---
_id: '10396'
abstract:
- lang: eng
  text: Stimfit is a free cross-platform software package for viewing and analyzing
    electrophysiological data. It supports most standard file types for cellular neurophysiology
    and other biomedical formats. Its analysis algorithms have been used and validated
    in several experimental laboratories. Its embedded Python scripting interface
    makes Stimfit highly extensible and customizable.
article_number: '000010151520134181'
article_processing_charge: No
article_type: original
author:
- first_name: Alois
  full_name: Schlögl, Alois
  id: 45BF87EE-F248-11E8-B48F-1D18A9856A87
  last_name: Schlögl
  orcid: 0000-0002-5621-8100
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
- first_name: C.
  full_name: Schmidt-Hieber, C.
  last_name: Schmidt-Hieber
- first_name: S. J.
  full_name: Guzman, S. J.
  last_name: Guzman
citation:
  ama: 'Schlögl A, Jonas PM, Schmidt-Hieber C, Guzman SJ. Stimfit: A fast visualization
    and analysis environment for cellular neurophysiology. <i>Biomedical Engineering
    / Biomedizinische Technik</i>. 2013;58(SI-1-Track-G). doi:<a href="https://doi.org/10.1515/bmt-2013-4181">10.1515/bmt-2013-4181</a>'
  apa: 'Schlögl, A., Jonas, P. M., Schmidt-Hieber, C., &#38; Guzman, S. J. (2013).
    Stimfit: A fast visualization and analysis environment for cellular neurophysiology.
    <i>Biomedical Engineering / Biomedizinische Technik</i>. Graz, Austria: De Gruyter.
    <a href="https://doi.org/10.1515/bmt-2013-4181">https://doi.org/10.1515/bmt-2013-4181</a>'
  chicago: 'Schlögl, Alois, Peter M Jonas, C. Schmidt-Hieber, and S. J. Guzman. “Stimfit:
    A Fast Visualization and Analysis Environment for Cellular Neurophysiology.” <i>Biomedical
    Engineering / Biomedizinische Technik</i>. De Gruyter, 2013. <a href="https://doi.org/10.1515/bmt-2013-4181">https://doi.org/10.1515/bmt-2013-4181</a>.'
  ieee: 'A. Schlögl, P. M. Jonas, C. Schmidt-Hieber, and S. J. Guzman, “Stimfit: A
    fast visualization and analysis environment for cellular neurophysiology,” <i>Biomedical
    Engineering / Biomedizinische Technik</i>, vol. 58, no. SI-1-Track-G. De Gruyter,
    2013.'
  ista: 'Schlögl A, Jonas PM, Schmidt-Hieber C, Guzman SJ. 2013. Stimfit: A fast visualization
    and analysis environment for cellular neurophysiology. Biomedical Engineering
    / Biomedizinische Technik. 58(SI-1-Track-G), 000010151520134181.'
  mla: 'Schlögl, Alois, et al. “Stimfit: A Fast Visualization and Analysis Environment
    for Cellular Neurophysiology.” <i>Biomedical Engineering / Biomedizinische Technik</i>,
    vol. 58, no. SI-1-Track-G, 000010151520134181, De Gruyter, 2013, doi:<a href="https://doi.org/10.1515/bmt-2013-4181">10.1515/bmt-2013-4181</a>.'
  short: A. Schlögl, P.M. Jonas, C. Schmidt-Hieber, S.J. Guzman, Biomedical Engineering
    / Biomedizinische Technik 58 (2013).
conference:
  end_date: 2013-09-21
  location: Graz, Austria
  name: 'BMT: Biomedizinische Technik '
  start_date: 2013-09-19
date_created: 2021-12-01T14:35:35Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2021-12-02T12:51:12Z
day: '01'
ddc:
- '005'
- '610'
department:
- _id: PeJo
doi: 10.1515/bmt-2013-4181
external_id:
  pmid:
  - '24042795'
file:
- access_level: open_access
  checksum: cdfc5339b530a25d6079f7223f0b1f16
  content_type: application/pdf
  creator: schloegl
  date_created: 2021-12-01T14:38:08Z
  date_updated: 2021-12-01T14:38:08Z
  file_id: '10397'
  file_name: Schloegl_Abstract-BMT2013.pdf
  file_size: 149825
  relation: main_file
  success: 1
file_date_updated: 2021-12-01T14:38:08Z
has_accepted_license: '1'
intvolume: '        58'
issue: SI-1-Track-G
keyword:
- biomedical engineering
- data analysis
- free software
language:
- iso: eng
month: '08'
oa: 1
oa_version: Submitted Version
pmid: 1
publication: Biomedical Engineering / Biomedizinische Technik
publication_identifier:
  eissn:
  - 1862-278X
  issn:
  - 0013-5585
publication_status: published
publisher: De Gruyter
quality_controlled: '1'
status: public
title: 'Stimfit: A fast visualization and analysis environment for cellular neurophysiology'
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 58
year: '2013'
...
---
_id: '9459'
abstract:
- lang: eng
  text: Nucleosome remodelers of the DDM1/Lsh family are required for DNA methylation
    of transposable elements, but the reason for this is unknown. How DDM1 interacts
    with other methylation pathways, such as small-RNA-directed DNA methylation (RdDM),
    which is thought to mediate plant asymmetric methylation through DRM enzymes,
    is also unclear. Here, we show that most asymmetric methylation is facilitated
    by DDM1 and mediated by the methyltransferase CMT2 separately from RdDM. We find
    that heterochromatic sequences preferentially require DDM1 for DNA methylation
    and that this preference depends on linker histone H1. RdDM is instead inhibited
    by heterochromatin and absolutely requires the nucleosome remodeler DRD1. Together,
    DDM1 and RdDM mediate nearly all transposon methylation and collaborate to repress
    transposition and regulate the methylation and expression of genes. Our results
    indicate that DDM1 provides DNA methyltransferases access to H1-containing heterochromatin
    to allow stable silencing of transposable elements in cooperation with the RdDM
    pathway.
article_processing_charge: No
article_type: original
author:
- first_name: Assaf
  full_name: Zemach, Assaf
  last_name: Zemach
- first_name: M. Yvonne
  full_name: Kim, M. Yvonne
  last_name: Kim
- first_name: Ping-Hung
  full_name: Hsieh, Ping-Hung
  last_name: Hsieh
- first_name: Devin
  full_name: Coleman-Derr, Devin
  last_name: Coleman-Derr
- first_name: Leor
  full_name: Eshed-Williams, Leor
  last_name: Eshed-Williams
- first_name: Ka
  full_name: Thao, Ka
  last_name: Thao
- first_name: Stacey L.
  full_name: Harmer, Stacey L.
  last_name: Harmer
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
citation:
  ama: Zemach A, Kim MY, Hsieh P-H, et al. The Arabidopsis nucleosome remodeler DDM1
    allows DNA methyltransferases to access H1-containing heterochromatin. <i>Cell</i>.
    2013;153(1):193-205. doi:<a href="https://doi.org/10.1016/j.cell.2013.02.033">10.1016/j.cell.2013.02.033</a>
  apa: Zemach, A., Kim, M. Y., Hsieh, P.-H., Coleman-Derr, D., Eshed-Williams, L.,
    Thao, K., … Zilberman, D. (2013). The Arabidopsis nucleosome remodeler DDM1 allows
    DNA methyltransferases to access H1-containing heterochromatin. <i>Cell</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.cell.2013.02.033">https://doi.org/10.1016/j.cell.2013.02.033</a>
  chicago: Zemach, Assaf, M. Yvonne Kim, Ping-Hung Hsieh, Devin Coleman-Derr, Leor
    Eshed-Williams, Ka Thao, Stacey L. Harmer, and Daniel Zilberman. “The Arabidopsis
    Nucleosome Remodeler DDM1 Allows DNA Methyltransferases to Access H1-Containing
    Heterochromatin.” <i>Cell</i>. Elsevier, 2013. <a href="https://doi.org/10.1016/j.cell.2013.02.033">https://doi.org/10.1016/j.cell.2013.02.033</a>.
  ieee: A. Zemach <i>et al.</i>, “The Arabidopsis nucleosome remodeler DDM1 allows
    DNA methyltransferases to access H1-containing heterochromatin,” <i>Cell</i>,
    vol. 153, no. 1. Elsevier, pp. 193–205, 2013.
  ista: Zemach A, Kim MY, Hsieh P-H, Coleman-Derr D, Eshed-Williams L, Thao K, Harmer
    SL, Zilberman D. 2013. The Arabidopsis nucleosome remodeler DDM1 allows DNA methyltransferases
    to access H1-containing heterochromatin. Cell. 153(1), 193–205.
  mla: Zemach, Assaf, et al. “The Arabidopsis Nucleosome Remodeler DDM1 Allows DNA
    Methyltransferases to Access H1-Containing Heterochromatin.” <i>Cell</i>, vol.
    153, no. 1, Elsevier, 2013, pp. 193–205, doi:<a href="https://doi.org/10.1016/j.cell.2013.02.033">10.1016/j.cell.2013.02.033</a>.
  short: A. Zemach, M.Y. Kim, P.-H. Hsieh, D. Coleman-Derr, L. Eshed-Williams, K.
    Thao, S.L. Harmer, D. Zilberman, Cell 153 (2013) 193–205.
date_created: 2021-06-04T12:23:28Z
date_published: 2013-03-28T00:00:00Z
date_updated: 2021-12-14T08:25:35Z
day: '28'
department:
- _id: DaZi
doi: 10.1016/j.cell.2013.02.033
extern: '1'
external_id:
  pmid:
  - '23540698'
intvolume: '       153'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.cell.2013.02.033
month: '03'
oa: 1
oa_version: Published Version
page: 193-205
pmid: 1
publication: Cell
publication_identifier:
  eissn:
  - 1097-4172
  issn:
  - 0092-8674
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: The Arabidopsis nucleosome remodeler DDM1 allows DNA methyltransferases to
  access H1-containing heterochromatin
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 153
year: '2013'
...
---
_id: '9481'
abstract:
- lang: eng
  text: Arabidopsis thaliana endosperm, a transient tissue that nourishes the embryo,
    exhibits extensive localized DNA demethylation on maternally inherited chromosomes.
    Demethylation mediates parent-of-origin–specific (imprinted) gene expression but
    is apparently unnecessary for the extensive accumulation of maternally biased
    small RNA (sRNA) molecules detected in seeds. Endosperm DNA in the distantly related
    monocots rice and maize is likewise locally hypomethylated, but whether this hypomethylation
    is generally parent-of-origin specific is unknown. Imprinted expression of sRNA
    also remains uninvestigated in monocot seeds. Here, we report high-coverage sequencing
    of the Kitaake rice cultivar that enabled us to show that localized hypomethylation
    in rice endosperm occurs solely on the maternal genome, preferring regions of
    high DNA accessibility. Maternally expressed imprinted genes are enriched for
    hypomethylation at putative promoter regions and transcriptional termini and paternally
    expressed genes at promoters and gene bodies, mirroring our recent results in
    A. thaliana. However, unlike in A. thaliana, rice endosperm sRNA populations are
    dominated by specific strong sRNA-producing loci, and imprinted 24-nt sRNAs are
    expressed from both parental genomes and correlate with hypomethylation. Overlaps
    between imprinted sRNA loci and imprinted genes expressed from opposite alleles
    suggest that sRNAs may regulate genomic imprinting. Whereas sRNAs in seedling
    tissues primarily originate from small class II (cut-and-paste) transposable elements,
    those in endosperm are more uniformly derived, including sequences from other
    transposon classes, as well as genic and intergenic regions. Our data indicate
    that the endosperm exhibits a unique pattern of sRNA expression and suggest that
    localized hypomethylation of maternal endosperm DNA is conserved in flowering
    plants.
article_processing_charge: No
article_type: original
author:
- first_name: Jessica A.
  full_name: Rodrigues, Jessica A.
  last_name: Rodrigues
- first_name: Randy
  full_name: Ruan, Randy
  last_name: Ruan
- first_name: Toshiro
  full_name: Nishimura, Toshiro
  last_name: Nishimura
- first_name: Manoj K.
  full_name: Sharma, Manoj K.
  last_name: Sharma
- first_name: Rita
  full_name: Sharma, Rita
  last_name: Sharma
- first_name: Pamela C
  full_name: Ronald, Pamela C
  last_name: Ronald
- first_name: Robert L.
  full_name: Fischer, Robert L.
  last_name: Fischer
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
citation:
  ama: Rodrigues JA, Ruan R, Nishimura T, et al. Imprinted expression of genes and
    small RNA is associated with localized hypomethylation of the maternal genome
    in rice endosperm. <i>Proceedings of the National Academy of Sciences</i>. 2013;110(19):7934-7939.
    doi:<a href="https://doi.org/10.1073/pnas.1306164110">10.1073/pnas.1306164110</a>
  apa: Rodrigues, J. A., Ruan, R., Nishimura, T., Sharma, M. K., Sharma, R., Ronald,
    P. C., … Zilberman, D. (2013). Imprinted expression of genes and small RNA is
    associated with localized hypomethylation of the maternal genome in rice endosperm.
    <i>Proceedings of the National Academy of Sciences</i>. National Academy of Sciences.
    <a href="https://doi.org/10.1073/pnas.1306164110">https://doi.org/10.1073/pnas.1306164110</a>
  chicago: Rodrigues, Jessica A., Randy Ruan, Toshiro Nishimura, Manoj K. Sharma,
    Rita Sharma, Pamela C Ronald, Robert L. Fischer, and Daniel Zilberman. “Imprinted
    Expression of Genes and Small RNA Is Associated with Localized Hypomethylation
    of the Maternal Genome in Rice Endosperm.” <i>Proceedings of the National Academy
    of Sciences</i>. National Academy of Sciences, 2013. <a href="https://doi.org/10.1073/pnas.1306164110">https://doi.org/10.1073/pnas.1306164110</a>.
  ieee: J. A. Rodrigues <i>et al.</i>, “Imprinted expression of genes and small RNA
    is associated with localized hypomethylation of the maternal genome in rice endosperm,”
    <i>Proceedings of the National Academy of Sciences</i>, vol. 110, no. 19. National
    Academy of Sciences, pp. 7934–7939, 2013.
  ista: Rodrigues JA, Ruan R, Nishimura T, Sharma MK, Sharma R, Ronald PC, Fischer
    RL, Zilberman D. 2013. Imprinted expression of genes and small RNA is associated
    with localized hypomethylation of the maternal genome in rice endosperm. Proceedings
    of the National Academy of Sciences. 110(19), 7934–7939.
  mla: Rodrigues, Jessica A., et al. “Imprinted Expression of Genes and Small RNA
    Is Associated with Localized Hypomethylation of the Maternal Genome in Rice Endosperm.”
    <i>Proceedings of the National Academy of Sciences</i>, vol. 110, no. 19, National
    Academy of Sciences, 2013, pp. 7934–39, doi:<a href="https://doi.org/10.1073/pnas.1306164110">10.1073/pnas.1306164110</a>.
  short: J.A. Rodrigues, R. Ruan, T. Nishimura, M.K. Sharma, R. Sharma, P.C. Ronald,
    R.L. Fischer, D. Zilberman, Proceedings of the National Academy of Sciences 110
    (2013) 7934–7939.
date_created: 2021-06-07T07:31:02Z
date_published: 2013-05-07T00:00:00Z
date_updated: 2021-12-14T08:26:44Z
day: '07'
department:
- _id: DaZi
doi: 10.1073/pnas.1306164110
extern: '1'
external_id:
  pmid:
  - '23613580'
intvolume: '       110'
issue: '19'
keyword:
- Multidisciplinary
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1073/pnas.1306164110
month: '05'
oa: 1
oa_version: Published Version
page: 7934-7939
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: Imprinted expression of genes and small RNA is associated with localized hypomethylation
  of the maternal genome in rice endosperm
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 110
year: '2013'
...
---
_id: '9520'
abstract:
- lang: eng
  text: Plants undergo alternation of generation in which reproductive cells develop
    in the plant body ("sporophytic generation") and then differentiate into a multicellular
    gamete-forming "gametophytic generation." Different populations of helper cells
    assist in this transgenerational journey, with somatic tissues supporting early
    development and single nurse cells supporting gametogenesis. New data reveal a
    two-way relationship between early reproductive cells and their helpers involving
    complex epigenetic and signaling networks determining cell number and fate. Later,
    the egg cell plays a central role in specifying accessory cells, whereas in both
    gametophytes, companion cells contribute non-cell-autonomously to the epigenetic
    landscape of the gamete genomes.
article_processing_charge: No
article_type: review
author:
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Hugh
  full_name: Dickinson, Hugh
  last_name: Dickinson
citation:
  ama: 'Feng X, Zilberman D, Dickinson H. A conversation across generations: Soma-germ
    cell crosstalk in plants. <i>Developmental Cell</i>. 2013;24(3):215-225. doi:<a
    href="https://doi.org/10.1016/j.devcel.2013.01.014">10.1016/j.devcel.2013.01.014</a>'
  apa: 'Feng, X., Zilberman, D., &#38; Dickinson, H. (2013). A conversation across
    generations: Soma-germ cell crosstalk in plants. <i>Developmental Cell</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.devcel.2013.01.014">https://doi.org/10.1016/j.devcel.2013.01.014</a>'
  chicago: 'Feng, Xiaoqi, Daniel Zilberman, and Hugh Dickinson. “A Conversation across
    Generations: Soma-Germ Cell Crosstalk in Plants.” <i>Developmental Cell</i>. Elsevier,
    2013. <a href="https://doi.org/10.1016/j.devcel.2013.01.014">https://doi.org/10.1016/j.devcel.2013.01.014</a>.'
  ieee: 'X. Feng, D. Zilberman, and H. Dickinson, “A conversation across generations:
    Soma-germ cell crosstalk in plants,” <i>Developmental Cell</i>, vol. 24, no. 3.
    Elsevier, pp. 215–225, 2013.'
  ista: 'Feng X, Zilberman D, Dickinson H. 2013. A conversation across generations:
    Soma-germ cell crosstalk in plants. Developmental Cell. 24(3), 215–225.'
  mla: 'Feng, Xiaoqi, et al. “A Conversation across Generations: Soma-Germ Cell Crosstalk
    in Plants.” <i>Developmental Cell</i>, vol. 24, no. 3, Elsevier, 2013, pp. 215–25,
    doi:<a href="https://doi.org/10.1016/j.devcel.2013.01.014">10.1016/j.devcel.2013.01.014</a>.'
  short: X. Feng, D. Zilberman, H. Dickinson, Developmental Cell 24 (2013) 215–225.
date_created: 2021-06-08T06:14:50Z
date_published: 2013-02-11T00:00:00Z
date_updated: 2023-05-08T11:00:59Z
day: '11'
department:
- _id: DaZi
- _id: XiFe
doi: 10.1016/j.devcel.2013.01.014
extern: '1'
external_id:
  pmid:
  - '23410937'
intvolume: '        24'
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.devcel.2013.01.014
month: '02'
oa: 1
oa_version: Published Version
page: 215-225
pmid: 1
publication: Developmental Cell
publication_identifier:
  eissn:
  - 1878-1551
  issn:
  - 1534-5807
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'A conversation across generations: Soma-germ cell crosstalk in plants'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2013'
...
---
_id: '9749'
abstract:
- lang: eng
  text: Cooperative behavior, where one individual incurs a cost to help another,
    is a wide spread phenomenon. Here we study direct reciprocity in the context of
    the alternating Prisoner's Dilemma. We consider all strategies that can be implemented
    by one and two-state automata. We calculate the payoff matrix of all pairwise
    encounters in the presence of noise. We explore deterministic selection dynamics
    with and without mutation. Using different error rates and payoff values, we observe
    convergence to a small number of distinct equilibria. Two of them are uncooperative
    strict Nash equilibria representing always-defect (ALLD) and Grim. The third equilibrium
    is mixed and represents a cooperative alliance of several strategies, dominated
    by a strategy which we call Forgiver. Forgiver cooperates whenever the opponent
    has cooperated; it defects once when the opponent has defected, but subsequently
    Forgiver attempts to re-establish cooperation even if the opponent has defected
    again. Forgiver is not an evolutionarily stable strategy, but the alliance, which
    it rules, is asymptotically stable. For a wide range of parameter values the most
    commonly observed outcome is convergence to the mixed equilibrium, dominated by
    Forgiver. Our results show that although forgiving might incur a short-term loss
    it can lead to a long-term gain. Forgiveness facilitates stable cooperation in
    the presence of exploitation and noise.
article_processing_charge: No
author:
- first_name: Benjamin
  full_name: Zagorsky, Benjamin
  last_name: Zagorsky
- first_name: Johannes
  full_name: Reiter, Johannes
  id: 4A918E98-F248-11E8-B48F-1D18A9856A87
  last_name: Reiter
  orcid: 0000-0002-0170-7353
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Martin
  full_name: Nowak, Martin
  last_name: Nowak
citation:
  ama: Zagorsky B, Reiter J, Chatterjee K, Nowak M. Forgiver triumphs in alternating
    prisoner’s dilemma . 2013. doi:<a href="https://doi.org/10.1371/journal.pone.0080814.s001">10.1371/journal.pone.0080814.s001</a>
  apa: Zagorsky, B., Reiter, J., Chatterjee, K., &#38; Nowak, M. (2013). Forgiver
    triumphs in alternating prisoner’s dilemma . Public Library of Science. <a href="https://doi.org/10.1371/journal.pone.0080814.s001">https://doi.org/10.1371/journal.pone.0080814.s001</a>
  chicago: Zagorsky, Benjamin, Johannes Reiter, Krishnendu Chatterjee, and Martin
    Nowak. “Forgiver Triumphs in Alternating Prisoner’s Dilemma .” Public Library
    of Science, 2013. <a href="https://doi.org/10.1371/journal.pone.0080814.s001">https://doi.org/10.1371/journal.pone.0080814.s001</a>.
  ieee: B. Zagorsky, J. Reiter, K. Chatterjee, and M. Nowak, “Forgiver triumphs in
    alternating prisoner’s dilemma .” Public Library of Science, 2013.
  ista: Zagorsky B, Reiter J, Chatterjee K, Nowak M. 2013. Forgiver triumphs in alternating
    prisoner’s dilemma , Public Library of Science, <a href="https://doi.org/10.1371/journal.pone.0080814.s001">10.1371/journal.pone.0080814.s001</a>.
  mla: Zagorsky, Benjamin, et al. <i>Forgiver Triumphs in Alternating Prisoner’s Dilemma
    </i>. Public Library of Science, 2013, doi:<a href="https://doi.org/10.1371/journal.pone.0080814.s001">10.1371/journal.pone.0080814.s001</a>.
  short: B. Zagorsky, J. Reiter, K. Chatterjee, M. Nowak, (2013).
date_created: 2021-07-28T15:45:07Z
date_published: 2013-12-12T00:00:00Z
date_updated: 2023-02-23T10:34:39Z
day: '12'
department:
- _id: KrCh
doi: 10.1371/journal.pone.0080814.s001
month: '12'
oa_version: Published Version
publisher: Public Library of Science
related_material:
  record:
  - id: '2247'
    relation: used_in_publication
    status: public
status: public
title: 'Forgiver triumphs in alternating prisoner''s dilemma '
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2013'
...
---
_id: '9751'
abstract:
- lang: eng
  text: High relatedness among interacting individuals has generally been considered
    a precondition for the evolution of altruism. However, kin-selection theory also
    predicts the evolution of altruism when relatedness is low, as long as the cost
    of the altruistic act is minor compared to its benefit. Here, we demonstrate evidence
    for a low-cost altruistic act in bacteria. We investigated Escherichia coli responding
    to the attack of an obligately lytic phage by committing suicide in order to prevent
    parasite transmission to nearby relatives. We found that bacterial suicide provides
    large benefits to survivors at marginal costs to committers. The cost of suicide
    was low because infected cells are moribund, rapidly dying upon phage infection,
    such that no more opportunity for reproduction remains. As a consequence of its
    marginal cost, host suicide was selectively favoured even when relatedness between
    committers and survivors approached zero. Altogether, our findings demonstrate
    that low-cost suicide can evolve with ease, represents an effective host-defence
    strategy, and seems to be widespread among microbes. Moreover, low-cost suicide
    might also occur in higher organisms as exemplified by infected social insect
    workers leaving the colony to die in isolation.
article_processing_charge: No
author:
- first_name: Dominik
  full_name: Refardt, Dominik
  last_name: Refardt
- first_name: Tobias
  full_name: Bergmiller, Tobias
  id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
  last_name: Bergmiller
  orcid: 0000-0001-5396-4346
- first_name: Rolf
  full_name: Kümmerli, Rolf
  last_name: Kümmerli
citation:
  ama: 'Refardt D, Bergmiller T, Kümmerli R. Data from: Altruism can evolve when relatedness
    is low: evidence from bacteria committing suicide upon phage infection. 2013.
    doi:<a href="https://doi.org/10.5061/dryad.b1q2n">10.5061/dryad.b1q2n</a>'
  apa: 'Refardt, D., Bergmiller, T., &#38; Kümmerli, R. (2013). Data from: Altruism
    can evolve when relatedness is low: evidence from bacteria committing suicide
    upon phage infection. Dryad. <a href="https://doi.org/10.5061/dryad.b1q2n">https://doi.org/10.5061/dryad.b1q2n</a>'
  chicago: 'Refardt, Dominik, Tobias Bergmiller, and Rolf Kümmerli. “Data from: Altruism
    Can Evolve When Relatedness Is Low: Evidence from Bacteria Committing Suicide
    upon Phage Infection.” Dryad, 2013. <a href="https://doi.org/10.5061/dryad.b1q2n">https://doi.org/10.5061/dryad.b1q2n</a>.'
  ieee: 'D. Refardt, T. Bergmiller, and R. Kümmerli, “Data from: Altruism can evolve
    when relatedness is low: evidence from bacteria committing suicide upon phage
    infection.” Dryad, 2013.'
  ista: 'Refardt D, Bergmiller T, Kümmerli R. 2013. Data from: Altruism can evolve
    when relatedness is low: evidence from bacteria committing suicide upon phage
    infection, Dryad, <a href="https://doi.org/10.5061/dryad.b1q2n">10.5061/dryad.b1q2n</a>.'
  mla: 'Refardt, Dominik, et al. <i>Data from: Altruism Can Evolve When Relatedness
    Is Low: Evidence from Bacteria Committing Suicide upon Phage Infection</i>. Dryad,
    2013, doi:<a href="https://doi.org/10.5061/dryad.b1q2n">10.5061/dryad.b1q2n</a>.'
  short: D. Refardt, T. Bergmiller, R. Kümmerli, (2013).
date_created: 2021-07-30T08:08:09Z
date_published: 2013-03-21T00:00:00Z
date_updated: 2023-10-18T06:43:22Z
day: '21'
department:
- _id: CaGu
doi: 10.5061/dryad.b1q2n
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.b1q2n
month: '03'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '2853'
    relation: used_in_publication
    status: public
status: public
title: 'Data from: Altruism can evolve when relatedness is low: evidence from bacteria
  committing suicide upon phage infection'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2013'
...
---
_id: '9754'
abstract:
- lang: eng
  text: Short-read sequencing technologies have in principle made it feasible to draw
    detailed inferences about the recent history of any organism. In practice, however,
    this remains challenging due to the difficulty of genome assembly in most organisms
    and the lack of statistical methods powerful enough to discriminate among recent,
    non-equilibrium histories. We address both the assembly and inference challenges.
    We develop a bioinformatic pipeline for generating outgroup-rooted alignments
    of orthologous sequence blocks from de novo low-coverage short-read data for a
    small number of genomes, and show how such sequence blocks can be used to fit
    explicit models of population divergence and admixture in a likelihood framework.
    To illustrate our approach, we reconstruct the Pleistocene history of an oak-feeding
    insect (the oak gallwasp Biorhiza pallida) which, in common with many other taxa,
    was restricted during Pleistocene ice ages to a longitudinal series of southern
    refugia spanning theWestern Palaearctic. Our analysis of sequence blocks sampled
    from a single genome from each of three major glacial refugia reveals support
    for an unexpected history dominated by recent admixture. Despite the fact that
    80% of the genome is affected by admixture during the last glacial cycle, we are
    able to infer the deeper divergence history of these populations. These inferences
    are robust to variation in block length, mutation model, and the sampling location
    of individual genomes within refugia. This combination of de novo assembly and
    numerical likelihood calculation provides a powerful framework for estimating
    recent population history that can be applied to any organism without the need
    for prior genetic resources.
article_processing_charge: No
author:
- first_name: Jack
  full_name: Hearn, Jack
  last_name: Hearn
- first_name: Graham
  full_name: Stone, Graham
  last_name: Stone
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
- first_name: Konrad
  full_name: Lohse, Konrad
  last_name: Lohse
- first_name: Lynsey
  full_name: Bunnefeld, Lynsey
  last_name: Bunnefeld
citation:
  ama: 'Hearn J, Stone G, Barton NH, Lohse K, Bunnefeld L. Data from: Likelihood-based
    inference of population history from low coverage de novo genome assemblies. 2013.
    doi:<a href="https://doi.org/10.5061/dryad.r3r60">10.5061/dryad.r3r60</a>'
  apa: 'Hearn, J., Stone, G., Barton, N. H., Lohse, K., &#38; Bunnefeld, L. (2013).
    Data from: Likelihood-based inference of population history from low coverage
    de novo genome assemblies. Dryad. <a href="https://doi.org/10.5061/dryad.r3r60">https://doi.org/10.5061/dryad.r3r60</a>'
  chicago: 'Hearn, Jack, Graham Stone, Nicholas H Barton, Konrad Lohse, and Lynsey
    Bunnefeld. “Data from: Likelihood-Based Inference of Population History from Low
    Coverage de Novo Genome Assemblies.” Dryad, 2013. <a href="https://doi.org/10.5061/dryad.r3r60">https://doi.org/10.5061/dryad.r3r60</a>.'
  ieee: 'J. Hearn, G. Stone, N. H. Barton, K. Lohse, and L. Bunnefeld, “Data from:
    Likelihood-based inference of population history from low coverage de novo genome
    assemblies.” Dryad, 2013.'
  ista: 'Hearn J, Stone G, Barton NH, Lohse K, Bunnefeld L. 2013. Data from: Likelihood-based
    inference of population history from low coverage de novo genome assemblies, Dryad,
    <a href="https://doi.org/10.5061/dryad.r3r60">10.5061/dryad.r3r60</a>.'
  mla: 'Hearn, Jack, et al. <i>Data from: Likelihood-Based Inference of Population
    History from Low Coverage de Novo Genome Assemblies</i>. Dryad, 2013, doi:<a href="https://doi.org/10.5061/dryad.r3r60">10.5061/dryad.r3r60</a>.'
  short: J. Hearn, G. Stone, N.H. Barton, K. Lohse, L. Bunnefeld, (2013).
date_created: 2021-07-30T08:31:22Z
date_published: 2013-10-01T00:00:00Z
date_updated: 2023-02-23T10:31:17Z
day: '01'
department:
- _id: NiBa
doi: 10.5061/dryad.r3r60
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.r3r60
month: '10'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '2170'
    relation: used_in_publication
    status: public
status: public
title: 'Data from: Likelihood-based inference of population history from low coverage
  de novo genome assemblies'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2013'
...
---
_id: '2443'
abstract:
- lang: eng
  text: The mode of action of auxin is based on its non-uniform distribution within
    tissues and organs. Despite the wide use of several auxin analogues in research
    and agriculture, little is known about the specificity of different auxin-related
    transport and signalling processes towards these compounds. Using seedlings of
    Arabidopsis thaliana and suspension-cultured cells of Nicotiana tabacum (BY-2),
    the physiological activity of several auxin analogues was investigated, together
    with their capacity to induce auxin-dependent gene expression, to inhibit endocytosis
    and to be transported across the plasma membrane. This study shows that the specificity
    criteria for different auxin-related processes vary widely. Notably, the special
    behaviour of some synthetic auxin analogues suggests that they might be useful
    tools in investigations of the molecular mechanism of auxin action. Thus, due
    to their differential stimulatory effects on DR5 expression, indole-3-propionic
    (IPA) and 2,4,5-trichlorophenoxy acetic (2,4,5-T) acids can serve in studies of
    TRANSPORT INHIBITOR RESPONSE 1/AUXIN SIGNALLING F-BOX (TIR1/AFB)-mediated auxin
    signalling, and 5-fluoroindole-3-acetic acid (5-F-IAA) can help to discriminate
    between transcriptional and non-transcriptional pathways of auxin signalling.
    The results demonstrate that the major determinants for the auxin-like physiological
    potential of a particular compound are very complex and involve its chemical and
    metabolic stability, its ability to distribute in tissues in a polar manner and
    its activity towards auxin signalling machinery.
acknowledgement: The authors thank Dr Christian Luschnig (University of Natural Resources
  and Life Sciences (BOKU), Vienna, Austria) for the anti-PIN2 antibody, Professor
  Mark Estelle (University of California, San Diego, CA, USA) for tir1-1 mutant seeds
  and, last but not least, to Dr David Morris for critical reading of the manuscript.
  We also thank Markéta Pařezová and Jana Stýblová for excellent technical assistance.
  This work was supported by the Grant Agency of the Czech Republic (P305/11/0797
  to E.Z. and 13-40637S to J.F.), the Central European Institute of Technology project
  CZ.1.05/1.1.00/02.0068 from the European Regional Development Fund and by a European
  Research Council starting independent research grant ERC-2011-StG-20101109-PSDP
  (to J.F.).
article_processing_charge: No
article_type: original
author:
- first_name: Sibu
  full_name: Simon, Sibu
  id: 4542EF9A-F248-11E8-B48F-1D18A9856A87
  last_name: Simon
  orcid: 0000-0002-1998-6741
- first_name: Martin
  full_name: Kubeš, Martin
  last_name: Kubeš
- first_name: Pawel
  full_name: Baster, Pawel
  id: 3028BD74-F248-11E8-B48F-1D18A9856A87
  last_name: Baster
- first_name: Stéphanie
  full_name: Robert, Stéphanie
  last_name: Robert
- first_name: Petre
  full_name: Dobrev, Petre
  last_name: Dobrev
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Jan
  full_name: Petrášek, Jan
  last_name: Petrášek
- first_name: Eva
  full_name: Zažímalová, Eva
  last_name: Zažímalová
citation:
  ama: 'Simon S, Kubeš M, Baster P, et al. Defining the selectivity of processes along
    the auxin response chain: A study using auxin analogues. <i>New Phytologist</i>.
    2013;200(4):1034-1048. doi:<a href="https://doi.org/10.1111/nph.12437">10.1111/nph.12437</a>'
  apa: 'Simon, S., Kubeš, M., Baster, P., Robert, S., Dobrev, P., Friml, J., … Zažímalová,
    E. (2013). Defining the selectivity of processes along the auxin response chain:
    A study using auxin analogues. <i>New Phytologist</i>. Wiley. <a href="https://doi.org/10.1111/nph.12437">https://doi.org/10.1111/nph.12437</a>'
  chicago: 'Simon, Sibu, Martin Kubeš, Pawel Baster, Stéphanie Robert, Petre Dobrev,
    Jiří Friml, Jan Petrášek, and Eva Zažímalová. “Defining the Selectivity of Processes
    along the Auxin Response Chain: A Study Using Auxin Analogues.” <i>New Phytologist</i>.
    Wiley, 2013. <a href="https://doi.org/10.1111/nph.12437">https://doi.org/10.1111/nph.12437</a>.'
  ieee: 'S. Simon <i>et al.</i>, “Defining the selectivity of processes along the
    auxin response chain: A study using auxin analogues,” <i>New Phytologist</i>,
    vol. 200, no. 4. Wiley, pp. 1034–1048, 2013.'
  ista: 'Simon S, Kubeš M, Baster P, Robert S, Dobrev P, Friml J, Petrášek J, Zažímalová
    E. 2013. Defining the selectivity of processes along the auxin response chain:
    A study using auxin analogues. New Phytologist. 200(4), 1034–1048.'
  mla: 'Simon, Sibu, et al. “Defining the Selectivity of Processes along the Auxin
    Response Chain: A Study Using Auxin Analogues.” <i>New Phytologist</i>, vol. 200,
    no. 4, Wiley, 2013, pp. 1034–48, doi:<a href="https://doi.org/10.1111/nph.12437">10.1111/nph.12437</a>.'
  short: S. Simon, M. Kubeš, P. Baster, S. Robert, P. Dobrev, J. Friml, J. Petrášek,
    E. Zažímalová, New Phytologist 200 (2013) 1034–1048.
das_tickbox: '1'
date_created: 2018-12-11T11:57:41Z
date_published: 2013-12-01T00:00:00Z
date_updated: 2026-06-18T07:49:41Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1111/nph.12437
ec_funded: 1
intvolume: '       200'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1111/nph.12437
month: '12'
oa: 1
oa_version: Published Version
page: 1034 - 1048
project:
- _id: 25716A02-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '282300'
  name: Polarity and subcellular dynamics in plants
publication: New Phytologist
publication_status: published
publisher: Wiley
publist_id: '4460'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Defining the selectivity of processes along the auxin response chain: A study
  using auxin analogues'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 200
year: '2013'
...
---
_id: '2444'
abstract:
- lang: eng
  text: 'We consider two core algorithmic problems for probabilistic verification:
    the maximal end-component decomposition and the almost-sure reachability set computation
    for Markov decision processes (MDPs). For MDPs with treewidth k, we present two
    improved static algorithms for both the problems that run in time O(n·k 2.38·2k
    ) and O(m·logn· k), respectively, where n is the number of states and m is the
    number of edges, significantly improving the previous known O(n·k·√n· k) bound
    for low treewidth. We also present decremental algorithms for both problems for
    MDPs with constant treewidth that run in amortized logarithmic time, which is
    a huge improvement over the previously known algorithms that require amortized
    linear time.'
alternative_title:
- LNCS
article_processing_charge: No
arxiv: 1
author:
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Jakub
  full_name: Ła̧Cki, Jakub
  last_name: Ła̧Cki
citation:
  ama: Chatterjee K, Ła̧Cki J. Faster algorithms for Markov decision processes with
    low treewidth. 2013;8044:543-558. doi:<a href="https://doi.org/10.1007/978-3-642-39799-8_36">10.1007/978-3-642-39799-8_36</a>
  apa: 'Chatterjee, K., &#38; Ła̧Cki, J. (2013). Faster algorithms for Markov decision
    processes with low treewidth. Presented at the CAV: Computer Aided Verification,
    St. Petersburg, Russia: Springer. <a href="https://doi.org/10.1007/978-3-642-39799-8_36">https://doi.org/10.1007/978-3-642-39799-8_36</a>'
  chicago: Chatterjee, Krishnendu, and Jakub Ła̧Cki. “Faster Algorithms for Markov
    Decision Processes with Low Treewidth.” Lecture Notes in Computer Science. Springer,
    2013. <a href="https://doi.org/10.1007/978-3-642-39799-8_36">https://doi.org/10.1007/978-3-642-39799-8_36</a>.
  ieee: K. Chatterjee and J. Ła̧Cki, “Faster algorithms for Markov decision processes
    with low treewidth,” vol. 8044. Springer, pp. 543–558, 2013.
  ista: Chatterjee K, Ła̧Cki J. 2013. Faster algorithms for Markov decision processes
    with low treewidth. 8044, 543–558.
  mla: Chatterjee, Krishnendu, and Jakub Ła̧Cki. <i>Faster Algorithms for Markov Decision
    Processes with Low Treewidth</i>. Vol. 8044, Springer, 2013, pp. 543–58, doi:<a
    href="https://doi.org/10.1007/978-3-642-39799-8_36">10.1007/978-3-642-39799-8_36</a>.
  short: K. Chatterjee, J. Ła̧Cki, 8044 (2013) 543–558.
conference:
  end_date: 2013-07-19
  location: St. Petersburg, Russia
  name: 'CAV: Computer Aided Verification'
  start_date: 2013-07-13
das_tickbox: '1'
date_created: 2018-12-11T11:57:42Z
date_published: 2013-07-01T00:00:00Z
date_updated: 2026-06-18T07:50:03Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1007/978-3-642-39799-8_36
ec_funded: 1
external_id:
  arxiv:
  - '1304.0084'
intvolume: '      8044'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1304.0084
month: '07'
oa: 1
oa_version: Preprint
page: 543 - 558
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: '4459'
quality_controlled: '1'
scopus_import: '1'
series_title: Lecture Notes in Computer Science
status: public
title: Faster algorithms for Markov decision processes with low treewidth
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8044
year: '2013'
...
---
_id: '3321'
author:
- first_name: Novi
  full_name: Quadrianto, Novi
  last_name: Quadrianto
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
citation:
  ama: 'Quadrianto N, Lampert C. Kernel based learning. In: Dubitzky W, Wolkenhauer
    O, Cho K, Yokota H, eds. <i>Encyclopedia of Systems Biology</i>. Vol 3. Springer;
    2013:1069-1069. doi:<a href="https://doi.org/10.1007/978-1-4419-9863-7_604">10.1007/978-1-4419-9863-7_604</a>'
  apa: Quadrianto, N., &#38; Lampert, C. (2013). Kernel based learning. In W. Dubitzky,
    O. Wolkenhauer, K. Cho, &#38; H. Yokota (Eds.), <i>Encyclopedia of Systems Biology</i>
    (Vol. 3, pp. 1069–1069). Springer. <a href="https://doi.org/10.1007/978-1-4419-9863-7_604">https://doi.org/10.1007/978-1-4419-9863-7_604</a>
  chicago: Quadrianto, Novi, and Christoph Lampert. “Kernel Based Learning.” In <i>Encyclopedia
    of Systems Biology</i>, edited by Werner Dubitzky, Olaf Wolkenhauer, Kwang Cho,
    and Hiroki Yokota, 3:1069–1069. Springer, 2013. <a href="https://doi.org/10.1007/978-1-4419-9863-7_604">https://doi.org/10.1007/978-1-4419-9863-7_604</a>.
  ieee: N. Quadrianto and C. Lampert, “Kernel based learning,” in <i>Encyclopedia
    of Systems Biology</i>, vol. 3, W. Dubitzky, O. Wolkenhauer, K. Cho, and H. Yokota,
    Eds. Springer, 2013, pp. 1069–1069.
  ista: 'Quadrianto N, Lampert C. 2013.Kernel based learning. In: Encyclopedia of
    Systems Biology. vol. 3, 1069–1069.'
  mla: Quadrianto, Novi, and Christoph Lampert. “Kernel Based Learning.” <i>Encyclopedia
    of Systems Biology</i>, edited by Werner Dubitzky et al., vol. 3, Springer, 2013,
    pp. 1069–1069, doi:<a href="https://doi.org/10.1007/978-1-4419-9863-7_604">10.1007/978-1-4419-9863-7_604</a>.
  short: N. Quadrianto, C. Lampert, in:, W. Dubitzky, O. Wolkenhauer, K. Cho, H. Yokota
    (Eds.), Encyclopedia of Systems Biology, Springer, 2013, pp. 1069–1069.
date_created: 2018-12-11T12:02:39Z
date_published: 2013-01-01T00:00:00Z
date_updated: 2021-01-12T07:42:38Z
day: '01'
department:
- _id: ChLa
doi: 10.1007/978-1-4419-9863-7_604
editor:
- first_name: Werner
  full_name: Dubitzky, Werner
  last_name: Dubitzky
- first_name: Olaf
  full_name: Wolkenhauer, Olaf
  last_name: Wolkenhauer
- first_name: Kwang
  full_name: Cho, Kwang
  last_name: Cho
- first_name: Hiroki
  full_name: Yokota, Hiroki
  last_name: Yokota
intvolume: '         3'
language:
- iso: eng
month: '01'
oa_version: None
page: 1069 - 1069
publication: Encyclopedia of Systems Biology
publication_status: published
publisher: Springer
publist_id: '3314'
quality_controlled: '1'
status: public
title: Kernel based learning
type: encyclopedia_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 3
year: '2013'
...
---
_id: '450'
abstract:
- lang: eng
  text: Understanding the relative importance of heterosis and outbreeding depression
    over multiple generations is a key question in evolutionary biology and is essential
    for identifying appropriate genetic sources for population and ecosystem restoration.
    Here we use 2455 experimental crosses between 12 population pairs of the rare
    perennial plant Rutidosis leptorrhynchoides (Asteraceae) to investigate the multi-generational
    (F1, F2, F3) fitness outcomes of inter-population hybridization. We detected no
    evidence of outbreeding depression, with inter-population hybrids and backcrosses
    showing either similar fitness or significant heterosis for fitness components
    across the three generations. Variation in heterosis among population pairs was
    best explained by characteristics of the foreign source or home population, and
    was greatest when the source population was large, with high genetic diversity
    and low inbreeding, and the home population was small and inbred. Our results
    indicate that the primary consideration for maximizing progeny fitness following
    population augmentation or restoration is the use of seed from large, genetically
    diverse populations.
article_number: '2058'
author:
- first_name: Melinda
  full_name: Pickup, Melinda
  id: 2C78037E-F248-11E8-B48F-1D18A9856A87
  last_name: Pickup
  orcid: 0000-0001-6118-0541
- first_name: David
  full_name: Field, David
  id: 419049E2-F248-11E8-B48F-1D18A9856A87
  last_name: Field
  orcid: 0000-0002-4014-8478
- first_name: David
  full_name: Rowell, David
  last_name: Rowell
- first_name: Andrew
  full_name: Young, Andrew
  last_name: Young
citation:
  ama: Pickup M, Field D, Rowell D, Young A. Source population characteristics affect
    heterosis following genetic rescue of fragmented plant populations. <i>Proceedings
    of the Royal Society of London Series B Biological Sciences</i>. 2013;280(1750).
    doi:<a href="https://doi.org/10.1098/rspb.2012.2058">10.1098/rspb.2012.2058</a>
  apa: Pickup, M., Field, D., Rowell, D., &#38; Young, A. (2013). Source population
    characteristics affect heterosis following genetic rescue of fragmented plant
    populations. <i>Proceedings of the Royal Society of London Series B Biological
    Sciences</i>. Royal Society, The. <a href="https://doi.org/10.1098/rspb.2012.2058">https://doi.org/10.1098/rspb.2012.2058</a>
  chicago: Pickup, Melinda, David Field, David Rowell, and Andrew Young. “Source Population
    Characteristics Affect Heterosis Following Genetic Rescue of Fragmented Plant
    Populations.” <i>Proceedings of the Royal Society of London Series B Biological
    Sciences</i>. Royal Society, The, 2013. <a href="https://doi.org/10.1098/rspb.2012.2058">https://doi.org/10.1098/rspb.2012.2058</a>.
  ieee: M. Pickup, D. Field, D. Rowell, and A. Young, “Source population characteristics
    affect heterosis following genetic rescue of fragmented plant populations,” <i>Proceedings
    of the Royal Society of London Series B Biological Sciences</i>, vol. 280, no.
    1750. Royal Society, The, 2013.
  ista: Pickup M, Field D, Rowell D, Young A. 2013. Source population characteristics
    affect heterosis following genetic rescue of fragmented plant populations. Proceedings
    of the Royal Society of London Series B Biological Sciences. 280(1750), 2058.
  mla: Pickup, Melinda, et al. “Source Population Characteristics Affect Heterosis
    Following Genetic Rescue of Fragmented Plant Populations.” <i>Proceedings of the
    Royal Society of London Series B Biological Sciences</i>, vol. 280, no. 1750,
    2058, Royal Society, The, 2013, doi:<a href="https://doi.org/10.1098/rspb.2012.2058">10.1098/rspb.2012.2058</a>.
  short: M. Pickup, D. Field, D. Rowell, A. Young, Proceedings of the Royal Society
    of London Series B Biological Sciences 280 (2013).
date_created: 2018-12-11T11:46:32Z
date_published: 2013-01-07T00:00:00Z
date_updated: 2021-01-12T07:57:25Z
day: '07'
department:
- _id: NiBa
doi: 10.1098/rspb.2012.2058
external_id:
  pmid:
  - '23173202'
intvolume: '       280'
issue: '1750'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574427/
month: '01'
oa: 1
oa_version: Submitted Version
pmid: 1
publication: Proceedings of the Royal Society of London Series B Biological Sciences
publication_status: published
publisher: Royal Society, The
publist_id: '7372'
quality_controlled: '1'
status: public
title: Source population characteristics affect heterosis following genetic rescue
  of fragmented plant populations
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 280
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
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
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'
...
---
_id: '509'
abstract:
- lang: eng
  text: 'Clathrin-mediated endocytosis (CME) regulates many aspects of plant development,
    including hormone signaling and responses to environmental stresses. Despite the
    importance of this process, the machinery that regulates CME in plants is largely
    unknown. In mammals, the heterotetrameric ADAPTOR PROTEIN COMPLEX-2 (AP-2) is
    required for the formation of clathrin-coated vesicles at the plasma membrane
    (PM). Although the existence of AP-2 has been predicted in Arabidopsis thaliana,
    the biochemistry and functionality of the complex is still uncharacterized. Here,
    we identified all the subunits of the Arabidopsis AP-2 by tandem affinity purification
    and found that one of the large AP-2 subunits, AP2A1, localized at the PM and
    interacted with clathrin. Furthermore, endocytosis of the leucine-rich repeat
    receptor kinase, BRASSINOSTEROID INSENSITIVE1 (BRI1), was shown to depend on AP-2.
    Knockdown of the two Arabidopsis AP2A genes or overexpression of a dominant-negative
    version of the medium AP-2 subunit, AP2M, impaired BRI1 endocytosis and enhanced
    the brassinosteroid signaling. Our data reveal that the CME machinery in Arabidopsis
    is evolutionarily conserved and that AP-2 functions in receptormediated endocytosis. '
author:
- first_name: Simone
  full_name: Di Rubbo, Simone
  last_name: Di Rubbo
- first_name: Niloufer
  full_name: Irani, Niloufer
  last_name: Irani
- first_name: Soo
  full_name: Kim, Soo
  last_name: Kim
- first_name: Zheng
  full_name: Xu, Zheng
  last_name: Xu
- first_name: Astrid
  full_name: Gadeyne, Astrid
  last_name: Gadeyne
- first_name: Wim
  full_name: Dejonghe, Wim
  last_name: Dejonghe
- first_name: Isabelle
  full_name: Vanhoutte, Isabelle
  last_name: Vanhoutte
- first_name: Geert
  full_name: Persiau, Geert
  last_name: Persiau
- first_name: Dominique
  full_name: Eeckhout, Dominique
  last_name: Eeckhout
- first_name: Sibu
  full_name: Simon, Sibu
  id: 4542EF9A-F248-11E8-B48F-1D18A9856A87
  last_name: Simon
  orcid: 0000-0002-1998-6741
- first_name: Kyungyoung
  full_name: Song, Kyungyoung
  last_name: Song
- first_name: Jürgen
  full_name: Kleine Vehn, Jürgen
  last_name: Kleine Vehn
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Geert
  full_name: De Jaeger, Geert
  last_name: De Jaeger
- first_name: Daniël
  full_name: Van Damme, Daniël
  last_name: Van Damme
- first_name: Inhwan
  full_name: Hwang, Inhwan
  last_name: Hwang
- first_name: Eugenia
  full_name: Russinova, Eugenia
  last_name: Russinova
citation:
  ama: Di Rubbo S, Irani N, Kim S, et al. The clathrin adaptor complex AP-2 mediates
    endocytosis of brassinosteroid INSENSITIVE1 in arabidopsis. <i>Plant Cell</i>.
    2013;25(8):2986-2997. doi:<a href="https://doi.org/10.1105/tpc.113.114058">10.1105/tpc.113.114058</a>
  apa: Di Rubbo, S., Irani, N., Kim, S., Xu, Z., Gadeyne, A., Dejonghe, W., … Russinova,
    E. (2013). The clathrin adaptor complex AP-2 mediates endocytosis of brassinosteroid
    INSENSITIVE1 in arabidopsis. <i>Plant Cell</i>. American Society of Plant Biologists.
    <a href="https://doi.org/10.1105/tpc.113.114058">https://doi.org/10.1105/tpc.113.114058</a>
  chicago: Di Rubbo, Simone, Niloufer Irani, Soo Kim, Zheng Xu, Astrid Gadeyne, Wim
    Dejonghe, Isabelle Vanhoutte, et al. “The Clathrin Adaptor Complex AP-2 Mediates
    Endocytosis of Brassinosteroid INSENSITIVE1 in Arabidopsis.” <i>Plant Cell</i>.
    American Society of Plant Biologists, 2013. <a href="https://doi.org/10.1105/tpc.113.114058">https://doi.org/10.1105/tpc.113.114058</a>.
  ieee: S. Di Rubbo <i>et al.</i>, “The clathrin adaptor complex AP-2 mediates endocytosis
    of brassinosteroid INSENSITIVE1 in arabidopsis,” <i>Plant Cell</i>, vol. 25, no.
    8. American Society of Plant Biologists, pp. 2986–2997, 2013.
  ista: Di Rubbo S, Irani N, Kim S, Xu Z, Gadeyne A, Dejonghe W, Vanhoutte I, Persiau
    G, Eeckhout D, Simon S, Song K, Kleine Vehn J, Friml J, De Jaeger G, Van Damme
    D, Hwang I, Russinova E. 2013. The clathrin adaptor complex AP-2 mediates endocytosis
    of brassinosteroid INSENSITIVE1 in arabidopsis. Plant Cell. 25(8), 2986–2997.
  mla: Di Rubbo, Simone, et al. “The Clathrin Adaptor Complex AP-2 Mediates Endocytosis
    of Brassinosteroid INSENSITIVE1 in Arabidopsis.” <i>Plant Cell</i>, vol. 25, no.
    8, American Society of Plant Biologists, 2013, pp. 2986–97, doi:<a href="https://doi.org/10.1105/tpc.113.114058">10.1105/tpc.113.114058</a>.
  short: S. Di Rubbo, N. Irani, S. Kim, Z. Xu, A. Gadeyne, W. Dejonghe, I. Vanhoutte,
    G. Persiau, D. Eeckhout, S. Simon, K. Song, J. Kleine Vehn, J. Friml, G. De Jaeger,
    D. Van Damme, I. Hwang, E. Russinova, Plant Cell 25 (2013) 2986–2997.
date_created: 2018-12-11T11:46:52Z
date_published: 2013-08-01T00:00:00Z
date_updated: 2021-01-12T08:01:13Z
day: '01'
department:
- _id: JiFr
doi: 10.1105/tpc.113.114058
external_id:
  pmid:
  - '23975899'
intvolume: '        25'
issue: '8'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784593/
month: '08'
oa: 1
oa_version: Submitted Version
page: 2986 - 2997
pmid: 1
publication: Plant Cell
publication_status: published
publisher: American Society of Plant Biologists
publist_id: '7311'
quality_controlled: '1'
scopus_import: 1
status: public
title: The clathrin adaptor complex AP-2 mediates endocytosis of brassinosteroid INSENSITIVE1
  in arabidopsis
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 25
year: '2013'
...
