---
_id: '2300'
abstract:
- lang: eng
  text: We consider Ising models in two and three dimensions with nearest neighbor
    ferromagnetic interactions and long-range, power law decaying, antiferromagnetic
    interactions. If the strength of the ferromagnetic coupling J is larger than a
    critical value Jc, then the ground state is homogeneous and ferromagnetic. As
    the critical value is approached from smaller values of J, it is believed that
    the ground state consists of a periodic array of stripes (d=2) or slabs (d=3),
    all of the same size and alternating magnetization. Here we prove rigorously that
    the ground state energy per site converges to that of the optimal periodic striped
    or slabbed state, in the limit that J tends to the ferromagnetic transition point.
    While this theorem does not prove rigorously that the ground state is precisely
    striped or slabbed, it does prove that in any suitably large box the ground state
    is striped or slabbed with high probability.
article_number: '064401'
arxiv: 1
author:
- first_name: Alessandro
  full_name: Giuliani, Alessandro
  last_name: Giuliani
- first_name: Élliott
  full_name: Lieb, Élliott
  last_name: Lieb
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
citation:
  ama: Giuliani A, Lieb É, Seiringer R. Realization of stripes and slabs in two and
    three dimensions. <i>Physical Review B</i>. 2013;88(6). doi:<a href="https://doi.org/10.1103/PhysRevB.88.064401">10.1103/PhysRevB.88.064401</a>
  apa: Giuliani, A., Lieb, É., &#38; Seiringer, R. (2013). Realization of stripes
    and slabs in two and three dimensions. <i>Physical Review B</i>. American Physical
    Society. <a href="https://doi.org/10.1103/PhysRevB.88.064401">https://doi.org/10.1103/PhysRevB.88.064401</a>
  chicago: Giuliani, Alessandro, Élliott Lieb, and Robert Seiringer. “Realization
    of Stripes and Slabs in Two and Three Dimensions.” <i>Physical Review B</i>. American
    Physical Society, 2013. <a href="https://doi.org/10.1103/PhysRevB.88.064401">https://doi.org/10.1103/PhysRevB.88.064401</a>.
  ieee: A. Giuliani, É. Lieb, and R. Seiringer, “Realization of stripes and slabs
    in two and three dimensions,” <i>Physical Review B</i>, vol. 88, no. 6. American
    Physical Society, 2013.
  ista: Giuliani A, Lieb É, Seiringer R. 2013. Realization of stripes and slabs in
    two and three dimensions. Physical Review B. 88(6), 064401.
  mla: Giuliani, Alessandro, et al. “Realization of Stripes and Slabs in Two and Three
    Dimensions.” <i>Physical Review B</i>, vol. 88, no. 6, 064401, American Physical
    Society, 2013, doi:<a href="https://doi.org/10.1103/PhysRevB.88.064401">10.1103/PhysRevB.88.064401</a>.
  short: A. Giuliani, É. Lieb, R. Seiringer, Physical Review B 88 (2013).
date_created: 2018-12-11T11:56:51Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2021-01-12T06:56:38Z
day: '01'
department:
- _id: RoSe
doi: 10.1103/PhysRevB.88.064401
external_id:
  arxiv:
  - '1305.5323'
intvolume: '        88'
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1305.5323
month: '08'
oa: 1
oa_version: Preprint
publication: Physical Review B
publication_status: published
publisher: American Physical Society
publist_id: '4627'
quality_controlled: '1'
scopus_import: 1
status: public
title: Realization of stripes and slabs in two and three dimensions
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 88
year: '2013'
...
---
_id: '2301'
abstract:
- lang: eng
  text: We describe the design and implementation of P, a domain-specific language
    to write asynchronous event driven code. P allows the programmer to specify the
    system as a collection of interacting state machines, which communicate with each
    other using events. P unifies modeling and programming into one activity for the
    programmer. Not only can a P program be compiled into executable code, but it
    can also be tested using model checking techniques. P allows the programmer to
    specify the environment, used to &quot;close&quot; the system during testing,
    as nondeterministic ghost machines. Ghost machines are erased during compilation
    to executable code; a type system ensures that the erasure is semantics preserving.
    The P language is designed so that a P program can be checked for responsiveness-the
    ability to handle every event in a timely manner. By default, a machine needs
    to handle every event that arrives in every state. But handling every event in
    every state is impractical. The language provides a notion of deferred events
    where the programmer can annotate when she wants to delay processing an event.
    The default safety checker looks for presence of unhan-dled events. The language
    also provides default liveness checks that an event cannot be potentially deferred
    forever. P was used to implement and verify the core of the USB device driver
    stack that ships with Microsoft Windows 8. The resulting driver is more reliable
    and performs better than its prior incarnation (which did not use P); we have
    more confidence in the robustness of its design due to the language abstractions
    and verification provided by P.
author:
- first_name: Ankush
  full_name: Desai, Ankush
  last_name: Desai
- first_name: Vivek
  full_name: Gupta, Vivek
  last_name: Gupta
- first_name: Ethan
  full_name: Jackson, Ethan
  last_name: Jackson
- first_name: Shaz
  full_name: Qadeer, Shaz
  last_name: Qadeer
- first_name: Sriram
  full_name: Rajamani, Sriram
  last_name: Rajamani
- first_name: Damien
  full_name: Zufferey, Damien
  id: 4397AC76-F248-11E8-B48F-1D18A9856A87
  last_name: Zufferey
  orcid: 0000-0002-3197-8736
citation:
  ama: 'Desai A, Gupta V, Jackson E, Qadeer S, Rajamani S, Zufferey D. P: Safe asynchronous
    event-driven programming. In: <i>Proceedings of the 34th ACM SIGPLAN Conference
    on Programming Language Design and Implementation</i>. ACM; 2013:321-331. doi:<a
    href="https://doi.org/10.1145/2491956.2462184">10.1145/2491956.2462184</a>'
  apa: 'Desai, A., Gupta, V., Jackson, E., Qadeer, S., Rajamani, S., &#38; Zufferey,
    D. (2013). P: Safe asynchronous event-driven programming. In <i>Proceedings of
    the 34th ACM SIGPLAN Conference on Programming Language Design and Implementation</i>
    (pp. 321–331). Seattle, WA, United States: ACM. <a href="https://doi.org/10.1145/2491956.2462184">https://doi.org/10.1145/2491956.2462184</a>'
  chicago: 'Desai, Ankush, Vivek Gupta, Ethan Jackson, Shaz Qadeer, Sriram Rajamani,
    and Damien Zufferey. “P: Safe Asynchronous Event-Driven Programming.” In <i>Proceedings
    of the 34th ACM SIGPLAN Conference on Programming Language Design and Implementation</i>,
    321–31. ACM, 2013. <a href="https://doi.org/10.1145/2491956.2462184">https://doi.org/10.1145/2491956.2462184</a>.'
  ieee: 'A. Desai, V. Gupta, E. Jackson, S. Qadeer, S. Rajamani, and D. Zufferey,
    “P: Safe asynchronous event-driven programming,” in <i>Proceedings of the 34th
    ACM SIGPLAN Conference on Programming Language Design and Implementation</i>,
    Seattle, WA, United States, 2013, pp. 321–331.'
  ista: 'Desai A, Gupta V, Jackson E, Qadeer S, Rajamani S, Zufferey D. 2013. P: Safe
    asynchronous event-driven programming. Proceedings of the 34th ACM SIGPLAN Conference
    on Programming Language Design and Implementation. PLDI: Programming Languages
    Design and Implementation, 321–331.'
  mla: 'Desai, Ankush, et al. “P: Safe Asynchronous Event-Driven Programming.” <i>Proceedings
    of the 34th ACM SIGPLAN Conference on Programming Language Design and Implementation</i>,
    ACM, 2013, pp. 321–31, doi:<a href="https://doi.org/10.1145/2491956.2462184">10.1145/2491956.2462184</a>.'
  short: A. Desai, V. Gupta, E. Jackson, S. Qadeer, S. Rajamani, D. Zufferey, in:,
    Proceedings of the 34th ACM SIGPLAN Conference on Programming Language Design
    and Implementation, ACM, 2013, pp. 321–331.
conference:
  end_date: 2013-06-19
  location: Seattle, WA, United States
  name: 'PLDI: Programming Languages Design and Implementation'
  start_date: 2013-06-16
date_created: 2018-12-11T11:56:52Z
date_published: 2013-06-01T00:00:00Z
date_updated: 2021-01-12T06:56:38Z
day: '01'
department:
- _id: ToHe
doi: 10.1145/2491956.2462184
ec_funded: 1
language:
- iso: eng
main_file_link:
- url: http://research.microsoft.com/pubs/191069/pldi212_desai.pdf
month: '06'
oa_version: None
page: 321 - 331
project:
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 25EE3708-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '267989'
  name: Quantitative Reactive Modeling
publication: Proceedings of the 34th ACM SIGPLAN Conference on Programming Language
  Design and Implementation
publication_status: published
publisher: ACM
publist_id: '4626'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'P: Safe asynchronous event-driven programming'
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2013'
...
---
_id: '2303'
abstract:
- lang: eng
  text: MADM (Mosaic Analysis with Double Markers) technology offers a genetic approach
    in mice to visualize and concomitantly manipulate genetically defined cells at
    clonal level and single cell resolution. MADM employs Cre recombinase/loxP-dependent
    interchromosomal mitotic recombination to reconstitute two split marker genes—green
    GFP and red tdTomato—and can label sparse clones of homozygous mutant cells in
    one color and wild-type cells in the other color in an otherwise unlabeled background.
    At present, major MADM applications include lineage tracing, single cell labeling,
    conditional knockouts in small populations of cells and induction of uniparental
    chromosome disomy to assess effects of genomic imprinting. MADM can be applied
    universally in the mouse with the sole limitation being the specificity of the
    promoter controlling Cre recombinase expression. Here I review recent developments
    and extensions of the MADM technique and give an overview of the major discoveries
    and progresses enabled by the implementation of the novel genetic MADM tools.
acknowledgement: This work was supported by IST Austria institutional funds.
article_type: review
author:
- first_name: Simon
  full_name: Hippenmeyer, Simon
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
citation:
  ama: Hippenmeyer S. Dissection of gene function at clonal level using mosaic analysis
    with double markers. <i>Frontiers in Biology</i>. 2013;8(6):557-568. doi:<a href="https://doi.org/10.1007/s11515-013-1279-6">10.1007/s11515-013-1279-6</a>
  apa: Hippenmeyer, S. (2013). Dissection of gene function at clonal level using mosaic
    analysis with double markers. <i>Frontiers in Biology</i>. Springer. <a href="https://doi.org/10.1007/s11515-013-1279-6">https://doi.org/10.1007/s11515-013-1279-6</a>
  chicago: Hippenmeyer, Simon. “Dissection of Gene Function at Clonal Level Using
    Mosaic Analysis with Double Markers.” <i>Frontiers in Biology</i>. Springer, 2013.
    <a href="https://doi.org/10.1007/s11515-013-1279-6">https://doi.org/10.1007/s11515-013-1279-6</a>.
  ieee: S. Hippenmeyer, “Dissection of gene function at clonal level using mosaic
    analysis with double markers,” <i>Frontiers in Biology</i>, vol. 8, no. 6. Springer,
    pp. 557–568, 2013.
  ista: Hippenmeyer S. 2013. Dissection of gene function at clonal level using mosaic
    analysis with double markers. Frontiers in Biology. 8(6), 557–568.
  mla: Hippenmeyer, Simon. “Dissection of Gene Function at Clonal Level Using Mosaic
    Analysis with Double Markers.” <i>Frontiers in Biology</i>, vol. 8, no. 6, Springer,
    2013, pp. 557–68, doi:<a href="https://doi.org/10.1007/s11515-013-1279-6">10.1007/s11515-013-1279-6</a>.
  short: S. Hippenmeyer, Frontiers in Biology 8 (2013) 557–568.
date_created: 2018-12-11T11:56:52Z
date_published: 2013-09-03T00:00:00Z
date_updated: 2021-01-12T06:56:39Z
day: '03'
department:
- _id: SiHi
doi: 10.1007/s11515-013-1279-6
intvolume: '         8'
issue: '6'
language:
- iso: eng
month: '09'
oa_version: None
page: 557 - 568
publication: Frontiers in Biology
publication_status: published
publisher: Springer
publist_id: '4624'
quality_controlled: '1'
scopus_import: 1
status: public
title: Dissection of gene function at clonal level using mosaic analysis with double
  markers
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2013'
...
---
_id: '2304'
abstract:
- lang: eng
  text: This extended abstract is concerned with the irregularities of distribution
    of one-dimensional permuted van der Corput sequences that are generated from linear
    permutations. We show how to obtain upper bounds for the discrepancy and diaphony
    of these sequences, by relating them to Kronecker sequences and applying earlier
    results of Faure and Niederreiter.
acknowledgement: This research is supported by the Graduate school of IST Austria
  (Institute of Science and Technology Austria).
author:
- first_name: Florian
  full_name: Pausinger, Florian
  id: 2A77D7A2-F248-11E8-B48F-1D18A9856A87
  last_name: Pausinger
  orcid: 0000-0002-8379-3768
citation:
  ama: Pausinger F. Van der Corput sequences and linear permutations. <i>Electronic
    Notes in Discrete Mathematics</i>. 2013;43:43-50. doi:<a href="https://doi.org/10.1016/j.endm.2013.07.008">10.1016/j.endm.2013.07.008</a>
  apa: Pausinger, F. (2013). Van der Corput sequences and linear permutations. <i>Electronic
    Notes in Discrete Mathematics</i>. Elsevier. <a href="https://doi.org/10.1016/j.endm.2013.07.008">https://doi.org/10.1016/j.endm.2013.07.008</a>
  chicago: Pausinger, Florian. “Van Der Corput Sequences and Linear Permutations.”
    <i>Electronic Notes in Discrete Mathematics</i>. Elsevier, 2013. <a href="https://doi.org/10.1016/j.endm.2013.07.008">https://doi.org/10.1016/j.endm.2013.07.008</a>.
  ieee: F. Pausinger, “Van der Corput sequences and linear permutations,” <i>Electronic
    Notes in Discrete Mathematics</i>, vol. 43. Elsevier, pp. 43–50, 2013.
  ista: Pausinger F. 2013. Van der Corput sequences and linear permutations. Electronic
    Notes in Discrete Mathematics. 43, 43–50.
  mla: Pausinger, Florian. “Van Der Corput Sequences and Linear Permutations.” <i>Electronic
    Notes in Discrete Mathematics</i>, vol. 43, Elsevier, 2013, pp. 43–50, doi:<a
    href="https://doi.org/10.1016/j.endm.2013.07.008">10.1016/j.endm.2013.07.008</a>.
  short: F. Pausinger, Electronic Notes in Discrete Mathematics 43 (2013) 43–50.
date_created: 2018-12-11T11:56:53Z
date_published: 2013-09-05T00:00:00Z
date_updated: 2021-01-12T06:56:39Z
day: '05'
department:
- _id: HeEd
doi: 10.1016/j.endm.2013.07.008
intvolume: '        43'
language:
- iso: eng
month: '09'
oa_version: None
page: 43 - 50
publication: Electronic Notes in Discrete Mathematics
publication_status: published
publisher: Elsevier
publist_id: '4623'
quality_controlled: '1'
scopus_import: 1
status: public
title: Van der Corput sequences and linear permutations
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 43
year: '2013'
...
---
_id: '2305'
abstract:
- lang: eng
  text: We study the complexity of central controller synthesis problems for finite-state
    Markov decision processes, where the objective is to optimize both the expected
    mean-payoff performance of the system and its stability. e argue that the basic
    theoretical notion of expressing the stability in terms of the variance of the
    mean-payoff (called global variance in our paper) is not always sufficient, since
    it ignores possible instabilities on respective runs. For this reason we propose
    alernative definitions of stability, which we call local and hybrid variance,
    and which express how rewards on each run deviate from the run's own mean-payoff
    and from the expected mean-payoff, respectively. We show that a strategy ensuring
    both the expected mean-payoff and the variance below given bounds requires randomization
    and memory, under all the above semantics of variance. We then look at the problem
    of determining whether there is a such a strategy. For the global variance, we
    show that the problem is in PSPACE, and that the answer can be approximated in
    pseudo-polynomial time. For the hybrid variance, the analogous decision problem
    is in NP, and a polynomial-time approximating algorithm also exists. For local
    variance, we show that the decision problem is in NP. Since the overall performance
    can be traded for stability (and vice versa), we also present algorithms for approximating
    the associated Pareto curve in all the three cases. Finally, we study a special
    case of the decision problems, where we require a given expected mean-payoff together
    with zero variance. Here we show that the problems can be all solved in polynomial
    time.
arxiv: 1
author:
- first_name: Tomáš
  full_name: Brázdil, Tomáš
  last_name: Brázdil
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Vojtěch
  full_name: Forejt, Vojtěch
  last_name: Forejt
- first_name: Antonín
  full_name: Kučera, Antonín
  last_name: Kučera
citation:
  ama: 'Brázdil T, Chatterjee K, Forejt V, Kučera A. Trading performance for stability
    in Markov decision processes. In: <i>28th Annual ACM/IEEE Symposium</i>. IEEE;
    2013:331-340. doi:<a href="https://doi.org/10.1109/LICS.2013.39">10.1109/LICS.2013.39</a>'
  apa: 'Brázdil, T., Chatterjee, K., Forejt, V., &#38; Kučera, A. (2013). Trading
    performance for stability in Markov decision processes. In <i>28th Annual ACM/IEEE
    Symposium</i> (pp. 331–340). New Orleans, LA, United States: IEEE. <a href="https://doi.org/10.1109/LICS.2013.39">https://doi.org/10.1109/LICS.2013.39</a>'
  chicago: Brázdil, Tomáš, Krishnendu Chatterjee, Vojtěch Forejt, and Antonín Kučera.
    “Trading Performance for Stability in Markov Decision Processes.” In <i>28th Annual
    ACM/IEEE Symposium</i>, 331–40. IEEE, 2013. <a href="https://doi.org/10.1109/LICS.2013.39">https://doi.org/10.1109/LICS.2013.39</a>.
  ieee: T. Brázdil, K. Chatterjee, V. Forejt, and A. Kučera, “Trading performance
    for stability in Markov decision processes,” in <i>28th Annual ACM/IEEE Symposium</i>,
    New Orleans, LA, United States, 2013, pp. 331–340.
  ista: 'Brázdil T, Chatterjee K, Forejt V, Kučera A. 2013. Trading performance for
    stability in Markov decision processes. 28th Annual ACM/IEEE Symposium. LICS:
    Logic in Computer Science, 331–340.'
  mla: Brázdil, Tomáš, et al. “Trading Performance for Stability in Markov Decision
    Processes.” <i>28th Annual ACM/IEEE Symposium</i>, IEEE, 2013, pp. 331–40, doi:<a
    href="https://doi.org/10.1109/LICS.2013.39">10.1109/LICS.2013.39</a>.
  short: T. Brázdil, K. Chatterjee, V. Forejt, A. Kučera, in:, 28th Annual ACM/IEEE
    Symposium, IEEE, 2013, pp. 331–340.
conference:
  end_date: 2013-06-28
  location: New Orleans, LA, United States
  name: 'LICS: Logic in Computer Science'
  start_date: 2013-06-25
date_created: 2018-12-11T11:56:53Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2023-09-20T11:15:30Z
day: '01'
department:
- _id: KrCh
doi: 10.1109/LICS.2013.39
ec_funded: 1
external_id:
  arxiv:
  - '1305.4103'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1305.4103
month: '08'
oa: 1
oa_version: Preprint
page: 331 - 340
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 23499-N23
  name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25863FF4-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11407
  name: Game Theory
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2587B514-B435-11E9-9278-68D0E5697425
  name: Microsoft Research Faculty Fellowship
publication: 28th Annual ACM/IEEE Symposium
publication_status: published
publisher: IEEE
publist_id: '4622'
quality_controlled: '1'
related_material:
  record:
  - id: '1294'
    relation: later_version
    status: public
scopus_import: 1
status: public
title: Trading performance for stability in Markov decision processes
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2013'
...
---
_id: '2306'
abstract:
- lang: ger
  text: Das Buch ist sowohl eine Einführung in die Themen Linked Data, Open Data und
    Open Linked Data als es auch den konkreten Bezug auf Bibliotheken behandelt. Hierzu
    werden konkrete Anwendungsprojekte beschrieben. Der Band wendet sich dabei sowohl
    an Personen aus der Bibliothekspraxis als auch an Personen aus dem Bibliotheksmanagement,
    die noch nicht mit dem Thema vertraut sind.
alternative_title:
- Bibliotheks- und Informationspraxis
article_processing_charge: No
author:
- first_name: Patrick
  full_name: Danowski, Patrick
  id: 2EBD1598-F248-11E8-B48F-1D18A9856A87
  last_name: Danowski
  orcid: 0000-0002-6026-4409
- first_name: Adrian
  full_name: Pohl, Adrian
  last_name: Pohl
citation:
  ama: Danowski P, Pohl A. <i>(Open) Linked Data in Bibliotheken</i>. Vol 50. De Gruyter;
    2013. doi:<a href="https://doi.org/10.1515/9783110278736">10.1515/9783110278736</a>
  apa: Danowski, P., &#38; Pohl, A. (2013). <i>(Open) Linked Data in Bibliotheken</i>
    (Vol. 50). De Gruyter. <a href="https://doi.org/10.1515/9783110278736">https://doi.org/10.1515/9783110278736</a>
  chicago: Danowski, Patrick, and Adrian Pohl. <i>(Open) Linked Data in Bibliotheken</i>.
    Vol. 50. De Gruyter, 2013. <a href="https://doi.org/10.1515/9783110278736">https://doi.org/10.1515/9783110278736</a>.
  ieee: P. Danowski and A. Pohl, <i>(Open) Linked Data in Bibliotheken</i>, vol. 50.
    De Gruyter, 2013.
  ista: Danowski P, Pohl A. 2013. (Open) Linked Data in Bibliotheken, De Gruyter,p.
  mla: Danowski, Patrick, and Adrian Pohl. <i>(Open) Linked Data in Bibliotheken</i>.
    Vol. 50, De Gruyter, 2013, doi:<a href="https://doi.org/10.1515/9783110278736">10.1515/9783110278736</a>.
  short: P. Danowski, A. Pohl, (Open) Linked Data in Bibliotheken, De Gruyter, 2013.
date_created: 2018-12-11T11:56:53Z
date_published: 2013-09-13T00:00:00Z
date_updated: 2021-12-21T12:17:19Z
day: '13'
ddc:
- '020'
department:
- _id: E-Lib
doi: 10.1515/9783110278736
file:
- access_level: open_access
  checksum: 807a408bbee519d792702828a32c6e85
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:09:49Z
  date_updated: 2020-07-14T12:45:38Z
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has_accepted_license: '1'
intvolume: '        50'
language:
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month: '09'
oa: 1
oa_version: Published Version
publication_identifier:
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  - 9-783-1102-7873-6
  isbn:
  - ' 978-3-11-027634-3'
  issn:
  - 2191-3587
publication_status: published
publisher: De Gruyter
publist_id: '4621'
pubrep_id: '725'
quality_controlled: '1'
status: public
title: (Open) Linked Data in Bibliotheken
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: book
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 50
year: '2013'
...
---
_id: '2327'
abstract:
- lang: eng
  text: 'We define the model-measuring problem: given a model M and specification
    φ, what is the maximal distance ρ such that all models M′ within distance ρ from
    M satisfy (or violate) φ. The model measuring problem presupposes a distance function
    on models. We concentrate on automatic distance functions, which are defined by
    weighted automata. The model-measuring problem subsumes several generalizations
    of the classical model-checking problem, in particular, quantitative model-checking
    problems that measure the degree of satisfaction of a specification, and robustness
    problems that measure how much a model can be perturbed without violating the
    specification. We show that for automatic distance functions, and ω-regular linear-time
    and branching-time specifications, the model-measuring problem can be solved.
    We use automata-theoretic model-checking methods for model measuring, replacing
    the emptiness question for standard word and tree automata by the optimal-weight
    question for the weighted versions of these automata. We consider weighted automata
    that accumulate weights by maximizing, summing, discounting, and limit averaging.
    We give several examples of using the model-measuring problem to compute various
    notions of robustness and quantitative satisfaction for temporal specifications.'
alternative_title:
- LNCS
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Jan
  full_name: Otop, Jan
  id: 2FC5DA74-F248-11E8-B48F-1D18A9856A87
  last_name: Otop
citation:
  ama: Henzinger TA, Otop J. From model checking to model measuring. 2013;8052:273-287.
    doi:<a href="https://doi.org/10.1007/978-3-642-40184-8_20">10.1007/978-3-642-40184-8_20</a>
  apa: 'Henzinger, T. A., &#38; Otop, J. (2013). From model checking to model measuring.
    Presented at the CONCUR: Concurrency Theory, Buenos Aires, Argentina: Springer.
    <a href="https://doi.org/10.1007/978-3-642-40184-8_20">https://doi.org/10.1007/978-3-642-40184-8_20</a>'
  chicago: Henzinger, Thomas A, and Jan Otop. “From Model Checking to Model Measuring.”
    Lecture Notes in Computer Science. Springer, 2013. <a href="https://doi.org/10.1007/978-3-642-40184-8_20">https://doi.org/10.1007/978-3-642-40184-8_20</a>.
  ieee: T. A. Henzinger and J. Otop, “From model checking to model measuring,” vol.
    8052. Springer, pp. 273–287, 2013.
  ista: Henzinger TA, Otop J. 2013. From model checking to model measuring. 8052,
    273–287.
  mla: Henzinger, Thomas A., and Jan Otop. <i>From Model Checking to Model Measuring</i>.
    Vol. 8052, Springer, 2013, pp. 273–87, doi:<a href="https://doi.org/10.1007/978-3-642-40184-8_20">10.1007/978-3-642-40184-8_20</a>.
  short: T.A. Henzinger, J. Otop, 8052 (2013) 273–287.
conference:
  end_date: 2013-08-30
  location: Buenos Aires, Argentina
  name: 'CONCUR: Concurrency Theory'
  start_date: 2013-08-27
date_created: 2018-12-11T11:57:00Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2023-02-23T12:25:26Z
day: '01'
ddc:
- '005'
- '000'
department:
- _id: ToHe
doi: 10.1007/978-3-642-40184-8_20
file:
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  creator: system
  date_created: 2018-12-12T10:17:45Z
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file_date_updated: 2020-07-14T12:45:38Z
has_accepted_license: '1'
intvolume: '      8052'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Submitted Version
page: 273 - 287
publication_status: published
publisher: Springer
publist_id: '4599'
pubrep_id: '129'
quality_controlled: '1'
related_material:
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  - id: '5417'
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    status: public
series_title: Lecture Notes in Computer Science
status: public
title: From model checking to model measuring
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8052
year: '2013'
...
---
_id: '2328'
abstract:
- lang: eng
  text: "Linearizability of concurrent data structures is usually proved by monolithic
    simulation arguments relying on identifying the so-called linearization points.
    Regrettably, such proofs, whether manual or automatic, are often complicated and
    scale poorly to advanced non-blocking concurrency patterns, such as helping and
    optimistic updates.\r\nIn response, we propose a more modular way of checking
    linearizability of concurrent queue algorithms that does not involve identifying
    linearization points. We reduce the task of proving linearizability with respect
    to the queue specification to establishing four basic properties, each of which
    can be proved independently by simpler arguments. As a demonstration of our approach,
    we verify the Herlihy and Wing queue, an algorithm that is challenging to verify
    by a simulation proof."
alternative_title:
- LNCS
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Ali
  full_name: Sezgin, Ali
  id: 4C7638DA-F248-11E8-B48F-1D18A9856A87
  last_name: Sezgin
- first_name: Viktor
  full_name: Vafeiadis, Viktor
  last_name: Vafeiadis
citation:
  ama: Henzinger TA, Sezgin A, Vafeiadis V. Aspect-oriented linearizability proofs.
    2013;8052:242-256. doi:<a href="https://doi.org/10.1007/978-3-642-40184-8_18">10.1007/978-3-642-40184-8_18</a>
  apa: 'Henzinger, T. A., Sezgin, A., &#38; Vafeiadis, V. (2013). Aspect-oriented
    linearizability proofs. Presented at the CONCUR: Concurrency Theory, Buenos Aires,
    Argentina: Schloss Dagstuhl - Leibniz-Zentrum für Informatik. <a href="https://doi.org/10.1007/978-3-642-40184-8_18">https://doi.org/10.1007/978-3-642-40184-8_18</a>'
  chicago: Henzinger, Thomas A, Ali Sezgin, and Viktor Vafeiadis. “Aspect-Oriented
    Linearizability Proofs.” Lecture Notes in Computer Science. Schloss Dagstuhl -
    Leibniz-Zentrum für Informatik, 2013. <a href="https://doi.org/10.1007/978-3-642-40184-8_18">https://doi.org/10.1007/978-3-642-40184-8_18</a>.
  ieee: T. A. Henzinger, A. Sezgin, and V. Vafeiadis, “Aspect-oriented linearizability
    proofs,” vol. 8052. Schloss Dagstuhl - Leibniz-Zentrum für Informatik, pp. 242–256,
    2013.
  ista: Henzinger TA, Sezgin A, Vafeiadis V. 2013. Aspect-oriented linearizability
    proofs. 8052, 242–256.
  mla: Henzinger, Thomas A., et al. <i>Aspect-Oriented Linearizability Proofs</i>.
    Vol. 8052, Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2013, pp. 242–56,
    doi:<a href="https://doi.org/10.1007/978-3-642-40184-8_18">10.1007/978-3-642-40184-8_18</a>.
  short: T.A. Henzinger, A. Sezgin, V. Vafeiadis, 8052 (2013) 242–256.
conference:
  end_date: 2013-08-30
  location: Buenos Aires, Argentina
  name: 'CONCUR: Concurrency Theory'
  start_date: 2013-08-27
date_created: 2018-12-11T11:57:01Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2023-02-23T10:16:27Z
day: '01'
ddc:
- '000'
- '004'
department:
- _id: ToHe
doi: 10.1007/978-3-642-40184-8_18
ec_funded: 1
file:
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  checksum: bdbb520de91751fe0136309ad4ef67e4
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:08:58Z
  date_updated: 2020-07-14T12:45:39Z
  file_id: '4721'
  file_name: IST-2014-197-v1+1_main-queue-verification.pdf
  file_size: 337059
  relation: main_file
file_date_updated: 2020-07-14T12:45:39Z
has_accepted_license: '1'
intvolume: '      8052'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Submitted Version
page: 242 - 256
project:
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 25EE3708-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '267989'
  name: Quantitative Reactive Modeling
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
publist_id: '4598'
pubrep_id: '197'
quality_controlled: '1'
related_material:
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  - id: '1832'
    relation: later_version
    status: public
scopus_import: 1
series_title: Lecture Notes in Computer Science
status: public
title: Aspect-oriented linearizability proofs
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8052
year: '2013'
...
---
_id: '2329'
abstract:
- lang: eng
  text: 'Two-player games on graphs are central in many problems in formal verification
    and program analysis such as synthesis and verification of open systems. In this
    work, we consider both finite-state game graphs, and recursive game graphs (or
    pushdown game graphs) that model the control flow of sequential programs with
    recursion. The objectives we study are multidimensional mean-payoff objectives,
    where the goal of player 1 is to ensure that the mean-payoff is non-negative in
    all dimensions. In pushdown games two types of strategies are relevant: (1) global
    strategies, that depend on the entire global history; and (2) modular strategies,
    that have only local memory and thus do not depend on the context of invocation.
    Our main contributions are as follows: (1) We show that finite-state multidimensional
    mean-payoff games can be solved in polynomial time if the number of dimensions
    and the maximal absolute value of the weights are fixed; whereas if the number
    of dimensions is arbitrary, then the problem is known to be coNP-complete. (2)
    We show that pushdown graphs with multidimensional mean-payoff objectives can
    be solved in polynomial time. For both (1) and (2) our algorithms are based on
    hyperplane separation technique. (3) For pushdown games under global strategies
    both one and multidimensional mean-payoff objectives problems are known to be
    undecidable, and we show that under modular strategies the multidimensional problem
    is also undecidable; under modular strategies the one-dimensional problem is NP-complete.
    We show that if the number of modules, the number of exits, and the maximal absolute
    value of the weights are fixed, then pushdown games under modular strategies with
    one-dimensional mean-payoff objectives can be solved in polynomial time, and if
    either the number of exits or the number of modules is unbounded, then the problem
    is NP-hard. (4) Finally we show that a fixed parameter tractable algorithm for
    finite-state multidimensional mean-payoff games or pushdown games under modular
    strategies with one-dimensional mean-payoff objectives would imply the fixed parameter
    tractability of parity games.'
alternative_title:
- LNCS
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: Yaron
  full_name: Velner, Yaron
  last_name: Velner
citation:
  ama: Chatterjee K, Velner Y. Hyperplane separation technique for multidimensional
    mean-payoff games. 2013;8052:500-515. doi:<a href="https://doi.org/10.1007/978-3-642-40184-8_35">10.1007/978-3-642-40184-8_35</a>
  apa: 'Chatterjee, K., &#38; Velner, Y. (2013). Hyperplane separation technique for
    multidimensional mean-payoff games. Presented at the CONCUR: Concurrency Theory,
    Buenos Aires, Argentinia: Springer. <a href="https://doi.org/10.1007/978-3-642-40184-8_35">https://doi.org/10.1007/978-3-642-40184-8_35</a>'
  chicago: Chatterjee, Krishnendu, and Yaron Velner. “Hyperplane Separation Technique
    for Multidimensional Mean-Payoff Games.” Lecture Notes in Computer Science. Springer,
    2013. <a href="https://doi.org/10.1007/978-3-642-40184-8_35">https://doi.org/10.1007/978-3-642-40184-8_35</a>.
  ieee: K. Chatterjee and Y. Velner, “Hyperplane separation technique for multidimensional
    mean-payoff games,” vol. 8052. Springer, pp. 500–515, 2013.
  ista: Chatterjee K, Velner Y. 2013. Hyperplane separation technique for multidimensional
    mean-payoff games. 8052, 500–515.
  mla: Chatterjee, Krishnendu, and Yaron Velner. <i>Hyperplane Separation Technique
    for Multidimensional Mean-Payoff Games</i>. Vol. 8052, Springer, 2013, pp. 500–15,
    doi:<a href="https://doi.org/10.1007/978-3-642-40184-8_35">10.1007/978-3-642-40184-8_35</a>.
  short: K. Chatterjee, Y. Velner, 8052 (2013) 500–515.
conference:
  end_date: 2013-08-30
  location: Buenos Aires, Argentinia
  name: 'CONCUR: Concurrency Theory'
  start_date: 2013-08-27
date_created: 2018-12-11T11:57:01Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2023-02-23T13:00:42Z
day: '01'
department:
- _id: KrCh
doi: 10.1007/978-3-642-40184-8_35
ec_funded: 1
external_id:
  arxiv:
  - '1210.3141'
intvolume: '      8052'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1210.3141
month: '08'
oa: 1
oa_version: Preprint
page: 500 - 515
project:
- _id: 2584A770-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 23499-N23
  name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 25863FF4-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11407
  name: Game Theory
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2587B514-B435-11E9-9278-68D0E5697425
  name: Microsoft Research Faculty Fellowship
publication_status: published
publisher: Springer
publist_id: '4597'
quality_controlled: '1'
related_material:
  record:
  - id: '717'
    relation: later_version
    status: public
scopus_import: 1
series_title: Lecture Notes in Computer Science
status: public
title: Hyperplane separation technique for multidimensional mean-payoff games
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8052
year: '2013'
...
---
_id: '2410'
abstract:
- lang: eng
  text: 'Here, we describe a novel virulent bacteriophage that infects Bacillus weihenstephanensis,
    isolated from soil in Austria. It is the first phage to be discovered that infects
    this species. Here, we present the complete genome sequence of this podovirus. '
author:
- 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: Anne
  full_name: Kupczok, Anne
  id: 2BB22BC2-F248-11E8-B48F-1D18A9856A87
  last_name: Kupczok
- first_name: Gertraud
  full_name: Stift, Gertraud
  id: 2DB195CA-F248-11E8-B48F-1D18A9856A87
  last_name: Stift
- first_name: Jonathan P
  full_name: Bollback, Jonathan P
  id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
  last_name: Bollback
  orcid: 0000-0002-4624-4612
citation:
  ama: Fernandes Redondo RA, Kupczok A, Stift G, Bollback JP. Complete genome sequence
    of the novel phage MG-B1 infecting bacillus weihenstephanensis. <i>Genome Announcements</i>.
    2013;1(3). doi:<a href="https://doi.org/10.1128/genomeA.00216-13">10.1128/genomeA.00216-13</a>
  apa: Fernandes Redondo, R. A., Kupczok, A., Stift, G., &#38; Bollback, J. P. (2013).
    Complete genome sequence of the novel phage MG-B1 infecting bacillus weihenstephanensis.
    <i>Genome Announcements</i>. American Society for Microbiology. <a href="https://doi.org/10.1128/genomeA.00216-13">https://doi.org/10.1128/genomeA.00216-13</a>
  chicago: Fernandes Redondo, Rodrigo A, Anne Kupczok, Gertraud Stift, and Jonathan
    P Bollback. “Complete Genome Sequence of the Novel Phage MG-B1 Infecting Bacillus
    Weihenstephanensis.” <i>Genome Announcements</i>. American Society for Microbiology,
    2013. <a href="https://doi.org/10.1128/genomeA.00216-13">https://doi.org/10.1128/genomeA.00216-13</a>.
  ieee: R. A. Fernandes Redondo, A. Kupczok, G. Stift, and J. P. Bollback, “Complete
    genome sequence of the novel phage MG-B1 infecting bacillus weihenstephanensis,”
    <i>Genome Announcements</i>, vol. 1, no. 3. American Society for Microbiology,
    2013.
  ista: Fernandes Redondo RA, Kupczok A, Stift G, Bollback JP. 2013. Complete genome
    sequence of the novel phage MG-B1 infecting bacillus weihenstephanensis. Genome
    Announcements. 1(3).
  mla: Fernandes Redondo, Rodrigo A., et al. “Complete Genome Sequence of the Novel
    Phage MG-B1 Infecting Bacillus Weihenstephanensis.” <i>Genome Announcements</i>,
    vol. 1, no. 3, American Society for Microbiology, 2013, doi:<a href="https://doi.org/10.1128/genomeA.00216-13">10.1128/genomeA.00216-13</a>.
  short: R.A. Fernandes Redondo, A. Kupczok, G. Stift, J.P. Bollback, Genome Announcements
    1 (2013).
date_created: 2018-12-11T11:57:30Z
date_published: 2013-06-13T00:00:00Z
date_updated: 2021-01-12T06:57:19Z
day: '13'
ddc:
- '576'
department:
- _id: JoBo
- _id: LifeSc
doi: 10.1128/genomeA.00216-13
file:
- access_level: open_access
  checksum: 0751ec74b695567e0cdf02aaf9c26829
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:17:36Z
  date_updated: 2020-07-14T12:45:40Z
  file_id: '5291'
  file_name: IST-2015-398-v1+1_Genome_Announc.-2013-Redondo-.pdf
  file_size: 130026
  relation: main_file
file_date_updated: 2020-07-14T12:45:40Z
has_accepted_license: '1'
intvolume: '         1'
issue: '3'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
publication: Genome Announcements
publication_status: published
publisher: American Society for Microbiology
publist_id: '4516'
pubrep_id: '398'
quality_controlled: '1'
scopus_import: 1
status: public
title: Complete genome sequence of the novel phage MG-B1 infecting bacillus weihenstephanensis
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 1
year: '2013'
...
---
_id: '2412'
abstract:
- lang: eng
  text: 'Background: The CRISPR/Cas system is known to act as an adaptive and heritable
    immune system in Eubacteria and Archaea. Immunity is encoded in an array of spacer
    sequences. Each spacer can provide specific immunity to invasive elements that
    carry the same or a similar sequence. Even in closely related strains, spacer
    content is very dynamic and evolves quickly. Standard models of nucleotide evolutioncannot
    be applied to quantify its rate of change since processes other than single nucleotide
    changes determine its evolution.Methods We present probabilistic models that are
    specific for spacer content evolution. They account for the different processes
    of insertion and deletion. Insertions can be constrained to occur on one end only
    or are allowed to occur throughout the array. One deletion event can affect one
    spacer or a whole fragment of adjacent spacers. Parameters of the underlying models
    are estimated for a pair of arrays by maximum likelihood using explicit ancestor
    enumeration.Results Simulations show that parameters are well estimated on average
    under the models presented here. There is a bias in the rate estimation when including
    fragment deletions. The models also estimate times between pairs of strains. But
    with increasing time, spacer overlap goes to zero, and thus there is an upper
    bound on the distance that can be estimated. Spacer content similarities are displayed
    in a distance based phylogeny using the estimated times.We use the presented models
    to analyze different Yersinia pestis data sets and find that the results among
    them are largely congruent. The models also capture the variation in diversity
    of spacers among the data sets. A comparison of spacer-based phylogenies and Cas
    gene phylogenies shows that they resolve very different time scales for this data
    set.Conclusions The simulations and data analyses show that the presented models
    are useful for quantifying spacer content evolution and for displaying spacer
    content similarities of closely related strains in a phylogeny. This allows for
    comparisons of different CRISPR arrays or for comparisons between CRISPR arrays
    and nucleotide substitution rates.'
author:
- first_name: Anne
  full_name: Kupczok, Anne
  id: 2BB22BC2-F248-11E8-B48F-1D18A9856A87
  last_name: Kupczok
- first_name: Jonathan P
  full_name: Bollback, Jonathan P
  id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
  last_name: Bollback
  orcid: 0000-0002-4624-4612
citation:
  ama: Kupczok A, Bollback JP. Probabilistic models for CRISPR spacer content evolution
    . <i>BMC Evolutionary Biology</i>. 2013;13(1):54-54. doi:<a href="https://doi.org/10.1186/1471-2148-13-54">10.1186/1471-2148-13-54</a>
  apa: Kupczok, A., &#38; Bollback, J. P. (2013). Probabilistic models for CRISPR
    spacer content evolution . <i>BMC Evolutionary Biology</i>. BioMed Central. <a
    href="https://doi.org/10.1186/1471-2148-13-54">https://doi.org/10.1186/1471-2148-13-54</a>
  chicago: Kupczok, Anne, and Jonathan P Bollback. “Probabilistic Models for CRISPR
    Spacer Content Evolution .” <i>BMC Evolutionary Biology</i>. BioMed Central, 2013.
    <a href="https://doi.org/10.1186/1471-2148-13-54">https://doi.org/10.1186/1471-2148-13-54</a>.
  ieee: A. Kupczok and J. P. Bollback, “Probabilistic models for CRISPR spacer content
    evolution ,” <i>BMC Evolutionary Biology</i>, vol. 13, no. 1. BioMed Central,
    pp. 54–54, 2013.
  ista: Kupczok A, Bollback JP. 2013. Probabilistic models for CRISPR spacer content
    evolution . BMC Evolutionary Biology. 13(1), 54–54.
  mla: Kupczok, Anne, and Jonathan P. Bollback. “Probabilistic Models for CRISPR Spacer
    Content Evolution .” <i>BMC Evolutionary Biology</i>, vol. 13, no. 1, BioMed Central,
    2013, pp. 54–54, doi:<a href="https://doi.org/10.1186/1471-2148-13-54">10.1186/1471-2148-13-54</a>.
  short: A. Kupczok, J.P. Bollback, BMC Evolutionary Biology 13 (2013) 54–54.
date_created: 2018-12-11T11:57:31Z
date_published: 2013-02-26T00:00:00Z
date_updated: 2021-01-12T06:57:20Z
day: '26'
ddc:
- '576'
department:
- _id: JoBo
doi: 10.1186/1471-2148-13-54
file:
- access_level: open_access
  checksum: 029c7e0b198c19312b66ecce3cabb22f
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:17:15Z
  date_updated: 2020-07-14T12:45:40Z
  file_id: '5268'
  file_name: IST-2015-397-v1+1_1471-2148-13-54.pdf
  file_size: 518729
  relation: main_file
file_date_updated: 2020-07-14T12:45:40Z
has_accepted_license: '1'
intvolume: '        13'
issue: '1'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 54 - 54
publication: BMC Evolutionary Biology
publication_status: published
publisher: BioMed Central
publist_id: '4514'
pubrep_id: '397'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'Probabilistic models for CRISPR spacer content evolution '
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: 13
year: '2013'
...
---
_id: '2413'
abstract:
- lang: eng
  text: 'Progress in understanding the global brain dynamics has remained slow to
    date in large part because of the highly multiscale nature of brain activity.
    Indeed, normal brain dynamics is characterized by complex interactions between
    multiple levels: from the microscopic scale of single neurons to the mesoscopic
    level of local groups of neurons, and finally to the macroscopic level of the
    whole brain. Among the most difficult tasks are those of identifying which scales
    are significant for a given particular function and describing how the scales
    affect each other. It is important to realize that the scales of time and space
    are linked together, or even intertwined, and that causal inference is far more
    ambiguous between than within levels. We approach this problem from the perspective
    of our recent work on simultaneous recording from micro- and macroelectrodes in
    the human brain. We propose a physiological description of these multilevel interactions,
    based on phase–amplitude coupling of neuronal oscillations that operate at multiple
    frequencies and on different spatial scales. Specifically, the amplitude of the
    oscillations on a particular spatial scale is modulated by phasic variations in
    neuronal excitability induced by lower frequency oscillations that emerge on a
    larger spatial scale. Following this general principle, it is possible to scale
    up or scale down the multiscale brain dynamics. It is expected that large-scale
    network oscillations in the low-frequency range, mediating downward effects, may
    play an important role in attention and consciousness.'
alternative_title:
- Reviews of Nonlinear Dynamics and Complexity
author:
- first_name: Mario
  full_name: Valderrama, Mario
  last_name: Valderrama
- first_name: Vicente
  full_name: Botella Soler, Vicente
  id: 421234E8-F248-11E8-B48F-1D18A9856A87
  last_name: Botella Soler
  orcid: 0000-0002-8790-1914
- first_name: Michel
  full_name: Le Van Quyen, Michel
  last_name: Le Van Quyen
citation:
  ama: 'Valderrama M, Botella Soler V, Le Van Quyen M. Neuronal oscillations scale
    up and scale down the brain dynamics . In: Meyer M, Pesenson Z, eds. <i>Multiscale
    Analysis and Nonlinear Dynamics: From Genes to the Brain</i>. Wiley-VCH; 2013.
    doi:<a href="https://doi.org/10.1002/9783527671632.ch08">10.1002/9783527671632.ch08</a>'
  apa: 'Valderrama, M., Botella Soler, V., &#38; Le Van Quyen, M. (2013). Neuronal
    oscillations scale up and scale down the brain dynamics . In M. Meyer &#38; Z.
    Pesenson (Eds.), <i>Multiscale Analysis and Nonlinear Dynamics: From Genes to
    the Brain</i>. Wiley-VCH. <a href="https://doi.org/10.1002/9783527671632.ch08">https://doi.org/10.1002/9783527671632.ch08</a>'
  chicago: 'Valderrama, Mario, Vicente Botella Soler, and Michel Le Van Quyen. “Neuronal
    Oscillations Scale up and Scale down the Brain Dynamics .” In <i>Multiscale Analysis
    and Nonlinear Dynamics: From Genes to the Brain</i>, edited by Misha Meyer and
    Z. Pesenson. Wiley-VCH, 2013. <a href="https://doi.org/10.1002/9783527671632.ch08">https://doi.org/10.1002/9783527671632.ch08</a>.'
  ieee: 'M. Valderrama, V. Botella Soler, and M. Le Van Quyen, “Neuronal oscillations
    scale up and scale down the brain dynamics ,” in <i>Multiscale Analysis and Nonlinear
    Dynamics: From Genes to the Brain</i>, M. Meyer and Z. Pesenson, Eds. Wiley-VCH,
    2013.'
  ista: 'Valderrama M, Botella Soler V, Le Van Quyen M. 2013.Neuronal oscillations
    scale up and scale down the brain dynamics . In: Multiscale Analysis and Nonlinear
    Dynamics: From Genes to the Brain. Reviews of Nonlinear Dynamics and Complexity,
    .'
  mla: 'Valderrama, Mario, et al. “Neuronal Oscillations Scale up and Scale down the
    Brain Dynamics .” <i>Multiscale Analysis and Nonlinear Dynamics: From Genes to
    the Brain</i>, edited by Misha Meyer and Z. Pesenson, Wiley-VCH, 2013, doi:<a
    href="https://doi.org/10.1002/9783527671632.ch08">10.1002/9783527671632.ch08</a>.'
  short: 'M. Valderrama, V. Botella Soler, M. Le Van Quyen, in:, M. Meyer, Z. Pesenson
    (Eds.), Multiscale Analysis and Nonlinear Dynamics: From Genes to the Brain, Wiley-VCH,
    2013.'
date_created: 2018-12-11T11:57:31Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2021-01-12T06:57:20Z
day: '01'
department:
- _id: GaTk
doi: 10.1002/9783527671632.ch08
editor:
- first_name: Misha
  full_name: Meyer, Misha
  last_name: Meyer
- first_name: Z.
  full_name: Pesenson, Z.
  last_name: Pesenson
language:
- iso: eng
month: '08'
oa_version: None
publication: 'Multiscale Analysis and Nonlinear Dynamics: From Genes to the Brain'
publication_identifier:
  eisbn:
  - '9783527671632'
  isbn:
  - '9783527411986 '
publication_status: published
publisher: Wiley-VCH
publist_id: '4513'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'Neuronal oscillations scale up and scale down the brain dynamics '
type: book_chapter
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
year: '2013'
...
---
_id: '476'
abstract:
- lang: eng
  text: 'Maternal exposure to infection occurring mid-gestation produces a three-fold
    increase in the risk of schizophrenia in the offspring. The critical initiating
    factor appears to be the maternal immune activation (MIA) that follows infection.
    This process can be induced in rodents by exposure of pregnant dams to the viral
    mimic Poly I:C, which triggers an immune response that results in structural,
    functional, behavioral, and electrophysiological phenotypes in the adult offspring
    that model those seen in schizophrenia. We used this model to explore the role
    of synchronization in brain neural networks, a process thought to be dysfunctional
    in schizophrenia and previously associated with positive, negative, and cognitive
    symptoms of schizophrenia. Exposure of pregnant dams to Poly I:C on GD15 produced
    an impairment in long-range neural synchrony in adult offspring between two regions
    implicated in schizophrenia pathology; the hippocampus and the medial prefrontal
    cortex (mPFC). This reduction in synchrony was ameliorated by acute doses of the
    antipsychotic clozapine. MIA animals have previously been shown to have impaired
    pre-pulse inhibition (PPI), a gold-standard measure of schizophrenia-like deficits
    in animal models. Our data showed that deficits in synchrony were positively correlated
    with the impairments in PPI. Subsequent analysis of LFP activity during the PPI
    response also showed that reduced coupling between the mPFC and the hippocampus
    following processing of the pre-pulse was associated with reduced PPI. The ability
    of the MIA intervention to model neurodevelopmental aspects of schizophrenia pathology
    provides a useful platform from which to investigate the ontogeny of aberrant
    synchronous processes. Further, the way in which the model expresses translatable
    deficits such as aberrant synchrony and reduced PPI will allow researchers to
    explore novel intervention strategies targeted to these changes. '
author:
- first_name: Desiree
  full_name: Dickerson, Desiree
  id: 444EB89E-F248-11E8-B48F-1D18A9856A87
  last_name: Dickerson
- first_name: David
  full_name: Bilkey, David
  last_name: Bilkey
citation:
  ama: 'Dickerson D, Bilkey D. Aberrant neural synchrony in the maternal immune activation
    model: Using translatable measures to explore targeted interventions. <i>Frontiers
    in Behavioral Neuroscience</i>. 2013;7(DEC). doi:<a href="https://doi.org/10.3389/fnbeh.2013.00217">10.3389/fnbeh.2013.00217</a>'
  apa: 'Dickerson, D., &#38; Bilkey, D. (2013). Aberrant neural synchrony in the maternal
    immune activation model: Using translatable measures to explore targeted interventions.
    <i>Frontiers in Behavioral Neuroscience</i>. Frontiers Research Foundation. <a
    href="https://doi.org/10.3389/fnbeh.2013.00217">https://doi.org/10.3389/fnbeh.2013.00217</a>'
  chicago: 'Dickerson, Desiree, and David Bilkey. “Aberrant Neural Synchrony in the
    Maternal Immune Activation Model: Using Translatable Measures to Explore Targeted
    Interventions.” <i>Frontiers in Behavioral Neuroscience</i>. Frontiers Research
    Foundation, 2013. <a href="https://doi.org/10.3389/fnbeh.2013.00217">https://doi.org/10.3389/fnbeh.2013.00217</a>.'
  ieee: 'D. Dickerson and D. Bilkey, “Aberrant neural synchrony in the maternal immune
    activation model: Using translatable measures to explore targeted interventions,”
    <i>Frontiers in Behavioral Neuroscience</i>, vol. 7, no. DEC. Frontiers Research
    Foundation, 2013.'
  ista: 'Dickerson D, Bilkey D. 2013. Aberrant neural synchrony in the maternal immune
    activation model: Using translatable measures to explore targeted interventions.
    Frontiers in Behavioral Neuroscience. 7(DEC).'
  mla: 'Dickerson, Desiree, and David Bilkey. “Aberrant Neural Synchrony in the Maternal
    Immune Activation Model: Using Translatable Measures to Explore Targeted Interventions.”
    <i>Frontiers in Behavioral Neuroscience</i>, vol. 7, no. DEC, Frontiers Research
    Foundation, 2013, doi:<a href="https://doi.org/10.3389/fnbeh.2013.00217">10.3389/fnbeh.2013.00217</a>.'
  short: D. Dickerson, D. Bilkey, Frontiers in Behavioral Neuroscience 7 (2013).
date_created: 2018-12-11T11:46:41Z
date_published: 2013-12-27T00:00:00Z
date_updated: 2021-01-12T08:00:53Z
day: '27'
ddc:
- '571'
department:
- _id: JoCs
doi: 10.3389/fnbeh.2013.00217
file:
- access_level: open_access
  checksum: cd7183121e56251176100ccac165c95c
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:15:10Z
  date_updated: 2020-07-14T12:46:35Z
  file_id: '5128'
  file_name: IST-2018-953-v1+1_2013_Dickerson_Aberrant_neural.pdf
  file_size: 530134
  relation: main_file
file_date_updated: 2020-07-14T12:46:35Z
has_accepted_license: '1'
intvolume: '         7'
issue: DEC
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
publication: Frontiers in Behavioral Neuroscience
publication_status: published
publisher: Frontiers Research Foundation
publist_id: '7346'
pubrep_id: '953'
quality_controlled: '1'
status: public
title: 'Aberrant neural synchrony in the maternal immune activation model: Using translatable
  measures to explore targeted interventions'
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: 7
year: '2013'
...
---
_id: '499'
abstract:
- lang: eng
  text: Exposure of an isogenic bacterial population to a cidal antibiotic typically
    fails to eliminate a small fraction of refractory cells. Historically, fractional
    killing has been attributed to infrequently dividing or nondividing &quot;persisters.&quot;
    Using microfluidic cultures and time-lapse microscopy, we found that Mycobacterium
    smegmatis persists by dividing in the presence of the drug isoniazid (INH). Although
    persistence in these studies was characterized by stable numbers of cells, this
    apparent stability was actually a dynamic state of balanced division and death.
    Single cells expressed catalase-peroxidase (KatG), which activates INH, in stochastic
    pulses that were negatively correlated with cell survival. These behaviors may
    reflect epigenetic effects, because KatG pulsing and death were correlated between
    sibling cells. Selection of lineages characterized by infrequent KatG pulsing
    could allow nonresponsive adaptation during prolonged drug exposure.
author:
- first_name: Yurichi
  full_name: Wakamoto, Yurichi
  last_name: Wakamoto
- first_name: Neraaj
  full_name: Dhar, Neraaj
  last_name: Dhar
- first_name: Remy P
  full_name: Chait, Remy P
  id: 3464AE84-F248-11E8-B48F-1D18A9856A87
  last_name: Chait
  orcid: 0000-0003-0876-3187
- first_name: Katrin
  full_name: Schneider, Katrin
  last_name: Schneider
- first_name: François
  full_name: Signorino Gelo, François
  last_name: Signorino Gelo
- first_name: Stanislas
  full_name: Leibler, Stanislas
  last_name: Leibler
- first_name: John
  full_name: Mckinney, John
  last_name: Mckinney
citation:
  ama: Wakamoto Y, Dhar N, Chait RP, et al. Dynamic persistence of antibiotic-stressed
    mycobacteria. <i>Science</i>. 2013;339(6115):91-95. doi:<a href="https://doi.org/10.1126/science.1229858">10.1126/science.1229858</a>
  apa: Wakamoto, Y., Dhar, N., Chait, R. P., Schneider, K., Signorino Gelo, F., Leibler,
    S., &#38; Mckinney, J. (2013). Dynamic persistence of antibiotic-stressed mycobacteria.
    <i>Science</i>. American Association for the Advancement of Science. <a href="https://doi.org/10.1126/science.1229858">https://doi.org/10.1126/science.1229858</a>
  chicago: Wakamoto, Yurichi, Neraaj Dhar, Remy P Chait, Katrin Schneider, François
    Signorino Gelo, Stanislas Leibler, and John Mckinney. “Dynamic Persistence of
    Antibiotic-Stressed Mycobacteria.” <i>Science</i>. American Association for the
    Advancement of Science, 2013. <a href="https://doi.org/10.1126/science.1229858">https://doi.org/10.1126/science.1229858</a>.
  ieee: Y. Wakamoto <i>et al.</i>, “Dynamic persistence of antibiotic-stressed mycobacteria,”
    <i>Science</i>, vol. 339, no. 6115. American Association for the Advancement of
    Science, pp. 91–95, 2013.
  ista: Wakamoto Y, Dhar N, Chait RP, Schneider K, Signorino Gelo F, Leibler S, Mckinney
    J. 2013. Dynamic persistence of antibiotic-stressed mycobacteria. Science. 339(6115),
    91–95.
  mla: Wakamoto, Yurichi, et al. “Dynamic Persistence of Antibiotic-Stressed Mycobacteria.”
    <i>Science</i>, vol. 339, no. 6115, American Association for the Advancement of
    Science, 2013, pp. 91–95, doi:<a href="https://doi.org/10.1126/science.1229858">10.1126/science.1229858</a>.
  short: Y. Wakamoto, N. Dhar, R.P. Chait, K. Schneider, F. Signorino Gelo, S. Leibler,
    J. Mckinney, Science 339 (2013) 91–95.
date_created: 2018-12-11T11:46:48Z
date_published: 2013-01-04T00:00:00Z
date_updated: 2021-01-12T08:01:06Z
day: '04'
department:
- _id: CaGu
- _id: GaTk
doi: 10.1126/science.1229858
intvolume: '       339'
issue: '6115'
language:
- iso: eng
month: '01'
oa_version: None
page: 91 - 95
publication: Science
publication_status: published
publisher: American Association for the Advancement of Science
publist_id: '7321'
quality_controlled: '1'
scopus_import: 1
status: public
title: Dynamic persistence of antibiotic-stressed mycobacteria
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 339
year: '2013'
...
---
_id: '500'
abstract:
- lang: eng
  text: 'Background: Reassortment between the RNA segments encoding haemagglutinin
    (HA) and neuraminidase (NA), the major antigenic influenza proteins, produces
    viruses with novel HA and NA subtype combinations and has preceded the emergence
    of pandemic strains. It has been suggested that productive viral infection requires
    a balance in the level of functional activity of HA and NA, arising from their
    closely interacting roles in the viral life cycle, and that this functional balance
    could be mediated by genetic changes in the HA and NA. Here, we investigate how
    the selective pressure varies for H7 avian influenza HA on different NA subtype
    backgrounds. Results: By extending Bayesian stochastic mutational mapping methods
    to calculate the ratio of the rate of non-synonymous change to the rate of synonymous
    change (d N/d S), we found the average d N/d S across the avian influenza H7 HA1
    region to be significantly greater on an N2 NA subtype background than on an N1,
    N3 or N7 background. Observed differences in evolutionary rates of H7 HA on different
    NA subtype backgrounds could not be attributed to underlying differences between
    avian host species or virus pathogenicity. Examination of d N/d S values for each
    subtype on a site-by-site basis indicated that the elevated d N/d S on the N2
    NA background was a result of increased selection, rather than a relaxation of
    selective constraint. Conclusions: Our results are consistent with the hypothesis
    that reassortment exposes influenza HA to significant changes in selective pressure
    through genetic interactions with NA. Such epistatic effects might be explicitly
    accounted for in future models of influenza evolution.'
acknowledgement: "This work was supported by the Biotechnology and Biological Sciences
  Research Council, the Government of the Republic of Panama, the Interdisciplinary
  Centre for Human and Avian Influenza Research (www.ichair-flu.org) funded by the
  Scottish Funding Council, and the Institute for Science and Technology Austria.\r\nCC
  BY 2.0\r\n"
article_number: '222'
author:
- first_name: Melissa
  full_name: Ward, Melissa
  last_name: Ward
- first_name: Samantha
  full_name: Lycett, Samantha
  last_name: Lycett
- first_name: Dorita
  full_name: Avila, Dorita
  last_name: Avila
- first_name: Jonathan P
  full_name: Bollback, Jonathan P
  id: 2C6FA9CC-F248-11E8-B48F-1D18A9856A87
  last_name: Bollback
  orcid: 0000-0002-4624-4612
- first_name: Andrew
  full_name: Leigh Brown, Andrew
  last_name: Leigh Brown
citation:
  ama: Ward M, Lycett S, Avila D, Bollback JP, Leigh Brown A. Evolutionary interactions
    between haemagglutinin and neuraminidase in avian influenza. <i>BMC Evolutionary
    Biology</i>. 2013;13(1). doi:<a href="https://doi.org/10.1186/1471-2148-13-222">10.1186/1471-2148-13-222</a>
  apa: Ward, M., Lycett, S., Avila, D., Bollback, J. P., &#38; Leigh Brown, A. (2013).
    Evolutionary interactions between haemagglutinin and neuraminidase in avian influenza.
    <i>BMC Evolutionary Biology</i>. BioMed Central. <a href="https://doi.org/10.1186/1471-2148-13-222">https://doi.org/10.1186/1471-2148-13-222</a>
  chicago: Ward, Melissa, Samantha Lycett, Dorita Avila, Jonathan P Bollback, and
    Andrew Leigh Brown. “Evolutionary Interactions between Haemagglutinin and Neuraminidase
    in Avian Influenza.” <i>BMC Evolutionary Biology</i>. BioMed Central, 2013. <a
    href="https://doi.org/10.1186/1471-2148-13-222">https://doi.org/10.1186/1471-2148-13-222</a>.
  ieee: M. Ward, S. Lycett, D. Avila, J. P. Bollback, and A. Leigh Brown, “Evolutionary
    interactions between haemagglutinin and neuraminidase in avian influenza,” <i>BMC
    Evolutionary Biology</i>, vol. 13, no. 1. BioMed Central, 2013.
  ista: Ward M, Lycett S, Avila D, Bollback JP, Leigh Brown A. 2013. Evolutionary
    interactions between haemagglutinin and neuraminidase in avian influenza. BMC
    Evolutionary Biology. 13(1), 222.
  mla: Ward, Melissa, et al. “Evolutionary Interactions between Haemagglutinin and
    Neuraminidase in Avian Influenza.” <i>BMC Evolutionary Biology</i>, vol. 13, no.
    1, 222, BioMed Central, 2013, doi:<a href="https://doi.org/10.1186/1471-2148-13-222">10.1186/1471-2148-13-222</a>.
  short: M. Ward, S. Lycett, D. Avila, J.P. Bollback, A. Leigh Brown, BMC Evolutionary
    Biology 13 (2013).
date_created: 2018-12-11T11:46:49Z
date_published: 2013-10-09T00:00:00Z
date_updated: 2021-01-12T08:01:08Z
day: '09'
ddc:
- '576'
department:
- _id: JoBo
doi: 10.1186/1471-2148-13-222
file:
- access_level: open_access
  checksum: 52cf48a7c1794676ae8b0029573a84a9
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:08:59Z
  date_updated: 2020-07-14T12:46:36Z
  file_id: '4722'
  file_name: IST-2018-941-v1+1_2013_Bollback_Evolutionary_interactionspdf.pdf
  file_size: 1150052
  relation: main_file
file_date_updated: 2020-07-14T12:46:36Z
has_accepted_license: '1'
intvolume: '        13'
issue: '1'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
publication: BMC Evolutionary Biology
publication_status: published
publisher: BioMed Central
publist_id: '7320'
pubrep_id: '941'
quality_controlled: '1'
scopus_import: 1
status: public
title: Evolutionary interactions between haemagglutinin and neuraminidase in avian
  influenza
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: 13
year: '2013'
...
---
_id: '501'
abstract:
- lang: eng
  text: 'All known species of extant tapirs are allopatric: 1 in southeastern Asia
    and 3 in Central and South America. The fossil record for tapirs, however, is
    much wider in geographical range, including Europe, Asia, and North and South
    America, going back to the late Oligocene, making the present distribution a relict
    of the original one. We here describe a new species of living Tapirus from the
    Amazon rain forest, the 1st since T. bairdii Gill, 1865, and the 1st new Perissodactyla
    in more than 100 years, from both morphological and molecular characters. It is
    shorter in stature than T. terrestris (Linnaeus, 1758) and has distinctive skull
    morphology, and it is basal to the clade formed by T. terrestris and T. pinchaque
    (Roulin, 1829). This highlights the unrecognized biodiversity in western Amazonia,
    where the biota faces increasing threats. Local peoples have long recognized our
    new species, suggesting a key role for traditional knowledge in understanding
    the biodiversity of the region.'
author:
- first_name: Mario
  full_name: Cozzuol, Mario
  last_name: Cozzuol
- first_name: Camila
  full_name: Clozato, Camila
  last_name: Clozato
- first_name: Elizete
  full_name: Holanda, Elizete
  last_name: Holanda
- first_name: Flávio
  full_name: Rodrigues, Flávio
  last_name: Rodrigues
- first_name: Samuel
  full_name: Nienow, Samuel
  last_name: Nienow
- first_name: Benoit
  full_name: De Thoisy, Benoit
  last_name: De Thoisy
- 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: Fabrício
  full_name: Santos, Fabrício
  last_name: Santos
citation:
  ama: Cozzuol M, Clozato C, Holanda E, et al. A new species of tapir from the Amazon.
    <i>Journal of Mammalogy</i>. 2013;94(6):1331-1345. doi:<a href="https://doi.org/10.1644/12-MAMM-A-169.1">10.1644/12-MAMM-A-169.1</a>
  apa: Cozzuol, M., Clozato, C., Holanda, E., Rodrigues, F., Nienow, S., De Thoisy,
    B., … Santos, F. (2013). A new species of tapir from the Amazon. <i>Journal of
    Mammalogy</i>. Oxford University Press. <a href="https://doi.org/10.1644/12-MAMM-A-169.1">https://doi.org/10.1644/12-MAMM-A-169.1</a>
  chicago: Cozzuol, Mario, Camila Clozato, Elizete Holanda, Flávio Rodrigues, Samuel
    Nienow, Benoit De Thoisy, Rodrigo A Fernandes Redondo, and Fabrício Santos. “A
    New Species of Tapir from the Amazon.” <i>Journal of Mammalogy</i>. Oxford University
    Press, 2013. <a href="https://doi.org/10.1644/12-MAMM-A-169.1">https://doi.org/10.1644/12-MAMM-A-169.1</a>.
  ieee: M. Cozzuol <i>et al.</i>, “A new species of tapir from the Amazon,” <i>Journal
    of Mammalogy</i>, vol. 94, no. 6. Oxford University Press, pp. 1331–1345, 2013.
  ista: Cozzuol M, Clozato C, Holanda E, Rodrigues F, Nienow S, De Thoisy B, Fernandes
    Redondo RA, Santos F. 2013. A new species of tapir from the Amazon. Journal of
    Mammalogy. 94(6), 1331–1345.
  mla: Cozzuol, Mario, et al. “A New Species of Tapir from the Amazon.” <i>Journal
    of Mammalogy</i>, vol. 94, no. 6, Oxford University Press, 2013, pp. 1331–45,
    doi:<a href="https://doi.org/10.1644/12-MAMM-A-169.1">10.1644/12-MAMM-A-169.1</a>.
  short: M. Cozzuol, C. Clozato, E. Holanda, F. Rodrigues, S. Nienow, B. De Thoisy,
    R.A. Fernandes Redondo, F. Santos, Journal of Mammalogy 94 (2013) 1331–1345.
date_created: 2018-12-11T11:46:49Z
date_published: 2013-12-01T00:00:00Z
date_updated: 2021-01-12T08:01:09Z
day: '01'
ddc:
- '570'
department:
- _id: JoBo
doi: 10.1644/12-MAMM-A-169.1
file:
- access_level: open_access
  checksum: 8007815078dccac21ecd1cf73a269dc6
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:12:59Z
  date_updated: 2020-07-14T12:46:36Z
  file_id: '4980'
  file_name: IST-2018-940-v1+1_2013_Redondo_A_new.pdf
  file_size: 1040765
  relation: main_file
file_date_updated: 2020-07-14T12:46:36Z
has_accepted_license: '1'
intvolume: '        94'
issue: '6'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 1331 - 1345
publication: Journal of Mammalogy
publication_status: published
publisher: Oxford University Press
publist_id: '7319'
pubrep_id: '940'
quality_controlled: '1'
scopus_import: 1
status: public
title: A new species of tapir from the Amazon
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 94
year: '2013'
...
---
_id: '502'
abstract:
- lang: eng
  text: 'Blind signatures allow users to obtain signatures on messages hidden from
    the signer; moreover, the signer cannot link the resulting message/signature pair
    to the signing session. This paper presents blind signature schemes, in which
    the number of interactions between the user and the signer is minimal and whose
    blind signatures are short. Our schemes are defined over bilinear groups and are
    proved secure in the common-reference-string model without random oracles and
    under standard assumptions: CDH and the decision-linear assumption. (We also give
    variants over asymmetric groups based on similar assumptions.) The blind signatures
    are Waters signatures, which consist of 2 group elements. Moreover, we instantiate
    partially blind signatures, where the message consists of a part hidden from the
    signer and a commonly known public part, and schemes achieving perfect blindness.
    We propose new variants of blind signatures, such as signer-friendly partially
    blind signatures, where the public part can be chosen by the signer without prior
    agreement, 3-party blind signatures, as well as blind signatures on multiple aggregated
    messages provided by independent sources. We also extend Waters signatures to
    non-binary alphabets by proving a new result on the underlying hash function. '
author:
- first_name: Olivier
  full_name: Blazy, Olivier
  last_name: Blazy
- first_name: Georg
  full_name: Fuchsbauer, Georg
  id: 46B4C3EE-F248-11E8-B48F-1D18A9856A87
  last_name: Fuchsbauer
- first_name: David
  full_name: Pointcheval, David
  last_name: Pointcheval
- first_name: Damien
  full_name: Vergnaud, Damien
  last_name: Vergnaud
citation:
  ama: Blazy O, Fuchsbauer G, Pointcheval D, Vergnaud D. Short blind signatures. <i>Journal
    of Computer Security</i>. 2013;21(5):627-661. doi:<a href="https://doi.org/10.3233/JCS-130477">10.3233/JCS-130477</a>
  apa: Blazy, O., Fuchsbauer, G., Pointcheval, D., &#38; Vergnaud, D. (2013). Short
    blind signatures. <i>Journal of Computer Security</i>. IOS Press. <a href="https://doi.org/10.3233/JCS-130477">https://doi.org/10.3233/JCS-130477</a>
  chicago: Blazy, Olivier, Georg Fuchsbauer, David Pointcheval, and Damien Vergnaud.
    “Short Blind Signatures.” <i>Journal of Computer Security</i>. IOS Press, 2013.
    <a href="https://doi.org/10.3233/JCS-130477">https://doi.org/10.3233/JCS-130477</a>.
  ieee: O. Blazy, G. Fuchsbauer, D. Pointcheval, and D. Vergnaud, “Short blind signatures,”
    <i>Journal of Computer Security</i>, vol. 21, no. 5. IOS Press, pp. 627–661, 2013.
  ista: Blazy O, Fuchsbauer G, Pointcheval D, Vergnaud D. 2013. Short blind signatures.
    Journal of Computer Security. 21(5), 627–661.
  mla: Blazy, Olivier, et al. “Short Blind Signatures.” <i>Journal of Computer Security</i>,
    vol. 21, no. 5, IOS Press, 2013, pp. 627–61, doi:<a href="https://doi.org/10.3233/JCS-130477">10.3233/JCS-130477</a>.
  short: O. Blazy, G. Fuchsbauer, D. Pointcheval, D. Vergnaud, Journal of Computer
    Security 21 (2013) 627–661.
date_created: 2018-12-11T11:46:50Z
date_published: 2013-11-22T00:00:00Z
date_updated: 2021-01-12T08:01:09Z
day: '22'
department:
- _id: KrPi
doi: 10.3233/JCS-130477
intvolume: '        21'
issue: '5'
language:
- iso: eng
month: '11'
oa_version: None
page: 627 - 661
publication: Journal of Computer Security
publication_status: published
publisher: IOS Press
publist_id: '7318'
quality_controlled: '1'
scopus_import: 1
status: public
title: Short blind signatures
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 21
year: '2013'
...
---
_id: '505'
abstract:
- lang: eng
  text: Alkyd resins are polyesters containing unsaturated fatty acids that are used
    as binding agents in paints and coatings. Chemical drying of these polyesters
    is based on heavy metal catalyzed cross-linking of the unsaturated fatty acid
    moieties. Among the heavy-metal catalysts, cobalt complexes are the most effective,
    yet they have been proven to be carcinogenic. Therefore, strategies to replace
    the cobalt-based catalyst by environmentally friendlier and less toxic alternatives
    are under development. Here, we demonstrate for the first time that a laccase-mediator
    system can effectively replace the heavy-metal catalyst and cross-link alkyd resins.
    Interestingly, the biocatalytic reaction does not only work in aqueous media,
    but also in a solid film, where enzyme diffusion is limited. Within the catalytic
    cycle, the mediator oxidizes the alkyd resin and is regenerated by the laccase,
    which is uniformly distributed within the drying film as evidenced by confocal
    laser scanning microscopy. During gradual build-up of molecular weight, there
    is a concomitant decrease of the oxygen content in the film. A new optical sensor
    to follow oxygen consumption during the cross-linking reaction was developed and
    validated with state of the art techniques. A remarkable feature is the low sample
    amount required, which allows faster screening of new catalysts.
acknowledgement: "This study was performed within the Austrian Centre of Indus-\r\ntrial
  Biotechnology ACIB and the COST Action 868. This work\r\nhas been supported by the
  Federal Ministry of Economy,\r\nFamily and Youth (BMWFJ), the Federal Ministry of
  Tra\r\nffi\r\nc,\r\nInnovation and Technology (bmvit), the Styrian Business\r\nPromotion
  Agency SFG, the Standortagentur Tirol and ZIT\r\n–\r\nTechnology  Agency  of  the
  \ City  of  Vienna  through  the\r\nCOMET-Funding Program managed by the Austrian
  Research\r\nPromotion Agency FFG. Dr Massimiliano Cardinale (Institute of\r\nEnvironmental
  Biotechnology, TU Graz) is gratefully acknowl-\r\nedged for technical support with
  the CLSM measurements."
author:
- first_name: Katrin
  full_name: Greimel, Katrin
  last_name: Greimel
- first_name: Veronika
  full_name: Perz, Veronika
  last_name: Perz
- first_name: Klaus
  full_name: Koren, Klaus
  id: 382FBD6A-F248-11E8-B48F-1D18A9856A87
  last_name: Koren
- first_name: Roland
  full_name: Feola, Roland
  last_name: Feola
- first_name: Armin
  full_name: Temel, Armin
  last_name: Temel
- first_name: Christian
  full_name: Sohar, Christian
  last_name: Sohar
- first_name: Enrique
  full_name: Herrero Acero, Enrique
  last_name: Herrero Acero
- first_name: Ingo
  full_name: Klimant, Ingo
  last_name: Klimant
- first_name: Georg
  full_name: Guebitz, Georg
  last_name: Guebitz
citation:
  ama: 'Greimel K, Perz V, Koren K, et al. Banning toxic heavy-metal catalysts from
    paints: Enzymatic cross-linking of alkyd resins. <i>Green Chemistry</i>. 2013;15(2):381-388.
    doi:<a href="https://doi.org/10.1039/c2gc36666e">10.1039/c2gc36666e</a>'
  apa: 'Greimel, K., Perz, V., Koren, K., Feola, R., Temel, A., Sohar, C., … Guebitz,
    G. (2013). Banning toxic heavy-metal catalysts from paints: Enzymatic cross-linking
    of alkyd resins. <i>Green Chemistry</i>. Royal Society of Chemistry. <a href="https://doi.org/10.1039/c2gc36666e">https://doi.org/10.1039/c2gc36666e</a>'
  chicago: 'Greimel, Katrin, Veronika Perz, Klaus Koren, Roland Feola, Armin Temel,
    Christian Sohar, Enrique Herrero Acero, Ingo Klimant, and Georg Guebitz. “Banning
    Toxic Heavy-Metal Catalysts from Paints: Enzymatic Cross-Linking of Alkyd Resins.”
    <i>Green Chemistry</i>. Royal Society of Chemistry, 2013. <a href="https://doi.org/10.1039/c2gc36666e">https://doi.org/10.1039/c2gc36666e</a>.'
  ieee: 'K. Greimel <i>et al.</i>, “Banning toxic heavy-metal catalysts from paints:
    Enzymatic cross-linking of alkyd resins,” <i>Green Chemistry</i>, vol. 15, no.
    2. Royal Society of Chemistry, pp. 381–388, 2013.'
  ista: 'Greimel K, Perz V, Koren K, Feola R, Temel A, Sohar C, Herrero Acero E, Klimant
    I, Guebitz G. 2013. Banning toxic heavy-metal catalysts from paints: Enzymatic
    cross-linking of alkyd resins. Green Chemistry. 15(2), 381–388.'
  mla: 'Greimel, Katrin, et al. “Banning Toxic Heavy-Metal Catalysts from Paints:
    Enzymatic Cross-Linking of Alkyd Resins.” <i>Green Chemistry</i>, vol. 15, no.
    2, Royal Society of Chemistry, 2013, pp. 381–88, doi:<a href="https://doi.org/10.1039/c2gc36666e">10.1039/c2gc36666e</a>.'
  short: K. Greimel, V. Perz, K. Koren, R. Feola, A. Temel, C. Sohar, E. Herrero Acero,
    I. Klimant, G. Guebitz, Green Chemistry 15 (2013) 381–388.
date_created: 2018-12-11T11:46:51Z
date_published: 2013-02-01T00:00:00Z
date_updated: 2021-01-12T08:01:11Z
day: '01'
department:
- _id: HaJa
doi: 10.1039/c2gc36666e
intvolume: '        15'
issue: '2'
language:
- iso: eng
month: '02'
oa_version: None
page: 381 - 388
publication: Green Chemistry
publication_status: published
publisher: Royal Society of Chemistry
publist_id: '7313'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'Banning toxic heavy-metal catalysts from paints: Enzymatic cross-linking of
  alkyd resins'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2013'
...
---
_id: '507'
abstract:
- lang: eng
  text: Fertilization in flowering plants requires the temporal and spatial coordination
    of many developmental processes, including pollen production, anther dehiscence,
    ovule production, and pollen tube elongation. However, it remains elusive as to
    how this coordination occurs during reproduction. Here, we present evidence that
    endocytosis, involving heterotetrameric adaptor protein complex 2 (AP-2), plays
    a crucial role in fertilization. An Arabidopsis thaliana mutant ap2m displays
    multiple defects in pollen production and viability, as well as elongation of
    staminal filaments and pollen tubes, all of which are pivotal processes needed
    for fertilization. Of these abnormalities, the defects in elongation of staminal
    filaments and pollen tubes were partially rescued by exogenous auxin. Moreover,
    DR5rev:GFP (for green fluorescent protein) expression was greatly reduced in filaments
    and anthers in ap2m mutant plants. At the cellular level, ap2m mutants displayed
    defects in both endocytosis of N-(3-triethylammonium-propyl)-4- (4-diethylaminophenylhexatrienyl)
    pyridinium dibromide, a lypophilic dye used as an endocytosis marker, and polar
    localization of auxin-efflux carrier PIN FORMED2 (PIN2) in the stamen filaments.
    Moreover, these defects were phenocopied by treatment with Tyrphostin A23, an
    inhibitor of endocytosis. Based on these results, we propose that AP-2-dependent
    endocytosis plays a crucial role in coordinating the multiple developmental aspects
    of male reproductive organs by modulating cellular auxin level through the regulation
    of the amount and polarity of PINs.
author:
- first_name: Soo
  full_name: Kim, Soo
  last_name: Kim
- first_name: Zheng
  full_name: Xu, Zheng
  last_name: Xu
- first_name: Kyungyoung
  full_name: Song, Kyungyoung
  last_name: Song
- first_name: Dae
  full_name: Kim, Dae
  last_name: Kim
- first_name: Hyangju
  full_name: Kang, Hyangju
  last_name: Kang
- first_name: Ilka
  full_name: Reichardt, Ilka
  last_name: Reichardt
- first_name: Eun
  full_name: Sohn, Eun
  last_name: Sohn
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Gerd
  full_name: Juergens, Gerd
  last_name: Juergens
- first_name: Inhwan
  full_name: Hwang, Inhwan
  last_name: Hwang
citation:
  ama: Kim S, Xu Z, Song K, et al. Adaptor protein complex 2-mediated endocytosis
    is crucial for male reproductive organ development in arabidopsis. <i>Plant Cell</i>.
    2013;25(8):2970-2985. doi:<a href="https://doi.org/10.1105/tpc.113.114264">10.1105/tpc.113.114264</a>
  apa: Kim, S., Xu, Z., Song, K., Kim, D., Kang, H., Reichardt, I., … Hwang, I. (2013).
    Adaptor protein complex 2-mediated endocytosis is crucial for male reproductive
    organ development in arabidopsis. <i>Plant Cell</i>. American Society of Plant
    Biologists. <a href="https://doi.org/10.1105/tpc.113.114264">https://doi.org/10.1105/tpc.113.114264</a>
  chicago: Kim, Soo, Zheng Xu, Kyungyoung Song, Dae Kim, Hyangju Kang, Ilka Reichardt,
    Eun Sohn, Jiří Friml, Gerd Juergens, and Inhwan Hwang. “Adaptor Protein Complex
    2-Mediated Endocytosis Is Crucial for Male Reproductive Organ Development in Arabidopsis.”
    <i>Plant Cell</i>. American Society of Plant Biologists, 2013. <a href="https://doi.org/10.1105/tpc.113.114264">https://doi.org/10.1105/tpc.113.114264</a>.
  ieee: S. Kim <i>et al.</i>, “Adaptor protein complex 2-mediated endocytosis is crucial
    for male reproductive organ development in arabidopsis,” <i>Plant Cell</i>, vol.
    25, no. 8. American Society of Plant Biologists, pp. 2970–2985, 2013.
  ista: Kim S, Xu Z, Song K, Kim D, Kang H, Reichardt I, Sohn E, Friml J, Juergens
    G, Hwang I. 2013. Adaptor protein complex 2-mediated endocytosis is crucial for
    male reproductive organ development in arabidopsis. Plant Cell. 25(8), 2970–2985.
  mla: Kim, Soo, et al. “Adaptor Protein Complex 2-Mediated Endocytosis Is Crucial
    for Male Reproductive Organ Development in Arabidopsis.” <i>Plant Cell</i>, vol.
    25, no. 8, American Society of Plant Biologists, 2013, pp. 2970–85, doi:<a href="https://doi.org/10.1105/tpc.113.114264">10.1105/tpc.113.114264</a>.
  short: S. Kim, Z. Xu, K. Song, D. Kim, H. Kang, I. Reichardt, E. Sohn, J. Friml,
    G. Juergens, I. Hwang, Plant Cell 25 (2013) 2970–2985.
date_created: 2018-12-11T11:46:52Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2021-01-12T08:01:12Z
day: '01'
department:
- _id: JiFr
doi: 10.1105/tpc.113.114264
external_id:
  pmid:
  - '23975898'
intvolume: '        25'
issue: '8'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784592/
month: '08'
oa: 1
oa_version: Submitted Version
page: 2970 - 2985
pmid: 1
publication: Plant Cell
publication_status: published
publisher: American Society of Plant Biologists
publist_id: '7312'
quality_controlled: '1'
scopus_import: 1
status: public
title: Adaptor protein complex 2-mediated endocytosis is crucial for male reproductive
  organ development in arabidopsis
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 25
year: '2013'
...
---
_id: '508'
abstract:
- lang: eng
  text: The phagocyte NADPH oxidase catalyzes the reduction of O2 to reactive oxygen
    species with microbicidal activity. It is composed of two membrane-spanning subunits,
    gp91-phox and p22-phox (encoded by CYBB and CYBA, respectively), and three cytoplasmic
    subunits, p40-phox, p47-phox, and p67-phox (encoded by NCF4, NCF1, and NCF2, respectively).
    Mutations in any of these genes can result in chronic granulomatous disease, a
    primary immunodeficiency characterized by recurrent infections. Using evolutionary
    mapping, we determined that episodes of adaptive natural selection have shaped
    the extracellular portion of gp91-phox during the evolution of mammals, which
    suggests that this region may have a function in host-pathogen interactions. On
    the basis of a resequencing analysis of approximately 35 kb of CYBB, CYBA, NCF2,
    and NCF4 in 102 ethnically diverse individuals (24 of African ancestry, 31 of
    European ancestry, 24 of Asian/Oceanians, and 23 US Hispanics), we show that the
    pattern of CYBA diversity is compatible with balancing natural selection, perhaps
    mediated by catalase-positive pathogens. NCF2 in Asian populations shows a pattern
    of diversity characterized by a differentiated haplotype structure. Our study
    provides insight into the role of pathogen-driven natural selection in an innate
    immune pathway and sheds light on the role of CYBA in endothelial, nonphagocytic
    NADPH oxidases, which are relevant in the pathogenesis of cardiovascular and other
    complex diseases.
author:
- first_name: Eduardo
  full_name: Tarazona Santos, Eduardo
  last_name: Tarazona Santos
- first_name: Moara
  full_name: Machado, Moara
  last_name: Machado
- first_name: Wagner
  full_name: Magalhães, Wagner
  last_name: Magalhães
- first_name: Renee
  full_name: Chen, Renee
  last_name: Chen
- first_name: Fernanda
  full_name: Lyon, Fernanda
  last_name: Lyon
- first_name: Laurie
  full_name: Burdett, Laurie
  last_name: Burdett
- first_name: Andrew
  full_name: Crenshaw, Andrew
  last_name: Crenshaw
- first_name: Cristina
  full_name: Fabbri, Cristina
  last_name: Fabbri
- first_name: Latife
  full_name: Pereira, Latife
  last_name: Pereira
- first_name: Laelia
  full_name: Pinto, Laelia
  last_name: Pinto
- 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: Ben
  full_name: Sestanovich, Ben
  last_name: Sestanovich
- first_name: Meredith
  full_name: Yeager, Meredith
  last_name: Yeager
- first_name: Stephen
  full_name: Chanock, Stephen
  last_name: Chanock
citation:
  ama: 'Tarazona Santos E, Machado M, Magalhães W, et al. Evolutionary dynamics of
    the human NADPH oxidase genes CYBB, CYBA, NCF2, and NCF4: Functional implications.
    <i>Molecular Biology and Evolution</i>. 2013;30(9):2157-2167. doi:<a href="https://doi.org/10.1093/molbev/mst119">10.1093/molbev/mst119</a>'
  apa: 'Tarazona Santos, E., Machado, M., Magalhães, W., Chen, R., Lyon, F., Burdett,
    L., … Chanock, S. (2013). Evolutionary dynamics of the human NADPH oxidase genes
    CYBB, CYBA, NCF2, and NCF4: Functional implications. <i>Molecular Biology and
    Evolution</i>. Oxford University Press. <a href="https://doi.org/10.1093/molbev/mst119">https://doi.org/10.1093/molbev/mst119</a>'
  chicago: 'Tarazona Santos, Eduardo, Moara Machado, Wagner Magalhães, Renee Chen,
    Fernanda Lyon, Laurie Burdett, Andrew Crenshaw, et al. “Evolutionary Dynamics
    of the Human NADPH Oxidase Genes CYBB, CYBA, NCF2, and NCF4: Functional Implications.”
    <i>Molecular Biology and Evolution</i>. Oxford University Press, 2013. <a href="https://doi.org/10.1093/molbev/mst119">https://doi.org/10.1093/molbev/mst119</a>.'
  ieee: 'E. Tarazona Santos <i>et al.</i>, “Evolutionary dynamics of the human NADPH
    oxidase genes CYBB, CYBA, NCF2, and NCF4: Functional implications,” <i>Molecular
    Biology and Evolution</i>, vol. 30, no. 9. Oxford University Press, pp. 2157–2167,
    2013.'
  ista: 'Tarazona Santos E, Machado M, Magalhães W, Chen R, Lyon F, Burdett L, Crenshaw
    A, Fabbri C, Pereira L, Pinto L, Fernandes Redondo RA, Sestanovich B, Yeager M,
    Chanock S. 2013. Evolutionary dynamics of the human NADPH oxidase genes CYBB,
    CYBA, NCF2, and NCF4: Functional implications. Molecular Biology and Evolution.
    30(9), 2157–2167.'
  mla: 'Tarazona Santos, Eduardo, et al. “Evolutionary Dynamics of the Human NADPH
    Oxidase Genes CYBB, CYBA, NCF2, and NCF4: Functional Implications.” <i>Molecular
    Biology and Evolution</i>, vol. 30, no. 9, Oxford University Press, 2013, pp.
    2157–67, doi:<a href="https://doi.org/10.1093/molbev/mst119">10.1093/molbev/mst119</a>.'
  short: E. Tarazona Santos, M. Machado, W. Magalhães, R. Chen, F. Lyon, L. Burdett,
    A. Crenshaw, C. Fabbri, L. Pereira, L. Pinto, R.A. Fernandes Redondo, B. Sestanovich,
    M. Yeager, S. Chanock, Molecular Biology and Evolution 30 (2013) 2157–2167.
date_created: 2018-12-11T11:46:52Z
date_published: 2013-09-01T00:00:00Z
date_updated: 2021-01-12T08:01:12Z
day: '01'
department:
- _id: JoBo
doi: 10.1093/molbev/mst119
external_id:
  pmid:
  - '23821607'
intvolume: '        30'
issue: '9'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748357/
month: '09'
oa: 1
oa_version: Submitted Version
page: 2157 - 2167
pmid: 1
publication: Molecular Biology and Evolution
publication_status: published
publisher: Oxford University Press
publist_id: '7310'
quality_controlled: '1'
scopus_import: 1
status: public
title: 'Evolutionary dynamics of the human NADPH oxidase genes CYBB, CYBA, NCF2, and
  NCF4: Functional implications'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 30
year: '2013'
...
