---
_id: '3158'
abstract:
- lang: eng
  text: We describe here the development and characterization of a conditionally inducible
    mouse model expressing Lifeact-GFP, a peptide that reports the dynamics of filamentous
    actin. We have used this model to study platelets, megakaryocytes and melanoblasts
    and we provide evidence that Lifeact-GFP is a useful reporter in these cell types
    ex vivo. In the case of platelets and megakaryocytes, these cells are not transfectable
    by traditional methods, so conditional activation of Lifeact allows the study
    of actin dynamics in these cells live. We studied melanoblasts in native skin
    explants from embryos, allowing the visualization of live actin dynamics during
    cytokinesis and migration. Our study revealed that melanoblasts lacking the small
    GTPase Rac1 show a delay in the formation of new pseudopodia following cytokinesis
    that accounts for the previously reported cytokinesis delay in these cells. Thus,
    through use of this mouse model, we were able to gain insights into the actin
    dynamics of cells that could only previously be studied using fixed specimens
    or following isolation from their native tissue environment.
author:
- first_name: Hannah
  full_name: Schachtner, Hannah
  last_name: Schachtner
- first_name: Ang
  full_name: Li, Ang
  last_name: Li
- first_name: David
  full_name: Stevenson, David
  last_name: Stevenson
- first_name: Simon
  full_name: Calaminus, Simon
  last_name: Calaminus
- first_name: Steven
  full_name: Thomas, Steven
  last_name: Thomas
- first_name: Steve
  full_name: Watson, Steve
  last_name: Watson
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
- first_name: Roland
  full_name: Wedlich Söldner, Roland
  last_name: Wedlich Söldner
- first_name: Douglas
  full_name: Strathdee, Douglas
  last_name: Strathdee
- first_name: Laura
  full_name: Machesky, Laura
  last_name: Machesky
citation:
  ama: Schachtner H, Li A, Stevenson D, et al. Tissue inducible Lifeact expression
    allows visualization of actin dynamics in vivo and ex vivo. <i>European Journal
    of Cell Biology</i>. 2012;91(11-12):923-929. doi:<a href="https://doi.org/10.1016/j.ejcb.2012.04.002">10.1016/j.ejcb.2012.04.002</a>
  apa: Schachtner, H., Li, A., Stevenson, D., Calaminus, S., Thomas, S., Watson, S.,
    … Machesky, L. (2012). Tissue inducible Lifeact expression allows visualization
    of actin dynamics in vivo and ex vivo. <i>European Journal of Cell Biology</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.ejcb.2012.04.002">https://doi.org/10.1016/j.ejcb.2012.04.002</a>
  chicago: Schachtner, Hannah, Ang Li, David Stevenson, Simon Calaminus, Steven Thomas,
    Steve Watson, Michael K Sixt, Roland Wedlich Söldner, Douglas Strathdee, and Laura
    Machesky. “Tissue Inducible Lifeact Expression Allows Visualization of Actin Dynamics
    in Vivo and Ex Vivo.” <i>European Journal of Cell Biology</i>. Elsevier, 2012.
    <a href="https://doi.org/10.1016/j.ejcb.2012.04.002">https://doi.org/10.1016/j.ejcb.2012.04.002</a>.
  ieee: H. Schachtner <i>et al.</i>, “Tissue inducible Lifeact expression allows visualization
    of actin dynamics in vivo and ex vivo,” <i>European Journal of Cell Biology</i>,
    vol. 91, no. 11–12. Elsevier, pp. 923–929, 2012.
  ista: Schachtner H, Li A, Stevenson D, Calaminus S, Thomas S, Watson S, Sixt MK,
    Wedlich Söldner R, Strathdee D, Machesky L. 2012. Tissue inducible Lifeact expression
    allows visualization of actin dynamics in vivo and ex vivo. European Journal of
    Cell Biology. 91(11–12), 923–929.
  mla: Schachtner, Hannah, et al. “Tissue Inducible Lifeact Expression Allows Visualization
    of Actin Dynamics in Vivo and Ex Vivo.” <i>European Journal of Cell Biology</i>,
    vol. 91, no. 11–12, Elsevier, 2012, pp. 923–29, doi:<a href="https://doi.org/10.1016/j.ejcb.2012.04.002">10.1016/j.ejcb.2012.04.002</a>.
  short: H. Schachtner, A. Li, D. Stevenson, S. Calaminus, S. Thomas, S. Watson, M.K.
    Sixt, R. Wedlich Söldner, D. Strathdee, L. Machesky, European Journal of Cell
    Biology 91 (2012) 923–929.
date_created: 2018-12-11T12:01:44Z
date_published: 2012-11-01T00:00:00Z
date_updated: 2021-01-12T07:41:27Z
day: '01'
department:
- _id: MiSi
doi: 10.1016/j.ejcb.2012.04.002
external_id:
  pmid:
  - '22658956'
intvolume: '        91'
issue: 11-12
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930012/
month: '11'
oa: 1
oa_version: Submitted Version
page: 923 - 929
pmid: 1
publication: European Journal of Cell Biology
publication_status: published
publisher: Elsevier
publist_id: '3534'
quality_controlled: '1'
scopus_import: 1
status: public
title: Tissue inducible Lifeact expression allows visualization of actin dynamics
  in vivo and ex vivo
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 91
year: '2012'
...
---
_id: '3159'
abstract:
- lang: eng
  text: The structure of hierarchical networks in biological and physical systems
    has long been characterized using the Horton-Strahler ordering scheme. The scheme
    assigns an integer order to each edge in the network based on the topology of
    branching such that the order increases from distal parts of the network (e.g.,
    mountain streams or capillaries) to the &quot;root&quot; of the network (e.g.,
    the river outlet or the aorta). However, Horton-Strahler ordering cannot be applied
    to networks with loops because they they create a contradiction in the edge ordering
    in terms of which edge precedes another in the hierarchy. Here, we present a generalization
    of the Horton-Strahler order to weighted planar reticular networks, where weights
    are assumed to correlate with the importance of network edges, e.g., weights estimated
    from edge widths may correlate to flow capacity. Our method assigns hierarchical
    levels not only to edges of the network, but also to its loops, and classifies
    the edges into reticular edges, which are responsible for loop formation, and
    tree edges. In addition, we perform a detailed and rigorous theoretical analysis
    of the sensitivity of the hierarchical levels to weight perturbations. In doing
    so, we show that the ordering of the reticular edges is more robust to noise in
    weight estimation than is the ordering of the tree edges. We discuss applications
    of this generalized Horton-Strahler ordering to the study of leaf venation and
    other biological networks.
acknowledgement: "his work was supported by the National Science Foundation Plant
  Genome Research Program (grant 0820624 to H.E. and J.S.W.), the Defense Advanced
  Projects Research Agency (grant HR0011-09-1-0055 to H.E. and J.S.W.), and the European
  Science Foundation (under the Research Networking Programme on “Applied and Computational
  Algebraic Topology” run by H.E.). Joshua S. Weitz, Ph.D., holds a Career Award at
  the Scientific Interface from the Burroughs Wellcome Fund.\r\n\r\n\r\n\r\nDuring
  preparation of this manuscript the authors became aware of a related work by Katifori
  and Magnasco (arXiv:1110.1412v1), concurrently submitted and accepted for publication
  in PLoS ONE."
article_number: e36715
author:
- first_name: Yuriy
  full_name: Mileyko, Yuriy
  last_name: Mileyko
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
- first_name: Charles
  full_name: Price, Charles
  last_name: Price
- first_name: Joshua
  full_name: Weitz, Joshua
  last_name: Weitz
citation:
  ama: Mileyko Y, Edelsbrunner H, Price C, Weitz J. Hierarchical ordering of reticular
    networks. <i>PLoS One</i>. 2012;7(6). doi:<a href="https://doi.org/10.1371/journal.pone.0036715">10.1371/journal.pone.0036715</a>
  apa: Mileyko, Y., Edelsbrunner, H., Price, C., &#38; Weitz, J. (2012). Hierarchical
    ordering of reticular networks. <i>PLoS One</i>. Public Library of Science. <a
    href="https://doi.org/10.1371/journal.pone.0036715">https://doi.org/10.1371/journal.pone.0036715</a>
  chicago: Mileyko, Yuriy, Herbert Edelsbrunner, Charles Price, and Joshua Weitz.
    “Hierarchical Ordering of Reticular Networks.” <i>PLoS One</i>. Public Library
    of Science, 2012. <a href="https://doi.org/10.1371/journal.pone.0036715">https://doi.org/10.1371/journal.pone.0036715</a>.
  ieee: Y. Mileyko, H. Edelsbrunner, C. Price, and J. Weitz, “Hierarchical ordering
    of reticular networks,” <i>PLoS One</i>, vol. 7, no. 6. Public Library of Science,
    2012.
  ista: Mileyko Y, Edelsbrunner H, Price C, Weitz J. 2012. Hierarchical ordering of
    reticular networks. PLoS One. 7(6), e36715.
  mla: Mileyko, Yuriy, et al. “Hierarchical Ordering of Reticular Networks.” <i>PLoS
    One</i>, vol. 7, no. 6, e36715, Public Library of Science, 2012, doi:<a href="https://doi.org/10.1371/journal.pone.0036715">10.1371/journal.pone.0036715</a>.
  short: Y. Mileyko, H. Edelsbrunner, C. Price, J. Weitz, PLoS One 7 (2012).
date_created: 2018-12-11T12:01:44Z
date_published: 2012-06-06T00:00:00Z
date_updated: 2021-01-12T07:41:28Z
day: '06'
ddc:
- '510'
department:
- _id: HeEd
doi: 10.1371/journal.pone.0036715
file:
- access_level: open_access
  checksum: 515a98ad72e470752f03f13663dcaff8
  content_type: application/pdf
  creator: kschuh
  date_created: 2019-02-05T12:38:43Z
  date_updated: 2020-07-14T12:46:01Z
  file_id: '5922'
  file_name: 2012_PLoS_Mileyko.PDF
  file_size: 541583
  relation: main_file
file_date_updated: 2020-07-14T12:46:01Z
has_accepted_license: '1'
intvolume: '         7'
issue: '6'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
publication: PLoS One
publication_status: published
publisher: Public Library of Science
publist_id: '3530'
pubrep_id: '385'
quality_controlled: '1'
scopus_import: 1
status: public
title: Hierarchical ordering of reticular networks
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2012'
...
---
_id: '3160'
abstract:
- lang: eng
  text: There is a long-running controversy about how early cell fate decisions are
    made in the developing mammalian embryo. 1,2 In particular, it is controversial
    when the first events that can predict the establishment of the pluripotent and
    extra-embryonic lineages in the blastocyst of the pre-implantation embryo occur.
    It has long been proposed that the position and polarity of cells at the 16- to
    32-cell stage embryo influence their decision to either give rise to the pluripotent
    cell lineage that eventually contributes to the inner cell mass (ICM), comprising
    the primitive endoderm (PE) and the epiblast (EPI), or the extra-embryonic trophectoderm
    (TE) surrounding the blastocoel. The positioning of cells in the embryo at this
    developmental stage could largely be the result of random events, making this
    a stochastic model of cell lineage allocation. Contrary to such a stochastic model,
    some studies have detected putative differences in the lineage potential of individual
    blastomeres before compaction, indicating that the first cell fate decisions may
    occur as early as at the 4-cell stage. Using a non-invasive, quantitative in vivo
    imaging assay to study the kinetic behavior of Oct4 (also known as POU5F1), a
    key transcription factor (TF) controlling pre-implantation development in the
    mouse embryo, 3-5 a recent study identifies Oct4 kinetics as a predictive measure
    of cell lineage patterning in the early mouse embryo. 6 Here, we discuss the implications
    of such molecular heterogeneities in early development and offer potential avenues
    toward a mechanistic understanding of these observations, contributing to the
    resolution of the controversy of developmental cell lineage allocation.
author:
- first_name: Periklis
  full_name: Pantazis, Periklis
  last_name: Pantazis
- first_name: Tobias
  full_name: Bollenbach, Tobias
  id: 3E6DB97A-F248-11E8-B48F-1D18A9856A87
  last_name: Bollenbach
  orcid: 0000-0003-4398-476X
citation:
  ama: Pantazis P, Bollenbach MT. Transcription factor kinetics and the emerging asymmetry
    in the early mammalian embryo. <i>Cell Cycle</i>. 2012;11(11):2055-2058. doi:<a
    href="https://doi.org/10.4161/cc.20118">10.4161/cc.20118</a>
  apa: Pantazis, P., &#38; Bollenbach, M. T. (2012). Transcription factor kinetics
    and the emerging asymmetry in the early mammalian embryo. <i>Cell Cycle</i>. Taylor
    and Francis. <a href="https://doi.org/10.4161/cc.20118">https://doi.org/10.4161/cc.20118</a>
  chicago: Pantazis, Periklis, and Mark Tobias Bollenbach. “Transcription Factor Kinetics
    and the Emerging Asymmetry in the Early Mammalian Embryo.” <i>Cell Cycle</i>.
    Taylor and Francis, 2012. <a href="https://doi.org/10.4161/cc.20118">https://doi.org/10.4161/cc.20118</a>.
  ieee: P. Pantazis and M. T. Bollenbach, “Transcription factor kinetics and the emerging
    asymmetry in the early mammalian embryo,” <i>Cell Cycle</i>, vol. 11, no. 11.
    Taylor and Francis, pp. 2055–2058, 2012.
  ista: Pantazis P, Bollenbach MT. 2012. Transcription factor kinetics and the emerging
    asymmetry in the early mammalian embryo. Cell Cycle. 11(11), 2055–2058.
  mla: Pantazis, Periklis, and Mark Tobias Bollenbach. “Transcription Factor Kinetics
    and the Emerging Asymmetry in the Early Mammalian Embryo.” <i>Cell Cycle</i>,
    vol. 11, no. 11, Taylor and Francis, 2012, pp. 2055–58, doi:<a href="https://doi.org/10.4161/cc.20118">10.4161/cc.20118</a>.
  short: P. Pantazis, M.T. Bollenbach, Cell Cycle 11 (2012) 2055–2058.
date_created: 2018-12-11T12:01:44Z
date_published: 2012-06-01T00:00:00Z
date_updated: 2021-01-12T07:41:28Z
day: '01'
department:
- _id: ToBo
doi: 10.4161/cc.20118
intvolume: '        11'
issue: '11'
language:
- iso: eng
month: '06'
oa_version: None
page: 2055 - 2058
publication: Cell Cycle
publication_status: published
publisher: Taylor and Francis
publist_id: '3531'
quality_controlled: '1'
scopus_import: 1
status: public
title: Transcription factor kinetics and the emerging asymmetry in the early mammalian
  embryo
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 11
year: '2012'
...
---
_id: '3161'
abstract:
- lang: eng
  text: 'Some inflammatory stimuli trigger activation of the NLRP3 inflammasome by
    inducing efflux of cellular potassium. Loss of cellular potassium is known to
    potently suppress protein synthesis, leading us to test whether the inhibition
    of protein synthesis itself serves as an activating signal for the NLRP3 inflammasome.
    Murine bone marrow-derived macrophages, either primed by LPS or unprimed, were
    exposed to a panel of inhibitors of ribosomal function: ricin, cycloheximide,
    puromycin, pactamycin, and anisomycin. Macrophages were also exposed to nigericin,
    ATP, monosodium urate (MSU), and poly I:C. Synthesis of pro-IL-ß and release of
    IL-1ß from cells in response to these agents was detected by immunoblotting and
    ELISA. Release of intracellular potassium was measured by mass spectrometry. Inhibition
    of translation by each of the tested translation inhibitors led to processing
    of IL-1ß, which was released from cells. Processing and release of IL-1ß was reduced
    or absent from cells deficient in NLRP3, ASC, or caspase-1, demonstrating the
    role of the NLRP3 inflammasome. Despite the inability of these inhibitors to trigger
    efflux of intracellular potassium, the addition of high extracellular potassium
    suppressed activation of the NLRP3 inflammasome. MSU and double-stranded RNA,
    which are known to activate the NLRP3 inflammasome, also substantially inhibited
    protein translation, supporting a close association between inhibition of translation
    and inflammasome activation. These data demonstrate that translational inhibition
    itself constitutes a heretofore-unrecognized mechanism underlying IL-1ß dependent
    inflammatory signaling and that other physical, chemical, or pathogen-associated
    agents that impair translation may lead to IL-1ß-dependent inflammation through
    activation of the NLRP3 inflammasome. For agents that inhibit translation through
    decreased cellular potassium, the application of high extracellular potassium
    restores protein translation and suppresses activation of the NLRP inflammasome.
    For agents that inhibit translation through mechanisms that do not involve loss
    of potassium, high extracellular potassium suppresses IL-1ß processing through
    a mechanism that remains undefined.'
acknowledgement: "Supported by National Institutes of Health grants GM071338 (ML)
  and AI059355 (BM).\r\nWe acknowledge the expertise of Dr. Martina Ralle in Department
  of Biochemistry and Molecular Biology at OHSU for measurements of potassium using
  inductively coupled plasma mass spectrometry."
article_number: e36044
author:
- first_name: Meghan
  full_name: Vyleta, Meghan
  id: 418901AA-F248-11E8-B48F-1D18A9856A87
  last_name: Vyleta
- first_name: John
  full_name: Wong, John
  last_name: Wong
- first_name: Bruce
  full_name: Magun, Bruce
  last_name: Magun
citation:
  ama: Vyleta M, Wong J, Magun B. Suppression of ribosomal function triggers innate
    immune signaling through activation of the NLRP3 inflammasome. <i>PLoS One</i>.
    2012;7(5). doi:<a href="https://doi.org/10.1371/journal.pone.0036044">10.1371/journal.pone.0036044</a>
  apa: Vyleta, M., Wong, J., &#38; Magun, B. (2012). Suppression of ribosomal function
    triggers innate immune signaling through activation of the NLRP3 inflammasome.
    <i>PLoS One</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pone.0036044">https://doi.org/10.1371/journal.pone.0036044</a>
  chicago: Vyleta, Meghan, John Wong, and Bruce Magun. “Suppression of Ribosomal Function
    Triggers Innate Immune Signaling through Activation of the NLRP3 Inflammasome.”
    <i>PLoS One</i>. Public Library of Science, 2012. <a href="https://doi.org/10.1371/journal.pone.0036044">https://doi.org/10.1371/journal.pone.0036044</a>.
  ieee: M. Vyleta, J. Wong, and B. Magun, “Suppression of ribosomal function triggers
    innate immune signaling through activation of the NLRP3 inflammasome,” <i>PLoS
    One</i>, vol. 7, no. 5. Public Library of Science, 2012.
  ista: Vyleta M, Wong J, Magun B. 2012. Suppression of ribosomal function triggers
    innate immune signaling through activation of the NLRP3 inflammasome. PLoS One.
    7(5), e36044.
  mla: Vyleta, Meghan, et al. “Suppression of Ribosomal Function Triggers Innate Immune
    Signaling through Activation of the NLRP3 Inflammasome.” <i>PLoS One</i>, vol.
    7, no. 5, e36044, Public Library of Science, 2012, doi:<a href="https://doi.org/10.1371/journal.pone.0036044">10.1371/journal.pone.0036044</a>.
  short: M. Vyleta, J. Wong, B. Magun, PLoS One 7 (2012).
date_created: 2018-12-11T12:01:45Z
date_published: 2012-05-14T00:00:00Z
date_updated: 2021-01-12T07:41:29Z
day: '14'
ddc:
- '610'
department:
- _id: SyCr
doi: 10.1371/journal.pone.0036044
file:
- access_level: open_access
  checksum: 30cef37e27eaa467f6571b3640282010
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:14:30Z
  date_updated: 2020-07-14T12:46:01Z
  file_id: '5082'
  file_name: IST-2012-97-v1+1_journal.pone.0036044.pdf
  file_size: 2984012
  relation: main_file
file_date_updated: 2020-07-14T12:46:01Z
has_accepted_license: '1'
intvolume: '         7'
issue: '5'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
publication: PLoS One
publication_status: published
publisher: Public Library of Science
publist_id: '3526'
pubrep_id: '97'
quality_controlled: '1'
scopus_import: 1
status: public
title: Suppression of ribosomal function triggers innate immune signaling through
  activation of the NLRP3 inflammasome
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2012'
...
---
_id: '3162'
abstract:
- lang: eng
  text: Given a dense-time real-valued signal and a parameterized temporal logic formula
    with both magnitude and timing parameters, we compute the subset of the parameter
    space that renders the formula satisfied by the trace. We provide two preliminary
    implementations, one which follows the exact semantics and attempts to compute
    the validity domain by quantifier elimination in linear arithmetics and one which
    conducts adaptive search in the parameter space.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Eugene
  full_name: Asarin, Eugene
  last_name: Asarin
- first_name: Alexandre
  full_name: Donzé, Alexandre
  last_name: Donzé
- first_name: Oded
  full_name: Maler, Oded
  last_name: Maler
- first_name: Dejan
  full_name: Nickovic, Dejan
  id: 41BCEE5C-F248-11E8-B48F-1D18A9856A87
  last_name: Nickovic
citation:
  ama: 'Asarin E, Donzé A, Maler O, Nickovic D. Parametric identification of temporal
    properties. In: Vol 7186. Springer; 2012:147-160. doi:<a href="https://doi.org/10.1007/978-3-642-29860-8_12">10.1007/978-3-642-29860-8_12</a>'
  apa: 'Asarin, E., Donzé, A., Maler, O., &#38; Nickovic, D. (2012). Parametric identification
    of temporal properties (Vol. 7186, pp. 147–160). Presented at the RV: Runtime
    Verification, San Francisco, CA, United States: Springer. <a href="https://doi.org/10.1007/978-3-642-29860-8_12">https://doi.org/10.1007/978-3-642-29860-8_12</a>'
  chicago: Asarin, Eugene, Alexandre Donzé, Oded Maler, and Dejan Nickovic. “Parametric
    Identification of Temporal Properties,” 7186:147–60. Springer, 2012. <a href="https://doi.org/10.1007/978-3-642-29860-8_12">https://doi.org/10.1007/978-3-642-29860-8_12</a>.
  ieee: 'E. Asarin, A. Donzé, O. Maler, and D. Nickovic, “Parametric identification
    of temporal properties,” presented at the RV: Runtime Verification, San Francisco,
    CA, United States, 2012, vol. 7186, pp. 147–160.'
  ista: 'Asarin E, Donzé A, Maler O, Nickovic D. 2012. Parametric identification of
    temporal properties. RV: Runtime Verification, LNCS, vol. 7186, 147–160.'
  mla: Asarin, Eugene, et al. <i>Parametric Identification of Temporal Properties</i>.
    Vol. 7186, Springer, 2012, pp. 147–60, doi:<a href="https://doi.org/10.1007/978-3-642-29860-8_12">10.1007/978-3-642-29860-8_12</a>.
  short: E. Asarin, A. Donzé, O. Maler, D. Nickovic, in:, Springer, 2012, pp. 147–160.
conference:
  end_date: 2011-09-30
  location: San Francisco, CA, United States
  name: 'RV: Runtime Verification'
  start_date: 2011-09-27
date_created: 2018-12-11T12:01:45Z
date_published: 2012-01-01T00:00:00Z
date_updated: 2021-01-12T07:41:29Z
day: '01'
ddc:
- '000'
department:
- _id: ToHe
doi: 10.1007/978-3-642-29860-8_12
file:
- access_level: open_access
  checksum: ba4a75287008fc64b8fbf78a7476ec32
  content_type: application/pdf
  creator: dernst
  date_created: 2020-05-15T12:50:15Z
  date_updated: 2020-07-14T12:46:01Z
  file_id: '7862'
  file_name: 2012_RV_Asarin.pdf
  file_size: 374726
  relation: main_file
file_date_updated: 2020-07-14T12:46:01Z
has_accepted_license: '1'
intvolume: '      7186'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Submitted Version
page: 147 - 160
publication_status: published
publisher: Springer
publist_id: '3525'
quality_controlled: '1'
scopus_import: 1
status: public
title: Parametric identification of temporal properties
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7186
year: '2012'
...
---
_id: '3164'
abstract:
- lang: eng
  text: Overview of the Special Issue on structured prediction and inference.
author:
- first_name: Matthew
  full_name: Blaschko, Matthew
  last_name: Blaschko
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
citation:
  ama: 'Blaschko M, Lampert C. Guest editorial: Special issue on structured prediction
    and inference. <i>International Journal of Computer Vision</i>. 2012;99(3):257-258.
    doi:<a href="https://doi.org/10.1007/s11263-012-0530-y">10.1007/s11263-012-0530-y</a>'
  apa: 'Blaschko, M., &#38; Lampert, C. (2012). Guest editorial: Special issue on
    structured prediction and inference. <i>International Journal of Computer Vision</i>.
    Springer. <a href="https://doi.org/10.1007/s11263-012-0530-y">https://doi.org/10.1007/s11263-012-0530-y</a>'
  chicago: 'Blaschko, Matthew, and Christoph Lampert. “Guest Editorial: Special Issue
    on Structured Prediction and Inference.” <i>International Journal of Computer
    Vision</i>. Springer, 2012. <a href="https://doi.org/10.1007/s11263-012-0530-y">https://doi.org/10.1007/s11263-012-0530-y</a>.'
  ieee: 'M. Blaschko and C. Lampert, “Guest editorial: Special issue on structured
    prediction and inference,” <i>International Journal of Computer Vision</i>, vol.
    99, no. 3. Springer, pp. 257–258, 2012.'
  ista: 'Blaschko M, Lampert C. 2012. Guest editorial: Special issue on structured
    prediction and inference. International Journal of Computer Vision. 99(3), 257–258.'
  mla: 'Blaschko, Matthew, and Christoph Lampert. “Guest Editorial: Special Issue
    on Structured Prediction and Inference.” <i>International Journal of Computer
    Vision</i>, vol. 99, no. 3, Springer, 2012, pp. 257–58, doi:<a href="https://doi.org/10.1007/s11263-012-0530-y">10.1007/s11263-012-0530-y</a>.'
  short: M. Blaschko, C. Lampert, International Journal of Computer Vision 99 (2012)
    257–258.
date_created: 2018-12-11T12:01:46Z
date_published: 2012-09-01T00:00:00Z
date_updated: 2021-01-12T07:41:30Z
day: '01'
department:
- _id: ChLa
doi: 10.1007/s11263-012-0530-y
intvolume: '        99'
issue: '3'
language:
- iso: eng
month: '09'
oa_version: None
page: 257 - 258
publication: International Journal of Computer Vision
publication_status: published
publisher: Springer
publist_id: '3521'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'Guest editorial: Special issue on structured prediction and inference'
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 99
year: '2012'
...
---
_id: '3165'
abstract:
- lang: eng
  text: Computing the winning set for Büchi objectives in alternating games on graphs
    is a central problem in computer aided verification with a large number of applications.
    The long standing best known upper bound for solving the problem is Õ(n·m), where
    n is the number of vertices and m is the number of edges in the graph. We are
    the first to break the Õ(n·m) boundary by presenting a new technique that reduces
    the running time to O(n 2). This bound also leads to O(n 2) time algorithms for
    computing the set of almost-sure winning vertices for Büchi objectives (1) in
    alternating games with probabilistic transitions (improving an earlier bound of
    Õ(n·m)), (2) in concurrent graph games with constant actions (improving an earlier
    bound of O(n 3)), and (3) in Markov decision processes (improving for m &gt; n
    4/3 an earlier bound of O(min(m 1.5, m·n 2/3)). We also show that the same technique
    can be used to compute the maximal end-component decomposition of a graph in time
    O(n 2), which is an improvement over earlier bounds for m &gt; n 4/3. Finally,
    we show how to maintain the winning set for Büchi objectives in alternating games
    under a sequence of edge insertions or a sequence of edge deletions in O(n) amortized
    time per operation. This is the first dynamic algorithm for this problem.
acknowledgement: 'The research was supported by Austrian Science Fund (FWF) Grant
  No P 23499-N23 on Modern Graph Algorithmic Techniques in Formal Verification, Vienna
  Science and Technology Fund (WWTF) Grant ICT10-002, FWF NFN Grant No S11407-N23
  (RiSE), ERC Start grant (279307: Graph Games), and Microsoft faculty fellows award.'
article_processing_charge: No
arxiv: 1
author:
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Monika H
  full_name: Henzinger, Monika H
  id: 540c9bbd-f2de-11ec-812d-d04a5be85630
  last_name: Henzinger
  orcid: 0000-0002-5008-6530
citation:
  ama: 'Chatterjee K, Henzinger MH. An O(n2) time algorithm for alternating Büchi
    games. In: <i>Proceedings of the Annual ACM-SIAM Symposium on Discrete Algorithms</i>.
    SIAM; 2012:1386-1399. doi:<a href="https://doi.org/10.1137/1.9781611973099.109">10.1137/1.9781611973099.109</a>'
  apa: 'Chatterjee, K., &#38; Henzinger, M. H. (2012). An O(n2) time algorithm for
    alternating Büchi games. In <i>Proceedings of the Annual ACM-SIAM Symposium on
    Discrete Algorithms</i> (pp. 1386–1399). Kyoto, Japan: SIAM. <a href="https://doi.org/10.1137/1.9781611973099.109">https://doi.org/10.1137/1.9781611973099.109</a>'
  chicago: Chatterjee, Krishnendu, and Monika H Henzinger. “An O(N2) Time Algorithm
    for Alternating Büchi Games.” In <i>Proceedings of the Annual ACM-SIAM Symposium
    on Discrete Algorithms</i>, 1386–99. SIAM, 2012. <a href="https://doi.org/10.1137/1.9781611973099.109">https://doi.org/10.1137/1.9781611973099.109</a>.
  ieee: K. Chatterjee and M. H. Henzinger, “An O(n2) time algorithm for alternating
    Büchi games,” in <i>Proceedings of the Annual ACM-SIAM Symposium on Discrete Algorithms</i>,
    Kyoto, Japan, 2012, pp. 1386–1399.
  ista: 'Chatterjee K, Henzinger MH. 2012. An O(n2) time algorithm for alternating
    Büchi games. Proceedings of the Annual ACM-SIAM Symposium on Discrete Algorithms.
    SODA: Symposium on Discrete Algorithms, 1386–1399.'
  mla: Chatterjee, Krishnendu, and Monika H. Henzinger. “An O(N2) Time Algorithm for
    Alternating Büchi Games.” <i>Proceedings of the Annual ACM-SIAM Symposium on Discrete
    Algorithms</i>, SIAM, 2012, pp. 1386–99, doi:<a href="https://doi.org/10.1137/1.9781611973099.109">10.1137/1.9781611973099.109</a>.
  short: K. Chatterjee, M.H. Henzinger, in:, Proceedings of the Annual ACM-SIAM Symposium
    on Discrete Algorithms, SIAM, 2012, pp. 1386–1399.
conference:
  end_date: 2012-01-19
  location: Kyoto, Japan
  name: 'SODA: Symposium on Discrete Algorithms'
  start_date: 2012-01-17
date_created: 2018-12-11T12:01:46Z
date_published: 2012-01-01T00:00:00Z
date_updated: 2025-06-02T08:53:48Z
day: '01'
department:
- _id: KrCh
doi: 10.1137/1.9781611973099.109
ec_funded: 1
external_id:
  arxiv:
  - '1109.5018'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1109.5018
month: '01'
oa: 1
oa_version: None
page: 1386 - 1399
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 23499-N23
  name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 2587B514-B435-11E9-9278-68D0E5697425
  name: Microsoft Research Faculty Fellowship
publication: Proceedings of the Annual ACM-SIAM Symposium on Discrete Algorithms
publication_status: published
publisher: SIAM
publist_id: '3519'
pubrep_id: '15'
quality_controlled: '1'
related_material:
  record:
  - id: '5379'
    relation: earlier_version
    status: public
  - id: '2141'
    relation: later_version
    status: public
status: public
title: An O(n2) time algorithm for alternating Büchi games
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2012'
...
---
_id: '3166'
abstract:
- lang: eng
  text: 'There is evidence that the genetic code was established prior to the existence
    of proteins, when metabolism was powered by ribozymes. Also, early proto-organisms
    had to rely on simple anaerobic bioenergetic processes. In this work I propose
    that amino acid fermentation powered metabolism in the RNA world, and that this
    was facilitated by proto-adapters, the precursors of the tRNAs. Amino acids were
    used as carbon sources rather than as catalytic or structural elements. In modern
    bacteria, amino acid fermentation is known as the Stickland reaction. This pathway
    involves two amino acids: the first undergoes oxidative deamination, and the second
    acts as an electron acceptor through reductive deamination. This redox reaction
    results in two keto acids that are employed to synthesise ATP via substrate-level
    phosphorylation. The Stickland reaction is the basic bioenergetic pathway of some
    bacteria of the genus Clostridium. Two other facts support Stickland fermentation
    in the RNA world. First, several Stickland amino acid pairs are synthesised in
    abiotic amino acid synthesis. This suggests that amino acids that could be used
    as an energy substrate were freely available. Second, anticodons that have complementary
    sequences often correspond to amino acids that form Stickland pairs. The main
    hypothesis of this paper is that pairs of complementary proto-adapters were assigned
    to Stickland amino acids pairs. There are signatures of this hypothesis in the
    genetic code. Furthermore, it is argued that the proto-adapters formed double
    strands that brought amino acid pairs into proximity to facilitate their mutual
    redox reaction, structurally constraining the anticodon pairs that are assigned
    to these amino acid pairs. Significance tests which randomise the code are performed
    to study the extent of the variability of the energetic (ATP) yield. Random assignments
    can lead to a substantial yield of ATP and maintain enough variability, thus selection
    can act and refine the assignments into a proto-code that optimises the energetic
    yield. Monte Carlo simulations are performed to evaluate the establishment of
    these simple proto-codes, based on amino acid substitutions and codon swapping.
    In all cases, donor amino acids are assigned to anticodons composed of U+G, and
    have low redundancy (1-2 codons), whereas acceptor amino acids are assigned to
    the the remaining codons. These bioenergetic and structural constraints allow
    for a metabolic role for amino acids before their co-option as catalyst cofactors.
    Reviewers: this article was reviewed by Prof. William Martin, Prof. Eors Szathmary
    (nominated by Dr. Gaspar Jekely) and Dr. Adam Kun (nominated by Dr. Sandor Pongor)'
acknowledgement: 'The author was supported by the ERC-2009-AdG Grant for project 250152
  SELECTIONINFORMATION. '
article_number: '6'
author:
- first_name: Harold
  full_name: Vladar, Harold
  id: 2A181218-F248-11E8-B48F-1D18A9856A87
  last_name: Vladar
  orcid: 0000-0002-5985-7653
citation:
  ama: de Vladar H. Amino acid fermentation at the origin of the genetic code. <i>Biology
    Direct</i>. 2012;7. doi:<a href="https://doi.org/10.1186/1745-6150-7-6">10.1186/1745-6150-7-6</a>
  apa: de Vladar, H. (2012). Amino acid fermentation at the origin of the genetic
    code. <i>Biology Direct</i>. BioMed Central. <a href="https://doi.org/10.1186/1745-6150-7-6">https://doi.org/10.1186/1745-6150-7-6</a>
  chicago: Vladar, Harold de. “Amino Acid Fermentation at the Origin of the Genetic
    Code.” <i>Biology Direct</i>. BioMed Central, 2012. <a href="https://doi.org/10.1186/1745-6150-7-6">https://doi.org/10.1186/1745-6150-7-6</a>.
  ieee: H. de Vladar, “Amino acid fermentation at the origin of the genetic code,”
    <i>Biology Direct</i>, vol. 7. BioMed Central, 2012.
  ista: de Vladar H. 2012. Amino acid fermentation at the origin of the genetic code.
    Biology Direct. 7, 6.
  mla: de Vladar, Harold. “Amino Acid Fermentation at the Origin of the Genetic Code.”
    <i>Biology Direct</i>, vol. 7, 6, BioMed Central, 2012, doi:<a href="https://doi.org/10.1186/1745-6150-7-6">10.1186/1745-6150-7-6</a>.
  short: H. de Vladar, Biology Direct 7 (2012).
date_created: 2018-12-11T12:01:46Z
date_published: 2012-02-10T00:00:00Z
date_updated: 2021-01-12T07:41:31Z
day: '10'
ddc:
- '570'
- '576'
department:
- _id: NiBa
doi: 10.1186/1745-6150-7-6
ec_funded: 1
file:
- access_level: open_access
  checksum: e511e401e239ef608a7fd79b21a06d78
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:15:44Z
  date_updated: 2020-07-14T12:46:02Z
  file_id: '5166'
  file_name: IST-2012-99-v1+1_1745-6150-7-6.pdf
  file_size: 4099536
  relation: main_file
file_date_updated: 2020-07-14T12:46:02Z
has_accepted_license: '1'
intvolume: '         7'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
project:
- _id: 25B07788-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '250152'
  name: Limits to selection in biology and in evolutionary computation
publication: Biology Direct
publication_status: published
publisher: BioMed Central
publist_id: '3518'
pubrep_id: '99'
quality_controlled: '1'
status: public
title: Amino acid fermentation at the origin of the genetic code
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2012'
...
---
_id: '3167'
article_type: letter_note
author:
- first_name: Michele
  full_name: Weber, Michele
  id: 3A3FC708-F248-11E8-B48F-1D18A9856A87
  last_name: Weber
citation:
  ama: Weber M. NextGen speaks 13 . <i>Science</i>. 2012;336(6077):32-34. doi:<a href="https://doi.org/10.1126/science.336.6077.32">10.1126/science.336.6077.32</a>
  apa: Weber, M. (2012). NextGen speaks 13 . <i>Science</i>. American Association
    for the Advancement of Science. <a href="https://doi.org/10.1126/science.336.6077.32">https://doi.org/10.1126/science.336.6077.32</a>
  chicago: Weber, Michele. “NextGen Speaks 13 .” <i>Science</i>. American Association
    for the Advancement of Science, 2012. <a href="https://doi.org/10.1126/science.336.6077.32">https://doi.org/10.1126/science.336.6077.32</a>.
  ieee: M. Weber, “NextGen speaks 13 ,” <i>Science</i>, vol. 336, no. 6077. American
    Association for the Advancement of Science, pp. 32–34, 2012.
  ista: Weber M. 2012. NextGen speaks 13 . Science. 336(6077), 32–34.
  mla: Weber, Michele. “NextGen Speaks 13 .” <i>Science</i>, vol. 336, no. 6077, American
    Association for the Advancement of Science, 2012, pp. 32–34, doi:<a href="https://doi.org/10.1126/science.336.6077.32">10.1126/science.336.6077.32</a>.
  short: M. Weber, Science 336 (2012) 32–34.
date_created: 2018-12-11T12:01:47Z
date_published: 2012-04-06T00:00:00Z
date_updated: 2021-01-12T07:41:32Z
day: '06'
department:
- _id: MiSi
doi: 10.1126/science.336.6077.32
external_id:
  pmid:
  - '22491839'
intvolume: '       336'
issue: '6077'
language:
- iso: eng
month: '04'
oa_version: None
page: 32-34
pmid: 1
popular_science: '1'
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '3516'
status: public
title: 'NextGen speaks 13 '
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 336
year: '2012'
...
---
_id: '3168'
abstract:
- lang: eng
  text: The induction of a signaling pathway is characterized by transient complex
    formation and mutual posttranslational modification of proteins. To faithfully
    capture this combinatorial process in a mathematical model is an important challenge
    in systems biology. Exploiting the limited context on which most binding and modification
    events are conditioned, attempts have been made to reduce the combinatorial complexity
    by quotienting the reachable set of molecular species into species aggregates
    while preserving the deterministic semantics of the thermodynamic limit. Recently,
    we proposed a quotienting that also preserves the stochastic semantics and that
    is complete in the sense that the semantics of individual species can be recovered
    from the aggregate semantics. In this paper, we prove that this quotienting yields
    a sufficient condition for weak lumpability (that is to say that the quotient
    system is still Markovian for a given set of initial distributions) and that it
    gives rise to a backward Markov bisimulation between the original and aggregated
    transition system (which means that the conditional probability of being in a
    given state in the original system knowing that we are in its equivalence class
    is an invariant of the system). We illustrate the framework on a case study of
    the epidermal growth factor (EGF)/insulin receptor crosstalk.
acknowledgement: "We would like to thank the anonymous reviewers for their comments
  on the different versions of the paper. We would also like to thank Ferdinanda Camporesi
  for her careful reading and the useful insights that she gave us about the paper.\r\nJérôme
  Feret’s contribution was partially supported by the AbstractCell ANR-Chair of Excellence.
  Heinz Koeppl’s research is supported by the Swiss National Science Foundation, grant
  no. 200020-117975/1. Tatjana Petrov’s research is supported by SystemsX.ch (the
  Swiss Initiative in Systems Biology)."
author:
- first_name: Jérôme
  full_name: Feret, Jérôme
  last_name: Feret
- 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: Heinz
  full_name: Koeppl, Heinz
  last_name: Koeppl
- first_name: Tatjana
  full_name: Petrov, Tatjana
  id: 3D5811FC-F248-11E8-B48F-1D18A9856A87
  last_name: Petrov
  orcid: 0000-0002-9041-0905
citation:
  ama: Feret J, Henzinger TA, Koeppl H, Petrov T. Lumpability abstractions of rule
    based systems. <i>Theoretical Computer Science</i>. 2012;431:137-164. doi:<a href="https://doi.org/10.1016/j.tcs.2011.12.059">10.1016/j.tcs.2011.12.059</a>
  apa: Feret, J., Henzinger, T. A., Koeppl, H., &#38; Petrov, T. (2012). Lumpability
    abstractions of rule based systems. <i>Theoretical Computer Science</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.tcs.2011.12.059">https://doi.org/10.1016/j.tcs.2011.12.059</a>
  chicago: Feret, Jérôme, Thomas A Henzinger, Heinz Koeppl, and Tatjana Petrov. “Lumpability
    Abstractions of Rule Based Systems.” <i>Theoretical Computer Science</i>. Elsevier,
    2012. <a href="https://doi.org/10.1016/j.tcs.2011.12.059">https://doi.org/10.1016/j.tcs.2011.12.059</a>.
  ieee: J. Feret, T. A. Henzinger, H. Koeppl, and T. Petrov, “Lumpability abstractions
    of rule based systems,” <i>Theoretical Computer Science</i>, vol. 431. Elsevier,
    pp. 137–164, 2012.
  ista: Feret J, Henzinger TA, Koeppl H, Petrov T. 2012. Lumpability abstractions
    of rule based systems. Theoretical Computer Science. 431, 137–164.
  mla: Feret, Jérôme, et al. “Lumpability Abstractions of Rule Based Systems.” <i>Theoretical
    Computer Science</i>, vol. 431, Elsevier, 2012, pp. 137–64, doi:<a href="https://doi.org/10.1016/j.tcs.2011.12.059">10.1016/j.tcs.2011.12.059</a>.
  short: J. Feret, T.A. Henzinger, H. Koeppl, T. Petrov, Theoretical Computer Science
    431 (2012) 137–164.
date_created: 2018-12-11T12:01:47Z
date_published: 2012-05-04T00:00:00Z
date_updated: 2023-02-23T11:39:40Z
day: '04'
department:
- _id: ToHe
doi: 10.1016/j.tcs.2011.12.059
intvolume: '       431'
language:
- iso: eng
month: '05'
oa_version: None
page: 137 - 164
publication: Theoretical Computer Science
publication_status: published
publisher: Elsevier
publist_id: '3515'
pubrep_id: '73'
quality_controlled: '1'
related_material:
  record:
  - id: '3719'
    relation: earlier_version
    status: public
scopus_import: 1
status: public
title: Lumpability abstractions of rule based systems
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 431
year: '2012'
...
---
_id: '3242'
abstract:
- lang: eng
  text: Due to the omnipresent risk of epidemics, insect societies have evolved sophisticated
    disease defences at the individual and colony level. An intriguing yet little
    understood phenomenon is that social contact to pathogen-exposed individuals reduces
    susceptibility of previously naive nestmates to this pathogen. We tested whether
    such social immunisation in Lasius ants against the entomopathogenic fungus Metarhizium
    anisopliae is based on active upregulation of the immune system of nestmates following
    contact to an infectious individual or passive protection via transfer of immune
    effectors among group members—that is, active versus passive immunisation. We
    found no evidence for involvement of passive immunisation via transfer of antimicrobials
    among colony members. Instead, intensive allogrooming behaviour between naive
    and pathogen-exposed ants before fungal conidia firmly attached to their cuticle
    suggested passage of the pathogen from the exposed individuals to their nestmates.
    By tracing fluorescence-labelled conidia we indeed detected frequent pathogen
    transfer to the nestmates, where they caused low-level infections as revealed
    by growth of small numbers of fungal colony forming units from their dissected
    body content. These infections rarely led to death, but instead promoted an enhanced
    ability to inhibit fungal growth and an active upregulation of immune genes involved
    in antifungal defences (defensin and prophenoloxidase, PPO). Contrarily, there
    was no upregulation of the gene cathepsin L, which is associated with antibacterial
    and antiviral defences, and we found no increased antibacterial activity of nestmates
    of fungus-exposed ants. This indicates that social immunisation after fungal exposure
    is specific, similar to recent findings for individual-level immune priming in
    invertebrates. Epidemiological modeling further suggests that active social immunisation
    is adaptive, as it leads to faster elimination of the disease and lower death
    rates than passive immunisation. Interestingly, humans have also utilised the
    protective effect of low-level infections to fight smallpox by intentional transfer
    of low pathogen doses (“variolation” or “inoculation”).
acknowledgement: Funding for this project was obtained by the German Research Foundation
  DFG (http://www.dfg.de/en/index.jsp) as an Individual Research Grant (CR118/2-1
  to SC) and the European Research Council (http://erc.europa.eu/) in form of two
  ERC Starting Grants (ERC-2009-StG240371-SocialVaccines to SC and ERC-2010-StG259294-LatentCauses
  to FJT). In addition, the Junge Akademie (Young Academy of the Berlin-Brandenburg
  Academy of Sciences and Humanities and the National Academy of Sciences Leopoldina
  (http://www.diejungeakademie.de/english/i​ndex.html) funded this joint Antnet project
  of SC and FJT. The funders had no role in study design, data collection and analysis,
  decision to publish, or preparation of the manuscript.
article_number: e1001300
author:
- first_name: Matthias
  full_name: Konrad, Matthias
  id: 46528076-F248-11E8-B48F-1D18A9856A87
  last_name: Konrad
- first_name: Meghan
  full_name: Vyleta, Meghan
  id: 418901AA-F248-11E8-B48F-1D18A9856A87
  last_name: Vyleta
- first_name: Fabian
  full_name: Theis, Fabian
  last_name: Theis
- first_name: Miriam
  full_name: Stock, Miriam
  id: 42462816-F248-11E8-B48F-1D18A9856A87
  last_name: Stock
- first_name: Simon
  full_name: Tragust, Simon
  id: 35A7A418-F248-11E8-B48F-1D18A9856A87
  last_name: Tragust
- first_name: Martina
  full_name: Klatt, Martina
  id: E60F29C6-E9AE-11E9-AF6E-D190C7302F38
  last_name: Klatt
- first_name: Verena
  full_name: Drescher, Verena
  last_name: Drescher
- first_name: Carsten
  full_name: Marr, Carsten
  last_name: Marr
- first_name: Line V
  full_name: Ugelvig, Line V
  id: 3DC97C8E-F248-11E8-B48F-1D18A9856A87
  last_name: Ugelvig
  orcid: 0000-0003-1832-8883
- first_name: Sylvia
  full_name: Cremer, Sylvia
  id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
  last_name: Cremer
  orcid: 0000-0002-2193-3868
citation:
  ama: Konrad M, Vyleta M, Theis F, et al. Social transfer of pathogenic fungus promotes
    active immunisation in ant colonies. <i>PLoS Biology</i>. 2012;10(4). doi:<a href="https://doi.org/10.1371/journal.pbio.1001300">10.1371/journal.pbio.1001300</a>
  apa: Konrad, M., Vyleta, M., Theis, F., Stock, M., Tragust, S., Klatt, M., … Cremer,
    S. (2012). Social transfer of pathogenic fungus promotes active immunisation in
    ant colonies. <i>PLoS Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.1001300">https://doi.org/10.1371/journal.pbio.1001300</a>
  chicago: Konrad, Matthias, Meghan Vyleta, Fabian Theis, Miriam Stock, Simon Tragust,
    Martina Klatt, Verena Drescher, Carsten Marr, Line V Ugelvig, and Sylvia Cremer.
    “Social Transfer of Pathogenic Fungus Promotes Active Immunisation in Ant Colonies.”
    <i>PLoS Biology</i>. Public Library of Science, 2012. <a href="https://doi.org/10.1371/journal.pbio.1001300">https://doi.org/10.1371/journal.pbio.1001300</a>.
  ieee: M. Konrad <i>et al.</i>, “Social transfer of pathogenic fungus promotes active
    immunisation in ant colonies,” <i>PLoS Biology</i>, vol. 10, no. 4. Public Library
    of Science, 2012.
  ista: Konrad M, Vyleta M, Theis F, Stock M, Tragust S, Klatt M, Drescher V, Marr
    C, Ugelvig LV, Cremer S. 2012. Social transfer of pathogenic fungus promotes active
    immunisation in ant colonies. PLoS Biology. 10(4), e1001300.
  mla: Konrad, Matthias, et al. “Social Transfer of Pathogenic Fungus Promotes Active
    Immunisation in Ant Colonies.” <i>PLoS Biology</i>, vol. 10, no. 4, e1001300,
    Public Library of Science, 2012, doi:<a href="https://doi.org/10.1371/journal.pbio.1001300">10.1371/journal.pbio.1001300</a>.
  short: M. Konrad, M. Vyleta, F. Theis, M. Stock, S. Tragust, M. Klatt, V. Drescher,
    C. Marr, L.V. Ugelvig, S. Cremer, PLoS Biology 10 (2012).
date_created: 2018-12-11T12:02:13Z
date_published: 2012-04-03T00:00:00Z
date_updated: 2023-02-23T14:07:11Z
day: '03'
ddc:
- '570'
- '579'
department:
- _id: SyCr
doi: 10.1371/journal.pbio.1001300
ec_funded: 1
file:
- access_level: open_access
  checksum: 4ebacefd9fbab5c68adf829124115fd1
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:08:28Z
  date_updated: 2020-07-14T12:46:04Z
  file_id: '4689'
  file_name: IST-2012-96-v1+1_journal.pbio.1001300.pdf
  file_size: 674228
  relation: main_file
file_date_updated: 2020-07-14T12:46:04Z
has_accepted_license: '1'
intvolume: '        10'
issue: '4'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
project:
- _id: 25DAF0B2-B435-11E9-9278-68D0E5697425
  grant_number: CR-118/3-1
  name: Host-Parasite Coevolution
- _id: 25DC711C-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '243071'
  name: 'Social Vaccination in Ant Colonies: from Individual Mechanisms to Society
    Effects'
- _id: 25E0E184-B435-11E9-9278-68D0E5697425
  name: Antnet
publication: PLoS Biology
publication_status: published
publisher: Public Library of Science
publist_id: '3434'
pubrep_id: '96'
quality_controlled: '1'
related_material:
  record:
  - id: '9755'
    relation: research_data
    status: public
scopus_import: 1
status: public
title: Social transfer of pathogenic fungus promotes active immunisation in ant colonies
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: 10
year: '2012'
...
---
_id: '3243'
abstract:
- lang: eng
  text: 'Wie wandelt sich das Berufsbild in Wissenschaftlichen Bibliotheken? Patrick
    Danowski gibt seine Einschätzung ab. '
article_processing_charge: No
article_type: letter_note
author:
- first_name: Patrick
  full_name: Danowski, Patrick
  id: 2EBD1598-F248-11E8-B48F-1D18A9856A87
  last_name: Danowski
  orcid: 0000-0002-6026-4409
citation:
  ama: Danowski P. Zwischen Technologie und Information. <i>Büchereiperspektiven</i>.
    2012;2012(1):11.
  apa: Danowski, P. (2012). Zwischen Technologie und Information. <i>Büchereiperspektiven</i>.
    Büchereiverband Österreichs.
  chicago: Danowski, Patrick. “Zwischen Technologie und Information.” <i>Büchereiperspektiven</i>.
    Büchereiverband Österreichs, 2012.
  ieee: P. Danowski, “Zwischen Technologie und Information,” <i>Büchereiperspektiven</i>,
    vol. 2012, no. 1. Büchereiverband Österreichs, p. 11, 2012.
  ista: Danowski P. 2012. Zwischen Technologie und Information. Büchereiperspektiven.
    2012(1), 11.
  mla: Danowski, Patrick. “Zwischen Technologie und Information.” <i>Büchereiperspektiven</i>,
    vol. 2012, no. 1, Büchereiverband Österreichs, 2012, p. 11.
  short: P. Danowski, Büchereiperspektiven 2012 (2012) 11.
date_created: 2018-12-11T12:02:13Z
date_published: 2012-03-01T00:00:00Z
date_updated: 2023-10-16T10:40:18Z
day: '01'
department:
- _id: E-Lib
intvolume: '      2012'
issue: '1'
language:
- iso: ger
main_file_link:
- open_access: '1'
  url: https://www.bvoe.at/sites/default/files/2022-07/BP_1_12.pdf
month: '03'
oa: 1
oa_version: Published Version
page: '11'
popular_science: '1'
publication: Büchereiperspektiven
publication_identifier:
  issn:
  - 1607-7172
publication_status: published
publisher: Büchereiverband Österreichs
publist_id: '3433'
status: public
title: Zwischen Technologie und Information
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 2012
year: '2012'
...
---
_id: '3244'
abstract:
- lang: eng
  text: "Bibliothekare haben die Aufgabe, sich mit neuen Medienformen auseinanderzusetzen.\r\n"
article_processing_charge: No
article_type: letter_note
author:
- first_name: Patrick
  full_name: Danowski, Patrick
  id: 2EBD1598-F248-11E8-B48F-1D18A9856A87
  last_name: Danowski
  orcid: 0000-0002-6026-4409
citation:
  ama: Danowski P. Die Zeit des Abwartens ist vorbei! <i>BuB - Forum Bibliothek und
    Information</i>. 2012;64(4):284.
  apa: Danowski, P. (2012). Die Zeit des Abwartens ist vorbei! <i>BuB - Forum Bibliothek
    und Information</i>. Fachzeitschrift des BIB – Berufsverband Information Bibliothek.
  chicago: Danowski, Patrick. “Die Zeit des Abwartens ist vorbei!” <i>BuB - Forum
    Bibliothek und Information</i>. Fachzeitschrift des BIB – Berufsverband Information
    Bibliothek, 2012.
  ieee: P. Danowski, “Die Zeit des Abwartens ist vorbei!,” <i>BuB - Forum Bibliothek
    und Information</i>, vol. 64, no. 4. Fachzeitschrift des BIB – Berufsverband Information
    Bibliothek, p. 284, 2012.
  ista: Danowski P. 2012. Die Zeit des Abwartens ist vorbei! BuB - Forum Bibliothek
    und Information. 64(4), 284.
  mla: Danowski, Patrick. “Die Zeit des Abwartens ist vorbei!” <i>BuB - Forum Bibliothek
    und Information</i>, vol. 64, no. 4, Fachzeitschrift des BIB – Berufsverband Information
    Bibliothek, 2012, p. 284.
  short: P. Danowski, BuB - Forum Bibliothek und Information 64 (2012) 284.
date_created: 2018-12-11T12:02:13Z
date_published: 2012-04-15T00:00:00Z
date_updated: 2023-10-16T10:19:14Z
day: '15'
department:
- _id: E-Lib
intvolume: '        64'
issue: '4'
language:
- iso: ger
main_file_link:
- open_access: '1'
  url: https://www.b-u-b.de/fileadmin/archiv/imports/pdf_files/2012/bub_2012_04_284.pdf
month: '04'
oa: 1
oa_version: Published Version
page: '284'
popular_science: '1'
publication: BuB - Forum Bibliothek und Information
publication_identifier:
  issn:
  - 1869 -1137
publication_status: published
publisher: Fachzeitschrift des BIB – Berufsverband Information Bibliothek
publist_id: '3432'
status: public
title: Die Zeit des Abwartens ist vorbei!
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 64
year: '2012'
...
---
_id: '3245'
abstract:
- lang: eng
  text: How cells orchestrate their behavior during collective migration is a long-standing
    question. Using magnetic tweezers to apply mechanical stimuli to Xenopus mesendoderm
    cells, Weber etal. (2012) now reveal, in this issue of Developmental Cell, a cadherin-mediated
    mechanosensitive response that promotes cell polarization and movement persistence
    during the collective mesendoderm migration in gastrulation.
author:
- first_name: Martin
  full_name: Behrndt, Martin
  id: 3ECECA3A-F248-11E8-B48F-1D18A9856A87
  last_name: Behrndt
- first_name: Carl-Philipp J
  full_name: Heisenberg, Carl-Philipp J
  id: 39427864-F248-11E8-B48F-1D18A9856A87
  last_name: Heisenberg
  orcid: 0000-0002-0912-4566
citation:
  ama: Behrndt M, Heisenberg C-PJ. Spurred by resistance mechanosensation in collective
    migration. <i>Developmental Cell</i>. 2012;22(1):3-4. doi:<a href="https://doi.org/10.1016/j.devcel.2011.12.018">10.1016/j.devcel.2011.12.018</a>
  apa: Behrndt, M., &#38; Heisenberg, C.-P. J. (2012). Spurred by resistance mechanosensation
    in collective migration. <i>Developmental Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.devcel.2011.12.018">https://doi.org/10.1016/j.devcel.2011.12.018</a>
  chicago: Behrndt, Martin, and Carl-Philipp J Heisenberg. “Spurred by Resistance
    Mechanosensation in Collective Migration.” <i>Developmental Cell</i>. Cell Press,
    2012. <a href="https://doi.org/10.1016/j.devcel.2011.12.018">https://doi.org/10.1016/j.devcel.2011.12.018</a>.
  ieee: M. Behrndt and C.-P. J. Heisenberg, “Spurred by resistance mechanosensation
    in collective migration,” <i>Developmental Cell</i>, vol. 22, no. 1. Cell Press,
    pp. 3–4, 2012.
  ista: Behrndt M, Heisenberg C-PJ. 2012. Spurred by resistance mechanosensation in
    collective migration. Developmental Cell. 22(1), 3–4.
  mla: Behrndt, Martin, and Carl-Philipp J. Heisenberg. “Spurred by Resistance Mechanosensation
    in Collective Migration.” <i>Developmental Cell</i>, vol. 22, no. 1, Cell Press,
    2012, pp. 3–4, doi:<a href="https://doi.org/10.1016/j.devcel.2011.12.018">10.1016/j.devcel.2011.12.018</a>.
  short: M. Behrndt, C.-P.J. Heisenberg, Developmental Cell 22 (2012) 3–4.
date_created: 2018-12-11T12:02:14Z
date_published: 2012-01-17T00:00:00Z
date_updated: 2021-01-12T07:42:05Z
day: '17'
department:
- _id: CaHe
doi: 10.1016/j.devcel.2011.12.018
intvolume: '        22'
issue: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 3 - 4
publication: Developmental Cell
publication_status: published
publisher: Cell Press
publist_id: '3426'
quality_controlled: '1'
scopus_import: 1
status: public
title: Spurred by resistance mechanosensation in collective migration
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 22
year: '2012'
...
---
_id: '3246'
abstract:
- lang: eng
  text: Visualizing and analyzing shape changes at various scales, ranging from single
    molecules to whole organisms, are essential for understanding complex morphogenetic
    processes, such as early embryonic development. Embryo morphogenesis relies on
    the interplay between different tissues, the properties of which are again determined
    by the interaction between their constituent cells. Cell interactions, on the
    other hand, are controlled by various molecules, such as signaling and adhesion
    molecules, which in order to exert their functions need to be spatiotemporally
    organized within and between the interacting cells. In this review, we will focus
    on the role of cell adhesion functioning at different scales to organize cell,
    tissue and embryo morphogenesis. We will specifically ask how the subcellular
    distribution of adhesion molecules controls the formation of cell-cell contacts,
    how cell-cell contacts determine tissue shape, and how tissue interactions regulate
    embryo morphogenesis.
acknowledgement: This review comes from a themed issue on Cell structure and dynamics
  Edited by Jason Swedlow and Gaudenz Danuser
author:
- first_name: Vanessa
  full_name: Barone, Vanessa
  id: 419EECCC-F248-11E8-B48F-1D18A9856A87
  last_name: Barone
  orcid: 0000-0003-2676-3367
- first_name: Carl-Philipp J
  full_name: Heisenberg, Carl-Philipp J
  id: 39427864-F248-11E8-B48F-1D18A9856A87
  last_name: Heisenberg
  orcid: 0000-0002-0912-4566
citation:
  ama: Barone V, Heisenberg C-PJ. Cell adhesion in embryo morphogenesis. <i>Current
    Opinion in Cell Biology</i>. 2012;24(1):148-153. doi:<a href="https://doi.org/10.1016/j.ceb.2011.11.006">10.1016/j.ceb.2011.11.006</a>
  apa: Barone, V., &#38; Heisenberg, C.-P. J. (2012). Cell adhesion in embryo morphogenesis.
    <i>Current Opinion in Cell Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.ceb.2011.11.006">https://doi.org/10.1016/j.ceb.2011.11.006</a>
  chicago: Barone, Vanessa, and Carl-Philipp J Heisenberg. “Cell Adhesion in Embryo
    Morphogenesis.” <i>Current Opinion in Cell Biology</i>. Elsevier, 2012. <a href="https://doi.org/10.1016/j.ceb.2011.11.006">https://doi.org/10.1016/j.ceb.2011.11.006</a>.
  ieee: V. Barone and C.-P. J. Heisenberg, “Cell adhesion in embryo morphogenesis,”
    <i>Current Opinion in Cell Biology</i>, vol. 24, no. 1. Elsevier, pp. 148–153,
    2012.
  ista: Barone V, Heisenberg C-PJ. 2012. Cell adhesion in embryo morphogenesis. Current
    Opinion in Cell Biology. 24(1), 148–153.
  mla: Barone, Vanessa, and Carl-Philipp J. Heisenberg. “Cell Adhesion in Embryo Morphogenesis.”
    <i>Current Opinion in Cell Biology</i>, vol. 24, no. 1, Elsevier, 2012, pp. 148–53,
    doi:<a href="https://doi.org/10.1016/j.ceb.2011.11.006">10.1016/j.ceb.2011.11.006</a>.
  short: V. Barone, C.-P.J. Heisenberg, Current Opinion in Cell Biology 24 (2012)
    148–153.
date_created: 2018-12-11T12:02:14Z
date_published: 2012-02-01T00:00:00Z
date_updated: 2023-09-07T12:05:08Z
day: '01'
department:
- _id: CaHe
doi: 10.1016/j.ceb.2011.11.006
intvolume: '        24'
issue: '1'
language:
- iso: eng
month: '02'
oa_version: None
page: 148 - 153
publication: Current Opinion in Cell Biology
publication_status: published
publisher: Elsevier
publist_id: '3423'
quality_controlled: '1'
related_material:
  record:
  - id: '961'
    relation: dissertation_contains
    status: public
scopus_import: 1
status: public
title: Cell adhesion in embryo morphogenesis
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2012'
...
---
_id: '3247'
abstract:
- lang: eng
  text: The Brazilian Merganser is a very rare and threatened species that nowadays
    inhabits only a few protected areas and their surroundings in the Brazilian territory.
    In order to estimate the remaining genetic diversity and population structure
    in this species, two mitochondrial genes were sequenced in 39 individuals belonging
    to two populations and in one individual collected in Argentina in 1950. We found
    a highly significant divergence between two major remaining populations of Mergus
    octosetaceus, which suggests a historical population structure in this species.
    Furthermore, two deeply divergent lineages were found in a single location, which
    could due to current or historical secondary contact. Based on the available genetic
    data, we point out future directions which would contribute to design strategies
    for conservation and management of this threatened species.
acknowledgement: "The present study received grants from FAPEMIG, CNPq, Petrobras
  Ambiental and Fundação O Boticário de Conservação da Natureza, and followed all
  ethical guidelines and legal requirements of Brazil for sampling and studying an
  endangered species.\r\nWe thank the Specialist Work Group for the Conservation of
  Brazilian Merganser for valuable discussions and opinions on this manuscript. We
  also thank all the staff from Instituto Terra Brasilis and Funatura (Vivian S. Braz
  and Gislaine Disconzi) for collecting the samples at Serra da Canastra and Chapada
  dos Veadeiros, respectively; Dario A. Lijtmaerand and Pablo Tubaro for providing
  the samples from Argentina, Bradley C. Livezey for sending copies of his papers,
  and Geoff M. Hilton and Paulo de Tarso Z. Antas for useful suggestions that greatly
  improved this manuscript."
author:
- first_name: Sibelle
  full_name: Vilaça, Sibelle
  last_name: Vilaça
- first_name: Rodrigo A
  full_name: Fernandes Redondo, Rodrigo A
  id: 409D5C96-F248-11E8-B48F-1D18A9856A87
  last_name: Fernandes Redondo
  orcid: 0000-0002-5837-2793
- first_name: Lívia
  full_name: Lins, Lívia
  last_name: Lins
- first_name: Fabrício
  full_name: Santos, Fabrício
  last_name: Santos
citation:
  ama: Vilaça S, Fernandes Redondo RA, Lins L, Santos F. Remaining genetic diversity
    in Brazilian Merganser (Mergus octosetaceus). <i>Conservation Genetics</i>. 2012;13(1):293-298.
    doi:<a href="https://doi.org/10.1007/s10592-011-0262-5">10.1007/s10592-011-0262-5</a>
  apa: Vilaça, S., Fernandes Redondo, R. A., Lins, L., &#38; Santos, F. (2012). Remaining
    genetic diversity in Brazilian Merganser (Mergus octosetaceus). <i>Conservation
    Genetics</i>. Springer. <a href="https://doi.org/10.1007/s10592-011-0262-5">https://doi.org/10.1007/s10592-011-0262-5</a>
  chicago: Vilaça, Sibelle, Rodrigo A Fernandes Redondo, Lívia Lins, and Fabrício
    Santos. “Remaining Genetic Diversity in Brazilian Merganser (Mergus Octosetaceus).”
    <i>Conservation Genetics</i>. Springer, 2012. <a href="https://doi.org/10.1007/s10592-011-0262-5">https://doi.org/10.1007/s10592-011-0262-5</a>.
  ieee: S. Vilaça, R. A. Fernandes Redondo, L. Lins, and F. Santos, “Remaining genetic
    diversity in Brazilian Merganser (Mergus octosetaceus),” <i>Conservation Genetics</i>,
    vol. 13, no. 1. Springer, pp. 293–298, 2012.
  ista: Vilaça S, Fernandes Redondo RA, Lins L, Santos F. 2012. Remaining genetic
    diversity in Brazilian Merganser (Mergus octosetaceus). Conservation Genetics.
    13(1), 293–298.
  mla: Vilaça, Sibelle, et al. “Remaining Genetic Diversity in Brazilian Merganser
    (Mergus Octosetaceus).” <i>Conservation Genetics</i>, vol. 13, no. 1, Springer,
    2012, pp. 293–98, doi:<a href="https://doi.org/10.1007/s10592-011-0262-5">10.1007/s10592-011-0262-5</a>.
  short: S. Vilaça, R.A. Fernandes Redondo, L. Lins, F. Santos, Conservation Genetics
    13 (2012) 293–298.
date_created: 2018-12-11T12:02:15Z
date_published: 2012-02-01T00:00:00Z
date_updated: 2021-01-12T07:42:05Z
day: '01'
department:
- _id: JoBo
doi: 10.1007/s10592-011-0262-5
intvolume: '        13'
issue: '1'
language:
- iso: eng
month: '02'
oa_version: None
page: 293 - 298
publication: Conservation Genetics
publication_status: published
publisher: Springer
publist_id: '3420'
quality_controlled: '1'
scopus_import: 1
status: public
title: Remaining genetic diversity in Brazilian Merganser (Mergus octosetaceus)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 13
year: '2012'
...
---
_id: '3248'
abstract:
- lang: eng
  text: We describe RTblob, a high speed vision system that detects objects in cluttered
    scenes based on their color and shape at a speed of over 800 frames/s. Because
    the system is available as open-source software and relies only on off-the-shelf
    PC hardware components, it can provide the basis for multiple application scenarios.
    As an illustrative example, we show how RTblob can be used in a robotic table
    tennis scenario to estimate ball trajectories through 3D space simultaneously
    from four cameras images at a speed of 200 Hz.
article_processing_charge: No
article_type: original
author:
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
- first_name: Jan
  full_name: Peters, Jan
  last_name: Peters
citation:
  ama: Lampert C, Peters J. Real-time detection of colored objects in multiple camera
    streams with off-the-shelf hardware components. <i>Journal of Real-Time Image
    Processing</i>. 2012;7(1):31-41. doi:<a href="https://doi.org/10.1007/s11554-010-0168-3">10.1007/s11554-010-0168-3</a>
  apa: Lampert, C., &#38; Peters, J. (2012). Real-time detection of colored objects
    in multiple camera streams with off-the-shelf hardware components. <i>Journal
    of Real-Time Image Processing</i>. Springer. <a href="https://doi.org/10.1007/s11554-010-0168-3">https://doi.org/10.1007/s11554-010-0168-3</a>
  chicago: Lampert, Christoph, and Jan Peters. “Real-Time Detection of Colored Objects
    in Multiple Camera Streams with off-the-Shelf Hardware Components.” <i>Journal
    of Real-Time Image Processing</i>. Springer, 2012. <a href="https://doi.org/10.1007/s11554-010-0168-3">https://doi.org/10.1007/s11554-010-0168-3</a>.
  ieee: C. Lampert and J. Peters, “Real-time detection of colored objects in multiple
    camera streams with off-the-shelf hardware components,” <i>Journal of Real-Time
    Image Processing</i>, vol. 7, no. 1. Springer, pp. 31–41, 2012.
  ista: Lampert C, Peters J. 2012. Real-time detection of colored objects in multiple
    camera streams with off-the-shelf hardware components. Journal of Real-Time Image
    Processing. 7(1), 31–41.
  mla: Lampert, Christoph, and Jan Peters. “Real-Time Detection of Colored Objects
    in Multiple Camera Streams with off-the-Shelf Hardware Components.” <i>Journal
    of Real-Time Image Processing</i>, vol. 7, no. 1, Springer, 2012, pp. 31–41, doi:<a
    href="https://doi.org/10.1007/s11554-010-0168-3">10.1007/s11554-010-0168-3</a>.
  short: C. Lampert, J. Peters, Journal of Real-Time Image Processing 7 (2012) 31–41.
date_created: 2018-12-11T12:02:15Z
date_published: 2012-03-01T00:00:00Z
date_updated: 2022-05-24T08:05:40Z
day: '01'
ddc:
- '000'
department:
- _id: ChLa
doi: 10.1007/s11554-010-0168-3
file:
- access_level: open_access
  checksum: 241be47ea50e81a283bcf4c45b07e8cc
  content_type: application/pdf
  creator: kschuh
  date_created: 2019-02-12T10:52:25Z
  date_updated: 2020-07-14T12:46:04Z
  file_id: '5958'
  file_name: 2012_Springer_Lampert.pdf
  file_size: 2933187
  relation: main_file
file_date_updated: 2020-07-14T12:46:04Z
has_accepted_license: '1'
intvolume: '         7'
issue: '1'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Submitted Version
page: 31 - 41
publication: Journal of Real-Time Image Processing
publication_identifier:
  eissn:
  - 1861-8219
  issn:
  - 1861-8200
publication_status: published
publisher: Springer
publist_id: '3417'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Real-time detection of colored objects in multiple camera streams with off-the-shelf
  hardware components
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2012'
...
---
_id: '3249'
abstract:
- lang: eng
  text: Boolean notions of correctness are formalized by preorders on systems. Quantitative
    measures of correctness can be formalized by real-valued distance functions between
    systems, where the distance between implementation and specification provides
    a measure of &quot;fit&quot; or &quot;desirability&quot;. We extend the simulation
    preorder to the quantitative setting by making each player of a simulation game
    pay a certain price for her choices. We use the resulting games with quantitative
    objectives to define three different simulation distances. The correctness distance
    measures how much the specification must be changed in order to be satisfied by
    the implementation. The coverage distance measures how much the implementation
    restricts the degrees of freedom offered by the specification. The robustness
    distance measures how much a system can deviate from the implementation description
    without violating the specification. We consider these distances for safety as
    well as liveness specifications. The distances can be computed in polynomial time
    for safety specifications, and for liveness specifications given by weak fairness
    constraints. We show that the distance functions satisfy the triangle inequality,
    that the distance between two systems does not increase under parallel composition
    with a third system, and that the distance between two systems can be bounded
    from above and below by distances between abstractions of the two systems. These
    properties suggest that our simulation distances provide an appropriate basis
    for a quantitative theory of discrete systems. We also demonstrate how the robustness
    distance can be used to measure how many transmission errors are tolerated by
    error correcting codes.
acknowledgement: This work was partially supported by the ERC Advanced Grant QUAREM,
  the FWF NFN Grant S11402-N23 (RiSE), the European Union project COMBEST and the
  European Network of Excellence Artist Design.
author:
- first_name: Pavol
  full_name: Cerny, Pavol
  id: 4DCBEFFE-F248-11E8-B48F-1D18A9856A87
  last_name: Cerny
- 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: Arjun
  full_name: Radhakrishna, Arjun
  id: 3B51CAC4-F248-11E8-B48F-1D18A9856A87
  last_name: Radhakrishna
citation:
  ama: Cerny P, Henzinger TA, Radhakrishna A. Simulation distances. <i>Theoretical
    Computer Science</i>. 2012;413(1):21-35. doi:<a href="https://doi.org/10.1016/j.tcs.2011.08.002">10.1016/j.tcs.2011.08.002</a>
  apa: Cerny, P., Henzinger, T. A., &#38; Radhakrishna, A. (2012). Simulation distances.
    <i>Theoretical Computer Science</i>. Elsevier. <a href="https://doi.org/10.1016/j.tcs.2011.08.002">https://doi.org/10.1016/j.tcs.2011.08.002</a>
  chicago: Cerny, Pavol, Thomas A Henzinger, and Arjun Radhakrishna. “Simulation Distances.”
    <i>Theoretical Computer Science</i>. Elsevier, 2012. <a href="https://doi.org/10.1016/j.tcs.2011.08.002">https://doi.org/10.1016/j.tcs.2011.08.002</a>.
  ieee: P. Cerny, T. A. Henzinger, and A. Radhakrishna, “Simulation distances,” <i>Theoretical
    Computer Science</i>, vol. 413, no. 1. Elsevier, pp. 21–35, 2012.
  ista: Cerny P, Henzinger TA, Radhakrishna A. 2012. Simulation distances. Theoretical
    Computer Science. 413(1), 21–35.
  mla: Cerny, Pavol, et al. “Simulation Distances.” <i>Theoretical Computer Science</i>,
    vol. 413, no. 1, Elsevier, 2012, pp. 21–35, doi:<a href="https://doi.org/10.1016/j.tcs.2011.08.002">10.1016/j.tcs.2011.08.002</a>.
  short: P. Cerny, T.A. Henzinger, A. Radhakrishna, Theoretical Computer Science 413
    (2012) 21–35.
date_created: 2018-12-11T12:02:15Z
date_published: 2012-01-06T00:00:00Z
date_updated: 2023-02-23T12:24:04Z
day: '06'
department:
- _id: ToHe
doi: 10.1016/j.tcs.2011.08.002
ec_funded: 1
intvolume: '       413'
issue: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 21 - 35
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: 25EFB36C-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '215543'
  name: COMponent-Based Embedded Systems design Techniques
- _id: 25F1337C-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '214373'
  name: Design for Embedded Systems
publication: Theoretical Computer Science
publication_status: published
publisher: Elsevier
publist_id: '3408'
pubrep_id: '42'
quality_controlled: '1'
related_material:
  record:
  - id: '4393'
    relation: earlier_version
    status: public
  - id: '5389'
    relation: earlier_version
    status: public
scopus_import: 1
status: public
title: Simulation distances
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 413
year: '2012'
...
---
_id: '3250'
abstract:
- lang: eng
  text: The Learning Parity with Noise (LPN) problem has recently found many applications
    in cryptography as the hardness assumption underlying the constructions of &quot;provably
    secure&quot; cryptographic schemes like encryption or authentication protocols.
    Being provably secure means that the scheme comes with a proof showing that the
    existence of an efficient adversary against the scheme implies that the underlying
    hardness assumption is wrong. LPN based schemes are appealing for theoretical
    and practical reasons. On the theoretical side, LPN based schemes offer a very
    strong security guarantee. The LPN problem is equivalent to the problem of decoding
    random linear codes, a problem that has been extensively studied in the last half
    century. The fastest known algorithms run in exponential time and unlike most
    number-theoretic problems used in cryptography, the LPN problem does not succumb
    to known quantum algorithms. On the practical side, LPN based schemes are often
    extremely simple and efficient in terms of code-size as well as time and space
    requirements. This makes them prime candidates for light-weight devices like RFID
    tags, which are too weak to implement standard cryptographic primitives like the
    AES block-cipher. This talk will be a gentle introduction to provable security
    using simple LPN based schemes as examples. Starting from pseudorandom generators
    and symmetric key encryption, over secret-key authentication protocols, and, if
    time admits, touching on recent constructions of public-key identification, commitments
    and zero-knowledge proofs.
alternative_title:
- LNCS
author:
- 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: 'Pietrzak KZ. Cryptography from learning parity with noise. In: Vol 7147. Springer;
    2012:99-114. doi:<a href="https://doi.org/10.1007/978-3-642-27660-6_9">10.1007/978-3-642-27660-6_9</a>'
  apa: 'Pietrzak, K. Z. (2012). Cryptography from learning parity with noise (Vol.
    7147, pp. 99–114). Presented at the SOFSEM: Current Trends in Theory and Practice
    of Computer Science, Špindlerův Mlýn, Czech Republic: Springer. <a href="https://doi.org/10.1007/978-3-642-27660-6_9">https://doi.org/10.1007/978-3-642-27660-6_9</a>'
  chicago: Pietrzak, Krzysztof Z. “Cryptography from Learning Parity with Noise,”
    7147:99–114. Springer, 2012. <a href="https://doi.org/10.1007/978-3-642-27660-6_9">https://doi.org/10.1007/978-3-642-27660-6_9</a>.
  ieee: 'K. Z. Pietrzak, “Cryptography from learning parity with noise,” presented
    at the SOFSEM: Current Trends in Theory and Practice of Computer Science, Špindlerův
    Mlýn, Czech Republic, 2012, vol. 7147, pp. 99–114.'
  ista: 'Pietrzak KZ. 2012. Cryptography from learning parity with noise. SOFSEM:
    Current Trends in Theory and Practice of Computer Science, LNCS, vol. 7147, 99–114.'
  mla: Pietrzak, Krzysztof Z. <i>Cryptography from Learning Parity with Noise</i>.
    Vol. 7147, Springer, 2012, pp. 99–114, doi:<a href="https://doi.org/10.1007/978-3-642-27660-6_9">10.1007/978-3-642-27660-6_9</a>.
  short: K.Z. Pietrzak, in:, Springer, 2012, pp. 99–114.
conference:
  end_date: 2012-01-27
  location: Špindlerův Mlýn, Czech Republic
  name: 'SOFSEM: Current Trends in Theory and Practice of Computer Science'
  start_date: 2012-01-21
date_created: 2018-12-11T12:02:15Z
date_published: 2012-02-19T00:00:00Z
date_updated: 2021-01-12T07:42:07Z
day: '19'
department:
- _id: KrPi
doi: 10.1007/978-3-642-27660-6_9
intvolume: '      7147'
language:
- iso: eng
month: '02'
oa_version: None
page: 99 - 114
publication_status: published
publisher: Springer
publist_id: '3407'
quality_controlled: '1'
scopus_import: 1
status: public
title: Cryptography from learning parity with noise
type: conference
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7147
year: '2012'
...
---
_id: '3251'
abstract:
- lang: eng
  text: Many infinite state systems can be seen as well-structured transition systems
    (WSTS), i.e., systems equipped with a well-quasi-ordering on states that is also
    a simulation relation. WSTS are an attractive target for formal analysis because
    there exist generic algorithms that decide interesting verification problems for
    this class. Among the most popular algorithms are acceleration-based forward analyses
    for computing the covering set. Termination of these algorithms can only be guaranteed
    for flattable WSTS. Yet, many WSTS of practical interest are not flattable and
    the question whether any given WSTS is flattable is itself undecidable. We therefore
    propose an analysis that computes the covering set and captures the essence of
    acceleration-based algorithms, but sacrifices precision for guaranteed termination.
    Our analysis is an abstract interpretation whose abstract domain builds on the
    ideal completion of the well-quasi-ordered state space, and a widening operator
    that mimics acceleration and controls the loss of precision of the analysis. We
    present instances of our framework for various classes of WSTS. Our experience
    with a prototype implementation indicates that, despite the inherent precision
    loss, our analysis often computes the precise covering set of the analyzed system.
acknowledgement: This research was supported in part by the European Research Council
  (ERC) Advanced Investigator Grant QUAREM and by the Austrian Science Fund (FWF)
  project S11402-N23.
alternative_title:
- LNCS
author:
- first_name: Damien
  full_name: Zufferey, Damien
  id: 4397AC76-F248-11E8-B48F-1D18A9856A87
  last_name: Zufferey
  orcid: 0000-0002-3197-8736
- first_name: Thomas
  full_name: Wies, Thomas
  id: 447BFB88-F248-11E8-B48F-1D18A9856A87
  last_name: Wies
- 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: 'Zufferey D, Wies T, Henzinger TA. Ideal abstractions for well structured transition
    systems. In: Vol 7148. Springer; 2012:445-460. doi:<a href="https://doi.org/10.1007/978-3-642-27940-9_29">10.1007/978-3-642-27940-9_29</a>'
  apa: 'Zufferey, D., Wies, T., &#38; Henzinger, T. A. (2012). Ideal abstractions
    for well structured transition systems (Vol. 7148, pp. 445–460). Presented at
    the VMCAI: Verification, Model Checking and Abstract Interpretation, Philadelphia,
    PA, USA: Springer. <a href="https://doi.org/10.1007/978-3-642-27940-9_29">https://doi.org/10.1007/978-3-642-27940-9_29</a>'
  chicago: Zufferey, Damien, Thomas Wies, and Thomas A Henzinger. “Ideal Abstractions
    for Well Structured Transition Systems,” 7148:445–60. Springer, 2012. <a href="https://doi.org/10.1007/978-3-642-27940-9_29">https://doi.org/10.1007/978-3-642-27940-9_29</a>.
  ieee: 'D. Zufferey, T. Wies, and T. A. Henzinger, “Ideal abstractions for well structured
    transition systems,” presented at the VMCAI: Verification, Model Checking and
    Abstract Interpretation, Philadelphia, PA, USA, 2012, vol. 7148, pp. 445–460.'
  ista: 'Zufferey D, Wies T, Henzinger TA. 2012. Ideal abstractions for well structured
    transition systems. VMCAI: Verification, Model Checking and Abstract Interpretation,
    LNCS, vol. 7148, 445–460.'
  mla: Zufferey, Damien, et al. <i>Ideal Abstractions for Well Structured Transition
    Systems</i>. Vol. 7148, Springer, 2012, pp. 445–60, doi:<a href="https://doi.org/10.1007/978-3-642-27940-9_29">10.1007/978-3-642-27940-9_29</a>.
  short: D. Zufferey, T. Wies, T.A. Henzinger, in:, Springer, 2012, pp. 445–460.
conference:
  end_date: 2012-01-24
  location: Philadelphia, PA, USA
  name: 'VMCAI: Verification, Model Checking and Abstract Interpretation'
  start_date: 2012-01-22
date_created: 2018-12-11T12:02:16Z
date_published: 2012-01-01T00:00:00Z
date_updated: 2023-09-07T11:36:36Z
day: '01'
ddc:
- '000'
- '005'
department:
- _id: ToHe
doi: 10.1007/978-3-642-27940-9_29
ec_funded: 1
file:
- access_level: open_access
  checksum: f2f0d55efa32309ad1fe65a5fcaad90c
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:09:35Z
  date_updated: 2020-07-14T12:46:05Z
  file_id: '4759'
  file_name: IST-2012-100-v1+1_Ideal_abstractions_for_well-structured_transition_systems.pdf
  file_size: 217104
  relation: main_file
file_date_updated: 2020-07-14T12:46:05Z
has_accepted_license: '1'
intvolume: '      7148'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Submitted Version
page: 445 - 460
project:
- _id: 25EE3708-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '267989'
  name: Quantitative Reactive Modeling
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
publication_status: published
publisher: Springer
publist_id: '3406'
pubrep_id: '100'
quality_controlled: '1'
related_material:
  record:
  - id: '1405'
    relation: dissertation_contains
    status: public
status: public
title: Ideal abstractions for well structured transition systems
type: conference
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 7148
year: '2012'
...
