---
_id: '1859'
abstract:
- lang: eng
  text: "Structural support vector machines (SSVMs) are amongst the best performing
    models for structured computer vision tasks, such as semantic image segmentation
    or human pose estimation. Training SSVMs, however, is computationally costly,
    because it requires repeated calls to a structured prediction subroutine (called
    \\emph{max-oracle}), which has to solve an optimization problem itself, e.g. a
    graph cut.\r\nIn this work, we introduce a new algorithm for SSVM training that
    is more efficient than earlier techniques when the max-oracle is computationally
    expensive, as it is frequently the case in computer vision tasks. The main idea
    is to (i) combine the recent stochastic Block-Coordinate Frank-Wolfe algorithm
    with efficient hyperplane caching, and (ii) use an automatic selection rule for
    deciding whether to call the exact max-oracle or to rely on an approximate one
    based on the cached hyperplanes.\r\nWe show experimentally that this strategy
    leads to faster convergence to the optimum with respect to the number of requires
    oracle calls, and that this translates into faster convergence with respect to
    the total runtime when the max-oracle is slow compared to the other steps of the
    algorithm. "
author:
- first_name: Neel
  full_name: Shah, Neel
  id: 31ABAF80-F248-11E8-B48F-1D18A9856A87
  last_name: Shah
- first_name: Vladimir
  full_name: Kolmogorov, Vladimir
  id: 3D50B0BA-F248-11E8-B48F-1D18A9856A87
  last_name: Kolmogorov
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
citation:
  ama: 'Shah N, Kolmogorov V, Lampert C. A multi-plane block-coordinate Frank-Wolfe
    algorithm for training structural SVMs with a costly max-oracle. In: IEEE; 2015:2737-2745.
    doi:<a href="https://doi.org/10.1109/CVPR.2015.7298890">10.1109/CVPR.2015.7298890</a>'
  apa: 'Shah, N., Kolmogorov, V., &#38; Lampert, C. (2015). A multi-plane block-coordinate
    Frank-Wolfe algorithm for training structural SVMs with a costly max-oracle (pp.
    2737–2745). Presented at the CVPR: Computer Vision and Pattern Recognition, Boston,
    MA, USA: IEEE. <a href="https://doi.org/10.1109/CVPR.2015.7298890">https://doi.org/10.1109/CVPR.2015.7298890</a>'
  chicago: Shah, Neel, Vladimir Kolmogorov, and Christoph Lampert. “A Multi-Plane
    Block-Coordinate Frank-Wolfe Algorithm for Training Structural SVMs with a Costly
    Max-Oracle,” 2737–45. IEEE, 2015. <a href="https://doi.org/10.1109/CVPR.2015.7298890">https://doi.org/10.1109/CVPR.2015.7298890</a>.
  ieee: 'N. Shah, V. Kolmogorov, and C. Lampert, “A multi-plane block-coordinate Frank-Wolfe
    algorithm for training structural SVMs with a costly max-oracle,” presented at
    the CVPR: Computer Vision and Pattern Recognition, Boston, MA, USA, 2015, pp.
    2737–2745.'
  ista: 'Shah N, Kolmogorov V, Lampert C. 2015. A multi-plane block-coordinate Frank-Wolfe
    algorithm for training structural SVMs with a costly max-oracle. CVPR: Computer
    Vision and Pattern Recognition, 2737–2745.'
  mla: Shah, Neel, et al. <i>A Multi-Plane Block-Coordinate Frank-Wolfe Algorithm
    for Training Structural SVMs with a Costly Max-Oracle</i>. IEEE, 2015, pp. 2737–45,
    doi:<a href="https://doi.org/10.1109/CVPR.2015.7298890">10.1109/CVPR.2015.7298890</a>.
  short: N. Shah, V. Kolmogorov, C. Lampert, in:, IEEE, 2015, pp. 2737–2745.
conference:
  end_date: 2015-06-12
  location: Boston, MA, USA
  name: 'CVPR: Computer Vision and Pattern Recognition'
  start_date: 2015-06-07
date_created: 2018-12-11T11:54:24Z
date_published: 2015-06-01T00:00:00Z
date_updated: 2021-01-12T06:53:40Z
day: '01'
department:
- _id: VlKo
- _id: ChLa
doi: 10.1109/CVPR.2015.7298890
ec_funded: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1408.6804
month: '06'
oa: 1
oa_version: Preprint
page: 2737 - 2745
project:
- _id: 2532554C-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '308036'
  name: Lifelong Learning of Visual Scene Understanding
- _id: 25FBA906-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '616160'
  name: 'Discrete Optimization in Computer Vision: Theory and Practice'
publication_status: published
publisher: IEEE
publist_id: '5240'
quality_controlled: '1'
scopus_import: 1
status: public
title: A multi-plane block-coordinate Frank-Wolfe algorithm for training structural
  SVMs with a costly max-oracle
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2015'
...
---
_id: '1860'
abstract:
- lang: eng
  text: Classifiers for object categorization are usually evaluated by their accuracy
    on a set of i.i.d. test examples. This provides us with an estimate of the expected
    error when applying the classifiers to a single new image. In real application,
    however, classifiers are rarely only used for a single image and then discarded.
    Instead, they are applied sequentially to many images, and these are typically
    not i.i.d. samples from a fixed data distribution, but they carry dependencies
    and their class distribution varies over time. In this work, we argue that the
    phenomenon of correlated data at prediction time is not a nuisance, but a blessing
    in disguise. We describe a probabilistic method for adapting classifiers at prediction
    time without having to retrain them. We also introduce a framework for creating
    realistically distributed image sequences, which offers a way to benchmark classifier
    adaptation methods, such as the one we propose. Experiments on the ILSVRC2010
    and ILSVRC2012 datasets show that adapting object classification systems at prediction
    time can significantly reduce their error rate, even with no additional human
    feedback.
author:
- first_name: Amélie
  full_name: Royer, Amélie
  last_name: Royer
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
citation:
  ama: 'Royer A, Lampert C. Classifier adaptation at prediction time. In: IEEE; 2015:1401-1409.
    doi:<a href="https://doi.org/10.1109/CVPR.2015.7298746">10.1109/CVPR.2015.7298746</a>'
  apa: 'Royer, A., &#38; Lampert, C. (2015). Classifier adaptation at prediction time
    (pp. 1401–1409). Presented at the CVPR: Computer Vision and Pattern Recognition,
    Boston, MA, United States: IEEE. <a href="https://doi.org/10.1109/CVPR.2015.7298746">https://doi.org/10.1109/CVPR.2015.7298746</a>'
  chicago: Royer, Amélie, and Christoph Lampert. “Classifier Adaptation at Prediction
    Time,” 1401–9. IEEE, 2015. <a href="https://doi.org/10.1109/CVPR.2015.7298746">https://doi.org/10.1109/CVPR.2015.7298746</a>.
  ieee: 'A. Royer and C. Lampert, “Classifier adaptation at prediction time,” presented
    at the CVPR: Computer Vision and Pattern Recognition, Boston, MA, United States,
    2015, pp. 1401–1409.'
  ista: 'Royer A, Lampert C. 2015. Classifier adaptation at prediction time. CVPR:
    Computer Vision and Pattern Recognition, 1401–1409.'
  mla: Royer, Amélie, and Christoph Lampert. <i>Classifier Adaptation at Prediction
    Time</i>. IEEE, 2015, pp. 1401–09, doi:<a href="https://doi.org/10.1109/CVPR.2015.7298746">10.1109/CVPR.2015.7298746</a>.
  short: A. Royer, C. Lampert, in:, IEEE, 2015, pp. 1401–1409.
conference:
  end_date: 2015-06-12
  location: Boston, MA, United States
  name: 'CVPR: Computer Vision and Pattern Recognition'
  start_date: 2015-06-07
date_created: 2018-12-11T11:54:24Z
date_published: 2015-06-01T00:00:00Z
date_updated: 2021-01-12T06:53:41Z
day: '01'
department:
- _id: ChLa
doi: 10.1109/CVPR.2015.7298746
ec_funded: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.cv-foundation.org/openaccess/content_cvpr_2015/papers/Royer_Classifier_Adaptation_at_2015_CVPR_paper.pdf
month: '06'
oa: 1
oa_version: Submitted Version
page: 1401 - 1409
project:
- _id: 2532554C-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '308036'
  name: Lifelong Learning of Visual Scene Understanding
publication_status: published
publisher: IEEE
publist_id: '5239'
quality_controlled: '1'
scopus_import: 1
status: public
title: Classifier adaptation at prediction time
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2015'
...
---
_id: '1861'
abstract:
- lang: eng
  text: Continuous-time Markov chains are commonly used in practice for modeling biochemical
    reaction networks in which the inherent randomness of themolecular interactions
    cannot be ignored. This has motivated recent research effort into methods for
    parameter inference and experiment design for such models. The major difficulty
    is that such methods usually require one to iteratively solve the chemical master
    equation that governs the time evolution of the probability distribution of the
    system. This, however, is rarely possible, and even approximation techniques remain
    limited to relatively small and simple systems. An alternative explored in this
    article is to base methods on only some low-order moments of the entire probability
    distribution. We summarize the theory behind such moment-based methods for parameter
    inference and experiment design and provide new case studies where we investigate
    their performance.
acknowledgement: "HYCON2; EC; European Commission\r\n"
article_number: '8'
author:
- first_name: Jakob
  full_name: Ruess, Jakob
  id: 4A245D00-F248-11E8-B48F-1D18A9856A87
  last_name: Ruess
  orcid: 0000-0003-1615-3282
- first_name: John
  full_name: Lygeros, John
  last_name: Lygeros
citation:
  ama: Ruess J, Lygeros J. Moment-based methods for parameter inference and experiment
    design for stochastic biochemical reaction networks. <i>ACM Transactions on Modeling
    and Computer Simulation</i>. 2015;25(2). doi:<a href="https://doi.org/10.1145/2688906">10.1145/2688906</a>
  apa: Ruess, J., &#38; Lygeros, J. (2015). Moment-based methods for parameter inference
    and experiment design for stochastic biochemical reaction networks. <i>ACM Transactions
    on Modeling and Computer Simulation</i>. ACM. <a href="https://doi.org/10.1145/2688906">https://doi.org/10.1145/2688906</a>
  chicago: Ruess, Jakob, and John Lygeros. “Moment-Based Methods for Parameter Inference
    and Experiment Design for Stochastic Biochemical Reaction Networks.” <i>ACM Transactions
    on Modeling and Computer Simulation</i>. ACM, 2015. <a href="https://doi.org/10.1145/2688906">https://doi.org/10.1145/2688906</a>.
  ieee: J. Ruess and J. Lygeros, “Moment-based methods for parameter inference and
    experiment design for stochastic biochemical reaction networks,” <i>ACM Transactions
    on Modeling and Computer Simulation</i>, vol. 25, no. 2. ACM, 2015.
  ista: Ruess J, Lygeros J. 2015. Moment-based methods for parameter inference and
    experiment design for stochastic biochemical reaction networks. ACM Transactions
    on Modeling and Computer Simulation. 25(2), 8.
  mla: Ruess, Jakob, and John Lygeros. “Moment-Based Methods for Parameter Inference
    and Experiment Design for Stochastic Biochemical Reaction Networks.” <i>ACM Transactions
    on Modeling and Computer Simulation</i>, vol. 25, no. 2, 8, ACM, 2015, doi:<a
    href="https://doi.org/10.1145/2688906">10.1145/2688906</a>.
  short: J. Ruess, J. Lygeros, ACM Transactions on Modeling and Computer Simulation
    25 (2015).
date_created: 2018-12-11T11:54:25Z
date_published: 2015-02-01T00:00:00Z
date_updated: 2021-01-12T06:53:41Z
day: '01'
department:
- _id: ToHe
- _id: GaTk
doi: 10.1145/2688906
intvolume: '        25'
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
publication: ACM Transactions on Modeling and Computer Simulation
publication_status: published
publisher: ACM
publist_id: '5238'
quality_controlled: '1'
scopus_import: 1
status: public
title: Moment-based methods for parameter inference and experiment design for stochastic
  biochemical reaction networks
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 25
year: '2015'
...
---
_id: '1864'
abstract:
- lang: eng
  text: "The Altshuler–Shklovskii formulas (Altshuler and Shklovskii, BZh Eksp Teor
    Fiz 91:200, 1986) predict, for any disordered quantum system in the diffusive
    regime, a universal power law behaviour for the correlation functions of the mesoscopic
    eigenvalue density. In this paper and its companion (Erdős and Knowles, The Altshuler–Shklovskii
    formulas for random band matrices I: the unimodular case, 2013), we prove these
    formulas for random band matrices. In (Erdős and Knowles, The Altshuler–Shklovskii
    formulas for random band matrices I: the unimodular case, 2013) we introduced
    a diagrammatic approach and presented robust estimates on general diagrams under
    certain simplifying assumptions. In this paper, we remove these assumptions by
    giving a general estimate of the subleading diagrams. We also give a precise analysis
    of the leading diagrams which give rise to the Altschuler–Shklovskii power laws.
    Moreover, we introduce a family of general random band matrices which interpolates
    between real symmetric (β = 1) and complex Hermitian (β = 2) models, and track
    the transition for the mesoscopic density–density correlation. Finally, we address
    the higher-order correlation functions by proving that they behave asymptotically
    according to a Gaussian process whose covariance is given by the Altshuler–Shklovskii
    formulas.\r\n"
author:
- first_name: László
  full_name: Erdös, László
  id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
  last_name: Erdös
  orcid: 0000-0001-5366-9603
- first_name: Antti
  full_name: Knowles, Antti
  last_name: Knowles
citation:
  ama: 'Erdös L, Knowles A. The Altshuler–Shklovskii formulas for random band matrices
    II: The general case. <i>Annales Henri Poincare</i>. 2015;16(3):709-799. doi:<a
    href="https://doi.org/10.1007/s00023-014-0333-5">10.1007/s00023-014-0333-5</a>'
  apa: 'Erdös, L., &#38; Knowles, A. (2015). The Altshuler–Shklovskii formulas for
    random band matrices II: The general case. <i>Annales Henri Poincare</i>. Springer.
    <a href="https://doi.org/10.1007/s00023-014-0333-5">https://doi.org/10.1007/s00023-014-0333-5</a>'
  chicago: 'Erdös, László, and Antti Knowles. “The Altshuler–Shklovskii Formulas for
    Random Band Matrices II: The General Case.” <i>Annales Henri Poincare</i>. Springer,
    2015. <a href="https://doi.org/10.1007/s00023-014-0333-5">https://doi.org/10.1007/s00023-014-0333-5</a>.'
  ieee: 'L. Erdös and A. Knowles, “The Altshuler–Shklovskii formulas for random band
    matrices II: The general case,” <i>Annales Henri Poincare</i>, vol. 16, no. 3.
    Springer, pp. 709–799, 2015.'
  ista: 'Erdös L, Knowles A. 2015. The Altshuler–Shklovskii formulas for random band
    matrices II: The general case. Annales Henri Poincare. 16(3), 709–799.'
  mla: 'Erdös, László, and Antti Knowles. “The Altshuler–Shklovskii Formulas for Random
    Band Matrices II: The General Case.” <i>Annales Henri Poincare</i>, vol. 16, no.
    3, Springer, 2015, pp. 709–99, doi:<a href="https://doi.org/10.1007/s00023-014-0333-5">10.1007/s00023-014-0333-5</a>.'
  short: L. Erdös, A. Knowles, Annales Henri Poincare 16 (2015) 709–799.
date_created: 2018-12-11T11:54:26Z
date_published: 2015-03-01T00:00:00Z
date_updated: 2021-01-12T06:53:42Z
day: '01'
department:
- _id: LaEr
doi: 10.1007/s00023-014-0333-5
ec_funded: 1
intvolume: '        16'
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1309.5107
month: '03'
oa: 1
oa_version: Preprint
page: 709 - 799
project:
- _id: 258DCDE6-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '338804'
  name: Random matrices, universality and disordered quantum systems
publication: Annales Henri Poincare
publication_status: published
publisher: Springer
publist_id: '5233'
scopus_import: 1
status: public
title: 'The Altshuler–Shklovskii formulas for random band matrices II: The general
  case'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2015'
...
---
_id: '1865'
abstract:
- lang: eng
  text: The plant hormone auxin and its directional transport are known to play a
    crucial role in defining the embryonic axis and subsequent development of the
    body plan. Although the role of PIN auxin efflux transporters has been clearly
    assigned during embryonic shoot and root specification, the role of the auxin
    influx carriers AUX1 and LIKE-AUX1 (LAX) proteins is not well established. Here,
    we used chemical and genetic tools on Brassica napus microspore-derived embryos
    and Arabidopsis thaliana zygotic embryos, and demonstrate that AUX1, LAX1 and
    LAX2 are required for both shoot and root pole formation, in concert with PIN
    efflux carriers. Furthermore, we uncovered a positive-feedback loop betweenMONOPTEROS(ARF5)-dependent
    auxin signalling and auxin transport. ThisMONOPTEROSdependent transcriptional
    regulation of auxin influx (AUX1, LAX1 and LAX2) and auxin efflux (PIN1 and PIN4)
    carriers by MONOPTEROS helps to maintain proper auxin transport to the root tip.
    These results indicate that auxin-dependent cell specification during embryo development
    requires balanced auxin transport involving both influx and efflux mechanisms,
    and that this transport is maintained by a positive transcriptional feedback on
    auxin signalling.
acknowledgement: W.G. is a post-doctoral fellow of the Research Foundation Flanders.
  H.S.R. is supported by Employment of Best Young Scientists for International Cooperation
  Empowerment [CZ.1.07/2.3.00/30.0037], co-financed by the European Social Fund and
  the state budget of the Czech Republic. Mi.S. was funded by the Ramón y Cajal program.
  This work was supported by the European Research Council [project ERC-2011-StG-20101109-PSDP],
  project ‘CEITEC – Central European Institute of Technology’ [CZ.1.05/1.1.00/02.0068],
  the European Social Fund [CZ.1.07/2.3.00/20.0043] and the Czech Science Foundation
  GACR [GA13-40637S] to J.F. We acknowledge funding from the Biological and Biotechnological
  Science Research Council (BBSRC) and Engineering Physics Science Research Council
  (EPSRC) to R.S. and M.B
author:
- first_name: Hélène
  full_name: Robert, Hélène
  last_name: Robert
- first_name: Wim
  full_name: Grunewald, Wim
  last_name: Grunewald
- first_name: Michael
  full_name: Sauer, Michael
  last_name: Sauer
- first_name: Bernard
  full_name: Cannoot, Bernard
  last_name: Cannoot
- first_name: Mercedes
  full_name: Soriano, Mercedes
  last_name: Soriano
- first_name: Ranjan
  full_name: Swarup, Ranjan
  last_name: Swarup
- first_name: Dolf
  full_name: Weijers, Dolf
  last_name: Weijers
- first_name: Malcolm
  full_name: Bennett, Malcolm
  last_name: Bennett
- first_name: Kim
  full_name: Boutilier, Kim
  last_name: Boutilier
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Robert H, Grunewald W, Sauer M, et al. Plant embryogenesis requires AUX/LAX-mediated
    auxin influx. <i>Development</i>. 2015;142(4):702-711. doi:<a href="https://doi.org/10.1242/dev.115832">10.1242/dev.115832</a>
  apa: Robert, H., Grunewald, W., Sauer, M., Cannoot, B., Soriano, M., Swarup, R.,
    … Friml, J. (2015). Plant embryogenesis requires AUX/LAX-mediated auxin influx.
    <i>Development</i>. Company of Biologists. <a href="https://doi.org/10.1242/dev.115832">https://doi.org/10.1242/dev.115832</a>
  chicago: Robert, Hélène, Wim Grunewald, Michael Sauer, Bernard Cannoot, Mercedes
    Soriano, Ranjan Swarup, Dolf Weijers, Malcolm Bennett, Kim Boutilier, and Jiří
    Friml. “Plant Embryogenesis Requires AUX/LAX-Mediated Auxin Influx.” <i>Development</i>.
    Company of Biologists, 2015. <a href="https://doi.org/10.1242/dev.115832">https://doi.org/10.1242/dev.115832</a>.
  ieee: H. Robert <i>et al.</i>, “Plant embryogenesis requires AUX/LAX-mediated auxin
    influx,” <i>Development</i>, vol. 142, no. 4. Company of Biologists, pp. 702–711,
    2015.
  ista: Robert H, Grunewald W, Sauer M, Cannoot B, Soriano M, Swarup R, Weijers D,
    Bennett M, Boutilier K, Friml J. 2015. Plant embryogenesis requires AUX/LAX-mediated
    auxin influx. Development. 142(4), 702–711.
  mla: Robert, Hélène, et al. “Plant Embryogenesis Requires AUX/LAX-Mediated Auxin
    Influx.” <i>Development</i>, vol. 142, no. 4, Company of Biologists, 2015, pp.
    702–11, doi:<a href="https://doi.org/10.1242/dev.115832">10.1242/dev.115832</a>.
  short: H. Robert, W. Grunewald, M. Sauer, B. Cannoot, M. Soriano, R. Swarup, D.
    Weijers, M. Bennett, K. Boutilier, J. Friml, Development 142 (2015) 702–711.
date_created: 2018-12-11T11:54:26Z
date_published: 2015-02-15T00:00:00Z
date_updated: 2021-01-12T06:53:43Z
day: '15'
department:
- _id: JiFr
doi: 10.1242/dev.115832
ec_funded: 1
intvolume: '       142'
issue: '4'
language:
- iso: eng
month: '02'
oa_version: None
page: 702 - 711
project:
- _id: 25716A02-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '282300'
  name: Polarity and subcellular dynamics in plants
publication: Development
publication_status: published
publisher: Company of Biologists
publist_id: '5231'
quality_controlled: '1'
scopus_import: 1
status: public
title: Plant embryogenesis requires AUX/LAX-mediated auxin influx
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 142
year: '2015'
...
---
_id: '1866'
author:
- 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: Jean
  full_name: Raskin, Jean
  last_name: Raskin
citation:
  ama: 'Henzinger TA, Raskin J. The equivalence problem for finite automata: Technical
    perspective. <i>Communications of the ACM</i>. 2015;58(2):86-86. doi:<a href="https://doi.org/10.1145/2701001">10.1145/2701001</a>'
  apa: 'Henzinger, T. A., &#38; Raskin, J. (2015). The equivalence problem for finite
    automata: Technical perspective. <i>Communications of the ACM</i>. ACM. <a href="https://doi.org/10.1145/2701001">https://doi.org/10.1145/2701001</a>'
  chicago: 'Henzinger, Thomas A, and Jean Raskin. “The Equivalence Problem for Finite
    Automata: Technical Perspective.” <i>Communications of the ACM</i>. ACM, 2015.
    <a href="https://doi.org/10.1145/2701001">https://doi.org/10.1145/2701001</a>.'
  ieee: 'T. A. Henzinger and J. Raskin, “The equivalence problem for finite automata:
    Technical perspective,” <i>Communications of the ACM</i>, vol. 58, no. 2. ACM,
    pp. 86–86, 2015.'
  ista: 'Henzinger TA, Raskin J. 2015. The equivalence problem for finite automata:
    Technical perspective. Communications of the ACM. 58(2), 86–86.'
  mla: 'Henzinger, Thomas A., and Jean Raskin. “The Equivalence Problem for Finite
    Automata: Technical Perspective.” <i>Communications of the ACM</i>, vol. 58, no.
    2, ACM, 2015, pp. 86–86, doi:<a href="https://doi.org/10.1145/2701001">10.1145/2701001</a>.'
  short: T.A. Henzinger, J. Raskin, Communications of the ACM 58 (2015) 86–86.
date_created: 2018-12-11T11:54:26Z
date_published: 2015-01-28T00:00:00Z
date_updated: 2021-01-12T06:53:43Z
day: '28'
department:
- _id: ToHe
doi: 10.1145/2701001
intvolume: '        58'
issue: '2'
language:
- iso: eng
month: '01'
oa_version: None
page: 86-86
publication: Communications of the ACM
publication_status: published
publisher: ACM
publist_id: '5232'
scopus_import: 1
status: public
title: 'The equivalence problem for finite automata: Technical perspective'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 58
year: '2015'
...
---
_id: '1867'
abstract:
- lang: eng
  text: Cultured mammalian cells essential are model systems in basic biology research,
    production platforms of proteins for medical use, and testbeds in synthetic biology.
    Flavin cofactors, in particular flavin mononucleotide (FMN) and flavin adenine
    dinucleotide (FAD), are critical for cellular redox reactions and sense light
    in naturally occurring photoreceptors and optogenetic tools. Here, we quantified
    flavin contents of commonly used mammalian cell lines. We first compared three
    procedures for extraction of free and noncovalently protein-bound flavins and
    verified extraction using fluorescence spectroscopy. For separation, two CE methods
    with different BGEs were established, and detection was performed by LED-induced
    fluorescence with limit of detections (LODs 0.5-3.8 nM). We found that riboflavin
    (RF), FMN, and FAD contents varied significantly between cell lines. RF (3.1-14
    amol/cell) and FAD (2.2-17.0 amol/cell) were the predominant flavins, while FMN
    (0.46-3.4 amol/cell) was found at markedly lower levels. Observed flavin contents
    agree with those previously extracted from mammalian tissues, yet reduced forms
    of RF were detected that were not described previously. Quantification of flavins
    in mammalian cell lines will allow a better understanding of cellular redox reactions
    and optogenetic tools.
author:
- first_name: Jens
  full_name: Hühner, Jens
  last_name: Hühner
- first_name: Álvaro
  full_name: Inglés Prieto, Álvaro
  id: 2A9DB292-F248-11E8-B48F-1D18A9856A87
  last_name: Inglés Prieto
  orcid: 0000-0002-5409-8571
- first_name: Christian
  full_name: Neusüß, Christian
  last_name: Neusüß
- first_name: Michael
  full_name: Lämmerhofer, Michael
  last_name: Lämmerhofer
- 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: Hühner J, Inglés Prieto Á, Neusüß C, Lämmerhofer M, Janovjak HL. Quantification
    of riboflavin, flavin mononucleotide, and flavin adenine dinucleotide in mammalian
    model cells by CE with LED-induced fluorescence detection. <i>Electrophoresis</i>.
    2015;36(4):518-525. doi:<a href="https://doi.org/10.1002/elps.201400451">10.1002/elps.201400451</a>
  apa: Hühner, J., Inglés Prieto, Á., Neusüß, C., Lämmerhofer, M., &#38; Janovjak,
    H. L. (2015). Quantification of riboflavin, flavin mononucleotide, and flavin
    adenine dinucleotide in mammalian model cells by CE with LED-induced fluorescence
    detection. <i>Electrophoresis</i>. Wiley. <a href="https://doi.org/10.1002/elps.201400451">https://doi.org/10.1002/elps.201400451</a>
  chicago: Hühner, Jens, Álvaro Inglés Prieto, Christian Neusüß, Michael Lämmerhofer,
    and Harald L Janovjak. “Quantification of Riboflavin, Flavin Mononucleotide, and
    Flavin Adenine Dinucleotide in Mammalian Model Cells by CE with LED-Induced Fluorescence
    Detection.” <i>Electrophoresis</i>. Wiley, 2015. <a href="https://doi.org/10.1002/elps.201400451">https://doi.org/10.1002/elps.201400451</a>.
  ieee: J. Hühner, Á. Inglés Prieto, C. Neusüß, M. Lämmerhofer, and H. L. Janovjak,
    “Quantification of riboflavin, flavin mononucleotide, and flavin adenine dinucleotide
    in mammalian model cells by CE with LED-induced fluorescence detection,” <i>Electrophoresis</i>,
    vol. 36, no. 4. Wiley, pp. 518–525, 2015.
  ista: Hühner J, Inglés Prieto Á, Neusüß C, Lämmerhofer M, Janovjak HL. 2015. Quantification
    of riboflavin, flavin mononucleotide, and flavin adenine dinucleotide in mammalian
    model cells by CE with LED-induced fluorescence detection. Electrophoresis. 36(4),
    518–525.
  mla: Hühner, Jens, et al. “Quantification of Riboflavin, Flavin Mononucleotide,
    and Flavin Adenine Dinucleotide in Mammalian Model Cells by CE with LED-Induced
    Fluorescence Detection.” <i>Electrophoresis</i>, vol. 36, no. 4, Wiley, 2015,
    pp. 518–25, doi:<a href="https://doi.org/10.1002/elps.201400451">10.1002/elps.201400451</a>.
  short: J. Hühner, Á. Inglés Prieto, C. Neusüß, M. Lämmerhofer, H.L. Janovjak, Electrophoresis
    36 (2015) 518–525.
date_created: 2018-12-11T11:54:26Z
date_published: 2015-02-01T00:00:00Z
date_updated: 2021-01-12T06:53:43Z
day: '01'
department:
- _id: HaJa
doi: 10.1002/elps.201400451
ec_funded: 1
intvolume: '        36'
issue: '4'
language:
- iso: eng
month: '02'
oa_version: None
page: 518 - 525
project:
- _id: 25548C20-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '303564'
  name: Microbial Ion Channels for Synthetic Neurobiology
- _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)
publication: Electrophoresis
publication_status: published
publisher: Wiley
publist_id: '5230'
pubrep_id: '836'
quality_controlled: '1'
scopus_import: 1
status: public
title: Quantification of riboflavin, flavin mononucleotide, and flavin adenine dinucleotide
  in mammalian model cells by CE with LED-induced fluorescence detection
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 36
year: '2015'
...
---
_id: '1868'
abstract:
- lang: eng
  text: We investigate high-dimensional nonlinear dynamical systems exhibiting multiple
    resonances under adiabatic parameter variations. Our motivations come from experimental
    considerations where time-dependent sweeping of parameters is a practical approach
    to probing and characterizing the bifurcations of the system. The question is
    whether bifurcations so detected are faithful representations of the bifurcations
    intrinsic to the original stationary system. Utilizing a harmonically forced,
    closed fluid flow system that possesses multiple resonances and solving the Navier-Stokes
    equation under proper boundary conditions, we uncover the phenomenon of the early
    effect. Specifically, as a control parameter, e.g., the driving frequency, is
    adiabatically increased from an initial value, resonances emerge at frequency
    values that are lower than those in the corresponding stationary system. The phenomenon
    is established by numerical characterization of physical quantities through the
    resonances, which include the kinetic energy and the vorticity field, and a heuristic
    analysis based on the concept of instantaneous frequency. A simple formula is
    obtained which relates the resonance points in the time-dependent and time-independent
    systems. Our findings suggest that, in general, any true bifurcation of a nonlinear
    dynamical system can be unequivocally uncovered through adiabatic parameter sweeping,
    in spite of a shift in the bifurcation point, which is of value to experimental
    studies of nonlinear dynamical systems.
article_number: '022906'
author:
- first_name: Youngyong
  full_name: Park, Youngyong
  last_name: Park
- first_name: Younghae
  full_name: Do, Younghae
  last_name: Do
- first_name: Sebastian
  full_name: Altmeyer, Sebastian
  id: 2EE67FDC-F248-11E8-B48F-1D18A9856A87
  last_name: Altmeyer
  orcid: 0000-0001-5964-0203
- first_name: Yingcheng
  full_name: Lai, Yingcheng
  last_name: Lai
- first_name: Gyuwon
  full_name: Lee, Gyuwon
  last_name: Lee
citation:
  ama: Park Y, Do Y, Altmeyer S, Lai Y, Lee G. Early effect in time-dependent, high-dimensional
    nonlinear dynamical systems with multiple resonances. <i>Physical Review E</i>.
    2015;91(2). doi:<a href="https://doi.org/10.1103/PhysRevE.91.022906">10.1103/PhysRevE.91.022906</a>
  apa: Park, Y., Do, Y., Altmeyer, S., Lai, Y., &#38; Lee, G. (2015). Early effect
    in time-dependent, high-dimensional nonlinear dynamical systems with multiple
    resonances. <i>Physical Review E</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevE.91.022906">https://doi.org/10.1103/PhysRevE.91.022906</a>
  chicago: Park, Youngyong, Younghae Do, Sebastian Altmeyer, Yingcheng Lai, and Gyuwon
    Lee. “Early Effect in Time-Dependent, High-Dimensional Nonlinear Dynamical Systems
    with Multiple Resonances.” <i>Physical Review E</i>. American Physical Society,
    2015. <a href="https://doi.org/10.1103/PhysRevE.91.022906">https://doi.org/10.1103/PhysRevE.91.022906</a>.
  ieee: Y. Park, Y. Do, S. Altmeyer, Y. Lai, and G. Lee, “Early effect in time-dependent,
    high-dimensional nonlinear dynamical systems with multiple resonances,” <i>Physical
    Review E</i>, vol. 91, no. 2. American Physical Society, 2015.
  ista: Park Y, Do Y, Altmeyer S, Lai Y, Lee G. 2015. Early effect in time-dependent,
    high-dimensional nonlinear dynamical systems with multiple resonances. Physical
    Review E. 91(2), 022906.
  mla: Park, Youngyong, et al. “Early Effect in Time-Dependent, High-Dimensional Nonlinear
    Dynamical Systems with Multiple Resonances.” <i>Physical Review E</i>, vol. 91,
    no. 2, 022906, American Physical Society, 2015, doi:<a href="https://doi.org/10.1103/PhysRevE.91.022906">10.1103/PhysRevE.91.022906</a>.
  short: Y. Park, Y. Do, S. Altmeyer, Y. Lai, G. Lee, Physical Review E 91 (2015).
date_created: 2018-12-11T11:54:27Z
date_published: 2015-02-09T00:00:00Z
date_updated: 2021-01-12T06:53:44Z
day: '09'
department:
- _id: BjHo
doi: 10.1103/PhysRevE.91.022906
intvolume: '        91'
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
publication: Physical Review E
publication_identifier:
  issn:
  - 1539-3755
publication_status: published
publisher: American Physical Society
publist_id: '5229'
quality_controlled: '1'
scopus_import: 1
status: public
title: Early effect in time-dependent, high-dimensional nonlinear dynamical systems
  with multiple resonances
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 91
year: '2015'
...
---
_id: '1871'
abstract:
- lang: eng
  text: The plant hormone auxin is a key regulator of plant growth and development.
    Differences in auxin distribution within tissues are mediated by the polar auxin
    transport machinery, and cellular auxin responses occur depending on changes in
    cellular auxin levels. Multiple receptor systems at the cell surface and in the
    interior operate to sense and interpret fluctuations in auxin distribution that
    occur during plant development. Until now, three proteins or protein complexes
    that can bind auxin have been identified. SCFTIR1 [a SKP1-cullin-1-F-box complex
    that contains transport inhibitor response 1 (TIR1) as the F-box protein] and
    S-phase-kinaseassociated protein 2 (SKP2) localize to the nucleus, whereas auxinbinding
    protein 1 (ABP1), predominantly associates with the endoplasmic reticulum and
    cell surface. In this Cell Science at a Glance article, we summarize recent discoveries
    in the field of auxin transport and signaling that have led to the identification
    of new components of these pathways, as well as their mutual interaction.
acknowledgement: This work was supported by the European Research Council [project
  ERC-2011-StG-20101109-PSDP]; European Social Fund [grant number CZ.1.07/2.3.00/20.0043]
  and the Czech Science Foundation GAČR [grant number GA13-40637S]
author:
- first_name: Peter
  full_name: Grones, Peter
  id: 399876EC-F248-11E8-B48F-1D18A9856A87
  last_name: Grones
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Grones P, Friml J. Auxin transporters and binding proteins at a glance. <i>Journal
    of Cell Science</i>. 2015;128(1):1-7. doi:<a href="https://doi.org/10.1242/jcs.159418">10.1242/jcs.159418</a>
  apa: Grones, P., &#38; Friml, J. (2015). Auxin transporters and binding proteins
    at a glance. <i>Journal of Cell Science</i>. Company of Biologists. <a href="https://doi.org/10.1242/jcs.159418">https://doi.org/10.1242/jcs.159418</a>
  chicago: Grones, Peter, and Jiří Friml. “Auxin Transporters and Binding Proteins
    at a Glance.” <i>Journal of Cell Science</i>. Company of Biologists, 2015. <a
    href="https://doi.org/10.1242/jcs.159418">https://doi.org/10.1242/jcs.159418</a>.
  ieee: P. Grones and J. Friml, “Auxin transporters and binding proteins at a glance,”
    <i>Journal of Cell Science</i>, vol. 128, no. 1. Company of Biologists, pp. 1–7,
    2015.
  ista: Grones P, Friml J. 2015. Auxin transporters and binding proteins at a glance.
    Journal of Cell Science. 128(1), 1–7.
  mla: Grones, Peter, and Jiří Friml. “Auxin Transporters and Binding Proteins at
    a Glance.” <i>Journal of Cell Science</i>, vol. 128, no. 1, Company of Biologists,
    2015, pp. 1–7, doi:<a href="https://doi.org/10.1242/jcs.159418">10.1242/jcs.159418</a>.
  short: P. Grones, J. Friml, Journal of Cell Science 128 (2015) 1–7.
date_created: 2018-12-11T11:54:28Z
date_published: 2015-01-01T00:00:00Z
date_updated: 2021-01-12T06:53:45Z
day: '01'
ddc:
- '570'
department:
- _id: JiFr
doi: 10.1242/jcs.159418
file:
- access_level: open_access
  checksum: 24c779f4cd9d549ca6833e26f486be27
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:11:00Z
  date_updated: 2020-07-14T12:45:19Z
  file_id: '4852'
  file_name: IST-2016-563-v1+1_1.full.pdf
  file_size: 1688844
  relation: main_file
file_date_updated: 2020-07-14T12:45:19Z
has_accepted_license: '1'
intvolume: '       128'
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Submitted Version
page: 1 - 7
publication: Journal of Cell Science
publication_status: published
publisher: Company of Biologists
publist_id: '5225'
pubrep_id: '563'
quality_controlled: '1'
scopus_import: 1
status: public
title: Auxin transporters and binding proteins at a glance
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 128
year: '2015'
...
---
_id: '1873'
abstract:
- lang: eng
  text: 'We consider partially observable Markov decision processes (POMDPs) with
    limit-average payoff, where a reward value in the interval [0,1] is associated
    with every transition, and the payoff of an infinite path is the long-run average
    of the rewards. We consider two types of path constraints: (i) a quantitative
    constraint defines the set of paths where the payoff is at least a given threshold
    λ1ε(0,1]; and (ii) a qualitative constraint which is a special case of the quantitative
    constraint with λ1=1. We consider the computation of the almost-sure winning set,
    where the controller needs to ensure that the path constraint is satisfied with
    probability 1. Our main results for qualitative path constraints are as follows:
    (i) the problem of deciding the existence of a finite-memory controller is EXPTIME-complete;
    and (ii) the problem of deciding the existence of an infinite-memory controller
    is undecidable. For quantitative path constraints we show that the problem of
    deciding the existence of a finite-memory controller is undecidable. We also present
    a prototype implementation of our EXPTIME algorithm and experimental results on
    several examples.'
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: Martin
  full_name: Chmelik, Martin
  id: 3624234E-F248-11E8-B48F-1D18A9856A87
  last_name: Chmelik
citation:
  ama: Chatterjee K, Chmelik M. POMDPs under probabilistic semantics. <i>Artificial
    Intelligence</i>. 2015;221:46-72. doi:<a href="https://doi.org/10.1016/j.artint.2014.12.009">10.1016/j.artint.2014.12.009</a>
  apa: Chatterjee, K., &#38; Chmelik, M. (2015). POMDPs under probabilistic semantics.
    <i>Artificial Intelligence</i>. Elsevier. <a href="https://doi.org/10.1016/j.artint.2014.12.009">https://doi.org/10.1016/j.artint.2014.12.009</a>
  chicago: Chatterjee, Krishnendu, and Martin Chmelik. “POMDPs under Probabilistic
    Semantics.” <i>Artificial Intelligence</i>. Elsevier, 2015. <a href="https://doi.org/10.1016/j.artint.2014.12.009">https://doi.org/10.1016/j.artint.2014.12.009</a>.
  ieee: K. Chatterjee and M. Chmelik, “POMDPs under probabilistic semantics,” <i>Artificial
    Intelligence</i>, vol. 221. Elsevier, pp. 46–72, 2015.
  ista: Chatterjee K, Chmelik M. 2015. POMDPs under probabilistic semantics. Artificial
    Intelligence. 221, 46–72.
  mla: Chatterjee, Krishnendu, and Martin Chmelik. “POMDPs under Probabilistic Semantics.”
    <i>Artificial Intelligence</i>, vol. 221, Elsevier, 2015, pp. 46–72, doi:<a href="https://doi.org/10.1016/j.artint.2014.12.009">10.1016/j.artint.2014.12.009</a>.
  short: K. Chatterjee, M. Chmelik, Artificial Intelligence 221 (2015) 46–72.
date_created: 2018-12-11T11:54:28Z
date_published: 2015-04-01T00:00:00Z
date_updated: 2021-01-12T06:53:46Z
day: '01'
department:
- _id: KrCh
doi: 10.1016/j.artint.2014.12.009
external_id:
  arxiv:
  - '1408.2058'
intvolume: '       221'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1408.2058
month: '04'
oa: 1
oa_version: Preprint
page: 46 - 72
publication: Artificial Intelligence
publication_status: published
publisher: Elsevier
publist_id: '5224'
quality_controlled: '1'
scopus_import: 1
status: public
title: POMDPs under probabilistic semantics
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 221
year: '2015'
...
---
_id: '1874'
abstract:
- lang: eng
  text: 'The hippocampal region, comprising the hippocampal formation and the parahippocampal
    region, has been one of the most intensively studied parts of the brain for decades.
    Better understanding of its functional diversity and complexity has led to an
    increased demand for specificity in experimental procedures and manipulations.
    In view of the complex 3D structure of the hippocampal region, precisely positioned
    experimental approaches require a fine-grained architectural description that
    is available and readable to experimentalists lacking detailed anatomical experience.
    In this paper, we provide the first cyto- and chemoarchitectural description of
    the hippocampal formation and parahippocampal region in the rat at high resolution
    and in the three standard sectional planes: coronal, horizontal and sagittal.
    The atlas uses a series of adjacent sections stained for neurons and for a number
    of chemical marker substances, particularly parvalbumin and calbindin. All the
    borders defined in one plane have been cross-checked against their counterparts
    in the other two planes. The entire dataset will be made available as a web-based
    interactive application through the Rodent Brain WorkBench (http://www.rbwb.org)
    which, together with this paper, provides a unique atlas resource.'
author:
- first_name: Charlotte
  full_name: Boccara, Charlotte
  id: 3FC06552-F248-11E8-B48F-1D18A9856A87
  last_name: Boccara
  orcid: 0000-0001-7237-5109
- first_name: Lisa
  full_name: Kjønigsen, Lisa
  last_name: Kjønigsen
- first_name: Ingvild
  full_name: Hammer, Ingvild
  last_name: Hammer
- first_name: Jan
  full_name: Bjaalie, Jan
  last_name: Bjaalie
- first_name: Trygve
  full_name: Leergaard, Trygve
  last_name: Leergaard
- first_name: Menno
  full_name: Witter, Menno
  last_name: Witter
citation:
  ama: Boccara CN, Kjønigsen L, Hammer I, Bjaalie J, Leergaard T, Witter M. A three-plane
    architectonic atlas of the rat hippocampal region. <i>Hippocampus</i>. 2015;25(7):838-857.
    doi:<a href="https://doi.org/10.1002/hipo.22407">10.1002/hipo.22407</a>
  apa: Boccara, C. N., Kjønigsen, L., Hammer, I., Bjaalie, J., Leergaard, T., &#38;
    Witter, M. (2015). A three-plane architectonic atlas of the rat hippocampal region.
    <i>Hippocampus</i>. Wiley. <a href="https://doi.org/10.1002/hipo.22407">https://doi.org/10.1002/hipo.22407</a>
  chicago: Boccara, Charlotte N., Lisa Kjønigsen, Ingvild Hammer, Jan Bjaalie, Trygve
    Leergaard, and Menno Witter. “A Three-Plane Architectonic Atlas of the Rat Hippocampal
    Region.” <i>Hippocampus</i>. Wiley, 2015. <a href="https://doi.org/10.1002/hipo.22407">https://doi.org/10.1002/hipo.22407</a>.
  ieee: C. N. Boccara, L. Kjønigsen, I. Hammer, J. Bjaalie, T. Leergaard, and M. Witter,
    “A three-plane architectonic atlas of the rat hippocampal region,” <i>Hippocampus</i>,
    vol. 25, no. 7. Wiley, pp. 838–857, 2015.
  ista: Boccara CN, Kjønigsen L, Hammer I, Bjaalie J, Leergaard T, Witter M. 2015.
    A three-plane architectonic atlas of the rat hippocampal region. Hippocampus.
    25(7), 838–857.
  mla: Boccara, Charlotte N., et al. “A Three-Plane Architectonic Atlas of the Rat
    Hippocampal Region.” <i>Hippocampus</i>, vol. 25, no. 7, Wiley, 2015, pp. 838–57,
    doi:<a href="https://doi.org/10.1002/hipo.22407">10.1002/hipo.22407</a>.
  short: C.N. Boccara, L. Kjønigsen, I. Hammer, J. Bjaalie, T. Leergaard, M. Witter,
    Hippocampus 25 (2015) 838–857.
date_created: 2018-12-11T11:54:29Z
date_published: 2015-07-01T00:00:00Z
date_updated: 2021-01-12T06:53:46Z
day: '01'
department:
- _id: JoCs
doi: 10.1002/hipo.22407
intvolume: '        25'
issue: '7'
language:
- iso: eng
month: '07'
oa_version: None
page: 838 - 857
publication: Hippocampus
publication_status: published
publisher: Wiley
publist_id: '5222'
quality_controlled: '1'
scopus_import: 1
status: public
title: A three-plane architectonic atlas of the rat hippocampal region
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 25
year: '2015'
...
---
_id: '1878'
abstract:
- lang: eng
  text: Petrocoptis is a small genus of chasmophytic plants endemic to the Iberian
    Peninsula, with some localized populations in the French Pyrenees. Within the
    genus, a dozen species have been recognized based on morphological diversity,
    most of them with limited distribution area, in small populations and frequently
    with potential threats to their survival. To date, however, a molecular evaluation
    of the current systematic treatments has not been carried out. The aim of the
    present study is to infer phylogenetic relationships among its subordinate taxa
    by using plastidial rps16 intron and nuclear internal transcribed spacer (ITS)
    DNA sequences; and evaluate the phylogenetic placement of the genus Petrocoptis
    within the family Caryophyllaceae. The monophyly of Petrocoptis is supported by
    both ITS and rps16 intron sequence analyses. Furthermore, time estimates using
    BEAST analyses indicate a Middle to Late Miocene diversification (10.59 Myr, 6.44–15.26
    Myr highest posterior densities [HPD], for ITS; 14.30 Myr, 8.61–21.00 Myr HPD,
    for rps16 intron).
author:
- first_name: Eduardo
  full_name: Cires Rodriguez, Eduardo
  id: 2AD56A7A-F248-11E8-B48F-1D18A9856A87
  last_name: Cires Rodriguez
- first_name: José
  full_name: Prieto, José
  last_name: Prieto
citation:
  ama: Cires Rodriguez E, Prieto J. Phylogenetic relationships of Petrocoptis A. Braun
    ex Endl. (Caryophyllaceae), a discussed genus from the Iberian Peninsula. <i>Journal
    of Plant Research</i>. 2015;128(2):223-238. doi:<a href="https://doi.org/10.1007/s10265-014-0691-6">10.1007/s10265-014-0691-6</a>
  apa: Cires Rodriguez, E., &#38; Prieto, J. (2015). Phylogenetic relationships of
    Petrocoptis A. Braun ex Endl. (Caryophyllaceae), a discussed genus from the Iberian
    Peninsula. <i>Journal of Plant Research</i>. Springer. <a href="https://doi.org/10.1007/s10265-014-0691-6">https://doi.org/10.1007/s10265-014-0691-6</a>
  chicago: Cires Rodriguez, Eduardo, and José Prieto. “Phylogenetic Relationships
    of Petrocoptis A. Braun Ex Endl. (Caryophyllaceae), a Discussed Genus from the
    Iberian Peninsula.” <i>Journal of Plant Research</i>. Springer, 2015. <a href="https://doi.org/10.1007/s10265-014-0691-6">https://doi.org/10.1007/s10265-014-0691-6</a>.
  ieee: E. Cires Rodriguez and J. Prieto, “Phylogenetic relationships of Petrocoptis
    A. Braun ex Endl. (Caryophyllaceae), a discussed genus from the Iberian Peninsula,”
    <i>Journal of Plant Research</i>, vol. 128, no. 2. Springer, pp. 223–238, 2015.
  ista: Cires Rodriguez E, Prieto J. 2015. Phylogenetic relationships of Petrocoptis
    A. Braun ex Endl. (Caryophyllaceae), a discussed genus from the Iberian Peninsula.
    Journal of Plant Research. 128(2), 223–238.
  mla: Cires Rodriguez, Eduardo, and José Prieto. “Phylogenetic Relationships of Petrocoptis
    A. Braun Ex Endl. (Caryophyllaceae), a Discussed Genus from the Iberian Peninsula.”
    <i>Journal of Plant Research</i>, vol. 128, no. 2, Springer, 2015, pp. 223–38,
    doi:<a href="https://doi.org/10.1007/s10265-014-0691-6">10.1007/s10265-014-0691-6</a>.
  short: E. Cires Rodriguez, J. Prieto, Journal of Plant Research 128 (2015) 223–238.
date_created: 2018-12-11T11:54:30Z
date_published: 2015-01-24T00:00:00Z
date_updated: 2021-01-12T06:53:47Z
day: '24'
department:
- _id: JiFr
doi: 10.1007/s10265-014-0691-6
intvolume: '       128'
issue: '2'
language:
- iso: eng
month: '01'
oa_version: None
page: 223 - 238
publication: Journal of Plant Research
publication_status: published
publisher: Springer
publist_id: '5217'
quality_controlled: '1'
scopus_import: 1
status: public
title: Phylogenetic relationships of Petrocoptis A. Braun ex Endl. (Caryophyllaceae),
  a discussed genus from the Iberian Peninsula
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 128
year: '2015'
...
---
_id: '1879'
abstract:
- lang: eng
  text: When electron microscopy (EM) was introduced in the 1930s it gave scientists
    their first look into the nanoworld of cells. Over the last 80 years EM has vastly
    increased our understanding of the complex cellular structures that underlie the
    diverse functions that cells need to maintain life. One drawback that has been
    difficult to overcome was the inherent lack of volume information, mainly due
    to the limit on the thickness of sections that could be viewed in a transmission
    electron microscope (TEM). For many years scientists struggled to achieve three-dimensional
    (3D) EM using serial section reconstructions, TEM tomography, and scanning EM
    (SEM) techniques such as freeze-fracture. Although each technique yielded some
    special information, they required a significant amount of time and specialist
    expertise to obtain even a very small 3D EM dataset. Almost 20 years ago scientists
    began to exploit SEMs to image blocks of embedded tissues and perform serial sectioning
    of these tissues inside the SEM chamber. Using first focused ion beams (FIB) and
    subsequently robotic ultramicrotomes (serial block-face, SBF-SEM) microscopists
    were able to collect large volumes of 3D EM information at resolutions that could
    address many important biological questions, and do so in an efficient manner.
    We present here some examples of 3D EM taken from the many diverse specimens that
    have been imaged in our core facility. We propose that the next major step forward
    will be to efficiently correlate functional information obtained using light microscopy
    (LM) with 3D EM datasets to more completely investigate the important links between
    cell structures and their functions.
acknowledgement: The Zeiss Merlin with Gatan 3View2XP and Zeiss Auriga were acquired
  through a CLEM grant from Minister Ingrid Lieten to the VIB Bio-Imaging-Core. Michiel
  Krols and Saskia Lippens are the recipients of a fellowship from the FWO (Fonds
  Wetenschappelijk Onderzoek) of Flanders.
author:
- first_name: A
  full_name: Kremer, A
  last_name: Kremer
- first_name: Stefaan
  full_name: Lippens, Stefaan
  last_name: Lippens
- first_name: Sonia
  full_name: Bartunkova, Sonia
  last_name: Bartunkova
- first_name: Bob
  full_name: Asselbergh, Bob
  last_name: Asselbergh
- first_name: Cendric
  full_name: Blanpain, Cendric
  last_name: Blanpain
- first_name: Matyas
  full_name: Fendrych, Matyas
  id: 43905548-F248-11E8-B48F-1D18A9856A87
  last_name: Fendrych
  orcid: 0000-0002-9767-8699
- first_name: A
  full_name: Goossens, A
  last_name: Goossens
- first_name: Matthew
  full_name: Holt, Matthew
  last_name: Holt
- first_name: Sophie
  full_name: Janssens, Sophie
  last_name: Janssens
- first_name: Michiel
  full_name: Krols, Michiel
  last_name: Krols
- first_name: Jean
  full_name: Larsimont, Jean
  last_name: Larsimont
- first_name: Conor
  full_name: Mc Guire, Conor
  last_name: Mc Guire
- first_name: Moritz
  full_name: Nowack, Moritz
  last_name: Nowack
- first_name: Xavier
  full_name: Saelens, Xavier
  last_name: Saelens
- first_name: Andreas
  full_name: Schertel, Andreas
  last_name: Schertel
- first_name: B
  full_name: Schepens, B
  last_name: Schepens
- first_name: M
  full_name: Slezak, M
  last_name: Slezak
- first_name: Vincent
  full_name: Timmerman, Vincent
  last_name: Timmerman
- first_name: Clara
  full_name: Theunis, Clara
  last_name: Theunis
- first_name: Ronald
  full_name: Van Brempt, Ronald
  last_name: Van Brempt
- first_name: Y
  full_name: Visser, Y
  last_name: Visser
- first_name: Christophe
  full_name: Guérin, Christophe
  last_name: Guérin
citation:
  ama: Kremer A, Lippens S, Bartunkova S, et al. Developing 3D SEM in a broad biological
    context. <i>Journal of Microscopy</i>. 2015;259(2):80-96. doi:<a href="https://doi.org/10.1111/jmi.12211">10.1111/jmi.12211</a>
  apa: Kremer, A., Lippens, S., Bartunkova, S., Asselbergh, B., Blanpain, C., Fendrych,
    M., … Guérin, C. (2015). Developing 3D SEM in a broad biological context. <i>Journal
    of Microscopy</i>. Wiley-Blackwell. <a href="https://doi.org/10.1111/jmi.12211">https://doi.org/10.1111/jmi.12211</a>
  chicago: Kremer, A, Stefaan Lippens, Sonia Bartunkova, Bob Asselbergh, Cendric Blanpain,
    Matyas Fendrych, A Goossens, et al. “Developing 3D SEM in a Broad Biological Context.”
    <i>Journal of Microscopy</i>. Wiley-Blackwell, 2015. <a href="https://doi.org/10.1111/jmi.12211">https://doi.org/10.1111/jmi.12211</a>.
  ieee: A. Kremer <i>et al.</i>, “Developing 3D SEM in a broad biological context,”
    <i>Journal of Microscopy</i>, vol. 259, no. 2. Wiley-Blackwell, pp. 80–96, 2015.
  ista: Kremer A, Lippens S, Bartunkova S, Asselbergh B, Blanpain C, Fendrych M, Goossens
    A, Holt M, Janssens S, Krols M, Larsimont J, Mc Guire C, Nowack M, Saelens X,
    Schertel A, Schepens B, Slezak M, Timmerman V, Theunis C, Van Brempt R, Visser
    Y, Guérin C. 2015. Developing 3D SEM in a broad biological context. Journal of
    Microscopy. 259(2), 80–96.
  mla: Kremer, A., et al. “Developing 3D SEM in a Broad Biological Context.” <i>Journal
    of Microscopy</i>, vol. 259, no. 2, Wiley-Blackwell, 2015, pp. 80–96, doi:<a href="https://doi.org/10.1111/jmi.12211">10.1111/jmi.12211</a>.
  short: A. Kremer, S. Lippens, S. Bartunkova, B. Asselbergh, C. Blanpain, M. Fendrych,
    A. Goossens, M. Holt, S. Janssens, M. Krols, J. Larsimont, C. Mc Guire, M. Nowack,
    X. Saelens, A. Schertel, B. Schepens, M. Slezak, V. Timmerman, C. Theunis, R.
    Van Brempt, Y. Visser, C. Guérin, Journal of Microscopy 259 (2015) 80–96.
date_created: 2018-12-11T11:54:30Z
date_published: 2015-08-01T00:00:00Z
date_updated: 2021-01-12T06:53:48Z
day: '01'
ddc:
- '570'
department:
- _id: JiFr
doi: 10.1111/jmi.12211
file:
- access_level: open_access
  checksum: 3649c5372d1644062d728ea9287e367f
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:11:19Z
  date_updated: 2020-07-14T12:45:19Z
  file_id: '4872'
  file_name: IST-2016-459-v1+1_KREMER_et_al-2015-Journal_of_Microscopy.pdf
  file_size: 2899898
  relation: main_file
file_date_updated: 2020-07-14T12:45:19Z
has_accepted_license: '1'
intvolume: '       259'
issue: '2'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: 80 - 96
publication: Journal of Microscopy
publication_status: published
publisher: Wiley-Blackwell
publist_id: '5218'
pubrep_id: '459'
quality_controlled: '1'
scopus_import: 1
status: public
title: Developing 3D SEM in a broad biological context
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: 259
year: '2015'
...
---
_id: '1880'
abstract:
- lang: eng
  text: We investigate the relation between Bose-Einstein condensation (BEC) and superfluidity
    in the ground state of a one-dimensional model of interacting bosons in a strong
    random potential. We prove rigorously that in a certain parameter regime the superfluid
    fraction can be arbitrarily small while complete BEC prevails. In another regime
    there is both complete BEC and complete superfluidity, despite the strong disorder
acknowledgement: Support from the Natural Sciences and Engineering Research Council
  of Canada NSERC (MK and RS) and from the Austrian Science Fund FWF (JY, under project
  P 22929-N16) is gratefully acknowledged
article_number: '013022'
author:
- first_name: Martin
  full_name: Könenberg, Martin
  last_name: Könenberg
- first_name: Thomas
  full_name: Moser, Thomas
  id: 2B5FC9A4-F248-11E8-B48F-1D18A9856A87
  last_name: Moser
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
- first_name: Jakob
  full_name: Yngvason, Jakob
  last_name: Yngvason
citation:
  ama: Könenberg M, Moser T, Seiringer R, Yngvason J. Superfluid behavior of a Bose-Einstein
    condensate in a random potential. <i>New Journal of Physics</i>. 2015;17. doi:<a
    href="https://doi.org/10.1088/1367-2630/17/1/013022">10.1088/1367-2630/17/1/013022</a>
  apa: Könenberg, M., Moser, T., Seiringer, R., &#38; Yngvason, J. (2015). Superfluid
    behavior of a Bose-Einstein condensate in a random potential. <i>New Journal of
    Physics</i>. IOP Publishing Ltd. <a href="https://doi.org/10.1088/1367-2630/17/1/013022">https://doi.org/10.1088/1367-2630/17/1/013022</a>
  chicago: Könenberg, Martin, Thomas Moser, Robert Seiringer, and Jakob Yngvason.
    “Superfluid Behavior of a Bose-Einstein Condensate in a Random Potential.” <i>New
    Journal of Physics</i>. IOP Publishing Ltd., 2015. <a href="https://doi.org/10.1088/1367-2630/17/1/013022">https://doi.org/10.1088/1367-2630/17/1/013022</a>.
  ieee: M. Könenberg, T. Moser, R. Seiringer, and J. Yngvason, “Superfluid behavior
    of a Bose-Einstein condensate in a random potential,” <i>New Journal of Physics</i>,
    vol. 17. IOP Publishing Ltd., 2015.
  ista: Könenberg M, Moser T, Seiringer R, Yngvason J. 2015. Superfluid behavior of
    a Bose-Einstein condensate in a random potential. New Journal of Physics. 17,
    013022.
  mla: Könenberg, Martin, et al. “Superfluid Behavior of a Bose-Einstein Condensate
    in a Random Potential.” <i>New Journal of Physics</i>, vol. 17, 013022, IOP Publishing
    Ltd., 2015, doi:<a href="https://doi.org/10.1088/1367-2630/17/1/013022">10.1088/1367-2630/17/1/013022</a>.
  short: M. Könenberg, T. Moser, R. Seiringer, J. Yngvason, New Journal of Physics
    17 (2015).
date_created: 2018-12-11T11:54:30Z
date_published: 2015-01-15T00:00:00Z
date_updated: 2021-01-12T06:53:48Z
day: '15'
ddc:
- '530'
department:
- _id: RoSe
doi: 10.1088/1367-2630/17/1/013022
file:
- access_level: open_access
  checksum: 38fdf2b5ac30445e26a5d613abd84b16
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:12:44Z
  date_updated: 2020-07-14T12:45:20Z
  file_id: '4963'
  file_name: IST-2016-447-v1+1_document_1_.pdf
  file_size: 768108
  relation: main_file
file_date_updated: 2020-07-14T12:45:20Z
has_accepted_license: '1'
intvolume: '        17'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: 26450934-B435-11E9-9278-68D0E5697425
  name: NSERC Postdoctoral fellowship
publication: New Journal of Physics
publication_status: published
publisher: IOP Publishing Ltd.
publist_id: '5214'
pubrep_id: '447'
quality_controlled: '1'
scopus_import: 1
status: public
title: Superfluid behavior of a Bose-Einstein condensate in a random potential
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: 17
year: '2015'
...
---
_id: '1882'
abstract:
- lang: eng
  text: We provide a framework for compositional and iterative design and verification
    of systems with quantitative information, such as rewards, time or energy. It
    is based on disjunctive modal transition systems where we allow actions to bear
    various types of quantitative information. Throughout the design process the actions
    can be further refined and the information made more precise. We show how to compute
    the results of standard operations on the systems, including the quotient (residual),
    which has not been previously considered for quantitative non-deterministic systems.
    Our quantitative framework has close connections to the modal nu-calculus and
    is compositional with respect to general notions of distances between systems
    and the standard operations.
acknowledgement: This research was funded in part by the European Research Council
  (ERC) under grant agreement 267989 (QUAREM), by the Austrian Science Fund (FWF)
  project S11402-N23 (RiSE), and by the Czech Science Foundation, grant No. P202/12/G061.
alternative_title:
- LNCS
author:
- first_name: Uli
  full_name: Fahrenberg, Uli
  last_name: Fahrenberg
- first_name: Jan
  full_name: Kretinsky, Jan
  id: 44CEF464-F248-11E8-B48F-1D18A9856A87
  last_name: Kretinsky
  orcid: 0000-0002-8122-2881
- first_name: Axel
  full_name: Legay, Axel
  last_name: Legay
- first_name: Louis
  full_name: Traonouez, Louis
  last_name: Traonouez
citation:
  ama: 'Fahrenberg U, Kretinsky J, Legay A, Traonouez L. Compositionality for quantitative
    specifications. In: Vol 8997. Springer; 2015:306-324. doi:<a href="https://doi.org/10.1007/978-3-319-15317-9_19">10.1007/978-3-319-15317-9_19</a>'
  apa: 'Fahrenberg, U., Kretinsky, J., Legay, A., &#38; Traonouez, L. (2015). Compositionality
    for quantitative specifications (Vol. 8997, pp. 306–324). Presented at the FACS:
    Formal Aspects of Component Software, Bertinoro, Italy: Springer. <a href="https://doi.org/10.1007/978-3-319-15317-9_19">https://doi.org/10.1007/978-3-319-15317-9_19</a>'
  chicago: Fahrenberg, Uli, Jan Kretinsky, Axel Legay, and Louis Traonouez. “Compositionality
    for Quantitative Specifications,” 8997:306–24. Springer, 2015. <a href="https://doi.org/10.1007/978-3-319-15317-9_19">https://doi.org/10.1007/978-3-319-15317-9_19</a>.
  ieee: 'U. Fahrenberg, J. Kretinsky, A. Legay, and L. Traonouez, “Compositionality
    for quantitative specifications,” presented at the FACS: Formal Aspects of Component
    Software, Bertinoro, Italy, 2015, vol. 8997, pp. 306–324.'
  ista: 'Fahrenberg U, Kretinsky J, Legay A, Traonouez L. 2015. Compositionality for
    quantitative specifications. FACS: Formal Aspects of Component Software, LNCS,
    vol. 8997, 306–324.'
  mla: Fahrenberg, Uli, et al. <i>Compositionality for Quantitative Specifications</i>.
    Vol. 8997, Springer, 2015, pp. 306–24, doi:<a href="https://doi.org/10.1007/978-3-319-15317-9_19">10.1007/978-3-319-15317-9_19</a>.
  short: U. Fahrenberg, J. Kretinsky, A. Legay, L. Traonouez, in:, Springer, 2015,
    pp. 306–324.
conference:
  end_date: 2014-09-12
  location: Bertinoro, Italy
  name: 'FACS: Formal Aspects of Component Software'
  start_date: 2014-09-10
date_created: 2018-12-11T11:54:31Z
date_published: 2015-01-30T00:00:00Z
date_updated: 2021-01-12T06:53:49Z
day: '30'
department:
- _id: ToHe
- _id: KrCh
doi: 10.1007/978-3-319-15317-9_19
ec_funded: 1
intvolume: '      8997'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1408.1256
month: '01'
oa: 1
oa_version: Preprint
page: 306 - 324
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_status: published
publisher: Springer
publist_id: '5216'
quality_controlled: '1'
scopus_import: 1
status: public
title: Compositionality for quantitative specifications
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8997
year: '2015'
...
---
_id: '1883'
abstract:
- lang: eng
  text: "We introduce a one-parametric family of tree growth models, in which branching
    probabilities decrease with branch age τ as τ-α. Depending on the exponent α,
    the scaling of tree depth with tree size n displays a transition between the logarithmic
    scaling of random trees and an algebraic growth. At the transition (α=1) tree
    depth grows as (logn)2. This anomalous scaling is in good agreement with the trend
    observed in evolution of biological species, thus providing a theoretical support
    for age-dependent speciation and associating it to the occurrence of a critical
    point.\r\n"
article_number: '022803'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Stephanie
  full_name: Keller-Schmidt, Stephanie
  last_name: Keller-Schmidt
- first_name: Murat
  full_name: Tugrul, Murat
  id: 37C323C6-F248-11E8-B48F-1D18A9856A87
  last_name: Tugrul
  orcid: 0000-0002-8523-0758
- first_name: Víctor
  full_name: Eguíluz, Víctor
  last_name: Eguíluz
- first_name: Emilio
  full_name: Hernandez Garcia, Emilio
  last_name: Hernandez Garcia
- first_name: Konstantin
  full_name: Klemm, Konstantin
  last_name: Klemm
citation:
  ama: Keller-Schmidt S, Tugrul M, Eguíluz V, Hernandez Garcia E, Klemm K. Anomalous
    scaling in an age-dependent branching model. <i>Physical Review E Statistical
    Nonlinear and Soft Matter Physics</i>. 2015;91(2). doi:<a href="https://doi.org/10.1103/PhysRevE.91.022803">10.1103/PhysRevE.91.022803</a>
  apa: Keller-Schmidt, S., Tugrul, M., Eguíluz, V., Hernandez Garcia, E., &#38; Klemm,
    K. (2015). Anomalous scaling in an age-dependent branching model. <i>Physical
    Review E Statistical Nonlinear and Soft Matter Physics</i>. American Institute
    of Physics. <a href="https://doi.org/10.1103/PhysRevE.91.022803">https://doi.org/10.1103/PhysRevE.91.022803</a>
  chicago: Keller-Schmidt, Stephanie, Murat Tugrul, Víctor Eguíluz, Emilio Hernandez
    Garcia, and Konstantin Klemm. “Anomalous Scaling in an Age-Dependent Branching
    Model.” <i>Physical Review E Statistical Nonlinear and Soft Matter Physics</i>.
    American Institute of Physics, 2015. <a href="https://doi.org/10.1103/PhysRevE.91.022803">https://doi.org/10.1103/PhysRevE.91.022803</a>.
  ieee: S. Keller-Schmidt, M. Tugrul, V. Eguíluz, E. Hernandez Garcia, and K. Klemm,
    “Anomalous scaling in an age-dependent branching model,” <i>Physical Review E
    Statistical Nonlinear and Soft Matter Physics</i>, vol. 91, no. 2. American Institute
    of Physics, 2015.
  ista: Keller-Schmidt S, Tugrul M, Eguíluz V, Hernandez Garcia E, Klemm K. 2015.
    Anomalous scaling in an age-dependent branching model. Physical Review E Statistical
    Nonlinear and Soft Matter Physics. 91(2), 022803.
  mla: Keller-Schmidt, Stephanie, et al. “Anomalous Scaling in an Age-Dependent Branching
    Model.” <i>Physical Review E Statistical Nonlinear and Soft Matter Physics</i>,
    vol. 91, no. 2, 022803, American Institute of Physics, 2015, doi:<a href="https://doi.org/10.1103/PhysRevE.91.022803">10.1103/PhysRevE.91.022803</a>.
  short: S. Keller-Schmidt, M. Tugrul, V. Eguíluz, E. Hernandez Garcia, K. Klemm,
    Physical Review E Statistical Nonlinear and Soft Matter Physics 91 (2015).
date_created: 2018-12-11T11:54:31Z
date_published: 2015-02-02T00:00:00Z
date_updated: 2021-01-12T06:53:49Z
day: '02'
department:
- _id: NiBa
doi: 10.1103/PhysRevE.91.022803
external_id:
  arxiv:
  - '1012.3298'
intvolume: '        91'
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1012.3298
month: '02'
oa: 1
oa_version: Preprint
publication: Physical Review E Statistical Nonlinear and Soft Matter Physics
publication_status: published
publisher: American Institute of Physics
publist_id: '5213'
quality_controlled: '1'
scopus_import: 1
status: public
title: Anomalous scaling in an age-dependent branching model
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 91
year: '2015'
...
---
_id: '1885'
abstract:
- lang: eng
  text: 'The concept of positional information is central to our understanding of
    how cells determine their location in a multicellular structure and thereby their
    developmental fates. Nevertheless, positional information has neither been defined
    mathematically nor quantified in a principled way. Here we provide an information-theoretic
    definition in the context of developmental gene expression patterns and examine
    the features of expression patterns that affect positional information quantitatively.
    We connect positional information with the concept of positional error and develop
    tools to directly measure information and error from experimental data. We illustrate
    our framework for the case of gap gene expression patterns in the early Drosophila
    embryo and show how information that is distributed among only four genes is sufficient
    to determine developmental fates with nearly single-cell resolution. Our approach
    can be generalized to a variety of different model systems; procedures and examples
    are discussed in detail. '
author:
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
- first_name: Julien
  full_name: Dubuis, Julien
  last_name: Dubuis
- first_name: Mariela
  full_name: Petkova, Mariela
  last_name: Petkova
- first_name: Thomas
  full_name: Gregor, Thomas
  last_name: Gregor
citation:
  ama: 'Tkačik G, Dubuis J, Petkova M, Gregor T. Positional information, positional
    error, and readout precision in morphogenesis: A mathematical framework. <i>Genetics</i>.
    2015;199(1):39-59. doi:<a href="https://doi.org/10.1534/genetics.114.171850">10.1534/genetics.114.171850</a>'
  apa: 'Tkačik, G., Dubuis, J., Petkova, M., &#38; Gregor, T. (2015). Positional information,
    positional error, and readout precision in morphogenesis: A mathematical framework.
    <i>Genetics</i>. Genetics Society of America. <a href="https://doi.org/10.1534/genetics.114.171850">https://doi.org/10.1534/genetics.114.171850</a>'
  chicago: 'Tkačik, Gašper, Julien Dubuis, Mariela Petkova, and Thomas Gregor. “Positional
    Information, Positional Error, and Readout Precision in Morphogenesis: A Mathematical
    Framework.” <i>Genetics</i>. Genetics Society of America, 2015. <a href="https://doi.org/10.1534/genetics.114.171850">https://doi.org/10.1534/genetics.114.171850</a>.'
  ieee: 'G. Tkačik, J. Dubuis, M. Petkova, and T. Gregor, “Positional information,
    positional error, and readout precision in morphogenesis: A mathematical framework,”
    <i>Genetics</i>, vol. 199, no. 1. Genetics Society of America, pp. 39–59, 2015.'
  ista: 'Tkačik G, Dubuis J, Petkova M, Gregor T. 2015. Positional information, positional
    error, and readout precision in morphogenesis: A mathematical framework. Genetics.
    199(1), 39–59.'
  mla: 'Tkačik, Gašper, et al. “Positional Information, Positional Error, and Readout
    Precision in Morphogenesis: A Mathematical Framework.” <i>Genetics</i>, vol. 199,
    no. 1, Genetics Society of America, 2015, pp. 39–59, doi:<a href="https://doi.org/10.1534/genetics.114.171850">10.1534/genetics.114.171850</a>.'
  short: G. Tkačik, J. Dubuis, M. Petkova, T. Gregor, Genetics 199 (2015) 39–59.
date_created: 2018-12-11T11:54:32Z
date_published: 2015-01-01T00:00:00Z
date_updated: 2021-01-12T06:53:50Z
day: '01'
department:
- _id: GaTk
doi: 10.1534/genetics.114.171850
intvolume: '       199'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1404.5599
month: '01'
oa: 1
oa_version: Preprint
page: 39 - 59
publication: Genetics
publication_status: published
publisher: Genetics Society of America
publist_id: '5210'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'Positional information, positional error, and readout precision in morphogenesis:
  A mathematical framework'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 199
year: '2015'
...
---
_id: '1938'
abstract:
- lang: eng
  text: 'We numerically investigate the distribution of extrema of ''chaotic'' Laplacian
    eigenfunctions on two-dimensional manifolds. Our contribution is two-fold: (a)
    we count extrema on grid graphs with a small number of randomly added edges and
    show the behavior to coincide with the 1957 prediction of Longuet-Higgins for
    the continuous case and (b) we compute the regularity of their spatial distribution
    using discrepancy, which is a classical measure from the theory of Monte Carlo
    integration. The first part suggests that grid graphs with randomly added edges
    should behave like two-dimensional surfaces with ergodic geodesic flow; in the
    second part we show that the extrema are more regularly distributed in space than
    the grid Z2.'
acknowledgement: "F.P. was supported by the Graduate School of IST Austria. S.S. was
  partially supported by CRC1060 of the DFG\r\nThe authors thank Olga Symonova and
  Michael Kerber for sharing their implementation of the persistence algorithm. "
author:
- first_name: Florian
  full_name: Pausinger, Florian
  id: 2A77D7A2-F248-11E8-B48F-1D18A9856A87
  last_name: Pausinger
  orcid: 0000-0002-8379-3768
- first_name: Stefan
  full_name: Steinerberger, Stefan
  last_name: Steinerberger
citation:
  ama: Pausinger F, Steinerberger S. On the distribution of local extrema in quantum
    chaos. <i>Physics Letters, Section A</i>. 2015;379(6):535-541. doi:<a href="https://doi.org/10.1016/j.physleta.2014.12.010">10.1016/j.physleta.2014.12.010</a>
  apa: Pausinger, F., &#38; Steinerberger, S. (2015). On the distribution of local
    extrema in quantum chaos. <i>Physics Letters, Section A</i>. Elsevier. <a href="https://doi.org/10.1016/j.physleta.2014.12.010">https://doi.org/10.1016/j.physleta.2014.12.010</a>
  chicago: Pausinger, Florian, and Stefan Steinerberger. “On the Distribution of Local
    Extrema in Quantum Chaos.” <i>Physics Letters, Section A</i>. Elsevier, 2015.
    <a href="https://doi.org/10.1016/j.physleta.2014.12.010">https://doi.org/10.1016/j.physleta.2014.12.010</a>.
  ieee: F. Pausinger and S. Steinerberger, “On the distribution of local extrema in
    quantum chaos,” <i>Physics Letters, Section A</i>, vol. 379, no. 6. Elsevier,
    pp. 535–541, 2015.
  ista: Pausinger F, Steinerberger S. 2015. On the distribution of local extrema in
    quantum chaos. Physics Letters, Section A. 379(6), 535–541.
  mla: Pausinger, Florian, and Stefan Steinerberger. “On the Distribution of Local
    Extrema in Quantum Chaos.” <i>Physics Letters, Section A</i>, vol. 379, no. 6,
    Elsevier, 2015, pp. 535–41, doi:<a href="https://doi.org/10.1016/j.physleta.2014.12.010">10.1016/j.physleta.2014.12.010</a>.
  short: F. Pausinger, S. Steinerberger, Physics Letters, Section A 379 (2015) 535–541.
date_created: 2018-12-11T11:54:49Z
date_published: 2015-03-06T00:00:00Z
date_updated: 2021-01-12T06:54:12Z
day: '06'
department:
- _id: HeEd
doi: 10.1016/j.physleta.2014.12.010
intvolume: '       379'
issue: '6'
language:
- iso: eng
month: '03'
oa_version: None
page: 535 - 541
publication: Physics Letters, Section A
publication_status: published
publisher: Elsevier
publist_id: '5152'
quality_controlled: '1'
scopus_import: 1
status: public
title: On the distribution of local extrema in quantum chaos
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 379
year: '2015'
...
---
_id: '1940'
abstract:
- lang: eng
  text: We typically think of cells as responding to external signals independently
    by regulating their gene expression levels, yet they often locally exchange information
    and coordinate. Can such spatial coupling be of benefit for conveying signals
    subject to gene regulatory noise? Here we extend our information-theoretic framework
    for gene regulation to spatially extended systems. As an example, we consider
    a lattice of nuclei responding to a concentration field of a transcriptional regulator
    (the &quot;input&quot;) by expressing a single diffusible target gene. When input
    concentrations are low, diffusive coupling markedly improves information transmission;
    optimal gene activation functions also systematically change. A qualitatively
    new regulatory strategy emerges where individual cells respond to the input in
    a nearly step-like fashion that is subsequently averaged out by strong diffusion.
    While motivated by early patterning events in the Drosophila embryo, our framework
    is generically applicable to spatially coupled stochastic gene expression models.
article_number: '062710'
author:
- first_name: Thomas R
  full_name: Sokolowski, Thomas R
  id: 3E999752-F248-11E8-B48F-1D18A9856A87
  last_name: Sokolowski
  orcid: 0000-0002-1287-3779
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
citation:
  ama: Sokolowski TR, Tkačik G. Optimizing information flow in small genetic networks.
    IV. Spatial coupling. <i>Physical Review E Statistical Nonlinear and Soft Matter
    Physics</i>. 2015;91(6). doi:<a href="https://doi.org/10.1103/PhysRevE.91.062710">10.1103/PhysRevE.91.062710</a>
  apa: Sokolowski, T. R., &#38; Tkačik, G. (2015). Optimizing information flow in
    small genetic networks. IV. Spatial coupling. <i>Physical Review E Statistical
    Nonlinear and Soft Matter Physics</i>. American Institute of Physics. <a href="https://doi.org/10.1103/PhysRevE.91.062710">https://doi.org/10.1103/PhysRevE.91.062710</a>
  chicago: Sokolowski, Thomas R, and Gašper Tkačik. “Optimizing Information Flow in
    Small Genetic Networks. IV. Spatial Coupling.” <i>Physical Review E Statistical
    Nonlinear and Soft Matter Physics</i>. American Institute of Physics, 2015. <a
    href="https://doi.org/10.1103/PhysRevE.91.062710">https://doi.org/10.1103/PhysRevE.91.062710</a>.
  ieee: T. R. Sokolowski and G. Tkačik, “Optimizing information flow in small genetic
    networks. IV. Spatial coupling,” <i>Physical Review E Statistical Nonlinear and
    Soft Matter Physics</i>, vol. 91, no. 6. American Institute of Physics, 2015.
  ista: Sokolowski TR, Tkačik G. 2015. Optimizing information flow in small genetic
    networks. IV. Spatial coupling. Physical Review E Statistical Nonlinear and Soft
    Matter Physics. 91(6), 062710.
  mla: Sokolowski, Thomas R., and Gašper Tkačik. “Optimizing Information Flow in Small
    Genetic Networks. IV. Spatial Coupling.” <i>Physical Review E Statistical Nonlinear
    and Soft Matter Physics</i>, vol. 91, no. 6, 062710, American Institute of Physics,
    2015, doi:<a href="https://doi.org/10.1103/PhysRevE.91.062710">10.1103/PhysRevE.91.062710</a>.
  short: T.R. Sokolowski, G. Tkačik, Physical Review E Statistical Nonlinear and Soft
    Matter Physics 91 (2015).
date_created: 2018-12-11T11:54:49Z
date_published: 2015-06-15T00:00:00Z
date_updated: 2021-01-12T06:54:13Z
day: '15'
department:
- _id: GaTk
doi: 10.1103/PhysRevE.91.062710
intvolume: '        91'
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1501.04015
month: '06'
oa: 1
oa_version: Preprint
publication: Physical Review E Statistical Nonlinear and Soft Matter Physics
publication_status: published
publisher: American Institute of Physics
publist_id: '5145'
quality_controlled: '1'
scopus_import: 1
status: public
title: Optimizing information flow in small genetic networks. IV. Spatial coupling
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 91
year: '2015'
...
---
_id: '1944'
acknowledgement: This work was supported by the European Research Council (project
  ERC-2011-StG-20101109-PSDP); the Agency for Innovation by Science and Technology
  (IWT) (predoctoral fellowship to H.R.); and the People Programme (Marie Curie Actions)
  of the European Union
author:
- first_name: Hana
  full_name: Rakusová, Hana
  last_name: Rakusová
- first_name: Matyas
  full_name: Fendrych, Matyas
  id: 43905548-F248-11E8-B48F-1D18A9856A87
  last_name: Fendrych
  orcid: 0000-0002-9767-8699
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Rakusová H, Fendrych M, Friml J. Intracellular trafficking and PIN-mediated
    cell polarity during tropic responses in plants. <i>Current Opinion in Plant Biology</i>.
    2015;23(2):116-123. doi:<a href="https://doi.org/10.1016/j.pbi.2014.12.002">10.1016/j.pbi.2014.12.002</a>
  apa: Rakusová, H., Fendrych, M., &#38; Friml, J. (2015). Intracellular trafficking
    and PIN-mediated cell polarity during tropic responses in plants. <i>Current Opinion
    in Plant Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.pbi.2014.12.002">https://doi.org/10.1016/j.pbi.2014.12.002</a>
  chicago: Rakusová, Hana, Matyas Fendrych, and Jiří Friml. “Intracellular Trafficking
    and PIN-Mediated Cell Polarity during Tropic Responses in Plants.” <i>Current
    Opinion in Plant Biology</i>. Elsevier, 2015. <a href="https://doi.org/10.1016/j.pbi.2014.12.002">https://doi.org/10.1016/j.pbi.2014.12.002</a>.
  ieee: H. Rakusová, M. Fendrych, and J. Friml, “Intracellular trafficking and PIN-mediated
    cell polarity during tropic responses in plants,” <i>Current Opinion in Plant
    Biology</i>, vol. 23, no. 2. Elsevier, pp. 116–123, 2015.
  ista: Rakusová H, Fendrych M, Friml J. 2015. Intracellular trafficking and PIN-mediated
    cell polarity during tropic responses in plants. Current Opinion in Plant Biology.
    23(2), 116–123.
  mla: Rakusová, Hana, et al. “Intracellular Trafficking and PIN-Mediated Cell Polarity
    during Tropic Responses in Plants.” <i>Current Opinion in Plant Biology</i>, vol.
    23, no. 2, Elsevier, 2015, pp. 116–23, doi:<a href="https://doi.org/10.1016/j.pbi.2014.12.002">10.1016/j.pbi.2014.12.002</a>.
  short: H. Rakusová, M. Fendrych, J. Friml, Current Opinion in Plant Biology 23 (2015)
    116–123.
date_created: 2018-12-11T11:54:51Z
date_published: 2015-02-01T00:00:00Z
date_updated: 2021-01-12T06:54:15Z
day: '01'
department:
- _id: JiFr
doi: 10.1016/j.pbi.2014.12.002
ec_funded: 1
intvolume: '        23'
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
page: 116 - 123
project:
- _id: 25716A02-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '282300'
  name: Polarity and subcellular dynamics in plants
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: Current Opinion in Plant Biology
publication_status: published
publisher: Elsevier
publist_id: '5140'
quality_controlled: '1'
scopus_import: 1
status: public
title: Intracellular trafficking and PIN-mediated cell polarity during tropic responses
  in plants
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 23
year: '2015'
...
