---
_id: '2949'
author:
- first_name: David
  full_name: Dupret, David
  last_name: Dupret
- 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, Csicsvari JL. The medial entorhinal cortex keeps Up. <i>Nature Neuroscience</i>.
    2012;15(11):1471-1472. doi:<a href="https://doi.org/10.1038/nn.3245">10.1038/nn.3245</a>
  apa: Dupret, D., &#38; Csicsvari, J. L. (2012). The medial entorhinal cortex keeps
    Up. <i>Nature Neuroscience</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/nn.3245">https://doi.org/10.1038/nn.3245</a>
  chicago: Dupret, David, and Jozsef L Csicsvari. “The Medial Entorhinal Cortex Keeps
    Up.” <i>Nature Neuroscience</i>. Nature Publishing Group, 2012. <a href="https://doi.org/10.1038/nn.3245">https://doi.org/10.1038/nn.3245</a>.
  ieee: D. Dupret and J. L. Csicsvari, “The medial entorhinal cortex keeps Up,” <i>Nature
    Neuroscience</i>, vol. 15, no. 11. Nature Publishing Group, pp. 1471–1472, 2012.
  ista: Dupret D, Csicsvari JL. 2012. The medial entorhinal cortex keeps Up. Nature
    Neuroscience. 15(11), 1471–1472.
  mla: Dupret, David, and Jozsef L. Csicsvari. “The Medial Entorhinal Cortex Keeps
    Up.” <i>Nature Neuroscience</i>, vol. 15, no. 11, Nature Publishing Group, 2012,
    pp. 1471–72, doi:<a href="https://doi.org/10.1038/nn.3245">10.1038/nn.3245</a>.
  short: D. Dupret, J.L. Csicsvari, Nature Neuroscience 15 (2012) 1471–1472.
date_created: 2018-12-11T12:00:30Z
date_published: 2012-11-01T00:00:00Z
date_updated: 2021-01-12T07:39:59Z
day: '01'
department:
- _id: JoCs
doi: 10.1038/nn.3245
intvolume: '        15'
issue: '11'
language:
- iso: eng
main_file_link:
- url: http://www.mrcbndu.ox.ac.uk/publications/medial-entorhinal-cortex-keeps
month: '11'
oa_version: None
page: 1471 - 1472
publication: Nature Neuroscience
publication_status: published
publisher: Nature Publishing Group
publist_id: '3782'
quality_controlled: '1'
scopus_import: 1
status: public
title: The medial entorhinal cortex keeps Up
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2012'
...
---
_id: '2950'
abstract:
- lang: eng
  text: Contractile actomyosin rings drive various fundamental morphogenetic processes
    ranging from cytokinesis to wound healing. Actomyosin rings are generally thought
    to function by circumferential contraction. Here, we show that the spreading of
    the enveloping cell layer (EVL) over the yolk cell during zebrafish gastrulation
    is driven by a contractile actomyosin ring. In contrast to previous suggestions,
    we find that this ring functions not only by circumferential contraction but also
    by a flow-friction mechanism. This generates a pulling force through resistance
    against retrograde actomyosin flow. EVL spreading proceeds normally in situations
    where circumferential contraction is unproductive, indicating that the flow-friction
    mechanism is sufficient. Thus, actomyosin rings can function in epithelial morphogenesis
    through a combination of cable-constriction and flow-friction mechanisms.
acknowledged_ssus:
- _id: SSU
author:
- first_name: Martin
  full_name: Behrndt, Martin
  id: 3ECECA3A-F248-11E8-B48F-1D18A9856A87
  last_name: Behrndt
- first_name: Guillaume
  full_name: Salbreux, Guillaume
  last_name: Salbreux
- first_name: Pedro
  full_name: Campinho, Pedro
  id: 3AFBBC42-F248-11E8-B48F-1D18A9856A87
  last_name: Campinho
  orcid: 0000-0002-8526-5416
- first_name: Robert
  full_name: Hauschild, Robert
  id: 4E01D6B4-F248-11E8-B48F-1D18A9856A87
  last_name: Hauschild
  orcid: 0000-0001-9843-3522
- first_name: Felix
  full_name: Oswald, Felix
  last_name: Oswald
- first_name: Julia
  full_name: Roensch, Julia
  id: 4220E59C-F248-11E8-B48F-1D18A9856A87
  last_name: Roensch
- first_name: Stephan
  full_name: Grill, Stephan
  last_name: Grill
- 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: Behrndt M, Salbreux G, Campinho P, et al. Forces driving epithelial spreading
    in zebrafish gastrulation. <i>Science</i>. 2012;338(6104):257-260. doi:<a href="https://doi.org/10.1126/science.1224143">10.1126/science.1224143</a>
  apa: Behrndt, M., Salbreux, G., Campinho, P., Hauschild, R., Oswald, F., Roensch,
    J., … Heisenberg, C.-P. J. (2012). Forces driving epithelial spreading in zebrafish
    gastrulation. <i>Science</i>. American Association for the Advancement of Science.
    <a href="https://doi.org/10.1126/science.1224143">https://doi.org/10.1126/science.1224143</a>
  chicago: Behrndt, Martin, Guillaume Salbreux, Pedro Campinho, Robert Hauschild,
    Felix Oswald, Julia Roensch, Stephan Grill, and Carl-Philipp J Heisenberg. “Forces
    Driving Epithelial Spreading in Zebrafish Gastrulation.” <i>Science</i>. American
    Association for the Advancement of Science, 2012. <a href="https://doi.org/10.1126/science.1224143">https://doi.org/10.1126/science.1224143</a>.
  ieee: M. Behrndt <i>et al.</i>, “Forces driving epithelial spreading in zebrafish
    gastrulation,” <i>Science</i>, vol. 338, no. 6104. American Association for the
    Advancement of Science, pp. 257–260, 2012.
  ista: Behrndt M, Salbreux G, Campinho P, Hauschild R, Oswald F, Roensch J, Grill
    S, Heisenberg C-PJ. 2012. Forces driving epithelial spreading in zebrafish gastrulation.
    Science. 338(6104), 257–260.
  mla: Behrndt, Martin, et al. “Forces Driving Epithelial Spreading in Zebrafish Gastrulation.”
    <i>Science</i>, vol. 338, no. 6104, American Association for the Advancement of
    Science, 2012, pp. 257–60, doi:<a href="https://doi.org/10.1126/science.1224143">10.1126/science.1224143</a>.
  short: M. Behrndt, G. Salbreux, P. Campinho, R. Hauschild, F. Oswald, J. Roensch,
    S. Grill, C.-P.J. Heisenberg, Science 338 (2012) 257–260.
date_created: 2018-12-11T12:00:30Z
date_published: 2012-10-12T00:00:00Z
date_updated: 2023-02-21T17:02:44Z
day: '12'
department:
- _id: CaHe
- _id: Bio
doi: 10.1126/science.1224143
intvolume: '       338'
issue: '6104'
language:
- iso: eng
month: '10'
oa_version: None
page: 257 - 260
project:
- _id: 252ABD0A-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I 930-B20
  name: Control of Epithelial Cell Layer Spreading in Zebrafish
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '3778'
quality_controlled: '1'
related_material:
  record:
  - id: '1403'
    relation: dissertation_contains
    status: public
scopus_import: 1
status: public
title: Forces driving epithelial spreading in zebrafish gastrulation
type: journal_article
user_id: 4435EBFC-F248-11E8-B48F-1D18A9856A87
volume: 338
year: '2012'
...
---
_id: '2951'
abstract:
- lang: eng
  text: Differential cell adhesion and cortex tension are thought to drive cell sorting
    by controlling cell-cell contact formation. Here, we show that cell adhesion and
    cortex tension have different mechanical functions in controlling progenitor cell-cell
    contact formation and sorting during zebrafish gastrulation. Cortex tension controls
    cell-cell contact expansion by modulating interfacial tension at the contact.
    By contrast, adhesion has little direct function in contact expansion, but instead
    is needed to mechanically couple the cortices of adhering cells at their contacts,
    allowing cortex tension to control contact expansion. The coupling function of
    adhesion is mediated by E-cadherin and limited by the mechanical anchoring of
    E-cadherin to the cortex. Thus, cell adhesion provides the mechanical scaffold
    for cell cortex tension to drive cell sorting during gastrulation.
acknowledged_ssus:
- _id: SSU
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. Adhesion functions in cell sorting
    by mechanically coupling the cortices of adhering cells. <i>Science</i>. 2012;338(6104):253-256.
    doi:<a href="https://doi.org/10.1126/science.1225399">10.1126/science.1225399</a>
  apa: Maître, J.-L., Berthoumieux, H., Krens, G., Salbreux, G., Julicher, F., Paluch,
    E., &#38; Heisenberg, C.-P. J. (2012). Adhesion functions in cell sorting by mechanically
    coupling the cortices of adhering cells. <i>Science</i>. American Association
    for the Advancement of Science. <a href="https://doi.org/10.1126/science.1225399">https://doi.org/10.1126/science.1225399</a>
  chicago: Maître, Jean-Léon, Hélène Berthoumieux, Gabriel Krens, Guillaume Salbreux,
    Frank Julicher, Ewa Paluch, and Carl-Philipp J Heisenberg. “Adhesion Functions
    in Cell Sorting by Mechanically Coupling the Cortices of Adhering Cells.” <i>Science</i>.
    American Association for the Advancement of Science, 2012. <a href="https://doi.org/10.1126/science.1225399">https://doi.org/10.1126/science.1225399</a>.
  ieee: J.-L. Maître <i>et al.</i>, “Adhesion functions in cell sorting by mechanically
    coupling the cortices of adhering cells,” <i>Science</i>, vol. 338, no. 6104.
    American Association for the Advancement of Science, pp. 253–256, 2012.
  ista: Maître J-L, Berthoumieux H, Krens G, Salbreux G, Julicher F, Paluch E, Heisenberg
    C-PJ. 2012. Adhesion functions in cell sorting by mechanically coupling the cortices
    of adhering cells. Science. 338(6104), 253–256.
  mla: Maître, Jean-Léon, et al. “Adhesion Functions in Cell Sorting by Mechanically
    Coupling the Cortices of Adhering Cells.” <i>Science</i>, vol. 338, no. 6104,
    American Association for the Advancement of Science, 2012, pp. 253–56, doi:<a
    href="https://doi.org/10.1126/science.1225399">10.1126/science.1225399</a>.
  short: J.-L. Maître, H. Berthoumieux, G. Krens, G. Salbreux, F. Julicher, E. Paluch,
    C.-P.J. Heisenberg, Science 338 (2012) 253–256.
date_created: 2018-12-11T12:00:31Z
date_published: 2012-10-12T00:00:00Z
date_updated: 2021-01-12T07:40:00Z
day: '12'
department:
- _id: CaHe
doi: 10.1126/science.1225399
intvolume: '       338'
issue: '6104'
language:
- iso: eng
month: '10'
oa_version: None
page: 253 - 256
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '3777'
quality_controlled: '1'
scopus_import: 1
status: public
title: Adhesion functions in cell sorting by mechanically coupling the cortices of
  adhering cells
type: journal_article
user_id: 4435EBFC-F248-11E8-B48F-1D18A9856A87
volume: 338
year: '2012'
...
---
_id: '2952'
abstract:
- lang: eng
  text: Body axis elongation represents a common and fundamental morphogenetic process
    in development. A key mechanism triggering body axis elongation without additional
    growth is convergent extension (CE), whereby a tissue undergoes simultaneous narrowing
    and extension. Both collective cell migration and cell intercalation are thought
    to drive CE and are used to different degrees in various species as they elongate
    their body axis. Here, we provide an overview of CE as a general strategy for
    body axis elongation and discuss conserved and divergent mechanisms underlying
    CE among different species.
acknowledgement: 'M.T. is supported by the UK Medical Research Council (MRC) and Royal
  Society and C.-P.H. by the Fonds zur Förderung der wissenschaftlichen Forschung
  (FWF), Deutsche Forschungsgemeinschaft (DFG) and Institute of Science and Technology
  Austria. '
author:
- first_name: Masazumi
  full_name: Tada, Masazumi
  last_name: Tada
- 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: Tada M, Heisenberg C-PJ. Convergent extension Using collective cell migration
    and cell intercalation to shape embryos. <i>Development</i>. 2012;139(21):3897-3904.
    doi:<a href="https://doi.org/10.1242/dev.073007">10.1242/dev.073007</a>
  apa: Tada, M., &#38; Heisenberg, C.-P. J. (2012). Convergent extension Using collective
    cell migration and cell intercalation to shape embryos. <i>Development</i>. Company
    of Biologists. <a href="https://doi.org/10.1242/dev.073007">https://doi.org/10.1242/dev.073007</a>
  chicago: Tada, Masazumi, and Carl-Philipp J Heisenberg. “Convergent Extension Using
    Collective Cell Migration and Cell Intercalation to Shape Embryos.” <i>Development</i>.
    Company of Biologists, 2012. <a href="https://doi.org/10.1242/dev.073007">https://doi.org/10.1242/dev.073007</a>.
  ieee: M. Tada and C.-P. J. Heisenberg, “Convergent extension Using collective cell
    migration and cell intercalation to shape embryos,” <i>Development</i>, vol. 139,
    no. 21. Company of Biologists, pp. 3897–3904, 2012.
  ista: Tada M, Heisenberg C-PJ. 2012. Convergent extension Using collective cell
    migration and cell intercalation to shape embryos. Development. 139(21), 3897–3904.
  mla: Tada, Masazumi, and Carl-Philipp J. Heisenberg. “Convergent Extension Using
    Collective Cell Migration and Cell Intercalation to Shape Embryos.” <i>Development</i>,
    vol. 139, no. 21, Company of Biologists, 2012, pp. 3897–904, doi:<a href="https://doi.org/10.1242/dev.073007">10.1242/dev.073007</a>.
  short: M. Tada, C.-P.J. Heisenberg, Development 139 (2012) 3897–3904.
date_created: 2018-12-11T12:00:31Z
date_published: 2012-11-01T00:00:00Z
date_updated: 2021-01-12T07:40:00Z
day: '01'
department:
- _id: CaHe
doi: 10.1242/dev.073007
intvolume: '       139'
issue: '21'
language:
- iso: eng
month: '11'
oa_version: None
page: 3897 - 3904
publication: Development
publication_status: published
publisher: Company of Biologists
publist_id: '3776'
quality_controlled: '1'
scopus_import: 1
status: public
title: Convergent extension Using collective cell migration and cell intercalation
  to shape embryos
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 139
year: '2012'
...
---
_id: '2953'
author:
- 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: Reinhard
  full_name: Fässler, Reinhard
  last_name: Fässler
citation:
  ama: Heisenberg C-PJ, Fässler R. Cell-cell adhesion and extracellular matrix diversity
    counts. <i>Current Opinion in Cell Biology</i>. 2012;24(5):559-561. doi:<a href="https://doi.org/10.1016/j.ceb.2012.09.002">10.1016/j.ceb.2012.09.002</a>
  apa: Heisenberg, C.-P. J., &#38; Fässler, R. (2012). Cell-cell adhesion and extracellular
    matrix diversity counts. <i>Current Opinion in Cell Biology</i>. Elsevier. <a
    href="https://doi.org/10.1016/j.ceb.2012.09.002">https://doi.org/10.1016/j.ceb.2012.09.002</a>
  chicago: Heisenberg, Carl-Philipp J, and Reinhard Fässler. “Cell-Cell Adhesion and
    Extracellular Matrix Diversity Counts.” <i>Current Opinion in Cell Biology</i>.
    Elsevier, 2012. <a href="https://doi.org/10.1016/j.ceb.2012.09.002">https://doi.org/10.1016/j.ceb.2012.09.002</a>.
  ieee: C.-P. J. Heisenberg and R. Fässler, “Cell-cell adhesion and extracellular
    matrix diversity counts,” <i>Current Opinion in Cell Biology</i>, vol. 24, no.
    5. Elsevier, pp. 559–561, 2012.
  ista: Heisenberg C-PJ, Fässler R. 2012. Cell-cell adhesion and extracellular matrix
    diversity counts. Current Opinion in Cell Biology. 24(5), 559–561.
  mla: Heisenberg, Carl-Philipp J., and Reinhard Fässler. “Cell-Cell Adhesion and
    Extracellular Matrix Diversity Counts.” <i>Current Opinion in Cell Biology</i>,
    vol. 24, no. 5, Elsevier, 2012, pp. 559–61, doi:<a href="https://doi.org/10.1016/j.ceb.2012.09.002">10.1016/j.ceb.2012.09.002</a>.
  short: C.-P.J. Heisenberg, R. Fässler, Current Opinion in Cell Biology 24 (2012)
    559–561.
date_created: 2018-12-11T12:00:31Z
date_published: 2012-10-01T00:00:00Z
date_updated: 2021-01-12T07:40:01Z
day: '01'
department:
- _id: CaHe
doi: 10.1016/j.ceb.2012.09.002
intvolume: '        24'
issue: '5'
language:
- iso: eng
month: '10'
oa_version: None
page: 559 - 561
publication: Current Opinion in Cell Biology
publication_status: published
publisher: Elsevier
publist_id: '3773'
quality_controlled: '1'
scopus_import: 1
status: public
title: Cell-cell adhesion and extracellular matrix diversity counts
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2012'
...
---
_id: '2954'
abstract:
- lang: eng
  text: Spontaneous postsynaptic currents (PSCs) provide key information about the
    mechanisms of synaptic transmission and the activity modes of neuronal networks.
    However, detecting spontaneous PSCs in vitro and in vivo has been challenging,
    because of the small amplitude, the variable kinetics, and the undefined time
    of generation of these events. Here, we describe a, to our knowledge, new method
    for detecting spontaneous synaptic events by deconvolution, using a template that
    approximates the average time course of spontaneous PSCs. A recorded PSC trace
    is deconvolved from the template, resulting in a series of delta-like functions.
    The maxima of these delta-like events are reliably detected, revealing the precise
    onset times of the spontaneous PSCs. Among all detection methods, the deconvolution-based
    method has a unique temporal resolution, allowing the detection of individual
    events in high-frequency bursts. Furthermore, the deconvolution-based method has
    a high amplitude resolution, because deconvolution can substantially increase
    the signal/noise ratio. When tested against previously published methods using
    experimental data, the deconvolution-based method was superior for spontaneous
    PSCs recorded in vivo. Using the high-resolution deconvolution-based detection
    algorithm, we show that the frequency of spontaneous excitatory postsynaptic currents
    in dentate gyrus granule cells is 4.5 times higher in vivo than in vitro.
acknowledgement: "This work was supported by the Deutsche Forschungsgemeinschaft (TR3/B10)
  and a European Research Council Advanced grant to P.J.\r\nWe thank H. Hu, S. J.
  Guzman, and C. Schmidt-Hieber for critically reading the manuscript, I. Koeva and
  F. Marr for technical support, and E. Kramberger for editorial assistance.\r\n"
author:
- first_name: Alejandro
  full_name: Pernia-Andrade, Alejandro
  id: 36963E98-F248-11E8-B48F-1D18A9856A87
  last_name: Pernia-Andrade
- first_name: Sarit
  full_name: Goswami, Sarit
  id: 3A578F32-F248-11E8-B48F-1D18A9856A87
  last_name: Goswami
- first_name: Yvonne
  full_name: Stickler, Yvonne
  id: 63B76600-E9CC-11E9-9B5F-82450873F7A1
  last_name: Stickler
- first_name: Ulrich
  full_name: Fröbe, Ulrich
  last_name: Fröbe
- first_name: Alois
  full_name: Schlögl, Alois
  id: 45BF87EE-F248-11E8-B48F-1D18A9856A87
  last_name: Schlögl
  orcid: 0000-0002-5621-8100
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
citation:
  ama: Pernia-Andrade A, Goswami S, Stickler Y, Fröbe U, Schlögl A, Jonas PM. A deconvolution
    based method with high sensitivity and temporal resolution for detection of spontaneous
    synaptic currents in vitro and in vivo. <i>Biophysical Journal</i>. 2012;103(7):1429-1439.
    doi:<a href="https://doi.org/10.1016/j.bpj.2012.08.039">10.1016/j.bpj.2012.08.039</a>
  apa: Pernia-Andrade, A., Goswami, S., Stickler, Y., Fröbe, U., Schlögl, A., &#38;
    Jonas, P. M. (2012). A deconvolution based method with high sensitivity and temporal
    resolution for detection of spontaneous synaptic currents in vitro and in vivo.
    <i>Biophysical Journal</i>. Biophysical. <a href="https://doi.org/10.1016/j.bpj.2012.08.039">https://doi.org/10.1016/j.bpj.2012.08.039</a>
  chicago: Pernia-Andrade, Alejandro, Sarit Goswami, Yvonne Stickler, Ulrich Fröbe,
    Alois Schlögl, and Peter M Jonas. “A Deconvolution Based Method with High Sensitivity
    and Temporal Resolution for Detection of Spontaneous Synaptic Currents in Vitro
    and in Vivo.” <i>Biophysical Journal</i>. Biophysical, 2012. <a href="https://doi.org/10.1016/j.bpj.2012.08.039">https://doi.org/10.1016/j.bpj.2012.08.039</a>.
  ieee: A. Pernia-Andrade, S. Goswami, Y. Stickler, U. Fröbe, A. Schlögl, and P. M.
    Jonas, “A deconvolution based method with high sensitivity and temporal resolution
    for detection of spontaneous synaptic currents in vitro and in vivo,” <i>Biophysical
    Journal</i>, vol. 103, no. 7. Biophysical, pp. 1429–1439, 2012.
  ista: Pernia-Andrade A, Goswami S, Stickler Y, Fröbe U, Schlögl A, Jonas PM. 2012.
    A deconvolution based method with high sensitivity and temporal resolution for
    detection of spontaneous synaptic currents in vitro and in vivo. Biophysical Journal.
    103(7), 1429–1439.
  mla: Pernia-Andrade, Alejandro, et al. “A Deconvolution Based Method with High Sensitivity
    and Temporal Resolution for Detection of Spontaneous Synaptic Currents in Vitro
    and in Vivo.” <i>Biophysical Journal</i>, vol. 103, no. 7, Biophysical, 2012,
    pp. 1429–39, doi:<a href="https://doi.org/10.1016/j.bpj.2012.08.039">10.1016/j.bpj.2012.08.039</a>.
  short: A. Pernia-Andrade, S. Goswami, Y. Stickler, U. Fröbe, A. Schlögl, P.M. Jonas,
    Biophysical Journal 103 (2012) 1429–1439.
date_created: 2018-12-11T12:00:32Z
date_published: 2012-10-03T00:00:00Z
date_updated: 2021-01-12T07:40:01Z
day: '03'
department:
- _id: PeJo
- _id: ScienComp
doi: 10.1016/j.bpj.2012.08.039
external_id:
  pmid:
  - '23062335'
intvolume: '       103'
issue: '7'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3471482/
month: '10'
oa: 1
oa_version: Submitted Version
page: 1429 - 1439
pmid: 1
project:
- _id: 25BDE9A4-B435-11E9-9278-68D0E5697425
  grant_number: SFB-TR3-TP10B
  name: Glutamaterge synaptische Übertragung und Plastizität in hippocampalen Mikroschaltkreisen
publication: Biophysical Journal
publication_status: published
publisher: Biophysical
publist_id: '3774'
quality_controlled: '1'
scopus_import: 1
status: public
title: A deconvolution based method with high sensitivity and temporal resolution
  for detection of spontaneous synaptic currents in vitro and in vivo
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 103
year: '2012'
...
---
_id: '2955'
abstract:
- lang: eng
  text: 'We consider two-player stochastic games played on finite graphs with reachability
    objectives where the first player tries to ensure a target state to be visited
    almost-surely (i.e., with probability 1), or positively (i.e., with positive probability),
    no matter the strategy of the second player. We classify such games according
    to the information and the power of randomization available to the players. On
    the basis of information, the game can be one-sided with either (a) player 1,
    or (b) player 2 having partial observation (and the other player has perfect observation),
    or two-sided with (c) both players having partial observation. On the basis of
    randomization, the players (a) may not be allowed to use randomization (pure strategies),
    or (b) may choose a probability distribution over actions but the actual random
    choice is external and not visible to the player (actions invisible), or (c) may
    use full randomization. Our main results for pure strategies are as follows. (1)
    For one-sided games with player 1 having partial observation we show that (in
    contrast to full randomized strategies) belief-based (subset-construction based)
    strategies are not sufficient, and we present an exponential upper bound on memory
    both for almostsure and positive winning strategies; we show that the problem
    of deciding the existence of almost-sure and positive winning strategies for player
    1 is EXPTIME-complete. (2) For one-sided games with player 2 having partial observation
    we show that non-elementary memory is both necessary and sufficient for both almost-sure
    and positive winning strategies. (3) We show that for the general (two-sided)
    case finite-memory strategies are sufficient for both positive and almost-sure
    winning, and at least non-elementary memory is required. We establish the equivalence
    of the almost-sure winning problems for pure strategies and for randomized strategies
    with actions invisible. Our equivalence result exhibits serious flaws in previous
    results of the literature: we show a non-elementary memory lower bound for almost-sure
    winning whereas an exponential upper bound was previously claimed.'
acknowledgement: 'This work was partially supported by FWF Grant No P 23499-N23, FWF
  NFN Grant No S11407-N23 (RiSE), ERC Start grant (279307: Graph Games), and Microsoft
  faculty fellows award.'
article_number: '6280436'
arxiv: 1
author:
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Laurent
  full_name: Doyen, Laurent
  last_name: Doyen
citation:
  ama: 'Chatterjee K, Doyen L. Partial-observation stochastic games: How to win when
    belief fails. In: <i>Proceedings of the 2012 27th Annual ACM/IEEE Symposium on
    Logic in Computer Science</i>. IEEE; 2012. doi:<a href="https://doi.org/10.1109/LICS.2012.28">10.1109/LICS.2012.28</a>'
  apa: 'Chatterjee, K., &#38; Doyen, L. (2012). Partial-observation stochastic games:
    How to win when belief fails. In <i>Proceedings of the 2012 27th Annual ACM/IEEE
    Symposium on Logic in Computer Science</i>. Dubrovnik, Croatia: IEEE. <a href="https://doi.org/10.1109/LICS.2012.28">https://doi.org/10.1109/LICS.2012.28</a>'
  chicago: 'Chatterjee, Krishnendu, and Laurent Doyen. “Partial-Observation Stochastic
    Games: How to Win When Belief Fails.” In <i>Proceedings of the 2012 27th Annual
    ACM/IEEE Symposium on Logic in Computer Science</i>. IEEE, 2012. <a href="https://doi.org/10.1109/LICS.2012.28">https://doi.org/10.1109/LICS.2012.28</a>.'
  ieee: 'K. Chatterjee and L. Doyen, “Partial-observation stochastic games: How to
    win when belief fails,” in <i>Proceedings of the 2012 27th Annual ACM/IEEE Symposium
    on Logic in Computer Science</i>, Dubrovnik, Croatia, 2012.'
  ista: 'Chatterjee K, Doyen L. 2012. Partial-observation stochastic games: How to
    win when belief fails. Proceedings of the 2012 27th Annual ACM/IEEE Symposium
    on Logic in Computer Science. LICS: Logic in Computer Science, 6280436.'
  mla: 'Chatterjee, Krishnendu, and Laurent Doyen. “Partial-Observation Stochastic
    Games: How to Win When Belief Fails.” <i>Proceedings of the 2012 27th Annual ACM/IEEE
    Symposium on Logic in Computer Science</i>, 6280436, IEEE, 2012, doi:<a href="https://doi.org/10.1109/LICS.2012.28">10.1109/LICS.2012.28</a>.'
  short: K. Chatterjee, L. Doyen, in:, Proceedings of the 2012 27th Annual ACM/IEEE
    Symposium on Logic in Computer Science, IEEE, 2012.
conference:
  end_date: 2012-06-28
  location: Dubrovnik, Croatia
  name: 'LICS: Logic in Computer Science'
  start_date: 2012-06-25
date_created: 2018-12-11T12:00:32Z
date_published: 2012-08-23T00:00:00Z
date_updated: 2023-02-23T12:23:43Z
day: '23'
department:
- _id: KrCh
doi: 10.1109/LICS.2012.28
ec_funded: 1
external_id:
  arxiv:
  - '1107.2141'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1107.2141
month: '08'
oa: 1
oa_version: Preprint
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 23499-N23
  name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2587B514-B435-11E9-9278-68D0E5697425
  name: Microsoft Research Faculty Fellowship
publication: Proceedings of the 2012 27th Annual ACM/IEEE Symposium on Logic in Computer
  Science
publication_status: published
publisher: IEEE
publist_id: '3771'
quality_controlled: '1'
related_material:
  record:
  - id: '2211'
    relation: later_version
    status: public
  - id: '5381'
    relation: earlier_version
    status: public
scopus_import: 1
status: public
title: 'Partial-observation stochastic games: How to win when belief fails'
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2012'
...
---
_id: '2956'
abstract:
- lang: eng
  text: 'Two-player games on graphs are central in many problems in formal verification
    and program analysis such as synthesis and verification of open systems. In this
    work we consider solving recursive game graphs (or pushdown game graphs) that
    can model the control flow of sequential programs with recursion. While pushdown
    games have been studied before with qualitative objectives, such as reachability
    and parity objectives, in this work we study for the first time such games with
    the most well-studied quantitative objective, namely, mean payoff objectives.
    In pushdown games two types of strategies are relevant: (1) global strategies,
    that depend on the entire global history; and (2) modular strategies, that have
    only local memory and thus do not depend on the context of invocation, but only
    on the history of the current invocation of the module. Our main results are as
    follows: (1) One-player pushdown games with mean-payoff objectives under global
    strategies are decidable in polynomial time. (2) Two-player pushdown games with
    mean-payoff objectives under global strategies are undecidable. (3) One-player
    pushdown games with mean-payoff objectives under modular strategies are NP-hard.
    (4) Two-player pushdown games with mean-payoff objectives under modular strategies
    can be solved in NP (i.e., both one-player and two-player pushdown games with
    mean-payoff objectives under modular strategies are NP-complete). We also establish
    the optimal strategy complexity showing that global strategies for mean-payoff
    objectives require infinite memory even in one-player pushdown games; and memoryless
    modular strategies are sufficient in two-player pushdown games. Finally we also
    show that all the problems have the same computational complexity if the stack
    boundedness condition is added, where along with the mean-payoff objective the
    player must also ensure that the stack height is bounded.'
acknowledgement: "The research was supported by Austrian Science Fund (FWF) Grant
  No P 23499-N23, FWF NFN Grant No S11407-N23 (RiSE), ERC Start grant (279307: Graph
  Games), Microsoft faculty fellows award, the Israeli Centers of Research Excellence
  (ICORE) program, (Center No. 4/11), the RICH Model Toolkit (ICT COST Action IC0901),
  and was carried out in partial fulfillment of the requirements for the Ph.D. degree
  of the second author.\r\nA Technical Report of this paper is available via internal
  link."
article_number: '6280438'
author:
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Yaron
  full_name: Velner, Yaron
  last_name: Velner
citation:
  ama: 'Chatterjee K, Velner Y. Mean payoff pushdown games. In: <i>Proceedings of
    the 2012 27th Annual ACM/IEEE Symposium on Logic in Computer Science</i>. IEEE;
    2012. doi:<a href="https://doi.org/10.1109/LICS.2012.30">10.1109/LICS.2012.30</a>'
  apa: 'Chatterjee, K., &#38; Velner, Y. (2012). Mean payoff pushdown games. In <i>Proceedings
    of the 2012 27th Annual ACM/IEEE Symposium on Logic in Computer Science</i>. Dubrovnik,
    Croatia : IEEE. <a href="https://doi.org/10.1109/LICS.2012.30">https://doi.org/10.1109/LICS.2012.30</a>'
  chicago: Chatterjee, Krishnendu, and Yaron Velner. “Mean Payoff Pushdown Games.”
    In <i>Proceedings of the 2012 27th Annual ACM/IEEE Symposium on Logic in Computer
    Science</i>. IEEE, 2012. <a href="https://doi.org/10.1109/LICS.2012.30">https://doi.org/10.1109/LICS.2012.30</a>.
  ieee: K. Chatterjee and Y. Velner, “Mean payoff pushdown games,” in <i>Proceedings
    of the 2012 27th Annual ACM/IEEE Symposium on Logic in Computer Science</i>, Dubrovnik,
    Croatia , 2012.
  ista: 'Chatterjee K, Velner Y. 2012. Mean payoff pushdown games. Proceedings of
    the 2012 27th Annual ACM/IEEE Symposium on Logic in Computer Science. LICS: Logic
    in Computer Science, 6280438.'
  mla: Chatterjee, Krishnendu, and Yaron Velner. “Mean Payoff Pushdown Games.” <i>Proceedings
    of the 2012 27th Annual ACM/IEEE Symposium on Logic in Computer Science</i>, 6280438,
    IEEE, 2012, doi:<a href="https://doi.org/10.1109/LICS.2012.30">10.1109/LICS.2012.30</a>.
  short: K. Chatterjee, Y. Velner, in:, Proceedings of the 2012 27th Annual ACM/IEEE
    Symposium on Logic in Computer Science, IEEE, 2012.
conference:
  end_date: 2012-06-28
  location: 'Dubrovnik, Croatia '
  name: 'LICS: Logic in Computer Science'
  start_date: 2012-06-25
date_created: 2018-12-11T12:00:32Z
date_published: 2012-08-23T00:00:00Z
date_updated: 2023-02-23T12:23:30Z
day: '23'
department:
- _id: KrCh
doi: 10.1109/LICS.2012.30
ec_funded: 1
language:
- iso: eng
month: '08'
oa_version: None
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 23499-N23
  name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2587B514-B435-11E9-9278-68D0E5697425
  name: Microsoft Research Faculty Fellowship
publication: Proceedings of the 2012 27th Annual ACM/IEEE Symposium on Logic in Computer
  Science
publication_status: published
publisher: IEEE
publist_id: '3770'
quality_controlled: '1'
related_material:
  record:
  - id: '5377'
    relation: earlier_version
    status: public
scopus_import: 1
status: public
title: Mean payoff pushdown games
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2012'
...
---
_id: '2957'
abstract:
- lang: eng
  text: 'We consider probabilistic automata on infinite words with acceptance defined
    by parity conditions. We consider three qualitative decision problems: (i) the
    positive decision problem asks whether there is a word that is accepted with positive
    probability; (ii) the almost decision problem asks whether there is a word that
    is accepted with probability 1; and (iii) the limit decision problem asks whether
    words are accepted with probability arbitrarily close to 1. We unify and generalize
    several decidability results for probabilistic automata over infinite words, and
    identify a robust (closed under union and intersection) subclass of probabilistic
    automata for which all the qualitative decision problems are decidable for parity
    conditions. We also show that if the input words are restricted to lasso shape
    (regular) words, then the positive and almost problems are decidable for all probabilistic
    automata with parity conditions. For most decidable problems we show an optimal
    PSPACE-complete complexity bound.'
article_number: '6280437'
arxiv: 1
author:
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Mathieu
  full_name: Tracol, Mathieu
  id: 3F54FA38-F248-11E8-B48F-1D18A9856A87
  last_name: Tracol
citation:
  ama: 'Chatterjee K, Tracol M. Decidable problems for probabilistic automata on infinite
    words. In: <i>Proceedings of the 2012 27th Annual ACM/IEEE Symposium on Logic
    in Computer Science</i>. IEEE; 2012. doi:<a href="https://doi.org/10.1109/LICS.2012.29">10.1109/LICS.2012.29</a>'
  apa: 'Chatterjee, K., &#38; Tracol, M. (2012). Decidable problems for probabilistic
    automata on infinite words. In <i>Proceedings of the 2012 27th Annual ACM/IEEE
    Symposium on Logic in Computer Science</i>. Dubrovnik, Croatia : IEEE. <a href="https://doi.org/10.1109/LICS.2012.29">https://doi.org/10.1109/LICS.2012.29</a>'
  chicago: Chatterjee, Krishnendu, and Mathieu Tracol. “Decidable Problems for Probabilistic
    Automata on Infinite Words.” In <i>Proceedings of the 2012 27th Annual ACM/IEEE
    Symposium on Logic in Computer Science</i>. IEEE, 2012. <a href="https://doi.org/10.1109/LICS.2012.29">https://doi.org/10.1109/LICS.2012.29</a>.
  ieee: K. Chatterjee and M. Tracol, “Decidable problems for probabilistic automata
    on infinite words,” in <i>Proceedings of the 2012 27th Annual ACM/IEEE Symposium
    on Logic in Computer Science</i>, Dubrovnik, Croatia , 2012.
  ista: 'Chatterjee K, Tracol M. 2012. Decidable problems for probabilistic automata
    on infinite words. Proceedings of the 2012 27th Annual ACM/IEEE Symposium on Logic
    in Computer Science. LICS: Logic in Computer Science, 6280437.'
  mla: Chatterjee, Krishnendu, and Mathieu Tracol. “Decidable Problems for Probabilistic
    Automata on Infinite Words.” <i>Proceedings of the 2012 27th Annual ACM/IEEE Symposium
    on Logic in Computer Science</i>, 6280437, IEEE, 2012, doi:<a href="https://doi.org/10.1109/LICS.2012.29">10.1109/LICS.2012.29</a>.
  short: K. Chatterjee, M. Tracol, in:, Proceedings of the 2012 27th Annual ACM/IEEE
    Symposium on Logic in Computer Science, IEEE, 2012.
conference:
  end_date: 2012-06-28
  location: 'Dubrovnik, Croatia '
  name: 'LICS: Logic in Computer Science'
  start_date: 2012-06-25
date_created: 2018-12-11T12:00:33Z
date_published: 2012-08-23T00:00:00Z
date_updated: 2023-02-23T12:23:51Z
day: '23'
department:
- _id: KrCh
doi: 10.1109/LICS.2012.29
ec_funded: 1
external_id:
  arxiv:
  - '1107.2091'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1107.2091
month: '08'
oa: 1
oa_version: Preprint
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 23499-N23
  name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2587B514-B435-11E9-9278-68D0E5697425
  name: Microsoft Research Faculty Fellowship
publication: Proceedings of the 2012 27th Annual ACM/IEEE Symposium on Logic in Computer
  Science
publication_status: published
publisher: IEEE
publist_id: '3769'
quality_controlled: '1'
related_material:
  record:
  - id: '5384'
    relation: earlier_version
    status: public
scopus_import: 1
status: public
title: Decidable problems for probabilistic automata on infinite words
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2012'
...
---
_id: '2958'
abstract:
- lang: eng
  text: 'The activity of hippocampal pyramidal cells reflects both the current position
    of the animal and information related to its current behavior. Here we investigated
    whether single hippocampal neurons can encode several independent features defining
    trials during a memory task. We also tested whether task-related information is
    represented by partial remapping of the place cell population or, instead, via
    firing rate modulation of spatially stable place cells. To address these two questions,
    the activity of hippocampal neurons was recorded in rats performing a conditional
    discrimination task on a modified T-maze in which the identity of a food reward
    guided behavior. When the rat was on the central arm of the maze, the firing rate
    of pyramidal cells changed depending on two independent factors: (1) the identity
    of the food reward given to the animal and (2) the previous location of the animal
    on the maze. Importantly, some pyramidal cells encoded information relative to
    both factors. This trial-type specific and retrospective coding did not interfere
    with the spatial representation of the maze: hippocampal cells had stable place
    fields and their theta-phase precession profiles were unaltered during the task,
    indicating that trial-related information was encoded via rate remapping. During
    error trials, encoding of both trial-related information and spatial location
    was impaired. Finally, we found that pyramidal cells also encode trial-related
    information via rate remapping during the continuous version of the rewarded alternation
    task without delays. These results suggest that hippocampal neurons can encode
    several task-related cognitive aspects via rate remapping.'
acknowledgement: J.C. was supported by a MRC Intramural Programme Grant (U138197111)
  and a European Research Council Starter Grant (281511). K.A. held a Wellcome Trust
  PhD studentship and a Humboldt Research Fellowship for Postdoctoral Researchers.
  D.M.B. was supported by Wellcome Trust Senior Fellowships (074385 and 087736).
author:
- first_name: Kevin
  full_name: Allen, Kevin
  last_name: Allen
- first_name: J Nick
  full_name: Rawlins, J Nick
  last_name: Rawlins
- first_name: David
  full_name: Bannerman, David
  last_name: Bannerman
- 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: Allen K, Rawlins JN, Bannerman D, Csicsvari JL. Hippocampal place cells can
    encode multiple trial-dependent features through rate remapping. <i>Journal of
    Neuroscience</i>. 2012;32(42):14752-14766. doi:<a href="https://doi.org/10.1523/JNEUROSCI.6175-11.2012">10.1523/JNEUROSCI.6175-11.2012</a>
  apa: Allen, K., Rawlins, J. N., Bannerman, D., &#38; Csicsvari, J. L. (2012). Hippocampal
    place cells can encode multiple trial-dependent features through rate remapping.
    <i>Journal of Neuroscience</i>. Society for Neuroscience. <a href="https://doi.org/10.1523/JNEUROSCI.6175-11.2012">https://doi.org/10.1523/JNEUROSCI.6175-11.2012</a>
  chicago: Allen, Kevin, J Nick Rawlins, David Bannerman, and Jozsef L Csicsvari.
    “Hippocampal Place Cells Can Encode Multiple Trial-Dependent Features through
    Rate Remapping.” <i>Journal of Neuroscience</i>. Society for Neuroscience, 2012.
    <a href="https://doi.org/10.1523/JNEUROSCI.6175-11.2012">https://doi.org/10.1523/JNEUROSCI.6175-11.2012</a>.
  ieee: K. Allen, J. N. Rawlins, D. Bannerman, and J. L. Csicsvari, “Hippocampal place
    cells can encode multiple trial-dependent features through rate remapping,” <i>Journal
    of Neuroscience</i>, vol. 32, no. 42. Society for Neuroscience, pp. 14752–14766,
    2012.
  ista: Allen K, Rawlins JN, Bannerman D, Csicsvari JL. 2012. Hippocampal place cells
    can encode multiple trial-dependent features through rate remapping. Journal of
    Neuroscience. 32(42), 14752–14766.
  mla: Allen, Kevin, et al. “Hippocampal Place Cells Can Encode Multiple Trial-Dependent
    Features through Rate Remapping.” <i>Journal of Neuroscience</i>, vol. 32, no.
    42, Society for Neuroscience, 2012, pp. 14752–66, doi:<a href="https://doi.org/10.1523/JNEUROSCI.6175-11.2012">10.1523/JNEUROSCI.6175-11.2012</a>.
  short: K. Allen, J.N. Rawlins, D. Bannerman, J.L. Csicsvari, Journal of Neuroscience
    32 (2012) 14752–14766.
date_created: 2018-12-11T12:00:33Z
date_published: 2012-10-17T00:00:00Z
date_updated: 2021-01-12T07:40:03Z
day: '17'
department:
- _id: JoCs
doi: 10.1523/JNEUROSCI.6175-11.2012
ec_funded: 1
external_id:
  pmid:
  - '23077060'
intvolume: '        32'
issue: '42'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531717/
month: '10'
oa: 1
oa_version: Submitted Version
page: 14752 - 14766
pmid: 1
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: Journal of Neuroscience
publication_status: published
publisher: Society for Neuroscience
publist_id: '3768'
quality_controlled: '1'
scopus_import: 1
status: public
title: Hippocampal place cells can encode multiple trial-dependent features through
  rate remapping
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 32
year: '2012'
...
---
_id: '2959'
abstract:
- lang: eng
  text: We study maximum likelihood estimation in Gaussian graphical models from a
    geometric point of view. An algebraic elimination criterion allows us to find
    exact lower bounds on the number of observations needed to ensure that the maximum
    likelihood estimator (MLE) exists with probability one. This is applied to bipartite
    graphs, grids and colored graphs. We also study the ML degree, and we present
    the first instance of a graph for which the MLE exists with probability one, even
    when the number of observations equals the treewidth.
acknowledgement: "I wish to thank Bernd Sturmfels for many helpful discus- sions and
  Steffen Lauritzen for introducing me to the problem of the existence of the MLE
  in Gaussian graphical models. I would also like to thank two referees who provided
  helpful comments on the original version of this paper.\r\n"
author:
- first_name: Caroline
  full_name: Uhler, Caroline
  id: 49ADD78E-F248-11E8-B48F-1D18A9856A87
  last_name: Uhler
  orcid: 0000-0002-7008-0216
citation:
  ama: Uhler C. Geometry of maximum likelihood estimation in Gaussian graphical models.
    <i>Annals of Statistics</i>. 2012;40(1):238-261. doi:<a href="https://doi.org/10.1214/11-AOS957">10.1214/11-AOS957</a>
  apa: Uhler, C. (2012). Geometry of maximum likelihood estimation in Gaussian graphical
    models. <i>Annals of Statistics</i>. Institute of Mathematical Statistics. <a
    href="https://doi.org/10.1214/11-AOS957">https://doi.org/10.1214/11-AOS957</a>
  chicago: Uhler, Caroline. “Geometry of Maximum Likelihood Estimation in Gaussian
    Graphical Models.” <i>Annals of Statistics</i>. Institute of Mathematical Statistics,
    2012. <a href="https://doi.org/10.1214/11-AOS957">https://doi.org/10.1214/11-AOS957</a>.
  ieee: C. Uhler, “Geometry of maximum likelihood estimation in Gaussian graphical
    models,” <i>Annals of Statistics</i>, vol. 40, no. 1. Institute of Mathematical
    Statistics, pp. 238–261, 2012.
  ista: Uhler C. 2012. Geometry of maximum likelihood estimation in Gaussian graphical
    models. Annals of Statistics. 40(1), 238–261.
  mla: Uhler, Caroline. “Geometry of Maximum Likelihood Estimation in Gaussian Graphical
    Models.” <i>Annals of Statistics</i>, vol. 40, no. 1, Institute of Mathematical
    Statistics, 2012, pp. 238–61, doi:<a href="https://doi.org/10.1214/11-AOS957">10.1214/11-AOS957</a>.
  short: C. Uhler, Annals of Statistics 40 (2012) 238–261.
date_created: 2018-12-11T12:00:33Z
date_published: 2012-02-01T00:00:00Z
date_updated: 2021-01-12T07:40:04Z
day: '01'
department:
- _id: CaUh
doi: 10.1214/11-AOS957
intvolume: '        40'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1012.2643
month: '02'
oa: 1
oa_version: Preprint
page: 238 - 261
publication: Annals of Statistics
publication_status: published
publisher: Institute of Mathematical Statistics
publist_id: '3767'
quality_controlled: '1'
scopus_import: 1
status: public
title: Geometry of maximum likelihood estimation in Gaussian graphical models
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 40
year: '2012'
...
---
_id: '2962'
abstract:
- lang: eng
  text: The choice of summary statistics is a crucial step in approximate Bayesian
    computation (ABC). Since statistics are often not sufficient, this choice involves
    a trade-off between loss of information and reduction of dimensionality. The latter
    may increase the efficiency of ABC. Here, we propose an approach for choosing
    summary statistics based on boosting, a technique from the machine learning literature.
    We consider different types of boosting and compare them to partial least squares
    regression as an alternative. To mitigate the lack of sufficiency, we also propose
    an approach for choosing summary statistics locally, in the putative neighborhood
    of the true parameter value. We study a demographic model motivated by the re-introduction
    of Alpine ibex (Capra ibex) into the Swiss Alps. The parameters of interest are
    the mean and standard deviation across microsatellites of the scaled ancestral
    mutation rate (θanc = 4 Ne u), and the proportion of males obtaining access to
    matings per breeding season (ω). By simulation, we assess the properties of the
    posterior distribution obtained with the various methods. According to our criteria,
    ABC with summary statistics chosen locally via boosting with the L2-loss performs
    best. Applying that method to the ibex data, we estimate θanc ≈ 1.288, and find
    that most of the variation across loci of the ancestral mutation rate u is between
    7.7×10−4 and 3.5×10−3 per locus per generation. The proportion of males with access
    to matings is estimated to ω ≈ 0.21, which is in good agreement with recent independent
    estimates.
acknowledged_ssus:
- _id: ScienComp
author:
- first_name: Simon
  full_name: Aeschbacher, Simon
  id: 2D35326E-F248-11E8-B48F-1D18A9856A87
  last_name: Aeschbacher
- first_name: Mark
  full_name: Beaumont, Mark
  last_name: Beaumont
- first_name: Andreas
  full_name: Futschik, Andreas
  last_name: Futschik
citation:
  ama: Aeschbacher S, Beaumont M, Futschik A. A novel approach for choosing summary
    statistics in approximate Bayesian computation. <i>Genetics</i>. 2012;192(3):1027-1047.
    doi:<a href="https://doi.org/10.1534/genetics.112.143164">10.1534/genetics.112.143164</a>
  apa: Aeschbacher, S., Beaumont, M., &#38; Futschik, A. (2012). A novel approach
    for choosing summary statistics in approximate Bayesian computation. <i>Genetics</i>.
    Genetics Society of America. <a href="https://doi.org/10.1534/genetics.112.143164">https://doi.org/10.1534/genetics.112.143164</a>
  chicago: Aeschbacher, Simon, Mark Beaumont, and Andreas Futschik. “A Novel Approach
    for Choosing Summary Statistics in Approximate Bayesian Computation.” <i>Genetics</i>.
    Genetics Society of America, 2012. <a href="https://doi.org/10.1534/genetics.112.143164">https://doi.org/10.1534/genetics.112.143164</a>.
  ieee: S. Aeschbacher, M. Beaumont, and A. Futschik, “A novel approach for choosing
    summary statistics in approximate Bayesian computation,” <i>Genetics</i>, vol.
    192, no. 3. Genetics Society of America, pp. 1027–1047, 2012.
  ista: Aeschbacher S, Beaumont M, Futschik A. 2012. A novel approach for choosing
    summary statistics in approximate Bayesian computation. Genetics. 192(3), 1027–1047.
  mla: Aeschbacher, Simon, et al. “A Novel Approach for Choosing Summary Statistics
    in Approximate Bayesian Computation.” <i>Genetics</i>, vol. 192, no. 3, Genetics
    Society of America, 2012, pp. 1027–47, doi:<a href="https://doi.org/10.1534/genetics.112.143164">10.1534/genetics.112.143164</a>.
  short: S. Aeschbacher, M. Beaumont, A. Futschik, Genetics 192 (2012) 1027–1047.
date_created: 2018-12-11T12:00:34Z
date_published: 2012-11-01T00:00:00Z
date_updated: 2021-01-12T07:40:05Z
day: '01'
department:
- _id: NiBa
doi: 10.1534/genetics.112.143164
external_id:
  pmid:
  - '22960215'
intvolume: '       192'
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522150/
month: '11'
oa: 1
oa_version: Submitted Version
page: 1027 - 1047
pmid: 1
publication: Genetics
publication_status: published
publisher: Genetics Society of America
publist_id: '3763'
quality_controlled: '1'
scopus_import: 1
status: public
title: A novel approach for choosing summary statistics in approximate Bayesian computation
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 192
year: '2012'
...
---
_id: '2963'
abstract:
- lang: eng
  text: 'Zebra finches are an ubiquitous model system for the study of vocal learning
    in animal communication. Their song has been well described, but its possible
    function(s) in social communication are only partly understood. The so-called
    ‘directed song’ is a high-intensity, high-performance song given during courtship
    in close proximity to the female, which is known to mediate mate choice and mating.
    However, this singing mode constitutes only a fraction of zebra finch males’ prolific
    song output. Potential communicative functions of their second, ‘undirected’ singing
    mode remain unresolved in the face of contradicting reports of both facilitating
    and inhibiting effects of social company on singing. We addressed this issue by
    experimentally manipulating social contexts in a within-subject design, comparing
    a solo versus male or female only company condition, each lasting for 24 hours.
    Males’ total song output was significantly higher when a conspecific was in audible
    and visible distance than when they were alone. Male and female company had an
    equally facilitating effect on song output. Our findings thus indicate that singing
    motivation is facilitated rather than inhibited by social company, suggesting
    that singing in zebra finches might function both in inter- and intrasexual communication. '
author:
- first_name: Fabienne
  full_name: Jesse, Fabienne
  id: 4C8C26A4-F248-11E8-B48F-1D18A9856A87
  last_name: Jesse
- first_name: Katharina
  full_name: Riebel, Katharina
  last_name: Riebel
citation:
  ama: Jesse F, Riebel K. Social facilitation of male song by male and female conspecifics
    in the zebra finch, Taeniopygia guttata. <i>Behavioural Processes</i>. 2012;91(3):262-266.
    doi:<a href="https://doi.org/10.1016/j.beproc.2012.09.006">10.1016/j.beproc.2012.09.006</a>
  apa: Jesse, F., &#38; Riebel, K. (2012). Social facilitation of male song by male
    and female conspecifics in the zebra finch, Taeniopygia guttata. <i>Behavioural
    Processes</i>. Elsevier. <a href="https://doi.org/10.1016/j.beproc.2012.09.006">https://doi.org/10.1016/j.beproc.2012.09.006</a>
  chicago: Jesse, Fabienne, and Katharina Riebel. “Social Facilitation of Male Song
    by Male and Female Conspecifics in the Zebra Finch, Taeniopygia Guttata.” <i>Behavioural
    Processes</i>. Elsevier, 2012. <a href="https://doi.org/10.1016/j.beproc.2012.09.006">https://doi.org/10.1016/j.beproc.2012.09.006</a>.
  ieee: F. Jesse and K. Riebel, “Social facilitation of male song by male and female
    conspecifics in the zebra finch, Taeniopygia guttata,” <i>Behavioural Processes</i>,
    vol. 91, no. 3. Elsevier, pp. 262–266, 2012.
  ista: Jesse F, Riebel K. 2012. Social facilitation of male song by male and female
    conspecifics in the zebra finch, Taeniopygia guttata. Behavioural Processes. 91(3),
    262–266.
  mla: Jesse, Fabienne, and Katharina Riebel. “Social Facilitation of Male Song by
    Male and Female Conspecifics in the Zebra Finch, Taeniopygia Guttata.” <i>Behavioural
    Processes</i>, vol. 91, no. 3, Elsevier, 2012, pp. 262–66, doi:<a href="https://doi.org/10.1016/j.beproc.2012.09.006">10.1016/j.beproc.2012.09.006</a>.
  short: F. Jesse, K. Riebel, Behavioural Processes 91 (2012) 262–266.
date_created: 2018-12-11T12:00:35Z
date_published: 2012-11-01T00:00:00Z
date_updated: 2021-01-12T07:40:06Z
day: '01'
department:
- _id: JoBo
doi: 10.1016/j.beproc.2012.09.006
intvolume: '        91'
issue: '3'
language:
- iso: eng
month: '11'
oa_version: None
page: 262 - 266
publication: Behavioural Processes
publication_status: published
publisher: Elsevier
publist_id: '3756'
quality_controlled: '1'
status: public
title: Social facilitation of male song by male and female conspecifics in the zebra
  finch, Taeniopygia guttata
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 91
year: '2012'
...
---
_id: '2964'
abstract:
- lang: eng
  text: 'CA3 pyramidal neurons are important for memory formation and pattern completion
    in the hippocampal network. These neurons receive multiple excitatory inputs from
    numerous sources. Therefore, the rules of spatiotemporal integration of multiple
    synaptic inputs and propagation of action potentials are important to understand
    how CA3 neurons contribute to higher brain functions at cellular level. By using
    confocally targeted patch-clamp recording techniques, we investigated the biophysical
    properties of rat CA3 pyramidal neuron dendrites. We found two distinct dendritic
    domains critical for action potential initiation and propagation: In the proximal
    domain, action potentials initiated in the axon backpropagate actively with large
    amplitude and fast time course. In the distal domain, Na+-channel mediated dendritic
    spikes are efficiently evoked by local dendritic depolarization or waveforms mimicking
    synaptic events. These findings can be explained by a high Na+-to-K+ conductance
    density ratio of CA3 pyramidal neuron dendrites. The results challenge the prevailing
    view that proximal mossy fiber inputs activate CA3 pyramidal neurons more efficiently
    than distal perforant inputs by showing that the distal synapses trigger a different
    form of activity represented by dendritic spikes. The high probability of dendritic
    spike initiation in the distal area may enhance the computational power of CA3
    pyramidal neurons in the hippocampal network.  '
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Sooyun
  full_name: Kim, Sooyun
  id: 394AB1C8-F248-11E8-B48F-1D18A9856A87
  last_name: Kim
citation:
  ama: Kim S. Active properties of hippocampal CA3 pyramidal neuron dendrites. 2012.
  apa: Kim, S. (2012). <i>Active properties of hippocampal CA3 pyramidal neuron dendrites</i>.
    Institute of Science and Technology Austria.
  chicago: Kim, Sooyun. “Active Properties of Hippocampal CA3 Pyramidal Neuron Dendrites.”
    Institute of Science and Technology Austria, 2012.
  ieee: S. Kim, “Active properties of hippocampal CA3 pyramidal neuron dendrites,”
    Institute of Science and Technology Austria, 2012.
  ista: Kim S. 2012. Active properties of hippocampal CA3 pyramidal neuron dendrites.
    Institute of Science and Technology Austria.
  mla: Kim, Sooyun. <i>Active Properties of Hippocampal CA3 Pyramidal Neuron Dendrites</i>.
    Institute of Science and Technology Austria, 2012.
  short: S. Kim, Active Properties of Hippocampal CA3 Pyramidal Neuron Dendrites,
    Institute of Science and Technology Austria, 2012.
date_created: 2018-12-11T12:00:35Z
date_published: 2012-06-01T00:00:00Z
date_updated: 2023-09-07T11:43:51Z
day: '01'
degree_awarded: PhD
department:
- _id: PeJo
- _id: GradSch
language:
- iso: eng
month: '06'
oa_version: None
page: '65'
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
publist_id: '3755'
related_material:
  record:
  - id: '3258'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
title: Active properties of hippocampal CA3 pyramidal neuron dendrites
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2012'
...
---
_id: '2965'
abstract:
- lang: eng
  text: Dieser Artikel soll die sechs verschiedenen Creative Commons Lizenzen erläutern
    und ihre Bedeutung im Rahmen des wissenschaftlichen Publizierens und des Open
    Access erklären (CC-BY, CC-BY-SA, CC-BY-NC, CC-BY-ND, CC-BYNC-SA, CC-BY-NC-ND).
author:
- first_name: Patrick
  full_name: Danowski, Patrick
  id: 2EBD1598-F248-11E8-B48F-1D18A9856A87
  last_name: Danowski
  orcid: 0000-0002-6026-4409
citation:
  ama: 'Danowski P. Kontext Open Access: Creative Commons. <i>Mitteilungen der Vereinigung
    Österreichischer Bibliothekarinnen &#38; Bibliothekare</i>. 2012;65(2):200-212.'
  apa: 'Danowski, P. (2012). Kontext Open Access: Creative Commons. <i>Mitteilungen
    der Vereinigung Österreichischer Bibliothekarinnen &#38; Bibliothekare</i>. VÖB.'
  chicago: 'Danowski, Patrick. “Kontext Open Access: Creative Commons.” <i>Mitteilungen
    der Vereinigung Österreichischer Bibliothekarinnen &#38; Bibliothekare</i>. VÖB,
    2012.'
  ieee: 'P. Danowski, “Kontext Open Access: Creative Commons,” <i>Mitteilungen der
    Vereinigung Österreichischer Bibliothekarinnen &#38; Bibliothekare</i>, vol. 65,
    no. 2. VÖB, pp. 200–212, 2012.'
  ista: 'Danowski P. 2012. Kontext Open Access: Creative Commons. Mitteilungen der
    Vereinigung Österreichischer Bibliothekarinnen &#38; Bibliothekare. 65(2), 200–212.'
  mla: 'Danowski, Patrick. “Kontext Open Access: Creative Commons.” <i>Mitteilungen
    der Vereinigung Österreichischer Bibliothekarinnen &#38; Bibliothekare</i>, vol.
    65, no. 2, VÖB, 2012, pp. 200–12.'
  short: P. Danowski, Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen
    &#38; Bibliothekare 65 (2012) 200–212.
date_created: 2018-12-11T12:00:35Z
date_published: 2012-09-01T00:00:00Z
date_updated: 2021-01-12T07:40:07Z
day: '01'
ddc:
- '020'
department:
- _id: E-Lib
file:
- access_level: open_access
  checksum: 162eea47d9d840c26b496ba6ae4d1c09
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:08:42Z
  date_updated: 2020-07-14T12:45:57Z
  file_id: '4703'
  file_name: IST-2012-95-v1+1_sp-beitrag_danowski_kontext_open_access_creative_commons.pdf
  file_size: 503345
  relation: main_file
file_date_updated: 2020-07-14T12:45:57Z
has_accepted_license: '1'
intvolume: '        65'
issue: '2'
language:
- iso: ger
main_file_link:
- open_access: '1'
  url: ' http://hdl.handle.net/10760/17625'
month: '09'
oa: 1
oa_version: Published Version
page: 200 - 212
popular_science: '1'
publication: Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare
publication_status: published
publisher: VÖB
publist_id: '3754'
pubrep_id: '95'
scopus_import: 1
status: public
title: 'Kontext Open Access: Creative Commons'
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: 65
year: '2012'
...
---
_id: '2966'
abstract:
- lang: eng
  text: 'Background: The outcome of male-male competition can be predicted from the
    relative fighting qualities of the opponents, which often depend on their age.
    In insects, freshly emerged and still sexually inactive males are morphologically
    indistinct from older, sexually active males. These young inactive males may thus
    be easy targets for older males if they cannot conceal themselves from their attacks.
    The ant Cardiocondyla obscurior is characterised by lethal fighting between wingless
    (&quot; ergatoid&quot; ) males. Here, we analyse for how long young males are
    defenceless after eclosion, and how early adult males can detect the presence
    of rival males.Results: We found that old ergatoid males consistently won fights
    against ergatoid males younger than two days. Old males did not differentiate
    between different types of unpigmented pupae several days before emergence, but
    had more frequent contact to ready-to-eclose pupae of female sexuals and winged
    males than of workers and ergatoid males. In rare cases, old ergatoid males displayed
    alleviated biting of pigmented ergatoid male pupae shortly before adult eclosion,
    as well as copulation attempts to dark pupae of female sexuals and winged males.
    Ergatoid male behaviour may be promoted by a closer similarity of the chemical
    profile of ready-to-eclose pupae to the profile of adults than that of young pupae
    several days prior to emergence.Conclusion: Young ergatoid males of C. obscurior
    would benefit greatly by hiding their identity from older, resident males, as
    they are highly vulnerable during the first two days of their adult lives. In
    contrast to the winged males of the same species, which are able to prevent ergatoid
    male attacks by chemical female mimicry, young ergatoids do not seem to be able
    to produce a protective chemical profile. Conflicts in male-male competition between
    ergatoid males of different age thus seem to be resolved in favour of the older
    males. This might represent selection at the colony level rather than the individual
    level. © 2012 Cremer et al.; licensee BioMed Central Ltd.'
article_number: '7'
author:
- first_name: Sylvia
  full_name: Cremer, Sylvia
  id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
  last_name: Cremer
  orcid: 0000-0002-2193-3868
- first_name: Masaki
  full_name: Suefuji, Masaki
  last_name: Suefuji
- first_name: Alexandra
  full_name: Schrempf, Alexandra
  last_name: Schrempf
- first_name: Jürgen
  full_name: Heinze, Jürgen
  last_name: Heinze
citation:
  ama: Cremer S, Suefuji M, Schrempf A, Heinze J. The dynamics of male-male competition
    in Cardiocondyla obscurior ants. <i>BMC Ecology</i>. 2012;12. doi:<a href="https://doi.org/10.1186/1472-6785-12-7">10.1186/1472-6785-12-7</a>
  apa: Cremer, S., Suefuji, M., Schrempf, A., &#38; Heinze, J. (2012). The dynamics
    of male-male competition in Cardiocondyla obscurior ants. <i>BMC Ecology</i>.
    BioMed Central. <a href="https://doi.org/10.1186/1472-6785-12-7">https://doi.org/10.1186/1472-6785-12-7</a>
  chicago: Cremer, Sylvia, Masaki Suefuji, Alexandra Schrempf, and Jürgen Heinze.
    “The Dynamics of Male-Male Competition in Cardiocondyla Obscurior Ants.” <i>BMC
    Ecology</i>. BioMed Central, 2012. <a href="https://doi.org/10.1186/1472-6785-12-7">https://doi.org/10.1186/1472-6785-12-7</a>.
  ieee: S. Cremer, M. Suefuji, A. Schrempf, and J. Heinze, “The dynamics of male-male
    competition in Cardiocondyla obscurior ants,” <i>BMC Ecology</i>, vol. 12. BioMed
    Central, 2012.
  ista: Cremer S, Suefuji M, Schrempf A, Heinze J. 2012. The dynamics of male-male
    competition in Cardiocondyla obscurior ants. BMC Ecology. 12, 7.
  mla: Cremer, Sylvia, et al. “The Dynamics of Male-Male Competition in Cardiocondyla
    Obscurior Ants.” <i>BMC Ecology</i>, vol. 12, 7, BioMed Central, 2012, doi:<a
    href="https://doi.org/10.1186/1472-6785-12-7">10.1186/1472-6785-12-7</a>.
  short: S. Cremer, M. Suefuji, A. Schrempf, J. Heinze, BMC Ecology 12 (2012).
date_created: 2018-12-11T12:00:35Z
date_published: 2012-06-15T00:00:00Z
date_updated: 2021-01-12T07:40:07Z
day: '15'
ddc:
- '570'
department:
- _id: SyCr
doi: 10.1186/1472-6785-12-7
file:
- access_level: open_access
  checksum: 03d004bdff3724fb1627e3f5004bad80
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:08:44Z
  date_updated: 2020-07-14T12:45:57Z
  file_id: '4706'
  file_name: IST-2012-94-v1+1_1472-6785-12-7.pdf
  file_size: 489994
  relation: main_file
file_date_updated: 2020-07-14T12:45:57Z
has_accepted_license: '1'
intvolume: '        12'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
publication: BMC Ecology
publication_status: published
publisher: BioMed Central
publist_id: '3753'
pubrep_id: '94'
quality_controlled: '1'
scopus_import: 1
status: public
title: The dynamics of male-male competition in Cardiocondyla obscurior ants
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: 12
year: '2012'
...
---
_id: '2967'
abstract:
- lang: eng
  text: For programs whose data variables range over Boolean or finite domains, program
    verification is decidable, and this forms the basis of recent tools for software
    model checking. In this article, we consider algorithmic verification of programs
    that use Boolean variables, and in addition, access a single read-only array whose
    length is potentially unbounded, and whose elements range over an unbounded data
    domain. We show that the reachability problem, while undecidable in general, is
    (1) PSPACE-complete for programs in which the array-accessing for-loops are not
    nested, (2) decidable for a restricted class of programs with doubly nested loops.
    The second result establishes connections to automata and logics defining languages
    over data words.
acknowledgement: This research was supported in part by the NSF Cybertrust award CNS
  0524059, by the European Research Council (ERC) Advanced Investigator Grant QUAREM,
  and by the Austrian Science Fund (FWF) project S11402-N23.
article_number: '27'
author:
- first_name: Rajeev
  full_name: Alur, Rajeev
  last_name: Alur
- first_name: Pavol
  full_name: Cerny, Pavol
  id: 4DCBEFFE-F248-11E8-B48F-1D18A9856A87
  last_name: Cerny
- first_name: Scott
  full_name: Weinstein, Scott
  last_name: Weinstein
citation:
  ama: Alur R, Cerny P, Weinstein S. Algorithmic analysis of array-accessing programs.
    <i>ACM Transactions on Computational Logic (TOCL)</i>. 2012;13(3). doi:<a href="https://doi.org/10.1145/2287718.2287727">10.1145/2287718.2287727</a>
  apa: Alur, R., Cerny, P., &#38; Weinstein, S. (2012). Algorithmic analysis of array-accessing
    programs. <i>ACM Transactions on Computational Logic (TOCL)</i>. ACM. <a href="https://doi.org/10.1145/2287718.2287727">https://doi.org/10.1145/2287718.2287727</a>
  chicago: Alur, Rajeev, Pavol Cerny, and Scott Weinstein. “Algorithmic Analysis of
    Array-Accessing Programs.” <i>ACM Transactions on Computational Logic (TOCL)</i>.
    ACM, 2012. <a href="https://doi.org/10.1145/2287718.2287727">https://doi.org/10.1145/2287718.2287727</a>.
  ieee: R. Alur, P. Cerny, and S. Weinstein, “Algorithmic analysis of array-accessing
    programs,” <i>ACM Transactions on Computational Logic (TOCL)</i>, vol. 13, no.
    3. ACM, 2012.
  ista: Alur R, Cerny P, Weinstein S. 2012. Algorithmic analysis of array-accessing
    programs. ACM Transactions on Computational Logic (TOCL). 13(3), 27.
  mla: Alur, Rajeev, et al. “Algorithmic Analysis of Array-Accessing Programs.” <i>ACM
    Transactions on Computational Logic (TOCL)</i>, vol. 13, no. 3, 27, ACM, 2012,
    doi:<a href="https://doi.org/10.1145/2287718.2287727">10.1145/2287718.2287727</a>.
  short: R. Alur, P. Cerny, S. Weinstein, ACM Transactions on Computational Logic
    (TOCL) 13 (2012).
date_created: 2018-12-11T12:00:36Z
date_published: 2012-08-01T00:00:00Z
date_updated: 2023-02-23T12:09:43Z
day: '01'
department:
- _id: ToHe
doi: 10.1145/2287718.2287727
ec_funded: 1
intvolume: '        13'
issue: '3'
language:
- iso: eng
month: '08'
oa_version: None
project:
- _id: 25EE3708-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '267989'
  name: Quantitative Reactive Modeling
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
publication: ACM Transactions on Computational Logic (TOCL)
publication_status: published
publisher: ACM
publist_id: '3748'
quality_controlled: '1'
related_material:
  record:
  - id: '4403'
    relation: earlier_version
    status: public
scopus_import: 1
status: public
title: Algorithmic analysis of array-accessing programs
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 13
year: '2012'
...
---
_id: '2968'
abstract:
- lang: eng
  text: Little is known about the stability of trophic relationships in complex natural
    communities over evolutionary timescales. Here, we use sequence data from 18 nuclear
    loci to reconstruct and compare the intraspecific histories of major Pleistocene
    refugial populations in the Middle East, the Balkans and Iberia in a guild of
    four Chalcid parasitoids (Cecidostiba fungosa, Cecidostiba semifascia, Hobbya
    stenonota and Mesopolobus amaenus) all attacking Cynipid oak galls. We develop
    a likelihood method to numerically estimate models of divergence between three
    populations from multilocus data. We investigate the power of this framework on
    simulated data, and-using triplet alignments of intronic loci-quantify the support
    for all possible divergence relationships between refugial populations in the
    four parasitoids. Although an East to West order of population divergence has
    highest support in all but one species, we cannot rule out alternative population
    tree topologies. Comparing the estimated times of population splits between species,
    we find that one species, M. amaenus, has a significantly older history than the
    rest of the guild and must have arrived in central Europe at least one glacial
    cycle prior to other guild members. This suggests that although all four species
    may share a common origin in the East, they expanded westwards into Europe at
    different times. © 2012 Blackwell Publishing Ltd.
acknowledgement: "This work was supported by funding from the UK Natural Environment
  Research Council to KL (NE/I020288/1) and GS (NE/H000038/1, NE/E014453/1, NER/B/504406/1,
  NER/B/S2003/00856) and a grant from the European Research Council (250152) to NB.\r\nWe
  thank Majide Tavakoli, Juli Pujade-Villar and Pablo-Fuentes Utrilla for contributing
  specimens. Mike Hickerson and three anonymous reviewers gave helpful comments on
  earlier versions of the manuscript. "
author:
- first_name: Konrad
  full_name: Lohse, Konrad
  last_name: Lohse
- 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: George
  full_name: Melika, George
  last_name: Melika
- first_name: Graham
  full_name: Stone, Graham
  last_name: Stone
citation:
  ama: Lohse K, Barton NH, Melika G, Stone G. A likelihood based comparison of population
    histories in a parasitoid guild. <i>Molecular Ecology</i>. 2012;21(18):4605-4617.
    doi:<a href="https://doi.org/10.1111/j.1365-294X.2012.05700.x">10.1111/j.1365-294X.2012.05700.x</a>
  apa: Lohse, K., Barton, N. H., Melika, G., &#38; Stone, G. (2012). A likelihood
    based comparison of population histories in a parasitoid guild. <i>Molecular Ecology</i>.
    Wiley-Blackwell. <a href="https://doi.org/10.1111/j.1365-294X.2012.05700.x">https://doi.org/10.1111/j.1365-294X.2012.05700.x</a>
  chicago: Lohse, Konrad, Nicholas H Barton, George Melika, and Graham Stone. “A Likelihood
    Based Comparison of Population Histories in a Parasitoid Guild.” <i>Molecular
    Ecology</i>. Wiley-Blackwell, 2012. <a href="https://doi.org/10.1111/j.1365-294X.2012.05700.x">https://doi.org/10.1111/j.1365-294X.2012.05700.x</a>.
  ieee: K. Lohse, N. H. Barton, G. Melika, and G. Stone, “A likelihood based comparison
    of population histories in a parasitoid guild,” <i>Molecular Ecology</i>, vol.
    21, no. 18. Wiley-Blackwell, pp. 4605–4617, 2012.
  ista: Lohse K, Barton NH, Melika G, Stone G. 2012. A likelihood based comparison
    of population histories in a parasitoid guild. Molecular Ecology. 21(18), 4605–4617.
  mla: Lohse, Konrad, et al. “A Likelihood Based Comparison of Population Histories
    in a Parasitoid Guild.” <i>Molecular Ecology</i>, vol. 21, no. 18, Wiley-Blackwell,
    2012, pp. 4605–17, doi:<a href="https://doi.org/10.1111/j.1365-294X.2012.05700.x">10.1111/j.1365-294X.2012.05700.x</a>.
  short: K. Lohse, N.H. Barton, G. Melika, G. Stone, Molecular Ecology 21 (2012) 4605–4617.
date_created: 2018-12-11T12:00:36Z
date_published: 2012-09-01T00:00:00Z
date_updated: 2023-05-30T13:07:47Z
day: '01'
ddc:
- '570'
- '579'
department:
- _id: NiBa
doi: 10.1111/j.1365-294X.2012.05700.x
ec_funded: 1
file:
- access_level: open_access
  checksum: c14ee4cb2a8ba9575bfd8a9bb7a883bb
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:17:47Z
  date_updated: 2020-07-14T12:45:57Z
  file_id: '5304'
  file_name: IST-2014-296-v1+1_4_wasps_revised3.pdf
  file_size: 235820
  relation: main_file
- access_level: open_access
  checksum: f00afc5b887c8222014b57375b8caece
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:17:48Z
  date_updated: 2020-07-14T12:45:57Z
  file_id: '5305'
  file_name: IST-2014-296-v1+2_4_wasps_Supporting2.pdf
  file_size: 41975
  relation: main_file
file_date_updated: 2020-07-14T12:45:57Z
has_accepted_license: '1'
intvolume: '        21'
issue: '18'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Submitted Version
page: 4605 - 4617
project:
- _id: 25B07788-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '250152'
  name: Limits to selection in biology and in evolutionary computation
publication: Molecular Ecology
publication_status: published
publisher: Wiley-Blackwell
publist_id: '3746'
pubrep_id: '296'
quality_controlled: '1'
related_material:
  record:
  - id: '13075'
    relation: research_data
    status: public
scopus_import: 1
status: public
title: A likelihood based comparison of population histories in a parasitoid guild
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 21
year: '2012'
...
---
_id: '2969'
abstract:
- lang: eng
  text: "The coupling between presynaptic Ca^(2+) channels and Ca^(2+) sensors of
    exocytosis is a key determinant of synaptic transmission. Evoked release from
    parvalbumin (PV)-expressing interneurons is triggered by nanodomain coupling of
    P/Q-type Ca^(2+) channels, whereas release from cholecystokinin (CCK)-containing
    interneurons is generated by microdomain coupling of N-type channels. Nanodomain
    coupling has several functional advantages, including speed and efficacy of transmission.
    One potential disadvantage is that stochastic\r\nopening of presynaptic Ca^(2+)
    channels may trigger spontaneous transmitter release. We addressed this possibility
    in rat hippocampal\r\ngranule cells, which receive converging inputs from different
    inhibitory sources. Both reduction of extracellular Ca^(2+) concentration and
    the unselective Ca^(2+) channel blocker Cd^(2+) reduced the frequency of miniature
    IPSCs (mIPSCs) in granule cells by ~50%, suggesting that the opening of presynaptic
    Ca^(2+) channels contributes to spontaneous release. Application of the selective
    P/Q-type Ca^(2+) channel blocker\r\nω-agatoxin IVa had no detectable effects,
    whereas both the N-type blocker ω-conotoxin GVIa and the L-type blocker nimodipine
    reduced\r\nmIPSC frequency. Furthermore, both the fast Ca^(2+) chelator BAPTA-AM
    and the slow chelator EGTA-AM reduced the mIPSC frequency,\r\nsuggesting that
    Ca^(2+)-dependent spontaneous release is triggered by microdomain rather than
    nanodomain coupling. The CB_(1) receptor\r\nagonist WIN 55212-2 also decreased
    spontaneous release; this effect was occluded by prior application of ω-conotoxin
    GVIa, suggesting that a major fraction of Ca^(2+)-dependent spontaneous release
    was generated at the terminals of CCK-expressing interneurons. Tonic inhibition
    generated by spontaneous opening of presynaptic N- and L-type Ca^(2+) channels
    may be important for hippocampal information processing.\r\n"
acknowledgement: This work was supported by grants from the Deutsche Forschungsgemeinschaft
  (TR 3/B10, Leibniz program, GSC-4 Spemann Graduate School) and the European Union
  (European Research Council Advanced Grant).
author:
- first_name: Sarit
  full_name: Goswami, Sarit
  id: 3A578F32-F248-11E8-B48F-1D18A9856A87
  last_name: Goswami
- first_name: Iancu
  full_name: Bucurenciu, Iancu
  last_name: Bucurenciu
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
citation:
  ama: Goswami S, Bucurenciu I, Jonas PM. Miniature IPSCs in hippocampal granule cells
    are triggered by voltage-gated Ca^(2+) channels via microdomain coupling. <i>Journal
    of Neuroscience</i>. 2012;32(41):14294-14304. doi:<a href="https://doi.org/10.1523/JNEUROSCI.6104-11.2012">10.1523/JNEUROSCI.6104-11.2012</a>
  apa: Goswami, S., Bucurenciu, I., &#38; Jonas, P. M. (2012). Miniature IPSCs in
    hippocampal granule cells are triggered by voltage-gated Ca^(2+) channels via
    microdomain coupling. <i>Journal of Neuroscience</i>. Society for Neuroscience.
    <a href="https://doi.org/10.1523/JNEUROSCI.6104-11.2012">https://doi.org/10.1523/JNEUROSCI.6104-11.2012</a>
  chicago: Goswami, Sarit, Iancu Bucurenciu, and Peter M Jonas. “Miniature IPSCs in
    Hippocampal Granule Cells Are Triggered by Voltage-Gated Ca^(2+) Channels via
    Microdomain Coupling.” <i>Journal of Neuroscience</i>. Society for Neuroscience,
    2012. <a href="https://doi.org/10.1523/JNEUROSCI.6104-11.2012">https://doi.org/10.1523/JNEUROSCI.6104-11.2012</a>.
  ieee: S. Goswami, I. Bucurenciu, and P. M. Jonas, “Miniature IPSCs in hippocampal
    granule cells are triggered by voltage-gated Ca^(2+) channels via microdomain
    coupling,” <i>Journal of Neuroscience</i>, vol. 32, no. 41. Society for Neuroscience,
    pp. 14294–14304, 2012.
  ista: Goswami S, Bucurenciu I, Jonas PM. 2012. Miniature IPSCs in hippocampal granule
    cells are triggered by voltage-gated Ca^(2+) channels via microdomain coupling.
    Journal of Neuroscience. 32(41), 14294–14304.
  mla: Goswami, Sarit, et al. “Miniature IPSCs in Hippocampal Granule Cells Are Triggered
    by Voltage-Gated Ca^(2+) Channels via Microdomain Coupling.” <i>Journal of Neuroscience</i>,
    vol. 32, no. 41, Society for Neuroscience, 2012, pp. 14294–304, doi:<a href="https://doi.org/10.1523/JNEUROSCI.6104-11.2012">10.1523/JNEUROSCI.6104-11.2012</a>.
  short: S. Goswami, I. Bucurenciu, P.M. Jonas, Journal of Neuroscience 32 (2012)
    14294–14304.
date_created: 2018-12-11T12:00:36Z
date_published: 2012-10-10T00:00:00Z
date_updated: 2021-01-12T07:40:08Z
day: '10'
department:
- _id: PeJo
doi: 10.1523/JNEUROSCI.6104-11.2012
external_id:
  pmid:
  - '23055500'
intvolume: '        32'
issue: '41'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3632771/
month: '10'
oa: 1
oa_version: Submitted Version
page: 14294 - 14304
pmid: 1
project:
- _id: 25BDE9A4-B435-11E9-9278-68D0E5697425
  grant_number: SFB-TR3-TP10B
  name: Glutamaterge synaptische Übertragung und Plastizität in hippocampalen Mikroschaltkreisen
publication: Journal of Neuroscience
publication_status: published
publisher: Society for Neuroscience
publist_id: '3744'
quality_controlled: '1'
scopus_import: 1
status: public
title: Miniature IPSCs in hippocampal granule cells are triggered by voltage-gated
  Ca^(2+) channels via microdomain coupling
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 32
year: '2012'
...
---
_id: '2970'
abstract:
- lang: eng
  text: Morphogen gradients regulate the patterning and growth of many tissues, hence
    a key question is how they are established and maintained during development.
    Theoretical descriptions have helped to explain how gradient shape is controlled
    by the rates of morphogen production, spreading and degradation. These effective
    rates have been measured using fluorescence recovery after photobleaching (FRAP)
    and photoactivation. To unravel which molecular events determine the effective
    rates, such tissue-level assays have been combined with genetic analysis, high-resolution
    assays, and models that take into account interactions with receptors, extracellular
    components and trafficking. Nevertheless, because of the natural and experimental
    data variability, and the underlying assumptions of transport models, it remains
    challenging to conclusively distinguish between cellular mechanisms.
acknowledgement: AK is currently supported by an MRC CDF. MGG and OW were supported
  by the Swiss National Science Foundation, grants from the Swiss SystemsX.ch initiative,
  LipidX-2008/011, an ERC advanced investigator grant and the Polish-Swiss research
  program.
author:
- first_name: Anna
  full_name: Kicheva, Anna
  id: 3959A2A0-F248-11E8-B48F-1D18A9856A87
  last_name: Kicheva
  orcid: 0000-0003-4509-4998
- 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: Ortrud
  full_name: Wartlick, Ortrud
  last_name: Wartlick
- first_name: Frank
  full_name: Julicher, Frank
  last_name: Julicher
- first_name: Marcos
  full_name: Gonzalez Gaitan, Marcos
  last_name: Gonzalez Gaitan
citation:
  ama: 'Kicheva A, Bollenbach MT, Wartlick O, Julicher F, Gonzalez Gaitan M. Investigating
    the principles of morphogen gradient formation: from tissues to cells. <i>Current
    Opinion in Genetics &#38; Development</i>. 2012;22(6):527-532. doi:<a href="https://doi.org/10.1016/j.gde.2012.08.004">10.1016/j.gde.2012.08.004</a>'
  apa: 'Kicheva, A., Bollenbach, M. T., Wartlick, O., Julicher, F., &#38; Gonzalez
    Gaitan, M. (2012). Investigating the principles of morphogen gradient formation:
    from tissues to cells. <i>Current Opinion in Genetics &#38; Development</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.gde.2012.08.004">https://doi.org/10.1016/j.gde.2012.08.004</a>'
  chicago: 'Kicheva, Anna, Mark Tobias Bollenbach, Ortrud Wartlick, Frank Julicher,
    and Marcos Gonzalez Gaitan. “Investigating the Principles of Morphogen Gradient
    Formation: From Tissues to Cells.” <i>Current Opinion in Genetics &#38; Development</i>.
    Elsevier, 2012. <a href="https://doi.org/10.1016/j.gde.2012.08.004">https://doi.org/10.1016/j.gde.2012.08.004</a>.'
  ieee: 'A. Kicheva, M. T. Bollenbach, O. Wartlick, F. Julicher, and M. Gonzalez Gaitan,
    “Investigating the principles of morphogen gradient formation: from tissues to
    cells,” <i>Current Opinion in Genetics &#38; Development</i>, vol. 22, no. 6.
    Elsevier, pp. 527–532, 2012.'
  ista: 'Kicheva A, Bollenbach MT, Wartlick O, Julicher F, Gonzalez Gaitan M. 2012.
    Investigating the principles of morphogen gradient formation: from tissues to
    cells. Current Opinion in Genetics &#38; Development. 22(6), 527–532.'
  mla: 'Kicheva, Anna, et al. “Investigating the Principles of Morphogen Gradient
    Formation: From Tissues to Cells.” <i>Current Opinion in Genetics &#38; Development</i>,
    vol. 22, no. 6, Elsevier, 2012, pp. 527–32, doi:<a href="https://doi.org/10.1016/j.gde.2012.08.004">10.1016/j.gde.2012.08.004</a>.'
  short: A. Kicheva, M.T. Bollenbach, O. Wartlick, F. Julicher, M. Gonzalez Gaitan,
    Current Opinion in Genetics &#38; Development 22 (2012) 527–532.
date_created: 2018-12-11T12:00:37Z
date_published: 2012-12-01T00:00:00Z
date_updated: 2021-01-12T07:40:09Z
day: '01'
department:
- _id: ToBo
doi: 10.1016/j.gde.2012.08.004
intvolume: '        22'
issue: '6'
language:
- iso: eng
month: '12'
oa_version: None
page: 527 - 532
publication: Current Opinion in Genetics & Development
publication_status: published
publisher: Elsevier
publist_id: '3739'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'Investigating the principles of morphogen gradient formation: from tissues
  to cells'
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 22
year: '2012'
...
