a href="https://doi.org/10.1093/cercor/bhs033">https://doi.org/10.1093/cercor/bhs033</a>.
  ieee: T. Van Cauter, J. Camon, A. Alvernhe, C. Elduayen, F. Sargolini, and É. Save,
    “Distinct roles of medial and lateral entorhinal cortex in spatial cognition,”
    <i>Cerebral Cortex</i>, vol. 23, no. 2. Oxford University Press, pp. 451–459,
    2013.
  ista: Van Cauter T, Camon J, Alvernhe A, Elduayen C, Sargolini F, Save É. 2013.
    Distinct roles of medial and lateral entorhinal cortex in spatial cognition. Cerebral
    Cortex. 23(2), 451–459.
  mla: Van Cauter, Tiffany, et al. “Distinct Roles of Medial and Lateral Entorhinal
    Cortex in Spatial Cognition.” <i>Cerebral Cortex</i>, vol. 23, no. 2, Oxford University
    Press, 2013, pp. 451–59, doi:<a href="https://doi.org/10.1093/cercor/bhs033">10.1093/cercor/bhs033</a>.
  short: T. Van Cauter, J. Camon, A. Alvernhe, C. Elduayen, F. Sargolini, É. Save,
    Cerebral Cortex 23 (2013) 451–459.
date_created: 2018-12-11T11:59:52Z
date_published: 2013-02-01T00:00:00Z
date_updated: 2025-09-29T13:45:23Z
day: '01'
department:
- _id: JoCs
doi: 10.1093/cercor/bhs033
external_id:
  isi:
  - '000313529600020'
intvolume: '        23'
isi: 1
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
page: 451 - 459
publication: Cerebral Cortex
publication_status: published
publisher: Oxford University Press
publist_id: '3958'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Distinct roles of medial and lateral entorhinal cortex in spatial cognition
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 23
year: '2013'
...
---
_id: '2841'
abstract:
- lang: eng
  text: In zebrafish early development, blastoderm cells undergo extensive radial
    intercalations, triggering the spreading of the blastoderm over the yolk cell
    and thereby initiating embryonic body axis formation. Now reporting in Developmental
    Cell, Song et al. (2013) demonstrate a critical function for EGF-dependent E-cadherin
    endocytosis in promoting blastoderm cell intercalations.
article_processing_charge: No
author:
- first_name: Hitoshi
  full_name: Morita, Hitoshi
  id: 4C6E54C6-F248-11E8-B48F-1D18A9856A87
  last_name: Morita
- first_name: Carl-Philipp J
  full_name: Heisenberg, Carl-Philipp J
  id: 39427864-F248-11E8-B48F-1D18A9856A87
  last_name: Heisenberg
  orcid: 0000-0002-0912-4566
citation:
  ama: 'Morita H, Heisenberg C-PJ. Holding on and letting go: Cadherin turnover in
    cell intercalation. <i>Developmental Cell</i>. 2013;24(6):567-569. doi:<a href="https://doi.org/10.1016/j.devcel.2013.03.007">10.1016/j.devcel.2013.03.007</a>'
  apa: 'Morita, H., &#38; Heisenberg, C.-P. J. (2013). Holding on and letting go:
    Cadherin turnover in cell intercalation. <i>Developmental Cell</i>. Cell Press.
    <a href="https://doi.org/10.1016/j.devcel.2013.03.007">https://doi.org/10.1016/j.devcel.2013.03.007</a>'
  chicago: 'Morita, Hitoshi, and Carl-Philipp J Heisenberg. “Holding on and Letting
    Go: Cadherin Turnover in Cell Intercalation.” <i>Developmental Cell</i>. Cell
    Press, 2013. <a href="https://doi.org/10.1016/j.devcel.2013.03.007">https://doi.org/10.1016/j.devcel.2013.03.007</a>.'
  ieee: 'H. Morita and C.-P. J. Heisenberg, “Holding on and letting go: Cadherin turnover
    in cell intercalation,” <i>Developmental Cell</i>, vol. 24, no. 6. Cell Press,
    pp. 567–569, 2013.'
  ista: 'Morita H, Heisenberg C-PJ. 2013. Holding on and letting go: Cadherin turnover
    in cell intercalation. Developmental Cell. 24(6), 567–569.'
  mla: 'Morita, Hitoshi, and Carl-Philipp J. Heisenberg. “Holding on and Letting Go:
    Cadherin Turnover in Cell Intercalation.” <i>Developmental Cell</i>, vol. 24,
    no. 6, Cell Press, 2013, pp. 567–69, doi:<a href="https://doi.org/10.1016/j.devcel.2013.03.007">10.1016/j.devcel.2013.03.007</a>.'
  short: H. Morita, C.-P.J. Heisenberg, Developmental Cell 24 (2013) 567–569.
corr_author: '1'
date_created: 2018-12-11T11:59:52Z
date_published: 2013-05-25T00:00:00Z
date_updated: 2025-09-29T13:44:50Z
day: '25'
department:
- _id: CaHe
doi: 10.1016/j.devcel.2013.03.007
external_id:
  isi:
  - '000317634500003'
intvolume: '        24'
isi: 1
issue: '6'
language:
- iso: eng
month: '05'
oa_version: None
page: 567 - 569
publication: Developmental Cell
publication_status: published
publisher: Cell Press
publist_id: '3956'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Holding on and letting go: Cadherin turnover in cell intercalation'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 24
year: '2013'
...
---
_id: '2842'
abstract:
- lang: eng
  text: 'We outline two approaches to inference of neighbourhood size, N, and dispersal
    rate, σ2, based on either allele frequencies or on the lengths of sequence blocks
    that are shared between genomes. Over intermediate timescales (10-100 generations,
    say), populations that live in two dimensions approach a quasi-equilibrium that
    is independent of both their local structure and their deeper history. Over such
    scales, the standardised covariance of allele frequencies (i.e. pairwise FS T)
    falls with the logarithm of distance, and depends only on neighbourhood size,
    N, and a ''local scale'', κ; the rate of gene flow, σ2, cannot be inferred. We
    show how spatial correlations can be accounted for, assuming a Gaussian distribution
    of allele frequencies, giving maximum likelihood estimates of N and κ. Alternatively,
    inferences can be based on the distribution of the lengths of sequence that are
    identical between blocks of genomes: long blocks (&gt;0.1 cM, say) tell us about
    intermediate timescales, over which we assume a quasi-equilibrium. For large neighbourhood
    size, the distribution of long blocks is given directly by the classical Wright-Malécot
    formula; this relationship can be used to infer both N and σ2. With small neighbourhood
    size, there is an appreciable chance that recombinant lineages will coalesce back
    before escaping into the distant past. For this case, we show that if genomes
    are sampled from some distance apart, then the distribution of lengths of blocks
    that are identical in state is geometric, with a mean that depends on N and σ2.'
article_processing_charge: No
author:
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
- first_name: Alison
  full_name: Etheridge, Alison
  last_name: Etheridge
- first_name: Jerome
  full_name: Kelleher, Jerome
  last_name: Kelleher
- first_name: Amandine
  full_name: Véber, Amandine
  last_name: Véber
citation:
  ama: 'Barton NH, Etheridge A, Kelleher J, Véber A. Inference in two dimensions:
    Allele frequencies versus lengths of shared sequence blocks. <i>Theoretical Population
    Biology</i>. 2013;87(1):105-119. doi:<a href="https://doi.org/10.1016/j.tpb.2013.03.001">10.1016/j.tpb.2013.03.001</a>'
  apa: 'Barton, N. H., Etheridge, A., Kelleher, J., &#38; Véber, A. (2013). Inference
    in two dimensions: Allele frequencies versus lengths of shared sequence blocks.
    <i>Theoretical Population Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.tpb.2013.03.001">https://doi.org/10.1016/j.tpb.2013.03.001</a>'
  chicago: 'Barton, Nicholas H, Alison Etheridge, Jerome Kelleher, and Amandine Véber.
    “Inference in Two Dimensions: Allele Frequencies versus Lengths of Shared Sequence
    Blocks.” <i>Theoretical Population Biology</i>. Elsevier, 2013. <a href="https://doi.org/10.1016/j.tpb.2013.03.001">https://doi.org/10.1016/j.tpb.2013.03.001</a>.'
  ieee: 'N. H. Barton, A. Etheridge, J. Kelleher, and A. Véber, “Inference in two
    dimensions: Allele frequencies versus lengths of shared sequence blocks,” <i>Theoretical
    Population Biology</i>, vol. 87, no. 1. Elsevier, pp. 105–119, 2013.'
  ista: 'Barton NH, Etheridge A, Kelleher J, Véber A. 2013. Inference in two dimensions:
    Allele frequencies versus lengths of shared sequence blocks. Theoretical Population
    Biology. 87(1), 105–119.'
  mla: 'Barton, Nicholas H., et al. “Inference in Two Dimensions: Allele Frequencies
    versus Lengths of Shared Sequence Blocks.” <i>Theoretical Population Biology</i>,
    vol. 87, no. 1, Elsevier, 2013, pp. 105–19, doi:<a href="https://doi.org/10.1016/j.tpb.2013.03.001">10.1016/j.tpb.2013.03.001</a>.'
  short: N.H. Barton, A. Etheridge, J. Kelleher, A. Véber, Theoretical Population
    Biology 87 (2013) 105–119.
date_created: 2018-12-11T11:59:53Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2025-09-29T13:44:19Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1016/j.tpb.2013.03.001
ec_funded: 1
external_id:
  isi:
  - '000322688800010'
file:
- access_level: open_access
  checksum: 9bf9d9a6fd03dd9df50906891f393bf8
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:17:33Z
  date_updated: 2020-07-14T12:45:50Z
  file_id: '5288'
  file_name: IST-2016-558-v1+1_inference_revised3101NB.pdf
  file_size: 1554712
  relation: main_file
- access_level: open_access
  checksum: 2bceddb76edacd0cd5fad73051e2a928
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:17:34Z
  date_updated: 2020-07-14T12:45:50Z
  file_id: '5289'
  file_name: IST-2016-558-v1+2_inference_revised3101NBApp.pdf
  file_size: 822964
  relation: main_file
file_date_updated: 2020-07-14T12:45:50Z
has_accepted_license: '1'
intvolume: '        87'
isi: 1
issue: '1'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Submitted Version
page: 105 - 119
project:
- _id: 25B07788-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '250152'
  name: Limits to selection in biology and in evolutionary computation
publication: Theoretical Population Biology
publication_status: published
publisher: Elsevier
publist_id: '3953'
pubrep_id: '558'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Inference in two dimensions: Allele frequencies versus lengths of shared sequence
  blocks'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 87
year: '2013'
...
---
_id: '2844'
abstract:
- lang: eng
  text: As soon as a seed germinates, plant growth relates to gravity to ensure that
    the root penetrates the soil and the shoot expands aerially. Whereas mechanisms
    of positive and negative orthogravitropism of primary roots and shoots are relatively
    well understood [1-3], lateral organs often show more complex growth behavior
    [4]. Lateral roots (LRs) seemingly suppress positive gravitropic growth and show
    a defined gravitropic set-point angle (GSA) that allows radial expansion of the
    root system (plagiotropism) [3, 4]. Despite its eminent importance for root architecture,
    it so far remains completely unknown how lateral organs partially suppress positive
    orthogravitropism. Here we show that the phytohormone auxin steers GSA formation
    and limits positive orthogravitropism in LR. Low and high auxin levels/signaling
    lead to radial or axial root systems, respectively. At a cellular level, it is
    the auxin transport-dependent regulation of asymmetric growth in the elongation
    zone that determines GSA. Our data suggest that strong repression of PIN4/PIN7
    and transient PIN3 expression limit auxin redistribution in young LR columella
    cells. We conclude that PIN activity, by temporally limiting the asymmetric auxin
    fluxes in the tip of LRs, induces transient, differential growth responses in
    the elongation zone and, consequently, controls root architecture.
article_processing_charge: No
author:
- first_name: Michel
  full_name: Rosquete, Michel
  last_name: Rosquete
- first_name: Daniel
  full_name: Von Wangenheim, Daniel
  id: 49E91952-F248-11E8-B48F-1D18A9856A87
  last_name: Von Wangenheim
  orcid: 0000-0002-6862-1247
- first_name: Peter
  full_name: Marhavy, Peter
  id: 3F45B078-F248-11E8-B48F-1D18A9856A87
  last_name: Marhavy
  orcid: 0000-0001-5227-5741
- first_name: Elke
  full_name: Barbez, Elke
  last_name: Barbez
- first_name: Ernst
  full_name: Stelzer, Ernst
  last_name: Stelzer
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Alexis
  full_name: Maizel, Alexis
  last_name: Maizel
- first_name: Jürgen
  full_name: Kleine Vehn, Jürgen
  last_name: Kleine Vehn
citation:
  ama: Rosquete M, von Wangenheim D, Marhavý P, et al. An auxin transport mechanism
    restricts positive orthogravitropism in lateral roots. <i>Current Biology</i>.
    2013;23(9):817-822. doi:<a href="https://doi.org/10.1016/j.cub.2013.03.064">10.1016/j.cub.2013.03.064</a>
  apa: Rosquete, M., von Wangenheim, D., Marhavý, P., Barbez, E., Stelzer, E., Benková,
    E., … Kleine Vehn, J. (2013). An auxin transport mechanism restricts positive
    orthogravitropism in lateral roots. <i>Current Biology</i>. Cell Press. <a href="https://doi.org/10.1016/j.cub.2013.03.064">https://doi.org/10.1016/j.cub.2013.03.064</a>
  chicago: Rosquete, Michel, Daniel von Wangenheim, Peter Marhavý, Elke Barbez, Ernst
    Stelzer, Eva Benková, Alexis Maizel, and Jürgen Kleine Vehn. “An Auxin Transport
    Mechanism Restricts Positive Orthogravitropism in Lateral Roots.” <i>Current Biology</i>.
    Cell Press, 2013. <a href="https://doi.org/10.1016/j.cub.2013.03.064">https://doi.org/10.1016/j.cub.2013.03.064</a>.
  ieee: M. Rosquete <i>et al.</i>, “An auxin transport mechanism restricts positive
    orthogravitropism in lateral roots,” <i>Current Biology</i>, vol. 23, no. 9. Cell
    Press, pp. 817–822, 2013.
  ista: Rosquete M, von Wangenheim D, Marhavý P, Barbez E, Stelzer E, Benková E, Maizel
    A, Kleine Vehn J. 2013. An auxin transport mechanism restricts positive orthogravitropism
    in lateral roots. Current Biology. 23(9), 817–822.
  mla: Rosquete, Michel, et al. “An Auxin Transport Mechanism Restricts Positive Orthogravitropism
    in Lateral Roots.” <i>Current Biology</i>, vol. 23, no. 9, Cell Press, 2013, pp.
    817–22, doi:<a href="https://doi.org/10.1016/j.cub.2013.03.064">10.1016/j.cub.2013.03.064</a>.
  short: M. Rosquete, D. von Wangenheim, P. Marhavý, E. Barbez, E. Stelzer, E. Benková,
    A. Maizel, J. Kleine Vehn, Current Biology 23 (2013) 817–822.
date_created: 2018-12-11T11:59:53Z
date_published: 2013-05-06T00:00:00Z
date_updated: 2025-09-29T13:43:30Z
day: '06'
department:
- _id: JiFr
- _id: EvBe
doi: 10.1016/j.cub.2013.03.064
ec_funded: 1
external_id:
  isi:
  - '000318750900035'
intvolume: '        23'
isi: 1
issue: '9'
language:
- iso: eng
month: '05'
oa_version: None
page: 817 - 822
project:
- _id: 253FCA6A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '207362'
  name: Hormonal cross-talk in plant organogenesis
publication: Current Biology
publication_status: published
publisher: Cell Press
publist_id: '3950'
quality_controlled: '1'
scopus_import: '1'
status: public
title: An auxin transport mechanism restricts positive orthogravitropism in lateral
  roots
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 23
year: '2013'
...
---
_id: '2845'
abstract:
- lang: eng
  text: At synapses formed between dissociated neurons, about half of all synaptic
    vesicles are refractory to evoked release, forming the so-called &quot;resting
    pool.&quot; Here, we use optical measurements of vesicular pH to study developmental
    changes in pool partitioning and vesicle cycling in cultured hippocampal slices.
    Two-photon imaging of a genetically encoded two-color release sensor (ratio-sypHy)
    allowed us to perform calibrated measurements at individual Schaffer collateral
    boutons. Mature boutons released a large fraction of their vesicles during simulated
    place field activity, and vesicle retrieval rates were 7-fold higher compared
    to immature boutons. Saturating stimulation mobilized essentially all vesicles
    at mature synapses. Resting pool formation and a concomitant reduction in evoked
    release was induced by chronic depolarization but not by acute inhibition of the
    protein phosphatase calcineurin. We conclude that synapses in CA1 undergo a prominent
    refinement of vesicle use during early postnatal development that is not recapitulated
    in dissociated neuronal culture.
article_processing_charge: No
author:
- first_name: Tobias
  full_name: Rose, Tobias
  last_name: Rose
- first_name: Philipp
  full_name: Schönenberger, Philipp
  id: 3B9D816C-F248-11E8-B48F-1D18A9856A87
  last_name: Schönenberger
- first_name: Karel
  full_name: Jezek, Karel
  last_name: Jezek
- first_name: Thomas
  full_name: Oertner, Thomas
  last_name: Oertner
citation:
  ama: Rose T, Schönenberger P, Jezek K, Oertner T. Developmental refinement of vesicle
    cycling at Schaffer collateral synapses. <i>Neuron</i>. 2013;77(6):1109-1121.
    doi:<a href="https://doi.org/10.1016/j.neuron.2013.01.021">10.1016/j.neuron.2013.01.021</a>
  apa: Rose, T., Schönenberger, P., Jezek, K., &#38; Oertner, T. (2013). Developmental
    refinement of vesicle cycling at Schaffer collateral synapses. <i>Neuron</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.neuron.2013.01.021">https://doi.org/10.1016/j.neuron.2013.01.021</a>
  chicago: Rose, Tobias, Philipp Schönenberger, Karel Jezek, and Thomas Oertner. “Developmental
    Refinement of Vesicle Cycling at Schaffer Collateral Synapses.” <i>Neuron</i>.
    Elsevier, 2013. <a href="https://doi.org/10.1016/j.neuron.2013.01.021">https://doi.org/10.1016/j.neuron.2013.01.021</a>.
  ieee: T. Rose, P. Schönenberger, K. Jezek, and T. Oertner, “Developmental refinement
    of vesicle cycling at Schaffer collateral synapses,” <i>Neuron</i>, vol. 77, no.
    6. Elsevier, pp. 1109–1121, 2013.
  ista: Rose T, Schönenberger P, Jezek K, Oertner T. 2013. Developmental refinement
    of vesicle cycling at Schaffer collateral synapses. Neuron. 77(6), 1109–1121.
  mla: Rose, Tobias, et al. “Developmental Refinement of Vesicle Cycling at Schaffer
    Collateral Synapses.” <i>Neuron</i>, vol. 77, no. 6, Elsevier, 2013, pp. 1109–21,
    doi:<a href="https://doi.org/10.1016/j.neuron.2013.01.021">10.1016/j.neuron.2013.01.021</a>.
  short: T. Rose, P. Schönenberger, K. Jezek, T. Oertner, Neuron 77 (2013) 1109–1121.
date_created: 2018-12-11T11:59:54Z
date_published: 2013-03-20T00:00:00Z
date_updated: 2025-09-29T13:42:59Z
day: '20'
department:
- _id: JoCs
doi: 10.1016/j.neuron.2013.01.021
external_id:
  isi:
  - '000316645000012'
intvolume: '        77'
isi: 1
issue: '6'
language:
- iso: eng
month: '03'
oa_version: None
page: 1109 - 1121
publication: Neuron
publication_status: published
publisher: Elsevier
publist_id: '3949'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Developmental refinement of vesicle cycling at Schaffer collateral synapses
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 77
year: '2013'
...
---
_id: '2846'
abstract:
- lang: eng
  text: The Red Queen hypothesis proposes that coevolving parasites select for outcrossing
    in the host. Outcrossing relies on males, which often show lower immune investment
    due to, for example, sexual selection. Here, we demonstrate that such sex differences
    in immunity interfere with parasite-mediated selection for outcrossing. Two independent
    coevolution experiments with Caenorhabditis elegans and its microparasite Bacillus
    thuringiensis produced decreased yet stable frequencies of outcrossing male hosts.
    A subsequent systematic analysis verified that male C. elegans suffered from a
    direct selective disadvantage under parasite pressure (i.e. lower resistance,
    decreased sexual activity, increased escape behaviour), which can reduce outcrossing
    and thus male frequencies. At the same time, males offered an indirect selective
    benefit, because male-mediated outcrossing increased offspring resistance, thus
    favouring male persistence in the evolving populations. As sex differences in
    immunity are widespread, such interference of opposing selective constraints is
    likely of central importance during host adaptation to a coevolving parasite.
article_processing_charge: No
author:
- first_name: Leila
  full_name: El Masri, Leila
  id: 349A6E66-F248-11E8-B48F-1D18A9856A87
  last_name: El Masri
- first_name: Rebecca
  full_name: Schulte, Rebecca
  last_name: Schulte
- first_name: Nadine
  full_name: Timmermeyer, Nadine
  last_name: Timmermeyer
- first_name: Stefanie
  full_name: Thanisch, Stefanie
  last_name: Thanisch
- first_name: Lena
  full_name: Crummenerl, Lena
  last_name: Crummenerl
- first_name: Gunther
  full_name: Jansen, Gunther
  last_name: Jansen
- first_name: Nico
  full_name: Michiels, Nico
  last_name: Michiels
- first_name: Hinrich
  full_name: Schulenburg, Hinrich
  last_name: Schulenburg
citation:
  ama: El Masri L, Schulte R, Timmermeyer N, et al. Sex differences in host defence
    interfere with parasite-mediated selection for outcrossing during host-parasite
    coevolution. <i>Ecology Letters</i>. 2013;16(4):461-468. doi:<a href="https://doi.org/10.1111/ele.12068">10.1111/ele.12068</a>
  apa: El Masri, L., Schulte, R., Timmermeyer, N., Thanisch, S., Crummenerl, L., Jansen,
    G., … Schulenburg, H. (2013). Sex differences in host defence interfere with parasite-mediated
    selection for outcrossing during host-parasite coevolution. <i>Ecology Letters</i>.
    Wiley-Blackwell. <a href="https://doi.org/10.1111/ele.12068">https://doi.org/10.1111/ele.12068</a>
  chicago: El Masri, Leila, Rebecca Schulte, Nadine Timmermeyer, Stefanie Thanisch,
    Lena Crummenerl, Gunther Jansen, Nico Michiels, and Hinrich Schulenburg. “Sex
    Differences in Host Defence Interfere with Parasite-Mediated Selection for Outcrossing
    during Host-Parasite Coevolution.” <i>Ecology Letters</i>. Wiley-Blackwell, 2013.
    <a href="https://doi.org/10.1111/ele.12068">https://doi.org/10.1111/ele.12068</a>.
  ieee: L. El Masri <i>et al.</i>, “Sex differences in host defence interfere with
    parasite-mediated selection for outcrossing during host-parasite coevolution,”
    <i>Ecology Letters</i>, vol. 16, no. 4. Wiley-Blackwell, pp. 461–468, 2013.
  ista: El Masri L, Schulte R, Timmermeyer N, Thanisch S, Crummenerl L, Jansen G,
    Michiels N, Schulenburg H. 2013. Sex differences in host defence interfere with
    parasite-mediated selection for outcrossing during host-parasite coevolution.
    Ecology Letters. 16(4), 461–468.
  mla: El Masri, Leila, et al. “Sex Differences in Host Defence Interfere with Parasite-Mediated
    Selection for Outcrossing during Host-Parasite Coevolution.” <i>Ecology Letters</i>,
    vol. 16, no. 4, Wiley-Blackwell, 2013, pp. 461–68, doi:<a href="https://doi.org/10.1111/ele.12068">10.1111/ele.12068</a>.
  short: L. El Masri, R. Schulte, N. Timmermeyer, S. Thanisch, L. Crummenerl, G. Jansen,
    N. Michiels, H. Schulenburg, Ecology Letters 16 (2013) 461–468.
date_created: 2018-12-11T11:59:54Z
date_published: 2013-04-04T00:00:00Z
date_updated: 2022-08-25T14:51:57Z
day: '04'
ddc:
- '570'
doi: 10.1111/ele.12068
extern: '1'
file:
- access_level: open_access
  checksum: aa7db788f7da7d7f102539a249ebce50
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:15:52Z
  date_updated: 2020-07-14T12:45:50Z
  file_id: '5176'
  file_name: IST-2016-404-v1+1_ele12068.pdf
  file_size: 763731
  relation: main_file
file_date_updated: 2020-07-14T12:45:50Z
has_accepted_license: '1'
intvolume: '        16'
issue: '4'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 461 - 468
publication: Ecology Letters
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3948'
pubrep_id: '404'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Sex differences in host defence interfere with parasite-mediated selection
  for outcrossing during host-parasite coevolution
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: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2013'
...
---
_id: '2850'
abstract:
- lang: eng
  text: "Recent work emphasizes that the maximum entropy principle provides a bridge
    between statistical mechanics models for collective behavior in neural networks
    and experiments on networks of real neurons. Most of this work has focused on
    capturing the measured correlations among pairs of neurons. Here we suggest an
    alternative, constructing models that are consistent with the distribution of
    global network activity, i.e. the probability that K out of N cells in the network
    generate action potentials in the same small time bin. The inverse problem that
    we need to solve in constructing the model is analytically tractable, and provides
    a natural 'thermodynamics' for the network in the limit of large N. We analyze
    the responses of neurons in a small patch of the retina to naturalistic stimuli,
    and find that the implied thermodynamics is very close to an unusual critical
    point, in which the entropy (in proper units) is exactly equal to the energy.
    © 2013 IOP Publishing Ltd and SISSA Medialab srl.\r\n"
acknowledgement: "his work was supported in part by NSF Grants IIS-0613435 and PHY-0957573,
  by NIH Grants R01 EY14196 and P50 GM071508, by the Fannie and John Hertz Foundation,
  by the Human Frontiers Science Program, by the Swartz Foundation, and by the WM
  Keck Foundation.\r\n"
article_number: P03011
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
- first_name: Olivier
  full_name: Marre, Olivier
  last_name: Marre
- first_name: Thierry
  full_name: Mora, Thierry
  last_name: Mora
- first_name: Dario
  full_name: Amodei, Dario
  last_name: Amodei
- first_name: Michael
  full_name: Berry, Michael
  last_name: Berry
- first_name: William
  full_name: Bialek, William
  last_name: Bialek
citation:
  ama: Tkačik G, Marre O, Mora T, Amodei D, Berry M, Bialek W. The simplest maximum
    entropy model for collective behavior in a neural network. <i>Journal of Statistical
    Mechanics Theory and Experiment</i>. 2013;2013(3). doi:<a href="https://doi.org/10.1088/1742-5468/2013/03/P03011">10.1088/1742-5468/2013/03/P03011</a>
  apa: Tkačik, G., Marre, O., Mora, T., Amodei, D., Berry, M., &#38; Bialek, W. (2013).
    The simplest maximum entropy model for collective behavior in a neural network.
    <i>Journal of Statistical Mechanics Theory and Experiment</i>. IOP Publishing.
    <a href="https://doi.org/10.1088/1742-5468/2013/03/P03011">https://doi.org/10.1088/1742-5468/2013/03/P03011</a>
  chicago: Tkačik, Gašper, Olivier Marre, Thierry Mora, Dario Amodei, Michael Berry,
    and William Bialek. “The Simplest Maximum Entropy Model for Collective Behavior
    in a Neural Network.” <i>Journal of Statistical Mechanics Theory and Experiment</i>.
    IOP Publishing, 2013. <a href="https://doi.org/10.1088/1742-5468/2013/03/P03011">https://doi.org/10.1088/1742-5468/2013/03/P03011</a>.
  ieee: G. Tkačik, O. Marre, T. Mora, D. Amodei, M. Berry, and W. Bialek, “The simplest
    maximum entropy model for collective behavior in a neural network,” <i>Journal
    of Statistical Mechanics Theory and Experiment</i>, vol. 2013, no. 3. IOP Publishing,
    2013.
  ista: Tkačik G, Marre O, Mora T, Amodei D, Berry M, Bialek W. 2013. The simplest
    maximum entropy model for collective behavior in a neural network. Journal of
    Statistical Mechanics Theory and Experiment. 2013(3), P03011.
  mla: Tkačik, Gašper, et al. “The Simplest Maximum Entropy Model for Collective Behavior
    in a Neural Network.” <i>Journal of Statistical Mechanics Theory and Experiment</i>,
    vol. 2013, no. 3, P03011, IOP Publishing, 2013, doi:<a href="https://doi.org/10.1088/1742-5468/2013/03/P03011">10.1088/1742-5468/2013/03/P03011</a>.
  short: G. Tkačik, O. Marre, T. Mora, D. Amodei, M. Berry, W. Bialek, Journal of
    Statistical Mechanics Theory and Experiment 2013 (2013).
date_created: 2018-12-11T11:59:55Z
date_published: 2013-03-12T00:00:00Z
date_updated: 2025-09-29T13:42:18Z
day: '12'
department:
- _id: GaTk
doi: 10.1088/1742-5468/2013/03/P03011
external_id:
  arxiv:
  - '1207.6319'
  isi:
  - '000316056900011'
intvolume: '      2013'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1207.6319
month: '03'
oa: 1
oa_version: Preprint
publication: Journal of Statistical Mechanics Theory and Experiment
publication_status: published
publisher: IOP Publishing
publist_id: '3942'
quality_controlled: '1'
scopus_import: '1'
status: public
title: The simplest maximum entropy model for collective behavior in a neural network
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 2013
year: '2013'
...
---
_id: '2851'
abstract:
- lang: eng
  text: The number of possible activity patterns in a population of neurons grows
    exponentially with the size of the population. Typical experiments explore only
    a tiny fraction of the large space of possible activity patterns in the case of
    populations with more than 10 or 20 neurons. It is thus impossible, in this undersampled
    regime, to estimate the probabilities with which most of the activity patterns
    occur. As a result, the corresponding entropy - which is a measure of the computational
    power of the neural population - cannot be estimated directly. We propose a simple
    scheme for estimating the entropy in the undersampled regime, which bounds its
    value from both below and above. The lower bound is the usual 'naive' entropy
    of the experimental frequencies. The upper bound results from a hybrid approximation
    of the entropy which makes use of the naive estimate, a maximum entropy fit, and
    a coverage adjustment. We apply our simple scheme to artificial data, in order
    to check their accuracy; we also compare its performance to those of several previously
    defined entropy estimators. We then apply it to actual measurements of neural
    activity in populations with up to 100 cells. Finally, we discuss the similarities
    and differences between the proposed simple estimation scheme and various earlier
    methods. © 2013 IOP Publishing Ltd and SISSA Medialab srl.
article_number: P03015
article_processing_charge: No
author:
- first_name: Michael
  full_name: Berry, Michael
  last_name: Berry
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
- first_name: Julien
  full_name: Dubuis, Julien
  last_name: Dubuis
- first_name: Olivier
  full_name: Marre, Olivier
  last_name: Marre
- first_name: Ravá
  full_name: Da Silveira, Ravá
  last_name: Da Silveira
citation:
  ama: Berry M, Tkačik G, Dubuis J, Marre O, Da Silveira R. A simple method for estimating
    the entropy of neural activity. <i>Journal of Statistical Mechanics Theory and
    Experiment</i>. 2013;2013(3). doi:<a href="https://doi.org/10.1088/1742-5468/2013/03/P03015">10.1088/1742-5468/2013/03/P03015</a>
  apa: Berry, M., Tkačik, G., Dubuis, J., Marre, O., &#38; Da Silveira, R. (2013).
    A simple method for estimating the entropy of neural activity. <i>Journal of Statistical
    Mechanics Theory and Experiment</i>. IOP Publishing. <a href="https://doi.org/10.1088/1742-5468/2013/03/P03015">https://doi.org/10.1088/1742-5468/2013/03/P03015</a>
  chicago: Berry, Michael, Gašper Tkačik, Julien Dubuis, Olivier Marre, and Ravá Da
    Silveira. “A Simple Method for Estimating the Entropy of Neural Activity.” <i>Journal
    of Statistical Mechanics Theory and Experiment</i>. IOP Publishing, 2013. <a href="https://doi.org/10.1088/1742-5468/2013/03/P03015">https://doi.org/10.1088/1742-5468/2013/03/P03015</a>.
  ieee: M. Berry, G. Tkačik, J. Dubuis, O. Marre, and R. Da Silveira, “A simple method
    for estimating the entropy of neural activity,” <i>Journal of Statistical Mechanics
    Theory and Experiment</i>, vol. 2013, no. 3. IOP Publishing, 2013.
  ista: Berry M, Tkačik G, Dubuis J, Marre O, Da Silveira R. 2013. A simple method
    for estimating the entropy of neural activity. Journal of Statistical Mechanics
    Theory and Experiment. 2013(3), P03015.
  mla: Berry, Michael, et al. “A Simple Method for Estimating the Entropy of Neural
    Activity.” <i>Journal of Statistical Mechanics Theory and Experiment</i>, vol.
    2013, no. 3, P03015, IOP Publishing, 2013, doi:<a href="https://doi.org/10.1088/1742-5468/2013/03/P03015">10.1088/1742-5468/2013/03/P03015</a>.
  short: M. Berry, G. Tkačik, J. Dubuis, O. Marre, R. Da Silveira, Journal of Statistical
    Mechanics Theory and Experiment 2013 (2013).
date_created: 2018-12-11T11:59:56Z
date_published: 2013-03-12T00:00:00Z
date_updated: 2025-09-29T13:41:46Z
day: '12'
department:
- _id: GaTk
doi: 10.1088/1742-5468/2013/03/P03015
external_id:
  isi:
  - '000316056900015'
intvolume: '      2013'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa_version: None
publication: Journal of Statistical Mechanics Theory and Experiment
publication_status: published
publisher: IOP Publishing
publist_id: '3941'
quality_controlled: '1'
scopus_import: '1'
status: public
title: A simple method for estimating the entropy of neural activity
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 2013
year: '2013'
...
---
_id: '2853'
abstract:
- lang: eng
  text: High relatedness among interacting individuals has generally been considered
    a precondition for the evolution of altruism. However, kin-selection theory also
    predicts the evolution of altruism when relatedness is low, as long as the cost
    of the altruistic act is minor compared with its benefit. Here, we demonstrate
    evidence for a low-cost altruistic act in bacteria. We investigated Escherichia
    coli responding to the attack of an obligately lytic phage by committing suicide
    in order to prevent parasite transmission to nearby relatives. We found that bacterial
    suicide provides large benefits to survivors at marginal costs to committers.
    The cost of suicide was low, because infected cells are moribund, rapidly dying
    upon phage infection, such that no more opportunity for reproduction remains.
    As a consequence of its marginal cost, host suicide was selectively favoured even
    when relatedness between committers and survivors approached zero. Altogether,
    our findings demonstrate that low-cost suicide can evolve with ease, represents
    an effective host-defence strategy, and seems to be widespread among microbes.
    Moreover, low-cost suicide might also occur in higher organisms as exemplified
    by infected social insect workers leaving the colony to die in isolation.
article_processing_charge: No
article_type: original
author:
- first_name: Dominik
  full_name: Refardt, Dominik
  last_name: Refardt
- first_name: Tobias
  full_name: Bergmiller, Tobias
  id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
  last_name: Bergmiller
  orcid: 0000-0001-5396-4346
- first_name: Rolf
  full_name: Kümmerli, Rolf
  last_name: Kümmerli
citation:
  ama: 'Refardt D, Bergmiller T, Kümmerli R. Altruism can evolve when relatedness
    is low: Evidence from bacteria committing suicide upon phage infection. <i>Proceedings
    of the Royal Society of London Series B Biological Sciences</i>. 2013;280(1759).
    doi:<a href="https://doi.org/10.1098/rspb.2012.3035">10.1098/rspb.2012.3035</a>'
  apa: 'Refardt, D., Bergmiller, T., &#38; Kümmerli, R. (2013). Altruism can evolve
    when relatedness is low: Evidence from bacteria committing suicide upon phage
    infection. <i>Proceedings of the Royal Society of London Series B Biological Sciences</i>.
    The Royal Society. <a href="https://doi.org/10.1098/rspb.2012.3035">https://doi.org/10.1098/rspb.2012.3035</a>'
  chicago: 'Refardt, Dominik, Tobias Bergmiller, and Rolf Kümmerli. “Altruism Can
    Evolve When Relatedness Is Low: Evidence from Bacteria Committing Suicide upon
    Phage Infection.” <i>Proceedings of the Royal Society of London Series B Biological
    Sciences</i>. The Royal Society, 2013. <a href="https://doi.org/10.1098/rspb.2012.3035">https://doi.org/10.1098/rspb.2012.3035</a>.'
  ieee: 'D. Refardt, T. Bergmiller, and R. Kümmerli, “Altruism can evolve when relatedness
    is low: Evidence from bacteria committing suicide upon phage infection,” <i>Proceedings
    of the Royal Society of London Series B Biological Sciences</i>, vol. 280, no.
    1759. The Royal Society, 2013.'
  ista: 'Refardt D, Bergmiller T, Kümmerli R. 2013. Altruism can evolve when relatedness
    is low: Evidence from bacteria committing suicide upon phage infection. Proceedings
    of the Royal Society of London Series B Biological Sciences. 280(1759).'
  mla: 'Refardt, Dominik, et al. “Altruism Can Evolve When Relatedness Is Low: Evidence
    from Bacteria Committing Suicide upon Phage Infection.” <i>Proceedings of the
    Royal Society of London Series B Biological Sciences</i>, vol. 280, no. 1759,
    The Royal Society, 2013, doi:<a href="https://doi.org/10.1098/rspb.2012.3035">10.1098/rspb.2012.3035</a>.'
  short: D. Refardt, T. Bergmiller, R. Kümmerli, Proceedings of the Royal Society
    of London Series B Biological Sciences 280 (2013).
corr_author: '1'
date_created: 2018-12-11T11:59:56Z
date_published: 2013-05-22T00:00:00Z
date_updated: 2025-09-29T13:41:12Z
day: '22'
department:
- _id: CaGu
doi: 10.1098/rspb.2012.3035
external_id:
  isi:
  - '000317482100005'
  pmid:
  - '23516238'
intvolume: '       280'
isi: 1
issue: '1759'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3619501/
month: '05'
oa: 1
oa_version: Submitted Version
pmid: 1
publication: Proceedings of the Royal Society of London Series B Biological Sciences
publication_identifier:
  eissn:
  - 1471-2954
publication_status: published
publisher: The Royal Society
publist_id: '3939'
quality_controlled: '1'
related_material:
  record:
  - id: '9751'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: 'Altruism can evolve when relatedness is low: Evidence from bacteria committing
  suicide upon phage infection'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 280
year: '2013'
...
---
_id: '2854'
abstract:
- lang: eng
  text: We consider concurrent games played on graphs. At every round of a game, each
    player simultaneously and independently selects a move; the moves jointly determine
    the transition to a successor state. Two basic objectives are the safety objective
    to stay forever in a given set of states, and its dual, the reachability objective
    to reach a given set of states. First, we present a simple proof of the fact that
    in concurrent reachability games, for all ε&gt;0, memoryless ε-optimal strategies
    exist. A memoryless strategy is independent of the history of plays, and an ε-optimal
    strategy achieves the objective with probability within ε of the value of the
    game. In contrast to previous proofs of this fact, our proof is more elementary
    and more combinatorial. Second, we present a strategy-improvement (a.k.a. policy-iteration)
    algorithm for concurrent games with reachability objectives. Finally, we present
    a strategy-improvement algorithm for turn-based stochastic games (where each player
    selects moves in turns) with safety objectives. Our algorithms yield sequences
    of player-1 strategies which ensure probabilities of winning that converge monotonically
    (from below) to the value of the game. © 2012 Elsevier Inc.
acknowledgement: This work was partially supported in part by the NSF grants CCR-0132780,
  CNS-0720884, CCR-0225610, by the Swiss National Science Foundation, ERC Start Grant
  Graph Games (Project No. 279307), FWF NFN Grant S11407-N23 (RiSE), and a Microsoft
  faculty fellows
article_processing_charge: No
article_type: original
author:
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Luca
  full_name: De Alfaro, Luca
  last_name: De Alfaro
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
citation:
  ama: Chatterjee K, De Alfaro L, Henzinger TA. Strategy improvement for concurrent
    reachability and turn based stochastic safety games. <i>Journal of Computer and
    System Sciences</i>. 2013;79(5):640-657. doi:<a href="https://doi.org/10.1016/j.jcss.2012.12.001">10.1016/j.jcss.2012.12.001</a>
  apa: Chatterjee, K., De Alfaro, L., &#38; Henzinger, T. A. (2013). Strategy improvement
    for concurrent reachability and turn based stochastic safety games. <i>Journal
    of Computer and System Sciences</i>. Elsevier. <a href="https://doi.org/10.1016/j.jcss.2012.12.001">https://doi.org/10.1016/j.jcss.2012.12.001</a>
  chicago: Chatterjee, Krishnendu, Luca De Alfaro, and Thomas A Henzinger. “Strategy
    Improvement for Concurrent Reachability and Turn Based Stochastic Safety Games.”
    <i>Journal of Computer and System Sciences</i>. Elsevier, 2013. <a href="https://doi.org/10.1016/j.jcss.2012.12.001">https://doi.org/10.1016/j.jcss.2012.12.001</a>.
  ieee: K. Chatterjee, L. De Alfaro, and T. A. Henzinger, “Strategy improvement for
    concurrent reachability and turn based stochastic safety games,” <i>Journal of
    Computer and System Sciences</i>, vol. 79, no. 5. Elsevier, pp. 640–657, 2013.
  ista: Chatterjee K, De Alfaro L, Henzinger TA. 2013. Strategy improvement for concurrent
    reachability and turn based stochastic safety games. Journal of Computer and System
    Sciences. 79(5), 640–657.
  mla: Chatterjee, Krishnendu, et al. “Strategy Improvement for Concurrent Reachability
    and Turn Based Stochastic Safety Games.” <i>Journal of Computer and System Sciences</i>,
    vol. 79, no. 5, Elsevier, 2013, pp. 640–57, doi:<a href="https://doi.org/10.1016/j.jcss.2012.12.001">10.1016/j.jcss.2012.12.001</a>.
  short: K. Chatterjee, L. De Alfaro, T.A. Henzinger, Journal of Computer and System
    Sciences 79 (2013) 640–657.
corr_author: '1'
date_created: 2018-12-11T11:59:57Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2025-09-29T13:40:38Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
- _id: ToHe
doi: 10.1016/j.jcss.2012.12.001
ec_funded: 1
external_id:
  isi:
  - '000316837300011'
file:
- access_level: open_access
  checksum: 6d3ee12cceb946a0abe69594b6a22409
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:18:48Z
  date_updated: 2020-07-14T12:45:51Z
  file_id: '5370'
  file_name: IST-2015-388-v1+1_1-s2.0-S0022000012001778-main.pdf
  file_size: 425488
  relation: main_file
file_date_updated: 2020-07-14T12:45:51Z
has_accepted_license: '1'
intvolume: '        79'
isi: 1
issue: '5'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '08'
oa: 1
oa_version: Published Version
page: 640 - 657
project:
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 25863FF4-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11407
  name: Game Theory
- _id: 2587B514-B435-11E9-9278-68D0E5697425
  name: Microsoft Research Faculty Fellowship
publication: Journal of Computer and System Sciences
publication_status: published
publisher: Elsevier
publist_id: '3938'
pubrep_id: '388'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Strategy improvement for concurrent reachability and turn based stochastic
  safety games
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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 79
year: '2013'
...
---
_id: '2855'
abstract:
- lang: eng
  text: Genomic imprinting leads to preferred expression of either the maternal or
    paternal alleles of a subset of genes. Imprinting is essential for mammalian development,
    and its deregulation causes many diseases. However, the functional relevance of
    imprinting at the cellular level is poorly understood for most imprinted genes.
    We used mosaic analysis with double markers (MADM) in mice to create uniparental
    disomies (UPDs) and to visualize imprinting effects with single-cell resolution.
    Although chromosome 12 UPD did not produce detectable phenotypes, chromosome 7
    UPD caused highly significant paternal growth dominance in the liver and lung,
    but not in the brain or heart. A single gene on chromosome 7, encoding the secreted
    insulin-like growth factor 2 (IGF2), accounts for most of the paternal dominance
    effect. Mosaic analyses implied additional imprinted loci on chromosome 7 acting
    cell autonomously to transmit the IGF2 signal. Our study reveals chromosome- and
    cell-type specificity of genomic imprinting effects.
article_processing_charge: No
author:
- first_name: Simon
  full_name: Hippenmeyer, Simon
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
- first_name: Randy
  full_name: Johnson, Randy
  last_name: Johnson
- first_name: Liqun
  full_name: Luo, Liqun
  last_name: Luo
citation:
  ama: Hippenmeyer S, Johnson R, Luo L. Mosaic analysis with double markers reveals
    cell type specific paternal growth dominance. <i>Cell Reports</i>. 2013;3(3):960-967.
    doi:<a href="https://doi.org/10.1016/j.celrep.2013.02.002">10.1016/j.celrep.2013.02.002</a>
  apa: Hippenmeyer, S., Johnson, R., &#38; Luo, L. (2013). Mosaic analysis with double
    markers reveals cell type specific paternal growth dominance. <i>Cell Reports</i>.
    Cell Press. <a href="https://doi.org/10.1016/j.celrep.2013.02.002">https://doi.org/10.1016/j.celrep.2013.02.002</a>
  chicago: Hippenmeyer, Simon, Randy Johnson, and Liqun Luo. “Mosaic Analysis with
    Double Markers Reveals Cell Type Specific Paternal Growth Dominance.” <i>Cell
    Reports</i>. Cell Press, 2013. <a href="https://doi.org/10.1016/j.celrep.2013.02.002">https://doi.org/10.1016/j.celrep.2013.02.002</a>.
  ieee: S. Hippenmeyer, R. Johnson, and L. Luo, “Mosaic analysis with double markers
    reveals cell type specific paternal growth dominance,” <i>Cell Reports</i>, vol.
    3, no. 3. Cell Press, pp. 960–967, 2013.
  ista: Hippenmeyer S, Johnson R, Luo L. 2013. Mosaic analysis with double markers
    reveals cell type specific paternal growth dominance. Cell Reports. 3(3), 960–967.
  mla: Hippenmeyer, Simon, et al. “Mosaic Analysis with Double Markers Reveals Cell
    Type Specific Paternal Growth Dominance.” <i>Cell Reports</i>, vol. 3, no. 3,
    Cell Press, 2013, pp. 960–67, doi:<a href="https://doi.org/10.1016/j.celrep.2013.02.002">10.1016/j.celrep.2013.02.002</a>.
  short: S. Hippenmeyer, R. Johnson, L. Luo, Cell Reports 3 (2013) 960–967.
corr_author: '1'
date_created: 2018-12-11T11:59:57Z
date_published: 2013-03-28T00:00:00Z
date_updated: 2025-09-29T13:40:05Z
day: '28'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.1016/j.celrep.2013.02.002
external_id:
  isi:
  - '000321896000036'
file:
- access_level: open_access
  checksum: 6e977b918e81384cd571ec5a9d812289
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:17:20Z
  date_updated: 2020-07-14T12:45:51Z
  file_id: '5274'
  file_name: IST-2016-405-v1+1_1-s2.0-S2211124713000612-main.pdf
  file_size: 1907211
  relation: main_file
file_date_updated: 2020-07-14T12:45:51Z
has_accepted_license: '1'
intvolume: '         3'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 960 - 967
publication: Cell Reports
publication_status: published
publisher: Cell Press
publist_id: '3937'
pubrep_id: '405'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mosaic analysis with double markers reveals cell type specific paternal growth
  dominance
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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 3
year: '2013'
...
---
_id: '2856'
abstract:
- lang: eng
  text: 'G protein–coupled receptors (GPCRs), the largest family of membrane signaling
    proteins, respond to neurotransmitters, hormones and small environmental molecules.
    The neuronal function of many GPCRs has been difficult to resolve because of an
    inability to gate them with subtype specificity, spatial precision, speed and
    reversibility. To address this, we developed an approach for opto-chemical engineering
    of native GPCRs. We applied this to the metabotropic glutamate receptors (mGluRs)
    to generate light-agonized and light-antagonized mGluRs (LimGluRs). The light-agonized
    LimGluR2, on which we focused, was fast, bistable and supported multiple rounds
    of on/off switching. Light gated two of the primary neuronal functions of mGluR2:
    suppression of excitability and inhibition of neurotransmitter release. We found
    that the light-antagonized tool LimGluR2-block was able to manipulate negative
    feedback of synaptically released glutamate on transmitter release. We generalized
    the optical control to two additional family members: mGluR3 and mGluR6. This
    system worked in rodent brain slices and in zebrafish in vivo, where we found
    that mGluR2 modulated the threshold for escape behavior. These light-gated mGluRs
    pave the way for determining the roles of mGluRs in synaptic plasticity, memory
    and disease.'
acknowledgement: National Science Foundation grants CHE-0233882 and CHE-0840505 (to
  the College of Chemistry at the University of California, Berkeley), a postdoctoral
  fellowship of the European Molecular Biology Organization (H.J.)
article_processing_charge: No
author:
- first_name: Joshua
  full_name: Levitz, Joshua
  last_name: Levitz
- first_name: Carlos
  full_name: Pantoja, Carlos
  last_name: Pantoja
- first_name: Benjamin
  full_name: Gaub, Benjamin
  last_name: Gaub
- first_name: Harald L
  full_name: Janovjak, Harald L
  id: 33BA6C30-F248-11E8-B48F-1D18A9856A87
  last_name: Janovjak
  orcid: 0000-0002-8023-9315
- first_name: Andreas
  full_name: Reiner, Andreas
  last_name: Reiner
- first_name: Adam
  full_name: Hoagland, Adam
  last_name: Hoagland
- first_name: David
  full_name: Schoppik, David
  last_name: Schoppik
- first_name: Brian
  full_name: Kane, Brian
  last_name: Kane
- first_name: Philipp
  full_name: Stawski, Philipp
  last_name: Stawski
- first_name: Alexander
  full_name: Schier, Alexander
  last_name: Schier
- first_name: Dirk
  full_name: Trauner, Dirk
  last_name: Trauner
- first_name: Ehud
  full_name: Isacoff, Ehud
  last_name: Isacoff
citation:
  ama: Levitz J, Pantoja C, Gaub B, et al. Optical control of metabotropic glutamate
    receptors. <i>Nature Neuroscience</i>. 2013;16:507-516. doi:<a href="https://doi.org/10.1038/nn.3346">10.1038/nn.3346</a>
  apa: Levitz, J., Pantoja, C., Gaub, B., Janovjak, H. L., Reiner, A., Hoagland, A.,
    … Isacoff, E. (2013). Optical control of metabotropic glutamate receptors. <i>Nature
    Neuroscience</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/nn.3346">https://doi.org/10.1038/nn.3346</a>
  chicago: Levitz, Joshua, Carlos Pantoja, Benjamin Gaub, Harald L Janovjak, Andreas
    Reiner, Adam Hoagland, David Schoppik, et al. “Optical Control of Metabotropic
    Glutamate Receptors.” <i>Nature Neuroscience</i>. Nature Publishing Group, 2013.
    <a href="https://doi.org/10.1038/nn.3346">https://doi.org/10.1038/nn.3346</a>.
  ieee: J. Levitz <i>et al.</i>, “Optical control of metabotropic glutamate receptors,”
    <i>Nature Neuroscience</i>, vol. 16. Nature Publishing Group, pp. 507–516, 2013.
  ista: Levitz J, Pantoja C, Gaub B, Janovjak HL, Reiner A, Hoagland A, Schoppik D,
    Kane B, Stawski P, Schier A, Trauner D, Isacoff E. 2013. Optical control of metabotropic
    glutamate receptors. Nature Neuroscience. 16, 507–516.
  mla: Levitz, Joshua, et al. “Optical Control of Metabotropic Glutamate Receptors.”
    <i>Nature Neuroscience</i>, vol. 16, Nature Publishing Group, 2013, pp. 507–16,
    doi:<a href="https://doi.org/10.1038/nn.3346">10.1038/nn.3346</a>.
  short: J. Levitz, C. Pantoja, B. Gaub, H.L. Janovjak, A. Reiner, A. Hoagland, D.
    Schoppik, B. Kane, P. Stawski, A. Schier, D. Trauner, E. Isacoff, Nature Neuroscience
    16 (2013) 507–516.
date_created: 2018-12-11T11:59:57Z
date_published: 2013-03-03T00:00:00Z
date_updated: 2025-09-29T13:39:33Z
day: '03'
department:
- _id: HaJa
doi: 10.1038/nn.3346
external_id:
  isi:
  - '000316723700023'
  pmid:
  - '23455609'
intvolume: '        16'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3681425/
month: '03'
oa: 1
oa_version: Submitted Version
page: 507 - 516
pmid: 1
publication: Nature Neuroscience
publication_status: published
publisher: Nature Publishing Group
publist_id: '3936'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Optical control of metabotropic glutamate receptors
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 16
year: '2013'
...
---
_id: '2857'
abstract:
- lang: eng
  text: In the vibrant field of optogenetics, optics and genetic targeting are combined
    to commandeer cellular functions, such as the neuronal action potential, by optically
    stimulating light-sensitive ion channels expressed in the cell membrane. One broadly
    applicable manifestation of this approach are covalently attached photochromic
    tethered ligands (PTLs) that allow activating ligand-gated ion channels with outstanding
    spatial and temporal resolution. Here, we describe all steps towards the successful
    development and application of PTL-gated ion channels in cell lines and primary
    cells. The basis for these experiments forms a combination of molecular modeling,
    genetic engineering, cell culture, and electrophysiology. The light-gated glutamate
    receptor (LiGluR), which consists of the PTL-functionalized GluK2 receptor, serves
    as a model.
alternative_title:
- MIMB
author:
- first_name: Stephanie
  full_name: Szobota, Stephanie
  last_name: Szobota
- first_name: Catherine
  full_name: Mckenzie, Catherine
  id: 3EEDE19A-F248-11E8-B48F-1D18A9856A87
  last_name: Mckenzie
- first_name: Harald L
  full_name: Janovjak, Harald L
  id: 33BA6C30-F248-11E8-B48F-1D18A9856A87
  last_name: Janovjak
  orcid: 0000-0002-8023-9315
citation:
  ama: Szobota S, Mckenzie C, Janovjak HL. Optical control of ligand-gated ion channels.
    <i>Methods in Molecular Biology</i>. 2013;998:417-435. doi:<a href="https://doi.org/10.1007/978-1-62703-351-0_32">10.1007/978-1-62703-351-0_32</a>
  apa: Szobota, S., Mckenzie, C., &#38; Janovjak, H. L. (2013). Optical control of
    ligand-gated ion channels. <i>Methods in Molecular Biology</i>. Springer. <a href="https://doi.org/10.1007/978-1-62703-351-0_32">https://doi.org/10.1007/978-1-62703-351-0_32</a>
  chicago: Szobota, Stephanie, Catherine Mckenzie, and Harald L Janovjak. “Optical
    Control of Ligand-Gated Ion Channels.” <i>Methods in Molecular Biology</i>. Springer,
    2013. <a href="https://doi.org/10.1007/978-1-62703-351-0_32">https://doi.org/10.1007/978-1-62703-351-0_32</a>.
  ieee: S. Szobota, C. Mckenzie, and H. L. Janovjak, “Optical control of ligand-gated
    ion channels,” <i>Methods in Molecular Biology</i>, vol. 998. Springer, pp. 417–435,
    2013.
  ista: Szobota S, Mckenzie C, Janovjak HL. 2013. Optical control of ligand-gated
    ion channels. Methods in Molecular Biology. 998, 417–435.
  mla: Szobota, Stephanie, et al. “Optical Control of Ligand-Gated Ion Channels.”
    <i>Methods in Molecular Biology</i>, vol. 998, Springer, 2013, pp. 417–35, doi:<a
    href="https://doi.org/10.1007/978-1-62703-351-0_32">10.1007/978-1-62703-351-0_32</a>.
  short: S. Szobota, C. Mckenzie, H.L. Janovjak, Methods in Molecular Biology 998
    (2013) 417–435.
date_created: 2018-12-11T11:59:57Z
date_published: 2013-02-22T00:00:00Z
date_updated: 2025-04-15T06:43:12Z
day: '22'
ddc:
- '570'
department:
- _id: HaJa
doi: 10.1007/978-1-62703-351-0_32
ec_funded: 1
file:
- access_level: open_access
  checksum: 1701f0d989f27ddac471b19a894ec0d1
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:12:34Z
  date_updated: 2020-07-14T12:45:51Z
  file_id: '4952'
  file_name: IST-2017-834-v1+1_szobota.pdf
  file_size: 336734
  relation: main_file
file_date_updated: 2020-07-14T12:45:51Z
has_accepted_license: '1'
intvolume: '       998'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Submitted Version
page: 417 - 435
project:
- _id: 255BFFFA-B435-11E9-9278-68D0E5697425
  grant_number: RGY0084/2012
  name: In situ real-time imaging of neurotransmitter signaling using designer optical
    sensors
- _id: 25548C20-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '303564'
  name: Microbial Ion Channels for Synthetic Neurobiology
publication: Methods in Molecular Biology
publication_status: published
publisher: Springer
publist_id: '3932'
pubrep_id: '834'
quality_controlled: '1'
scopus_import: 1
status: public
title: Optical control of ligand-gated ion channels
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 998
year: '2013'
...
---
_id: '2859'
abstract:
- lang: eng
  text: Given a continuous function f:X-R on a topological space, we consider the
    preimages of intervals and their homology groups and show how to read the ranks
    of these groups from the extended persistence diagram of f. In addition, we quantify
    the robustness of the homology classes under perturbations of f using well groups,
    and we show how to read the ranks of these groups from the same extended persistence
    diagram. The special case X=R3 has ramifications in the fields of medical imaging
    and scientific visualization.
article_processing_charge: No
arxiv: 1
author:
- first_name: Paul
  full_name: Bendich, Paul
  id: 43F6EC54-F248-11E8-B48F-1D18A9856A87
  last_name: Bendich
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
- first_name: Dmitriy
  full_name: Morozov, Dmitriy
  last_name: Morozov
- first_name: Amit
  full_name: Patel, Amit
  id: 34A254A0-F248-11E8-B48F-1D18A9856A87
  last_name: Patel
citation:
  ama: Bendich P, Edelsbrunner H, Morozov D, Patel A. Homology and robustness of level
    and interlevel sets. <i>Homology, Homotopy and Applications</i>. 2013;15(1):51-72.
    doi:<a href="https://doi.org/10.4310/HHA.2013.v15.n1.a3">10.4310/HHA.2013.v15.n1.a3</a>
  apa: Bendich, P., Edelsbrunner, H., Morozov, D., &#38; Patel, A. (2013). Homology
    and robustness of level and interlevel sets. <i>Homology, Homotopy and Applications</i>.
    International Press. <a href="https://doi.org/10.4310/HHA.2013.v15.n1.a3">https://doi.org/10.4310/HHA.2013.v15.n1.a3</a>
  chicago: Bendich, Paul, Herbert Edelsbrunner, Dmitriy Morozov, and Amit Patel. “Homology
    and Robustness of Level and Interlevel Sets.” <i>Homology, Homotopy and Applications</i>.
    International Press, 2013. <a href="https://doi.org/10.4310/HHA.2013.v15.n1.a3">https://doi.org/10.4310/HHA.2013.v15.n1.a3</a>.
  ieee: P. Bendich, H. Edelsbrunner, D. Morozov, and A. Patel, “Homology and robustness
    of level and interlevel sets,” <i>Homology, Homotopy and Applications</i>, vol.
    15, no. 1. International Press, pp. 51–72, 2013.
  ista: Bendich P, Edelsbrunner H, Morozov D, Patel A. 2013. Homology and robustness
    of level and interlevel sets. Homology, Homotopy and Applications. 15(1), 51–72.
  mla: Bendich, Paul, et al. “Homology and Robustness of Level and Interlevel Sets.”
    <i>Homology, Homotopy and Applications</i>, vol. 15, no. 1, International Press,
    2013, pp. 51–72, doi:<a href="https://doi.org/10.4310/HHA.2013.v15.n1.a3">10.4310/HHA.2013.v15.n1.a3</a>.
  short: P. Bendich, H. Edelsbrunner, D. Morozov, A. Patel, Homology, Homotopy and
    Applications 15 (2013) 51–72.
date_created: 2018-12-11T11:59:58Z
date_published: 2013-05-01T00:00:00Z
date_updated: 2025-09-29T13:38:09Z
day: '01'
department:
- _id: HeEd
doi: 10.4310/HHA.2013.v15.n1.a3
external_id:
  arxiv:
  - '1102.3389'
  isi:
  - '000322423600003'
intvolume: '        15'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1102.3389v1
month: '05'
oa: 1
oa_version: Preprint
page: 51 - 72
publication: Homology, Homotopy and Applications
publication_status: published
publisher: International Press
publist_id: '3930'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Homology and robustness of level and interlevel sets
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 15
year: '2013'
...
---
_id: '2860'
abstract:
- lang: eng
  text: 'In the hippocampus, cell assemblies forming mnemonic representations of space
    are thought to arise as a result of changes in functional connections of pyramidal
    cells. We have found that CA1 interneuron circuits are also reconfigured during
    goal-oriented spatial learning through modification of inputs from pyramidal cells.
    As learning progressed, new pyramidal assemblies expressed in theta cycles alternated
    with previously established ones, and eventually overtook them. The firing patterns
    of interneurons developed a relationship to new, learning-related assemblies:
    some interneurons associated their activity with new pyramidal assemblies while
    some others dissociated from them. These firing associations were explained by
    changes in the weight of monosynaptic inputs received by interneurons from new
    pyramidal assemblies, as these predicted the associational changes. Spatial learning
    thus engages circuit modifications in the hippocampus that incorporate a redistribution
    of inhibitory activity that might assist in the segregation of competing pyramidal
    cell assembly patterns in space and time.'
acknowledgement: D.D. and J.C. were supported by a MRC Intramural Programme Grant
  U138197111
article_processing_charge: No
author:
- first_name: David
  full_name: Dupret, David
  last_name: Dupret
- first_name: Joseph
  full_name: O'Neill, Joseph
  id: 426376DC-F248-11E8-B48F-1D18A9856A87
  last_name: O'Neill
- 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: Dupret D, O’Neill J, Csicsvari JL. Dynamic reconfiguration of hippocampal interneuron
    circuits during spatial learning. <i>Neuron</i>. 2013;78(1):166-180. doi:<a href="https://doi.org/10.1016/j.neuron.2013.01.033">10.1016/j.neuron.2013.01.033</a>
  apa: Dupret, D., O’Neill, J., &#38; Csicsvari, J. L. (2013). Dynamic reconfiguration
    of hippocampal interneuron circuits during spatial learning. <i>Neuron</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.neuron.2013.01.033">https://doi.org/10.1016/j.neuron.2013.01.033</a>
  chicago: Dupret, David, Joseph O’Neill, and Jozsef L Csicsvari. “Dynamic Reconfiguration
    of Hippocampal Interneuron Circuits during Spatial Learning.” <i>Neuron</i>. Elsevier,
    2013. <a href="https://doi.org/10.1016/j.neuron.2013.01.033">https://doi.org/10.1016/j.neuron.2013.01.033</a>.
  ieee: D. Dupret, J. O’Neill, and J. L. Csicsvari, “Dynamic reconfiguration of hippocampal
    interneuron circuits during spatial learning,” <i>Neuron</i>, vol. 78, no. 1.
    Elsevier, pp. 166–180, 2013.
  ista: Dupret D, O’Neill J, Csicsvari JL. 2013. Dynamic reconfiguration of hippocampal
    interneuron circuits during spatial learning. Neuron. 78(1), 166–180.
  mla: Dupret, David, et al. “Dynamic Reconfiguration of Hippocampal Interneuron Circuits
    during Spatial Learning.” <i>Neuron</i>, vol. 78, no. 1, Elsevier, 2013, pp. 166–80,
    doi:<a href="https://doi.org/10.1016/j.neuron.2013.01.033">10.1016/j.neuron.2013.01.033</a>.
  short: D. Dupret, J. O’Neill, J.L. Csicsvari, Neuron 78 (2013) 166–180.
corr_author: '1'
date_created: 2018-12-11T11:59:59Z
date_published: 2013-03-21T00:00:00Z
date_updated: 2025-09-29T13:37:37Z
day: '21'
ddc:
- '570'
department:
- _id: JoCs
doi: 10.1016/j.neuron.2013.01.033
ec_funded: 1
external_id:
  isi:
  - '000317556000015'
file:
- access_level: open_access
  checksum: 0e18cb8561153ddb50bb5af16e7c9e97
  content_type: application/pdf
  creator: dernst
  date_created: 2019-01-23T08:08:07Z
  date_updated: 2020-07-14T12:45:52Z
  file_id: '5877'
  file_name: 2013_Neuron_Dupret.pdf
  file_size: 2637837
  relation: main_file
file_date_updated: 2020-07-14T12:45:52Z
has_accepted_license: '1'
intvolume: '        78'
isi: 1
issue: '1'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 166 - 180
project:
- _id: 257A4776-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '281511'
  name: Memory-related information processing in neuronal circuits of the hippocampus
    and entorhinal cortex
publication: Neuron
publication_status: published
publisher: Elsevier
publist_id: '3929'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Dynamic reconfiguration of hippocampal interneuron circuits during spatial
  learning
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 78
year: '2013'
...
---
_id: '2861'
abstract:
- lang: eng
  text: We consider a two-parameter family of piecewise linear maps in which the moduli
    of the two slopes take different values. We provide numerical evidence of the
    existence of some parameter regions in which the Lyapunov exponent and the topological
    entropy remain constant. Analytical proof of this phenomenon is also given for
    certain cases. Surprisingly however, the systems with that property are not conjugate
    as we prove by using kneading theory.
article_number: '125101'
article_processing_charge: No
author:
- first_name: Vicente
  full_name: Botella Soler, Vicente
  id: 421234E8-F248-11E8-B48F-1D18A9856A87
  last_name: Botella Soler
  orcid: 0000-0002-8790-1914
- first_name: José
  full_name: Oteo, José
  last_name: Oteo
- first_name: Javier
  full_name: Ros, Javier
  last_name: Ros
- first_name: Paul
  full_name: Glendinning, Paul
  last_name: Glendinning
citation:
  ama: 'Botella Soler V, Oteo J, Ros J, Glendinning P. Lyapunov exponent and topological
    entropy plateaus in piecewise linear maps. <i>Journal of Physics A: Mathematical
    and Theoretical</i>. 2013;46(12). doi:<a href="https://doi.org/10.1088/1751-8113/46/12/125101">10.1088/1751-8113/46/12/125101</a>'
  apa: 'Botella Soler, V., Oteo, J., Ros, J., &#38; Glendinning, P. (2013). Lyapunov
    exponent and topological entropy plateaus in piecewise linear maps. <i>Journal
    of Physics A: Mathematical and Theoretical</i>. IOP Publishing. <a href="https://doi.org/10.1088/1751-8113/46/12/125101">https://doi.org/10.1088/1751-8113/46/12/125101</a>'
  chicago: 'Botella Soler, Vicente, José Oteo, Javier Ros, and Paul Glendinning. “Lyapunov
    Exponent and Topological Entropy Plateaus in Piecewise Linear Maps.” <i>Journal
    of Physics A: Mathematical and Theoretical</i>. IOP Publishing, 2013. <a href="https://doi.org/10.1088/1751-8113/46/12/125101">https://doi.org/10.1088/1751-8113/46/12/125101</a>.'
  ieee: 'V. Botella Soler, J. Oteo, J. Ros, and P. Glendinning, “Lyapunov exponent
    and topological entropy plateaus in piecewise linear maps,” <i>Journal of Physics
    A: Mathematical and Theoretical</i>, vol. 46, no. 12. IOP Publishing, 2013.'
  ista: 'Botella Soler V, Oteo J, Ros J, Glendinning P. 2013. Lyapunov exponent and
    topological entropy plateaus in piecewise linear maps. Journal of Physics A: Mathematical
    and Theoretical. 46(12), 125101.'
  mla: 'Botella Soler, Vicente, et al. “Lyapunov Exponent and Topological Entropy
    Plateaus in Piecewise Linear Maps.” <i>Journal of Physics A: Mathematical and
    Theoretical</i>, vol. 46, no. 12, 125101, IOP Publishing, 2013, doi:<a href="https://doi.org/10.1088/1751-8113/46/12/125101">10.1088/1751-8113/46/12/125101</a>.'
  short: 'V. Botella Soler, J. Oteo, J. Ros, P. Glendinning, Journal of Physics A:
    Mathematical and Theoretical 46 (2013).'
corr_author: '1'
date_created: 2018-12-11T11:59:59Z
date_published: 2013-03-29T00:00:00Z
date_updated: 2025-09-29T13:36:56Z
day: '29'
department:
- _id: GaTk
doi: 10.1088/1751-8113/46/12/125101
external_id:
  isi:
  - '000316058200010'
intvolume: '        46'
isi: 1
issue: '12'
language:
- iso: eng
month: '03'
oa_version: None
publication: 'Journal of Physics A: Mathematical and Theoretical'
publication_status: published
publisher: IOP Publishing
publist_id: '3928'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Lyapunov exponent and topological entropy plateaus in piecewise linear maps
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 46
year: '2013'
...
---
_id: '2862'
abstract:
- lang: eng
  text: Motile cilia perform crucial functions during embryonic development and throughout
    adult life. Development of organs containing motile cilia involves regulation
    of cilia formation (ciliogenesis) and formation of a luminal space (lumenogenesis)
    in which cilia generate fluid flows. Control of ciliogenesis and lumenogenesis
    is not yet fully understood, and it remains unclear whether these processes are
    coupled. In the zebrafish embryo, lethal giant larvae 2 (lgl2) is expressed prominently
    in ciliated organs. Lgl proteins are involved in establishing cell polarity and
    have been implicated in vesicle trafficking. Here, we identified a role for Lgl2
    in development of ciliated epithelia in Kupffer's vesicle, which directs left-right
    asymmetry of the embryo; the otic vesicles, which give rise to the inner ear;
    and the pronephric ducts of the kidney. Using Kupffer's vesicle as a model ciliated
    organ, we found that depletion of Lgl2 disrupted lumen formation and reduced cilia
    number and length. Immunofluorescence and time-lapse imaging of Kupffer's vesicle
    morphogenesis in Lgl2-deficient embryos suggested cell adhesion defects and revealed
    loss of the adherens junction component E-cadherin at lateral membranes. Genetic
    interaction experiments indicate that Lgl2 interacts with Rab11a to regulate E-cadherin
    and mediate lumen formation that is uncoupled from cilia formation. These results
    uncover new roles and interactions for Lgl2 that are crucial for both lumenogenesis
    and ciliogenesis and indicate that these processes are genetically separable in
    zebrafish.
acknowledgement: Deposited in PMC for release after 12 months. We thank members of
  the Amack lab for helpful discussions and Mahendra Sonawane for donating reagents.
article_processing_charge: No
author:
- first_name: Hwee
  full_name: Tay, Hwee
  last_name: Tay
- first_name: Sabrina
  full_name: Schulze, Sabrina
  last_name: Schulze
- first_name: Julien
  full_name: Compagnon, Julien
  id: 2E3E0988-F248-11E8-B48F-1D18A9856A87
  last_name: Compagnon
- first_name: Fiona
  full_name: Foley, Fiona
  last_name: Foley
- first_name: Carl-Philipp J
  full_name: Heisenberg, Carl-Philipp J
  id: 39427864-F248-11E8-B48F-1D18A9856A87
  last_name: Heisenberg
  orcid: 0000-0002-0912-4566
- first_name: H Joseph
  full_name: Yost, H Joseph
  last_name: Yost
- first_name: Salim
  full_name: Abdelilah Seyfried, Salim
  last_name: Abdelilah Seyfried
- first_name: Jeffrey
  full_name: Amack, Jeffrey
  last_name: Amack
citation:
  ama: Tay H, Schulze S, Compagnon J, et al. Lethal giant larvae 2 regulates development
    of the ciliated organ Kupffer’s vesicle. <i>Development</i>. 2013;140(7):1550-1559.
    doi:<a href="https://doi.org/10.1242/dev.087130">10.1242/dev.087130</a>
  apa: Tay, H., Schulze, S., Compagnon, J., Foley, F., Heisenberg, C.-P. J., Yost,
    H. J., … Amack, J. (2013). Lethal giant larvae 2 regulates development of the
    ciliated organ Kupffer’s vesicle. <i>Development</i>. Company of Biologists. <a
    href="https://doi.org/10.1242/dev.087130">https://doi.org/10.1242/dev.087130</a>
  chicago: Tay, Hwee, Sabrina Schulze, Julien Compagnon, Fiona Foley, Carl-Philipp
    J Heisenberg, H Joseph Yost, Salim Abdelilah Seyfried, and Jeffrey Amack. “Lethal
    Giant Larvae 2 Regulates Development of the Ciliated Organ Kupffer’s Vesicle.”
    <i>Development</i>. Company of Biologists, 2013. <a href="https://doi.org/10.1242/dev.087130">https://doi.org/10.1242/dev.087130</a>.
  ieee: H. Tay <i>et al.</i>, “Lethal giant larvae 2 regulates development of the
    ciliated organ Kupffer’s vesicle,” <i>Development</i>, vol. 140, no. 7. Company
    of Biologists, pp. 1550–1559, 2013.
  ista: Tay H, Schulze S, Compagnon J, Foley F, Heisenberg C-PJ, Yost HJ, Abdelilah
    Seyfried S, Amack J. 2013. Lethal giant larvae 2 regulates development of the
    ciliated organ Kupffer’s vesicle. Development. 140(7), 1550–1559.
  mla: Tay, Hwee, et al. “Lethal Giant Larvae 2 Regulates Development of the Ciliated
    Organ Kupffer’s Vesicle.” <i>Development</i>, vol. 140, no. 7, Company of Biologists,
    2013, pp. 1550–59, doi:<a href="https://doi.org/10.1242/dev.087130">10.1242/dev.087130</a>.
  short: H. Tay, S. Schulze, J. Compagnon, F. Foley, C.-P.J. Heisenberg, H.J. Yost,
    S. Abdelilah Seyfried, J. Amack, Development 140 (2013) 1550–1559.
date_created: 2018-12-11T11:59:59Z
date_published: 2013-04-01T00:00:00Z
date_updated: 2025-09-29T13:36:20Z
day: '01'
department:
- _id: CaHe
doi: 10.1242/dev.087130
external_id:
  isi:
  - '000316096400018'
  pmid:
  - '23482490'
intvolume: '       140'
isi: 1
issue: '7'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596994/
month: '04'
oa: 1
oa_version: Submitted Version
page: 1550 - 1559
pmid: 1
publication: Development
publication_status: published
publisher: Company of Biologists
publist_id: '3927'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Lethal giant larvae 2 regulates development of the ciliated organ Kupffer’s
  vesicle
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 140
year: '2013'
...
