---
_id: '1218'
abstract:
- lang: eng
  text: Investigating the physiology of cyanobacteria cultured under a diel light
    regime is relevant for a better understanding of the resulting growth characteristics
    and for specific biotechnological applications that are foreseen for these photosynthetic
    organisms. Here, we present the results of a multiomics study of the model cyanobacterium
    Synechocystis sp. strain PCC 6803, cultured in a lab-scale photobioreactor in
    physiological conditions relevant for large-scale culturing. The culture was sparged
    withN2 andCO2, leading to an anoxic environment during the dark period. Growth
    followed the availability of light. Metabolite analysis performed with 1Hnuclear
    magnetic resonance analysis showed that amino acids involved in nitrogen and sulfur
    assimilation showed elevated levels in the light. Most protein levels, analyzed
    through mass spectrometry, remained rather stable. However, several high-light-response
    proteins and stress-response proteins showed distinct changes at the onset of
    the light period. Microarray-based transcript analysis found common patterns of~56%
    of the transcriptome following the diel regime. These oscillating transcripts
    could be grouped coarsely into genes that were upregulated and downregulated in
    the dark period. The accumulated glycogen was degraded in the anaerobic environment
    in the dark. A small part was degraded gradually, reflecting basic maintenance
    requirements of the cells in darkness. Surprisingly, the largest part was degraded
    rapidly in a short time span at the end of the dark period. This degradation could
    allow rapid formation of metabolic intermediates at the end of the dark period,
    preparing the cells for the resumption of growth at the start of the light period.
acknowledgement: "Dutch Ministry of Economic Affairs, Agriculture, and Innovation
  through the program BioSolar CellsS. Andreas Angermayr,Pascal van Alphen, Klaas
  J. Hellingwerf\r\nWe thank Naira Quintana (presently at Rousselot, Belgium) for
  the ini-\r\ntiative  at  the  10th  Cyanobacterial  Molecular  Biology  Workshop\r\n(CMBW),
  June 2010, Lake Arrowhead, Los Angeles, CA, USA, to start the\r\ncollaborative endeavor
  reported here. We thank Timo Maarleveld from\r\nCWI/VU (Amsterdam) for a custom-made
  Python script handling the output from the NMR analysis and for evaluating and visualizing
  the\r\nseparate metabolites for their evaluation. We thank Rob Verpoorte from\r\nLeiden
  University (metabolome analysis) and Hans Aerts from the AMC\r\n(proteome analysis)
  for lab space and equipment. We thank Robert Leh-\r\nmann (Humboldt University Berlin)
  and Ilka Axmann (University of\r\nDüsseldorf) for sharing the R-code for the LOS
  transformation of the\r\ntranscript data. We thank Hans C. P. Matthijs from IBED
  for inspiring\r\ndialogues and insightful thoughts on continuous culturing of cyanobac-\r\nteria.
  We thank Sandra Waaijenborg for performing the transcript nor-\r\nmalization and
  Johan Westerhuis from BDA, Jeroen van der Steen and\r\nFilipe Branco dos Santos
  from MMP, and Lucas Stal from IBED/NIOZ for\r\nhelpful discussions. We thank Milou
  Schuurmans from MMP for help\r\nwith sampling and glycogen determination. We thank
  the members of the\r\nRNA Biology & Applied Bioinformatics group at SILS, in particular
  Selina\r\nvan Leeuwen, Elisa Hoekstra, and Martijs Jonker, for the microarray anal-\r\nysis.
  We thank the reviewers of this work for their insightful comments\r\nwhich improved
  the quality of the manuscript. This work, including the efforts of S. Andreas Angermayr,
  Pascal van\r\nAlphen, and Klaas J. Hellingwerf, was funded by Dutch Ministry of
  Eco-\r\nnomic Affairs, Agriculture, and Innovation through the program BioSolar\r\nCells."
article_processing_charge: No
author:
- first_name: Andreas
  full_name: Angermayr, Andreas
  id: 4677C796-F248-11E8-B48F-1D18A9856A87
  last_name: Angermayr
  orcid: 0000-0001-8619-2223
- first_name: Pascal
  full_name: Van Alphen, Pascal
  last_name: Van Alphen
- first_name: Dicle
  full_name: Hasdemir, Dicle
  last_name: Hasdemir
- first_name: Gertjan
  full_name: Kramer, Gertjan
  last_name: Kramer
- first_name: Muzamal
  full_name: Iqbal, Muzamal
  last_name: Iqbal
- first_name: Wilmar
  full_name: Van Grondelle, Wilmar
  last_name: Van Grondelle
- first_name: Huub
  full_name: Hoefsloot, Huub
  last_name: Hoefsloot
- first_name: Younghae
  full_name: Choi, Younghae
  last_name: Choi
- first_name: Klaas
  full_name: Hellingwerf, Klaas
  last_name: Hellingwerf
citation:
  ama: Angermayr A, Van Alphen P, Hasdemir D, et al. Culturing synechocystis sp. Strain
    pcc 6803 with N2 and CO2 in a diel regime reveals multiphase glycogen dynamics
    with low maintenance costs. <i>Applied and Environmental Microbiology</i>. 2016;82(14):4180-4189.
    doi:<a href="https://doi.org/10.1128/AEM.00256-16">10.1128/AEM.00256-16</a>
  apa: Angermayr, A., Van Alphen, P., Hasdemir, D., Kramer, G., Iqbal, M., Van Grondelle,
    W., … Hellingwerf, K. (2016). Culturing synechocystis sp. Strain pcc 6803 with
    N2 and CO2 in a diel regime reveals multiphase glycogen dynamics with low maintenance
    costs. <i>Applied and Environmental Microbiology</i>. American Society for Microbiology.
    <a href="https://doi.org/10.1128/AEM.00256-16">https://doi.org/10.1128/AEM.00256-16</a>
  chicago: Angermayr, Andreas, Pascal Van Alphen, Dicle Hasdemir, Gertjan Kramer,
    Muzamal Iqbal, Wilmar Van Grondelle, Huub Hoefsloot, Younghae Choi, and Klaas
    Hellingwerf. “Culturing Synechocystis Sp. Strain Pcc 6803 with N2 and CO2 in a
    Diel Regime Reveals Multiphase Glycogen Dynamics with Low Maintenance Costs.”
    <i>Applied and Environmental Microbiology</i>. American Society for Microbiology,
    2016. <a href="https://doi.org/10.1128/AEM.00256-16">https://doi.org/10.1128/AEM.00256-16</a>.
  ieee: A. Angermayr <i>et al.</i>, “Culturing synechocystis sp. Strain pcc 6803 with
    N2 and CO2 in a diel regime reveals multiphase glycogen dynamics with low maintenance
    costs,” <i>Applied and Environmental Microbiology</i>, vol. 82, no. 14. American
    Society for Microbiology, pp. 4180–4189, 2016.
  ista: Angermayr A, Van Alphen P, Hasdemir D, Kramer G, Iqbal M, Van Grondelle W,
    Hoefsloot H, Choi Y, Hellingwerf K. 2016. Culturing synechocystis sp. Strain pcc
    6803 with N2 and CO2 in a diel regime reveals multiphase glycogen dynamics with
    low maintenance costs. Applied and Environmental Microbiology. 82(14), 4180–4189.
  mla: Angermayr, Andreas, et al. “Culturing Synechocystis Sp. Strain Pcc 6803 with
    N2 and CO2 in a Diel Regime Reveals Multiphase Glycogen Dynamics with Low Maintenance
    Costs.” <i>Applied and Environmental Microbiology</i>, vol. 82, no. 14, American
    Society for Microbiology, 2016, pp. 4180–89, doi:<a href="https://doi.org/10.1128/AEM.00256-16">10.1128/AEM.00256-16</a>.
  short: A. Angermayr, P. Van Alphen, D. Hasdemir, G. Kramer, M. Iqbal, W. Van Grondelle,
    H. Hoefsloot, Y. Choi, K. Hellingwerf, Applied and Environmental Microbiology
    82 (2016) 4180–4189.
date_created: 2018-12-11T11:50:46Z
date_published: 2016-07-01T00:00:00Z
date_updated: 2025-09-22T09:35:22Z
day: '01'
department:
- _id: ToBo
doi: 10.1128/AEM.00256-16
external_id:
  isi:
  - '000379345100012'
intvolume: '        82'
isi: 1
issue: '14'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959195/
month: '07'
oa: 1
oa_version: Submitted Version
page: 4180 - 4189
publication: Applied and Environmental Microbiology
publication_status: published
publisher: American Society for Microbiology
publist_id: '6117'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Culturing synechocystis sp. Strain pcc 6803 with N2 and CO2 in a diel regime
  reveals multiphase glycogen dynamics with low maintenance costs
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 82
year: '2016'
...
---
_id: '1219'
abstract:
- lang: eng
  text: We consider N×N random matrices of the form H = W + V where W is a real symmetric
    or complex Hermitian Wigner matrix and V is a random or deterministic, real, diagonal
    matrix whose entries are independent of W. We assume subexponential decay for
    the matrix entries of W, and we choose V so that the eigenvalues ofW and V are
    typically of the same order. For a large class of diagonal matrices V , we show
    that the local statistics in the bulk of the spectrum are universal in the limit
    of large N.
acknowledgement: "J.C. was supported in part by National Research Foundation of Korea
  Grant 2011-0013474 and TJ Park Junior Faculty Fellowship.\r\nK.S. was supported
  by ERC Advanced Grant RANMAT, No. 338804, and the \"Fund for Math.\"\r\nB.S. was
  supported by NSF GRFP Fellowship DGE-1144152.\r\nH.Y. was supported in part by NSF
  Grant DMS-13-07444 and Simons investigator fellowship. We thank Paul Bourgade, László
  Erd ̋os and Antti Knowles for helpful comments. We are grateful to the Taida Institute
  for Mathematical\r\nSciences and National Taiwan Universality for their hospitality
  during part of this\r\nresearch. We thank Thomas Spencer and the Institute for Advanced
  Study for their\r\nhospitality during the academic year 2013–2014.  "
article_processing_charge: No
arxiv: 1
author:
- first_name: Jioon
  full_name: Lee, Jioon
  last_name: Lee
- first_name: Kevin
  full_name: Schnelli, Kevin
  id: 434AD0AE-F248-11E8-B48F-1D18A9856A87
  last_name: Schnelli
  orcid: 0000-0003-0954-3231
- first_name: Ben
  full_name: Stetler, Ben
  last_name: Stetler
- first_name: Horngtzer
  full_name: Yau, Horngtzer
  last_name: Yau
citation:
  ama: Lee J, Schnelli K, Stetler B, Yau H. Bulk universality for deformed wigner
    matrices. <i>Annals of Probability</i>. 2016;44(3):2349-2425. doi:<a href="https://doi.org/10.1214/15-AOP1023">10.1214/15-AOP1023</a>
  apa: Lee, J., Schnelli, K., Stetler, B., &#38; Yau, H. (2016). Bulk universality
    for deformed wigner matrices. <i>Annals of Probability</i>. Institute of Mathematical
    Statistics. <a href="https://doi.org/10.1214/15-AOP1023">https://doi.org/10.1214/15-AOP1023</a>
  chicago: Lee, Jioon, Kevin Schnelli, Ben Stetler, and Horngtzer Yau. “Bulk Universality
    for Deformed Wigner Matrices.” <i>Annals of Probability</i>. Institute of Mathematical
    Statistics, 2016. <a href="https://doi.org/10.1214/15-AOP1023">https://doi.org/10.1214/15-AOP1023</a>.
  ieee: J. Lee, K. Schnelli, B. Stetler, and H. Yau, “Bulk universality for deformed
    wigner matrices,” <i>Annals of Probability</i>, vol. 44, no. 3. Institute of Mathematical
    Statistics, pp. 2349–2425, 2016.
  ista: Lee J, Schnelli K, Stetler B, Yau H. 2016. Bulk universality for deformed
    wigner matrices. Annals of Probability. 44(3), 2349–2425.
  mla: Lee, Jioon, et al. “Bulk Universality for Deformed Wigner Matrices.” <i>Annals
    of Probability</i>, vol. 44, no. 3, Institute of Mathematical Statistics, 2016,
    pp. 2349–425, doi:<a href="https://doi.org/10.1214/15-AOP1023">10.1214/15-AOP1023</a>.
  short: J. Lee, K. Schnelli, B. Stetler, H. Yau, Annals of Probability 44 (2016)
    2349–2425.
date_created: 2018-12-11T11:50:47Z
date_published: 2016-01-01T00:00:00Z
date_updated: 2025-09-22T09:33:43Z
day: '01'
department:
- _id: LaEr
doi: 10.1214/15-AOP1023
ec_funded: 1
external_id:
  arxiv:
  - '1405.6634'
  isi:
  - '000376180700016'
intvolume: '        44'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1405.6634
month: '01'
oa: 1
oa_version: Preprint
page: 2349 - 2425
project:
- _id: 258DCDE6-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '338804'
  name: Random matrices, universality and disordered quantum systems
publication: Annals of Probability
publication_status: published
publisher: Institute of Mathematical Statistics
publist_id: '6115'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Bulk universality for deformed wigner matrices
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 44
year: '2016'
...
---
_id: '1220'
abstract:
- lang: eng
  text: Theoretical and numerical aspects of aerodynamic efficiency of propulsion
    systems coupled to the boundary layer of a fuselage are studied. We discuss the
    effects of local flow fields, which are affected both by conservative flow acceleration
    as well as total pressure losses, on the efficiency of boundary layer immersed
    propulsion devices. We introduce the concept of a boundary layer retardation turbine
    that helps reduce skin friction over the fuselage. We numerically investigate
    efficiency gains offered by boundary layer and wake interacting devices. We discuss
    the results in terms of a total energy consumption framework and show that efficiency
    gains of any device depend on all the other elements of the propulsion system.
author:
- first_name: Gregor
  full_name: Mikić, Gregor
  last_name: Mikić
- first_name: Alex
  full_name: Stoll, Alex
  last_name: Stoll
- first_name: Joe
  full_name: Bevirt, Joe
  last_name: Bevirt
- first_name: Rok
  full_name: Grah, Rok
  id: 483E70DE-F248-11E8-B48F-1D18A9856A87
  last_name: Grah
  orcid: 0000-0003-2539-3560
- first_name: Mark
  full_name: Moore, Mark
  last_name: Moore
citation:
  ama: 'Mikić G, Stoll A, Bevirt J, Grah R, Moore M. Fuselage boundary layer ingestion
    propulsion applied to a thin haul commuter aircraft for optimal efficiency. In:
    AIAA; 2016:1-19. doi:<a href="https://doi.org/10.2514/6.2016-3764">10.2514/6.2016-3764</a>'
  apa: 'Mikić, G., Stoll, A., Bevirt, J., Grah, R., &#38; Moore, M. (2016). Fuselage
    boundary layer ingestion propulsion applied to a thin haul commuter aircraft for
    optimal efficiency (pp. 1–19). Presented at the AIAA: Aviation Technology, Integration,
    and Operations Conference, Washington, D.C., USA: AIAA. <a href="https://doi.org/10.2514/6.2016-3764">https://doi.org/10.2514/6.2016-3764</a>'
  chicago: Mikić, Gregor, Alex Stoll, Joe Bevirt, Rok Grah, and Mark Moore. “Fuselage
    Boundary Layer Ingestion Propulsion Applied to a Thin Haul Commuter Aircraft for
    Optimal Efficiency,” 1–19. AIAA, 2016. <a href="https://doi.org/10.2514/6.2016-3764">https://doi.org/10.2514/6.2016-3764</a>.
  ieee: 'G. Mikić, A. Stoll, J. Bevirt, R. Grah, and M. Moore, “Fuselage boundary
    layer ingestion propulsion applied to a thin haul commuter aircraft for optimal
    efficiency,” presented at the AIAA: Aviation Technology, Integration, and Operations
    Conference, Washington, D.C., USA, 2016, pp. 1–19.'
  ista: 'Mikić G, Stoll A, Bevirt J, Grah R, Moore M. 2016. Fuselage boundary layer
    ingestion propulsion applied to a thin haul commuter aircraft for optimal efficiency.
    AIAA: Aviation Technology, Integration, and Operations Conference, 1–19.'
  mla: Mikić, Gregor, et al. <i>Fuselage Boundary Layer Ingestion Propulsion Applied
    to a Thin Haul Commuter Aircraft for Optimal Efficiency</i>. AIAA, 2016, pp. 1–19,
    doi:<a href="https://doi.org/10.2514/6.2016-3764">10.2514/6.2016-3764</a>.
  short: G. Mikić, A. Stoll, J. Bevirt, R. Grah, M. Moore, in:, AIAA, 2016, pp. 1–19.
conference:
  end_date: 2016-06-17
  location: Washington, D.C., USA
  name: 'AIAA: Aviation Technology, Integration, and Operations Conference'
  start_date: 2016-06-13
date_created: 2018-12-11T11:50:47Z
date_published: 2016-06-01T00:00:00Z
date_updated: 2023-02-21T10:17:50Z
day: '01'
department:
- _id: CaGu
- _id: GaTk
doi: 10.2514/6.2016-3764
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://ntrs.nasa.gov/search.jsp?R=20160010167&amp;hterms=Fuselage+boundary+layer+ingestion+propulsion+applied+thin+haul+commuter+aircraft+optimal+efficiency&amp;qs=N%3D0%26Ntk%3DAll%26Ntt%3DFuselage%2520boundary%2520layer%2520ingestion%2520propulsion%2520applied%2520to%2520a%2520thin%2520haul%2520commuter%2520aircraft%2520for%2520optimal%2520efficiency%26Ntx%3Dmode%2520matchallpartial%26Nm%3D123%7CCollection%7CNASA%2520STI%7C%7C17%7CCollection%7CNACA
month: '06'
oa: 1
oa_version: Preprint
page: 1 - 19
publication_status: published
publisher: AIAA
publist_id: '6114'
quality_controlled: '1'
scopus_import: 1
status: public
title: Fuselage boundary layer ingestion propulsion applied to a thin haul commuter
  aircraft for optimal efficiency
type: conference
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
year: '2016'
...
---
_id: '1221'
abstract:
- lang: eng
  text: The Auxin Binding Protein 1 (ABP1) is one of the most studied proteins in
    plants. Since decades ago, it has been the prime receptor candidate for the plant
    hormone auxin with a plethora of described functions in auxin signaling and development.
    The developmental importance of ABP1 has recently been questioned by identification
    of Arabidopsis thaliana abp1 knock-out alleles that show no obvious phenotypes
    under normal growth conditions. In this study, we examined the contradiction between
    the normal growth and development of the abp1 knock-outs and the strong morphological
    defects observed in three different ethanol-inducible abp1 knock-down mutants
    ( abp1-AS, SS12K, SS12S). By analyzing segregating populations of abp1 knock-out
    vs. abp1 knock-down crosses we show that the strong morphological defects that
    were believed to be the result of conditional down-regulation of ABP1 can be reproduced
    also in the absence of the functional ABP1 protein. This data suggests that the
    phenotypes in abp1 knock-down lines are due to the off-target effects and asks
    for further reflections on the biological function of ABP1 or alternative explanations
    for the missing phenotypic defects in the abp1 loss-of-function alleles.
acknowledgement: "This work was supported by ERC Independent Research grant (ERC-2011-StG-20101109-PSDP
  to JF). JM internship was supported by the grant “Action Austria – Slovakia”. MG
  was supported by the scholarship \"Stipendien der Stipendienstiftung der Republik
  Österreich\". Work by EH and CPR were supported by ANR blanc ANR-14-CE11-0018. We
  would like to thank Mark Estelle and Yunde Zhao for provid\r\n-\r\ning \r\nabp1-c1\r\n,
  \r\nabp1-TD1 \r\nand \r\nabp1-WTc1 \r\nseeds. We thank Emeline \r\nHuault for technical
  assistance."
article_number: '86'
article_processing_charge: No
article_type: original
author:
- first_name: Jaroslav
  full_name: Michalko, Jaroslav
  id: 483727CA-F248-11E8-B48F-1D18A9856A87
  last_name: Michalko
- first_name: Matous
  full_name: Glanc, Matous
  id: 1AE1EA24-02D0-11E9-9BAA-DAF4881429F2
  last_name: Glanc
  orcid: 0000-0003-0619-7783
- first_name: Catherine
  full_name: Perrot Rechenmann, Catherine
  last_name: Perrot Rechenmann
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Michalko J, Glanc M, Perrot Rechenmann C, Friml J. Strong morphological defects
    in conditional Arabidopsis abp1 knock-down mutants generated in absence of functional
    ABP1 protein. <i>F1000 Research </i>. 2016;5. doi:<a href="https://doi.org/10.12688/f1000research.7654.1">10.12688/f1000research.7654.1</a>
  apa: Michalko, J., Glanc, M., Perrot Rechenmann, C., &#38; Friml, J. (2016). Strong
    morphological defects in conditional Arabidopsis abp1 knock-down mutants generated
    in absence of functional ABP1 protein. <i>F1000 Research </i>. F1000 Research.
    <a href="https://doi.org/10.12688/f1000research.7654.1">https://doi.org/10.12688/f1000research.7654.1</a>
  chicago: Michalko, Jaroslav, Matous Glanc, Catherine Perrot Rechenmann, and Jiří
    Friml. “Strong Morphological Defects in Conditional Arabidopsis Abp1 Knock-down
    Mutants Generated in Absence of Functional ABP1 Protein.” <i>F1000 Research </i>.
    F1000 Research, 2016. <a href="https://doi.org/10.12688/f1000research.7654.1">https://doi.org/10.12688/f1000research.7654.1</a>.
  ieee: J. Michalko, M. Glanc, C. Perrot Rechenmann, and J. Friml, “Strong morphological
    defects in conditional Arabidopsis abp1 knock-down mutants generated in absence
    of functional ABP1 protein,” <i>F1000 Research </i>, vol. 5. F1000 Research, 2016.
  ista: Michalko J, Glanc M, Perrot Rechenmann C, Friml J. 2016. Strong morphological
    defects in conditional Arabidopsis abp1 knock-down mutants generated in absence
    of functional ABP1 protein. F1000 Research . 5, 86.
  mla: Michalko, Jaroslav, et al. “Strong Morphological Defects in Conditional Arabidopsis
    Abp1 Knock-down Mutants Generated in Absence of Functional ABP1 Protein.” <i>F1000
    Research </i>, vol. 5, 86, F1000 Research, 2016, doi:<a href="https://doi.org/10.12688/f1000research.7654.1">10.12688/f1000research.7654.1</a>.
  short: J. Michalko, M. Glanc, C. Perrot Rechenmann, J. Friml, F1000 Research  5
    (2016).
date_created: 2018-12-11T11:50:47Z
date_published: 2016-01-20T00:00:00Z
date_updated: 2025-04-15T07:48:02Z
day: '20'
ddc:
- '581'
department:
- _id: JiFr
doi: 10.12688/f1000research.7654.1
ec_funded: 1
file:
- access_level: open_access
  checksum: c9e50bb6096a7ba4a832969935820f19
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:15:33Z
  date_updated: 2020-07-14T12:44:39Z
  file_id: '5154'
  file_name: IST-2016-711-v1+1_770cf1e0-612f-4e85-a500-54b6349fbbab_7654_-_jaroslav_michalko.pdf
  file_size: 2990459
  relation: main_file
file_date_updated: 2020-07-14T12:44:39Z
has_accepted_license: '1'
intvolume: '         5'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: 25716A02-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '282300'
  name: Polarity and subcellular dynamics in plants
publication: 'F1000 Research '
publication_status: published
publisher: F1000 Research
publist_id: '6113'
pubrep_id: '711'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Strong morphological defects in conditional Arabidopsis abp1 knock-down mutants
  generated in absence of functional ABP1 protein
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: 5
year: '2016'
...
---
_id: '1222'
abstract:
- lang: eng
  text: We consider packings of congruent circles on a square flat torus, i.e., periodic
    (w.r.t. a square lattice) planar circle packings, with the maximal circle radius.
    This problem is interesting due to a practical reason—the problem of “super resolution
    of images.” We have found optimal arrangements for N=6, 7 and 8 circles. Surprisingly,
    for the case N=7 there are three different optimal arrangements. Our proof is
    based on a computer enumeration of toroidal irreducible contact graphs.
acknowledgement: We wish to thank Alexey Tarasov, Vladislav Volkov and Brittany Fasy
  for some useful comments and remarks, and especially Thom Sulanke for modifying
  surftri to suit our purposes. Oleg R. Musin was partially supported by the NSF Grant
  DMS-1400876 and by the RFBR Grant 15-01-99563. Anton V. Nikitenko was supported
  by the Chebyshev Laboratory (Department of Mathematics and Mechanics, St. Petersburg
  State University) under RF Government Grant 11.G34.31.0026.
article_processing_charge: No
arxiv: 1
author:
- first_name: Oleg
  full_name: Musin, Oleg
  last_name: Musin
- first_name: Anton
  full_name: Nikitenko, Anton
  id: 3E4FF1BA-F248-11E8-B48F-1D18A9856A87
  last_name: Nikitenko
  orcid: 0000-0002-0659-3201
citation:
  ama: Musin O, Nikitenko A. Optimal packings of congruent circles on a square flat
    torus. <i>Discrete &#38; Computational Geometry</i>. 2016;55(1):1-20. doi:<a href="https://doi.org/10.1007/s00454-015-9742-6">10.1007/s00454-015-9742-6</a>
  apa: Musin, O., &#38; Nikitenko, A. (2016). Optimal packings of congruent circles
    on a square flat torus. <i>Discrete &#38; Computational Geometry</i>. Springer.
    <a href="https://doi.org/10.1007/s00454-015-9742-6">https://doi.org/10.1007/s00454-015-9742-6</a>
  chicago: Musin, Oleg, and Anton Nikitenko. “Optimal Packings of Congruent Circles
    on a Square Flat Torus.” <i>Discrete &#38; Computational Geometry</i>. Springer,
    2016. <a href="https://doi.org/10.1007/s00454-015-9742-6">https://doi.org/10.1007/s00454-015-9742-6</a>.
  ieee: O. Musin and A. Nikitenko, “Optimal packings of congruent circles on a square
    flat torus,” <i>Discrete &#38; Computational Geometry</i>, vol. 55, no. 1. Springer,
    pp. 1–20, 2016.
  ista: Musin O, Nikitenko A. 2016. Optimal packings of congruent circles on a square
    flat torus. Discrete &#38; Computational Geometry. 55(1), 1–20.
  mla: Musin, Oleg, and Anton Nikitenko. “Optimal Packings of Congruent Circles on
    a Square Flat Torus.” <i>Discrete &#38; Computational Geometry</i>, vol. 55, no.
    1, Springer, 2016, pp. 1–20, doi:<a href="https://doi.org/10.1007/s00454-015-9742-6">10.1007/s00454-015-9742-6</a>.
  short: O. Musin, A. Nikitenko, Discrete &#38; Computational Geometry 55 (2016) 1–20.
date_created: 2018-12-11T11:50:48Z
date_published: 2016-01-01T00:00:00Z
date_updated: 2025-09-22T09:32:23Z
day: '01'
department:
- _id: HeEd
doi: 10.1007/s00454-015-9742-6
external_id:
  arxiv:
  - '1212.0649'
  isi:
  - '000367625500001'
intvolume: '        55'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1212.0649
month: '01'
oa: 1
oa_version: Preprint
page: 1 - 20
publication: Discrete & Computational Geometry
publication_status: published
publisher: Springer
publist_id: '6111'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Optimal packings of congruent circles on a square flat torus
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 55
year: '2016'
...
---
_id: '1224'
abstract:
- lang: eng
  text: Sexual dimorphism in resource allocation is expected to change during the
    life cycle of dioecious plants because of temporal differences between the sexes
    in reproductive investment. Given the potential for sex-specific differences in
    reproductive costs, resource availability may contribute to variation in reproductive
    allocation in females and males. Here, we used Rumex hastatulus, a dioecious,
    wind-pollinated annual plant, to investigate whether sexual dimorphism varies
    with life-history stage and nutrient availability, and determine whether allocation
    patterns differ depending on reproductive commitment. To examine if the costs
    of reproduction varied between the sexes, reproduction was either allowed or prevented
    through bud removal, and biomass allocation was measured at maturity. In a second
    experiment to assess variation in sexual dimorphism across the life cycle, and
    whether this varied with resource availability, plants were grown in high and
    low nutrients and allocation to roots, aboveground vegetative growth and reproduction
    were measured at three developmental stages. Males prevented from reproducing
    compensated with increased above- and belowground allocation to a much larger
    degree than females, suggesting that male reproductive costs reduce vegetative
    growth. The proportional allocation to roots, reproductive structures and aboveground
    vegetative growth varied between the sexes and among life-cycle stages, but not
    with nutrient treatment. Females allocated proportionally more resources to roots
    than males at peak flowering, but this pattern was reversed at reproductive maturity
    under low-nutrient conditions. Our study illustrates the importance of temporal
    dynamics in sex-specific resource allocation and provides support for high male
    reproductive costs in wind-pollinated plants.
article_processing_charge: No
author:
- first_name: Zachary
  full_name: Teitel, Zachary
  last_name: Teitel
- first_name: Melinda
  full_name: Pickup, Melinda
  id: 2C78037E-F248-11E8-B48F-1D18A9856A87
  last_name: Pickup
  orcid: 0000-0001-6118-0541
- first_name: David
  full_name: Field, David
  id: 419049E2-F248-11E8-B48F-1D18A9856A87
  last_name: Field
  orcid: 0000-0002-4014-8478
- first_name: Spencer
  full_name: Barrett, Spencer
  last_name: Barrett
citation:
  ama: Teitel Z, Pickup M, Field D, Barrett S. The dynamics of resource allocation
    and costs of reproduction in a sexually dimorphic, wind-pollinated dioecious plant.
    <i>Plant Biology</i>. 2016;18(1):98-103. doi:<a href="https://doi.org/10.1111/plb.12336">10.1111/plb.12336</a>
  apa: Teitel, Z., Pickup, M., Field, D., &#38; Barrett, S. (2016). The dynamics of
    resource allocation and costs of reproduction in a sexually dimorphic, wind-pollinated
    dioecious plant. <i>Plant Biology</i>. Wiley-Blackwell. <a href="https://doi.org/10.1111/plb.12336">https://doi.org/10.1111/plb.12336</a>
  chicago: Teitel, Zachary, Melinda Pickup, David Field, and Spencer Barrett. “The
    Dynamics of Resource Allocation and Costs of Reproduction in a Sexually Dimorphic,
    Wind-Pollinated Dioecious Plant.” <i>Plant Biology</i>. Wiley-Blackwell, 2016.
    <a href="https://doi.org/10.1111/plb.12336">https://doi.org/10.1111/plb.12336</a>.
  ieee: Z. Teitel, M. Pickup, D. Field, and S. Barrett, “The dynamics of resource
    allocation and costs of reproduction in a sexually dimorphic, wind-pollinated
    dioecious plant,” <i>Plant Biology</i>, vol. 18, no. 1. Wiley-Blackwell, pp. 98–103,
    2016.
  ista: Teitel Z, Pickup M, Field D, Barrett S. 2016. The dynamics of resource allocation
    and costs of reproduction in a sexually dimorphic, wind-pollinated dioecious plant.
    Plant Biology. 18(1), 98–103.
  mla: Teitel, Zachary, et al. “The Dynamics of Resource Allocation and Costs of Reproduction
    in a Sexually Dimorphic, Wind-Pollinated Dioecious Plant.” <i>Plant Biology</i>,
    vol. 18, no. 1, Wiley-Blackwell, 2016, pp. 98–103, doi:<a href="https://doi.org/10.1111/plb.12336">10.1111/plb.12336</a>.
  short: Z. Teitel, M. Pickup, D. Field, S. Barrett, Plant Biology 18 (2016) 98–103.
date_created: 2018-12-11T11:50:48Z
date_published: 2016-01-01T00:00:00Z
date_updated: 2025-09-22T09:31:49Z
day: '01'
department:
- _id: NiBa
doi: 10.1111/plb.12336
external_id:
  isi:
  - '000369975700011'
intvolume: '        18'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 98 - 103
publication: Plant Biology
publication_status: published
publisher: Wiley-Blackwell
publist_id: '6110'
quality_controlled: '1'
scopus_import: '1'
status: public
title: The dynamics of resource allocation and costs of reproduction in a sexually
  dimorphic, wind-pollinated dioecious plant
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 18
year: '2016'
...
---
_id: '1225'
abstract:
- lang: eng
  text: At Crypto 2015 Fuchsbauer, Hanser and Slamanig (FHS) presented the first standard-model
    construction of efficient roundoptimal blind signatures that does not require
    complexity leveraging. It is conceptually simple and builds on the primitive of
    structure-preserving signatures on equivalence classes (SPS-EQ). FHS prove the
    unforgeability of their scheme assuming EUF-CMA security of the SPS-EQ scheme
    and hardness of a version of the DH inversion problem. Blindness under adversarially
    chosen keys is proven under an interactive variant of the DDH assumption. We propose
    a variant of their scheme whose blindness can be proven under a non-interactive
    assumption, namely a variant of the bilinear DDH assumption. We moreover prove
    its unforgeability assuming only unforgeability of the underlying SPS-EQ but no
    additional assumptions as needed for the FHS scheme.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Georg
  full_name: Fuchsbauer, Georg
  id: 46B4C3EE-F248-11E8-B48F-1D18A9856A87
  last_name: Fuchsbauer
- first_name: Christian
  full_name: Hanser, Christian
  last_name: Hanser
- first_name: Chethan
  full_name: Kamath Hosdurg, Chethan
  id: 4BD3F30E-F248-11E8-B48F-1D18A9856A87
  last_name: Kamath Hosdurg
- first_name: Daniel
  full_name: Slamanig, Daniel
  last_name: Slamanig
citation:
  ama: 'Fuchsbauer G, Hanser C, Kamath Hosdurg C, Slamanig D. Practical round-optimal
    blind signatures in the standard model from weaker assumptions. In: Vol 9841.
    Springer; 2016:391-408. doi:<a href="https://doi.org/10.1007/978-3-319-44618-9_21">10.1007/978-3-319-44618-9_21</a>'
  apa: 'Fuchsbauer, G., Hanser, C., Kamath Hosdurg, C., &#38; Slamanig, D. (2016).
    Practical round-optimal blind signatures in the standard model from weaker assumptions
    (Vol. 9841, pp. 391–408). Presented at the SCN: Security and Cryptography for
    Networks, Amalfi, Italy: Springer. <a href="https://doi.org/10.1007/978-3-319-44618-9_21">https://doi.org/10.1007/978-3-319-44618-9_21</a>'
  chicago: Fuchsbauer, Georg, Christian Hanser, Chethan Kamath Hosdurg, and Daniel
    Slamanig. “Practical Round-Optimal Blind Signatures in the Standard Model from
    Weaker Assumptions,” 9841:391–408. Springer, 2016. <a href="https://doi.org/10.1007/978-3-319-44618-9_21">https://doi.org/10.1007/978-3-319-44618-9_21</a>.
  ieee: 'G. Fuchsbauer, C. Hanser, C. Kamath Hosdurg, and D. Slamanig, “Practical
    round-optimal blind signatures in the standard model from weaker assumptions,”
    presented at the SCN: Security and Cryptography for Networks, Amalfi, Italy, 2016,
    vol. 9841, pp. 391–408.'
  ista: 'Fuchsbauer G, Hanser C, Kamath Hosdurg C, Slamanig D. 2016. Practical round-optimal
    blind signatures in the standard model from weaker assumptions. SCN: Security
    and Cryptography for Networks, LNCS, vol. 9841, 391–408.'
  mla: Fuchsbauer, Georg, et al. <i>Practical Round-Optimal Blind Signatures in the
    Standard Model from Weaker Assumptions</i>. Vol. 9841, Springer, 2016, pp. 391–408,
    doi:<a href="https://doi.org/10.1007/978-3-319-44618-9_21">10.1007/978-3-319-44618-9_21</a>.
  short: G. Fuchsbauer, C. Hanser, C. Kamath Hosdurg, D. Slamanig, in:, Springer,
    2016, pp. 391–408.
conference:
  end_date: 2016-09-02
  location: Amalfi, Italy
  name: 'SCN: Security and Cryptography for Networks'
  start_date: 2016-08-31
date_created: 2018-12-11T11:50:49Z
date_published: 2016-08-11T00:00:00Z
date_updated: 2025-09-23T09:53:45Z
day: '11'
department:
- _id: KrPi
doi: 10.1007/978-3-319-44618-9_21
ec_funded: 1
external_id:
  isi:
  - '000389516500021'
intvolume: '      9841'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://eprint.iacr.org/2016/662
month: '08'
oa: 1
oa_version: Submitted Version
page: 391 - 408
project:
- _id: 258C570E-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '259668'
  name: Provable Security for Physical Cryptography
- _id: 258AA5B2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '682815'
  name: Teaching Old Crypto New Tricks
publication_status: published
publisher: Springer
publist_id: '6109'
quality_controlled: '1'
related_material:
  record:
  - id: '1647'
    relation: earlier_version
    status: public
scopus_import: '1'
status: public
title: Practical round-optimal blind signatures in the standard model from weaker
  assumptions
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 9841
year: '2016'
...
---
_id: '1226'
abstract:
- lang: eng
  text: Mitochondrial complex I (also known as NADH:ubiquinone oxidoreductase) contributes
    to cellular energy production by transferring electrons from NADH to ubiquinone
    coupled to proton translocation across the membrane. It is the largest protein
    assembly of the respiratory chain with a total mass of 970 kilodaltons. Here we
    present a nearly complete atomic structure of ovine (Ovis aries) mitochondrial
    complex I at 3.9 Å resolution, solved by cryo-electron microscopy with cross-linking
    and mass-spectrometry mapping experiments. All 14 conserved core subunits and
    31 mitochondria-specific supernumerary subunits are resolved within the L-shaped
    molecule. The hydrophilic matrix arm comprises flavin mononucleotide and 8 iron-sulfur
    clusters involved in electron transfer, and the membrane arm contains 78 transmembrane
    helices, mostly contributed by antiporter-like subunits involved in proton translocation.
    Supernumerary subunits form an interlinked, stabilizing shell around the conserved
    core. Tightly bound lipids (including cardiolipins) further stabilize interactions
    between the hydrophobic subunits. Subunits with possible regulatory roles contain
    additional cofactors, NADPH and two phosphopantetheine molecules, which are shown
    to be involved in inter-subunit interactions. We observe two different conformations
    of the complex, which may be related to the conformationally driven coupling mechanism
    and to the active-deactive transition of the enzyme. Our structure provides insight
    into the mechanism, assembly, maturation and dysfunction of mitochondrial complex
    I, and allows detailed molecular analysis of disease-causing mutations.
article_processing_charge: No
article_type: original
author:
- first_name: Karol
  full_name: Fiedorczuk, Karol
  id: 5BFF67CE-02D1-11E9-B11A-A5A4D7DFFFD0
  last_name: Fiedorczuk
- first_name: James A
  full_name: Letts, James A
  id: 322DA418-F248-11E8-B48F-1D18A9856A87
  last_name: Letts
  orcid: 0000-0002-9864-3586
- first_name: Gianluca
  full_name: Degliesposti, Gianluca
  last_name: Degliesposti
- first_name: Karol
  full_name: Kaszuba, Karol
  id: 3FDF9472-F248-11E8-B48F-1D18A9856A87
  last_name: Kaszuba
- first_name: Mark
  full_name: Skehel, Mark
  last_name: Skehel
- first_name: Leonid A
  full_name: Sazanov, Leonid A
  id: 338D39FE-F248-11E8-B48F-1D18A9856A87
  last_name: Sazanov
  orcid: 0000-0002-0977-7989
citation:
  ama: Fiedorczuk K, Letts JA, Degliesposti G, Kaszuba K, Skehel M, Sazanov LA. Atomic
    structure of the entire mammalian mitochondrial complex i. <i>Nature</i>. 2016;538(7625):406-410.
    doi:<a href="https://doi.org/10.1038/nature19794">10.1038/nature19794</a>
  apa: Fiedorczuk, K., Letts, J. A., Degliesposti, G., Kaszuba, K., Skehel, M., &#38;
    Sazanov, L. A. (2016). Atomic structure of the entire mammalian mitochondrial
    complex i. <i>Nature</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/nature19794">https://doi.org/10.1038/nature19794</a>
  chicago: Fiedorczuk, Karol, James A Letts, Gianluca Degliesposti, Karol Kaszuba,
    Mark Skehel, and Leonid A Sazanov. “Atomic Structure of the Entire Mammalian Mitochondrial
    Complex I.” <i>Nature</i>. Nature Publishing Group, 2016. <a href="https://doi.org/10.1038/nature19794">https://doi.org/10.1038/nature19794</a>.
  ieee: K. Fiedorczuk, J. A. Letts, G. Degliesposti, K. Kaszuba, M. Skehel, and L.
    A. Sazanov, “Atomic structure of the entire mammalian mitochondrial complex i,”
    <i>Nature</i>, vol. 538, no. 7625. Nature Publishing Group, pp. 406–410, 2016.
  ista: Fiedorczuk K, Letts JA, Degliesposti G, Kaszuba K, Skehel M, Sazanov LA. 2016.
    Atomic structure of the entire mammalian mitochondrial complex i. Nature. 538(7625),
    406–410.
  mla: Fiedorczuk, Karol, et al. “Atomic Structure of the Entire Mammalian Mitochondrial
    Complex I.” <i>Nature</i>, vol. 538, no. 7625, Nature Publishing Group, 2016,
    pp. 406–10, doi:<a href="https://doi.org/10.1038/nature19794">10.1038/nature19794</a>.
  short: K. Fiedorczuk, J.A. Letts, G. Degliesposti, K. Kaszuba, M. Skehel, L.A. Sazanov,
    Nature 538 (2016) 406–410.
date_created: 2018-12-11T11:50:49Z
date_published: 2016-10-20T00:00:00Z
date_updated: 2025-09-22T09:29:26Z
day: '20'
department:
- _id: LeSa
doi: 10.1038/nature19794
ec_funded: 1
external_id:
  isi:
  - '000386673100044'
  pmid:
  - '27595392'
intvolume: '       538'
isi: 1
issue: '7625'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5164932/
month: '10'
oa: 1
oa_version: Submitted Version
page: 406 - 410
pmid: 1
project:
- _id: 2593EBD6-B435-11E9-9278-68D0E5697425
  name: Atomic-Resolution Structures of Mitochondrial Respiratory Chain Supercomplexes
- _id: 2590DB08-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '701309'
  name: Atomic Resolution Structures of Mitochondrial Respiratory Chain Supercomplexes
publication: Nature
publication_status: published
publisher: Nature Publishing Group
publist_id: '6108'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Atomic structure of the entire mammalian mitochondrial complex i
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 538
year: '2016'
...
---
_id: '1227'
abstract:
- lang: eng
  text: Many biological systems can be modeled as multiaffine hybrid systems. Due
    to the nonlinearity of multiaffine systems, it is difficult to verify their properties
    of interest directly. A common strategy to tackle this problem is to construct
    and analyze a discrete overapproximation of the original system. However, the
    conservativeness of a discrete abstraction significantly determines the level
    of confidence we can have in the properties of the original system. In this paper,
    in order to reduce the conservativeness of a discrete abstraction, we propose
    a new method based on a sufficient and necessary decision condition for computing
    discrete transitions between states in the abstract system. We assume the state
    space partition of a multiaffine system to be based on a set of multivariate polynomials.
    Hence, a rectangular partition defined in terms of polynomials of the form (xi
    − c) is just a simple case of multivariate polynomial partition, and the new decision
    condition applies naturally. We analyze and demonstrate the improvement of our
    method over the existing methods using some examples.
acknowledgement: This research was supported in part by the Austrian Science Fund
  (FWF) under grants S11402-N23, S11405-N23 and S11412-N23 (RiSE/SHiNE) and Z211-N23
  (Wittgenstein Award).
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Hui
  full_name: Kong, Hui
  id: 3BDE25AA-F248-11E8-B48F-1D18A9856A87
  last_name: Kong
  orcid: 0000-0002-3066-6941
- first_name: Ezio
  full_name: Bartocci, Ezio
  last_name: Bartocci
- first_name: Sergiy
  full_name: Bogomolov, Sergiy
  id: 369D9A44-F248-11E8-B48F-1D18A9856A87
  last_name: Bogomolov
  orcid: 0000-0002-0686-0365
- first_name: Radu
  full_name: Grosu, Radu
  last_name: Grosu
- 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: Yu
  full_name: Jiang, Yu
  last_name: Jiang
- first_name: Christian
  full_name: Schilling, Christian
  id: 3A2F4DCE-F248-11E8-B48F-1D18A9856A87
  last_name: Schilling
  orcid: 0000-0003-3658-1065
citation:
  ama: 'Kong H, Bartocci E, Bogomolov S, et al. Discrete abstraction of multiaffine
    systems. In: Vol 9957. Springer; 2016:128-144. doi:<a href="https://doi.org/10.1007/978-3-319-47151-8_9">10.1007/978-3-319-47151-8_9</a>'
  apa: 'Kong, H., Bartocci, E., Bogomolov, S., Grosu, R., Henzinger, T. A., Jiang,
    Y., &#38; Schilling, C. (2016). Discrete abstraction of multiaffine systems (Vol.
    9957, pp. 128–144). Presented at the HSB: Hybrid Systems Biology, Grenoble, France:
    Springer. <a href="https://doi.org/10.1007/978-3-319-47151-8_9">https://doi.org/10.1007/978-3-319-47151-8_9</a>'
  chicago: Kong, Hui, Ezio Bartocci, Sergiy Bogomolov, Radu Grosu, Thomas A Henzinger,
    Yu Jiang, and Christian Schilling. “Discrete Abstraction of Multiaffine Systems,”
    9957:128–44. Springer, 2016. <a href="https://doi.org/10.1007/978-3-319-47151-8_9">https://doi.org/10.1007/978-3-319-47151-8_9</a>.
  ieee: 'H. Kong <i>et al.</i>, “Discrete abstraction of multiaffine systems,” presented
    at the HSB: Hybrid Systems Biology, Grenoble, France, 2016, vol. 9957, pp. 128–144.'
  ista: 'Kong H, Bartocci E, Bogomolov S, Grosu R, Henzinger TA, Jiang Y, Schilling
    C. 2016. Discrete abstraction of multiaffine systems. HSB: Hybrid Systems Biology,
    LNCS, vol. 9957, 128–144.'
  mla: Kong, Hui, et al. <i>Discrete Abstraction of Multiaffine Systems</i>. Vol.
    9957, Springer, 2016, pp. 128–44, doi:<a href="https://doi.org/10.1007/978-3-319-47151-8_9">10.1007/978-3-319-47151-8_9</a>.
  short: H. Kong, E. Bartocci, S. Bogomolov, R. Grosu, T.A. Henzinger, Y. Jiang, C.
    Schilling, in:, Springer, 2016, pp. 128–144.
conference:
  end_date: 2016-10-21
  location: Grenoble, France
  name: 'HSB: Hybrid Systems Biology'
  start_date: 2016-10-20
date_created: 2018-12-11T11:50:49Z
date_published: 2016-09-25T00:00:00Z
date_updated: 2025-09-22T09:24:50Z
day: '25'
ddc:
- '005'
department:
- _id: ToHe
doi: 10.1007/978-3-319-47151-8_9
external_id:
  isi:
  - '000389928100009'
file:
- access_level: open_access
  checksum: 994e164b558c47bacf8dc066dd27c8fc
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:10:49Z
  date_updated: 2020-07-14T12:44:39Z
  file_id: '4840'
  file_name: IST-2017-781-v1+1_main.pdf
  file_size: 683955
  relation: main_file
file_date_updated: 2020-07-14T12:44:39Z
has_accepted_license: '1'
intvolume: '      9957'
isi: 1
language:
- iso: eng
month: '09'
oa: 1
oa_version: Submitted Version
page: 128 - 144
project:
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
- _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: '6107'
pubrep_id: '781'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Discrete abstraction of multiaffine systems
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 9957
year: '2016'
...
---
_id: '1230'
abstract:
- lang: eng
  text: Concolic testing is a promising method for generating test suites for large
    programs. However, it suffers from the path-explosion problem and often fails
    to find tests that cover difficult-to-reach parts of programs. In contrast, model
    checkers based on counterexample-guided abstraction refinement explore programs
    exhaustively, while failing to scale on large programs with precision. In this
    paper, we present a novel method that iteratively combines concolic testing and
    model checking to find a test suite for a given coverage criterion. If concolic
    testing fails to cover some test goals, then the model checker refines its program
    abstraction to prove more paths infeasible, which reduces the search space for
    concolic testing. We have implemented our method on top of the concolictesting
    tool Crest and the model checker CpaChecker. We evaluated our tool on a collection
    of programs and a category of SvComp benchmarks. In our experiments, we observed
    an improvement in branch coverage compared to Crest from 48% to 63% in the best
    case, and from 66% to 71% on average.
acknowledgement: "We thank Andrey Kupriyanov for feedback on the manuscript,\r\nand
  Michael Tautschnig for help with preparing the experiments. This research was supported
  in part by the European Research Council (ERC) under grant 267989 (QUAREM) and by
  the Austrian Science Fund (FWF) under grants S11402-N23 (RiSE) and Z211-N23 (Wittgenstein
  Award)."
alternative_title:
- LNCS
article_processing_charge: No
arxiv: 1
author:
- first_name: Przemyslaw
  full_name: Daca, Przemyslaw
  id: 49351290-F248-11E8-B48F-1D18A9856A87
  last_name: Daca
- first_name: Ashutosh
  full_name: Gupta, Ashutosh
  id: 335E5684-F248-11E8-B48F-1D18A9856A87
  last_name: Gupta
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
citation:
  ama: 'Daca P, Gupta A, Henzinger TA. Abstraction-driven concolic testing. In: Vol
    9583. Springer; 2016:328-347. doi:<a href="https://doi.org/10.1007/978-3-662-49122-5_16">10.1007/978-3-662-49122-5_16</a>'
  apa: 'Daca, P., Gupta, A., &#38; Henzinger, T. A. (2016). Abstraction-driven concolic
    testing (Vol. 9583, pp. 328–347). Presented at the VMCAI: Verification, Model
    Checking and Abstract Interpretation, St. Petersburg, FL, USA: Springer. <a href="https://doi.org/10.1007/978-3-662-49122-5_16">https://doi.org/10.1007/978-3-662-49122-5_16</a>'
  chicago: Daca, Przemyslaw, Ashutosh Gupta, and Thomas A Henzinger. “Abstraction-Driven
    Concolic Testing,” 9583:328–47. Springer, 2016. <a href="https://doi.org/10.1007/978-3-662-49122-5_16">https://doi.org/10.1007/978-3-662-49122-5_16</a>.
  ieee: 'P. Daca, A. Gupta, and T. A. Henzinger, “Abstraction-driven concolic testing,”
    presented at the VMCAI: Verification, Model Checking and Abstract Interpretation,
    St. Petersburg, FL, USA, 2016, vol. 9583, pp. 328–347.'
  ista: 'Daca P, Gupta A, Henzinger TA. 2016. Abstraction-driven concolic testing.
    VMCAI: Verification, Model Checking and Abstract Interpretation, LNCS, vol. 9583,
    328–347.'
  mla: Daca, Przemyslaw, et al. <i>Abstraction-Driven Concolic Testing</i>. Vol. 9583,
    Springer, 2016, pp. 328–47, doi:<a href="https://doi.org/10.1007/978-3-662-49122-5_16">10.1007/978-3-662-49122-5_16</a>.
  short: P. Daca, A. Gupta, T.A. Henzinger, in:, Springer, 2016, pp. 328–347.
conference:
  end_date: 2016-01-19
  location: St. Petersburg, FL, USA
  name: 'VMCAI: Verification, Model Checking and Abstract Interpretation'
  start_date: 2016-01-17
date_created: 2018-12-11T11:50:50Z
date_published: 2016-01-01T00:00:00Z
date_updated: 2026-04-15T10:02:12Z
day: '01'
department:
- _id: ToHe
doi: 10.1007/978-3-662-49122-5_16
ec_funded: 1
external_id:
  arxiv:
  - '1511.02615'
  isi:
  - '000375148800016'
intvolume: '      9583'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1511.02615
month: '01'
oa: 1
oa_version: Preprint
page: 328 - 347
project:
- _id: 25EE3708-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '267989'
  name: Quantitative Reactive Modeling
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
- _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: '6104'
quality_controlled: '1'
related_material:
  record:
  - id: '1155'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Abstraction-driven concolic testing
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 9583
year: '2016'
...
---
_id: '1231'
abstract:
- lang: eng
  text: 'We study the time-and memory-complexities of the problem of computing labels
    of (multiple) randomly selected challenge-nodes in a directed acyclic graph. The
    w-bit label of a node is the hash of the labels of its parents, and the hash function
    is modeled as a random oracle. Specific instances of this problem underlie both
    proofs of space [Dziembowski et al. CRYPTO’15] as well as popular memory-hard
    functions like scrypt. As our main tool, we introduce the new notion of a probabilistic
    parallel entangled pebbling game, a new type of combinatorial pebbling game on
    a graph, which is closely related to the labeling game on the same graph. As a
    first application of our framework, we prove that for scrypt, when the underlying
    hash function is invoked n times, the cumulative memory complexity (CMC) (a notion
    recently introduced by Alwen and Serbinenko (STOC’15) to capture amortized memory-hardness
    for parallel adversaries) is at least Ω(w · (n/ log(n))2). This bound holds for
    adversaries that can store many natural functions of the labels (e.g., linear
    combinations), but still not arbitrary functions thereof. We then introduce and
    study a combinatorial quantity, and show how a sufficiently small upper bound
    on it (which we conjecture) extends our CMC bound for scrypt to hold against arbitrary
    adversaries. We also show that such an upper bound solves the main open problem
    for proofs-of-space protocols: namely, establishing that the time complexity of
    computing the label of a random node in a graph on n nodes (given an initial kw-bit
    state) reduces tightly to the time complexity for black pebbling on the same graph
    (given an initial k-node pebbling).'
acknowledgement: "Joël Alwen, Chethan Kamath, and Krzysztof Pietrzak’s research is
  partially supported by an ERC starting grant (259668-PSPC). Vladimir Kolmogorov
  is partially supported by an ERC consolidator grant (616160-DOICV). Binyi Chen was
  partially supported by NSF grants CNS-1423566 and CNS-1514526, and a gift from the
  Gareatis Foundation. Stefano Tessaro was partially supported by NSF grants CNS-1423566,
  CNS-1528178, a Hellman Fellowship, and the Glen and Susanne Culler Chair.\r\n\r\nThis
  work was done in part while the authors were visiting the Simons Institute for the
  Theory of Computing, supported by the Simons Foundation and by the DIMACS/Simons
  Collaboration in Cryptography through NSF grant CNS-1523467."
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: Binyi
  full_name: Chen, Binyi
  last_name: Chen
- first_name: Chethan
  full_name: Kamath Hosdurg, Chethan
  id: 4BD3F30E-F248-11E8-B48F-1D18A9856A87
  last_name: Kamath Hosdurg
- first_name: Vladimir
  full_name: Kolmogorov, Vladimir
  id: 3D50B0BA-F248-11E8-B48F-1D18A9856A87
  last_name: Kolmogorov
- first_name: Krzysztof Z
  full_name: Pietrzak, Krzysztof Z
  id: 3E04A7AA-F248-11E8-B48F-1D18A9856A87
  last_name: Pietrzak
  orcid: 0000-0002-9139-1654
- first_name: Stefano
  full_name: Tessaro, Stefano
  last_name: Tessaro
citation:
  ama: 'Alwen JF, Chen B, Kamath Hosdurg C, Kolmogorov V, Pietrzak KZ, Tessaro S.
    On the complexity of scrypt and proofs of space in the parallel random oracle
    model. In: Vol 9666. Springer; 2016:358-387. doi:<a href="https://doi.org/10.1007/978-3-662-49896-5_13">10.1007/978-3-662-49896-5_13</a>'
  apa: 'Alwen, J. F., Chen, B., Kamath Hosdurg, C., Kolmogorov, V., Pietrzak, K. Z.,
    &#38; Tessaro, S. (2016). On the complexity of scrypt and proofs of space in the
    parallel random oracle model (Vol. 9666, pp. 358–387). Presented at the EUROCRYPT:
    Theory and Applications of Cryptographic Techniques, Vienna, Austria: Springer.
    <a href="https://doi.org/10.1007/978-3-662-49896-5_13">https://doi.org/10.1007/978-3-662-49896-5_13</a>'
  chicago: Alwen, Joel F, Binyi Chen, Chethan Kamath Hosdurg, Vladimir Kolmogorov,
    Krzysztof Z Pietrzak, and Stefano Tessaro. “On the Complexity of Scrypt and Proofs
    of Space in the Parallel Random Oracle Model,” 9666:358–87. Springer, 2016. <a
    href="https://doi.org/10.1007/978-3-662-49896-5_13">https://doi.org/10.1007/978-3-662-49896-5_13</a>.
  ieee: 'J. F. Alwen, B. Chen, C. Kamath Hosdurg, V. Kolmogorov, K. Z. Pietrzak, and
    S. Tessaro, “On the complexity of scrypt and proofs of space in the parallel random
    oracle model,” presented at the EUROCRYPT: Theory and Applications of Cryptographic
    Techniques, Vienna, Austria, 2016, vol. 9666, pp. 358–387.'
  ista: 'Alwen JF, Chen B, Kamath Hosdurg C, Kolmogorov V, Pietrzak KZ, Tessaro S.
    2016. On the complexity of scrypt and proofs of space in the parallel random oracle
    model. EUROCRYPT: Theory and Applications of Cryptographic Techniques, LNCS, vol.
    9666, 358–387.'
  mla: Alwen, Joel F., et al. <i>On the Complexity of Scrypt and Proofs of Space in
    the Parallel Random Oracle Model</i>. Vol. 9666, Springer, 2016, pp. 358–87, doi:<a
    href="https://doi.org/10.1007/978-3-662-49896-5_13">10.1007/978-3-662-49896-5_13</a>.
  short: J.F. Alwen, B. Chen, C. Kamath Hosdurg, V. Kolmogorov, K.Z. Pietrzak, S.
    Tessaro, in:, Springer, 2016, pp. 358–387.
conference:
  end_date: 2016-05-12
  location: Vienna, Austria
  name: 'EUROCRYPT: Theory and Applications of Cryptographic Techniques'
  start_date: 2016-05-08
date_created: 2018-12-11T11:50:51Z
date_published: 2016-04-28T00:00:00Z
date_updated: 2025-09-22T09:22:54Z
day: '28'
department:
- _id: KrPi
- _id: VlKo
doi: 10.1007/978-3-662-49896-5_13
ec_funded: 1
external_id:
  isi:
  - '000389727200013'
intvolume: '      9666'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://eprint.iacr.org/2016/100
month: '04'
oa: 1
oa_version: Submitted Version
page: 358 - 387
project:
- _id: 258C570E-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '259668'
  name: Provable Security for Physical Cryptography
- _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: Springer
publist_id: '6103'
quality_controlled: '1'
scopus_import: '1'
status: public
title: On the complexity of scrypt and proofs of space in the parallel random oracle
  model
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 9666
year: '2016'
...
---
_id: '1232'
abstract:
- lang: eng
  text: Mitochondrial electron transport chain complexes are organized into supercomplexes
    responsible for carrying out cellular respiration. Here we present three architectures
    of mammalian (ovine) supercomplexes determined by cryo-electron microscopy. We
    identify two distinct arrangements of supercomplex CICIII 2 CIV (the respirasome)
    - a major 'tight' form and a minor 'loose' form (resolved at the resolution of
    5.8 Å and 6.7 Å, respectively), which may represent different stages in supercomplex
    assembly or disassembly. We have also determined an architecture of supercomplex
    CICIII 2 at 7.8 Å resolution. All observed density can be attributed to the known
    80 subunits of the individual complexes, including 132 transmembrane helices.
    The individual complexes form tight interactions that vary between the architectures,
    with complex IV subunit COX7a switching contact from complex III to complex I.
    The arrangement of active sites within the supercomplex may help control reactive
    oxygen species production. To our knowledge, these are the first complete architectures
    of the dominant, physiologically relevant state of the electron transport chain.
acknowledgement: We thank the MRC LMB Cambridge for the use of the Titan Krios microscope.
  Data processing was performed using the IST high-performance computer cluster. J.A.L.
  holds a long-term fellowship from FEBS. K.F. is partially funded by a MRC UK PhD
  fellowship.
article_processing_charge: No
author:
- first_name: James A
  full_name: Letts, James A
  id: 322DA418-F248-11E8-B48F-1D18A9856A87
  last_name: Letts
  orcid: 0000-0002-9864-3586
- first_name: Karol
  full_name: Fiedorczuk, Karol
  id: 5BFF67CE-02D1-11E9-B11A-A5A4D7DFFFD0
  last_name: Fiedorczuk
- first_name: Leonid A
  full_name: Sazanov, Leonid A
  id: 338D39FE-F248-11E8-B48F-1D18A9856A87
  last_name: Sazanov
  orcid: 0000-0002-0977-7989
citation:
  ama: Letts JA, Fiedorczuk K, Sazanov LA. The architecture of respiratory supercomplexes.
    <i>Nature</i>. 2016;537(7622):644-648. doi:<a href="https://doi.org/10.1038/nature19774">10.1038/nature19774</a>
  apa: Letts, J. A., Fiedorczuk, K., &#38; Sazanov, L. A. (2016). The architecture
    of respiratory supercomplexes. <i>Nature</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/nature19774">https://doi.org/10.1038/nature19774</a>
  chicago: Letts, James A, Karol Fiedorczuk, and Leonid A Sazanov. “The Architecture
    of Respiratory Supercomplexes.” <i>Nature</i>. Nature Publishing Group, 2016.
    <a href="https://doi.org/10.1038/nature19774">https://doi.org/10.1038/nature19774</a>.
  ieee: J. A. Letts, K. Fiedorczuk, and L. A. Sazanov, “The architecture of respiratory
    supercomplexes,” <i>Nature</i>, vol. 537, no. 7622. Nature Publishing Group, pp.
    644–648, 2016.
  ista: Letts JA, Fiedorczuk K, Sazanov LA. 2016. The architecture of respiratory
    supercomplexes. Nature. 537(7622), 644–648.
  mla: Letts, James A., et al. “The Architecture of Respiratory Supercomplexes.” <i>Nature</i>,
    vol. 537, no. 7622, Nature Publishing Group, 2016, pp. 644–48, doi:<a href="https://doi.org/10.1038/nature19774">10.1038/nature19774</a>.
  short: J.A. Letts, K. Fiedorczuk, L.A. Sazanov, Nature 537 (2016) 644–648.
date_created: 2018-12-11T11:50:51Z
date_published: 2016-09-29T00:00:00Z
date_updated: 2025-09-22T09:22:23Z
day: '29'
department:
- _id: LeSa
doi: 10.1038/nature19774
external_id:
  isi:
  - '000384331700042'
intvolume: '       537'
isi: 1
issue: '7622'
language:
- iso: eng
month: '09'
oa_version: None
page: 644 - 648
project:
- _id: 2593EBD6-B435-11E9-9278-68D0E5697425
  name: Atomic-Resolution Structures of Mitochondrial Respiratory Chain Supercomplexes
publication: Nature
publication_status: published
publisher: Nature Publishing Group
publist_id: '6102'
quality_controlled: '1'
scopus_import: '1'
status: public
title: The architecture of respiratory supercomplexes
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 537
year: '2016'
...
---
_id: '1233'
abstract:
- lang: eng
  text: About three decades ago it was realized that implementing private channels
    between parties which can be adaptively corrupted requires an encryption scheme
    that is secure against selective opening attacks. Whether standard (IND-CPA) security
    implies security against selective opening attacks has been a major open question
    since. The only known reduction from selective opening to IND-CPA security loses
    an exponential factor. A polynomial reduction is only known for the very special
    case where the distribution considered in the selective opening security experiment
    is a product distribution, i.e., the messages are sampled independently from each
    other. In this paper we give a reduction whose loss is quantified via the dependence
    graph (where message dependencies correspond to edges) of the underlying message
    distribution. In particular, for some concrete distributions including Markov
    distributions, our reduction is polynomial.
acknowledgement: G. Fuchsbauer and K. Pietrzak are supported by the European Research
  Council, ERC Starting Grant (259668-PSPC). F. Heuer is funded by a Sofja Kovalevskaja
  Award of the Alexander von Humboldt Foundation and DFG SPP 1736, Algorithms for
  BIG DATA. E. Kiltz is supported by a Sofja Kovalevskaja Award of the Alexander von
  Humboldt Foundation, the German Israel Foundation, and ERC Project ERCC (FP7/615074).
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Georg
  full_name: Fuchsbauer, Georg
  id: 46B4C3EE-F248-11E8-B48F-1D18A9856A87
  last_name: Fuchsbauer
- first_name: Felix
  full_name: Heuer, Felix
  last_name: Heuer
- first_name: Eike
  full_name: Kiltz, Eike
  last_name: Kiltz
- 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: 'Fuchsbauer G, Heuer F, Kiltz E, Pietrzak KZ. Standard security does imply
    security against selective opening for markov distributions. In: Vol 9562. Springer;
    2016:282-305. doi:<a href="https://doi.org/10.1007/978-3-662-49096-9_12">10.1007/978-3-662-49096-9_12</a>'
  apa: 'Fuchsbauer, G., Heuer, F., Kiltz, E., &#38; Pietrzak, K. Z. (2016). Standard
    security does imply security against selective opening for markov distributions
    (Vol. 9562, pp. 282–305). Presented at the TCC: Theory of Cryptography Conference,
    Tel Aviv, Israel: Springer. <a href="https://doi.org/10.1007/978-3-662-49096-9_12">https://doi.org/10.1007/978-3-662-49096-9_12</a>'
  chicago: Fuchsbauer, Georg, Felix Heuer, Eike Kiltz, and Krzysztof Z Pietrzak. “Standard
    Security Does Imply Security against Selective Opening for Markov Distributions,”
    9562:282–305. Springer, 2016. <a href="https://doi.org/10.1007/978-3-662-49096-9_12">https://doi.org/10.1007/978-3-662-49096-9_12</a>.
  ieee: 'G. Fuchsbauer, F. Heuer, E. Kiltz, and K. Z. Pietrzak, “Standard security
    does imply security against selective opening for markov distributions,” presented
    at the TCC: Theory of Cryptography Conference, Tel Aviv, Israel, 2016, vol. 9562,
    pp. 282–305.'
  ista: 'Fuchsbauer G, Heuer F, Kiltz E, Pietrzak KZ. 2016. Standard security does
    imply security against selective opening for markov distributions. TCC: Theory
    of Cryptography Conference, LNCS, vol. 9562, 282–305.'
  mla: Fuchsbauer, Georg, et al. <i>Standard Security Does Imply Security against
    Selective Opening for Markov Distributions</i>. Vol. 9562, Springer, 2016, pp.
    282–305, doi:<a href="https://doi.org/10.1007/978-3-662-49096-9_12">10.1007/978-3-662-49096-9_12</a>.
  short: G. Fuchsbauer, F. Heuer, E. Kiltz, K.Z. Pietrzak, in:, Springer, 2016, pp.
    282–305.
conference:
  end_date: 2016-01-13
  location: Tel Aviv, Israel
  name: 'TCC: Theory of Cryptography Conference'
  start_date: 2016-01-10
date_created: 2018-12-11T11:50:51Z
date_published: 2016-01-01T00:00:00Z
date_updated: 2025-09-22T09:21:52Z
day: '01'
department:
- _id: KrPi
doi: 10.1007/978-3-662-49096-9_12
ec_funded: 1
external_id:
  isi:
  - '000376041100012'
intvolume: '      9562'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://eprint.iacr.org/2015/853
month: '01'
oa: 1
oa_version: Submitted Version
page: 282 - 305
project:
- _id: 258C570E-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '259668'
  name: Provable Security for Physical Cryptography
publication_status: published
publisher: Springer
publist_id: '6100'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Standard security does imply security against selective opening for markov
  distributions
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 9562
year: '2016'
...
---
_id: '1234'
abstract:
- lang: eng
  text: We present a new algorithm for the statistical model checking of Markov chains
    with respect to unbounded temporal properties, including full linear temporal
    logic. The main idea is that we monitor each simulation run on the fly, in order
    to detect quickly if a bottom strongly connected component is entered with high
    probability, in which case the simulation run can be terminated early. As a result,
    our simulation runs are often much shorter than required by termination bounds
    that are computed a priori for a desired level of confidence on a large state
    space. In comparison to previous algorithms for statistical model checking our
    method is not only faster in many cases but also requires less information about
    the system, namely, only the minimum transition probability that occurs in the
    Markov chain. In addition, our method can be generalised to unbounded quantitative
    properties such as mean-payoff bounds.
acknowledgement: "This research was funded in part by the European Research Council
  (ERC) under\r\ngrant  agreement  267989  (QUAREM),  the  Austrian  Science  Fund
  \ (FWF)  under\r\ngrants project S11402-N23 (RiSE) and Z211-N23 (Wittgenstein Award),
  the Peo-\r\nple Programme (Marie Curie Actions) of the European Union’s Seventh
  Framework\r\nProgramme (FP7/2007-2013) REA Grant No 291734, the SNSF Advanced Postdoc.\r\nMobility
  Fellowship – grant number P300P2\r\n161067, and the Czech Science Foun-\r\ndation
  under grant agreement P202/12/G061."
alternative_title:
- LNCS
article_processing_charge: No
arxiv: 1
author:
- first_name: Przemyslaw
  full_name: Daca, Przemyslaw
  id: 49351290-F248-11E8-B48F-1D18A9856A87
  last_name: Daca
- 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: Jan
  full_name: Kretinsky, Jan
  id: 44CEF464-F248-11E8-B48F-1D18A9856A87
  last_name: Kretinsky
  orcid: 0000-0002-8122-2881
- first_name: Tatjana
  full_name: Petrov, Tatjana
  id: 3D5811FC-F248-11E8-B48F-1D18A9856A87
  last_name: Petrov
  orcid: 0000-0002-9041-0905
citation:
  ama: 'Daca P, Henzinger TA, Kretinsky J, Petrov T. Faster statistical model checking
    for unbounded temporal properties. In: Vol 9636. Springer; 2016:112-129. doi:<a
    href="https://doi.org/10.1007/978-3-662-49674-9_7">10.1007/978-3-662-49674-9_7</a>'
  apa: 'Daca, P., Henzinger, T. A., Kretinsky, J., &#38; Petrov, T. (2016). Faster
    statistical model checking for unbounded temporal properties (Vol. 9636, pp. 112–129).
    Presented at the TACAS: Tools and Algorithms for the Construction and Analysis
    of Systems, Eindhoven, The Netherlands: Springer. <a href="https://doi.org/10.1007/978-3-662-49674-9_7">https://doi.org/10.1007/978-3-662-49674-9_7</a>'
  chicago: Daca, Przemyslaw, Thomas A Henzinger, Jan Kretinsky, and Tatjana Petrov.
    “Faster Statistical Model Checking for Unbounded Temporal Properties,” 9636:112–29.
    Springer, 2016. <a href="https://doi.org/10.1007/978-3-662-49674-9_7">https://doi.org/10.1007/978-3-662-49674-9_7</a>.
  ieee: 'P. Daca, T. A. Henzinger, J. Kretinsky, and T. Petrov, “Faster statistical
    model checking for unbounded temporal properties,” presented at the TACAS: Tools
    and Algorithms for the Construction and Analysis of Systems, Eindhoven, The Netherlands,
    2016, vol. 9636, pp. 112–129.'
  ista: 'Daca P, Henzinger TA, Kretinsky J, Petrov T. 2016. Faster statistical model
    checking for unbounded temporal properties. TACAS: Tools and Algorithms for the
    Construction and Analysis of Systems, LNCS, vol. 9636, 112–129.'
  mla: Daca, Przemyslaw, et al. <i>Faster Statistical Model Checking for Unbounded
    Temporal Properties</i>. Vol. 9636, Springer, 2016, pp. 112–29, doi:<a href="https://doi.org/10.1007/978-3-662-49674-9_7">10.1007/978-3-662-49674-9_7</a>.
  short: P. Daca, T.A. Henzinger, J. Kretinsky, T. Petrov, in:, Springer, 2016, pp.
    112–129.
conference:
  end_date: 2016-04-08
  location: Eindhoven, The Netherlands
  name: 'TACAS: Tools and Algorithms for the Construction and Analysis of Systems'
  start_date: 2016-04-02
date_created: 2018-12-11T11:50:51Z
date_published: 2016-01-01T00:00:00Z
date_updated: 2026-04-15T10:02:12Z
day: '01'
department:
- _id: ToHe
- _id: CaGu
doi: 10.1007/978-3-662-49674-9_7
ec_funded: 1
external_id:
  arxiv:
  - '1504.05739'
  isi:
  - '000406428000007'
intvolume: '      9636'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1504.05739
month: '01'
oa: 1
oa_version: Preprint
page: 112 - 129
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
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication_status: published
publisher: Springer
publist_id: '6099'
quality_controlled: '1'
related_material:
  record:
  - id: '471'
    relation: later_version
    status: public
  - id: '1155'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Faster statistical model checking for unbounded temporal properties
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 9636
year: '2016'
...
---
_id: '1237'
abstract:
- lang: eng
  text: 'Bitmap images of arbitrary dimension may be formally perceived as unions
    of m-dimensional boxes aligned with respect to a rectangular grid in ℝm. Cohomology
    and homology groups are well known topological invariants of such sets. Cohomological
    operations, such as the cup product, provide higher-order algebraic topological
    invariants, especially important for digital images of dimension higher than 3.
    If such an operation is determined at the level of simplicial chains [see e.g.
    González-Díaz, Real, Homology, Homotopy Appl, 2003, 83-93], then it is effectively
    computable. However, decomposing a cubical complex into a simplicial one deleteriously
    affects the efficiency of such an approach. In order to avoid this overhead, a
    direct cubical approach was applied in [Pilarczyk, Real, Adv. Comput. Math., 2015,
    253-275] for the cup product in cohomology, and implemented in the ChainCon software
    package [http://www.pawelpilarczyk.com/chaincon/]. We establish a formula for
    the Steenrod square operations [see Steenrod, Annals of Mathematics. Second Series,
    1947, 290-320] directly at the level of cubical chains, and we prove the correctness
    of this formula. An implementation of this formula is programmed in C++ within
    the ChainCon software framework. We provide a few examples and discuss the effectiveness
    of this approach. One specific application follows from the fact that Steenrod
    squares yield tests for the topological extension problem: Can a given map A →
    Sd to a sphere Sd be extended to a given super-complex X of A? In particular,
    the ROB-SAT problem, which is to decide for a given function f: X → ℝm and a value
    r &gt; 0 whether every g: X → ℝm with ∥g - f ∥∞ ≤ r has a root, reduces to the
    extension problem.'
acknowledgement: The research conducted by both authors has received funding from
  the People Programme (Marie Curie Actions) of the European Union’s Seventh Framework
  Programme (FP7/2007-2013) under REA grant agreements no. 291734 (for M. K.) and
  no. 622033 (for P. P.).
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Marek
  full_name: Krcál, Marek
  id: 33E21118-F248-11E8-B48F-1D18A9856A87
  last_name: Krcál
- first_name: Pawel
  full_name: Pilarczyk, Pawel
  id: 3768D56A-F248-11E8-B48F-1D18A9856A87
  last_name: Pilarczyk
citation:
  ama: 'Krcál M, Pilarczyk P. Computation of cubical Steenrod squares. In: Vol 9667.
    Springer; 2016:140-151. doi:<a href="https://doi.org/10.1007/978-3-319-39441-1_13">10.1007/978-3-319-39441-1_13</a>'
  apa: 'Krcál, M., &#38; Pilarczyk, P. (2016). Computation of cubical Steenrod squares
    (Vol. 9667, pp. 140–151). Presented at the CTIC: Computational Topology in Image
    Context, Marseille, France: Springer. <a href="https://doi.org/10.1007/978-3-319-39441-1_13">https://doi.org/10.1007/978-3-319-39441-1_13</a>'
  chicago: Krcál, Marek, and Pawel Pilarczyk. “Computation of Cubical Steenrod Squares,”
    9667:140–51. Springer, 2016. <a href="https://doi.org/10.1007/978-3-319-39441-1_13">https://doi.org/10.1007/978-3-319-39441-1_13</a>.
  ieee: 'M. Krcál and P. Pilarczyk, “Computation of cubical Steenrod squares,” presented
    at the CTIC: Computational Topology in Image Context, Marseille, France, 2016,
    vol. 9667, pp. 140–151.'
  ista: 'Krcál M, Pilarczyk P. 2016. Computation of cubical Steenrod squares. CTIC:
    Computational Topology in Image Context, LNCS, vol. 9667, 140–151.'
  mla: Krcál, Marek, and Pawel Pilarczyk. <i>Computation of Cubical Steenrod Squares</i>.
    Vol. 9667, Springer, 2016, pp. 140–51, doi:<a href="https://doi.org/10.1007/978-3-319-39441-1_13">10.1007/978-3-319-39441-1_13</a>.
  short: M. Krcál, P. Pilarczyk, in:, Springer, 2016, pp. 140–151.
conference:
  end_date: 2016-06-17
  location: Marseille, France
  name: 'CTIC: Computational Topology in Image Context'
  start_date: 2016-06-15
date_created: 2018-12-11T11:50:52Z
date_published: 2016-06-02T00:00:00Z
date_updated: 2025-09-22T09:19:17Z
day: '02'
department:
- _id: UlWa
- _id: HeEd
doi: 10.1007/978-3-319-39441-1_13
ec_funded: 1
external_id:
  isi:
  - '000389805800013'
intvolume: '      9667'
isi: 1
language:
- iso: eng
month: '06'
oa_version: None
page: 140 - 151
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
- _id: 255F06BE-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '622033'
  name: Persistent Homology - Images, Data and Maps
publication_status: published
publisher: Springer
publist_id: '6096'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Computation of cubical Steenrod squares
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 9667
year: '2016'
...
---
_id: '1238'
abstract:
- lang: eng
  text: The dynamic localization of endosomal compartments labeled with targeted fluorescent
    protein tags is routinely followed by time lapse fluorescence microscopy approaches
    and single particle tracking algorithms. In this way trajectories of individual
    endosomes can be mapped and linked to physiological processes as cell growth.
    However, other aspects of dynamic behavior including endosomal interactions are
    difficult to follow in this manner. Therefore, we characterized the localization
    and dynamic properties of early and late endosomes throughout the entire course
    of root hair formation by means of spinning disc time lapse imaging and post-acquisition
    automated multitracking and quantitative analysis. Our results show differential
    motile behavior of early and late endosomes and interactions of late endosomes
    that may be specified to particular root hair domains. Detailed data analysis
    revealed a particular transient interaction between late endosomes—termed herein
    as dancing-endosomes—which is not concluding to vesicular fusion. Endosomes preferentially
    located in the root hair tip interacted as dancing-endosomes and traveled short
    distances during this interaction. Finally, sizes of early and late endosomes
    were addressed by means of super-resolution structured illumination microscopy
    (SIM) to corroborate measurements on the spinning disc. This is a first study
    providing quantitative microscopic data on dynamic spatio-temporal interactions
    of endosomes during root hair tip growth.
acknowledgement: "This work was supported by National Program for Sustainability I
  (grant no. LO1204) provided by the Czech Ministry of Education and by Institutional
  Fund of Palacký University Olomouc (GK and OŠ).\r\nWe thank Sabine Fischer for help
  with the statistics."
article_number: '1262'
article_processing_charge: No
author:
- first_name: Daniel
  full_name: Von Wangenheim, Daniel
  id: 49E91952-F248-11E8-B48F-1D18A9856A87
  last_name: Von Wangenheim
  orcid: 0000-0002-6862-1247
- first_name: Amparo
  full_name: Rosero, Amparo
  last_name: Rosero
- first_name: George
  full_name: Komis, George
  last_name: Komis
- first_name: Olga
  full_name: Šamajová, Olga
  last_name: Šamajová
- first_name: Miroslav
  full_name: Ovečka, Miroslav
  last_name: Ovečka
- first_name: Boris
  full_name: Voigt, Boris
  last_name: Voigt
- first_name: Jozef
  full_name: Šamaj, Jozef
  last_name: Šamaj
citation:
  ama: von Wangenheim D, Rosero A, Komis G, et al. Endosomal interactions during root
    hair growth. <i>Frontiers in Plant Science</i>. 2016;6(JAN2016). doi:<a href="https://doi.org/10.3389/fpls.2015.01262">10.3389/fpls.2015.01262</a>
  apa: von Wangenheim, D., Rosero, A., Komis, G., Šamajová, O., Ovečka, M., Voigt,
    B., &#38; Šamaj, J. (2016). Endosomal interactions during root hair growth. <i>Frontiers
    in Plant Science</i>. Frontiers Research Foundation. <a href="https://doi.org/10.3389/fpls.2015.01262">https://doi.org/10.3389/fpls.2015.01262</a>
  chicago: Wangenheim, Daniel von, Amparo Rosero, George Komis, Olga Šamajová, Miroslav
    Ovečka, Boris Voigt, and Jozef Šamaj. “Endosomal Interactions during Root Hair
    Growth.” <i>Frontiers in Plant Science</i>. Frontiers Research Foundation, 2016.
    <a href="https://doi.org/10.3389/fpls.2015.01262">https://doi.org/10.3389/fpls.2015.01262</a>.
  ieee: D. von Wangenheim <i>et al.</i>, “Endosomal interactions during root hair
    growth,” <i>Frontiers in Plant Science</i>, vol. 6, no. JAN2016. Frontiers Research
    Foundation, 2016.
  ista: von Wangenheim D, Rosero A, Komis G, Šamajová O, Ovečka M, Voigt B, Šamaj
    J. 2016. Endosomal interactions during root hair growth. Frontiers in Plant Science.
    6(JAN2016), 1262.
  mla: von Wangenheim, Daniel, et al. “Endosomal Interactions during Root Hair Growth.”
    <i>Frontiers in Plant Science</i>, vol. 6, no. JAN2016, 1262, Frontiers Research
    Foundation, 2016, doi:<a href="https://doi.org/10.3389/fpls.2015.01262">10.3389/fpls.2015.01262</a>.
  short: D. von Wangenheim, A. Rosero, G. Komis, O. Šamajová, M. Ovečka, B. Voigt,
    J. Šamaj, Frontiers in Plant Science 6 (2016).
date_created: 2018-12-11T11:50:53Z
date_published: 2016-01-29T00:00:00Z
date_updated: 2025-09-22T09:18:11Z
day: '29'
ddc:
- '581'
department:
- _id: JiFr
doi: 10.3389/fpls.2015.01262
external_id:
  isi:
  - '000368891500001'
file:
- access_level: open_access
  checksum: 3127eab844d53564bf47e2b6b42f1ca0
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:09:36Z
  date_updated: 2020-07-14T12:44:41Z
  file_id: '4760'
  file_name: IST-2016-710-v1+1_fpls-06-01262.pdf
  file_size: 1640550
  relation: main_file
file_date_updated: 2020-07-14T12:44:41Z
has_accepted_license: '1'
intvolume: '         6'
isi: 1
issue: JAN2016
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
publication: Frontiers in Plant Science
publication_status: published
publisher: Frontiers Research Foundation
publist_id: '6094'
pubrep_id: '710'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Endosomal interactions during root hair growth
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: '2016'
...
---
_id: '1239'
abstract:
- lang: eng
  text: Nonadherent polarized cells have been observed to have a pearlike, elongated
    shape. Using a minimal model that describes the cell cortex as a thin layer of
    contractile active gel, we show that the anisotropy of active stresses, controlled
    by cortical viscosity and filament ordering, can account for this morphology.
    The predicted shapes can be determined from the flow pattern only; they prove
    to be independent of the mechanism at the origin of the cortical flow, and are
    only weakly sensitive to the cytoplasmic rheology. In the case of actin flows
    resulting from a contractile instability, we propose a phase diagram of three-dimensional
    cell shapes that encompasses nonpolarized spherical, elongated, as well as oblate
    shapes, all of which have been observed in experiment.
acknowledgement: 'V. R. acknowledges support by the Austrian Science Fund (FWF): (Grant
  No. T560-B17).'
article_number: '028102'
article_processing_charge: No
author:
- first_name: Andrew
  full_name: Callan Jones, Andrew
  last_name: Callan Jones
- first_name: Verena
  full_name: Ruprecht, Verena
  id: 4D71A03A-F248-11E8-B48F-1D18A9856A87
  last_name: Ruprecht
  orcid: 0000-0003-4088-8633
- first_name: Stefan
  full_name: Wieser, Stefan
  id: 355AA5A0-F248-11E8-B48F-1D18A9856A87
  last_name: Wieser
  orcid: 0000-0002-2670-2217
- first_name: Carl-Philipp J
  full_name: Heisenberg, Carl-Philipp J
  id: 39427864-F248-11E8-B48F-1D18A9856A87
  last_name: Heisenberg
  orcid: 0000-0002-0912-4566
- first_name: Raphaël
  full_name: Voituriez, Raphaël
  last_name: Voituriez
citation:
  ama: Callan Jones A, Ruprecht V, Wieser S, Heisenberg C-PJ, Voituriez R. Cortical
    flow-driven shapes of nonadherent cells. <i>Physical Review Letters</i>. 2016;116(2).
    doi:<a href="https://doi.org/10.1103/PhysRevLett.116.028102">10.1103/PhysRevLett.116.028102</a>
  apa: Callan Jones, A., Ruprecht, V., Wieser, S., Heisenberg, C.-P. J., &#38; Voituriez,
    R. (2016). Cortical flow-driven shapes of nonadherent cells. <i>Physical Review
    Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevLett.116.028102">https://doi.org/10.1103/PhysRevLett.116.028102</a>
  chicago: Callan Jones, Andrew, Verena Ruprecht, Stefan Wieser, Carl-Philipp J Heisenberg,
    and Raphaël Voituriez. “Cortical Flow-Driven Shapes of Nonadherent Cells.” <i>Physical
    Review Letters</i>. American Physical Society, 2016. <a href="https://doi.org/10.1103/PhysRevLett.116.028102">https://doi.org/10.1103/PhysRevLett.116.028102</a>.
  ieee: A. Callan Jones, V. Ruprecht, S. Wieser, C.-P. J. Heisenberg, and R. Voituriez,
    “Cortical flow-driven shapes of nonadherent cells,” <i>Physical Review Letters</i>,
    vol. 116, no. 2. American Physical Society, 2016.
  ista: Callan Jones A, Ruprecht V, Wieser S, Heisenberg C-PJ, Voituriez R. 2016.
    Cortical flow-driven shapes of nonadherent cells. Physical Review Letters. 116(2),
    028102.
  mla: Callan Jones, Andrew, et al. “Cortical Flow-Driven Shapes of Nonadherent Cells.”
    <i>Physical Review Letters</i>, vol. 116, no. 2, 028102, American Physical Society,
    2016, doi:<a href="https://doi.org/10.1103/PhysRevLett.116.028102">10.1103/PhysRevLett.116.028102</a>.
  short: A. Callan Jones, V. Ruprecht, S. Wieser, C.-P.J. Heisenberg, R. Voituriez,
    Physical Review Letters 116 (2016).
date_created: 2018-12-11T11:50:53Z
date_published: 2016-01-15T00:00:00Z
date_updated: 2025-09-22T09:18:45Z
day: '15'
department:
- _id: CaHe
doi: 10.1103/PhysRevLett.116.028102
external_id:
  isi:
  - '000368286300022'
intvolume: '       116'
isi: 1
issue: '2'
language:
- iso: eng
month: '01'
oa_version: None
project:
- _id: 2529486C-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: T 560-B17
  name: Cell- and Tissue Mechanics in Zebrafish Germ Layer Formation
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '6095'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Cortical flow-driven shapes of nonadherent cells
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 116
year: '2016'
...
---
_id: '1240'
abstract:
- lang: eng
  text: 'Background: Long non-coding RNAs (lncRNAs) are increasingly implicated as
    gene regulators and may ultimately be more numerous than protein-coding genes
    in the human genome. Despite large numbers of reported lncRNAs, reference annotations
    are likely incomplete due to their lower and tighter tissue-specific expression
    compared to mRNAs. An unexplored factor potentially confounding lncRNA identification
    is inter-individual expression variability. Here, we characterize lncRNA natural
    expression variability in human primary granulocytes. Results: We annotate granulocyte
    lncRNAs and mRNAs in RNA-seq data from 10 healthy individuals, identifying multiple
    lncRNAs absent from reference annotations, and use this to investigate three known
    features (higher tissue-specificity, lower expression, and reduced splicing efficiency)
    of lncRNAs relative to mRNAs. Expression variability was examined in seven individuals
    sampled three times at 1- or more than 1-month intervals. We show that lncRNAs
    display significantly more inter-individual expression variability compared to
    mRNAs. We confirm this finding in two independent human datasets by analyzing
    multiple tissues from the GTEx project and lymphoblastoid cell lines from the
    GEUVADIS project. Using the latter dataset we also show that including more human
    donors into the transcriptome annotation pipeline allows identification of an
    increasing number of lncRNAs, but minimally affects mRNA gene number. Conclusions:
    A comprehensive annotation of lncRNAs is known to require an approach that is
    sensitive to low and tight tissue-specific expression. Here we show that increased
    inter-individual expression variability is an additional general lncRNA feature
    to consider when creating a comprehensive annotation of human lncRNAs or proposing
    their use as prognostic or disease markers.'
acknowledgement: "This study was partly funded by the Austrian Science Fund (FWF F43-B09,
  FWF W1207-B09). PMG is a recipient of a DOC Fellowship of the Austrian Academy of
  Sciences.\r\nWe thank Ruth Klement, Tomasz Kulinski, Elisangela Valente, Elisabeth
  Salzer,\r\nand Roland Jäger for technical/bioinformatic assistance and advice, the
  CeMM\r\nIT department and José Manuel Molero for help and advice on software usage,\r\nthe
  Biomedical Sequencing Facility (http://biomedical-sequencing.at/) for\r\nsequencing
  and advice, Jacques Colinge, Daniel Andergassen, and Tomasz\r\nKulinski for discussions,
  Quanah Hudson and Jörg Menche for reading and\r\ncommenting on the manuscript."
article_number: '14'
article_processing_charge: No
author:
- first_name: Aleksandra
  full_name: Kornienko, Aleksandra
  last_name: Kornienko
- first_name: Christoph
  full_name: Dotter, Christoph
  id: 4C66542E-F248-11E8-B48F-1D18A9856A87
  last_name: Dotter
  orcid: 0000-0002-9033-9096
- first_name: Philipp
  full_name: Guenzl, Philipp
  last_name: Guenzl
- first_name: Heinz
  full_name: Gisslinger, Heinz
  last_name: Gisslinger
- first_name: Bettina
  full_name: Gisslinger, Bettina
  last_name: Gisslinger
- first_name: Ciara
  full_name: Cleary, Ciara
  last_name: Cleary
- first_name: Robert
  full_name: Kralovics, Robert
  last_name: Kralovics
- first_name: Florian
  full_name: Pauler, Florian
  id: 48EA0138-F248-11E8-B48F-1D18A9856A87
  last_name: Pauler
  orcid: 0000-0002-7462-0048
- first_name: Denise
  full_name: Barlow, Denise
  last_name: Barlow
citation:
  ama: Kornienko A, Dotter C, Guenzl P, et al. Long non-coding RNAs display higher
    natural expression variation than protein-coding genes in healthy humans. <i>Genome
    Biology</i>. 2016;17(1). doi:<a href="https://doi.org/10.1186/s13059-016-0873-8">10.1186/s13059-016-0873-8</a>
  apa: Kornienko, A., Dotter, C., Guenzl, P., Gisslinger, H., Gisslinger, B., Cleary,
    C., … Barlow, D. (2016). Long non-coding RNAs display higher natural expression
    variation than protein-coding genes in healthy humans. <i>Genome Biology</i>.
    BioMed Central. <a href="https://doi.org/10.1186/s13059-016-0873-8">https://doi.org/10.1186/s13059-016-0873-8</a>
  chicago: Kornienko, Aleksandra, Christoph Dotter, Philipp Guenzl, Heinz Gisslinger,
    Bettina Gisslinger, Ciara Cleary, Robert Kralovics, Florian Pauler, and Denise
    Barlow. “Long Non-Coding RNAs Display Higher Natural Expression Variation than
    Protein-Coding Genes in Healthy Humans.” <i>Genome Biology</i>. BioMed Central,
    2016. <a href="https://doi.org/10.1186/s13059-016-0873-8">https://doi.org/10.1186/s13059-016-0873-8</a>.
  ieee: A. Kornienko <i>et al.</i>, “Long non-coding RNAs display higher natural expression
    variation than protein-coding genes in healthy humans,” <i>Genome Biology</i>,
    vol. 17, no. 1. BioMed Central, 2016.
  ista: Kornienko A, Dotter C, Guenzl P, Gisslinger H, Gisslinger B, Cleary C, Kralovics
    R, Pauler F, Barlow D. 2016. Long non-coding RNAs display higher natural expression
    variation than protein-coding genes in healthy humans. Genome Biology. 17(1),
    14.
  mla: Kornienko, Aleksandra, et al. “Long Non-Coding RNAs Display Higher Natural
    Expression Variation than Protein-Coding Genes in Healthy Humans.” <i>Genome Biology</i>,
    vol. 17, no. 1, 14, BioMed Central, 2016, doi:<a href="https://doi.org/10.1186/s13059-016-0873-8">10.1186/s13059-016-0873-8</a>.
  short: A. Kornienko, C. Dotter, P. Guenzl, H. Gisslinger, B. Gisslinger, C. Cleary,
    R. Kralovics, F. Pauler, D. Barlow, Genome Biology 17 (2016).
date_created: 2018-12-11T11:50:53Z
date_published: 2016-01-29T00:00:00Z
date_updated: 2025-09-22T09:17:40Z
day: '29'
ddc:
- '576'
department:
- _id: GaNo
doi: 10.1186/s13059-016-0873-8
external_id:
  isi:
  - '000368904100001'
file:
- access_level: open_access
  checksum: a268beee1a690801c83ec6729f9ebc5b
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:10:05Z
  date_updated: 2020-07-14T12:44:41Z
  file_id: '4789'
  file_name: IST-2016-709-v1+1_s13059-016-0873-8.pdf
  file_size: 2914601
  relation: main_file
file_date_updated: 2020-07-14T12:44:41Z
has_accepted_license: '1'
intvolume: '        17'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
publication: Genome Biology
publication_status: published
publisher: BioMed Central
publist_id: '6093'
pubrep_id: '709'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Long non-coding RNAs display higher natural expression variation than protein-coding
  genes in healthy humans
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: 17
year: '2016'
...
---
_id: '1241'
abstract:
- lang: eng
  text: 'How likely is it that a population escapes extinction through adaptive evolution?
    The answer to this question is of great relevance in conservation biology, where
    we aim at species’ rescue and the maintenance of biodiversity, and in agriculture
    and medicine, where we seek to hamper the emergence of pesticide or drug resistance.
    By reshuffling the genome, recombination has two antagonistic effects on the probability
    of evolutionary rescue: It generates and it breaks up favorable gene combinations.
    Which of the two effects prevails depends on the fitness effects of mutations
    and on the impact of stochasticity on the allele frequencies. In this article,
    we analyze a mathematical model for rescue after a sudden environmental change
    when adaptation is contingent on mutations at two loci. The analysis reveals a
    complex nonlinear dependence of population survival on recombination. We moreover
    find that, counterintuitively, a fast eradication of the wild type can promote
    rescue in the presence of recombination. The model also shows that two-step rescue
    is not unlikely to happen and can even be more likely than single-step rescue
    (where adaptation relies on a single mutation), depending on the circumstances.'
acknowledgement: This work was made possible by a “For Women in Science” fellowship
  (L’Oréal Österreich in cooperation with the Austrian Commission for the United Nations
  Educational, Scientific, and Cultural Organization and the Austrian Academy of Sciences
  with financial support from the Federal Ministry for Science and Research Austria)
  and European Research Council grant 250152 (to Nick Barton).
article_processing_charge: No
author:
- first_name: Hildegard
  full_name: Uecker, Hildegard
  id: 2DB8F68A-F248-11E8-B48F-1D18A9856A87
  last_name: Uecker
  orcid: 0000-0001-9435-2813
- first_name: Joachim
  full_name: Hermisson, Joachim
  last_name: Hermisson
biorxivid: 1
citation:
  ama: Uecker H, Hermisson J. The role of recombination in evolutionary rescue. <i>Genetics</i>.
    2016;202(2):721-732. doi:<a href="https://doi.org/10.1534/genetics.115.180299">10.1534/genetics.115.180299</a>
  apa: Uecker, H., &#38; Hermisson, J. (2016). The role of recombination in evolutionary
    rescue. <i>Genetics</i>. Genetics Society of America. <a href="https://doi.org/10.1534/genetics.115.180299">https://doi.org/10.1534/genetics.115.180299</a>
  chicago: Uecker, Hildegard, and Joachim Hermisson. “The Role of Recombination in
    Evolutionary Rescue.” <i>Genetics</i>. Genetics Society of America, 2016. <a href="https://doi.org/10.1534/genetics.115.180299">https://doi.org/10.1534/genetics.115.180299</a>.
  ieee: H. Uecker and J. Hermisson, “The role of recombination in evolutionary rescue,”
    <i>Genetics</i>, vol. 202, no. 2. Genetics Society of America, pp. 721–732, 2016.
  ista: Uecker H, Hermisson J. 2016. The role of recombination in evolutionary rescue.
    Genetics. 202(2), 721–732.
  mla: Uecker, Hildegard, and Joachim Hermisson. “The Role of Recombination in Evolutionary
    Rescue.” <i>Genetics</i>, vol. 202, no. 2, Genetics Society of America, 2016,
    pp. 721–32, doi:<a href="https://doi.org/10.1534/genetics.115.180299">10.1534/genetics.115.180299</a>.
  short: H. Uecker, J. Hermisson, Genetics 202 (2016) 721–732.
das_tickbox: '1'
date_created: 2018-12-11T11:50:54Z
date_published: 2016-02-01T00:00:00Z
date_updated: 2026-06-22T14:07:01Z
day: '01'
department:
- _id: NiBa
doi: 10.1534/genetics.115.180299
ec_funded: 1
external_id:
  biorxivid:
  - 10.1101/022020
  isi:
  - '000371304600028'
intvolume: '       202'
isi: 1
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/022020
month: '02'
oa: 1
oa_version: Preprint
page: 721 - 732
project:
- _id: 25B07788-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '250152'
  name: Limits to selection in biology and in evolutionary computation
- _id: 25B67606-B435-11E9-9278-68D0E5697425
  name: Evolutionary rescue
publication: Genetics
publication_status: published
publisher: Genetics Society of America
publist_id: '6091'
quality_controlled: '1'
scopus_import: '1'
status: public
title: The role of recombination in evolutionary rescue
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 202
year: '2016'
...
---
_id: '1243'
abstract:
- lang: eng
  text: Restriction-modification (RM) systems represent a minimal and ubiquitous biological
    system of self/non-self discrimination in prokaryotes [1], which protects hosts
    from exogenous DNA [2]. The mechanism is based on the balance between methyltransferase
    (M) and cognate restriction endonuclease (R). M tags endogenous DNA as self by
    methylating short specific DNA sequences called restriction sites, whereas R recognizes
    unmethylated restriction sites as non-self and introduces a double-stranded DNA
    break [3]. Restriction sites are significantly underrepresented in prokaryotic
    genomes [4-7], suggesting that the discrimination mechanism is imperfect and occasionally
    leads to autoimmunity due to self-DNA cleavage (self-restriction) [8]. Furthermore,
    RM systems can promote DNA recombination [9] and contribute to genetic variation
    in microbial populations, thus facilitating adaptive evolution [10]. However,
    cleavage of self-DNA by RM systems as elements shaping prokaryotic genomes has
    not been directly detected, and its cause, frequency, and outcome are unknown.
    We quantify self-restriction caused by two RM systems of Escherichia coli and
    find that, in agreement with levels of restriction site avoidance, EcoRI, but
    not EcoRV, cleaves self-DNA at a measurable rate. Self-restriction is a stochastic
    process, which temporarily induces the SOS response, and is followed by DNA repair,
    maintaining cell viability. We find that RM systems with higher restriction efficiency
    against bacteriophage infections exhibit a higher rate of self-restriction, and
    that this rate can be further increased by stochastic imbalance between R and
    M. Our results identify molecular noise in RM systems as a factor shaping prokaryotic
    genomes.
acknowledgement: This work was funded by an HFSP Young Investigators’ grant. M.P.
  is a recipient of a DOC Fellowship of the Austrian Academy of Science at the Institute
  of Science and Technology Austria. R.O. and Y.W. were supported by the Platform
  for Dynamic Approaches to Living System from MEXT, Japan. We wish to thank I. Kobayashi
  for providing us with the EcoRI and EcoRV plasmids, and A. Campbell for providing
  us with the λ vir phage. We thank D. Siekhaus and C. Uhler and members of the C.C.G.
  and J.P. Bollback laboratories for in-depth discussions. We thank B. Stern for comments
  on an earlier version of the manuscript. We especially thank B.R. Levin for advice
  and comments, and the anonymous reviewers for significantly improving the manuscript.
article_processing_charge: No
author:
- first_name: Maros
  full_name: Pleska, Maros
  id: 4569785E-F248-11E8-B48F-1D18A9856A87
  last_name: Pleska
  orcid: 0000-0001-7460-7479
- first_name: Long
  full_name: Qian, Long
  last_name: Qian
- first_name: Reiko
  full_name: Okura, Reiko
  last_name: Okura
- first_name: Tobias
  full_name: Bergmiller, Tobias
  id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
  last_name: Bergmiller
  orcid: 0000-0001-5396-4346
- first_name: Yuichi
  full_name: Wakamoto, Yuichi
  last_name: Wakamoto
- first_name: Edo
  full_name: Kussell, Edo
  last_name: Kussell
- 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, Qian L, Okura R, et al. Bacterial autoimmunity due to a restriction-modification
    system. <i>Current Biology</i>. 2016;26(3):404-409. doi:<a href="https://doi.org/10.1016/j.cub.2015.12.041">10.1016/j.cub.2015.12.041</a>
  apa: Pleska, M., Qian, L., Okura, R., Bergmiller, T., Wakamoto, Y., Kussell, E.,
    &#38; Guet, C. C. (2016). Bacterial autoimmunity due to a restriction-modification
    system. <i>Current Biology</i>. Cell Press. <a href="https://doi.org/10.1016/j.cub.2015.12.041">https://doi.org/10.1016/j.cub.2015.12.041</a>
  chicago: Pleska, Maros, Long Qian, Reiko Okura, Tobias Bergmiller, Yuichi Wakamoto,
    Edo Kussell, and Calin C Guet. “Bacterial Autoimmunity Due to a Restriction-Modification
    System.” <i>Current Biology</i>. Cell Press, 2016. <a href="https://doi.org/10.1016/j.cub.2015.12.041">https://doi.org/10.1016/j.cub.2015.12.041</a>.
  ieee: M. Pleska <i>et al.</i>, “Bacterial autoimmunity due to a restriction-modification
    system,” <i>Current Biology</i>, vol. 26, no. 3. Cell Press, pp. 404–409, 2016.
  ista: Pleska M, Qian L, Okura R, Bergmiller T, Wakamoto Y, Kussell E, Guet CC. 2016.
    Bacterial autoimmunity due to a restriction-modification system. Current Biology.
    26(3), 404–409.
  mla: Pleska, Maros, et al. “Bacterial Autoimmunity Due to a Restriction-Modification
    System.” <i>Current Biology</i>, vol. 26, no. 3, Cell Press, 2016, pp. 404–09,
    doi:<a href="https://doi.org/10.1016/j.cub.2015.12.041">10.1016/j.cub.2015.12.041</a>.
  short: M. Pleska, L. Qian, R. Okura, T. Bergmiller, Y. Wakamoto, E. Kussell, C.C.
    Guet, Current Biology 26 (2016) 404–409.
date_created: 2018-12-11T11:50:54Z
date_published: 2016-02-08T00:00:00Z
date_updated: 2026-04-08T14:19:43Z
day: '08'
department:
- _id: CaGu
doi: 10.1016/j.cub.2015.12.041
external_id:
  isi:
  - '000369502900034'
intvolume: '        26'
isi: 1
issue: '3'
language:
- iso: eng
month: '02'
oa_version: None
page: 404 - 409
project:
- _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: Current Biology
publication_status: published
publisher: Cell Press
publist_id: '6087'
quality_controlled: '1'
related_material:
  record:
  - id: '202'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Bacterial autoimmunity due to a restriction-modification system
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 26
year: '2016'
...
