---
_id: '5563'
abstract:
- lang: eng
  text: "MATLAB code and processed datasets available for reproducing the results
    in: \r\nLukačišin, M.*, Landon, M.*, Jajoo, R*. (2016) Sequence-Specific Thermodynamic
    Properties of Nucleic Acids Influence Both Transcriptional Pausing and Backtracking
    in Yeast.\r\n*equal contributions"
article_processing_charge: No
author:
- first_name: Martin
  full_name: Lukacisin, Martin
  id: 298FFE8C-F248-11E8-B48F-1D18A9856A87
  last_name: Lukacisin
  orcid: 0000-0001-6549-4177
citation:
  ama: Lukacisin M. MATLAB analysis code for “Sequence-Specific Thermodynamic Properties
    of Nucleic Acids Influence Both Transcriptional Pausing and Backtracking in Yeast.”
    2017. doi:<a href="https://doi.org/10.15479/AT:ISTA:64">10.15479/AT:ISTA:64</a>
  apa: Lukacisin, M. (2017). MATLAB analysis code for “Sequence-Specific Thermodynamic
    Properties of Nucleic Acids Influence Both Transcriptional Pausing and Backtracking
    in Yeast.” Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:64">https://doi.org/10.15479/AT:ISTA:64</a>
  chicago: Lukacisin, Martin. “MATLAB Analysis Code for ‘Sequence-Specific Thermodynamic
    Properties of Nucleic Acids Influence Both Transcriptional Pausing and Backtracking
    in Yeast.’” Institute of Science and Technology Austria, 2017. <a href="https://doi.org/10.15479/AT:ISTA:64">https://doi.org/10.15479/AT:ISTA:64</a>.
  ieee: M. Lukacisin, “MATLAB analysis code for ‘Sequence-Specific Thermodynamic Properties
    of Nucleic Acids Influence Both Transcriptional Pausing and Backtracking in Yeast.’”
    Institute of Science and Technology Austria, 2017.
  ista: Lukacisin M. 2017. MATLAB analysis code for ‘Sequence-Specific Thermodynamic
    Properties of Nucleic Acids Influence Both Transcriptional Pausing and Backtracking
    in Yeast’, Institute of Science and Technology Austria, <a href="https://doi.org/10.15479/AT:ISTA:64">10.15479/AT:ISTA:64</a>.
  mla: Lukacisin, Martin. <i>MATLAB Analysis Code for “Sequence-Specific Thermodynamic
    Properties of Nucleic Acids Influence Both Transcriptional Pausing and Backtracking
    in Yeast.”</i> Institute of Science and Technology Austria, 2017, doi:<a href="https://doi.org/10.15479/AT:ISTA:64">10.15479/AT:ISTA:64</a>.
  short: M. Lukacisin, (2017).
datarep_id: '64'
date_created: 2018-12-12T12:31:33Z
date_published: 2017-03-20T00:00:00Z
date_updated: 2024-02-21T13:46:47Z
day: '20'
ddc:
- '571'
department:
- _id: ToBo
doi: 10.15479/AT:ISTA:64
file:
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  date_updated: 2020-07-14T12:47:03Z
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  file_name: IST-2016-45-v1+1_PaperCode.zip
  file_size: 296722548
  relation: main_file
file_date_updated: 2020-07-14T12:47:03Z
has_accepted_license: '1'
license: https://creativecommons.org/licenses/by-sa/4.0/
month: '03'
oa: 1
oa_version: Published Version
publisher: Institute of Science and Technology Austria
status: public
title: MATLAB analysis code for 'Sequence-Specific Thermodynamic Properties of Nucleic
  Acids Influence Both Transcriptional Pausing and Backtracking in Yeast'
tmp:
  image: /images/cc_by_sa.png
  legal_code_url: https://creativecommons.org/licenses/by-sa/4.0/legalcode
  name: Creative Commons Attribution-ShareAlike 4.0 International Public License (CC
    BY-SA 4.0)
  short: CC BY-SA (4.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2017'
...
---
_id: '5564'
abstract:
- lang: eng
  text: Compressed Fastq files with whole-genome sequencing data of IS-wt strain D
    and clones from four evolved populations (A11, C08, C10, D08). Information on
    this data collection is available in the Methods Section of the primary publication.
article_processing_charge: No
author:
- first_name: Magdalena
  full_name: Steinrück, Magdalena
  id: 2C023F40-F248-11E8-B48F-1D18A9856A87
  last_name: Steinrück
  orcid: 0000-0003-1229-9719
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
citation:
  ama: Steinrück M, Guet CC. Fastq files for “Complex chromosomal neighborhood effects
    determine the adaptive potential of a gene under selection.” 2017. doi:<a href="https://doi.org/10.15479/AT:ISTA:65">10.15479/AT:ISTA:65</a>
  apa: Steinrück, M., &#38; Guet, C. C. (2017). Fastq files for “Complex chromosomal
    neighborhood effects determine the adaptive potential of a gene under selection.”
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:65">https://doi.org/10.15479/AT:ISTA:65</a>
  chicago: Steinrück, Magdalena, and Calin C Guet. “Fastq Files for ‘Complex Chromosomal
    Neighborhood Effects Determine the Adaptive Potential of a Gene under Selection.’”
    Institute of Science and Technology Austria, 2017. <a href="https://doi.org/10.15479/AT:ISTA:65">https://doi.org/10.15479/AT:ISTA:65</a>.
  ieee: M. Steinrück and C. C. Guet, “Fastq files for ‘Complex chromosomal neighborhood
    effects determine the adaptive potential of a gene under selection.’” Institute
    of Science and Technology Austria, 2017.
  ista: Steinrück M, Guet CC. 2017. Fastq files for ‘Complex chromosomal neighborhood
    effects determine the adaptive potential of a gene under selection’, Institute
    of Science and Technology Austria, <a href="https://doi.org/10.15479/AT:ISTA:65">10.15479/AT:ISTA:65</a>.
  mla: Steinrück, Magdalena, and Calin C. Guet. <i>Fastq Files for “Complex Chromosomal
    Neighborhood Effects Determine the Adaptive Potential of a Gene under Selection.”</i>
    Institute of Science and Technology Austria, 2017, doi:<a href="https://doi.org/10.15479/AT:ISTA:65">10.15479/AT:ISTA:65</a>.
  short: M. Steinrück, C.C. Guet, (2017).
datarep_id: '65'
date_created: 2018-12-12T12:31:33Z
date_published: 2017-04-11T00:00:00Z
date_updated: 2025-09-10T11:06:52Z
day: '11'
ddc:
- '576'
department:
- _id: CaGu
doi: 10.15479/AT:ISTA:65
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  date_updated: 2020-07-14T12:47:03Z
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file_date_updated: 2020-07-14T12:47:03Z
has_accepted_license: '1'
license: https://creativecommons.org/publicdomain/zero/1.0/
month: '04'
oa: 1
oa_version: Published Version
publisher: Institute of Science and Technology Austria
related_material:
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  - id: '704'
    relation: research_paper
    status: public
status: public
title: Fastq files for "Complex chromosomal neighborhood effects determine the adaptive
  potential of a gene under selection"
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user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2017'
...
---
_id: '5567'
abstract:
- lang: eng
  text: Immunological synapse DC-Tcells
article_processing_charge: No
author:
- first_name: Alexander F
  full_name: Leithner, Alexander F
  id: 3B1B77E4-F248-11E8-B48F-1D18A9856A87
  last_name: Leithner
  orcid: 0000-0002-1073-744X
citation:
  ama: Leithner AF. Immunological synapse DC-Tcells. 2017. doi:<a href="https://doi.org/10.15479/AT:ISTA:71">10.15479/AT:ISTA:71</a>
  apa: Leithner, A. F. (2017). Immunological synapse DC-Tcells. Institute of Science
    and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:71">https://doi.org/10.15479/AT:ISTA:71</a>
  chicago: Leithner, Alexander F. “Immunological Synapse DC-Tcells.” Institute of
    Science and Technology Austria, 2017. <a href="https://doi.org/10.15479/AT:ISTA:71">https://doi.org/10.15479/AT:ISTA:71</a>.
  ieee: A. F. Leithner, “Immunological synapse DC-Tcells.” Institute of Science and
    Technology Austria, 2017.
  ista: Leithner AF. 2017. Immunological synapse DC-Tcells, Institute of Science and
    Technology Austria, <a href="https://doi.org/10.15479/AT:ISTA:71">10.15479/AT:ISTA:71</a>.
  mla: Leithner, Alexander F. <i>Immunological Synapse DC-Tcells</i>. Institute of
    Science and Technology Austria, 2017, doi:<a href="https://doi.org/10.15479/AT:ISTA:71">10.15479/AT:ISTA:71</a>.
  short: A.F. Leithner, (2017).
datarep_id: '71'
date_created: 2018-12-12T12:31:34Z
date_published: 2017-08-09T00:00:00Z
date_updated: 2024-02-21T13:47:00Z
day: '09'
ddc:
- '570'
department:
- _id: MiSi
doi: 10.15479/AT:ISTA:71
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  date_created: 2018-12-12T13:02:47Z
  date_updated: 2020-07-14T12:47:04Z
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  creator: system
  date_created: 2018-12-12T13:02:51Z
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  file_size: 226232496
  relation: main_file
file_date_updated: 2020-07-14T12:47:04Z
has_accepted_license: '1'
keyword:
- Immunological synapse
month: '08'
oa: 1
oa_version: Published Version
publisher: Institute of Science and Technology Austria
status: public
title: Immunological synapse DC-Tcells
tmp:
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type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2017'
...
---
_id: '5571'
abstract:
- lang: eng
  text: "This folder contains all the data used in each of the main figures of \"The
    genomic characterization of the t-haplotype, a mouse meiotic driver, highlights
    its complex history and specialized biology\" (Kelemen, R., Vicoso, B.), as well
    as in the supplementary figures. \r\n"
article_processing_charge: No
author:
- first_name: Beatriz
  full_name: Vicoso, Beatriz
  id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
  last_name: Vicoso
  orcid: 0000-0002-4579-8306
citation:
  ama: Vicoso B. Data for “The genomic characterization of the t-haplotype, a mouse
    meiotic driver, highlights its complex history and specialized biology.” 2017.
    doi:<a href="https://doi.org/10.15479/AT:ISTA:78">10.15479/AT:ISTA:78</a>
  apa: Vicoso, B. (2017). Data for “The genomic characterization of the t-haplotype,
    a mouse meiotic driver, highlights its complex history and specialized biology.”
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:78">https://doi.org/10.15479/AT:ISTA:78</a>
  chicago: Vicoso, Beatriz. “Data for ‘The Genomic Characterization of the t-Haplotype,
    a Mouse Meiotic Driver, Highlights Its Complex History and Specialized Biology.’”
    Institute of Science and Technology Austria, 2017. <a href="https://doi.org/10.15479/AT:ISTA:78">https://doi.org/10.15479/AT:ISTA:78</a>.
  ieee: B. Vicoso, “Data for ‘The genomic characterization of the t-haplotype, a mouse
    meiotic driver, highlights its complex history and specialized biology.’” Institute
    of Science and Technology Austria, 2017.
  ista: Vicoso B. 2017. Data for ‘The genomic characterization of the t-haplotype,
    a mouse meiotic driver, highlights its complex history and specialized biology’,
    Institute of Science and Technology Austria, <a href="https://doi.org/10.15479/AT:ISTA:78">10.15479/AT:ISTA:78</a>.
  mla: Vicoso, Beatriz. <i>Data for “The Genomic Characterization of the t-Haplotype,
    a Mouse Meiotic Driver, Highlights Its Complex History and Specialized Biology.”</i>
    Institute of Science and Technology Austria, 2017, doi:<a href="https://doi.org/10.15479/AT:ISTA:78">10.15479/AT:ISTA:78</a>.
  short: B. Vicoso, (2017).
contributor:
- contributor_type: contact_person
  first_name: Beatriz
  id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
  last_name: Vicoso
datarep_id: '78'
date_created: 2018-12-12T12:31:36Z
date_published: 2017-11-06T00:00:00Z
date_updated: 2025-04-15T07:49:49Z
day: '06'
ddc:
- '576'
department:
- _id: BeVi
doi: 10.15479/AT:ISTA:78
file:
- access_level: open_access
  checksum: 4520eb2b8379417ee916995719158f16
  content_type: application/zip
  creator: system
  date_created: 2018-12-12T13:03:00Z
  date_updated: 2020-07-14T12:47:04Z
  file_id: '5618'
  file_name: IST-2017-78-v1+1_Data.zip
  file_size: 143697895
  relation: main_file
file_date_updated: 2020-07-14T12:47:04Z
has_accepted_license: '1'
month: '11'
oa: 1
oa_version: Submitted Version
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '542'
    relation: research_paper
    status: public
status: public
title: Data for "The genomic characterization of the t-haplotype, a mouse meiotic
  driver, highlights its complex history and specialized biology"
tmp:
  image: /images/cc_0.png
  legal_code_url: https://creativecommons.org/publicdomain/zero/1.0/legalcode
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type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2017'
...
---
_id: '5572'
abstract:
- lang: eng
  text: Code described in the Supplementary Methods of "The genomic characterization
    of the t-haplotype, a mouse meiotic driver, highlights its complex history and
    specialized biology" (Kelemen, R., Vicoso, B.)
article_processing_charge: No
author:
- first_name: Beatriz
  full_name: Vicoso, Beatriz
  id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
  last_name: Vicoso
  orcid: 0000-0002-4579-8306
citation:
  ama: Vicoso B. Code for “The genomic characterization of the t-haplotype, a mouse
    meiotic driver, highlights its complex history and specialized biology.” 2017.
    doi:<a href="https://doi.org/10.15479/AT:ISTA:79 ">10.15479/AT:ISTA:79 </a>
  apa: Vicoso, B. (2017). Code for “The genomic characterization of the t-haplotype,
    a mouse meiotic driver, highlights its complex history and specialized biology.”
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:79
    ">https://doi.org/10.15479/AT:ISTA:79 </a>
  chicago: Vicoso, Beatriz. “Code for ‘The Genomic Characterization of the t-Haplotype,
    a Mouse Meiotic Driver, Highlights Its Complex History and Specialized Biology.’”
    Institute of Science and Technology Austria, 2017. <a href="https://doi.org/10.15479/AT:ISTA:79
    ">https://doi.org/10.15479/AT:ISTA:79 </a>.
  ieee: B. Vicoso, “Code for ‘The genomic characterization of the t-haplotype, a mouse
    meiotic driver, highlights its complex history and specialized biology.’” Institute
    of Science and Technology Austria, 2017.
  ista: Vicoso B. 2017. Code for ‘The genomic characterization of the t-haplotype,
    a mouse meiotic driver, highlights its complex history and specialized biology’,
    Institute of Science and Technology Austria, <a href="https://doi.org/10.15479/AT:ISTA:79
    ">10.15479/AT:ISTA:79 </a>.
  mla: Vicoso, Beatriz. <i>Code for “The Genomic Characterization of the t-Haplotype,
    a Mouse Meiotic Driver, Highlights Its Complex History and Specialized Biology.”</i>
    Institute of Science and Technology Austria, 2017, doi:<a href="https://doi.org/10.15479/AT:ISTA:79
    ">10.15479/AT:ISTA:79 </a>.
  short: B. Vicoso, (2017).
datarep_id: '79'
date_created: 2018-12-12T12:31:36Z
date_published: 2017-11-06T00:00:00Z
date_updated: 2025-04-15T07:49:49Z
day: '06'
ddc:
- '576'
department:
- _id: BeVi
doi: '10.15479/AT:ISTA:79 '
file:
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  checksum: 3e70a7bcd6ff0c38b79e4c8a7d137034
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  date_created: 2018-12-12T13:05:15Z
  date_updated: 2020-07-14T12:47:05Z
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  file_name: IST-2017-79-v1+1_Code.zip
  file_size: 49823
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file_date_updated: 2020-07-14T12:47:05Z
has_accepted_license: '1'
month: '11'
oa: 1
oa_version: Submitted Version
publisher: Institute of Science and Technology Austria
related_material:
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  - id: '542'
    relation: research_paper
    status: public
status: public
title: Code for "The genomic characterization of the t-haplotype, a mouse meiotic
  driver, highlights its complex history and specialized biology"
tmp:
  image: /images/cc_0.png
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type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2017'
...
---
_id: '558'
abstract:
- lang: eng
  text: Immune specificity is the degree to which a host’s immune system discriminates
    among various pathogens or antigenic variants. Vertebrate immune memory is highly
    specific due to antibody responses. On the other hand, some invertebrates show
    immune priming, i.e. improved survival after secondary exposure to a previously
    encountered pathogen. Until now, specificity of priming has only been demonstrated
    via the septic infection route or when live pathogens were used for priming. Therefore,
    we tested for specificity in the oral priming route in the red flour beetle, Tribolium
    castaneum. For priming, we used pathogen-free supernatants derived from three
    different strains of the entomopathogen, Bacillus thuringiensis, which express
    different Cry toxin variants known for their toxicity against this beetle. Subsequent
    exposure to the infective spores showed that oral priming was specific for two
    naturally occurring strains, while a third engineered strain did not induce any
    priming effect. Our data demonstrate that oral immune priming with a non-infectious
    bacterial agent can be specific, but the priming effect is not universal across
    all bacterial strains.
article_number: '0632'
article_processing_charge: No
article_type: original
author:
- first_name: Momir
  full_name: Futo, Momir
  last_name: Futo
- first_name: Marie
  full_name: Sell, Marie
  last_name: Sell
- first_name: Megan
  full_name: Kutzer, Megan
  id: 29D0B332-F248-11E8-B48F-1D18A9856A87
  last_name: Kutzer
  orcid: 0000-0002-8696-6978
- first_name: Joachim
  full_name: Kurtz, Joachim
  last_name: Kurtz
citation:
  ama: Futo M, Sell M, Kutzer M, Kurtz J. Specificity of oral immune priming in the
    red flour beetle Tribolium castaneum. <i>Biology Letters</i>. 2017;13(12). doi:<a
    href="https://doi.org/10.1098/rsbl.2017.0632">10.1098/rsbl.2017.0632</a>
  apa: Futo, M., Sell, M., Kutzer, M., &#38; Kurtz, J. (2017). Specificity of oral
    immune priming in the red flour beetle Tribolium castaneum. <i>Biology Letters</i>.
    The Royal Society. <a href="https://doi.org/10.1098/rsbl.2017.0632">https://doi.org/10.1098/rsbl.2017.0632</a>
  chicago: Futo, Momir, Marie Sell, Megan Kutzer, and Joachim Kurtz. “Specificity
    of Oral Immune Priming in the Red Flour Beetle Tribolium Castaneum.” <i>Biology
    Letters</i>. The Royal Society, 2017. <a href="https://doi.org/10.1098/rsbl.2017.0632">https://doi.org/10.1098/rsbl.2017.0632</a>.
  ieee: M. Futo, M. Sell, M. Kutzer, and J. Kurtz, “Specificity of oral immune priming
    in the red flour beetle Tribolium castaneum,” <i>Biology Letters</i>, vol. 13,
    no. 12. The Royal Society, 2017.
  ista: Futo M, Sell M, Kutzer M, Kurtz J. 2017. Specificity of oral immune priming
    in the red flour beetle Tribolium castaneum. Biology Letters. 13(12), 0632.
  mla: Futo, Momir, et al. “Specificity of Oral Immune Priming in the Red Flour Beetle
    Tribolium Castaneum.” <i>Biology Letters</i>, vol. 13, no. 12, 0632, The Royal
    Society, 2017, doi:<a href="https://doi.org/10.1098/rsbl.2017.0632">10.1098/rsbl.2017.0632</a>.
  short: M. Futo, M. Sell, M. Kutzer, J. Kurtz, Biology Letters 13 (2017).
date_created: 2018-12-11T11:47:10Z
date_published: 2017-12-01T00:00:00Z
date_updated: 2025-09-11T08:07:58Z
day: '01'
department:
- _id: SyCr
doi: 10.1098/rsbl.2017.0632
external_id:
  isi:
  - '000418695400010'
  pmid:
  - '29237813'
intvolume: '        13'
isi: 1
issue: '12'
language:
- iso: eng
month: '12'
oa_version: None
pmid: 1
publication: Biology Letters
publication_identifier:
  issn:
  - 1744-9561
publication_status: published
publisher: The Royal Society
publist_id: '7255'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Specificity of oral immune priming in the red flour beetle Tribolium castaneum
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 13
year: '2017'
...
---
_id: '560'
abstract:
- lang: eng
  text: In a recent article (Jentzen et al. 2016 Commun. Math. Sci. 14, 1477–1500
    (doi:10.4310/CMS.2016.v14. n6.a1)), it has been established that, for every arbitrarily
    slow convergence speed and every natural number d ? {4, 5, . . .}, there exist
    d-dimensional stochastic differential equations with infinitely often differentiable
    and globally bounded coefficients such that no approximation method based on finitely
    many observations of the driving Brownian motion can converge in absolute mean
    to the solution faster than the given speed of convergence. In this paper, we
    strengthen the above result by proving that this slow convergence phenomenon also
    arises in two (d = 2) and three (d = 3) space dimensions.
article_number: '0104'
article_processing_charge: No
arxiv: 1
author:
- first_name: Mate
  full_name: Gerencser, Mate
  id: 44ECEDF2-F248-11E8-B48F-1D18A9856A87
  last_name: Gerencser
- first_name: Arnulf
  full_name: Jentzen, Arnulf
  last_name: Jentzen
- first_name: Diyora
  full_name: Salimova, Diyora
  last_name: Salimova
citation:
  ama: 'Gerencser M, Jentzen A, Salimova D. On stochastic differential equations with
    arbitrarily slow convergence rates for strong approximation in two space dimensions.
    <i>Proceedings of the Royal Society A: Mathematical, Physical and Engineering
    Sciences</i>. 2017;473(2207). doi:<a href="https://doi.org/10.1098/rspa.2017.0104">10.1098/rspa.2017.0104</a>'
  apa: 'Gerencser, M., Jentzen, A., &#38; Salimova, D. (2017). On stochastic differential
    equations with arbitrarily slow convergence rates for strong approximation in
    two space dimensions. <i>Proceedings of the Royal Society A: Mathematical, Physical
    and Engineering Sciences</i>. Royal Society of London. <a href="https://doi.org/10.1098/rspa.2017.0104">https://doi.org/10.1098/rspa.2017.0104</a>'
  chicago: 'Gerencser, Mate, Arnulf Jentzen, and Diyora Salimova. “On Stochastic Differential
    Equations with Arbitrarily Slow Convergence Rates for Strong Approximation in
    Two Space Dimensions.” <i>Proceedings of the Royal Society A: Mathematical, Physical
    and Engineering Sciences</i>. Royal Society of London, 2017. <a href="https://doi.org/10.1098/rspa.2017.0104">https://doi.org/10.1098/rspa.2017.0104</a>.'
  ieee: 'M. Gerencser, A. Jentzen, and D. Salimova, “On stochastic differential equations
    with arbitrarily slow convergence rates for strong approximation in two space
    dimensions,” <i>Proceedings of the Royal Society A: Mathematical, Physical and
    Engineering Sciences</i>, vol. 473, no. 2207. Royal Society of London, 2017.'
  ista: 'Gerencser M, Jentzen A, Salimova D. 2017. On stochastic differential equations
    with arbitrarily slow convergence rates for strong approximation in two space
    dimensions. Proceedings of the Royal Society A: Mathematical, Physical and Engineering
    Sciences. 473(2207), 0104.'
  mla: 'Gerencser, Mate, et al. “On Stochastic Differential Equations with Arbitrarily
    Slow Convergence Rates for Strong Approximation in Two Space Dimensions.” <i>Proceedings
    of the Royal Society A: Mathematical, Physical and Engineering Sciences</i>, vol.
    473, no. 2207, 0104, Royal Society of London, 2017, doi:<a href="https://doi.org/10.1098/rspa.2017.0104">10.1098/rspa.2017.0104</a>.'
  short: 'M. Gerencser, A. Jentzen, D. Salimova, Proceedings of the Royal Society
    A: Mathematical, Physical and Engineering Sciences 473 (2017).'
date_created: 2018-12-11T11:47:11Z
date_published: 2017-11-01T00:00:00Z
date_updated: 2025-09-18T07:33:24Z
day: '01'
department:
- _id: JaMa
doi: 10.1098/rspa.2017.0104
ec_funded: 1
external_id:
  arxiv:
  - '1702.03229'
  isi:
  - '000416736700003'
intvolume: '       473'
isi: 1
issue: '2207'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1702.03229
month: '11'
oa: 1
oa_version: Submitted Version
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: 'Proceedings of the Royal Society A: Mathematical, Physical and Engineering
  Sciences'
publication_identifier:
  issn:
  - 1364-5021
publication_status: published
publisher: Royal Society of London
publist_id: '7256'
quality_controlled: '1'
scopus_import: '1'
status: public
title: On stochastic differential equations with arbitrarily slow convergence rates
  for strong approximation in two space dimensions
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 473
year: '2017'
...
---
_id: '561'
abstract:
- lang: eng
  text: Restriction–modification systems are widespread genetic elements that protect
    bacteria from bacteriophage infections by recognizing and cleaving heterologous
    DNA at short, well-defined sequences called restriction sites. Bioinformatic evidence
    shows that restriction sites are significantly underrepresented in bacteriophage
    genomes, presumably because bacteriophages with fewer restriction sites are more
    likely to escape cleavage by restriction–modification systems. However, how mutations
    in restriction sites affect the likelihood of bacteriophage escape is unknown.
    Using the bacteriophage l and the restriction–modification system EcoRI, we show
    that while mutation effects at different restriction sites are unequal, they are
    independent. As a result, the probability of bacteriophage escape increases with
    each mutated restriction site. Our results experimentally support the role of
    restriction site avoidance as a response to selection imposed by restriction–modification
    systems and offer an insight into the events underlying the process of bacteriophage
    escape.
acknowledgement: This work was funded by an HFSP Young Investigators' grant RGY0079/2011
  (C.C.G.). M.P. is a recipient of a DOC Fellowship of the Austrian Academy of Science
  at the Institute of Science and Technology Austria.
article_number: '20170646'
article_processing_charge: No
article_type: original
author:
- first_name: Maros
  full_name: Pleska, Maros
  id: 4569785E-F248-11E8-B48F-1D18A9856A87
  last_name: Pleska
  orcid: 0000-0001-7460-7479
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
citation:
  ama: Pleska M, Guet CC. Effects of mutations in phage restriction sites during escape
    from restriction–modification. <i>Biology Letters</i>. 2017;13(12). doi:<a href="https://doi.org/10.1098/rsbl.2017.0646">10.1098/rsbl.2017.0646</a>
  apa: Pleska, M., &#38; Guet, C. C. (2017). Effects of mutations in phage restriction
    sites during escape from restriction–modification. <i>Biology Letters</i>. The
    Royal Society. <a href="https://doi.org/10.1098/rsbl.2017.0646">https://doi.org/10.1098/rsbl.2017.0646</a>
  chicago: Pleska, Maros, and Calin C Guet. “Effects of Mutations in Phage Restriction
    Sites during Escape from Restriction–Modification.” <i>Biology Letters</i>. The
    Royal Society, 2017. <a href="https://doi.org/10.1098/rsbl.2017.0646">https://doi.org/10.1098/rsbl.2017.0646</a>.
  ieee: M. Pleska and C. C. Guet, “Effects of mutations in phage restriction sites
    during escape from restriction–modification,” <i>Biology Letters</i>, vol. 13,
    no. 12. The Royal Society, 2017.
  ista: Pleska M, Guet CC. 2017. Effects of mutations in phage restriction sites during
    escape from restriction–modification. Biology Letters. 13(12), 20170646.
  mla: Pleska, Maros, and Calin C. Guet. “Effects of Mutations in Phage Restriction
    Sites during Escape from Restriction–Modification.” <i>Biology Letters</i>, vol.
    13, no. 12, 20170646, The Royal Society, 2017, doi:<a href="https://doi.org/10.1098/rsbl.2017.0646">10.1098/rsbl.2017.0646</a>.
  short: M. Pleska, C.C. Guet, Biology Letters 13 (2017).
corr_author: '1'
date_created: 2018-12-11T11:47:11Z
date_published: 2017-12-01T00:00:00Z
date_updated: 2026-06-18T18:54:20Z
day: '01'
ddc:
- '570'
department:
- _id: CaGu
doi: 10.1098/rsbl.2017.0646
external_id:
  isi:
  - '000418695400012'
  pmid:
  - '29237814'
intvolume: '        13'
isi: 1
issue: '12'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1098/rsbl.2017.0646
month: '12'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 251BCBEC-B435-11E9-9278-68D0E5697425
  grant_number: RGY0079/2011
  name: Multi-Level Conflicts in Evolutionary Dynamics of Restriction-Modification
    Systems
- _id: 251D65D8-B435-11E9-9278-68D0E5697425
  grant_number: '24210'
  name: Effects of Stochasticity on the Function of Restriction-Modi cation Systems
    at the Single-Cell Level
publication: Biology Letters
publication_identifier:
  issn:
  - 1744-9561
publication_status: published
publisher: The Royal Society
publist_id: '7253'
quality_controlled: '1'
related_material:
  record:
  - id: '9847'
    relation: research_data
    status: public
  - id: '202'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Effects of mutations in phage restriction sites during escape from restriction–modification
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 13
year: '2017'
...
---
_id: '567'
abstract:
- lang: eng
  text: "This book is a concise and self-contained introduction of recent techniques
    to prove local spectral universality for large random matrices. Random matrix
    theory is a fast expanding research area, and this book mainly focuses on the
    methods that the authors participated in developing over the past few years. Many
    other interesting topics are not included, and neither are several new developments
    within the framework of these methods. The authors have chosen instead to present
    key concepts that they believe are the core of these methods and should be relevant
    for future applications. They keep technicalities to a minimum to make the book
    accessible to graduate students. With this in mind, they include in this book
    the basic notions and tools for high-dimensional analysis, such as large deviation,
    entropy, Dirichlet form, and the logarithmic Sobolev inequality.\r\n"
alternative_title:
- Courant Lecture Notes
article_processing_charge: No
author:
- first_name: László
  full_name: Erdös, László
  id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
  last_name: Erdös
  orcid: 0000-0001-5366-9603
- first_name: Horng
  full_name: Yau, Horng
  last_name: Yau
citation:
  ama: Erdös L, Yau H. <i>A Dynamical Approach to Random Matrix Theory</i>. Vol 28.
    American Mathematical Society; 2017. doi:<a href="https://doi.org/10.1090/cln/028">10.1090/cln/028</a>
  apa: Erdös, L., &#38; Yau, H. (2017). <i>A Dynamical Approach to Random Matrix Theory</i>
    (Vol. 28). American Mathematical Society. <a href="https://doi.org/10.1090/cln/028">https://doi.org/10.1090/cln/028</a>
  chicago: Erdös, László, and Horng Yau. <i>A Dynamical Approach to Random Matrix
    Theory</i>. Vol. 28. Courant Lecture Notes. American Mathematical Society, 2017.
    <a href="https://doi.org/10.1090/cln/028">https://doi.org/10.1090/cln/028</a>.
  ieee: L. Erdös and H. Yau, <i>A Dynamical Approach to Random Matrix Theory</i>,
    vol. 28. American Mathematical Society, 2017.
  ista: Erdös L, Yau H. 2017. A Dynamical Approach to Random Matrix Theory, American
    Mathematical Society, 226p.
  mla: Erdös, László, and Horng Yau. <i>A Dynamical Approach to Random Matrix Theory</i>.
    Vol. 28, American Mathematical Society, 2017, doi:<a href="https://doi.org/10.1090/cln/028">10.1090/cln/028</a>.
  short: L. Erdös, H. Yau, A Dynamical Approach to Random Matrix Theory, American
    Mathematical Society, 2017.
corr_author: '1'
date_created: 2018-12-11T11:47:13Z
date_published: 2017-01-01T00:00:00Z
date_updated: 2025-04-15T08:05:02Z
day: '01'
department:
- _id: LaEr
doi: 10.1090/cln/028
ec_funded: 1
intvolume: '        28'
language:
- iso: eng
month: '01'
oa_version: None
page: '226'
project:
- _id: 258DCDE6-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '338804'
  name: Random matrices, universality and disordered quantum systems
publication_identifier:
  eisbn:
  - 978-1-4704-4194-4
  isbn:
  - 9-781-4704-3648-3
publication_status: published
publisher: American Mathematical Society
publist_id: '7247'
quality_controlled: '1'
series_title: Courant Lecture Notes
status: public
title: A Dynamical Approach to Random Matrix Theory
type: book
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 28
year: '2017'
...
---
_id: '569'
abstract:
- lang: eng
  text: The actomyosin ring generates force to ingress the cytokinetic cleavage furrow
    in animal cells, yet its filament organization and the mechanism of contractility
    is not well understood. We quantified actin filament order in human cells using
    fluorescence polarization microscopy and found that cleavage furrow ingression
    initiates by contraction of an equatorial actin network with randomly oriented
    filaments. The network subsequently gradually reoriented actin filaments along
    the cell equator. This strictly depended on myosin II activity, suggesting local
    network reorganization by mechanical forces. Cortical laser microsurgery revealed
    that during cytokinesis progression, mechanical tension increased substantially
    along the direction of the cell equator, while the network contracted laterally
    along the pole-to-pole axis without a detectable increase in tension. Our data
    suggest that an asymmetric increase in cortical tension promotes filament reorientation
    along the cytokinetic cleavage furrow, which might have implications for diverse
    other biological processes involving actomyosin rings.
article_number: e30867
article_processing_charge: No
author:
- first_name: Felix
  full_name: Spira, Felix
  last_name: Spira
- first_name: Sara
  full_name: Cuylen Haering, Sara
  last_name: Cuylen Haering
- first_name: Shalin
  full_name: Mehta, Shalin
  last_name: Mehta
- first_name: Matthias
  full_name: Samwer, Matthias
  last_name: Samwer
- first_name: Anne
  full_name: Reversat, Anne
  id: 35B76592-F248-11E8-B48F-1D18A9856A87
  last_name: Reversat
  orcid: 0000-0003-0666-8928
- first_name: Amitabh
  full_name: Verma, Amitabh
  last_name: Verma
- first_name: Rudolf
  full_name: Oldenbourg, Rudolf
  last_name: Oldenbourg
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
- first_name: Daniel
  full_name: Gerlich, Daniel
  last_name: Gerlich
citation:
  ama: Spira F, Cuylen Haering S, Mehta S, et al. Cytokinesis in vertebrate cells
    initiates by contraction of an equatorial actomyosin network composed of randomly
    oriented filaments. <i>eLife</i>. 2017;6. doi:<a href="https://doi.org/10.7554/eLife.30867">10.7554/eLife.30867</a>
  apa: Spira, F., Cuylen Haering, S., Mehta, S., Samwer, M., Reversat, A., Verma,
    A., … Gerlich, D. (2017). Cytokinesis in vertebrate cells initiates by contraction
    of an equatorial actomyosin network composed of randomly oriented filaments. <i>ELife</i>.
    eLife Sciences Publications. <a href="https://doi.org/10.7554/eLife.30867">https://doi.org/10.7554/eLife.30867</a>
  chicago: Spira, Felix, Sara Cuylen Haering, Shalin Mehta, Matthias Samwer, Anne
    Reversat, Amitabh Verma, Rudolf Oldenbourg, Michael K Sixt, and Daniel Gerlich.
    “Cytokinesis in Vertebrate Cells Initiates by Contraction of an Equatorial Actomyosin
    Network Composed of Randomly Oriented Filaments.” <i>ELife</i>. eLife Sciences
    Publications, 2017. <a href="https://doi.org/10.7554/eLife.30867">https://doi.org/10.7554/eLife.30867</a>.
  ieee: F. Spira <i>et al.</i>, “Cytokinesis in vertebrate cells initiates by contraction
    of an equatorial actomyosin network composed of randomly oriented filaments,”
    <i>eLife</i>, vol. 6. eLife Sciences Publications, 2017.
  ista: Spira F, Cuylen Haering S, Mehta S, Samwer M, Reversat A, Verma A, Oldenbourg
    R, Sixt MK, Gerlich D. 2017. Cytokinesis in vertebrate cells initiates by contraction
    of an equatorial actomyosin network composed of randomly oriented filaments. eLife.
    6, e30867.
  mla: Spira, Felix, et al. “Cytokinesis in Vertebrate Cells Initiates by Contraction
    of an Equatorial Actomyosin Network Composed of Randomly Oriented Filaments.”
    <i>ELife</i>, vol. 6, e30867, eLife Sciences Publications, 2017, doi:<a href="https://doi.org/10.7554/eLife.30867">10.7554/eLife.30867</a>.
  short: F. Spira, S. Cuylen Haering, S. Mehta, M. Samwer, A. Reversat, A. Verma,
    R. Oldenbourg, M.K. Sixt, D. Gerlich, ELife 6 (2017).
date_created: 2018-12-11T11:47:14Z
date_published: 2017-11-06T00:00:00Z
date_updated: 2025-09-11T07:41:10Z
day: '06'
ddc:
- '570'
department:
- _id: MiSi
doi: 10.7554/eLife.30867
external_id:
  isi:
  - '000414407700001'
file:
- access_level: open_access
  checksum: ba09c1451153d39e4f4b7cee013e314c
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:10:40Z
  date_updated: 2020-07-14T12:47:10Z
  file_id: '4829'
  file_name: IST-2017-919-v1+1_elife-30867-figures-v1.pdf
  file_size: 9666973
  relation: main_file
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  checksum: 01eb51f1d6ad679947415a51c988e137
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:10:41Z
  date_updated: 2020-07-14T12:47:10Z
  file_id: '4830'
  file_name: IST-2017-919-v1+2_elife-30867-v1.pdf
  file_size: 5951246
  relation: main_file
file_date_updated: 2020-07-14T12:47:10Z
has_accepted_license: '1'
intvolume: '         6'
isi: 1
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
publication: eLife
publication_identifier:
  issn:
  - 2050-084X
publication_status: published
publisher: eLife Sciences Publications
publist_id: '7245'
pubrep_id: '919'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Cytokinesis in vertebrate cells initiates by contraction of an equatorial actomyosin
  network composed of randomly oriented filaments
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 6
year: '2017'
...
---
_id: '570'
abstract:
- lang: eng
  text: 'Most phenotypes are determined by molecular systems composed of specifically
    interacting molecules. However, unlike for individual components, little is known
    about the distributions of mutational effects of molecular systems as a whole.
    We ask how the distribution of mutational effects of a transcriptional regulatory
    system differs from the distributions of its components, by first independently,
    and then simultaneously, mutating a transcription factor and the associated promoter
    it represses. We find that the system distribution exhibits increased phenotypic
    variation compared to individual component distributions - an effect arising from
    intermolecular epistasis between the transcription factor and its DNA-binding
    site. In large part, this epistasis can be qualitatively attributed to the structure
    of the transcriptional regulatory system and could therefore be a common feature
    in prokaryotes. Counter-intuitively, intermolecular epistasis can alleviate the
    constraints of individual components, thereby increasing phenotypic variation
    that selection could act on and facilitating adaptive evolution. '
article_number: e28921
article_processing_charge: No
author:
- first_name: Mato
  full_name: Lagator, Mato
  id: 345D25EC-F248-11E8-B48F-1D18A9856A87
  last_name: Lagator
- first_name: Srdjan
  full_name: Sarikas, Srdjan
  id: 35F0286E-F248-11E8-B48F-1D18A9856A87
  last_name: Sarikas
- first_name: Hande
  full_name: Acar, Hande
  id: 2DDF136A-F248-11E8-B48F-1D18A9856A87
  last_name: Acar
  orcid: 0000-0003-1986-9753
- first_name: Jonathan P
  full_name: Bollback, Jonathan P
  id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
  last_name: Bollback
  orcid: 0000-0002-4624-4612
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
citation:
  ama: Lagator M, Sarikas S, Acar H, Bollback JP, Guet CC. Regulatory network structure
    determines patterns of intermolecular epistasis. <i>eLife</i>. 2017;6. doi:<a
    href="https://doi.org/10.7554/eLife.28921">10.7554/eLife.28921</a>
  apa: Lagator, M., Sarikas, S., Acar, H., Bollback, J. P., &#38; Guet, C. C. (2017).
    Regulatory network structure determines patterns of intermolecular epistasis.
    <i>ELife</i>. eLife Sciences Publications. <a href="https://doi.org/10.7554/eLife.28921">https://doi.org/10.7554/eLife.28921</a>
  chicago: Lagator, Mato, Srdjan Sarikas, Hande Acar, Jonathan P Bollback, and Calin
    C Guet. “Regulatory Network Structure Determines Patterns of Intermolecular Epistasis.”
    <i>ELife</i>. eLife Sciences Publications, 2017. <a href="https://doi.org/10.7554/eLife.28921">https://doi.org/10.7554/eLife.28921</a>.
  ieee: M. Lagator, S. Sarikas, H. Acar, J. P. Bollback, and C. C. Guet, “Regulatory
    network structure determines patterns of intermolecular epistasis,” <i>eLife</i>,
    vol. 6. eLife Sciences Publications, 2017.
  ista: Lagator M, Sarikas S, Acar H, Bollback JP, Guet CC. 2017. Regulatory network
    structure determines patterns of intermolecular epistasis. eLife. 6, e28921.
  mla: Lagator, Mato, et al. “Regulatory Network Structure Determines Patterns of
    Intermolecular Epistasis.” <i>ELife</i>, vol. 6, e28921, eLife Sciences Publications,
    2017, doi:<a href="https://doi.org/10.7554/eLife.28921">10.7554/eLife.28921</a>.
  short: M. Lagator, S. Sarikas, H. Acar, J.P. Bollback, C.C. Guet, ELife 6 (2017).
corr_author: '1'
date_created: 2018-12-11T11:47:14Z
date_published: 2017-11-13T00:00:00Z
date_updated: 2025-09-11T07:40:30Z
day: '13'
ddc:
- '576'
department:
- _id: CaGu
- _id: JoBo
- _id: NiBa
doi: 10.7554/eLife.28921
ec_funded: 1
external_id:
  isi:
  - '000425868200001'
file:
- access_level: open_access
  checksum: 273ab17f33305e4eaafd911ff88e7c5b
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:14:42Z
  date_updated: 2020-07-14T12:47:10Z
  file_id: '5096'
  file_name: IST-2017-918-v1+1_elife-28921-figures-v3.pdf
  file_size: 8453470
  relation: main_file
- access_level: open_access
  checksum: b433f90576c7be597cd43367946f8e7f
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:14:43Z
  date_updated: 2020-07-14T12:47:10Z
  file_id: '5097'
  file_name: IST-2017-918-v1+2_elife-28921-v3.pdf
  file_size: 1953221
  relation: main_file
file_date_updated: 2020-07-14T12:47:10Z
has_accepted_license: '1'
intvolume: '         6'
isi: 1
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
- _id: 2578D616-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '648440'
  name: Selective Barriers to Horizontal Gene Transfer
publication: eLife
publication_identifier:
  issn:
  - 2050-084X
publication_status: published
publisher: eLife Sciences Publications
publist_id: '7244'
pubrep_id: '918'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Regulatory network structure determines patterns of intermolecular epistasis
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 6
year: '2017'
...
---
_id: '571'
abstract:
- lang: eng
  text: Blood platelets are critical for hemostasis and thrombosis and play diverse
    roles during immune responses. Despite these versatile tasks in mammalian biology,
    their skills on a cellular level are deemed limited, mainly consisting in rolling,
    adhesion, and aggregate formation. Here, we identify an unappreciated asset of
    platelets and show that adherent platelets use adhesion receptors to mechanically
    probe the adhesive substrate in their local microenvironment. When actomyosin-dependent
    traction forces overcome substrate resistance, platelets migrate and pile up the
    adhesive substrate together with any bound particulate material. They use this
    ability to act as cellular scavengers, scanning the vascular surface for potential
    invaders and collecting deposited bacteria. Microbe collection by migrating platelets
    boosts the activity of professional phagocytes, exacerbating inflammatory tissue
    injury in sepsis. This assigns platelets a central role in innate immune responses
    and identifies them as potential targets to dampen inflammatory tissue damage
    in clinical scenarios of severe systemic infection. In addition to their role
    in thrombosis and hemostasis, platelets can also migrate to sites of infection
    to help trap bacteria and clear the vascular surface.
article_processing_charge: No
author:
- first_name: Florian R
  full_name: Gärtner, Florian R
  id: 397A88EE-F248-11E8-B48F-1D18A9856A87
  last_name: Gärtner
  orcid: 0000-0001-6120-3723
- first_name: Zerkah
  full_name: Ahmad, Zerkah
  last_name: Ahmad
- first_name: Gerhild
  full_name: Rosenberger, Gerhild
  last_name: Rosenberger
- first_name: Shuxia
  full_name: Fan, Shuxia
  last_name: Fan
- first_name: Leo
  full_name: Nicolai, Leo
  last_name: Nicolai
- first_name: Benjamin
  full_name: Busch, Benjamin
  last_name: Busch
- first_name: Gökce
  full_name: Yavuz, Gökce
  last_name: Yavuz
- first_name: Manja
  full_name: Luckner, Manja
  last_name: Luckner
- first_name: Hellen
  full_name: Ishikawa Ankerhold, Hellen
  last_name: Ishikawa Ankerhold
- first_name: Roman
  full_name: Hennel, Roman
  last_name: Hennel
- first_name: Alexandre
  full_name: Benechet, Alexandre
  last_name: Benechet
- first_name: Michael
  full_name: Lorenz, Michael
  last_name: Lorenz
- first_name: Sue
  full_name: Chandraratne, Sue
  last_name: Chandraratne
- first_name: Irene
  full_name: Schubert, Irene
  last_name: Schubert
- first_name: Sebastian
  full_name: Helmer, Sebastian
  last_name: Helmer
- first_name: Bianca
  full_name: Striednig, Bianca
  last_name: Striednig
- first_name: Konstantin
  full_name: Stark, Konstantin
  last_name: Stark
- first_name: Marek
  full_name: Janko, Marek
  last_name: Janko
- first_name: Ralph
  full_name: Böttcher, Ralph
  last_name: Böttcher
- first_name: Admar
  full_name: Verschoor, Admar
  last_name: Verschoor
- first_name: Catherine
  full_name: Leon, Catherine
  last_name: Leon
- first_name: Christian
  full_name: Gachet, Christian
  last_name: Gachet
- first_name: Thomas
  full_name: Gudermann, Thomas
  last_name: Gudermann
- first_name: Michael
  full_name: Mederos Y Schnitzler, Michael
  last_name: Mederos Y Schnitzler
- first_name: Zachary
  full_name: Pincus, Zachary
  last_name: Pincus
- first_name: Matteo
  full_name: Iannacone, Matteo
  last_name: Iannacone
- first_name: Rainer
  full_name: Haas, Rainer
  last_name: Haas
- first_name: Gerhard
  full_name: Wanner, Gerhard
  last_name: Wanner
- first_name: Kirsten
  full_name: Lauber, Kirsten
  last_name: Lauber
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
- first_name: Steffen
  full_name: Massberg, Steffen
  last_name: Massberg
citation:
  ama: Gärtner FR, Ahmad Z, Rosenberger G, et al. Migrating platelets are mechano
    scavengers that collect and bundle bacteria. <i>Cell Press</i>. 2017;171(6):1368-1382.
    doi:<a href="https://doi.org/10.1016/j.cell.2017.11.001">10.1016/j.cell.2017.11.001</a>
  apa: Gärtner, F. R., Ahmad, Z., Rosenberger, G., Fan, S., Nicolai, L., Busch, B.,
    … Massberg, S. (2017). Migrating platelets are mechano scavengers that collect
    and bundle bacteria. <i>Cell Press</i>. Cell Press. <a href="https://doi.org/10.1016/j.cell.2017.11.001">https://doi.org/10.1016/j.cell.2017.11.001</a>
  chicago: Gärtner, Florian R, Zerkah Ahmad, Gerhild Rosenberger, Shuxia Fan, Leo
    Nicolai, Benjamin Busch, Gökce Yavuz, et al. “Migrating Platelets Are Mechano
    Scavengers That Collect and Bundle Bacteria.” <i>Cell Press</i>. Cell Press, 2017.
    <a href="https://doi.org/10.1016/j.cell.2017.11.001">https://doi.org/10.1016/j.cell.2017.11.001</a>.
  ieee: F. R. Gärtner <i>et al.</i>, “Migrating platelets are mechano scavengers that
    collect and bundle bacteria,” <i>Cell Press</i>, vol. 171, no. 6. Cell Press,
    pp. 1368–1382, 2017.
  ista: Gärtner FR, Ahmad Z, Rosenberger G, Fan S, Nicolai L, Busch B, Yavuz G, Luckner
    M, Ishikawa Ankerhold H, Hennel R, Benechet A, Lorenz M, Chandraratne S, Schubert
    I, Helmer S, Striednig B, Stark K, Janko M, Böttcher R, Verschoor A, Leon C, Gachet
    C, Gudermann T, Mederos Y Schnitzler M, Pincus Z, Iannacone M, Haas R, Wanner
    G, Lauber K, Sixt MK, Massberg S. 2017. Migrating platelets are mechano scavengers
    that collect and bundle bacteria. Cell Press. 171(6), 1368–1382.
  mla: Gärtner, Florian R., et al. “Migrating Platelets Are Mechano Scavengers That
    Collect and Bundle Bacteria.” <i>Cell Press</i>, vol. 171, no. 6, Cell Press,
    2017, pp. 1368–82, doi:<a href="https://doi.org/10.1016/j.cell.2017.11.001">10.1016/j.cell.2017.11.001</a>.
  short: F.R. Gärtner, Z. Ahmad, G. Rosenberger, S. Fan, L. Nicolai, B. Busch, G.
    Yavuz, M. Luckner, H. Ishikawa Ankerhold, R. Hennel, A. Benechet, M. Lorenz, S.
    Chandraratne, I. Schubert, S. Helmer, B. Striednig, K. Stark, M. Janko, R. Böttcher,
    A. Verschoor, C. Leon, C. Gachet, T. Gudermann, M. Mederos Y Schnitzler, Z. Pincus,
    M. Iannacone, R. Haas, G. Wanner, K. Lauber, M.K. Sixt, S. Massberg, Cell Press
    171 (2017) 1368–1382.
date_created: 2018-12-11T11:47:15Z
date_published: 2017-11-30T00:00:00Z
date_updated: 2025-09-11T07:39:45Z
day: '30'
department:
- _id: MiSi
doi: 10.1016/j.cell.2017.11.001
ec_funded: 1
external_id:
  isi:
  - '000417362700018'
intvolume: '       171'
isi: 1
issue: '6'
language:
- iso: eng
month: '11'
oa_version: None
page: 1368 - 1382
project:
- _id: 260AA4E2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '747687'
  name: Mechanical Adaptation of Lamellipodial Actin Networks in Migrating Cells
publication: Cell Press
publication_identifier:
  issn:
  - 0092-8674
publication_status: published
publisher: Cell Press
publist_id: '7243'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Migrating platelets are mechano scavengers that collect and bundle bacteria
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 171
year: '2017'
...
---
_id: '572'
abstract:
- lang: eng
  text: In this review, we summarize the different biosynthesis-related pathways that
    contribute to the regulation of endogenous auxin in plants. We demonstrate that
    all known genes involved in auxin biosynthesis also have a role in root formation,
    from the initiation of a root meristem during embryogenesis to the generation
    of a functional root system with a primary root, secondary lateral root branches
    and adventitious roots. Furthermore, the versatile adaptation of root development
    in response to environmental challenges is mediated by both local and distant
    control of auxin biosynthesis. In conclusion, auxin homeostasis mediated by spatial
    and temporal regulation of auxin biosynthesis plays a central role in determining
    root architecture.
article_number: '2587'
article_processing_charge: No
author:
- first_name: Damilola
  full_name: Olatunji, Damilola
  last_name: Olatunji
- first_name: Danny
  full_name: Geelen, Danny
  last_name: Geelen
- first_name: Inge
  full_name: Verstraeten, Inge
  id: 362BF7FE-F248-11E8-B48F-1D18A9856A87
  last_name: Verstraeten
  orcid: 0000-0001-7241-2328
citation:
  ama: Olatunji D, Geelen D, Verstraeten I. Control of endogenous auxin levels in
    plant root development. <i>International Journal of Molecular Sciences</i>. 2017;18(12).
    doi:<a href="https://doi.org/10.3390/ijms18122587">10.3390/ijms18122587</a>
  apa: Olatunji, D., Geelen, D., &#38; Verstraeten, I. (2017). Control of endogenous
    auxin levels in plant root development. <i>International Journal of Molecular
    Sciences</i>. MDPI. <a href="https://doi.org/10.3390/ijms18122587">https://doi.org/10.3390/ijms18122587</a>
  chicago: Olatunji, Damilola, Danny Geelen, and Inge Verstraeten. “Control of Endogenous
    Auxin Levels in Plant Root Development.” <i>International Journal of Molecular
    Sciences</i>. MDPI, 2017. <a href="https://doi.org/10.3390/ijms18122587">https://doi.org/10.3390/ijms18122587</a>.
  ieee: D. Olatunji, D. Geelen, and I. Verstraeten, “Control of endogenous auxin levels
    in plant root development,” <i>International Journal of Molecular Sciences</i>,
    vol. 18, no. 12. MDPI, 2017.
  ista: Olatunji D, Geelen D, Verstraeten I. 2017. Control of endogenous auxin levels
    in plant root development. International Journal of Molecular Sciences. 18(12),
    2587.
  mla: Olatunji, Damilola, et al. “Control of Endogenous Auxin Levels in Plant Root
    Development.” <i>International Journal of Molecular Sciences</i>, vol. 18, no.
    12, 2587, MDPI, 2017, doi:<a href="https://doi.org/10.3390/ijms18122587">10.3390/ijms18122587</a>.
  short: D. Olatunji, D. Geelen, I. Verstraeten, International Journal of Molecular
    Sciences 18 (2017).
corr_author: '1'
date_created: 2018-12-11T11:47:15Z
date_published: 2017-12-01T00:00:00Z
date_updated: 2025-09-11T07:38:50Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.3390/ijms18122587
external_id:
  isi:
  - '000418896700091'
file:
- access_level: open_access
  checksum: 82d51f11e493f7eec02976d9a9a9805e
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:08:55Z
  date_updated: 2020-07-14T12:47:10Z
  file_id: '4718'
  file_name: IST-2017-917-v1+1_ijms-18-02587.pdf
  file_size: 920962
  relation: main_file
file_date_updated: 2020-07-14T12:47:10Z
has_accepted_license: '1'
intvolume: '        18'
isi: 1
issue: '12'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
publication: International Journal of Molecular Sciences
publication_status: published
publisher: MDPI
publist_id: '7242'
pubrep_id: '917'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Control of endogenous auxin levels in plant root development
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 18
year: '2017'
...
---
_id: '5803'
abstract:
- lang: eng
  text: Different distance metrics produce Voronoi diagrams with different properties.
    It is a well-known that on the (real) 2D plane or even on any 3D plane, a Voronoi
    diagram (VD) based on the Euclidean distance metric produces convex Voronoi regions.
    In this paper, we first show that this metric produces a persistent VD on the
    2D digital plane, as it comprises digitally convex Voronoi regions and hence correctly
    approximates the corresponding VD on the 2D real plane. Next, we show that on
    a 3D digital plane D, the Euclidean metric spanning over its voxel set does not
    guarantee a digital VD which is persistent with the real-space VD. As a solution,
    we introduce a novel concept of functional-plane-convexity, which is ensured by
    the Euclidean metric spanning over the pedal set of D. Necessary proofs and some
    visual result have been provided to adjudge the merit and usefulness of the proposed
    concept.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Ranita
  full_name: Biswas, Ranita
  id: 3C2B033E-F248-11E8-B48F-1D18A9856A87
  last_name: Biswas
  orcid: 0000-0002-5372-7890
- first_name: Partha
  full_name: Bhowmick, Partha
  last_name: Bhowmick
citation:
  ama: 'Biswas R, Bhowmick P. Construction of persistent Voronoi diagram on 3D digital
    plane. In: <i>Combinatorial Image Analysis</i>. Vol 10256. Cham: Springer Nature;
    2017:93-104. doi:<a href="https://doi.org/10.1007/978-3-319-59108-7_8">10.1007/978-3-319-59108-7_8</a>'
  apa: 'Biswas, R., &#38; Bhowmick, P. (2017). Construction of persistent Voronoi
    diagram on 3D digital plane. In <i>Combinatorial image analysis</i> (Vol. 10256,
    pp. 93–104). Cham: Springer Nature. <a href="https://doi.org/10.1007/978-3-319-59108-7_8">https://doi.org/10.1007/978-3-319-59108-7_8</a>'
  chicago: 'Biswas, Ranita, and Partha Bhowmick. “Construction of Persistent Voronoi
    Diagram on 3D Digital Plane.” In <i>Combinatorial Image Analysis</i>, 10256:93–104.
    Cham: Springer Nature, 2017. <a href="https://doi.org/10.1007/978-3-319-59108-7_8">https://doi.org/10.1007/978-3-319-59108-7_8</a>.'
  ieee: 'R. Biswas and P. Bhowmick, “Construction of persistent Voronoi diagram on
    3D digital plane,” in <i>Combinatorial image analysis</i>, vol. 10256, Cham: Springer
    Nature, 2017, pp. 93–104.'
  ista: 'Biswas R, Bhowmick P. 2017.Construction of persistent Voronoi diagram on
    3D digital plane. In: Combinatorial image analysis. LNCS, vol. 10256, 93–104.'
  mla: Biswas, Ranita, and Partha Bhowmick. “Construction of Persistent Voronoi Diagram
    on 3D Digital Plane.” <i>Combinatorial Image Analysis</i>, vol. 10256, Springer
    Nature, 2017, pp. 93–104, doi:<a href="https://doi.org/10.1007/978-3-319-59108-7_8">10.1007/978-3-319-59108-7_8</a>.
  short: R. Biswas, P. Bhowmick, in:, Combinatorial Image Analysis, Springer Nature,
    Cham, 2017, pp. 93–104.
conference:
  end_date: 2017-06-21
  location: Plovdiv, Bulgaria
  name: 'IWCIA: International Workshop on Combinatorial Image Analysis'
  start_date: 2017-06-19
date_created: 2019-01-08T20:42:56Z
date_published: 2017-05-17T00:00:00Z
date_updated: 2022-01-28T07:48:24Z
day: '17'
department:
- _id: HeEd
doi: 10.1007/978-3-319-59108-7_8
extern: '1'
intvolume: '     10256'
language:
- iso: eng
month: '05'
oa_version: None
page: 93-104
place: Cham
publication: Combinatorial image analysis
publication_identifier:
  isbn:
  - 978-3-319-59107-0
  - 978-3-319-59108-7
  issn:
  - 0302-9743
  - 1611-3349
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Construction of persistent Voronoi diagram on 3D digital plane
type: book_chapter
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 10256
year: '2017'
...
---
_id: '6013'
abstract:
- lang: eng
  text: The first hundred attoseconds of the electron dynamics during strong field
    tunneling ionization are investigated. We quantify theoretically how the electron’s
    classical trajectories in the continuum emerge from the tunneling process and
    test the results with those achieved in parallel from attoclock measurements.
    An especially high sensitivity on the tunneling barrier is accomplished here by
    comparing the momentum distributions of two atomic species of slightly deviating
    atomic potentials (argon and krypton) being ionized under absolutely identical
    conditions with near-infrared laser pulses (1300 nm). The agreement between experiment
    and theory provides clear evidence for a nonzero tunneling time delay and a nonvanishing
    longitudinal momentum of the electron at the “tunnel exit.”
article_number: '023201'
article_processing_charge: No
arxiv: 1
author:
- first_name: Nicolas
  full_name: Camus, Nicolas
  last_name: Camus
- first_name: Enderalp
  full_name: Yakaboylu, Enderalp
  id: 38CB71F6-F248-11E8-B48F-1D18A9856A87
  last_name: Yakaboylu
  orcid: 0000-0001-5973-0874
- first_name: Lutz
  full_name: Fechner, Lutz
  last_name: Fechner
- first_name: Michael
  full_name: Klaiber, Michael
  last_name: Klaiber
- first_name: Martin
  full_name: Laux, Martin
  last_name: Laux
- first_name: Yonghao
  full_name: Mi, Yonghao
  last_name: Mi
- first_name: Karen Z.
  full_name: Hatsagortsyan, Karen Z.
  last_name: Hatsagortsyan
- first_name: Thomas
  full_name: Pfeifer, Thomas
  last_name: Pfeifer
- first_name: Christoph H.
  full_name: Keitel, Christoph H.
  last_name: Keitel
- first_name: Robert
  full_name: Moshammer, Robert
  last_name: Moshammer
citation:
  ama: Camus N, Yakaboylu E, Fechner L, et al. Experimental evidence for quantum tunneling
    time. <i>Physical Review Letters</i>. 2017;119(2). doi:<a href="https://doi.org/10.1103/PhysRevLett.119.023201">10.1103/PhysRevLett.119.023201</a>
  apa: Camus, N., Yakaboylu, E., Fechner, L., Klaiber, M., Laux, M., Mi, Y., … Moshammer,
    R. (2017). Experimental evidence for quantum tunneling time. <i>Physical Review
    Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevLett.119.023201">https://doi.org/10.1103/PhysRevLett.119.023201</a>
  chicago: Camus, Nicolas, Enderalp Yakaboylu, Lutz Fechner, Michael Klaiber, Martin
    Laux, Yonghao Mi, Karen Z. Hatsagortsyan, Thomas Pfeifer, Christoph H. Keitel,
    and Robert Moshammer. “Experimental Evidence for Quantum Tunneling Time.” <i>Physical
    Review Letters</i>. American Physical Society, 2017. <a href="https://doi.org/10.1103/PhysRevLett.119.023201">https://doi.org/10.1103/PhysRevLett.119.023201</a>.
  ieee: N. Camus <i>et al.</i>, “Experimental evidence for quantum tunneling time,”
    <i>Physical Review Letters</i>, vol. 119, no. 2. American Physical Society, 2017.
  ista: Camus N, Yakaboylu E, Fechner L, Klaiber M, Laux M, Mi Y, Hatsagortsyan KZ,
    Pfeifer T, Keitel CH, Moshammer R. 2017. Experimental evidence for quantum tunneling
    time. Physical Review Letters. 119(2), 023201.
  mla: Camus, Nicolas, et al. “Experimental Evidence for Quantum Tunneling Time.”
    <i>Physical Review Letters</i>, vol. 119, no. 2, 023201, American Physical Society,
    2017, doi:<a href="https://doi.org/10.1103/PhysRevLett.119.023201">10.1103/PhysRevLett.119.023201</a>.
  short: N. Camus, E. Yakaboylu, L. Fechner, M. Klaiber, M. Laux, Y. Mi, K.Z. Hatsagortsyan,
    T. Pfeifer, C.H. Keitel, R. Moshammer, Physical Review Letters 119 (2017).
date_created: 2019-02-14T15:24:13Z
date_published: 2017-07-14T00:00:00Z
date_updated: 2025-09-18T10:29:08Z
day: '14'
department:
- _id: MiLe
doi: 10.1103/PhysRevLett.119.023201
external_id:
  arxiv:
  - '1611.03701'
  isi:
  - '000405514700003'
intvolume: '       119'
isi: 1
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1611.03701
month: '07'
oa: 1
oa_version: Preprint
publication: Physical Review Letters
publication_identifier:
  eissn:
  - 1079-7114
  issn:
  - 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
related_material:
  record:
  - id: '313'
    relation: earlier_version
    status: public
scopus_import: '1'
status: public
title: Experimental evidence for quantum tunneling time
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 119
year: '2017'
...
---
_id: '605'
abstract:
- lang: eng
  text: 'Position based cryptography (PBC), proposed in the seminal work of Chandran,
    Goyal, Moriarty, and Ostrovsky (SIAM J. Computing, 2014), aims at constructing
    cryptographic schemes in which the identity of the user is his geographic position.
    Chandran et al. construct PBC schemes for secure positioning and position-based
    key agreement in the bounded-storage model (Maurer, J. Cryptology, 1992). Apart
    from bounded memory, their security proofs need a strong additional restriction
    on the power of the adversary: he cannot compute joint functions of his inputs.
    Removing this assumption is left as an open problem. We show that an answer to
    this question would resolve a long standing open problem in multiparty communication
    complexity: finding a function that is hard to compute with low communication
    complexity in the simultaneous message model, but easy to compute in the fully
    adaptive model. On a more positive side: we also show some implications in the
    other direction, i.e.: we prove that lower bounds on the communication complexity
    of certain multiparty problems imply existence of PBC primitives. Using this result
    we then show two attractive ways to “bypass” our hardness result: the first uses
    the random oracle model, the second weakens the locality requirement in the bounded-storage
    model to online computability. The random oracle construction is arguably one
    of the simplest proposed so far in this area. Our results indicate that constructing
    improved provably secure protocols for PBC requires a better understanding of
    multiparty communication complexity. This is yet another example where negative
    results in one area (in our case: lower bounds in multiparty communication complexity)
    can be used to construct secure cryptographic schemes.'
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Joshua
  full_name: Brody, Joshua
  last_name: Brody
- first_name: Stefan
  full_name: Dziembowski, Stefan
  last_name: Dziembowski
- first_name: Sebastian
  full_name: Faust, Sebastian
  last_name: Faust
- first_name: Krzysztof Z
  full_name: Pietrzak, Krzysztof Z
  id: 3E04A7AA-F248-11E8-B48F-1D18A9856A87
  last_name: Pietrzak
  orcid: 0000-0002-9139-1654
citation:
  ama: 'Brody J, Dziembowski S, Faust S, Pietrzak KZ. Position based cryptography
    and multiparty communication complexity. In: Kalai Y, Reyzin L, eds. Vol 10677.
    Springer; 2017:56-81. doi:<a href="https://doi.org/10.1007/978-3-319-70500-2_3">10.1007/978-3-319-70500-2_3</a>'
  apa: 'Brody, J., Dziembowski, S., Faust, S., &#38; Pietrzak, K. Z. (2017). Position
    based cryptography and multiparty communication complexity. In Y. Kalai &#38;
    L. Reyzin (Eds.) (Vol. 10677, pp. 56–81). Presented at the TCC: Theory of Cryptography
    Conference, Baltimore, MD, United States: Springer. <a href="https://doi.org/10.1007/978-3-319-70500-2_3">https://doi.org/10.1007/978-3-319-70500-2_3</a>'
  chicago: Brody, Joshua, Stefan Dziembowski, Sebastian Faust, and Krzysztof Z Pietrzak.
    “Position Based Cryptography and Multiparty Communication Complexity.” edited
    by Yael Kalai and Leonid Reyzin, 10677:56–81. Springer, 2017. <a href="https://doi.org/10.1007/978-3-319-70500-2_3">https://doi.org/10.1007/978-3-319-70500-2_3</a>.
  ieee: 'J. Brody, S. Dziembowski, S. Faust, and K. Z. Pietrzak, “Position based cryptography
    and multiparty communication complexity,” presented at the TCC: Theory of Cryptography
    Conference, Baltimore, MD, United States, 2017, vol. 10677, pp. 56–81.'
  ista: 'Brody J, Dziembowski S, Faust S, Pietrzak KZ. 2017. Position based cryptography
    and multiparty communication complexity. TCC: Theory of Cryptography Conference,
    LNCS, vol. 10677, 56–81.'
  mla: Brody, Joshua, et al. <i>Position Based Cryptography and Multiparty Communication
    Complexity</i>. Edited by Yael Kalai and Leonid Reyzin, vol. 10677, Springer,
    2017, pp. 56–81, doi:<a href="https://doi.org/10.1007/978-3-319-70500-2_3">10.1007/978-3-319-70500-2_3</a>.
  short: J. Brody, S. Dziembowski, S. Faust, K.Z. Pietrzak, in:, Y. Kalai, L. Reyzin
    (Eds.), Springer, 2017, pp. 56–81.
conference:
  end_date: 2017-11-15
  location: Baltimore, MD, United States
  name: 'TCC: Theory of Cryptography Conference'
  start_date: 2017-11-12
date_created: 2018-12-11T11:47:27Z
date_published: 2017-11-05T00:00:00Z
date_updated: 2025-09-11T07:36:46Z
day: '05'
department:
- _id: KrPi
doi: 10.1007/978-3-319-70500-2_3
ec_funded: 1
editor:
- first_name: Yael
  full_name: Kalai, Yael
  last_name: Kalai
- first_name: Leonid
  full_name: Reyzin, Leonid
  last_name: Reyzin
external_id:
  isi:
  - '000739735000003'
intvolume: '     10677'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://eprint.iacr.org/2016/536
month: '11'
oa: 1
oa_version: Submitted Version
page: 56 - 81
project:
- _id: 258AA5B2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '682815'
  name: Teaching Old Crypto New Tricks
publication_identifier:
  isbn:
  - 978-331970499-9
publication_status: published
publisher: Springer
publist_id: '7200'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Position based cryptography and multiparty communication complexity
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 10677
year: '2017'
...
---
_id: '609'
abstract:
- lang: eng
  text: Several cryptographic schemes and applications are based on functions that
    are both reasonably efficient to compute and moderately hard to invert, including
    client puzzles for Denial-of-Service protection, password protection via salted
    hashes, or recent proof-of-work blockchain systems. Despite their wide use, a
    definition of this concept has not yet been distilled and formalized explicitly.
    Instead, either the applications are proven directly based on the assumptions
    underlying the function, or some property of the function is proven, but the security
    of the application is argued only informally. The goal of this work is to provide
    a (universal) definition that decouples the efforts of designing new moderately
    hard functions and of building protocols based on them, serving as an interface
    between the two. On a technical level, beyond the mentioned definitions, we instantiate
    the model for four different notions of hardness. We extend the work of Alwen
    and Serbinenko (STOC 2015) by providing a general tool for proving security for
    the first notion of memory-hard functions that allows for provably secure applications.
    The tool allows us to recover all of the graph-theoretic techniques developed
    for proving security under the older, non-composable, notion of security used
    by Alwen and Serbinenko. As an application of our definition of moderately hard
    functions, we prove the security of two different schemes for proofs of effort
    (PoE). We also formalize and instantiate the concept of a non-interactive proof
    of effort (niPoE), in which the proof is not bound to a particular communication
    context but rather any bit-string chosen by the prover.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Joel F
  full_name: Alwen, Joel F
  id: 2A8DFA8C-F248-11E8-B48F-1D18A9856A87
  last_name: Alwen
- first_name: Björn
  full_name: Tackmann, Björn
  last_name: Tackmann
citation:
  ama: 'Alwen JF, Tackmann B. Moderately hard functions: Definition, instantiations,
    and applications. In: Kalai Y, Reyzin L, eds. Vol 10677. Springer; 2017:493-526.
    doi:<a href="https://doi.org/10.1007/978-3-319-70500-2_17">10.1007/978-3-319-70500-2_17</a>'
  apa: 'Alwen, J. F., &#38; Tackmann, B. (2017). Moderately hard functions: Definition,
    instantiations, and applications. In Y. Kalai &#38; L. Reyzin (Eds.) (Vol. 10677,
    pp. 493–526). Presented at the TCC: Theory of Cryptography, Baltimore, MD, United
    States: Springer. <a href="https://doi.org/10.1007/978-3-319-70500-2_17">https://doi.org/10.1007/978-3-319-70500-2_17</a>'
  chicago: 'Alwen, Joel F, and Björn Tackmann. “Moderately Hard Functions: Definition,
    Instantiations, and Applications.” edited by Yael Kalai and Leonid Reyzin, 10677:493–526.
    Springer, 2017. <a href="https://doi.org/10.1007/978-3-319-70500-2_17">https://doi.org/10.1007/978-3-319-70500-2_17</a>.'
  ieee: 'J. F. Alwen and B. Tackmann, “Moderately hard functions: Definition, instantiations,
    and applications,” presented at the TCC: Theory of Cryptography, Baltimore, MD,
    United States, 2017, vol. 10677, pp. 493–526.'
  ista: 'Alwen JF, Tackmann B. 2017. Moderately hard functions: Definition, instantiations,
    and applications. TCC: Theory of Cryptography, LNCS, vol. 10677, 493–526.'
  mla: 'Alwen, Joel F., and Björn Tackmann. <i>Moderately Hard Functions: Definition,
    Instantiations, and Applications</i>. Edited by Yael Kalai and Leonid Reyzin,
    vol. 10677, Springer, 2017, pp. 493–526, doi:<a href="https://doi.org/10.1007/978-3-319-70500-2_17">10.1007/978-3-319-70500-2_17</a>.'
  short: J.F. Alwen, B. Tackmann, in:, Y. Kalai, L. Reyzin (Eds.), Springer, 2017,
    pp. 493–526.
conference:
  end_date: 2017-11-15
  location: Baltimore, MD, United States
  name: 'TCC: Theory of Cryptography'
  start_date: 2017-11-12
date_created: 2018-12-11T11:47:28Z
date_published: 2017-11-05T00:00:00Z
date_updated: 2025-09-11T07:36:16Z
day: '05'
department:
- _id: KrPi
doi: 10.1007/978-3-319-70500-2_17
editor:
- first_name: Yael
  full_name: Kalai, Yael
  last_name: Kalai
- first_name: Leonid
  full_name: Reyzin, Leonid
  last_name: Reyzin
external_id:
  isi:
  - '000739735000017'
intvolume: '     10677'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://eprint.iacr.org/2017/945
month: '11'
oa: 1
oa_version: Submitted Version
page: 493 - 526
publication_identifier:
  isbn:
  - 978-331970499-9
publication_status: published
publisher: Springer
publist_id: '7196'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Moderately hard functions: Definition, instantiations, and applications'
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 10677
year: '2017'
...
---
_id: '610'
abstract:
- lang: eng
  text: 'The fact that the complete graph K5 does not embed in the plane has been
    generalized in two independent directions. On the one hand, the solution of the
    classical Heawood problem for graphs on surfaces established that the complete
    graph Kn embeds in a closed surface M (other than the Klein bottle) if and only
    if (n−3)(n−4) ≤ 6b1(M), where b1(M) is the first Z2-Betti number of M. On the
    other hand, van Kampen and Flores proved that the k-skeleton of the n-dimensional
    simplex (the higher-dimensional analogue of Kn+1) embeds in R2k if and only if
    n ≤ 2k + 1. Two decades ago, Kühnel conjectured that the k-skeleton of the n-simplex
    embeds in a compact, (k − 1)-connected 2k-manifold with kth Z2-Betti number bk
    only if the following generalized Heawood inequality holds: (k+1 n−k−1) ≤ (k+1
    2k+1)bk. This is a common generalization of the case of graphs on surfaces as
    well as the van Kampen–Flores theorem. In the spirit of Kühnel’s conjecture, we
    prove that if the k-skeleton of the n-simplex embeds in a compact 2k-manifold
    with kth Z2-Betti number bk, then n ≤ 2bk(k 2k+2)+2k+4. This bound is weaker than
    the generalized Heawood inequality, but does not require the assumption that M
    is (k−1)-connected. Our results generalize to maps without q-covered points, in
    the spirit of Tverberg’s theorem, for q a prime power. Our proof uses a result
    of Volovikov about maps that satisfy a certain homological triviality condition.'
acknowledgement: The work by Z. P. was partially supported by the Israel Science Foundation
  grant ISF-768/12. The work by Z. P. and M. T. was partially supported by the project
  CE-ITI (GACR P202/12/G061) of the Czech Science Foundation and by the ERC Advanced
  Grant No. 267165. Part of the research work of M.T. was conducted at IST Austria,
  supported by an IST Fellowship. The research of P. P. was supported by the ERC Advanced
  grant no. 320924. The work by I. M. and U. W. was supported by the Swiss National
  Science Foundation (grants SNSF-200020-138230 and SNSF-PP00P2-138948). The collaboration
  between U. W. and X. G. was partially supported by the LabEx Bézout (ANR-10-LABX-58).
article_processing_charge: No
arxiv: 1
author:
- first_name: Xavier
  full_name: Goaoc, Xavier
  last_name: Goaoc
- first_name: Isaac
  full_name: Mabillard, Isaac
  id: 32BF9DAA-F248-11E8-B48F-1D18A9856A87
  last_name: Mabillard
- first_name: Pavel
  full_name: Paták, Pavel
  last_name: Paták
- first_name: Zuzana
  full_name: Patakova, Zuzana
  id: 48B57058-F248-11E8-B48F-1D18A9856A87
  last_name: Patakova
  orcid: 0000-0002-3975-1683
- first_name: Martin
  full_name: Tancer, Martin
  id: 38AC689C-F248-11E8-B48F-1D18A9856A87
  last_name: Tancer
  orcid: 0000-0002-1191-6714
- first_name: Uli
  full_name: Wagner, Uli
  id: 36690CA2-F248-11E8-B48F-1D18A9856A87
  last_name: Wagner
  orcid: 0000-0002-1494-0568
citation:
  ama: 'Goaoc X, Mabillard I, Paták P, Patakova Z, Tancer M, Wagner U. On generalized
    Heawood inequalities for manifolds: A van Kampen–Flores type nonembeddability
    result. <i>Israel Journal of Mathematics</i>. 2017;222(2):841-866. doi:<a href="https://doi.org/10.1007/s11856-017-1607-7">10.1007/s11856-017-1607-7</a>'
  apa: 'Goaoc, X., Mabillard, I., Paták, P., Patakova, Z., Tancer, M., &#38; Wagner,
    U. (2017). On generalized Heawood inequalities for manifolds: A van Kampen–Flores
    type nonembeddability result. <i>Israel Journal of Mathematics</i>. Springer.
    <a href="https://doi.org/10.1007/s11856-017-1607-7">https://doi.org/10.1007/s11856-017-1607-7</a>'
  chicago: 'Goaoc, Xavier, Isaac Mabillard, Pavel Paták, Zuzana Patakova, Martin Tancer,
    and Uli Wagner. “On Generalized Heawood Inequalities for Manifolds: A van Kampen–Flores
    Type Nonembeddability Result.” <i>Israel Journal of Mathematics</i>. Springer,
    2017. <a href="https://doi.org/10.1007/s11856-017-1607-7">https://doi.org/10.1007/s11856-017-1607-7</a>.'
  ieee: 'X. Goaoc, I. Mabillard, P. Paták, Z. Patakova, M. Tancer, and U. Wagner,
    “On generalized Heawood inequalities for manifolds: A van Kampen–Flores type nonembeddability
    result,” <i>Israel Journal of Mathematics</i>, vol. 222, no. 2. Springer, pp.
    841–866, 2017.'
  ista: 'Goaoc X, Mabillard I, Paták P, Patakova Z, Tancer M, Wagner U. 2017. On generalized
    Heawood inequalities for manifolds: A van Kampen–Flores type nonembeddability
    result. Israel Journal of Mathematics. 222(2), 841–866.'
  mla: 'Goaoc, Xavier, et al. “On Generalized Heawood Inequalities for Manifolds:
    A van Kampen–Flores Type Nonembeddability Result.” <i>Israel Journal of Mathematics</i>,
    vol. 222, no. 2, Springer, 2017, pp. 841–66, doi:<a href="https://doi.org/10.1007/s11856-017-1607-7">10.1007/s11856-017-1607-7</a>.'
  short: X. Goaoc, I. Mabillard, P. Paták, Z. Patakova, M. Tancer, U. Wagner, Israel
    Journal of Mathematics 222 (2017) 841–866.
date_created: 2018-12-11T11:47:29Z
date_published: 2017-10-01T00:00:00Z
date_updated: 2025-09-11T07:35:36Z
day: '01'
department:
- _id: UlWa
doi: 10.1007/s11856-017-1607-7
ec_funded: 1
external_id:
  arxiv:
  - '1610.09063'
  isi:
  - '000415195500009'
intvolume: '       222'
isi: 1
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1610.09063
month: '10'
oa: 1
oa_version: Preprint
page: 841 - 866
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: Israel Journal of Mathematics
publication_status: published
publisher: Springer
publist_id: '7194'
quality_controlled: '1'
related_material:
  record:
  - id: '1511'
    relation: earlier_version
    status: public
scopus_import: '1'
status: public
title: 'On generalized Heawood inequalities for manifolds: A van Kampen–Flores type
  nonembeddability result'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 222
year: '2017'
...
---
_id: '611'
abstract:
- lang: eng
  text: Small RNAs (sRNAs) regulate genes in plants and animals. Here, we show that
    population-wide differences in color patterns in snapdragon flowers are caused
    by an inverted duplication that generates sRNAs. The complexity and size of the
    transcripts indicate that the duplication represents an intermediate on the pathway
    to microRNA evolution. The sRNAs repress a pigment biosynthesis gene, creating
    a yellow highlight at the site of pollinator entry. The inverted duplication exhibits
    steep clines in allele frequency in a natural hybrid zone, showing that the allele
    is under selection. Thus, regulatory interactions of evolutionarily recent sRNAs
    can be acted upon by selection and contribute to the evolution of phenotypic diversity.
article_processing_charge: No
author:
- first_name: Desmond
  full_name: Bradley, Desmond
  last_name: Bradley
- first_name: Ping
  full_name: Xu, Ping
  last_name: Xu
- first_name: Irina
  full_name: Mohorianu, Irina
  last_name: Mohorianu
- first_name: Annabel
  full_name: Whibley, Annabel
  last_name: Whibley
- first_name: David
  full_name: Field, David
  id: 419049E2-F248-11E8-B48F-1D18A9856A87
  last_name: Field
  orcid: 0000-0002-4014-8478
- first_name: Hugo
  full_name: Tavares, Hugo
  last_name: Tavares
- first_name: Matthew
  full_name: Couchman, Matthew
  last_name: Couchman
- first_name: Lucy
  full_name: Copsey, Lucy
  last_name: Copsey
- first_name: Rosemary
  full_name: Carpenter, Rosemary
  last_name: Carpenter
- first_name: Miaomiao
  full_name: Li, Miaomiao
  last_name: Li
- first_name: Qun
  full_name: Li, Qun
  last_name: Li
- first_name: Yongbiao
  full_name: Xue, Yongbiao
  last_name: Xue
- first_name: Tamas
  full_name: Dalmay, Tamas
  last_name: Dalmay
- first_name: Enrico
  full_name: Coen, Enrico
  last_name: Coen
citation:
  ama: Bradley D, Xu P, Mohorianu I, et al. Evolution of flower color pattern through
    selection on regulatory small RNAs. <i>Science</i>. 2017;358(6365):925-928. doi:<a
    href="https://doi.org/10.1126/science.aao3526">10.1126/science.aao3526</a>
  apa: Bradley, D., Xu, P., Mohorianu, I., Whibley, A., Field, D., Tavares, H., …
    Coen, E. (2017). Evolution of flower color pattern through selection on regulatory
    small RNAs. <i>Science</i>. American Association for the Advancement of Science.
    <a href="https://doi.org/10.1126/science.aao3526">https://doi.org/10.1126/science.aao3526</a>
  chicago: Bradley, Desmond, Ping Xu, Irina Mohorianu, Annabel Whibley, David Field,
    Hugo Tavares, Matthew Couchman, et al. “Evolution of Flower Color Pattern through
    Selection on Regulatory Small RNAs.” <i>Science</i>. American Association for
    the Advancement of Science, 2017. <a href="https://doi.org/10.1126/science.aao3526">https://doi.org/10.1126/science.aao3526</a>.
  ieee: D. Bradley <i>et al.</i>, “Evolution of flower color pattern through selection
    on regulatory small RNAs,” <i>Science</i>, vol. 358, no. 6365. American Association
    for the Advancement of Science, pp. 925–928, 2017.
  ista: Bradley D, Xu P, Mohorianu I, Whibley A, Field D, Tavares H, Couchman M, Copsey
    L, Carpenter R, Li M, Li Q, Xue Y, Dalmay T, Coen E. 2017. Evolution of flower
    color pattern through selection on regulatory small RNAs. Science. 358(6365),
    925–928.
  mla: Bradley, Desmond, et al. “Evolution of Flower Color Pattern through Selection
    on Regulatory Small RNAs.” <i>Science</i>, vol. 358, no. 6365, American Association
    for the Advancement of Science, 2017, pp. 925–28, doi:<a href="https://doi.org/10.1126/science.aao3526">10.1126/science.aao3526</a>.
  short: D. Bradley, P. Xu, I. Mohorianu, A. Whibley, D. Field, H. Tavares, M. Couchman,
    L. Copsey, R. Carpenter, M. Li, Q. Li, Y. Xue, T. Dalmay, E. Coen, Science 358
    (2017) 925–928.
date_created: 2018-12-11T11:47:29Z
date_published: 2017-11-17T00:00:00Z
date_updated: 2025-09-11T07:34:49Z
day: '17'
department:
- _id: NiBa
doi: 10.1126/science.aao3526
external_id:
  isi:
  - '000415293000047'
intvolume: '       358'
isi: 1
issue: '6365'
language:
- iso: eng
month: '11'
oa_version: None
page: 925 - 928
publication: Science
publication_identifier:
  issn:
  - 0036-8075
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '7193'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Evolution of flower color pattern through selection on regulatory small RNAs
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 358
year: '2017'
...
---
_id: '613'
abstract:
- lang: eng
  text: 'Bacteria in groups vary individually, and interact with other bacteria and
    the environment to produce population-level patterns of gene expression. Investigating
    such behavior in detail requires measuring and controlling populations at the
    single-cell level alongside precisely specified interactions and environmental
    characteristics. Here we present an automated, programmable platform that combines
    image-based gene expression and growth measurements with on-line optogenetic expression
    control for hundreds of individual Escherichia coli cells over days, in a dynamically
    adjustable environment. This integrated platform broadly enables experiments that
    bridge individual and population behaviors. We demonstrate: (i) population structuring
    by independent closed-loop control of gene expression in many individual cells,
    (ii) cell-cell variation control during antibiotic perturbation, (iii) hybrid
    bio-digital circuits in single cells, and freely specifiable digital communication
    between individual bacteria. These examples showcase the potential for real-time
    integration of theoretical models with measurement and control of many individual
    cells to investigate and engineer microbial population behavior.'
acknowledgement: We are grateful to M. Lang, H. Janovjak, M. Khammash, A. Milias-Argeitis,
  M. Rullan, G. Batt, A. Bosma-Moody, Aryan, S. Leibler, and members of the Guet and
  Tkačik groups for helpful discussion, comments, and suggestions. We thank A. Moglich,
  T. Mathes, J. Tabor, and S. Schmidl for kind gifts of strains, and R. Hauschild,
  B. Knep, M. Lang, T. Asenov, E. Papusheva, T. Menner, T. Adletzberger, and J. Merrin
  for technical assistance. The research leading to these results has received funding
  from the People Programme (Marie Curie Actions) of the European Union’s Seventh
  Framework Programme (FP7/2007–2013) under REA grant agreement no. [291734]. (to
  R.C. and J.R.), Austrian Science Fund grant FWF P28844 (to G.T.), and internal IST
  Austria Interdisciplinary Project Support. J.R. acknowledges support from the Agence
  Nationale de la Recherche (ANR) under Grant Nos. ANR-16-CE33-0018 (MEMIP), ANR-16-CE12-0025
  (COGEX) and ANR-10-BINF-06-01 (ICEBERG).
article_number: '1535'
article_processing_charge: Yes (in subscription journal)
author:
- first_name: Remy P
  full_name: Chait, Remy P
  id: 3464AE84-F248-11E8-B48F-1D18A9856A87
  last_name: Chait
  orcid: 0000-0003-0876-3187
- first_name: Jakob
  full_name: Ruess, Jakob
  id: 4A245D00-F248-11E8-B48F-1D18A9856A87
  last_name: Ruess
  orcid: 0000-0003-1615-3282
- first_name: Tobias
  full_name: Bergmiller, Tobias
  id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
  last_name: Bergmiller
  orcid: 0000-0001-5396-4346
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
citation:
  ama: Chait RP, Ruess J, Bergmiller T, Tkačik G, Guet CC. Shaping bacterial population
    behavior through computer interfaced control of individual cells. <i>Nature Communications</i>.
    2017;8(1). doi:<a href="https://doi.org/10.1038/s41467-017-01683-1">10.1038/s41467-017-01683-1</a>
  apa: Chait, R. P., Ruess, J., Bergmiller, T., Tkačik, G., &#38; Guet, C. C. (2017).
    Shaping bacterial population behavior through computer interfaced control of individual
    cells. <i>Nature Communications</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/s41467-017-01683-1">https://doi.org/10.1038/s41467-017-01683-1</a>
  chicago: Chait, Remy P, Jakob Ruess, Tobias Bergmiller, Gašper Tkačik, and Calin
    C Guet. “Shaping Bacterial Population Behavior through Computer Interfaced Control
    of Individual Cells.” <i>Nature Communications</i>. Nature Publishing Group, 2017.
    <a href="https://doi.org/10.1038/s41467-017-01683-1">https://doi.org/10.1038/s41467-017-01683-1</a>.
  ieee: R. P. Chait, J. Ruess, T. Bergmiller, G. Tkačik, and C. C. Guet, “Shaping
    bacterial population behavior through computer interfaced control of individual
    cells,” <i>Nature Communications</i>, vol. 8, no. 1. Nature Publishing Group,
    2017.
  ista: Chait RP, Ruess J, Bergmiller T, Tkačik G, Guet CC. 2017. Shaping bacterial
    population behavior through computer interfaced control of individual cells. Nature
    Communications. 8(1), 1535.
  mla: Chait, Remy P., et al. “Shaping Bacterial Population Behavior through Computer
    Interfaced Control of Individual Cells.” <i>Nature Communications</i>, vol. 8,
    no. 1, 1535, Nature Publishing Group, 2017, doi:<a href="https://doi.org/10.1038/s41467-017-01683-1">10.1038/s41467-017-01683-1</a>.
  short: R.P. Chait, J. Ruess, T. Bergmiller, G. Tkačik, C.C. Guet, Nature Communications
    8 (2017).
corr_author: '1'
date_created: 2018-12-11T11:47:30Z
date_published: 2017-12-01T00:00:00Z
date_updated: 2025-09-11T07:34:12Z
day: '01'
ddc:
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department:
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doi: 10.1038/s41467-017-01683-1
ec_funded: 1
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title: Shaping bacterial population behavior through computer interfaced control of
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