---
_id: '9458'
abstract:
- lang: eng
  text: Dnmt1 epigenetically propagates symmetrical CG methylation in many eukaryotes.
    Their genomes are typically depleted of CG dinucleotides because of imperfect
    repair of deaminated methylcytosines. Here, we extensively survey diverse species
    lacking Dnmt1 and show that, surprisingly, symmetrical CG methylation is nonetheless
    frequently present and catalyzed by a different DNA methyltransferase family,
    Dnmt5. Numerous Dnmt5-containing organisms that diverged more than a billion years
    ago exhibit clustered methylation, specifically in nucleosome linkers. Clustered
    methylation occurs at unprecedented densities and directly disfavors nucleosomes,
    contributing to nucleosome positioning between clusters. Dense methylation is
    enabled by a regime of genomic sequence evolution that enriches CG dinucleotides
    and drives the highest CG frequencies known. Species with linker methylation have
    small, transcriptionally active nuclei that approach the physical limits of chromatin
    compaction. These features constitute a previously unappreciated genome architecture,
    in which dense methylation influences nucleosome positions, likely facilitating
    nuclear processes under extreme spatial constraints.
article_processing_charge: No
article_type: original
author:
- first_name: Jason T.
  full_name: Huff, Jason T.
  last_name: Huff
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
citation:
  ama: Huff JT, Zilberman D. Dnmt1-independent CG methylation contributes to nucleosome
    positioning in diverse eukaryotes. <i>Cell</i>. 2014;156(6):1286-1297. doi:<a
    href="https://doi.org/10.1016/j.cell.2014.01.029">10.1016/j.cell.2014.01.029</a>
  apa: Huff, J. T., &#38; Zilberman, D. (2014). Dnmt1-independent CG methylation contributes
    to nucleosome positioning in diverse eukaryotes. <i>Cell</i>. Elsevier. <a href="https://doi.org/10.1016/j.cell.2014.01.029">https://doi.org/10.1016/j.cell.2014.01.029</a>
  chicago: Huff, Jason T., and Daniel Zilberman. “Dnmt1-Independent CG Methylation
    Contributes to Nucleosome Positioning in Diverse Eukaryotes.” <i>Cell</i>. Elsevier,
    2014. <a href="https://doi.org/10.1016/j.cell.2014.01.029">https://doi.org/10.1016/j.cell.2014.01.029</a>.
  ieee: J. T. Huff and D. Zilberman, “Dnmt1-independent CG methylation contributes
    to nucleosome positioning in diverse eukaryotes,” <i>Cell</i>, vol. 156, no. 6.
    Elsevier, pp. 1286–1297, 2014.
  ista: Huff JT, Zilberman D. 2014. Dnmt1-independent CG methylation contributes to
    nucleosome positioning in diverse eukaryotes. Cell. 156(6), 1286–1297.
  mla: Huff, Jason T., and Daniel Zilberman. “Dnmt1-Independent CG Methylation Contributes
    to Nucleosome Positioning in Diverse Eukaryotes.” <i>Cell</i>, vol. 156, no. 6,
    Elsevier, 2014, pp. 1286–97, doi:<a href="https://doi.org/10.1016/j.cell.2014.01.029">10.1016/j.cell.2014.01.029</a>.
  short: J.T. Huff, D. Zilberman, Cell 156 (2014) 1286–1297.
date_created: 2021-06-04T12:00:16Z
date_published: 2014-03-13T00:00:00Z
date_updated: 2021-12-14T08:22:36Z
day: '13'
department:
- _id: DaZi
doi: 10.1016/j.cell.2014.01.029
extern: '1'
external_id:
  pmid:
  - '24630728'
fulldoi: https://doi.org/10.1016/j.cell.2014.01.029
intvolume: '       156'
issue: '6'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.cell.2014.01.029
month: '03'
oa: 1
oa_version: Published Version
page: 1286-1297
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: Dnmt1-independent CG methylation contributes to nucleosome positioning in diverse
  eukaryotes
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 156
year: '2014'
...
---
_id: '9479'
abstract:
- lang: eng
  text: Centromeres mediate chromosome segregation and are defined by the centromere-specific
    histone H3 variant (CenH3)/centromere protein A (CENP-A). Removal of CenH3 from
    centromeres is a general property of terminally differentiated cells, and the
    persistence of CenH3 increases the risk of diseases such as cancer. However, active
    mechanisms of centromere disassembly are unknown. Nondividing Arabidopsis pollen
    vegetative cells, which transport engulfed sperm by extended tip growth, undergo
    loss of CenH3; centromeric heterochromatin decondensation; and bulk activation
    of silent rRNA genes, accompanied by their translocation into the nucleolus. Here,
    we show that these processes are blocked by mutations in the evolutionarily conserved
    AAA-ATPase molecular chaperone, CDC48A, homologous to yeast Cdc48 and human p97
    proteins, both of which are implicated in ubiquitin/small ubiquitin-like modifier
    (SUMO)-targeted protein degradation. We demonstrate that CDC48A physically associates
    with its heterodimeric cofactor UFD1-NPL4, known to bind ubiquitin and SUMO, as
    well as with SUMO1-modified CenH3 and mutations in NPL4 phenocopy cdc48a mutations.
    In WT vegetative cell nuclei, genetically unlinked ribosomal DNA (rDNA) loci are
    uniquely clustered together within the nucleolus and all major rRNA gene variants,
    including those rDNA variants silenced in leaves, are transcribed. In cdc48a mutant
    vegetative cell nuclei, however, these rDNA loci frequently colocalized with condensed
    centromeric heterochromatin at the external periphery of the nucleolus. Our results
    indicate that the CDC48ANPL4 complex actively removes sumoylated CenH3 from centromeres
    and disrupts centromeric heterochromatin to release bulk rRNA genes into the nucleolus
    for ribosome production, which fuels single nucleus-driven pollen tube growth
    and is essential for plant reproduction.
article_processing_charge: No
article_type: original
author:
- first_name: Zsuzsanna
  full_name: Mérai, Zsuzsanna
  last_name: Mérai
- first_name: Nina
  full_name: Chumak, Nina
  last_name: Chumak
- first_name: Marcelina
  full_name: García-Aguilar, Marcelina
  last_name: García-Aguilar
- first_name: Tzung-Fu
  full_name: Hsieh, Tzung-Fu
  last_name: Hsieh
- first_name: Toshiro
  full_name: Nishimura, Toshiro
  last_name: Nishimura
- first_name: Vera K.
  full_name: Schoft, Vera K.
  last_name: Schoft
- first_name: János
  full_name: Bindics, János
  last_name: Bindics
- first_name: Lucyna
  full_name: Ślusarz, Lucyna
  last_name: Ślusarz
- first_name: Stéphanie
  full_name: Arnoux, Stéphanie
  last_name: Arnoux
- first_name: Susanne
  full_name: Opravil, Susanne
  last_name: Opravil
- first_name: Karl
  full_name: Mechtler, Karl
  last_name: Mechtler
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Robert L.
  full_name: Fischer, Robert L.
  last_name: Fischer
- first_name: Hisashi
  full_name: Tamaru, Hisashi
  last_name: Tamaru
citation:
  ama: Mérai Z, Chumak N, García-Aguilar M, et al. The AAA-ATPase molecular chaperone
    Cdc48/p97 disassembles sumoylated centromeres, decondenses heterochromatin, and
    activates ribosomal RNA genes. <i>Proceedings of the National Academy of Sciences</i>.
    2014;111(45):16166-16171. doi:<a href="https://doi.org/10.1073/pnas.1418564111">10.1073/pnas.1418564111</a>
  apa: Mérai, Z., Chumak, N., García-Aguilar, M., Hsieh, T.-F., Nishimura, T., Schoft,
    V. K., … Tamaru, H. (2014). The AAA-ATPase molecular chaperone Cdc48/p97 disassembles
    sumoylated centromeres, decondenses heterochromatin, and activates ribosomal RNA
    genes. <i>Proceedings of the National Academy of Sciences</i>. National Academy
    of Sciences. <a href="https://doi.org/10.1073/pnas.1418564111">https://doi.org/10.1073/pnas.1418564111</a>
  chicago: Mérai, Zsuzsanna, Nina Chumak, Marcelina García-Aguilar, Tzung-Fu Hsieh,
    Toshiro Nishimura, Vera K. Schoft, János Bindics, et al. “The AAA-ATPase Molecular
    Chaperone Cdc48/P97 Disassembles Sumoylated Centromeres, Decondenses Heterochromatin,
    and Activates Ribosomal RNA Genes.” <i>Proceedings of the National Academy of
    Sciences</i>. National Academy of Sciences, 2014. <a href="https://doi.org/10.1073/pnas.1418564111">https://doi.org/10.1073/pnas.1418564111</a>.
  ieee: Z. Mérai <i>et al.</i>, “The AAA-ATPase molecular chaperone Cdc48/p97 disassembles
    sumoylated centromeres, decondenses heterochromatin, and activates ribosomal RNA
    genes,” <i>Proceedings of the National Academy of Sciences</i>, vol. 111, no.
    45. National Academy of Sciences, pp. 16166–16171, 2014.
  ista: Mérai Z, Chumak N, García-Aguilar M, Hsieh T-F, Nishimura T, Schoft VK, Bindics
    J, Ślusarz L, Arnoux S, Opravil S, Mechtler K, Zilberman D, Fischer RL, Tamaru
    H. 2014. The AAA-ATPase molecular chaperone Cdc48/p97 disassembles sumoylated
    centromeres, decondenses heterochromatin, and activates ribosomal RNA genes. Proceedings
    of the National Academy of Sciences. 111(45), 16166–16171.
  mla: Mérai, Zsuzsanna, et al. “The AAA-ATPase Molecular Chaperone Cdc48/P97 Disassembles
    Sumoylated Centromeres, Decondenses Heterochromatin, and Activates Ribosomal RNA
    Genes.” <i>Proceedings of the National Academy of Sciences</i>, vol. 111, no.
    45, National Academy of Sciences, 2014, pp. 16166–71, doi:<a href="https://doi.org/10.1073/pnas.1418564111">10.1073/pnas.1418564111</a>.
  short: Z. Mérai, N. Chumak, M. García-Aguilar, T.-F. Hsieh, T. Nishimura, V.K. Schoft,
    J. Bindics, L. Ślusarz, S. Arnoux, S. Opravil, K. Mechtler, D. Zilberman, R.L.
    Fischer, H. Tamaru, Proceedings of the National Academy of Sciences 111 (2014)
    16166–16171.
date_created: 2021-06-07T07:23:43Z
date_published: 2014-11-11T00:00:00Z
date_updated: 2021-12-14T08:23:26Z
day: '11'
department:
- _id: DaZi
doi: 10.1073/pnas.1418564111
extern: '1'
external_id:
  pmid:
  - '25344531'
fulldoi: https://doi.org/10.1073/pnas.1418564111
intvolume: '       111'
issue: '45'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1073/pnas.1418564111
month: '11'
oa: 1
oa_version: Published Version
page: 16166-16171
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: The AAA-ATPase molecular chaperone Cdc48/p97 disassembles sumoylated centromeres,
  decondenses heterochromatin, and activates ribosomal RNA genes
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 111
year: '2014'
...
---
_id: '9519'
abstract:
- lang: eng
  text: Transposons are selfish genetic sequences that can increase their copy number
    and inflict substantial damage on their hosts. To combat these genomic parasites,
    plants have evolved multiple pathways to identify and silence transposons by methylating
    their DNA. Plants have also evolved mechanisms to limit the collateral damage
    from the antitransposon machinery. In this review, we examine recent developments
    that have elucidated many of the molecular workings of these pathways. We also
    highlight the evidence that the methylation and demethylation pathways interact,
    indicating that plants have a highly sophisticated, integrated system of transposon
    defense that has an important role in the regulation of gene expression.
article_processing_charge: No
article_type: review
author:
- first_name: M. Yvonne
  full_name: Kim, M. Yvonne
  last_name: Kim
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
citation:
  ama: Kim MY, Zilberman D. DNA methylation as a system of plant genomic immunity.
    <i>Trends in Plant Science</i>. 2014;19(5):320-326. doi:<a href="https://doi.org/10.1016/j.tplants.2014.01.014">10.1016/j.tplants.2014.01.014</a>
  apa: Kim, M. Y., &#38; Zilberman, D. (2014). DNA methylation as a system of plant
    genomic immunity. <i>Trends in Plant Science</i>. Elsevier. <a href="https://doi.org/10.1016/j.tplants.2014.01.014">https://doi.org/10.1016/j.tplants.2014.01.014</a>
  chicago: Kim, M. Yvonne, and Daniel Zilberman. “DNA Methylation as a System of Plant
    Genomic Immunity.” <i>Trends in Plant Science</i>. Elsevier, 2014. <a href="https://doi.org/10.1016/j.tplants.2014.01.014">https://doi.org/10.1016/j.tplants.2014.01.014</a>.
  ieee: M. Y. Kim and D. Zilberman, “DNA methylation as a system of plant genomic
    immunity,” <i>Trends in Plant Science</i>, vol. 19, no. 5. Elsevier, pp. 320–326,
    2014.
  ista: Kim MY, Zilberman D. 2014. DNA methylation as a system of plant genomic immunity.
    Trends in Plant Science. 19(5), 320–326.
  mla: Kim, M. Yvonne, and Daniel Zilberman. “DNA Methylation as a System of Plant
    Genomic Immunity.” <i>Trends in Plant Science</i>, vol. 19, no. 5, Elsevier, 2014,
    pp. 320–26, doi:<a href="https://doi.org/10.1016/j.tplants.2014.01.014">10.1016/j.tplants.2014.01.014</a>.
  short: M.Y. Kim, D. Zilberman, Trends in Plant Science 19 (2014) 320–326.
date_created: 2021-06-07T14:38:09Z
date_published: 2014-05-04T00:00:00Z
date_updated: 2021-12-14T08:24:48Z
day: '04'
department:
- _id: DaZi
doi: 10.1016/j.tplants.2014.01.014
extern: '1'
external_id:
  pmid:
  - '24618094 '
fulldoi: https://doi.org/10.1016/j.tplants.2014.01.014
intvolume: '        19'
issue: '5'
language:
- iso: eng
month: '05'
oa_version: None
page: 320-326
pmid: 1
publication: Trends in Plant Science
publication_identifier:
  eissn:
  - 1878-4372
  issn:
  - 1360-1385
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: DNA methylation as a system of plant genomic immunity
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 19
year: '2014'
...
---
_id: '9722'
article_processing_charge: No
author:
- first_name: Anna
  full_name: Lovrics, Anna
  last_name: Lovrics
- first_name: Yu
  full_name: Gao, Yu
  last_name: Gao
- first_name: Bianka
  full_name: Juhász, Bianka
  last_name: Juhász
- first_name: István
  full_name: Bock, István
  last_name: Bock
- first_name: Helen M.
  full_name: Byrne, Helen M.
  last_name: Byrne
- first_name: András
  full_name: Dinnyés, András
  last_name: Dinnyés
- first_name: Krisztián
  full_name: Kovács, Krisztián
  id: 2AB5821E-F248-11E8-B48F-1D18A9856A87
  last_name: Kovács
citation:
  ama: Lovrics A, Gao Y, Juhász B, et al. Transition probability between TF expression
    states when Dbx2 inhibits Nkx2.2. 2014. doi:<a href="https://doi.org/10.1371/journal.pone.0111430.s006">10.1371/journal.pone.0111430.s006</a>
  apa: Lovrics, A., Gao, Y., Juhász, B., Bock, I., Byrne, H. M., Dinnyés, A., &#38;
    Kovács, K. (2014). Transition probability between TF expression states when Dbx2
    inhibits Nkx2.2. Public Library of Science. <a href="https://doi.org/10.1371/journal.pone.0111430.s006">https://doi.org/10.1371/journal.pone.0111430.s006</a>
  chicago: Lovrics, Anna, Yu Gao, Bianka Juhász, István Bock, Helen M. Byrne, András
    Dinnyés, and Krisztián Kovács. “Transition Probability between TF Expression States
    When Dbx2 Inhibits Nkx2.2.” Public Library of Science, 2014. <a href="https://doi.org/10.1371/journal.pone.0111430.s006">https://doi.org/10.1371/journal.pone.0111430.s006</a>.
  ieee: A. Lovrics <i>et al.</i>, “Transition probability between TF expression states
    when Dbx2 inhibits Nkx2.2.” Public Library of Science, 2014.
  ista: Lovrics A, Gao Y, Juhász B, Bock I, Byrne HM, Dinnyés A, Kovács K. 2014. Transition
    probability between TF expression states when Dbx2 inhibits Nkx2.2, Public Library
    of Science, <a href="https://doi.org/10.1371/journal.pone.0111430.s006">10.1371/journal.pone.0111430.s006</a>.
  mla: Lovrics, Anna, et al. <i>Transition Probability between TF Expression States
    When Dbx2 Inhibits Nkx2.2</i>. Public Library of Science, 2014, doi:<a href="https://doi.org/10.1371/journal.pone.0111430.s006">10.1371/journal.pone.0111430.s006</a>.
  short: A. Lovrics, Y. Gao, B. Juhász, I. Bock, H.M. Byrne, A. Dinnyés, K. Kovács,
    (2014).
date_created: 2021-07-26T14:35:00Z
date_published: 2014-11-14T00:00:00Z
date_updated: 2025-09-29T12:02:47Z
day: '14'
department:
- _id: JoCs
doi: 10.1371/journal.pone.0111430.s006
fulldoi: https://doi.org/10.1371/journal.pone.0111430.s006
month: '11'
oa_version: Published Version
publisher: Public Library of Science
related_material:
  record:
  - id: '2004'
    relation: used_in_publication
    status: public
status: public
title: Transition probability between TF expression states when Dbx2 inhibits Nkx2.2
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2014'
...
---
_id: '9739'
article_processing_charge: No
author:
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Andreas
  full_name: Pavlogiannis, Andreas
  id: 49704004-F248-11E8-B48F-1D18A9856A87
  last_name: Pavlogiannis
  orcid: 0000-0002-8943-0722
- first_name: Ben
  full_name: Adlam, Ben
  last_name: Adlam
- first_name: Martin
  full_name: Novak, Martin
  last_name: Novak
citation:
  ama: Chatterjee K, Pavlogiannis A, Adlam B, Novak M. Detailed proofs for “The time
    scale of evolutionary innovation.” 2014. doi:<a href="https://doi.org/10.1371/journal.pcbi.1003818.s001">10.1371/journal.pcbi.1003818.s001</a>
  apa: Chatterjee, K., Pavlogiannis, A., Adlam, B., &#38; Novak, M. (2014). Detailed
    proofs for “The time scale of evolutionary innovation.” Public Library of Science.
    <a href="https://doi.org/10.1371/journal.pcbi.1003818.s001">https://doi.org/10.1371/journal.pcbi.1003818.s001</a>
  chicago: Chatterjee, Krishnendu, Andreas Pavlogiannis, Ben Adlam, and Martin Novak.
    “Detailed Proofs for ‘The Time Scale of Evolutionary Innovation.’” Public Library
    of Science, 2014. <a href="https://doi.org/10.1371/journal.pcbi.1003818.s001">https://doi.org/10.1371/journal.pcbi.1003818.s001</a>.
  ieee: K. Chatterjee, A. Pavlogiannis, B. Adlam, and M. Novak, “Detailed proofs for
    ‘The time scale of evolutionary innovation.’” Public Library of Science, 2014.
  ista: Chatterjee K, Pavlogiannis A, Adlam B, Novak M. 2014. Detailed proofs for
    “The time scale of evolutionary innovation”, Public Library of Science, <a href="https://doi.org/10.1371/journal.pcbi.1003818.s001">10.1371/journal.pcbi.1003818.s001</a>.
  mla: Chatterjee, Krishnendu, et al. <i>Detailed Proofs for “The Time Scale of Evolutionary
    Innovation.”</i> Public Library of Science, 2014, doi:<a href="https://doi.org/10.1371/journal.pcbi.1003818.s001">10.1371/journal.pcbi.1003818.s001</a>.
  short: K. Chatterjee, A. Pavlogiannis, B. Adlam, M. Novak, (2014).
date_created: 2021-07-28T08:13:57Z
date_published: 2014-09-11T00:00:00Z
date_updated: 2025-09-29T11:53:46Z
day: '11'
department:
- _id: KrCh
doi: 10.1371/journal.pcbi.1003818.s001
fulldoi: https://doi.org/10.1371/journal.pcbi.1003818.s001
month: '09'
oa_version: Published Version
publisher: Public Library of Science
related_material:
  record:
  - id: '2039'
    relation: used_in_publication
    status: public
status: public
title: Detailed proofs for “The time scale of evolutionary innovation”
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2014'
...
---
_id: '9740'
abstract:
- lang: eng
  text: The fitness effects of symbionts on their hosts can be context-dependent,
    with usually benign symbionts causing detrimental effects when their hosts are
    stressed, or typically parasitic symbionts providing protection towards their
    hosts (e.g. against pathogen infection). Here, we studied the novel association
    between the invasive garden ant Lasius neglectus and its fungal ectosymbiont Laboulbenia
    formicarum for potential costs and benefits. We tested ants with different Laboulbenia
    levels for their survival and immunity under resource limitation and exposure
    to the obligate killing entomopathogen Metarhizium brunneum. While survival of
    L. neglectus workers under starvation was significantly decreased with increasing
    Laboulbenia levels, host survival under Metarhizium exposure increased with higher
    levels of the ectosymbiont, suggesting a symbiont-mediated anti-pathogen protection,
    which seems to be driven mechanistically by both improved sanitary behaviours
    and an upregulated immune system. Ants with high Laboulbenia levels showed significantly
    longer self-grooming and elevated expression of immune genes relevant for wound
    repair and antifungal responses (β-1,3-glucan binding protein, Prophenoloxidase),
    compared with ants carrying low Laboulbenia levels. This suggests that the ectosymbiont
    Laboulbenia formicarum weakens its ant host by either direct resource exploitation
    or the costs of an upregulated behavioural and immunological response, which,
    however, provides a prophylactic protection upon later exposure to pathogens.
article_processing_charge: No
author:
- first_name: Matthias
  full_name: Konrad, Matthias
  id: 46528076-F248-11E8-B48F-1D18A9856A87
  last_name: Konrad
- first_name: Anna V
  full_name: Grasse, Anna V
  id: 406F989C-F248-11E8-B48F-1D18A9856A87
  last_name: Grasse
- first_name: Simon
  full_name: Tragust, Simon
  id: 35A7A418-F248-11E8-B48F-1D18A9856A87
  last_name: Tragust
- first_name: Sylvia
  full_name: Cremer, Sylvia
  id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
  last_name: Cremer
  orcid: 0000-0002-2193-3868
citation:
  ama: 'Konrad M, Grasse AV, Tragust S, Cremer S. Data from: Anti-pathogen protection
    versus survival costs mediated by an ectosymbiont in an ant host. 2014. doi:<a
    href="https://doi.org/10.5061/dryad.vm0vc">10.5061/dryad.vm0vc</a>'
  apa: 'Konrad, M., Grasse, A. V., Tragust, S., &#38; Cremer, S. (2014). Data from:
    Anti-pathogen protection versus survival costs mediated by an ectosymbiont in
    an ant host. Dryad. <a href="https://doi.org/10.5061/dryad.vm0vc">https://doi.org/10.5061/dryad.vm0vc</a>'
  chicago: 'Konrad, Matthias, Anna V Grasse, Simon Tragust, and Sylvia Cremer. “Data
    from: Anti-Pathogen Protection versus Survival Costs Mediated by an Ectosymbiont
    in an Ant Host.” Dryad, 2014. <a href="https://doi.org/10.5061/dryad.vm0vc">https://doi.org/10.5061/dryad.vm0vc</a>.'
  ieee: 'M. Konrad, A. V. Grasse, S. Tragust, and S. Cremer, “Data from: Anti-pathogen
    protection versus survival costs mediated by an ectosymbiont in an ant host.”
    Dryad, 2014.'
  ista: 'Konrad M, Grasse AV, Tragust S, Cremer S. 2014. Data from: Anti-pathogen
    protection versus survival costs mediated by an ectosymbiont in an ant host, Dryad,
    <a href="https://doi.org/10.5061/dryad.vm0vc">10.5061/dryad.vm0vc</a>.'
  mla: 'Konrad, Matthias, et al. <i>Data from: Anti-Pathogen Protection versus Survival
    Costs Mediated by an Ectosymbiont in an Ant Host</i>. Dryad, 2014, doi:<a href="https://doi.org/10.5061/dryad.vm0vc">10.5061/dryad.vm0vc</a>.'
  short: M. Konrad, A.V. Grasse, S. Tragust, S. Cremer, (2014).
corr_author: '1'
date_created: 2021-07-28T08:38:40Z
date_published: 2014-11-13T00:00:00Z
date_updated: 2025-09-23T07:55:02Z
day: '13'
department:
- _id: SyCr
doi: 10.5061/dryad.vm0vc
fulldoi: https://doi.org/10.5061/dryad.vm0vc
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.vm0vc
month: '11'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '1993'
    relation: used_in_publication
    status: public
status: public
title: 'Data from: Anti-pathogen protection versus survival costs mediated by an ectosymbiont
  in an ant host'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2014'
...
---
_id: '9747'
abstract:
- lang: eng
  text: Understanding the effects of sex and migration on adaptation to novel environments
    remains a key problem in evolutionary biology. Using a single-cell alga Chlamydomonas
    reinhardtii, we investigated how sex and migration affected rates of evolutionary
    rescue in a sink environment, and subsequent changes in fitness following evolutionary
    rescue. We show that sex and migration affect both the rate of evolutionary rescue
    and subsequent adaptation. However, their combined effects change as the populations
    adapt to a sink habitat. Both sex and migration independently increased rates
    of evolutionary rescue, but the effect of sex on subsequent fitness improvements,
    following initial rescue, changed with migration, as sex was beneficial in the
    absence of migration but constraining adaptation when combined with migration.
    These results suggest that sex and migration are beneficial during the initial
    stages of adaptation, but can become detrimental as the population adapts to its
    environment.
article_processing_charge: No
author:
- first_name: Mato
  full_name: Lagator, Mato
  id: 345D25EC-F248-11E8-B48F-1D18A9856A87
  last_name: Lagator
- first_name: Andrew
  full_name: Morgan, Andrew
  last_name: Morgan
- first_name: Paul
  full_name: Neve, Paul
  last_name: Neve
- first_name: Nick
  full_name: Colegrave, Nick
  last_name: Colegrave
citation:
  ama: 'Lagator M, Morgan A, Neve P, Colegrave N. Data from: Role of sex and migration
    in adaptation to sink environments. 2014. doi:<a href="https://doi.org/10.5061/dryad.s42n1">10.5061/dryad.s42n1</a>'
  apa: 'Lagator, M., Morgan, A., Neve, P., &#38; Colegrave, N. (2014). Data from:
    Role of sex and migration in adaptation to sink environments. Dryad. <a href="https://doi.org/10.5061/dryad.s42n1">https://doi.org/10.5061/dryad.s42n1</a>'
  chicago: 'Lagator, Mato, Andrew Morgan, Paul Neve, and Nick Colegrave. “Data from:
    Role of Sex and Migration in Adaptation to Sink Environments.” Dryad, 2014. <a
    href="https://doi.org/10.5061/dryad.s42n1">https://doi.org/10.5061/dryad.s42n1</a>.'
  ieee: 'M. Lagator, A. Morgan, P. Neve, and N. Colegrave, “Data from: Role of sex
    and migration in adaptation to sink environments.” Dryad, 2014.'
  ista: 'Lagator M, Morgan A, Neve P, Colegrave N. 2014. Data from: Role of sex and
    migration in adaptation to sink environments, Dryad, <a href="https://doi.org/10.5061/dryad.s42n1">10.5061/dryad.s42n1</a>.'
  mla: 'Lagator, Mato, et al. <i>Data from: Role of Sex and Migration in Adaptation
    to Sink Environments</i>. Dryad, 2014, doi:<a href="https://doi.org/10.5061/dryad.s42n1">10.5061/dryad.s42n1</a>.'
  short: M. Lagator, A. Morgan, P. Neve, N. Colegrave, (2014).
date_created: 2021-07-28T15:32:55Z
date_published: 2014-04-17T00:00:00Z
date_updated: 2025-09-29T11:46:47Z
day: '17'
department:
- _id: CaGu
doi: 10.5061/dryad.s42n1
fulldoi: https://doi.org/10.5061/dryad.s42n1
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.s42n1
month: '04'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '2083'
    relation: used_in_publication
    status: public
status: public
title: 'Data from: Role of sex and migration in adaptation to sink environments'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2014'
...
---
_id: '9752'
abstract:
- lang: eng
  text: Redundancies and correlations in the responses of sensory neurons may seem
    to waste neural resources, but they can also carry cues about structured stimuli
    and may help the brain to correct for response errors. To investigate the effect
    of stimulus structure on redundancy in retina, we measured simultaneous responses
    from populations of retinal ganglion cells presented with natural and artificial
    stimuli that varied greatly in correlation structure; these stimuli and recordings
    are publicly available online. Responding to spatio-temporally structured stimuli
    such as natural movies, pairs of ganglion cells were modestly more correlated
    than in response to white noise checkerboards, but they were much less correlated
    than predicted by a non-adapting functional model of retinal response. Meanwhile,
    responding to stimuli with purely spatial correlations, pairs of ganglion cells
    showed increased correlations consistent with a static, non-adapting receptive
    field and nonlinearity. We found that in response to spatio-temporally correlated
    stimuli, ganglion cells had faster temporal kernels and tended to have stronger
    surrounds. These properties of individual cells, along with gain changes that
    opposed changes in effective contrast at the ganglion cell input, largely explained
    the pattern of pairwise correlations across stimuli where receptive field measurements
    were possible.
article_processing_charge: No
author:
- first_name: Kristina
  full_name: Simmons, Kristina
  last_name: Simmons
- first_name: Jason
  full_name: Prentice, Jason
  last_name: Prentice
- first_name: Gašper
  full_name: Tkačik, Gašper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkačik
  orcid: 0000-0002-6699-1455
- first_name: Jan
  full_name: Homann, Jan
  last_name: Homann
- first_name: Heather
  full_name: Yee, Heather
  last_name: Yee
- first_name: Stephanie
  full_name: Palmer, Stephanie
  last_name: Palmer
- first_name: Philip
  full_name: Nelson, Philip
  last_name: Nelson
- first_name: Vijay
  full_name: Balasubramanian, Vijay
  last_name: Balasubramanian
citation:
  ama: 'Simmons K, Prentice J, Tkačik G, et al. Data from: Transformation of stimulus
    correlations by the retina. 2014. doi:<a href="https://doi.org/10.5061/dryad.246qg">10.5061/dryad.246qg</a>'
  apa: 'Simmons, K., Prentice, J., Tkačik, G., Homann, J., Yee, H., Palmer, S., …
    Balasubramanian, V. (2014). Data from: Transformation of stimulus correlations
    by the retina. Dryad. <a href="https://doi.org/10.5061/dryad.246qg">https://doi.org/10.5061/dryad.246qg</a>'
  chicago: 'Simmons, Kristina, Jason Prentice, Gašper Tkačik, Jan Homann, Heather
    Yee, Stephanie Palmer, Philip Nelson, and Vijay Balasubramanian. “Data from: Transformation
    of Stimulus Correlations by the Retina.” Dryad, 2014. <a href="https://doi.org/10.5061/dryad.246qg">https://doi.org/10.5061/dryad.246qg</a>.'
  ieee: 'K. Simmons <i>et al.</i>, “Data from: Transformation of stimulus correlations
    by the retina.” Dryad, 2014.'
  ista: 'Simmons K, Prentice J, Tkačik G, Homann J, Yee H, Palmer S, Nelson P, Balasubramanian
    V. 2014. Data from: Transformation of stimulus correlations by the retina, Dryad,
    <a href="https://doi.org/10.5061/dryad.246qg">10.5061/dryad.246qg</a>.'
  mla: 'Simmons, Kristina, et al. <i>Data from: Transformation of Stimulus Correlations
    by the Retina</i>. Dryad, 2014, doi:<a href="https://doi.org/10.5061/dryad.246qg">10.5061/dryad.246qg</a>.'
  short: K. Simmons, J. Prentice, G. Tkačik, J. Homann, H. Yee, S. Palmer, P. Nelson,
    V. Balasubramanian, (2014).
date_created: 2021-07-30T08:13:52Z
date_published: 2014-11-07T00:00:00Z
date_updated: 2025-09-29T14:27:23Z
day: '07'
department:
- _id: GaTk
doi: 10.5061/dryad.246qg
fulldoi: https://doi.org/10.5061/dryad.246qg
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.246qg
month: '11'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '2277'
    relation: used_in_publication
    status: public
status: public
title: 'Data from: Transformation of stimulus correlations by the retina'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2014'
...
---
_id: '6853'
abstract:
- lang: eng
  text: This monograph presents a short course in computational geometry and topology.
    In the first part the book covers Voronoi diagrams and Delaunay triangulations,
    then it presents the theory of alpha complexes which play a crucial role in biology.
    The central part of the book is the homology theory and their computation, including
    the theory of persistence which is indispensable for applications, e.g. shape
    reconstruction. The target audience comprises researchers and practitioners in
    mathematics, biology, neuroscience and computer science, but the book may also
    be beneficial to graduate students of these fields.
alternative_title:
- SpringerBriefs in Applied Sciences and Technology
article_processing_charge: No
author:
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
citation:
  ama: 'Edelsbrunner H. <i>A Short Course in Computational Geometry and Topology</i>.
    1st ed. Cham: Springer Nature; 2014. doi:<a href="https://doi.org/10.1007/978-3-319-05957-0">10.1007/978-3-319-05957-0</a>'
  apa: 'Edelsbrunner, H. (2014). <i>A Short Course in Computational Geometry and Topology</i>
    (1st ed.). Cham: Springer Nature. <a href="https://doi.org/10.1007/978-3-319-05957-0">https://doi.org/10.1007/978-3-319-05957-0</a>'
  chicago: 'Edelsbrunner, Herbert. <i>A Short Course in Computational Geometry and
    Topology</i>. 1st ed. SpringerBriefs in Applied Sciences and Technology. Cham:
    Springer Nature, 2014. <a href="https://doi.org/10.1007/978-3-319-05957-0">https://doi.org/10.1007/978-3-319-05957-0</a>.'
  ieee: 'H. Edelsbrunner, <i>A Short Course in Computational Geometry and Topology</i>,
    1st ed. Cham: Springer Nature, 2014.'
  ista: 'Edelsbrunner H. 2014. A Short Course in Computational Geometry and Topology
    1st ed., Cham: Springer Nature, IX, 110p.'
  mla: Edelsbrunner, Herbert. <i>A Short Course in Computational Geometry and Topology</i>.
    1st ed., Springer Nature, 2014, doi:<a href="https://doi.org/10.1007/978-3-319-05957-0">10.1007/978-3-319-05957-0</a>.
  short: H. Edelsbrunner, A Short Course in Computational Geometry and Topology, 1st
    ed., Springer Nature, Cham, 2014.
date_created: 2019-09-06T09:22:33Z
date_published: 2014-01-01T00:00:00Z
date_updated: 2022-03-04T07:47:54Z
day: '01'
department:
- _id: HeEd
doi: 10.1007/978-3-319-05957-0
edition: '1'
fulldoi: https://doi.org/10.1007/978-3-319-05957-0
language:
- iso: eng
month: '01'
oa_version: None
page: IX, 110
place: Cham
publication_identifier:
  eisbn:
  - 9-783-3190-5957-0
  eissn:
  - 2191-5318
  isbn:
  - 9-783-3190-5956-3
  issn:
  - 2191-530X
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  link:
  - description: available as eBook via catalog IST BookList
    relation: other
    url: https://koha.app.ist.ac.at/cgi-bin/koha/opac-detail.pl?biblionumber=356106
  - description: available via catalog IST BookList
    relation: other
    url: https://koha.app.ist.ac.at/cgi-bin/koha/opac-detail.pl?biblionumber=373842
scopus_import: '1'
series_title: SpringerBriefs in Applied Sciences and Technology
status: public
title: A Short Course in Computational Geometry and Topology
type: book
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2014'
...
---
_id: '7038'
article_processing_charge: No
author:
- first_name: Kristóf
  full_name: Huszár, Kristóf
  id: 33C26278-F248-11E8-B48F-1D18A9856A87
  last_name: Huszár
  orcid: 0000-0002-5445-5057
- first_name: Michal
  full_name: Rolinek, Michal
  id: 3CB3BC06-F248-11E8-B48F-1D18A9856A87
  last_name: Rolinek
citation:
  ama: Huszár K, Rolinek M. <i>Playful Math - An Introduction to Mathematical Games</i>.
    IST Austria
  apa: Huszár, K., &#38; Rolinek, M. (n.d.). <i>Playful Math - An introduction to
    mathematical games</i>. IST Austria.
  chicago: Huszár, Kristóf, and Michal Rolinek. <i>Playful Math - An Introduction
    to Mathematical Games</i>. IST Austria, n.d.
  ieee: K. Huszár and M. Rolinek, <i>Playful Math - An introduction to mathematical
    games</i>. IST Austria.
  ista: Huszár K, Rolinek M. Playful Math - An introduction to mathematical games,
    IST Austria, 5p.
  mla: Huszár, Kristóf, and Michal Rolinek. <i>Playful Math - An Introduction to Mathematical
    Games</i>. IST Austria.
  short: K. Huszár, M. Rolinek, Playful Math - An Introduction to Mathematical Games,
    IST Austria, n.d.
corr_author: '1'
date_created: 2019-11-18T15:57:05Z
date_published: 2014-06-30T00:00:00Z
date_updated: 2025-06-26T12:38:53Z
day: '30'
ddc:
- '510'
department:
- _id: VlKo
- _id: UlWa
file:
- access_level: open_access
  checksum: 2b94e5e1f4c3fe8ab89b12806276fb09
  content_type: application/pdf
  creator: dernst
  date_created: 2019-11-18T15:57:51Z
  date_updated: 2020-07-14T12:47:48Z
  file_id: '7039'
  file_name: 2014_Playful_Math_Huszar.pdf
  file_size: 511233
  relation: main_file
file_date_updated: 2020-07-14T12:47:48Z
has_accepted_license: '1'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
page: '5'
publication_status: draft
publisher: IST Austria
status: public
title: Playful Math - An introduction to mathematical games
type: working_paper
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2014'
...
---
_id: '9888'
abstract:
- lang: eng
  text: Detailed description of the experimental prodedures, data analyses and additional
    statistical analyses of the results.
article_processing_charge: No
author:
- first_name: Stephan
  full_name: Wolf, Stephan
  last_name: Wolf
- first_name: Dino
  full_name: Mcmahon, Dino
  last_name: Mcmahon
- first_name: Ka
  full_name: Lim, Ka
  last_name: Lim
- first_name: Christopher
  full_name: Pull, Christopher
  id: 3C7F4840-F248-11E8-B48F-1D18A9856A87
  last_name: Pull
  orcid: 0000-0003-1122-3982
- first_name: Suzanne
  full_name: Clark, Suzanne
  last_name: Clark
- first_name: Robert
  full_name: Paxton, Robert
  last_name: Paxton
- first_name: Juliet
  full_name: Osborne, Juliet
  last_name: Osborne
citation:
  ama: Wolf S, Mcmahon D, Lim K, et al. Supporting information. 2014. doi:<a href="https://doi.org/10.1371/journal.pone.0103989.s003">10.1371/journal.pone.0103989.s003</a>
  apa: Wolf, S., Mcmahon, D., Lim, K., Pull, C., Clark, S., Paxton, R., &#38; Osborne,
    J. (2014). Supporting information. Public Library of Science. <a href="https://doi.org/10.1371/journal.pone.0103989.s003">https://doi.org/10.1371/journal.pone.0103989.s003</a>
  chicago: Wolf, Stephan, Dino Mcmahon, Ka Lim, Christopher Pull, Suzanne Clark, Robert
    Paxton, and Juliet Osborne. “Supporting Information.” Public Library of Science,
    2014. <a href="https://doi.org/10.1371/journal.pone.0103989.s003">https://doi.org/10.1371/journal.pone.0103989.s003</a>.
  ieee: S. Wolf <i>et al.</i>, “Supporting information.” Public Library of Science,
    2014.
  ista: Wolf S, Mcmahon D, Lim K, Pull C, Clark S, Paxton R, Osborne J. 2014. Supporting
    information, Public Library of Science, <a href="https://doi.org/10.1371/journal.pone.0103989.s003">10.1371/journal.pone.0103989.s003</a>.
  mla: Wolf, Stephan, et al. <i>Supporting Information</i>. Public Library of Science,
    2014, doi:<a href="https://doi.org/10.1371/journal.pone.0103989.s003">10.1371/journal.pone.0103989.s003</a>.
  short: S. Wolf, D. Mcmahon, K. Lim, C. Pull, S. Clark, R. Paxton, J. Osborne, (2014).
date_created: 2021-08-11T14:17:53Z
date_updated: 2025-09-29T11:45:40Z
day: '06'
department:
- _id: SyCr
doi: 10.1371/journal.pone.0103989.s003
fulldoi: https://doi.org/10.1371/journal.pone.0103989.s003
month: '08'
oa_version: Published Version
publisher: Public Library of Science
related_material:
  record:
  - id: '2086'
    relation: used_in_publication
    status: public
status: public
title: Supporting information
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2014'
...
---
_id: '9931'
abstract:
- lang: eng
  text: Gene duplication is important in evolution, because it provides new raw material
    for evolutionary adaptations. Several existing hypotheses about the causes of
    duplicate retention and diversification differ in their emphasis on gene dosage,
    subfunctionalization, and neofunctionalization. Little experimental data exist
    on the relative importance of gene expression changes and changes in coding regions
    for the evolution of duplicate genes. Furthermore, we do not know how strongly
    the environment could affect this importance. To address these questions, we performed
    evolution experiments with the TEM-1 beta lactamase gene in Escherichia coli to
    study the initial stages of duplicate gene evolution in the laboratory. We mimicked
    tandem duplication by inserting two copies of the TEM-1 gene on the same plasmid.
    We then subjected these copies to repeated cycles of mutagenesis and selection
    in various environments that contained antibiotics in different combinations and
    concentrations. Our experiments showed that gene dosage is the most important
    factor in the initial stages of duplicate gene evolution, and overshadows the
    importance of point mutations in the coding region.
acknowledgement: We thank the Functional Genomics Center Zurich for its service in
  generating sequencing data, M. Ackermann and E. Hayden for helpful discussions,
  A. de Visser for comments on earlier versions of this manuscript, and M. Moser for
  help with quantitative PCR. This work was supported by Swiss National Science Foundation
  (grant 315230–129708), as well as through the YeastX project of SystemsX.ch, and
  the University Priority Research Program in Systems Biology at the University of
  Zurich. RD acknowledges support from the Forschungskredit program of the University
  of Zurich. The authors declare no conflict of interest.
article_processing_charge: No
article_type: original
author:
- first_name: Riddhiman
  full_name: Dhar, Riddhiman
  last_name: Dhar
- first_name: Tobias
  full_name: Bergmiller, Tobias
  id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
  last_name: Bergmiller
  orcid: 0000-0001-5396-4346
- first_name: Andreas
  full_name: Wagner, Andreas
  last_name: Wagner
citation:
  ama: Dhar R, Bergmiller T, Wagner A. Increased gene dosage plays a predominant role
    in the initial stages of evolution of duplicate TEM-1 beta lactamase genes. <i>Evolution</i>.
    2014;68(6):1775-1791. doi:<a href="https://doi.org/10.1111/evo.12373">10.1111/evo.12373</a>
  apa: Dhar, R., Bergmiller, T., &#38; Wagner, A. (2014). Increased gene dosage plays
    a predominant role in the initial stages of evolution of duplicate TEM-1 beta
    lactamase genes. <i>Evolution</i>. Wiley. <a href="https://doi.org/10.1111/evo.12373">https://doi.org/10.1111/evo.12373</a>
  chicago: Dhar, Riddhiman, Tobias Bergmiller, and Andreas Wagner. “Increased Gene
    Dosage Plays a Predominant Role in the Initial Stages of Evolution of Duplicate
    TEM-1 Beta Lactamase Genes.” <i>Evolution</i>. Wiley, 2014. <a href="https://doi.org/10.1111/evo.12373">https://doi.org/10.1111/evo.12373</a>.
  ieee: R. Dhar, T. Bergmiller, and A. Wagner, “Increased gene dosage plays a predominant
    role in the initial stages of evolution of duplicate TEM-1 beta lactamase genes,”
    <i>Evolution</i>, vol. 68, no. 6. Wiley, pp. 1775–1791, 2014.
  ista: Dhar R, Bergmiller T, Wagner A. 2014. Increased gene dosage plays a predominant
    role in the initial stages of evolution of duplicate TEM-1 beta lactamase genes.
    Evolution. 68(6), 1775–1791.
  mla: Dhar, Riddhiman, et al. “Increased Gene Dosage Plays a Predominant Role in
    the Initial Stages of Evolution of Duplicate TEM-1 Beta Lactamase Genes.” <i>Evolution</i>,
    vol. 68, no. 6, Wiley, 2014, pp. 1775–91, doi:<a href="https://doi.org/10.1111/evo.12373">10.1111/evo.12373</a>.
  short: R. Dhar, T. Bergmiller, A. Wagner, Evolution 68 (2014) 1775–1791.
date_created: 2021-08-17T09:03:09Z
date_published: 2014-06-03T00:00:00Z
date_updated: 2025-09-29T13:20:48Z
day: '03'
department:
- _id: CaGu
doi: 10.1111/evo.12373
external_id:
  isi:
  - '000337558900019'
  pmid:
  - '24495000'
fulldoi: https://doi.org/10.1111/evo.12373
intvolume: '        68'
isi: 1
issue: '6'
language:
- iso: eng
month: '06'
oa_version: None
page: 1775-1791
pmid: 1
publication: Evolution
publication_identifier:
  eissn:
  - 1558-5646
  issn:
  - 0014-3820
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
  record:
  - id: '9932'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Increased gene dosage plays a predominant role in the initial stages of evolution
  of duplicate TEM-1 beta lactamase genes
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 68
year: '2014'
...
---
_id: '9932'
abstract:
- lang: eng
  text: Gene duplication is important in evolution, because it provides new raw material
    for evolutionary adaptations. Several existing hypotheses about the causes of
    duplicate retention and diversification differ in their emphasis on gene dosage,
    sub-functionalization, and neo-functionalization. Little experimental data exists
    on the relative importance of gene expression changes and changes in coding regions
    for the evolution of duplicate genes. Furthermore, we do not know how strongly
    the environment could affect this importance. To address these questions, we performed
    evolution experiments with the TEM-1 beta lactamase gene in E. coli to study the
    initial stages of duplicate gene evolution in the laboratory. We mimicked tandem
    duplication by inserting two copies of the TEM-1 gene on the same plasmid. We
    then subjected these copies to repeated cycles of mutagenesis and selection in
    various environments that contained antibiotics in different combinations and
    concentrations. Our experiments showed that gene dosage is the most important
    factor in the initial stages of duplicate gene evolution, and overshadows the
    importance of point mutations in the coding region.
article_processing_charge: No
author:
- first_name: Riddhiman
  full_name: Dhar, Riddhiman
  last_name: Dhar
- first_name: Tobias
  full_name: Bergmiller, Tobias
  id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
  last_name: Bergmiller
  orcid: 0000-0001-5396-4346
- first_name: Andreas
  full_name: Wagner, Andreas
  last_name: Wagner
citation:
  ama: 'Dhar R, Bergmiller T, Wagner A. Data from: Increased gene dosage plays a predominant
    role in the initial stages of evolution of duplicate TEM-1 beta lactamase genes.
    2014. doi:<a href="https://doi.org/10.5061/dryad.jc402">10.5061/dryad.jc402</a>'
  apa: 'Dhar, R., Bergmiller, T., &#38; Wagner, A. (2014). Data from: Increased gene
    dosage plays a predominant role in the initial stages of evolution of duplicate
    TEM-1 beta lactamase genes. Dryad. <a href="https://doi.org/10.5061/dryad.jc402">https://doi.org/10.5061/dryad.jc402</a>'
  chicago: 'Dhar, Riddhiman, Tobias Bergmiller, and Andreas Wagner. “Data from: Increased
    Gene Dosage Plays a Predominant Role in the Initial Stages of Evolution of Duplicate
    TEM-1 Beta Lactamase Genes.” Dryad, 2014. <a href="https://doi.org/10.5061/dryad.jc402">https://doi.org/10.5061/dryad.jc402</a>.'
  ieee: 'R. Dhar, T. Bergmiller, and A. Wagner, “Data from: Increased gene dosage
    plays a predominant role in the initial stages of evolution of duplicate TEM-1
    beta lactamase genes.” Dryad, 2014.'
  ista: 'Dhar R, Bergmiller T, Wagner A. 2014. Data from: Increased gene dosage plays
    a predominant role in the initial stages of evolution of duplicate TEM-1 beta
    lactamase genes, Dryad, <a href="https://doi.org/10.5061/dryad.jc402">10.5061/dryad.jc402</a>.'
  mla: 'Dhar, Riddhiman, et al. <i>Data from: Increased Gene Dosage Plays a Predominant
    Role in the Initial Stages of Evolution of Duplicate TEM-1 Beta Lactamase Genes</i>.
    Dryad, 2014, doi:<a href="https://doi.org/10.5061/dryad.jc402">10.5061/dryad.jc402</a>.'
  short: R. Dhar, T. Bergmiller, A. Wagner, (2014).
date_created: 2021-08-17T09:11:40Z
date_published: 2014-01-27T00:00:00Z
date_updated: 2025-09-29T13:20:47Z
day: '27'
department:
- _id: CaGu
doi: 10.5061/dryad.jc402
fulldoi: https://doi.org/10.5061/dryad.jc402
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.jc402
month: '01'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '9931'
    relation: used_in_publication
    status: public
status: public
title: 'Data from: Increased gene dosage plays a predominant role in the initial stages
  of evolution of duplicate TEM-1 beta lactamase genes'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2014'
...
---
_id: '3263'
abstract:
- lang: eng
  text: Adaptation in the retina is thought to optimize the encoding of natural light
    signals into sequences of spikes sent to the brain. While adaptive changes in
    retinal processing to the variations of the mean luminance level and second-order
    stimulus statistics have been documented before, no such measurements have been
    performed when higher-order moments of the light distribution change. We therefore
    measured the ganglion cell responses in the tiger salamander retina to controlled
    changes in the second (contrast), third (skew) and fourth (kurtosis) moments of
    the light intensity distribution of spatially uniform temporally independent stimuli.
    The skew and kurtosis of the stimuli were chosen to cover the range observed in
    natural scenes. We quantified adaptation in ganglion cells by studying linear-nonlinear
    models that capture well the retinal encoding properties across all stimuli. We
    found that the encoding properties of retinal ganglion cells change only marginally
    when higher-order statistics change, compared to the changes observed in response
    to the variation in contrast. By analyzing optimal coding in LN-type models, we
    showed that neurons can maintain a high information rate without large dynamic
    adaptation to changes in skew or kurtosis. This is because, for uncorrelated stimuli,
    spatio-temporal summation within the receptive field averages away non-gaussian
    aspects of the light intensity distribution.
acknowledgement: "This work was supported by The Israel Science Foundation and The
  Human Frontiers Science Program.\r\nWe thank the referees for helping significantly
  improve this paper. We also thank Vijay Balasubramanian, Kristina Simmons, and Jason
  Prentice for stimulating discussions. GT wishes to thank the faculty and students
  of the “Methods in Computational Neuroscience” course at Marine Biological Laboratory,
  Woods Hole.\r\n"
article_number: e85841
article_processing_charge: No
author:
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
- first_name: Anandamohan
  full_name: Ghosh, Anandamohan
  last_name: Ghosh
- first_name: Elad
  full_name: Schneidman, Elad
  last_name: Schneidman
- first_name: Ronen
  full_name: Segev, Ronen
  last_name: Segev
citation:
  ama: Tkačik G, Ghosh A, Schneidman E, Segev R. Adaptation to changes in higher-order
    stimulus statistics in the salamander retina. <i>PLoS One</i>. 2014;9(1). doi:<a
    href="https://doi.org/10.1371/journal.pone.0085841">10.1371/journal.pone.0085841</a>
  apa: Tkačik, G., Ghosh, A., Schneidman, E., &#38; Segev, R. (2014). Adaptation to
    changes in higher-order stimulus statistics in the salamander retina. <i>PLoS
    One</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pone.0085841">https://doi.org/10.1371/journal.pone.0085841</a>
  chicago: Tkačik, Gašper, Anandamohan Ghosh, Elad Schneidman, and Ronen Segev. “Adaptation
    to Changes in Higher-Order Stimulus Statistics in the Salamander Retina.” <i>PLoS
    One</i>. Public Library of Science, 2014. <a href="https://doi.org/10.1371/journal.pone.0085841">https://doi.org/10.1371/journal.pone.0085841</a>.
  ieee: G. Tkačik, A. Ghosh, E. Schneidman, and R. Segev, “Adaptation to changes in
    higher-order stimulus statistics in the salamander retina,” <i>PLoS One</i>, vol.
    9, no. 1. Public Library of Science, 2014.
  ista: Tkačik G, Ghosh A, Schneidman E, Segev R. 2014. Adaptation to changes in higher-order
    stimulus statistics in the salamander retina. PLoS One. 9(1), e85841.
  mla: Tkačik, Gašper, et al. “Adaptation to Changes in Higher-Order Stimulus Statistics
    in the Salamander Retina.” <i>PLoS One</i>, vol. 9, no. 1, e85841, Public Library
    of Science, 2014, doi:<a href="https://doi.org/10.1371/journal.pone.0085841">10.1371/journal.pone.0085841</a>.
  short: G. Tkačik, A. Ghosh, E. Schneidman, R. Segev, PLoS One 9 (2014).
corr_author: '1'
date_created: 2018-12-11T12:02:20Z
date_published: 2014-01-21T00:00:00Z
date_updated: 2025-09-29T11:09:18Z
day: '21'
ddc:
- '570'
department:
- _id: GaTk
doi: 10.1371/journal.pone.0085841
external_id:
  isi:
  - '000330244500130'
file:
- access_level: open_access
  checksum: 1d5816b343abe5eadc3eb419bcece971
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:13:28Z
  date_updated: 2020-07-14T12:46:06Z
  file_id: '5011'
  file_name: IST-2016-432-v1+1_journal.pone.0085841.pdf
  file_size: 1568524
  relation: main_file
file_date_updated: 2020-07-14T12:46:06Z
fulldoi: https://doi.org/10.1371/journal.pone.0085841
has_accepted_license: '1'
intvolume: '         9'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
publication: PLoS One
publication_status: published
publisher: Public Library of Science
publist_id: '3385'
pubrep_id: '432'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Adaptation to changes in higher-order stimulus statistics in the salamander
  retina
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 9
year: '2014'
...
---
_id: '1733'
abstract:
- lang: eng
  text: The classical (boolean) notion of refinement for behavioral interfaces of
    system components is the alternating refinement preorder. In this paper, we define
    a distance for interfaces, called interface simulation distance. It makes the
    alternating refinement preorder quantitative by, intuitively, tolerating errors
    (while counting them) in the alternating simulation game. We show that the interface
    simulation distance satisfies the triangle inequality, that the distance between
    two interfaces does not increase under parallel composition with a third interface,
    that the distance between two interfaces can be bounded from above and below by
    distances between abstractions of the two interfaces, and how to synthesize an
    interface from incompatible requirements. We illustrate the framework, and the
    properties of the distances under composition of interfaces, with two case studies.
article_processing_charge: No
arxiv: 1
author:
- first_name: Pavol
  full_name: Cerny, Pavol
  last_name: Cerny
- first_name: Martin
  full_name: Chmelik, Martin
  id: 3624234E-F248-11E8-B48F-1D18A9856A87
  last_name: Chmelik
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Arjun
  full_name: Radhakrishna, Arjun
  id: 3B51CAC4-F248-11E8-B48F-1D18A9856A87
  last_name: Radhakrishna
citation:
  ama: Cerny P, Chmelik M, Henzinger TA, Radhakrishna A. Interface simulation distances.
    <i>Theoretical Computer Science</i>. 2014;560(3):348-363. doi:<a href="https://doi.org/10.1016/j.tcs.2014.08.019">10.1016/j.tcs.2014.08.019</a>
  apa: Cerny, P., Chmelik, M., Henzinger, T. A., &#38; Radhakrishna, A. (2014). Interface
    simulation distances. <i>Theoretical Computer Science</i>. Elsevier. <a href="https://doi.org/10.1016/j.tcs.2014.08.019">https://doi.org/10.1016/j.tcs.2014.08.019</a>
  chicago: Cerny, Pavol, Martin Chmelik, Thomas A Henzinger, and Arjun Radhakrishna.
    “Interface Simulation Distances.” <i>Theoretical Computer Science</i>. Elsevier,
    2014. <a href="https://doi.org/10.1016/j.tcs.2014.08.019">https://doi.org/10.1016/j.tcs.2014.08.019</a>.
  ieee: P. Cerny, M. Chmelik, T. A. Henzinger, and A. Radhakrishna, “Interface simulation
    distances,” <i>Theoretical Computer Science</i>, vol. 560, no. 3. Elsevier, pp.
    348–363, 2014.
  ista: Cerny P, Chmelik M, Henzinger TA, Radhakrishna A. 2014. Interface simulation
    distances. Theoretical Computer Science. 560(3), 348–363.
  mla: Cerny, Pavol, et al. “Interface Simulation Distances.” <i>Theoretical Computer
    Science</i>, vol. 560, no. 3, Elsevier, 2014, pp. 348–63, doi:<a href="https://doi.org/10.1016/j.tcs.2014.08.019">10.1016/j.tcs.2014.08.019</a>.
  short: P. Cerny, M. Chmelik, T.A. Henzinger, A. Radhakrishna, Theoretical Computer
    Science 560 (2014) 348–363.
corr_author: '1'
date_created: 2018-12-11T11:53:43Z
date_published: 2014-12-04T00:00:00Z
date_updated: 2025-09-29T13:14:25Z
day: '04'
department:
- _id: ToHe
- _id: KrCh
doi: 10.1016/j.tcs.2014.08.019
ec_funded: 1
external_id:
  arxiv:
  - '1210.2450'
  isi:
  - '000347601300009'
fulldoi: https://doi.org/10.1016/j.tcs.2014.08.019
intvolume: '       560'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1210.2450
month: '12'
oa: 1
oa_version: Submitted Version
page: 348 - 363
project:
- _id: 25EE3708-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '267989'
  name: Quantitative Reactive Modeling
- _id: 25F5A88A-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11402-N23
  name: Moderne Concurrency Paradigms
- _id: 25863FF4-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11407
  name: Game Theory
- _id: 2584A770-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P 23499-N23
  name: Modern Graph Algorithmic Techniques in Formal Verification
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 2587B514-B435-11E9-9278-68D0E5697425
  name: Microsoft Research Faculty Fellowship
publication: Theoretical Computer Science
publication_status: published
publisher: Elsevier
publist_id: '5392'
quality_controlled: '1'
related_material:
  record:
  - id: '2916'
    relation: earlier_version
    status: public
scopus_import: '1'
status: public
title: Interface simulation distances
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 560
year: '2014'
...
---
_id: '1806'
abstract:
- lang: eng
  text: The generation of asymmetry, at both cellular and tissue level, is one of
    the most essential capabilities of all eukaryotic organisms. It mediates basically
    all multicellular development ranging from embryogenesis and de novo organ formation
    till responses to various environmental stimuli. In plants, the awe-inspiring
    number of such processes is regulated by phytohormone auxin and its directional,
    cell-to-cell transport. The mediators of this transport, PIN auxin transporters,
    are asymmetrically localized at the plasma membrane, and this polar localization
    determines the directionality of intercellular auxin flow. Thus, auxin transport
    contributes crucially to the generation of local auxin gradients or maxima, which
    instruct given cell to change its developmental program. Here, we introduce and
    discuss the molecular components and cellular mechanisms regulating the generation
    and maintenance of cellular PIN polarity, as the general hallmarks of cell polarity
    in plants.
author:
- first_name: Pawel
  full_name: Baster, Pawel
  id: 3028BD74-F248-11E8-B48F-1D18A9856A87
  last_name: Baster
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: 'Baster P, Friml J. Auxin on the road navigated by cellular PIN polarity. In:
    Zažímalová E, Petrášek J, Benková E, eds. <i>Auxin and Its Role in Plant Development</i>.
    Springer; 2014:143-170. doi:<a href="https://doi.org/10.1007/978-3-7091-1526-8_8">10.1007/978-3-7091-1526-8_8</a>'
  apa: Baster, P., &#38; Friml, J. (2014). Auxin on the road navigated by cellular
    PIN polarity. In E. Zažímalová, J. Petrášek, &#38; E. Benková (Eds.), <i>Auxin
    and Its Role in Plant Development</i> (pp. 143–170). Springer. <a href="https://doi.org/10.1007/978-3-7091-1526-8_8">https://doi.org/10.1007/978-3-7091-1526-8_8</a>
  chicago: Baster, Pawel, and Jiří Friml. “Auxin on the Road Navigated by Cellular
    PIN Polarity.” In <i>Auxin and Its Role in Plant Development</i>, edited by Eva
    Zažímalová, Jan Petrášek, and Eva Benková, 143–70. Springer, 2014. <a href="https://doi.org/10.1007/978-3-7091-1526-8_8">https://doi.org/10.1007/978-3-7091-1526-8_8</a>.
  ieee: P. Baster and J. Friml, “Auxin on the road navigated by cellular PIN polarity,”
    in <i>Auxin and Its Role in Plant Development</i>, E. Zažímalová, J. Petrášek,
    and E. Benková, Eds. Springer, 2014, pp. 143–170.
  ista: 'Baster P, Friml J. 2014.Auxin on the road navigated by cellular PIN polarity.
    In: Auxin and Its Role in Plant Development. , 143–170.'
  mla: Baster, Pawel, and Jiří Friml. “Auxin on the Road Navigated by Cellular PIN
    Polarity.” <i>Auxin and Its Role in Plant Development</i>, edited by Eva Zažímalová
    et al., Springer, 2014, pp. 143–70, doi:<a href="https://doi.org/10.1007/978-3-7091-1526-8_8">10.1007/978-3-7091-1526-8_8</a>.
  short: P. Baster, J. Friml, in:, E. Zažímalová, J. Petrášek, E. Benková (Eds.),
    Auxin and Its Role in Plant Development, Springer, 2014, pp. 143–170.
corr_author: '1'
date_created: 2018-12-11T11:54:07Z
date_published: 2014-04-01T00:00:00Z
date_updated: 2024-10-09T20:55:54Z
day: '01'
department:
- _id: JiFr
doi: 10.1007/978-3-7091-1526-8_8
editor:
- first_name: Eva
  full_name: Zažímalová, Eva
  last_name: Zažímalová
- first_name: Jan
  full_name: Petrášek, Jan
  last_name: Petrášek
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
fulldoi: https://doi.org/10.1007/978-3-7091-1526-8_8
language:
- iso: eng
month: '04'
oa_version: None
page: 143 - 170
publication: Auxin and Its Role in Plant Development
publication_status: published
publisher: Springer
publist_id: '5304'
quality_controlled: '1'
scopus_import: 1
status: public
title: Auxin on the road navigated by cellular PIN polarity
type: book_chapter
user_id: 4435EBFC-F248-11E8-B48F-1D18A9856A87
year: '2014'
...
---
_id: '1816'
abstract:
- lang: eng
  text: Watermarking techniques for vector graphics dislocate vertices in order to
    embed imperceptible, yet detectable, statistical features into the input data.
    The embedding process may result in a change of the topology of the input data,
    e.g., by introducing self-intersections, which is undesirable or even disastrous
    for many applications. In this paper we present a watermarking framework for two-dimensional
    vector graphics that employs conventional watermarking techniques but still provides
    the guarantee that the topology of the input data is preserved. The geometric
    part of this framework computes so-called maximum perturbation regions (MPR) of
    vertices. We propose two efficient algorithms to compute MPRs based on Voronoi
    diagrams and constrained triangulations. Furthermore, we present two algorithms
    to conditionally correct the watermarked data in order to increase the watermark
    embedding capacity and still guarantee topological correctness. While we focus
    on the watermarking of input formed by straight-line segments, one of our approaches
    can also be extended to circular arcs. We conclude the paper by demonstrating
    and analyzing the applicability of our framework in conjunction with two well-known
    watermarking techniques.
acknowledgement: 'Work by Martin Held and Stefan Huber was supported by Austrian Science
  Fund (FWF): L367-N15 and P25816-N15.'
author:
- first_name: Stefan
  full_name: Huber, Stefan
  id: 4700A070-F248-11E8-B48F-1D18A9856A87
  last_name: Huber
  orcid: 0000-0002-8871-5814
- first_name: Martin
  full_name: Held, Martin
  last_name: Held
- first_name: Peter
  full_name: Meerwald, Peter
  last_name: Meerwald
- first_name: Roland
  full_name: Kwitt, Roland
  last_name: Kwitt
citation:
  ama: Huber S, Held M, Meerwald P, Kwitt R. Topology-preserving watermarking of vector
    graphics. <i>International Journal of Computational Geometry and Applications</i>.
    2014;24(1):61-86. doi:<a href="https://doi.org/10.1142/S0218195914500034">10.1142/S0218195914500034</a>
  apa: Huber, S., Held, M., Meerwald, P., &#38; Kwitt, R. (2014). Topology-preserving
    watermarking of vector graphics. <i>International Journal of Computational Geometry
    and Applications</i>. World Scientific Publishing. <a href="https://doi.org/10.1142/S0218195914500034">https://doi.org/10.1142/S0218195914500034</a>
  chicago: Huber, Stefan, Martin Held, Peter Meerwald, and Roland Kwitt. “Topology-Preserving
    Watermarking of Vector Graphics.” <i>International Journal of Computational Geometry
    and Applications</i>. World Scientific Publishing, 2014. <a href="https://doi.org/10.1142/S0218195914500034">https://doi.org/10.1142/S0218195914500034</a>.
  ieee: S. Huber, M. Held, P. Meerwald, and R. Kwitt, “Topology-preserving watermarking
    of vector graphics,” <i>International Journal of Computational Geometry and Applications</i>,
    vol. 24, no. 1. World Scientific Publishing, pp. 61–86, 2014.
  ista: Huber S, Held M, Meerwald P, Kwitt R. 2014. Topology-preserving watermarking
    of vector graphics. International Journal of Computational Geometry and Applications.
    24(1), 61–86.
  mla: Huber, Stefan, et al. “Topology-Preserving Watermarking of Vector Graphics.”
    <i>International Journal of Computational Geometry and Applications</i>, vol.
    24, no. 1, World Scientific Publishing, 2014, pp. 61–86, doi:<a href="https://doi.org/10.1142/S0218195914500034">10.1142/S0218195914500034</a>.
  short: S. Huber, M. Held, P. Meerwald, R. Kwitt, International Journal of Computational
    Geometry and Applications 24 (2014) 61–86.
corr_author: '1'
date_created: 2018-12-11T11:54:10Z
date_published: 2014-03-16T00:00:00Z
date_updated: 2024-10-09T20:55:54Z
day: '16'
ddc:
- '000'
department:
- _id: HeEd
doi: 10.1142/S0218195914500034
file:
- access_level: open_access
  checksum: be45c133ab4d43351260e21beaa8f4b1
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:08:43Z
  date_updated: 2020-07-14T12:45:17Z
  file_id: '4704'
  file_name: IST-2016-443-v1+1_S0218195914500034.pdf
  file_size: 991734
  relation: main_file
file_date_updated: 2020-07-14T12:45:17Z
fulldoi: https://doi.org/10.1142/S0218195914500034
has_accepted_license: '1'
intvolume: '        24'
issue: '1'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 61 - 86
publication: International Journal of Computational Geometry and Applications
publication_status: published
publisher: World Scientific Publishing
publist_id: '5290'
pubrep_id: '443'
quality_controlled: '1'
scopus_import: 1
status: public
title: Topology-preserving watermarking of vector graphics
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2014'
...
---
_id: '1829'
abstract:
- lang: eng
  text: Hitting and batting tasks, such as tennis forehands, ping-pong strokes, or
    baseball batting, depend on predictions where the ball can be intercepted and
    how it can properly be returned to the opponent. These predictions get more accurate
    over time, hence the behaviors need to be continuously modified. As a result,
    movement templates with a learned global shape need to be adapted during the execution
    so that the racket reaches a target position and velocity that will return the
    ball over to the other side of the net or court. It requires altering learned
    movements to hit a varying target with the necessary velocity at a specific instant
    in time. Such a task cannot be incorporated straightforwardly in most movement
    representations suitable for learning. For example, the standard formulation of
    the dynamical system based motor primitives (introduced by Ijspeert et al (2002b))
    does not satisfy this property despite their flexibility which has allowed learning
    tasks ranging from locomotion to kendama. In order to fulfill this requirement,
    we reformulate the Ijspeert framework to incorporate the possibility of specifying
    a desired hitting point and a desired hitting velocity while maintaining all advantages
    of the original formulation.We show that the proposed movement template formulation
    works well in two scenarios, i.e., for hitting a ball on a string with a table
    tennis racket at a specified velocity and for returning balls launched by a ball
    gun successfully over the net using forehand movements.
alternative_title:
- Springer Tracts in Advanced Robotics
author:
- first_name: Katharina
  full_name: Muelling, Katharina
  last_name: Muelling
- first_name: Oliver
  full_name: Kroemer, Oliver
  last_name: Kroemer
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
- first_name: Bernhard
  full_name: Schölkopf, Bernhard
  last_name: Schölkopf
citation:
  ama: 'Muelling K, Kroemer O, Lampert C, Schölkopf B. Movement templates for learning
    of hitting and batting. In: Kober J, Peters J, eds. <i>Learning Motor Skills</i>.
    Vol 97. From Algorithms to Robot Experiments. Springer; 2014:69-82. doi:<a href="https://doi.org/10.1007/978-3-319-03194-1_3">10.1007/978-3-319-03194-1_3</a>'
  apa: Muelling, K., Kroemer, O., Lampert, C., &#38; Schölkopf, B. (2014). Movement
    templates for learning of hitting and batting. In J. Kober &#38; J. Peters (Eds.),
    <i>Learning Motor Skills</i> (Vol. 97, pp. 69–82). Springer. <a href="https://doi.org/10.1007/978-3-319-03194-1_3">https://doi.org/10.1007/978-3-319-03194-1_3</a>
  chicago: Muelling, Katharina, Oliver Kroemer, Christoph Lampert, and Bernhard Schölkopf.
    “Movement Templates for Learning of Hitting and Batting.” In <i>Learning Motor
    Skills</i>, edited by Jens Kober and Jan Peters, 97:69–82. From Algorithms to
    Robot Experiments. Springer, 2014. <a href="https://doi.org/10.1007/978-3-319-03194-1_3">https://doi.org/10.1007/978-3-319-03194-1_3</a>.
  ieee: K. Muelling, O. Kroemer, C. Lampert, and B. Schölkopf, “Movement templates
    for learning of hitting and batting,” in <i>Learning Motor Skills</i>, vol. 97,
    J. Kober and J. Peters, Eds. Springer, 2014, pp. 69–82.
  ista: 'Muelling K, Kroemer O, Lampert C, Schölkopf B. 2014.Movement templates for
    learning of hitting and batting. In: Learning Motor Skills. Springer Tracts in
    Advanced Robotics, vol. 97, 69–82.'
  mla: Muelling, Katharina, et al. “Movement Templates for Learning of Hitting and
    Batting.” <i>Learning Motor Skills</i>, edited by Jens Kober and Jan Peters, vol.
    97, Springer, 2014, pp. 69–82, doi:<a href="https://doi.org/10.1007/978-3-319-03194-1_3">10.1007/978-3-319-03194-1_3</a>.
  short: K. Muelling, O. Kroemer, C. Lampert, B. Schölkopf, in:, J. Kober, J. Peters
    (Eds.), Learning Motor Skills, Springer, 2014, pp. 69–82.
date_created: 2018-12-11T11:54:14Z
date_published: 2014-01-01T00:00:00Z
date_updated: 2021-01-12T06:53:28Z
day: '01'
department:
- _id: ChLa
doi: 10.1007/978-3-319-03194-1_3
editor:
- first_name: Jens
  full_name: Kober, Jens
  last_name: Kober
- first_name: Jan
  full_name: Peters, Jan
  last_name: Peters
fulldoi: https://doi.org/10.1007/978-3-319-03194-1_3
intvolume: '        97'
language:
- iso: eng
month: '01'
oa_version: None
page: 69 - 82
publication: Learning Motor Skills
publication_status: published
publisher: Springer
publist_id: '5274'
quality_controlled: '1'
scopus_import: 1
series_title: From Algorithms to Robot Experiments
status: public
title: Movement templates for learning of hitting and batting
type: book_chapter
user_id: 4435EBFC-F248-11E8-B48F-1D18A9856A87
volume: 97
year: '2014'
...
---
_id: '1842'
abstract:
- lang: eng
  text: We prove polynomial upper bounds of geometric Ramsey numbers of pathwidth-2
    outerplanar triangulations in both convex and general cases. We also prove that
    the geometric Ramsey numbers of the ladder graph on 2n vertices are bounded by
    O(n3) and O(n10), in the convex and general case, respectively. We then apply
    similar methods to prove an (Formula presented.) upper bound on the Ramsey number
    of a path with n ordered vertices.
acknowledgement: Marek Krčál was supported by the ERC Advanced Grant No. 267165.
article_processing_charge: No
arxiv: 1
author:
- first_name: Josef
  full_name: Cibulka, Josef
  last_name: Cibulka
- first_name: Pu
  full_name: Gao, Pu
  last_name: Gao
- first_name: Marek
  full_name: Krcál, Marek
  id: 33E21118-F248-11E8-B48F-1D18A9856A87
  last_name: Krcál
- first_name: Tomáš
  full_name: Valla, Tomáš
  last_name: Valla
- first_name: Pavel
  full_name: Valtr, Pavel
  last_name: Valtr
citation:
  ama: Cibulka J, Gao P, Krcál M, Valla T, Valtr P. On the geometric ramsey number
    of outerplanar graphs. <i>Discrete &#38; Computational Geometry</i>. 2014;53(1):64-79.
    doi:<a href="https://doi.org/10.1007/s00454-014-9646-x">10.1007/s00454-014-9646-x</a>
  apa: Cibulka, J., Gao, P., Krcál, M., Valla, T., &#38; Valtr, P. (2014). On the
    geometric ramsey number of outerplanar graphs. <i>Discrete &#38; Computational
    Geometry</i>. Springer. <a href="https://doi.org/10.1007/s00454-014-9646-x">https://doi.org/10.1007/s00454-014-9646-x</a>
  chicago: Cibulka, Josef, Pu Gao, Marek Krcál, Tomáš Valla, and Pavel Valtr. “On
    the Geometric Ramsey Number of Outerplanar Graphs.” <i>Discrete &#38; Computational
    Geometry</i>. Springer, 2014. <a href="https://doi.org/10.1007/s00454-014-9646-x">https://doi.org/10.1007/s00454-014-9646-x</a>.
  ieee: J. Cibulka, P. Gao, M. Krcál, T. Valla, and P. Valtr, “On the geometric ramsey
    number of outerplanar graphs,” <i>Discrete &#38; Computational Geometry</i>, vol.
    53, no. 1. Springer, pp. 64–79, 2014.
  ista: Cibulka J, Gao P, Krcál M, Valla T, Valtr P. 2014. On the geometric ramsey
    number of outerplanar graphs. Discrete &#38; Computational Geometry. 53(1), 64–79.
  mla: Cibulka, Josef, et al. “On the Geometric Ramsey Number of Outerplanar Graphs.”
    <i>Discrete &#38; Computational Geometry</i>, vol. 53, no. 1, Springer, 2014,
    pp. 64–79, doi:<a href="https://doi.org/10.1007/s00454-014-9646-x">10.1007/s00454-014-9646-x</a>.
  short: J. Cibulka, P. Gao, M. Krcál, T. Valla, P. Valtr, Discrete &#38; Computational
    Geometry 53 (2014) 64–79.
date_created: 2018-12-11T11:54:18Z
date_published: 2014-11-14T00:00:00Z
date_updated: 2025-09-29T13:11:56Z
day: '14'
department:
- _id: UlWa
- _id: HeEd
doi: 10.1007/s00454-014-9646-x
external_id:
  arxiv:
  - '1310.7004'
  isi:
  - '000346774600005'
fulldoi: https://doi.org/10.1007/s00454-014-9646-x
intvolume: '        53'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1310.7004
month: '11'
oa: 1
oa_version: Submitted Version
page: 64 - 79
publication: Discrete & Computational Geometry
publication_status: published
publisher: Springer
publist_id: '5260'
scopus_import: '1'
status: public
title: On the geometric ramsey number of outerplanar graphs
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 53
year: '2014'
...
---
_id: '1844'
abstract:
- lang: eng
  text: 'Local protein interactions (&quot;molecular context&quot; effects) dictate
    amino acid replacements and can be described in terms of site-specific, energetic
    preferences for any different amino acid. It has been recently debated whether
    these preferences remain approximately constant during evolution or whether, due
    to coevolution of sites, they change strongly. Such research highlights an unresolved
    and fundamental issue with far-reaching implications for phylogenetic analysis
    and molecular evolution modeling. Here, we take advantage of the recent availability
    of phenotypically supported laboratory resurrections of Precambrian thioredoxins
    and β-lactamases to experimentally address the change of site-specific amino acid
    preferences over long geological timescales. Extensive mutational analyses support
    the notion that evolutionary adjustment to a new amino acid may occur, but to
    a large extent this is insufficient to erase the primitive preference for amino
    acid replacements. Generally, site-specific amino acid preferences appear to remain
    conserved throughout evolutionary history despite local sequence divergence. We
    show such preference conservation to be readily understandable in molecular terms
    and we provide crystallographic evidence for an intriguing structural-switch mechanism:
    Energetic preference for an ancestral amino acid in a modern protein can be linked
    to reorganization upon mutation to the ancestral local structure around the mutated
    site. Finally, we point out that site-specific preference conservation naturally
    leads to one plausible evolutionary explanation for the existence of intragenic
    global suppressor mutations.'
article_processing_charge: No
author:
- first_name: Valeria
  full_name: Risso, Valeria
  last_name: Risso
- first_name: Fadia
  full_name: Manssour Triedo, Fadia
  last_name: Manssour Triedo
- first_name: Asuncion
  full_name: Delgado Delgado, Asuncion
  last_name: Delgado Delgado
- first_name: Rocio
  full_name: Arco, Rocio
  last_name: Arco
- first_name: Alicia
  full_name: Barroso Deljesús, Alicia
  last_name: Barroso Deljesús
- first_name: Álvaro
  full_name: Inglés Prieto, Álvaro
  id: 2A9DB292-F248-11E8-B48F-1D18A9856A87
  last_name: Inglés Prieto
  orcid: 0000-0002-5409-8571
- first_name: Raquel
  full_name: Godoy Ruiz, Raquel
  last_name: Godoy Ruiz
- first_name: Josè
  full_name: Gavira, Josè
  last_name: Gavira
- first_name: Eric
  full_name: Gaucher, Eric
  last_name: Gaucher
- first_name: Beatriz
  full_name: Ibarra Molero, Beatriz
  last_name: Ibarra Molero
- first_name: Jose
  full_name: Sánchez Ruiz, Jose
  last_name: Sánchez Ruiz
citation:
  ama: Risso V, Manssour Triedo F, Delgado Delgado A, et al. Mutational studies on
    resurrected ancestral proteins reveal conservation of site-specific amino acid
    preferences throughout evolutionary history. <i>Molecular Biology and Evolution</i>.
    2014;32(2):440-455. doi:<a href="https://doi.org/10.1093/molbev/msu312">10.1093/molbev/msu312</a>
  apa: Risso, V., Manssour Triedo, F., Delgado Delgado, A., Arco, R., Barroso Deljesús,
    A., Inglés Prieto, Á., … Sánchez Ruiz, J. (2014). Mutational studies on resurrected
    ancestral proteins reveal conservation of site-specific amino acid preferences
    throughout evolutionary history. <i>Molecular Biology and Evolution</i>. Oxford
    University Press. <a href="https://doi.org/10.1093/molbev/msu312">https://doi.org/10.1093/molbev/msu312</a>
  chicago: Risso, Valeria, Fadia Manssour Triedo, Asuncion Delgado Delgado, Rocio
    Arco, Alicia Barroso Deljesús, Álvaro Inglés Prieto, Raquel Godoy Ruiz, et al.
    “Mutational Studies on Resurrected Ancestral Proteins Reveal Conservation of Site-Specific
    Amino Acid Preferences throughout Evolutionary History.” <i>Molecular Biology
    and Evolution</i>. Oxford University Press, 2014. <a href="https://doi.org/10.1093/molbev/msu312">https://doi.org/10.1093/molbev/msu312</a>.
  ieee: V. Risso <i>et al.</i>, “Mutational studies on resurrected ancestral proteins
    reveal conservation of site-specific amino acid preferences throughout evolutionary
    history,” <i>Molecular Biology and Evolution</i>, vol. 32, no. 2. Oxford University
    Press, pp. 440–455, 2014.
  ista: Risso V, Manssour Triedo F, Delgado Delgado A, Arco R, Barroso Deljesús A,
    Inglés Prieto Á, Godoy Ruiz R, Gavira J, Gaucher E, Ibarra Molero B, Sánchez Ruiz
    J. 2014. Mutational studies on resurrected ancestral proteins reveal conservation
    of site-specific amino acid preferences throughout evolutionary history. Molecular
    Biology and Evolution. 32(2), 440–455.
  mla: Risso, Valeria, et al. “Mutational Studies on Resurrected Ancestral Proteins
    Reveal Conservation of Site-Specific Amino Acid Preferences throughout Evolutionary
    History.” <i>Molecular Biology and Evolution</i>, vol. 32, no. 2, Oxford University
    Press, 2014, pp. 440–55, doi:<a href="https://doi.org/10.1093/molbev/msu312">10.1093/molbev/msu312</a>.
  short: V. Risso, F. Manssour Triedo, A. Delgado Delgado, R. Arco, A. Barroso Deljesús,
    Á. Inglés Prieto, R. Godoy Ruiz, J. Gavira, E. Gaucher, B. Ibarra Molero, J. Sánchez
    Ruiz, Molecular Biology and Evolution 32 (2014) 440–455.
date_created: 2018-12-11T11:54:19Z
date_published: 2014-11-12T00:00:00Z
date_updated: 2025-09-29T13:11:19Z
day: '12'
ddc:
- '571'
department:
- _id: HaJa
doi: 10.1093/molbev/msu312
external_id:
  isi:
  - '000350050700012'
file:
- access_level: open_access
  checksum: 06215318e66be8f3e0c33abb07e9d3da
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:16:56Z
  date_updated: 2020-07-14T12:45:19Z
  file_id: '5247'
  file_name: IST-2016-430-v1+1_Mol_Biol_Evol-2015-Risso-440-55.pdf
  file_size: 1545246
  relation: main_file
file_date_updated: 2020-07-14T12:45:19Z
fulldoi: https://doi.org/10.1093/molbev/msu312
has_accepted_license: '1'
intvolume: '        32'
isi: 1
issue: '2'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: 440 - 455
publication: Molecular Biology and Evolution
publication_status: published
publisher: Oxford University Press
publist_id: '5257'
pubrep_id: '430'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mutational studies on resurrected ancestral proteins reveal conservation of
  site-specific amino acid preferences throughout evolutionary history
tmp:
  image: /images/cc_by_nc.png
  legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
  short: CC BY-NC (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 32
year: '2014'
...
