---
_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).
date_created: 2018-12-11T11:59:56Z
date_published: 2013-05-22T00:00:00Z
date_updated: 2023-10-18T06:43:23Z
day: '22'
department:
- _id: CaGu
doi: 10.1098/rspb.2012.3035
external_id:
  pmid:
  - '23516238'
intvolume: '       280'
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
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.
date_created: 2018-12-11T11:59:57Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2021-01-12T07:00:16Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
- _id: ToHe
doi: 10.1016/j.jcss.2012.12.001
ec_funded: 1
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'
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
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.
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.
date_created: 2018-12-11T11:59:57Z
date_published: 2013-03-28T00:00:00Z
date_updated: 2021-01-12T07:00:16Z
day: '28'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.1016/j.celrep.2013.02.002
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'
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
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.)
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: 2021-01-12T07:00:16Z
day: '03'
department:
- _id: HaJa
doi: 10.1038/nn.3346
external_id:
  pmid:
  - '23455609'
intvolume: '        16'
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
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: 2021-01-12T07:00:17Z
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
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  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
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  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 (HFSP Young Investigator)
- _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: '2858'
abstract:
- lang: eng
  text: Tumor growth is caused by the acquisition of driver mutations, which enhance
    the net reproductive rate of cells. Driver mutations may increase cell division,
    reduce cell death, or allow cells to overcome density-limiting effects. We study
    the dynamics of tumor growth as one additional driver mutation is acquired. Our
    models are based on two-type branching processes that terminate in either tumor
    disappearance or tumor detection. In our first model, both cell types grow exponentially,
    with a faster rate for cells carrying the additional driver. We find that the
    additional driver mutation does not affect the survival probability of the lesion,
    but can substantially reduce the time to reach the detectable size if the lesion
    is slow growing. In our second model, cells lacking the additional driver cannot
    exceed a fixed carrying capacity, due to density limitations. In this case, the
    time to detection depends strongly on this carrying capacity. Our model provides
    a quantitative framework for studying tumor dynamics during different stages of
    progression. We observe that early, small lesions need additional drivers, while
    late stage metastases are only marginally affected by them. These results help
    to explain why additional driver mutations are typically not detected in fast-growing
    metastases.
author:
- first_name: Johannes
  full_name: Reiter, Johannes
  id: 4A918E98-F248-11E8-B48F-1D18A9856A87
  last_name: Reiter
  orcid: 0000-0002-0170-7353
- first_name: Ivana
  full_name: Božić, Ivana
  last_name: Božić
- first_name: Benjamin
  full_name: Allen, Benjamin
  id: 135B5B70-E9D2-11E9-BD74-BB415DA2B523
  last_name: Allen
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Martin
  full_name: Nowak, Martin
  last_name: Nowak
citation:
  ama: Reiter J, Božić I, Allen B, Chatterjee K, Nowak M. The effect of one additional
    driver mutation on tumor progression. <i>Evolutionary Applications</i>. 2013;6(1):34-45.
    doi:<a href="https://doi.org/10.1111/eva.12020">10.1111/eva.12020</a>
  apa: Reiter, J., Božić, I., Allen, B., Chatterjee, K., &#38; Nowak, M. (2013). The
    effect of one additional driver mutation on tumor progression. <i>Evolutionary
    Applications</i>. Wiley-Blackwell. <a href="https://doi.org/10.1111/eva.12020">https://doi.org/10.1111/eva.12020</a>
  chicago: Reiter, Johannes, Ivana Božić, Benjamin Allen, Krishnendu Chatterjee, and
    Martin Nowak. “The Effect of One Additional Driver Mutation on Tumor Progression.”
    <i>Evolutionary Applications</i>. Wiley-Blackwell, 2013. <a href="https://doi.org/10.1111/eva.12020">https://doi.org/10.1111/eva.12020</a>.
  ieee: J. Reiter, I. Božić, B. Allen, K. Chatterjee, and M. Nowak, “The effect of
    one additional driver mutation on tumor progression,” <i>Evolutionary Applications</i>,
    vol. 6, no. 1. Wiley-Blackwell, pp. 34–45, 2013.
  ista: Reiter J, Božić I, Allen B, Chatterjee K, Nowak M. 2013. The effect of one
    additional driver mutation on tumor progression. Evolutionary Applications. 6(1),
    34–45.
  mla: Reiter, Johannes, et al. “The Effect of One Additional Driver Mutation on Tumor
    Progression.” <i>Evolutionary Applications</i>, vol. 6, no. 1, Wiley-Blackwell,
    2013, pp. 34–45, doi:<a href="https://doi.org/10.1111/eva.12020">10.1111/eva.12020</a>.
  short: J. Reiter, I. Božić, B. Allen, K. Chatterjee, M. Nowak, Evolutionary Applications
    6 (2013) 34–45.
date_created: 2018-12-11T11:59:58Z
date_published: 2013-01-01T00:00:00Z
date_updated: 2023-09-07T11:40:43Z
day: '01'
ddc:
- '570'
department:
- _id: KrCh
doi: 10.1111/eva.12020
ec_funded: 1
file:
- access_level: open_access
  checksum: e2955b3889f8a823c3d5a72cb16f8957
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:15:50Z
  date_updated: 2020-07-14T12:45:51Z
  file_id: '5173'
  file_name: IST-2016-415-v1+1_Reiter_et_al-2013-Evolutionary_Applications.pdf
  file_size: 1172037
  relation: main_file
file_date_updated: 2020-07-14T12:45:51Z
has_accepted_license: '1'
intvolume: '         6'
issue: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '01'
oa: 1
oa_version: Published Version
page: 34 - 45
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
publication: Evolutionary Applications
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3931'
pubrep_id: '415'
quality_controlled: '1'
related_material:
  record:
  - id: '1400'
    relation: dissertation_contains
    status: public
scopus_import: 1
status: public
title: The effect of one additional driver mutation on tumor progression
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 6
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.
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: 2021-01-12T07:00:18Z
day: '01'
department:
- _id: HeEd
doi: 10.4310/HHA.2013.v15.n1.a3
external_id:
  arxiv:
  - '1102.3389'
intvolume: '        15'
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
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
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.
date_created: 2018-12-11T11:59:59Z
date_published: 2013-03-21T00:00:00Z
date_updated: 2021-01-12T07:00:19Z
day: '21'
ddc:
- '570'
department:
- _id: JoCs
doi: 10.1016/j.neuron.2013.01.033
ec_funded: 1
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'
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
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'
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 Ltd. <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 Ltd., 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 Ltd., 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 Ltd., 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).'
date_created: 2018-12-11T11:59:59Z
date_published: 2013-03-29T00:00:00Z
date_updated: 2021-01-12T07:00:19Z
day: '29'
department:
- _id: GaTk
doi: 10.1088/1751-8113/46/12/125101
intvolume: '        46'
issue: '12'
language:
- iso: eng
month: '03'
oa_version: None
publication: 'Journal of Physics A: Mathematical and Theoretical'
publication_status: published
publisher: IOP Publishing Ltd.
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: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
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.
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: 2021-01-12T07:00:20Z
day: '01'
department:
- _id: CaHe
doi: 10.1242/dev.087130
external_id:
  pmid:
  - '23482490'
intvolume: '       140'
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: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 140
year: '2013'
...
---
_id: '2863'
abstract:
- lang: eng
  text: Neural populations encode information about their stimulus in a collective
    fashion, by joint activity patterns of spiking and silence. A full account of
    this mapping from stimulus to neural activity is given by the conditional probability
    distribution over neural codewords given the sensory input. For large populations,
    direct sampling of these distributions is impossible, and so we must rely on constructing
    appropriate models. We show here that in a population of 100 retinal ganglion
    cells in the salamander retina responding to temporal white-noise stimuli, dependencies
    between cells play an important encoding role. We introduce the stimulus-dependent
    maximum entropy (SDME) model—a minimal extension of the canonical linear-nonlinear
    model of a single neuron, to a pairwise-coupled neural population. We find that
    the SDME model gives a more accurate account of single cell responses and in particular
    significantly outperforms uncoupled models in reproducing the distributions of
    population codewords emitted in response to a stimulus. We show how the SDME model,
    in conjunction with static maximum entropy models of population vocabulary, can
    be used to estimate information-theoretic quantities like average surprise and
    information transmission in a neural population.
article_number: e1002922
author:
- first_name: Einat
  full_name: Granot Atedgi, Einat
  last_name: Granot Atedgi
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
- first_name: Ronen
  full_name: Segev, Ronen
  last_name: Segev
- first_name: Elad
  full_name: Schneidman, Elad
  last_name: Schneidman
citation:
  ama: Granot Atedgi E, Tkačik G, Segev R, Schneidman E. Stimulus-dependent maximum
    entropy models of neural population codes. <i>PLoS Computational Biology</i>.
    2013;9(3). doi:<a href="https://doi.org/10.1371/journal.pcbi.1002922">10.1371/journal.pcbi.1002922</a>
  apa: Granot Atedgi, E., Tkačik, G., Segev, R., &#38; Schneidman, E. (2013). Stimulus-dependent
    maximum entropy models of neural population codes. <i>PLoS Computational Biology</i>.
    Public Library of Science. <a href="https://doi.org/10.1371/journal.pcbi.1002922">https://doi.org/10.1371/journal.pcbi.1002922</a>
  chicago: Granot Atedgi, Einat, Gašper Tkačik, Ronen Segev, and Elad Schneidman.
    “Stimulus-Dependent Maximum Entropy Models of Neural Population Codes.” <i>PLoS
    Computational Biology</i>. Public Library of Science, 2013. <a href="https://doi.org/10.1371/journal.pcbi.1002922">https://doi.org/10.1371/journal.pcbi.1002922</a>.
  ieee: E. Granot Atedgi, G. Tkačik, R. Segev, and E. Schneidman, “Stimulus-dependent
    maximum entropy models of neural population codes,” <i>PLoS Computational Biology</i>,
    vol. 9, no. 3. Public Library of Science, 2013.
  ista: Granot Atedgi E, Tkačik G, Segev R, Schneidman E. 2013. Stimulus-dependent
    maximum entropy models of neural population codes. PLoS Computational Biology.
    9(3), e1002922.
  mla: Granot Atedgi, Einat, et al. “Stimulus-Dependent Maximum Entropy Models of
    Neural Population Codes.” <i>PLoS Computational Biology</i>, vol. 9, no. 3, e1002922,
    Public Library of Science, 2013, doi:<a href="https://doi.org/10.1371/journal.pcbi.1002922">10.1371/journal.pcbi.1002922</a>.
  short: E. Granot Atedgi, G. Tkačik, R. Segev, E. Schneidman, PLoS Computational
    Biology 9 (2013).
date_created: 2018-12-11T12:00:00Z
date_published: 2013-03-01T00:00:00Z
date_updated: 2021-01-12T07:00:20Z
day: '01'
ddc:
- '570'
department:
- _id: GaTk
doi: 10.1371/journal.pcbi.1002922
file:
- access_level: open_access
  checksum: 5a30876c193209fa05b26db71845dd16
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:14:45Z
  date_updated: 2020-07-14T12:45:52Z
  file_id: '5099'
  file_name: IST-2013-120-v1+1_journal.pcbi.1002922.pdf
  file_size: 1548120
  relation: main_file
file_date_updated: 2020-07-14T12:45:52Z
has_accepted_license: '1'
intvolume: '         9'
issue: '3'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
publication: PLoS Computational Biology
publication_status: published
publisher: Public Library of Science
publist_id: '3926'
pubrep_id: '120'
quality_controlled: '1'
scopus_import: 1
status: public
title: Stimulus-dependent maximum entropy models of neural population codes
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 9
year: '2013'
...
---
_id: '2877'
abstract:
- lang: eng
  text: 'Premise of the study: To reach favorable conditions for photosynthesis, seedlings
    grow upward when deprived of light upon underground germination. To direct their
    growth, they use their negative gravitropic capacity. Negative gravitropism is
    under tight control of multiple hormones. • Methods: By counting the number of
    standing plants in a population or by real time monitoring of the reorientation
    of gravistimulated seedlings of Arabidopsis thaliana, we evaluated the negative
    gravitropism of ethylene or brassinosteroid (BR) treated plants. Meta-analysis
    of transcriptomic data on AUX / IAA genes was gathered, and subsequent mutant
    analysis was performed. • Key results: Ethylene and BR have opposite effects in
    regulating shoot gravitropism. Lack of BR enhances gravitropic reorientation in
    2-d-old seedlings, whereas ethylene does not. Lack of ethylene signaling results
    in enhanced BR sensitivity. Ethylene and BRs regulate overlapping sets of AUX
    / IAA genes. BRs regulate a wider range of auxin signaling components than ethylene.
    • Conclusions: Upward growth in seedlings depends strongly on the internal hormonal
    balance. Endogenous ethylene stimulates, whereas BRs reduce negative gravitropism
    in a manner that depends on the function of different, yet overlapping sets of
    auxin signaling components.'
author:
- first_name: Filip
  full_name: Vandenbussche, Filip
  last_name: Vandenbussche
- first_name: Pieter
  full_name: Callebert, Pieter
  last_name: Callebert
- first_name: Petra
  full_name: Žádníková, Petra
  last_name: Žádníková
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Dominique
  full_name: Van Der Straeten, Dominique
  last_name: Van Der Straeten
citation:
  ama: Vandenbussche F, Callebert P, Žádníková P, Benková E, Van Der Straeten D. Brassinosteroid
    control of shoot gravitropism interacts with ethylene and depends on auxin signaling
    components. <i>American Journal of Botany</i>. 2013;100(1):215-225. doi:<a href="https://doi.org/10.3732/ajb.1200264">10.3732/ajb.1200264</a>
  apa: Vandenbussche, F., Callebert, P., Žádníková, P., Benková, E., &#38; Van Der
    Straeten, D. (2013). Brassinosteroid control of shoot gravitropism interacts with
    ethylene and depends on auxin signaling components. <i>American Journal of Botany</i>.
    Botanical Society of America. <a href="https://doi.org/10.3732/ajb.1200264">https://doi.org/10.3732/ajb.1200264</a>
  chicago: Vandenbussche, Filip, Pieter Callebert, Petra Žádníková, Eva Benková, and
    Dominique Van Der Straeten. “Brassinosteroid Control of Shoot Gravitropism Interacts
    with Ethylene and Depends on Auxin Signaling Components.” <i>American Journal
    of Botany</i>. Botanical Society of America, 2013. <a href="https://doi.org/10.3732/ajb.1200264">https://doi.org/10.3732/ajb.1200264</a>.
  ieee: F. Vandenbussche, P. Callebert, P. Žádníková, E. Benková, and D. Van Der Straeten,
    “Brassinosteroid control of shoot gravitropism interacts with ethylene and depends
    on auxin signaling components,” <i>American Journal of Botany</i>, vol. 100, no.
    1. Botanical Society of America, pp. 215–225, 2013.
  ista: Vandenbussche F, Callebert P, Žádníková P, Benková E, Van Der Straeten D.
    2013. Brassinosteroid control of shoot gravitropism interacts with ethylene and
    depends on auxin signaling components. American Journal of Botany. 100(1), 215–225.
  mla: Vandenbussche, Filip, et al. “Brassinosteroid Control of Shoot Gravitropism
    Interacts with Ethylene and Depends on Auxin Signaling Components.” <i>American
    Journal of Botany</i>, vol. 100, no. 1, Botanical Society of America, 2013, pp.
    215–25, doi:<a href="https://doi.org/10.3732/ajb.1200264">10.3732/ajb.1200264</a>.
  short: F. Vandenbussche, P. Callebert, P. Žádníková, E. Benková, D. Van Der Straeten,
    American Journal of Botany 100 (2013) 215–225.
date_created: 2018-12-11T12:00:06Z
date_published: 2013-01-01T00:00:00Z
date_updated: 2021-01-12T07:00:25Z
day: '01'
doi: 10.3732/ajb.1200264
extern: 1
intvolume: '       100'
issue: '1'
month: '01'
page: 215 - 225
publication: American Journal of Botany
publication_status: published
publisher: Botanical Society of America
publist_id: '3883'
quality_controlled: 0
status: public
title: Brassinosteroid control of shoot gravitropism interacts with ethylene and depends
  on auxin signaling components
type: journal_article
volume: 100
year: '2013'
...
---
_id: '2880'
abstract:
- lang: eng
  text: Lateral root (LR) formation is initiated when pericycle cells accumulate auxin,
    thereby acquiring founder cell (FC) status and triggering asymmetric cell divisions,
    giving rise to a new primordium. How this auxin maximum in pericycle cells builds
    up and remains focused is not understood. We report that the endodermis plays
    an active role in the regulation of auxin accumulation and is instructive for
    FCs to progress during the LR initiation (LRI) phase. We describe the functional
    importance of a PIN3 (PIN-formed) auxin efflux carrier-dependent hormone reflux
    pathway between overlaying endodermal and pericycle FCs. Disrupting this reflux
    pathway causes dramatic defects in the progress of FCs towards the next initiation
    phase. Our data identify an unexpected regulatory function for the endodermis
    in LRI as part of the fine-tuning mechanism that appears to act as a check point
    in LR organogenesis after FCs are specified.
author:
- first_name: Peter
  full_name: Marhavy, Peter
  id: 3F45B078-F248-11E8-B48F-1D18A9856A87
  last_name: Marhavy
  orcid: 0000-0001-5227-5741
- first_name: Marleen
  full_name: Vanstraelen, Marleen
  last_name: Vanstraelen
- first_name: Bert
  full_name: De Rybel, Bert
  last_name: De Rybel
- first_name: Ding
  full_name: Zhaojun, Ding
  last_name: Zhaojun
- first_name: Malcolm
  full_name: Bennett, Malcolm
  last_name: Bennett
- first_name: Tom
  full_name: Beeckman, Tom
  last_name: Beeckman
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
citation:
  ama: Marhavý P, Vanstraelen M, De Rybel B, et al. Auxin reflux between the endodermis
    and pericycle promotes lateral root initiation. <i>EMBO Journal</i>. 2013;32(1):149-158.
    doi:<a href="https://doi.org/10.1038/emboj.2012.303">10.1038/emboj.2012.303</a>
  apa: Marhavý, P., Vanstraelen, M., De Rybel, B., Zhaojun, D., Bennett, M., Beeckman,
    T., &#38; Benková, E. (2013). Auxin reflux between the endodermis and pericycle
    promotes lateral root initiation. <i>EMBO Journal</i>. Wiley-Blackwell. <a href="https://doi.org/10.1038/emboj.2012.303">https://doi.org/10.1038/emboj.2012.303</a>
  chicago: Marhavý, Peter, Marleen Vanstraelen, Bert De Rybel, Ding Zhaojun, Malcolm
    Bennett, Tom Beeckman, and Eva Benková. “Auxin Reflux between the Endodermis and
    Pericycle Promotes Lateral Root Initiation.” <i>EMBO Journal</i>. Wiley-Blackwell,
    2013. <a href="https://doi.org/10.1038/emboj.2012.303">https://doi.org/10.1038/emboj.2012.303</a>.
  ieee: P. Marhavý <i>et al.</i>, “Auxin reflux between the endodermis and pericycle
    promotes lateral root initiation,” <i>EMBO Journal</i>, vol. 32, no. 1. Wiley-Blackwell,
    pp. 149–158, 2013.
  ista: Marhavý P, Vanstraelen M, De Rybel B, Zhaojun D, Bennett M, Beeckman T, Benková
    E. 2013. Auxin reflux between the endodermis and pericycle promotes lateral root
    initiation. EMBO Journal. 32(1), 149–158.
  mla: Marhavý, Peter, et al. “Auxin Reflux between the Endodermis and Pericycle Promotes
    Lateral Root Initiation.” <i>EMBO Journal</i>, vol. 32, no. 1, Wiley-Blackwell,
    2013, pp. 149–58, doi:<a href="https://doi.org/10.1038/emboj.2012.303">10.1038/emboj.2012.303</a>.
  short: P. Marhavý, M. Vanstraelen, B. De Rybel, D. Zhaojun, M. Bennett, T. Beeckman,
    E. Benková, EMBO Journal 32 (2013) 149–158.
date_created: 2018-12-11T12:00:07Z
date_published: 2013-01-09T00:00:00Z
date_updated: 2021-01-12T07:00:27Z
day: '09'
department:
- _id: EvBe
doi: 10.1038/emboj.2012.303
ec_funded: 1
external_id:
  pmid:
  - '23178590'
intvolume: '        32'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3545298/
month: '01'
oa: 1
oa_version: Submitted Version
page: 149 - 158
pmid: 1
project:
- _id: 253FCA6A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '207362'
  name: Hormonal cross-talk in plant organogenesis
publication: EMBO Journal
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3882'
quality_controlled: '1'
scopus_import: 1
status: public
title: Auxin reflux between the endodermis and pericycle promotes lateral root initiation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 32
year: '2013'
...
---
_id: '2881'
abstract:
- lang: eng
  text: The puzzle piece-shaped Arabidopsis leaf pavement cells (PCs) with interdigitated
    lobes and indents is a good model system to investigate the mechanisms that coordinate
    cell polarity and shape formation within a tissue. Auxin has been shown to coordinate
    the interdigitation by activating ROP GTPase-dependent signaling pathways. To
    identify additional components or mechanisms, we screened for mutants with abnormal
    PC morphogenesis and found that cytokinin signaling regulates the PC interdigitation
    pattern. Reduction in cytokinin accumulation and defects in cytokinin signaling
    (such as in ARR7-over-expressing lines, the ahk3cre1 cytokinin receptor mutant,
    and the ahp12345 cytokinin signaling mutant) enhanced PC interdigitation, whereas
    over-production of cytokinin and over-activation of cytokinin signaling in an
    ARR20 over-expression line delayed or abolished PC interdigitation throughout
    the cotyledon. Genetic and biochemical analyses suggest that cytokinin signaling
    acts upstream of ROPs to suppress the formation of interdigitated pattern. Our
    results provide novel mechanistic understanding of the pathways controlling PC
    shape and uncover a new role for cytokinin signaling in cell morphogenesis.
acknowledgement: is work was supported by grants from the US National Institute of
  General Medical Sciences (GM081451 and GM081451-03S2) to ZY. We thank National Science
  Foundation grant (IOS-1147250) to GVR and MX. HL and DL were partially supported
  by the Chinese Scholarship Council.
author:
- first_name: Hongjiang
  full_name: Hongjiang Li
  id: 33CA54A6-F248-11E8-B48F-1D18A9856A87
  last_name: Li
  orcid: 0000-0001-5039-9660
- first_name: Tongda
  full_name: Xu, Tongda
  last_name: Xu
- first_name: Deshu
  full_name: Lin, Deshu
  last_name: Lin
- first_name: Mingzhang
  full_name: Wen, Mingzhang
  last_name: Wen
- first_name: Mingtang
  full_name: Xie, Mingtang
  last_name: Xie
- first_name: Jérôme
  full_name: Duclercq, Jérôme
  last_name: Duclercq
- first_name: Agnieszka
  full_name: Bielach, Agnieszka
  last_name: Bielach
- first_name: Jungmook
  full_name: Kim, Jungmook
  last_name: Kim
- first_name: G Venugopala
  full_name: Reddy, G Venugopala
  last_name: Reddy
- first_name: Jianru
  full_name: Zuo, Jianru
  last_name: Zuo
- first_name: Eva
  full_name: Eva Benková
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Jirí
  full_name: Jirí Friml
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Hongwei
  full_name: Guo, Hongwei
  last_name: Guo
- first_name: Zhenbiao
  full_name: Yang, Zhenbiao
  last_name: Yang
citation:
  ama: Li H, Xu T, Lin D, et al. Cytokinin signaling regulates pavement cell morphogenesis
    in Arabidopsis. <i>Cell Research</i>. 2013;23(2):290-299. doi:<a href="https://doi.org/10.1038/cr.2012.146">10.1038/cr.2012.146</a>
  apa: Li, H., Xu, T., Lin, D., Wen, M., Xie, M., Duclercq, J., … Yang, Z. (2013).
    Cytokinin signaling regulates pavement cell morphogenesis in Arabidopsis. <i>Cell
    Research</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/cr.2012.146">https://doi.org/10.1038/cr.2012.146</a>
  chicago: Li, Hongjiang, Tongda Xu, Deshu Lin, Mingzhang Wen, Mingtang Xie, Jérôme
    Duclercq, Agnieszka Bielach, et al. “Cytokinin Signaling Regulates Pavement Cell
    Morphogenesis in Arabidopsis.” <i>Cell Research</i>. Nature Publishing Group,
    2013. <a href="https://doi.org/10.1038/cr.2012.146">https://doi.org/10.1038/cr.2012.146</a>.
  ieee: H. Li <i>et al.</i>, “Cytokinin signaling regulates pavement cell morphogenesis
    in Arabidopsis,” <i>Cell Research</i>, vol. 23, no. 2. Nature Publishing Group,
    pp. 290–299, 2013.
  ista: Li H, Xu T, Lin D, Wen M, Xie M, Duclercq J, Bielach A, Kim J, Reddy GV, Zuo
    J, Benková E, Friml J, Guo H, Yang Z. 2013. Cytokinin signaling regulates pavement
    cell morphogenesis in Arabidopsis. Cell Research. 23(2), 290–299.
  mla: Li, Hongjiang, et al. “Cytokinin Signaling Regulates Pavement Cell Morphogenesis
    in Arabidopsis.” <i>Cell Research</i>, vol. 23, no. 2, Nature Publishing Group,
    2013, pp. 290–99, doi:<a href="https://doi.org/10.1038/cr.2012.146">10.1038/cr.2012.146</a>.
  short: H. Li, T. Xu, D. Lin, M. Wen, M. Xie, J. Duclercq, A. Bielach, J. Kim, G.V.
    Reddy, J. Zuo, E. Benková, J. Friml, H. Guo, Z. Yang, Cell Research 23 (2013)
    290–299.
date_created: 2018-12-11T12:00:07Z
date_published: 2013-02-01T00:00:00Z
date_updated: 2021-01-12T07:00:27Z
day: '01'
doi: 10.1038/cr.2012.146
extern: 1
intvolume: '        23'
issue: '2'
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3567823/
month: '02'
oa: 1
page: 290 - 299
publication: Cell Research
publication_status: published
publisher: Nature Publishing Group
publist_id: '3881'
quality_controlled: 0
status: public
title: Cytokinin signaling regulates pavement cell morphogenesis in Arabidopsis
type: journal_article
volume: 23
year: '2013'
...
---
_id: '2882'
abstract:
- lang: eng
  text: Gravitropic bending of plant organs is mediated by an asymmetric signaling
    of the plant hormone auxin between the upper and lower side of the respective
    organ. Here, we show that also another plant hormone, gibberellic acid (GA), shows
    asymmetric action during gravitropic responses. Immunodetection using an antibody
    against GA and monitoring GA signaling output by downstream degradation of DELLA
    proteins revealed an asymmetric GA distribution and response with the maximum
    at the lower side of gravistimulated roots. Genetic or pharmacological manipulation
    of GA levels or response affects gravity-mediated auxin redistribution and root
    bending response. The higher GA levels at the lower side of the root correlate
    with increased amounts of PIN-FORMED2 (PIN2) auxin transporter at the plasma membrane.
    The observed increase in PIN2 stability is caused by a specific GA effect on trafficking
    of PIN proteins to lytic vacuoles that presumably occurs downstream of brefeldin
    A-sensitive endosomes. Our results suggest that asymmetric auxin distribution
    instructive for gravity-induced differential growth is consolidated by the asymmetric
    action of GA that stabilizes the PIN-dependent auxin stream along the lower side
    of gravistimulated roots.
author:
- first_name: Christian
  full_name: Löfke, Christian
  last_name: Löfke
- first_name: Marta
  full_name: Zwiewka, Marta
  last_name: Zwiewka
- first_name: Ingo
  full_name: Heilmann, Ingo
  last_name: Heilmann
- first_name: Marc
  full_name: Van Montagu, Marc
  last_name: Van Montagu
- first_name: Thomas
  full_name: Teichmann, Thomas
  last_name: Teichmann
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Löfke C, Zwiewka M, Heilmann I, Van Montagu M, Teichmann T, Friml J. Asymmetric
    gibberellin signaling regulates vacuolar trafficking of PIN auxin transporters
    during root gravitropism. <i>PNAS</i>. 2013;110(9):3627-3632. doi:<a href="https://doi.org/10.1073/pnas.1300107110">10.1073/pnas.1300107110</a>
  apa: Löfke, C., Zwiewka, M., Heilmann, I., Van Montagu, M., Teichmann, T., &#38;
    Friml, J. (2013). Asymmetric gibberellin signaling regulates vacuolar trafficking
    of PIN auxin transporters during root gravitropism. <i>PNAS</i>. National Academy
    of Sciences. <a href="https://doi.org/10.1073/pnas.1300107110">https://doi.org/10.1073/pnas.1300107110</a>
  chicago: Löfke, Christian, Marta Zwiewka, Ingo Heilmann, Marc Van Montagu, Thomas
    Teichmann, and Jiří Friml. “Asymmetric Gibberellin Signaling Regulates Vacuolar
    Trafficking of PIN Auxin Transporters during Root Gravitropism.” <i>PNAS</i>.
    National Academy of Sciences, 2013. <a href="https://doi.org/10.1073/pnas.1300107110">https://doi.org/10.1073/pnas.1300107110</a>.
  ieee: C. Löfke, M. Zwiewka, I. Heilmann, M. Van Montagu, T. Teichmann, and J. Friml,
    “Asymmetric gibberellin signaling regulates vacuolar trafficking of PIN auxin
    transporters during root gravitropism,” <i>PNAS</i>, vol. 110, no. 9. National
    Academy of Sciences, pp. 3627–3632, 2013.
  ista: Löfke C, Zwiewka M, Heilmann I, Van Montagu M, Teichmann T, Friml J. 2013.
    Asymmetric gibberellin signaling regulates vacuolar trafficking of PIN auxin transporters
    during root gravitropism. PNAS. 110(9), 3627–3632.
  mla: Löfke, Christian, et al. “Asymmetric Gibberellin Signaling Regulates Vacuolar
    Trafficking of PIN Auxin Transporters during Root Gravitropism.” <i>PNAS</i>,
    vol. 110, no. 9, National Academy of Sciences, 2013, pp. 3627–32, doi:<a href="https://doi.org/10.1073/pnas.1300107110">10.1073/pnas.1300107110</a>.
  short: C. Löfke, M. Zwiewka, I. Heilmann, M. Van Montagu, T. Teichmann, J. Friml,
    PNAS 110 (2013) 3627–3632.
date_created: 2018-12-11T12:00:07Z
date_published: 2013-02-26T00:00:00Z
date_updated: 2021-01-12T07:00:27Z
day: '26'
department:
- _id: JiFr
doi: 10.1073/pnas.1300107110
external_id:
  pmid:
  - '23391733'
intvolume: '       110'
issue: '9'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3587205/
month: '02'
oa: 1
oa_version: Submitted Version
page: 3627 - 3632
pmid: 1
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
publist_id: '3879'
quality_controlled: '1'
scopus_import: 1
status: public
title: Asymmetric gibberellin signaling regulates vacuolar trafficking of PIN auxin
  transporters during root gravitropism
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 110
year: '2013'
...
---
_id: '2883'
abstract:
- lang: eng
  text: Plant architecture is influenced by the polar, cell-to-cell transport of auxin
    that is primarily provided and regulated by plasma membrane efflux catalysts of
    the PIN-FORMED and B family of ABC transporter (ABCB) classes. The latter were
    shown to require the functionality of the FK506 binding protein42 TWISTED DWARF1
    (TWD1), although underlying mechanisms are unclear. By genetic manipulation of
    TWD1 expression, we show here that TWD1 affects shootward root auxin reflux and,
    thus, downstream developmental traits, such as epidermal twisting and gravitropism
    of the root. Using immunological assays, we demonstrate a predominant lateral,
    mainly outward-facing, plasma membrane location for TWD1 in the root epidermis
    characterized by the lateral marker ABC transporter G36/PLEIOTROPIC DRUG-RESISTANCE8/PENETRATION3.
    At these epidermal plasma membrane domains, TWD1 colocalizes with nonpolar ABCB1.
    In planta bioluminescence resonance energy transfer analysis was used to verify
    specific ABC transporter B1 (ABCB1)-TWD1 interaction. Our data support a model
    in which TWD1 promotes lateral ABCB-mediated auxin efflux via protein-protein
    interaction at the plasma membrane, minimizing reflux from the root apoplast into
    the cytoplasm.
acknowledgement: We would thank Vincent Vincenzetti and Laurence Charrier for excellent
  technical assistance, A. von Arnim for the donation of BRET vectors, E. Spalding
  for TWD1-CFP, TWD1-CFP/29-1-GFP/ER-YFP, and ABCB4-GFP lines, M. Palmgren for discussion
  and support, and E. Martinoia for TT12 cDNA, support, and mentorship. Imaging data
  were partially collected at the Center for Advanced Bioimaging, University of Copenhagen,
  Denmark. This work was supported by grants from the Novartis Foundation (to M.G.),
  from the Danish Research School for Biotechnology (to M.G. and A.S.), from the Forschungskredit
  of the University of Zurich (to A.B.), from the Pool de Recherche of the University
  of Fribourg (to M.G.), and from the Swiss National Funds (to M.G.). M.G. dedicates
  this work to his father, who passed away during the resubmission process.
author:
- first_name: Bangjun
  full_name: Wang, Bangjun
  last_name: Wang
- first_name: Aurélien
  full_name: Bailly, Aurélien
  last_name: Bailly
- first_name: Marta
  full_name: Zwiewk, Marta
  last_name: Zwiewk
- first_name: Sina
  full_name: Henrichs, Sina
  last_name: Henrichs
- first_name: Elisa
  full_name: Azzarello, Elisa
  last_name: Azzarello
- first_name: Stefano
  full_name: Mancuso, Stefano
  last_name: Mancuso
- first_name: Masayoshi
  full_name: Maeshima, Masayoshi
  last_name: Maeshima
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Alexander
  full_name: Schulz, Alexander
  last_name: Schulz
- first_name: Markus
  full_name: Geisler, Markus
  last_name: Geisler
citation:
  ama: Wang B, Bailly A, Zwiewk M, et al. Arabidopsis TWISTED DWARF1 functionally
    interacts with auxin exporter ABCB1 on the root plasma membrane. <i>Plant Cell</i>.
    2013;25(1):202-214. doi:<a href="https://doi.org/10.1105/tpc.112.105999">10.1105/tpc.112.105999</a>
  apa: Wang, B., Bailly, A., Zwiewk, M., Henrichs, S., Azzarello, E., Mancuso, S.,
    … Geisler, M. (2013). Arabidopsis TWISTED DWARF1 functionally interacts with auxin
    exporter ABCB1 on the root plasma membrane. <i>Plant Cell</i>. American Society
    of Plant Biologists. <a href="https://doi.org/10.1105/tpc.112.105999">https://doi.org/10.1105/tpc.112.105999</a>
  chicago: Wang, Bangjun, Aurélien Bailly, Marta Zwiewk, Sina Henrichs, Elisa Azzarello,
    Stefano Mancuso, Masayoshi Maeshima, Jiří Friml, Alexander Schulz, and Markus
    Geisler. “Arabidopsis TWISTED DWARF1 Functionally Interacts with Auxin Exporter
    ABCB1 on the Root Plasma Membrane.” <i>Plant Cell</i>. American Society of Plant
    Biologists, 2013. <a href="https://doi.org/10.1105/tpc.112.105999">https://doi.org/10.1105/tpc.112.105999</a>.
  ieee: B. Wang <i>et al.</i>, “Arabidopsis TWISTED DWARF1 functionally interacts
    with auxin exporter ABCB1 on the root plasma membrane,” <i>Plant Cell</i>, vol.
    25, no. 1. American Society of Plant Biologists, pp. 202–214, 2013.
  ista: Wang B, Bailly A, Zwiewk M, Henrichs S, Azzarello E, Mancuso S, Maeshima M,
    Friml J, Schulz A, Geisler M. 2013. Arabidopsis TWISTED DWARF1 functionally interacts
    with auxin exporter ABCB1 on the root plasma membrane. Plant Cell. 25(1), 202–214.
  mla: Wang, Bangjun, et al. “Arabidopsis TWISTED DWARF1 Functionally Interacts with
    Auxin Exporter ABCB1 on the Root Plasma Membrane.” <i>Plant Cell</i>, vol. 25,
    no. 1, American Society of Plant Biologists, 2013, pp. 202–14, doi:<a href="https://doi.org/10.1105/tpc.112.105999">10.1105/tpc.112.105999</a>.
  short: B. Wang, A. Bailly, M. Zwiewk, S. Henrichs, E. Azzarello, S. Mancuso, M.
    Maeshima, J. Friml, A. Schulz, M. Geisler, Plant Cell 25 (2013) 202–214.
date_created: 2018-12-11T12:00:08Z
date_published: 2013-01-01T00:00:00Z
date_updated: 2021-01-12T07:00:28Z
day: '01'
department:
- _id: JiFr
doi: 10.1105/tpc.112.105999
external_id:
  pmid:
  - '23321285'
intvolume: '        25'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3584535/
month: '01'
oa: 1
oa_version: Submitted Version
page: 202 - 214
pmid: 1
publication: Plant Cell
publication_status: published
publisher: American Society of Plant Biologists
publist_id: '3878'
quality_controlled: '1'
scopus_import: 1
status: public
title: Arabidopsis TWISTED DWARF1 functionally interacts with auxin exporter ABCB1
  on the root plasma membrane
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 25
year: '2013'
...
---
_id: '2884'
author:
- first_name: Jean-Léon
  full_name: Maître, Jean-Léon
  id: 48F1E0D8-F248-11E8-B48F-1D18A9856A87
  last_name: Maître
  orcid: 0000-0002-3688-1474
- first_name: Hélène
  full_name: Berthoumieux, Hélène
  last_name: Berthoumieux
- first_name: Gabriel
  full_name: Krens, Gabriel
  id: 2B819732-F248-11E8-B48F-1D18A9856A87
  last_name: Krens
  orcid: 0000-0003-4761-5996
- first_name: Guillaume
  full_name: Salbreux, Guillaume
  last_name: Salbreux
- first_name: Frank
  full_name: Julicher, Frank
  last_name: Julicher
- first_name: Ewa
  full_name: Paluch, Ewa
  last_name: Paluch
- 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: Maître J-L, Berthoumieux H, Krens G, et al. Cell adhesion mechanics of zebrafish
    gastrulation. <i>Medecine Sciences</i>. 2013;29(2):147-150. doi:<a href="https://doi.org/10.1051/medsci/2013292011">10.1051/medsci/2013292011</a>
  apa: Maître, J.-L., Berthoumieux, H., Krens, G., Salbreux, G., Julicher, F., Paluch,
    E., &#38; Heisenberg, C.-P. J. (2013). Cell adhesion mechanics of zebrafish gastrulation.
    <i>Medecine Sciences</i>. Éditions Médicales et Scientifiques. <a href="https://doi.org/10.1051/medsci/2013292011">https://doi.org/10.1051/medsci/2013292011</a>
  chicago: Maître, Jean-Léon, Hélène Berthoumieux, Gabriel Krens, Guillaume Salbreux,
    Frank Julicher, Ewa Paluch, and Carl-Philipp J Heisenberg. “Cell Adhesion Mechanics
    of Zebrafish Gastrulation.” <i>Medecine Sciences</i>. Éditions Médicales et Scientifiques,
    2013. <a href="https://doi.org/10.1051/medsci/2013292011">https://doi.org/10.1051/medsci/2013292011</a>.
  ieee: J.-L. Maître <i>et al.</i>, “Cell adhesion mechanics of zebrafish gastrulation,”
    <i>Medecine Sciences</i>, vol. 29, no. 2. Éditions Médicales et Scientifiques,
    pp. 147–150, 2013.
  ista: Maître J-L, Berthoumieux H, Krens G, Salbreux G, Julicher F, Paluch E, Heisenberg
    C-PJ. 2013. Cell adhesion mechanics of zebrafish gastrulation. Medecine Sciences.
    29(2), 147–150.
  mla: Maître, Jean-Léon, et al. “Cell Adhesion Mechanics of Zebrafish Gastrulation.”
    <i>Medecine Sciences</i>, vol. 29, no. 2, Éditions Médicales et Scientifiques,
    2013, pp. 147–50, doi:<a href="https://doi.org/10.1051/medsci/2013292011">10.1051/medsci/2013292011</a>.
  short: J.-L. Maître, H. Berthoumieux, G. Krens, G. Salbreux, F. Julicher, E. Paluch,
    C.-P.J. Heisenberg, Medecine Sciences 29 (2013) 147–150.
date_created: 2018-12-11T12:00:08Z
date_published: 2013-02-01T00:00:00Z
date_updated: 2021-01-12T07:00:28Z
day: '01'
department:
- _id: CaHe
doi: 10.1051/medsci/2013292011
intvolume: '        29'
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
page: 147 - 150
project:
- _id: 252064B8-B435-11E9-9278-68D0E5697425
  grant_number: HE_3231/6-1
  name: Analysis of the Formation and Function of Different Cell Protusion Types During
    Cell Migration in Vivo
- _id: 2527D5CC-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I 812-B12
  name: Cell Cortex and Germ Layer Formation in Zebrafish Gastrulation
publication: Medecine Sciences
publication_status: published
publisher: Éditions Médicales et Scientifiques
publist_id: '3877'
quality_controlled: '1'
scopus_import: 1
status: public
title: Cell adhesion mechanics of zebrafish gastrulation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 29
year: '2013'
...
---
_id: '2885'
abstract:
- lang: eng
  text: 'This volume contains the post-proceedings of the 8th Doctoral Workshop on
    Mathematical and Engineering Methods in Computer Science, MEMICS 2012, held in
    Znojmo, Czech Republic, in October, 2012. The 13 thoroughly revised papers were
    carefully selected out of 31 submissions and are presented together with 6 invited
    papers. The topics covered by the papers include: computer-aided analysis and
    verification, applications of game theory in computer science, networks and security,
    modern trends of graph theory in computer science, electronic systems design and
    testing, and quantum information processing.'
acknowledgement: Red Hat Czech Republic, Y Soft
alternative_title:
- LNCS
citation:
  ama: Kucera A, Henzinger TA, Nesetril J, Vojnar T, Antos D, eds. <i>Mathematical
    and Engineering Methods in Computer Science</i>. Vol 7721. Springer; 2013:1-228.
    doi:<a href="https://doi.org/10.1007/978-3-642-36046-6">10.1007/978-3-642-36046-6</a>
  apa: 'Kucera, A., Henzinger, T. A., Nesetril, J., Vojnar, T., &#38; Antos, D. (Eds.).
    (2013). <i>Mathematical and Engineering Methods in Computer Science</i> (Vol.
    7721, pp. 1–228). Presented at the MEMICS: Mathematical and Engineering methods
    in computer science, Znojmo, Czech Republic: Springer. <a href="https://doi.org/10.1007/978-3-642-36046-6">https://doi.org/10.1007/978-3-642-36046-6</a>'
  chicago: Kucera, Antonin, Thomas A Henzinger, Jaroslav Nesetril, Tomas Vojnar, and
    David Antos, eds. <i>Mathematical and Engineering Methods in Computer Science</i>.
    Vol. 7721. Lecture Notes in Computer Science. Springer, 2013. <a href="https://doi.org/10.1007/978-3-642-36046-6">https://doi.org/10.1007/978-3-642-36046-6</a>.
  ieee: A. Kucera, T. A. Henzinger, J. Nesetril, T. Vojnar, and D. Antos, Eds., <i>Mathematical
    and Engineering Methods in Computer Science</i>, vol. 7721. Springer, 2013, pp.
    1–228.
  ista: Kucera A, Henzinger TA, Nesetril J, Vojnar T, Antos D eds. 2013. Mathematical
    and Engineering Methods in Computer Science, Springer,p.
  mla: Kucera, Antonin, et al., editors. <i>Mathematical and Engineering Methods in
    Computer Science</i>. Vol. 7721, Springer, 2013, pp. 1–228, doi:<a href="https://doi.org/10.1007/978-3-642-36046-6">10.1007/978-3-642-36046-6</a>.
  short: A. Kucera, T.A. Henzinger, J. Nesetril, T. Vojnar, D. Antos, eds., Mathematical
    and Engineering Methods in Computer Science, Springer, 2013.
conference:
  end_date: 2012-10-28
  location: Znojmo, Czech Republic
  name: 'MEMICS: Mathematical and Engineering methods in computer science'
  start_date: 2012-10-25
date_created: 2018-12-11T12:00:08Z
date_published: 2013-01-09T00:00:00Z
date_updated: 2019-08-02T12:37:55Z
day: '09'
department:
- _id: ToHe
doi: 10.1007/978-3-642-36046-6
editor:
- first_name: Antonin
  full_name: Kucera, Antonin
  last_name: Kucera
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Jaroslav
  full_name: Nesetril, Jaroslav
  last_name: Nesetril
- first_name: Tomas
  full_name: Vojnar, Tomas
  last_name: Vojnar
- first_name: David
  full_name: Antos, David
  last_name: Antos
intvolume: '      7721'
language:
- iso: eng
month: '01'
oa_version: None
page: 1 - 228
publication_status: published
publisher: Springer
publist_id: '3874'
quality_controlled: '1'
series_title: Lecture Notes in Computer Science
status: public
title: Mathematical and Engineering Methods in Computer Science
type: conference_editor
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7721
year: '2013'
...
---
_id: '2886'
abstract:
- lang: eng
  text: We focus on the realizability problem of Message Sequence Graphs (MSG), i.e.
    the problem whether a given MSG specification is correctly distributable among
    parallel components communicating via messages. This fundamental problem of MSG
    is known to be undecidable. We introduce a well motivated restricted class of
    MSG, so called controllable-choice MSG, and show that all its models are realizable
    and moreover it is decidable whether a given MSG model is a member of this class.
    In more detail, this class of MSG specifications admits a deadlock-free realization
    by overloading existing messages with additional bounded control data. We also
    show that the presented class is the largest known subclass of MSG that allows
    for deadlock-free realization.
alternative_title:
- LNCS
author:
- first_name: Martin
  full_name: Chmelik, Martin
  id: 3624234E-F248-11E8-B48F-1D18A9856A87
  last_name: Chmelik
- first_name: Vojtěch
  full_name: Řehák, Vojtěch
  last_name: Řehák
citation:
  ama: Chmelik M, Řehák V. Controllable-choice message sequence graphs. 2013;7721:118-130.
    doi:<a href="https://doi.org/10.1007/978-3-642-36046-6_12">10.1007/978-3-642-36046-6_12</a>
  apa: 'Chmelik, M., &#38; Řehák, V. (2013). Controllable-choice message sequence
    graphs. Presented at the MEMICS: Mathematical and Engineering Methods in Computer
    Science, Znojmo, Czech Republic: Springer. <a href="https://doi.org/10.1007/978-3-642-36046-6_12">https://doi.org/10.1007/978-3-642-36046-6_12</a>'
  chicago: Chmelik, Martin, and Vojtěch Řehák. “Controllable-Choice Message Sequence
    Graphs.” Lecture Notes in Computer Science. Springer, 2013. <a href="https://doi.org/10.1007/978-3-642-36046-6_12">https://doi.org/10.1007/978-3-642-36046-6_12</a>.
  ieee: M. Chmelik and V. Řehák, “Controllable-choice message sequence graphs,” vol.
    7721. Springer, pp. 118–130, 2013.
  ista: Chmelik M, Řehák V. 2013. Controllable-choice message sequence graphs. 7721,
    118–130.
  mla: Chmelik, Martin, and Vojtěch Řehák. <i>Controllable-Choice Message Sequence
    Graphs</i>. Vol. 7721, Springer, 2013, pp. 118–30, doi:<a href="https://doi.org/10.1007/978-3-642-36046-6_12">10.1007/978-3-642-36046-6_12</a>.
  short: M. Chmelik, V. Řehák, 7721 (2013) 118–130.
conference:
  end_date: 2012-10-28
  location: Znojmo, Czech Republic
  name: 'MEMICS: Mathematical and Engineering Methods in Computer Science'
  start_date: 2012-10-25
date_created: 2018-12-11T12:00:09Z
date_published: 2013-01-09T00:00:00Z
date_updated: 2020-08-11T10:09:52Z
day: '09'
department:
- _id: KrCh
doi: 10.1007/978-3-642-36046-6_12
ec_funded: 1
intvolume: '      7721'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1209.4499
month: '01'
oa: 1
oa_version: Submitted Version
page: 118 - 130
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 23499-N23
  name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25863FF4-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11407
  name: Game Theory
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2587B514-B435-11E9-9278-68D0E5697425
  name: Microsoft Research Faculty Fellowship
publication_status: published
publisher: Springer
publist_id: '3873'
quality_controlled: '1'
scopus_import: 1
series_title: Lecture Notes in Computer Science
status: public
title: Controllable-choice message sequence graphs
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7721
year: '2013'
...
---
_id: '2887'
abstract:
- lang: eng
  text: 'Root system growth and development is highly plastic and is influenced by
    the surrounding environment. Roots frequently grow in heterogeneous environments
    that include interactions from neighboring plants and physical impediments in
    the rhizosphere. To investigate how planting density and physical objects affect
    root system growth, we grew rice in a transparent gel system in close proximity
    with another plant or a physical object. Root systems were imaged and reconstructed
    in three dimensions. Root-root interaction strength was calculated using quantitative
    metrics that characterize the extent towhich the reconstructed root systems overlap
    each other. Surprisingly, we found the overlap of root systems of the same genotype
    was significantly higher than that of root systems of different genotypes. Root
    systems of the same genotype tended to grow toward each other but those of different
    genotypes appeared to avoid each other. Shoot separation experiments excluded
    the possibility of aerial interactions, suggesting root communication. Staggered
    plantings indicated that interactions likely occur at root tips in close proximity.
    Recognition of obstacles also occurred through root tips, but through physical
    contact in a size-dependent manner. These results indicate that root systems use
    two different forms of communication to recognize objects and alter root architecture:
    root-root recognition, possibly mediated through root exudates, and root-object
    recognition mediated by physical contact at the root tips. This finding suggests
    that root tips act as local sensors that integrate rhizosphere information into
    global root architectural changes.'
article_processing_charge: No
article_type: original
author:
- first_name: Suqin
  full_name: Fang, Suqin
  last_name: Fang
- first_name: Randy
  full_name: Clark, Randy
  last_name: Clark
- first_name: Ying
  full_name: Zheng, Ying
  last_name: Zheng
- first_name: Anjali
  full_name: Iyer Pascuzzi, Anjali
  last_name: Iyer Pascuzzi
- first_name: Joshua
  full_name: Weitz, Joshua
  last_name: Weitz
- first_name: Leon
  full_name: Kochian, Leon
  last_name: Kochian
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
- first_name: Hong
  full_name: Liao, Hong
  last_name: Liao
- first_name: Philip
  full_name: Benfey, Philip
  last_name: Benfey
citation:
  ama: Fang S, Clark R, Zheng Y, et al. Genotypic recognition and spatial responses
    by rice roots. <i>PNAS</i>. 2013;110(7):2670-2675. doi:<a href="https://doi.org/10.1073/pnas.1222821110">10.1073/pnas.1222821110</a>
  apa: Fang, S., Clark, R., Zheng, Y., Iyer Pascuzzi, A., Weitz, J., Kochian, L.,
    … Benfey, P. (2013). Genotypic recognition and spatial responses by rice roots.
    <i>PNAS</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1222821110">https://doi.org/10.1073/pnas.1222821110</a>
  chicago: Fang, Suqin, Randy Clark, Ying Zheng, Anjali Iyer Pascuzzi, Joshua Weitz,
    Leon Kochian, Herbert Edelsbrunner, Hong Liao, and Philip Benfey. “Genotypic Recognition
    and Spatial Responses by Rice Roots.” <i>PNAS</i>. National Academy of Sciences,
    2013. <a href="https://doi.org/10.1073/pnas.1222821110">https://doi.org/10.1073/pnas.1222821110</a>.
  ieee: S. Fang <i>et al.</i>, “Genotypic recognition and spatial responses by rice
    roots,” <i>PNAS</i>, vol. 110, no. 7. National Academy of Sciences, pp. 2670–2675,
    2013.
  ista: Fang S, Clark R, Zheng Y, Iyer Pascuzzi A, Weitz J, Kochian L, Edelsbrunner
    H, Liao H, Benfey P. 2013. Genotypic recognition and spatial responses by rice
    roots. PNAS. 110(7), 2670–2675.
  mla: Fang, Suqin, et al. “Genotypic Recognition and Spatial Responses by Rice Roots.”
    <i>PNAS</i>, vol. 110, no. 7, National Academy of Sciences, 2013, pp. 2670–75,
    doi:<a href="https://doi.org/10.1073/pnas.1222821110">10.1073/pnas.1222821110</a>.
  short: S. Fang, R. Clark, Y. Zheng, A. Iyer Pascuzzi, J. Weitz, L. Kochian, H. Edelsbrunner,
    H. Liao, P. Benfey, PNAS 110 (2013) 2670–2675.
date_created: 2018-12-11T12:00:09Z
date_published: 2013-02-12T00:00:00Z
date_updated: 2021-01-12T07:00:29Z
day: '12'
department:
- _id: HeEd
doi: 10.1073/pnas.1222821110
external_id:
  pmid:
  - '23362379'
intvolume: '       110'
issue: '7'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574932/
month: '02'
oa: 1
oa_version: Published Version
page: 2670 - 2675
pmid: 1
publication: PNAS
publication_status: published
publisher: National Academy of Sciences
publist_id: '3872'
quality_controlled: '1'
scopus_import: 1
status: public
title: Genotypic recognition and spatial responses by rice roots
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 110
year: '2013'
...
