---
_id: '10815'
abstract:
- lang: eng
  text: In the last several decades, developmental biology has clarified the molecular
    mechanisms of embryogenesis and organogenesis. In particular, it has demonstrated
    that the “tool-kit genes” essential for regulating developmental processes are
    not only highly conserved among species, but are also used as systems at various
    times and places in an organism to control distinct developmental events. Therefore,
    mutations in many of these tool-kit genes may cause congenital diseases involving
    morphological abnormalities. This link between genes and abnormal morphological
    phenotypes underscores the importance of understanding how cells behave and contribute
    to morphogenesis as a result of gene function. Recent improvements in live imaging
    and in quantitative analyses of cellular dynamics will advance our understanding
    of the cellular pathogenesis of congenital diseases associated with aberrant morphologies.
    In these studies, it is critical to select an appropriate model organism for the
    particular phenomenon of interest.
acknowledgement: The authors thank all the members of the Division of Morphogenesis,
  National Institute for Basic Biology, for their contributions to the research, their
  encouragement, and helpful discussions, particularly Dr M. Suzuki for his critical
  reading of the manuscript. We also thank the Model Animal Research and Spectrography
  and Bioimaging Facilities, NIBB Core Research Facilities, for technical support.
  M.H. was supported by a research fellowship from the Japan Society for the Promotion
  of Science (JSPS). Our work introduced in this review was supported by a Grant-in-Aid
  for Scientific Research on Innovative Areas from the Ministry of Education, Culture,
  Sports, Science, and Technology (MEXT), Japan, to N.U.
article_processing_charge: No
article_type: original
author:
- first_name: Masakazu
  full_name: Hashimoto, Masakazu
  last_name: Hashimoto
- first_name: Hitoshi
  full_name: Morita, Hitoshi
  id: 4C6E54C6-F248-11E8-B48F-1D18A9856A87
  last_name: Morita
- first_name: Naoto
  full_name: Ueno, Naoto
  last_name: Ueno
citation:
  ama: Hashimoto M, Morita H, Ueno N. Molecular and cellular mechanisms of development
    underlying congenital diseases. <i>Congenital Anomalies</i>. 2014;54(1):1-7. doi:<a
    href="https://doi.org/10.1111/cga.12039">10.1111/cga.12039</a>
  apa: Hashimoto, M., Morita, H., &#38; Ueno, N. (2014). Molecular and cellular mechanisms
    of development underlying congenital diseases. <i>Congenital Anomalies</i>. Wiley.
    <a href="https://doi.org/10.1111/cga.12039">https://doi.org/10.1111/cga.12039</a>
  chicago: Hashimoto, Masakazu, Hitoshi Morita, and Naoto Ueno. “Molecular and Cellular
    Mechanisms of Development Underlying Congenital Diseases.” <i>Congenital Anomalies</i>.
    Wiley, 2014. <a href="https://doi.org/10.1111/cga.12039">https://doi.org/10.1111/cga.12039</a>.
  ieee: M. Hashimoto, H. Morita, and N. Ueno, “Molecular and cellular mechanisms of
    development underlying congenital diseases,” <i>Congenital Anomalies</i>, vol.
    54, no. 1. Wiley, pp. 1–7, 2014.
  ista: Hashimoto M, Morita H, Ueno N. 2014. Molecular and cellular mechanisms of
    development underlying congenital diseases. Congenital Anomalies. 54(1), 1–7.
  mla: Hashimoto, Masakazu, et al. “Molecular and Cellular Mechanisms of Development
    Underlying Congenital Diseases.” <i>Congenital Anomalies</i>, vol. 54, no. 1,
    Wiley, 2014, pp. 1–7, doi:<a href="https://doi.org/10.1111/cga.12039">10.1111/cga.12039</a>.
  short: M. Hashimoto, H. Morita, N. Ueno, Congenital Anomalies 54 (2014) 1–7.
date_created: 2022-03-04T08:17:25Z
date_published: 2014-02-01T00:00:00Z
date_updated: 2022-03-04T08:26:05Z
day: '01'
department:
- _id: CaHe
doi: 10.1111/cga.12039
external_id:
  pmid:
  - '24666178'
intvolume: '        54'
issue: '1'
keyword:
- Developmental Biology
- Embryology
- General Medicine
- Pediatrics
- Perinatology
- and Child Health
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1111/cga.12039
month: '02'
oa: 1
oa_version: None
page: 1-7
pmid: 1
publication: Congenital Anomalies
publication_identifier:
  issn:
  - 0914-3505
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Molecular and cellular mechanisms of development underlying congenital diseases
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 54
year: '2014'
...
---
_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'
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'
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 '
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: '9594'
abstract:
- lang: eng
  text: Let d≥3 be a fixed integer. We give an asympotic formula for the expected
    number of spanning trees in a uniformly random d-regular graph with n vertices.
    (The asymptotics are as n→∞, restricted to even n if d is odd.) We also obtain
    the asymptotic distribution of the number of spanning trees in a uniformly random
    cubic graph, and conjecture that the corresponding result holds for arbitrary
    (fixed) d. Numerical evidence is presented which supports our conjecture.
article_number: P1.45
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Catherine
  full_name: Greenhill, Catherine
  last_name: Greenhill
- first_name: Matthew Alan
  full_name: Kwan, Matthew Alan
  id: 5fca0887-a1db-11eb-95d1-ca9d5e0453b3
  last_name: Kwan
  orcid: 0000-0002-4003-7567
- first_name: David
  full_name: Wind, David
  last_name: Wind
citation:
  ama: Greenhill C, Kwan MA, Wind D. On the number of spanning trees in random regular
    graphs. <i>The Electronic Journal of Combinatorics</i>. 2014;21(1). doi:<a href="https://doi.org/10.37236/3752">10.37236/3752</a>
  apa: Greenhill, C., Kwan, M. A., &#38; Wind, D. (2014). On the number of spanning
    trees in random regular graphs. <i>The Electronic Journal of Combinatorics</i>.
    The Electronic Journal of Combinatorics. <a href="https://doi.org/10.37236/3752">https://doi.org/10.37236/3752</a>
  chicago: Greenhill, Catherine, Matthew Alan Kwan, and David Wind. “On the Number
    of Spanning Trees in Random Regular Graphs.” <i>The Electronic Journal of Combinatorics</i>.
    The Electronic Journal of Combinatorics, 2014. <a href="https://doi.org/10.37236/3752">https://doi.org/10.37236/3752</a>.
  ieee: C. Greenhill, M. A. Kwan, and D. Wind, “On the number of spanning trees in
    random regular graphs,” <i>The Electronic Journal of Combinatorics</i>, vol. 21,
    no. 1. The Electronic Journal of Combinatorics, 2014.
  ista: Greenhill C, Kwan MA, Wind D. 2014. On the number of spanning trees in random
    regular graphs. The Electronic Journal of Combinatorics. 21(1), P1.45.
  mla: Greenhill, Catherine, et al. “On the Number of Spanning Trees in Random Regular
    Graphs.” <i>The Electronic Journal of Combinatorics</i>, vol. 21, no. 1, P1.45,
    The Electronic Journal of Combinatorics, 2014, doi:<a href="https://doi.org/10.37236/3752">10.37236/3752</a>.
  short: C. Greenhill, M.A. Kwan, D. Wind, The Electronic Journal of Combinatorics
    21 (2014).
date_created: 2021-06-23T06:29:35Z
date_published: 2014-02-28T00:00:00Z
date_updated: 2023-02-23T14:02:12Z
day: '28'
doi: 10.37236/3752
extern: '1'
external_id:
  arxiv:
  - '1309.6710'
intvolume: '        21'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.37236/3752
month: '02'
oa: 1
oa_version: Published Version
publication: The Electronic Journal of Combinatorics
publication_identifier:
  eissn:
  - 1077-8926
publication_status: published
publisher: The Electronic Journal of Combinatorics
quality_controlled: '1'
scopus_import: '1'
status: public
title: On the number of spanning trees in random regular graphs
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 21
year: '2014'
...
---
_id: '96'
abstract:
- lang: eng
  text: Multielectron spin qubits are demonstrated, and performance examined by comparing
    coherent exchange oscillations in coupled single-electron and multielectron quantum
    dots, measured in the same device. Fast (&gt;1 GHz) exchange oscillations with
    a quality factor Q∼15 are found for the multielectron case, compared to Q∼2 for
    the single-electron case, the latter consistent with experiments in the literature.
    A model of dephasing that includes voltage and hyperfine noise is developed that
    is in good agreement with both single- and multielectron data, though in both
    cases additional exchange-independent dephasing is needed to obtain quantitative
    agreement across a broad parameter range.
acknowledgement: The research is supported by the Intelligence Advanced Research Projects
  Activity (IARPA), through the Army Research Office Grant No. W911NF-12-1-0354, the
  DARPA QuEST Program, the Department of Energy, Office of Science, and the Danish
  National Research Foundation.
article_number: '026801'
arxiv: 1
author:
- first_name: Andrew P
  full_name: Higginbotham, Andrew P
  id: 4AD6785A-F248-11E8-B48F-1D18A9856A87
  last_name: Higginbotham
  orcid: 0000-0003-2607-2363
- first_name: Ferdinand
  full_name: Kuemmeth, Ferdinand
  last_name: Kuemmeth
- first_name: Micah
  full_name: Hanson, Micah
  last_name: Hanson
- first_name: Arthur
  full_name: Gossard, Arthur
  last_name: Gossard
- first_name: Charles
  full_name: Marcus, Charles
  last_name: Marcus
citation:
  ama: Higginbotham AP, Kuemmeth F, Hanson M, Gossard A, Marcus C. Coherent operations
    and screening in multielectron spin qubits. <i>APS Physics, Physical Review Letters</i>.
    2014;112(2). doi:<a href="https://doi.org/10.1103/PhysRevLett.112.026801">10.1103/PhysRevLett.112.026801</a>
  apa: Higginbotham, A. P., Kuemmeth, F., Hanson, M., Gossard, A., &#38; Marcus, C.
    (2014). Coherent operations and screening in multielectron spin qubits. <i>APS
    Physics, Physical Review Letters</i>. American Physiological Society. <a href="https://doi.org/10.1103/PhysRevLett.112.026801">https://doi.org/10.1103/PhysRevLett.112.026801</a>
  chicago: Higginbotham, Andrew P, Ferdinand Kuemmeth, Micah Hanson, Arthur Gossard,
    and Charles Marcus. “Coherent Operations and Screening in Multielectron Spin Qubits.”
    <i>APS Physics, Physical Review Letters</i>. American Physiological Society, 2014.
    <a href="https://doi.org/10.1103/PhysRevLett.112.026801">https://doi.org/10.1103/PhysRevLett.112.026801</a>.
  ieee: A. P. Higginbotham, F. Kuemmeth, M. Hanson, A. Gossard, and C. Marcus, “Coherent
    operations and screening in multielectron spin qubits,” <i>APS Physics, Physical
    Review Letters</i>, vol. 112, no. 2. American Physiological Society, 2014.
  ista: Higginbotham AP, Kuemmeth F, Hanson M, Gossard A, Marcus C. 2014. Coherent
    operations and screening in multielectron spin qubits. APS Physics, Physical Review
    Letters. 112(2), 026801.
  mla: Higginbotham, Andrew P., et al. “Coherent Operations and Screening in Multielectron
    Spin Qubits.” <i>APS Physics, Physical Review Letters</i>, vol. 112, no. 2, 026801,
    American Physiological Society, 2014, doi:<a href="https://doi.org/10.1103/PhysRevLett.112.026801">10.1103/PhysRevLett.112.026801</a>.
  short: A.P. Higginbotham, F. Kuemmeth, M. Hanson, A. Gossard, C. Marcus, APS Physics,
    Physical Review Letters 112 (2014).
date_created: 2018-12-11T11:44:36Z
date_published: 2014-01-14T00:00:00Z
date_updated: 2021-01-12T08:22:14Z
day: '14'
doi: 10.1103/PhysRevLett.112.026801
extern: '1'
external_id:
  arxiv:
  - '1306.2720'
intvolume: '       112'
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1306.2720
month: '01'
oa: 1
oa_version: Preprint
publication: APS Physics, Physical Review Letters
publication_status: published
publisher: American Physiological Society
publist_id: '7958'
quality_controlled: '1'
status: public
title: Coherent operations and screening in multielectron spin qubits
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 112
year: '2014'
...
---
_id: '9655'
abstract:
- lang: eng
  text: Correlative microscopy incorporates the specificity of fluorescent protein
    labeling into high-resolution electron micrographs. Several approaches exist for
    correlative microscopy, most of which have used the green fluorescent protein
    (GFP) as the label for light microscopy. Here we use chemical tagging and synthetic
    fluorophores instead, in order to achieve protein-specific labeling, and to perform
    multicolor imaging. We show that synthetic fluorophores preserve their post-embedding
    fluorescence in the presence of uranyl acetate. Post-embedding fluorescence is
    of such quality that the specimen can be prepared with identical protocols for
    scanning electron microscopy (SEM) and transmission electron microscopy (TEM);
    this is particularly valuable when singular or otherwise difficult samples are
    examined. We show that synthetic fluorophores give bright, well-resolved signals
    in super-resolution light microscopy, enabling us to superimpose light microscopic
    images with a precision of up to 25 nm in the x–y plane on electron micrographs.
    To exemplify the preservation quality of our new method we visualize the molecular
    arrangement of cadherins in adherens junctions of mouse epithelial cells.
article_processing_charge: No
article_type: original
author:
- first_name: Mario
  full_name: Perkovic, Mario
  last_name: Perkovic
- first_name: Michael
  full_name: Kunz, Michael
  last_name: Kunz
- first_name: Ulrike
  full_name: Endesfelder, Ulrike
  last_name: Endesfelder
- first_name: Stefanie
  full_name: Bunse, Stefanie
  last_name: Bunse
- first_name: Christoph
  full_name: Wigge, Christoph
  last_name: Wigge
- first_name: Zhou
  full_name: Yu, Zhou
  last_name: Yu
- first_name: Victor-Valentin
  full_name: Hodirnau, Victor-Valentin
  id: 3661B498-F248-11E8-B48F-1D18A9856A87
  last_name: Hodirnau
- first_name: Margot P.
  full_name: Scheffer, Margot P.
  last_name: Scheffer
- first_name: Anja
  full_name: Seybert, Anja
  last_name: Seybert
- first_name: Sebastian
  full_name: Malkusch, Sebastian
  last_name: Malkusch
- first_name: Erin M.
  full_name: Schuman, Erin M.
  last_name: Schuman
- first_name: Mike
  full_name: Heilemann, Mike
  last_name: Heilemann
- first_name: Achilleas S.
  full_name: Frangakis, Achilleas S.
  last_name: Frangakis
citation:
  ama: Perkovic M, Kunz M, Endesfelder U, et al. Correlative light- and electron microscopy
    with chemical tags. <i>Journal of Structural Biology</i>. 2014;186(2):205-213.
    doi:<a href="https://doi.org/10.1016/j.jsb.2014.03.018">10.1016/j.jsb.2014.03.018</a>
  apa: Perkovic, M., Kunz, M., Endesfelder, U., Bunse, S., Wigge, C., Yu, Z., … Frangakis,
    A. S. (2014). Correlative light- and electron microscopy with chemical tags. <i>Journal
    of Structural Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.jsb.2014.03.018">https://doi.org/10.1016/j.jsb.2014.03.018</a>
  chicago: Perkovic, Mario, Michael Kunz, Ulrike Endesfelder, Stefanie Bunse, Christoph
    Wigge, Zhou Yu, Victor-Valentin Hodirnau, et al. “Correlative Light- and Electron
    Microscopy with Chemical Tags.” <i>Journal of Structural Biology</i>. Elsevier,
    2014. <a href="https://doi.org/10.1016/j.jsb.2014.03.018">https://doi.org/10.1016/j.jsb.2014.03.018</a>.
  ieee: M. Perkovic <i>et al.</i>, “Correlative light- and electron microscopy with
    chemical tags,” <i>Journal of Structural Biology</i>, vol. 186, no. 2. Elsevier,
    pp. 205–213, 2014.
  ista: Perkovic M, Kunz M, Endesfelder U, Bunse S, Wigge C, Yu Z, Hodirnau V-V, Scheffer
    MP, Seybert A, Malkusch S, Schuman EM, Heilemann M, Frangakis AS. 2014. Correlative
    light- and electron microscopy with chemical tags. Journal of Structural Biology.
    186(2), 205–213.
  mla: Perkovic, Mario, et al. “Correlative Light- and Electron Microscopy with Chemical
    Tags.” <i>Journal of Structural Biology</i>, vol. 186, no. 2, Elsevier, 2014,
    pp. 205–13, doi:<a href="https://doi.org/10.1016/j.jsb.2014.03.018">10.1016/j.jsb.2014.03.018</a>.
  short: M. Perkovic, M. Kunz, U. Endesfelder, S. Bunse, C. Wigge, Z. Yu, V.-V. Hodirnau,
    M.P. Scheffer, A. Seybert, S. Malkusch, E.M. Schuman, M. Heilemann, A.S. Frangakis,
    Journal of Structural Biology 186 (2014) 205–213.
date_created: 2021-07-14T09:05:42Z
date_published: 2014-05-01T00:00:00Z
date_updated: 2021-07-22T08:26:32Z
day: '01'
ddc:
- '570'
doi: 10.1016/j.jsb.2014.03.018
extern: '1'
external_id:
  pmid:
  - '24698954'
file:
- access_level: open_access
  checksum: a322991b43cdc5935c99db88d285aa3a
  content_type: application/pdf
  creator: asandaue
  date_created: 2021-07-22T08:06:34Z
  date_updated: 2021-07-22T08:06:34Z
  file_id: '9701'
  file_name: 2014_JournalOfStructuralBiology_Perkovic.pdf
  file_size: 3454628
  relation: main_file
  success: 1
file_date_updated: 2021-07-22T08:06:34Z
has_accepted_license: '1'
intvolume: '       186'
issue: '2'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: 205-213
pmid: 1
publication: Journal of Structural Biology
publication_identifier:
  issn:
  - 1047-8477
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Correlative light- and electron microscopy with chemical tags
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/3.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported (CC BY-NC-ND
    3.0)
  short: CC BY-NC-ND (3.0)
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 186
year: '2014'
...
---
_id: '9662'
abstract:
- lang: eng
  text: Fractionation of isotopes among distinct molecules or phases is a quantum
    effect which is often exploited to obtain insights on reaction mechanisms, biochemical,
    geochemical, and atmospheric phenomena. Accurate evaluation of isotope ratios
    in atomistic simulations is challenging, because one needs to perform a thermodynamic
    integration with respect to the isotope mass, along with time-consuming path integral
    calculations. By re-formulating the problem as a particle exchange in the ring
    polymer partition function, we derive new estimators giving direct access to the
    differential partitioning of isotopes, which can simplify the calculations by
    avoiding thermodynamic integration. We demonstrate the efficiency of these estimators
    by applying them to investigate the isotope fractionation ratios in the gas-phase
    Zundel cation, and in a few simple hydrocarbons.
article_number: '244112'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Bingqing
  full_name: Cheng, Bingqing
  id: cbe3cda4-d82c-11eb-8dc7-8ff94289fcc9
  last_name: Cheng
  orcid: 0000-0002-3584-9632
- first_name: Michele
  full_name: Ceriotti, Michele
  last_name: Ceriotti
citation:
  ama: Cheng B, Ceriotti M. Direct path integral estimators for isotope fractionation
    ratios. <i>The Journal of Chemical Physics</i>. 2014;141(24). doi:<a href="https://doi.org/10.1063/1.4904293">10.1063/1.4904293</a>
  apa: Cheng, B., &#38; Ceriotti, M. (2014). Direct path integral estimators for isotope
    fractionation ratios. <i>The Journal of Chemical Physics</i>. AIP Publishing.
    <a href="https://doi.org/10.1063/1.4904293">https://doi.org/10.1063/1.4904293</a>
  chicago: Cheng, Bingqing, and Michele Ceriotti. “Direct Path Integral Estimators
    for Isotope Fractionation Ratios.” <i>The Journal of Chemical Physics</i>. AIP
    Publishing, 2014. <a href="https://doi.org/10.1063/1.4904293">https://doi.org/10.1063/1.4904293</a>.
  ieee: B. Cheng and M. Ceriotti, “Direct path integral estimators for isotope fractionation
    ratios,” <i>The Journal of Chemical Physics</i>, vol. 141, no. 24. AIP Publishing,
    2014.
  ista: Cheng B, Ceriotti M. 2014. Direct path integral estimators for isotope fractionation
    ratios. The Journal of Chemical Physics. 141(24), 244112.
  mla: Cheng, Bingqing, and Michele Ceriotti. “Direct Path Integral Estimators for
    Isotope Fractionation Ratios.” <i>The Journal of Chemical Physics</i>, vol. 141,
    no. 24, 244112, AIP Publishing, 2014, doi:<a href="https://doi.org/10.1063/1.4904293">10.1063/1.4904293</a>.
  short: B. Cheng, M. Ceriotti, The Journal of Chemical Physics 141 (2014).
date_created: 2021-07-15T09:22:49Z
date_published: 2014-12-28T00:00:00Z
date_updated: 2021-08-09T12:32:24Z
day: '28'
doi: 10.1063/1.4904293
extern: '1'
external_id:
  arxiv:
  - '1412.1308'
  pmid:
  - '25554138'
intvolume: '       141'
issue: '24'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1412.1308
month: '12'
oa: 1
oa_version: Preprint
pmid: 1
publication: The Journal of Chemical Physics
publication_identifier:
  eissn:
  - 1089-7690
  issn:
  - 0021-9606
publication_status: published
publisher: AIP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Direct path integral estimators for isotope fractionation ratios
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 141
year: '2014'
...
---
_id: '9686'
abstract:
- lang: eng
  text: It is well known that ultrasonic vibration can soften metals, and this phenomenon
    has been widely exploited in industrial applications concerning metal forming
    and bonding. Recent experiments show that the simultaneous application of oscillatory
    stresses from audible to ultrasonic frequency ranges can lead to not only softening
    but also significant dislocation annihilation and subgrain formation in metal
    samples from the nano- to macro-size range. These findings indicate that the existing
    understanding of ultrasound softening – that the vibrations either impose additional
    stress waves to augment the quasi-static applied load, or cause heating of the
    metal, whereas the metal’s intrinsic deformation resistance or mechanism remains
    unaltered – is far from complete. To understand the softening and the associated
    enhanced subgrain formation and dislocation annihilation, a new simulator based
    on the dynamics of dislocation-density functions is employed. This new simulator
    considers the flux, production and annihilation, as well as the Taylor and elastic
    interactions between dislocation densities. Softening during vibrations as well
    as enhanced cell formation is predicted. The simulations reveal the main mechanism
    for subcell formation under oscillatory loadings to be the enhanced elimination
    of statistically stored dislocations (SSDs) by the oscillatory stress, leaving
    behind geometrically necessary dislocations with low Schmid factors which then
    form the subgrain walls. The oscillatory stress helps the depletion of the SSDs,
    because the chance for them to meet up and annihilate is increased with reversals
    of dislocation motions. This is the first simulation effort to successfully predict
    the cell formation phenomenon under vibratory loadings.
article_processing_charge: No
article_type: original
author:
- first_name: Bingqing
  full_name: Cheng, Bingqing
  id: cbe3cda4-d82c-11eb-8dc7-8ff94289fcc9
  last_name: Cheng
  orcid: 0000-0002-3584-9632
- first_name: H.S.
  full_name: Leung, H.S.
  last_name: Leung
- first_name: A.H.W.
  full_name: Ngan, A.H.W.
  last_name: Ngan
citation:
  ama: Cheng B, Leung HS, Ngan AHW. Strength of metals under vibrations – dislocation-density-function
    dynamics simulations. <i>Philosophical Magazine</i>. 2014;95(16-18):1845-1865.
    doi:<a href="https://doi.org/10.1080/14786435.2014.897008">10.1080/14786435.2014.897008</a>
  apa: Cheng, B., Leung, H. S., &#38; Ngan, A. H. W. (2014). Strength of metals under
    vibrations – dislocation-density-function dynamics simulations. <i>Philosophical
    Magazine</i>. Taylor &#38; Francis. <a href="https://doi.org/10.1080/14786435.2014.897008">https://doi.org/10.1080/14786435.2014.897008</a>
  chicago: Cheng, Bingqing, H.S. Leung, and A.H.W. Ngan. “Strength of Metals under
    Vibrations – Dislocation-Density-Function Dynamics Simulations.” <i>Philosophical
    Magazine</i>. Taylor &#38; Francis, 2014. <a href="https://doi.org/10.1080/14786435.2014.897008">https://doi.org/10.1080/14786435.2014.897008</a>.
  ieee: B. Cheng, H. S. Leung, and A. H. W. Ngan, “Strength of metals under vibrations
    – dislocation-density-function dynamics simulations,” <i>Philosophical Magazine</i>,
    vol. 95, no. 16–18. Taylor &#38; Francis, pp. 1845–1865, 2014.
  ista: Cheng B, Leung HS, Ngan AHW. 2014. Strength of metals under vibrations – dislocation-density-function
    dynamics simulations. Philosophical Magazine. 95(16–18), 1845–1865.
  mla: Cheng, Bingqing, et al. “Strength of Metals under Vibrations – Dislocation-Density-Function
    Dynamics Simulations.” <i>Philosophical Magazine</i>, vol. 95, no. 16–18, Taylor
    &#38; Francis, 2014, pp. 1845–65, doi:<a href="https://doi.org/10.1080/14786435.2014.897008">10.1080/14786435.2014.897008</a>.
  short: B. Cheng, H.S. Leung, A.H.W. Ngan, Philosophical Magazine 95 (2014) 1845–1865.
date_created: 2021-07-19T09:27:15Z
date_published: 2014-06-23T00:00:00Z
date_updated: 2023-02-23T14:04:59Z
day: '23'
doi: 10.1080/14786435.2014.897008
extern: '1'
intvolume: '        95'
issue: 16-18
language:
- iso: eng
month: '06'
oa_version: None
page: 1845-1865
publication: Philosophical Magazine
publication_identifier:
  eissn:
  - 1478-6443
  issn:
  - 1478-6435
publication_status: published
publisher: Taylor & Francis
quality_controlled: '1'
scopus_import: '1'
status: public
title: Strength of metals under vibrations – dislocation-density-function dynamics
  simulations
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 95
year: '2014'
...
---
_id: '97'
abstract:
- lang: eng
  text: The distribution of Coulomb blockade peak heights as a function of magnetic
    field is investigated experimentally in a Ge-Si nanowire quantum dot. Strong spin-orbit
    coupling in this hole-gas system leads to antilocalization of Coulomb blockade
    peaks, consistent with theory. In particular, the peak height distribution has
    its maximum away from zero at zero magnetic field, with an average that decreases
    with increasing field. Magnetoconductance in the open-wire regime places a bound
    on the spin-orbit length (lso < 20 nm), consistent with values extracted in the
    Coulomb blockade regime (lso < 25 nm).
acknowledgement: Research supported by the Danish National Research Foundation, the
  Office of Science at the U.S. Department of Energy, the National Science Foundation
  (PHY-1104528), and the Defense Advanced Research Projects Agency through the QuEST
  Program.
article_number: '216806'
arxiv: 1
author:
- first_name: Andrew P
  full_name: Higginbotham, Andrew P
  id: 4AD6785A-F248-11E8-B48F-1D18A9856A87
  last_name: Higginbotham
  orcid: 0000-0003-2607-2363
- first_name: Ferdinand
  full_name: Kuemmeth, Ferdinand
  last_name: Kuemmeth
- first_name: Thorvald
  full_name: Larsen, Thorvald
  last_name: Larsen
- first_name: Mattias
  full_name: Fitzpatrick, Mattias
  last_name: Fitzpatrick
- first_name: Jun
  full_name: Yao, Jun
  last_name: Yao
- first_name: Hao
  full_name: Yan, Hao
  last_name: Yan
- first_name: Charles
  full_name: Lieber, Charles
  last_name: Lieber
- first_name: Charles
  full_name: Marcus, Charles
  last_name: Marcus
citation:
  ama: Higginbotham AP, Kuemmeth F, Larsen T, et al. Antilocalization of coulomb blockade
    in a Ge/Si nanowire. <i>APS Physics, Physical Review Letters</i>. 2014;112(21).
    doi:<a href="https://doi.org/10.1103/PhysRevLett.112.216806">10.1103/PhysRevLett.112.216806</a>
  apa: Higginbotham, A. P., Kuemmeth, F., Larsen, T., Fitzpatrick, M., Yao, J., Yan,
    H., … Marcus, C. (2014). Antilocalization of coulomb blockade in a Ge/Si nanowire.
    <i>APS Physics, Physical Review Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevLett.112.216806">https://doi.org/10.1103/PhysRevLett.112.216806</a>
  chicago: Higginbotham, Andrew P, Ferdinand Kuemmeth, Thorvald Larsen, Mattias Fitzpatrick,
    Jun Yao, Hao Yan, Charles Lieber, and Charles Marcus. “Antilocalization of Coulomb
    Blockade in a Ge/Si Nanowire.” <i>APS Physics, Physical Review Letters</i>. American
    Physical Society, 2014. <a href="https://doi.org/10.1103/PhysRevLett.112.216806">https://doi.org/10.1103/PhysRevLett.112.216806</a>.
  ieee: A. P. Higginbotham <i>et al.</i>, “Antilocalization of coulomb blockade in
    a Ge/Si nanowire,” <i>APS Physics, Physical Review Letters</i>, vol. 112, no.
    21. American Physical Society, 2014.
  ista: Higginbotham AP, Kuemmeth F, Larsen T, Fitzpatrick M, Yao J, Yan H, Lieber
    C, Marcus C. 2014. Antilocalization of coulomb blockade in a Ge/Si nanowire. APS
    Physics, Physical Review Letters. 112(21), 216806.
  mla: Higginbotham, Andrew P., et al. “Antilocalization of Coulomb Blockade in a
    Ge/Si Nanowire.” <i>APS Physics, Physical Review Letters</i>, vol. 112, no. 21,
    216806, American Physical Society, 2014, doi:<a href="https://doi.org/10.1103/PhysRevLett.112.216806">10.1103/PhysRevLett.112.216806</a>.
  short: A.P. Higginbotham, F. Kuemmeth, T. Larsen, M. Fitzpatrick, J. Yao, H. Yan,
    C. Lieber, C. Marcus, APS Physics, Physical Review Letters 112 (2014).
date_created: 2018-12-11T11:44:36Z
date_published: 2014-05-29T00:00:00Z
date_updated: 2021-01-12T08:22:19Z
day: '29'
doi: 10.1103/PhysRevLett.112.216806
extern: '1'
external_id:
  arxiv:
  - '1401.2948'
intvolume: '       112'
issue: '21'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1401.2948
month: '05'
oa: 1
oa_version: None
publication: APS Physics, Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '7957'
quality_controlled: '1'
status: public
title: Antilocalization of coulomb blockade in a Ge/Si nanowire
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 112
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: 2023-02-23T10:24:07Z
day: '14'
department:
- _id: JoCs
doi: 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: 2023-02-23T10:25:37Z
day: '11'
department:
- _id: KrCh
doi: 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).
date_created: 2021-07-28T08:38:40Z
date_published: 2014-11-13T00:00:00Z
date_updated: 2023-02-23T10:23:32Z
day: '13'
department:
- _id: SyCr
doi: 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: '9741'
abstract:
- lang: eng
  text: In rapidly changing environments, selection history may impact the dynamics
    of adaptation. Mutations selected in one environment may result in pleiotropic
    fitness trade-offs in subsequent novel environments, slowing the rates of adaptation.
    Epistatic interactions between mutations selected in sequential stressful environments
    may slow or accelerate subsequent rates of adaptation, depending on the nature
    of that interaction. We explored the dynamics of adaptation during sequential
    exposure to herbicides with different modes of action in Chlamydomonas reinhardtii.
    Evolution of resistance to two of the herbicides was largely independent of selection
    history. For carbetamide, previous adaptation to other herbicide modes of action
    positively impacted the likelihood of adaptation to this herbicide. Furthermore,
    while adaptation to all individual herbicides was associated with pleiotropic
    fitness costs in stress-free environments, we observed that accumulation of resistance
    mechanisms was accompanied by a reduction in overall fitness costs. We suggest
    that antagonistic epistasis may be a driving mechanism that enables populations
    to more readily adapt in novel environments. These findings highlight the potential
    for sequences of xenobiotics to facilitate the rapid evolution of multiple-drug
    and -pesticide resistance, as well as the potential for epistatic interactions
    between adaptive mutations to facilitate evolutionary rescue in rapidly changing
    environments.
article_processing_charge: No
author:
- first_name: Mato
  full_name: Lagator, Mato
  id: 345D25EC-F248-11E8-B48F-1D18A9856A87
  last_name: Lagator
- first_name: Nick
  full_name: Colegrave, Nick
  last_name: Colegrave
- first_name: Paul
  full_name: Neve, Paul
  last_name: Neve
citation:
  ama: 'Lagator M, Colegrave N, Neve P. Data from: Selection history and epistatic
    interactions impact dynamics of adaptation to novel environmental stresses. 2014.
    doi:<a href="https://doi.org/10.5061/dryad.85dn7">10.5061/dryad.85dn7</a>'
  apa: 'Lagator, M., Colegrave, N., &#38; Neve, P. (2014). Data from: Selection history
    and epistatic interactions impact dynamics of adaptation to novel environmental
    stresses. Dryad. <a href="https://doi.org/10.5061/dryad.85dn7">https://doi.org/10.5061/dryad.85dn7</a>'
  chicago: 'Lagator, Mato, Nick Colegrave, and Paul Neve. “Data from: Selection History
    and Epistatic Interactions Impact Dynamics of Adaptation to Novel Environmental
    Stresses.” Dryad, 2014. <a href="https://doi.org/10.5061/dryad.85dn7">https://doi.org/10.5061/dryad.85dn7</a>.'
  ieee: 'M. Lagator, N. Colegrave, and P. Neve, “Data from: Selection history and
    epistatic interactions impact dynamics of adaptation to novel environmental stresses.”
    Dryad, 2014.'
  ista: 'Lagator M, Colegrave N, Neve P. 2014. Data from: Selection history and epistatic
    interactions impact dynamics of adaptation to novel environmental stresses, Dryad,
    <a href="https://doi.org/10.5061/dryad.85dn7">10.5061/dryad.85dn7</a>.'
  mla: 'Lagator, Mato, et al. <i>Data from: Selection History and Epistatic Interactions
    Impact Dynamics of Adaptation to Novel Environmental Stresses</i>. Dryad, 2014,
    doi:<a href="https://doi.org/10.5061/dryad.85dn7">10.5061/dryad.85dn7</a>.'
  short: M. Lagator, N. Colegrave, P. Neve, (2014).
date_created: 2021-07-28T08:48:06Z
date_published: 2014-08-21T00:00:00Z
date_updated: 2023-02-23T10:25:31Z
day: '21'
department:
- _id: CaGu
doi: 10.5061/dryad.85dn7
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.85dn7
month: '08'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '2036'
    relation: used_in_publication
    status: public
status: public
title: 'Data from: Selection history and epistatic interactions impact dynamics of
  adaptation to novel environmental stresses'
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: 2023-02-23T10:27:31Z
day: '17'
department:
- _id: CaGu
doi: 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: 2023-02-23T10:35:57Z
day: '07'
department:
- _id: GaTk
doi: 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: '9753'
abstract:
- lang: eng
  text: 'Background: The brood of ants and other social insects is highly susceptible
    to pathogens, particularly those that penetrate the soft larval and pupal cuticle.
    We here test whether the presence of a pupal cocoon, which occurs in some ant
    species but not in others, affects the sanitary brood care and fungal infection
    patterns after exposure to the entomopathogenic fungus Metarhizium brunneum. We
    use a) a comparative approach analysing four species with either naked or cocooned
    pupae and b) a within-species analysis of a single ant species, in which both
    pupal types co-exist in the same colony. Results: We found that the presence of
    a cocoon did not compromise fungal pathogen detection by the ants and that species
    with cocooned pupae increased brood grooming after pathogen exposure. All tested
    ant species further removed brood from their nests, which was predominantly expressed
    towards larvae and naked pupae treated with the live fungal pathogen. In contrast,
    cocooned pupae exposed to live fungus were not removed at higher rates than cocooned
    pupae exposed to dead fungus or a sham control. Consistent with this, exposure
    to the live fungus caused high numbers of infections and fungal outgrowth in larvae
    and naked pupae, but not in cocooned pupae. Moreover, the ants consistently removed
    the brood prior to fungal outgrowth, ensuring a clean brood chamber. Conclusion:
    Our study suggests that the pupal cocoon has a protective effect against fungal
    infection, causing an adaptive change in sanitary behaviours by the ants. It further
    demonstrates that brood removal - originally described for honeybees as “hygienic
    behaviour” – is a widespread sanitary behaviour in ants, which likely has important
    implications on disease dynamics in social insect colonies.'
article_processing_charge: No
author:
- first_name: Simon
  full_name: Tragust, Simon
  id: 35A7A418-F248-11E8-B48F-1D18A9856A87
  last_name: Tragust
- first_name: Line V
  full_name: Ugelvig, Line V
  id: 3DC97C8E-F248-11E8-B48F-1D18A9856A87
  last_name: Ugelvig
  orcid: 0000-0003-1832-8883
- first_name: Michel
  full_name: Chapuisat, Michel
  last_name: Chapuisat
- first_name: Jürgen
  full_name: Heinze, Jürgen
  last_name: Heinze
- first_name: Sylvia
  full_name: Cremer, Sylvia
  id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
  last_name: Cremer
  orcid: 0000-0002-2193-3868
citation:
  ama: 'Tragust S, Ugelvig LV, Chapuisat M, Heinze J, Cremer S. Data from: Pupal cocoons
    affect sanitary brood care and limit fungal infections in ant colonies. 2014.
    doi:<a href="https://doi.org/10.5061/dryad.nc0gc">10.5061/dryad.nc0gc</a>'
  apa: 'Tragust, S., Ugelvig, L. V., Chapuisat, M., Heinze, J., &#38; Cremer, S. (2014).
    Data from: Pupal cocoons affect sanitary brood care and limit fungal infections
    in ant colonies. Dryad. <a href="https://doi.org/10.5061/dryad.nc0gc">https://doi.org/10.5061/dryad.nc0gc</a>'
  chicago: 'Tragust, Simon, Line V Ugelvig, Michel Chapuisat, Jürgen Heinze, and Sylvia
    Cremer. “Data from: Pupal Cocoons Affect Sanitary Brood Care and Limit Fungal
    Infections in Ant Colonies.” Dryad, 2014. <a href="https://doi.org/10.5061/dryad.nc0gc">https://doi.org/10.5061/dryad.nc0gc</a>.'
  ieee: 'S. Tragust, L. V. Ugelvig, M. Chapuisat, J. Heinze, and S. Cremer, “Data
    from: Pupal cocoons affect sanitary brood care and limit fungal infections in
    ant colonies.” Dryad, 2014.'
  ista: 'Tragust S, Ugelvig LV, Chapuisat M, Heinze J, Cremer S. 2014. Data from:
    Pupal cocoons affect sanitary brood care and limit fungal infections in ant colonies,
    Dryad, <a href="https://doi.org/10.5061/dryad.nc0gc">10.5061/dryad.nc0gc</a>.'
  mla: 'Tragust, Simon, et al. <i>Data from: Pupal Cocoons Affect Sanitary Brood Care
    and Limit Fungal Infections in Ant Colonies</i>. Dryad, 2014, doi:<a href="https://doi.org/10.5061/dryad.nc0gc">10.5061/dryad.nc0gc</a>.'
  short: S. Tragust, L.V. Ugelvig, M. Chapuisat, J. Heinze, S. Cremer, (2014).
date_created: 2021-07-30T08:24:11Z
date_published: 2014-10-08T00:00:00Z
date_updated: 2023-02-23T10:36:17Z
day: '08'
department:
- _id: SyCr
doi: 10.5061/dryad.nc0gc
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5061/dryad.nc0gc
month: '10'
oa: 1
oa_version: Published Version
publisher: Dryad
related_material:
  record:
  - id: '2284'
    relation: used_in_publication
    status: public
status: public
title: 'Data from: Pupal cocoons affect sanitary brood care and limit fungal infections
  in ant colonies'
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2014'
...
---
_id: '977'
abstract:
- lang: eng
  text: We propose a method for detecting many-body localization (MBL) in disordered
    spin systems. The method involves pulsed coherent spin manipulations that probe
    the dephasing of a given spin due to its entanglement with a set of distant spins.
    It allows one to distinguish the MBL phase from a noninteracting localized phase
    and a delocalized phase. In particular, we show that for a properly chosen pulse
    sequence the MBL phase exhibits a characteristic power-law decay reflecting its
    slow growth of entanglement. We find that this power-law decay is robust with
    respect to thermal and disorder averaging, provide numerical simulations supporting
    our results, and discuss possible experimental realizations in solid-state and
    cold-atom systems.
acknowledgement: |-
  We thank E. Altman, Y. Bahri, I. Bloch, T. Giamarchi, D. Huse, V. Oganesyan, A. Pal, D. Pekker, and G. Refael for insightful discussions. The authors acknowledge support from the Harvard Quantum Optics Center, Harvard-MIT CUA, the DARPA OLE program, AFOSR Quantum Simulation MURI, ARO-MURI on Atomtronics, the ARO-MURI Quism program, the Austrian Science Fund (FWF) Project No. J 3361-N20, NSERC grant, and Sloan Research Fellowship. Simulations presented in this article were performed on computational resources supported by the High Performance Computing Center (PICSciE) at Princeton University and the Research Computing Center at Harvard University. Research at Perimeter Institute was supported by the Government of Canada and by the Province of Ontario.

  M. S., M. K., and S. G. contributed equally to this work.
author:
- first_name: Maksym
  full_name: Maksym Serbyn
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
- first_name: Michael
  full_name: Knap, Michael J
  last_name: Knap
- first_name: Sarang
  full_name: Gopalakrishnan, Sarang
  last_name: Gopalakrishnan
- first_name: Zlatko
  full_name: Papić, Zlatko
  last_name: Papić
- first_name: Norman
  full_name: Yao, Norman Y
  last_name: Yao
- first_name: Chris
  full_name: Laumann, Chris R
  last_name: Laumann
- first_name: Dmitry
  full_name: Abanin, Dmitry A
  last_name: Abanin
- first_name: Mikhail
  full_name: Lukin, Mikhail D
  last_name: Lukin
- first_name: Eugene
  full_name: Demler, Eugene A
  last_name: Demler
citation:
  ama: Serbyn M, Knap M, Gopalakrishnan S, et al. Interferometric probes of many-body
    localization. <i>Physical Review Letters</i>. 2014;113(14). doi:<a href="https://doi.org/10.1103/PhysRevLett.113.147204">10.1103/PhysRevLett.113.147204</a>
  apa: Serbyn, M., Knap, M., Gopalakrishnan, S., Papić, Z., Yao, N., Laumann, C.,
    … Demler, E. (2014). Interferometric probes of many-body localization. <i>Physical
    Review Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevLett.113.147204">https://doi.org/10.1103/PhysRevLett.113.147204</a>
  chicago: Serbyn, Maksym, Michael Knap, Sarang Gopalakrishnan, Zlatko Papić, Norman
    Yao, Chris Laumann, Dmitry Abanin, Mikhail Lukin, and Eugene Demler. “Interferometric
    Probes of Many-Body Localization.” <i>Physical Review Letters</i>. American Physical
    Society, 2014. <a href="https://doi.org/10.1103/PhysRevLett.113.147204">https://doi.org/10.1103/PhysRevLett.113.147204</a>.
  ieee: M. Serbyn <i>et al.</i>, “Interferometric probes of many-body localization,”
    <i>Physical Review Letters</i>, vol. 113, no. 14. American Physical Society, 2014.
  ista: Serbyn M, Knap M, Gopalakrishnan S, Papić Z, Yao N, Laumann C, Abanin D, Lukin
    M, Demler E. 2014. Interferometric probes of many-body localization. Physical
    Review Letters. 113(14).
  mla: Serbyn, Maksym, et al. “Interferometric Probes of Many-Body Localization.”
    <i>Physical Review Letters</i>, vol. 113, no. 14, American Physical Society, 2014,
    doi:<a href="https://doi.org/10.1103/PhysRevLett.113.147204">10.1103/PhysRevLett.113.147204</a>.
  short: M. Serbyn, M. Knap, S. Gopalakrishnan, Z. Papić, N. Yao, C. Laumann, D. Abanin,
    M. Lukin, E. Demler, Physical Review Letters 113 (2014).
date_created: 2018-12-11T11:49:30Z
date_published: 2014-10-03T00:00:00Z
date_updated: 2021-01-12T08:22:22Z
day: '03'
doi: 10.1103/PhysRevLett.113.147204
extern: 1
intvolume: '       113'
issue: '14'
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1403.0693
month: '10'
oa: 1
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '6421'
quality_controlled: 0
status: public
title: Interferometric probes of many-body localization
type: journal_article
volume: 113
year: '2014'
...
---
_id: '978'
abstract:
- lang: eng
  text: The newly discovered topological crystalline insulators feature a complex
    band structure involving multiple Dirac cones, and are potentially highly tunable
    by external electric field, temperature or strain. Theoretically, it has been
    predicted that the various Dirac cones, which are offset in energy and momentum,
    might harbour vastly different orbital character. However, their orbital texture,
    which is of immense importance in determining a variety of a materialâ €™ s properties
    remains elusive. Here, we unveil the orbital texture of Pb 1â ̂'x Sn x Se, a prototypical
    topological crystalline insulator. By using Fourier-transform scanning tunnelling
    spectroscopy we measure the interference patterns produced by the scattering of
    surface-state electrons. We discover that the intensity and energy dependences
    of the Fourier transforms show distinct characteristics, which can be directly
    attributed to orbital effects. Our experiments reveal a complex band topology
    involving two Lifshitz transitions and establish the orbital nature of the Dirac
    bands, which could provide an alternative pathway towards future quantum applications.
acknowledgement: V.M. gratefully acknowledges funding from the US Department of Energy,
  Scanned Probe Division under Award Number DE-FG02-12ER46880 for the primary support
  of I.Z. and Y.O. (experiments, data analysis and writing the paper) and NSF-ECCS-1232105
  for the partial support of W.Z. and D.W. (data acquisition). Work at Massachusetts
  Institute of Technology is supported by US Department of Energy, Office of Basic
  Energy Sciences, Division of Materials Sciences and Engineering under Award DE-SC0010526
  (L.F.), and NSF DMR 1104498 (M.S.). H.L. acknowledges the Singapore National Research
  Foundation for support under NRF Award No. NRF-NRFF2013-03. The work at Northeastern
  University is supported by the US Department of Energy grant number DE-FG02-07ER46352,
  and benefited from Northeastern University’s Advanced Scientific Computation Center
  (ASCC), theory support at the Advanced Light Source, Berkeley and the allocation
  of time at the NERSC supercomputing centre through DOE grant number DE-AC02-05CH11231.
  W-F.T. and C-Y.H. were supported by the NSC in Taiwan under Grant No. 102-2112-M-110-009.
  W-F.T. also thanks C. Fang for useful discussions. Work at Princeton University
  is supported by the US National Science Foundation Grant, NSF-DMR-1006492. F.C.
  acknowledges the support provided by MOST-Taiwan under project number NSC-102-2119-M-002-004.
author:
- first_name: Ilija
  full_name: Zeljkovic, Ilija
  last_name: Zeljkovic
- first_name: Yoshinori
  full_name: Okada, Yoshinori
  last_name: Okada
- first_name: Chengyi
  full_name: Huang, Chengyi
  last_name: Huang
- first_name: Raman
  full_name: Sankar, Raman
  last_name: Sankar
- first_name: Daniel
  full_name: Walkup, Daniel
  last_name: Walkup
- first_name: Wenwen
  full_name: Zhou, Wenwen
  last_name: Zhou
- first_name: Maksym
  full_name: Maksym Serbyn
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
- first_name: Fangcheng
  full_name: Chou, Fangcheng
  last_name: Chou
- first_name: Wei
  full_name: Tsai, Wei-Feng
  last_name: Tsai
- first_name: Hsin
  full_name: Lin, Hsin
  last_name: Lin
- first_name: Arun
  full_name: Bansil, Arun
  last_name: Bansil
- first_name: Liang
  full_name: Fu, Liang
  last_name: Fu
- first_name: Md
  full_name: Hasan, Md Z
  last_name: Hasan
- first_name: Vidya
  full_name: Madhavan, Vidya
  last_name: Madhavan
citation:
  ama: Zeljkovic I, Okada Y, Huang C, et al. Mapping the unconventional orbital texture
    in topological crystalline insulators. <i>Nature Physics</i>. 2014;10(8):572-577.
    doi:<a href="https://doi.org/10.1038/nphys3012">10.1038/nphys3012</a>
  apa: Zeljkovic, I., Okada, Y., Huang, C., Sankar, R., Walkup, D., Zhou, W., … Madhavan,
    V. (2014). Mapping the unconventional orbital texture in topological crystalline
    insulators. <i>Nature Physics</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/nphys3012">https://doi.org/10.1038/nphys3012</a>
  chicago: Zeljkovic, Ilija, Yoshinori Okada, Chengyi Huang, Raman Sankar, Daniel
    Walkup, Wenwen Zhou, Maksym Serbyn, et al. “Mapping the Unconventional Orbital
    Texture in Topological Crystalline Insulators.” <i>Nature Physics</i>. Nature
    Publishing Group, 2014. <a href="https://doi.org/10.1038/nphys3012">https://doi.org/10.1038/nphys3012</a>.
  ieee: I. Zeljkovic <i>et al.</i>, “Mapping the unconventional orbital texture in
    topological crystalline insulators,” <i>Nature Physics</i>, vol. 10, no. 8. Nature
    Publishing Group, pp. 572–577, 2014.
  ista: Zeljkovic I, Okada Y, Huang C, Sankar R, Walkup D, Zhou W, Serbyn M, Chou
    F, Tsai W, Lin H, Bansil A, Fu L, Hasan M, Madhavan V. 2014. Mapping the unconventional
    orbital texture in topological crystalline insulators. Nature Physics. 10(8),
    572–577.
  mla: Zeljkovic, Ilija, et al. “Mapping the Unconventional Orbital Texture in Topological
    Crystalline Insulators.” <i>Nature Physics</i>, vol. 10, no. 8, Nature Publishing
    Group, 2014, pp. 572–77, doi:<a href="https://doi.org/10.1038/nphys3012">10.1038/nphys3012</a>.
  short: I. Zeljkovic, Y. Okada, C. Huang, R. Sankar, D. Walkup, W. Zhou, M. Serbyn,
    F. Chou, W. Tsai, H. Lin, A. Bansil, L. Fu, M. Hasan, V. Madhavan, Nature Physics
    10 (2014) 572–577.
date_created: 2018-12-11T11:49:30Z
date_published: 2014-08-01T00:00:00Z
date_updated: 2021-01-12T08:22:23Z
day: '01'
doi: 10.1038/nphys3012
extern: 1
intvolume: '        10'
issue: '8'
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1312.0164
month: '08'
oa: 1
page: 572 - 577
publication: Nature Physics
publication_status: published
publisher: Nature Publishing Group
publist_id: '6423'
quality_controlled: 0
status: public
title: Mapping the unconventional orbital texture in topological crystalline insulators
type: journal_article
volume: 10
year: '2014'
...
---
_id: '979'
abstract:
- lang: eng
  text: In the recently discovered topological crystalline insulators SnTe and Pb1-xSnx(Te,
    Se), crystal symmetry and electronic topology intertwine to create topological
    surface states with many interesting features including Lifshitz transition, Van-Hove
    singularity, and fermion mass generation. These surface states are protected by
    mirror symmetry with respect to the (110) plane. In this work we present a comprehensive
    study of the effects of different mirror-symmetry-breaking perturbations on the
    (001) surface band structure. Pristine (001) surface states have four branches
    of Dirac fermions at low energy. We show that ferroelectric-type structural distortion
    generates a mass and gaps out some or all of these Dirac points, while strain
    shifts Dirac points in the Brillouin zone. An in-plane magnetic field leaves the
    surface state gapless, but introduces asymmetry between Dirac points. Finally,
    an out-of-plane magnetic field leads to discrete Landau levels. We show that the
    Landau level spectrum has an unusual pattern of degeneracy and interesting features
    due to the unique underlying band structure. This suggests that Landau level spectroscopy
    can detect and distinguish between different mechanisms of symmetry breaking in
    topological crystalline insulators.
acknowledgement: We thank V. Madhavan and Y. Okada for related collaborations, and
  P. A. Lee for discussions. M.S. was supported by P. A. Lee via Grant No. NSF DMR
  1104498. L.F. is supported by the DOE Office of Basic Energy Sciences, Division
  of Materials Sciences and Engineering under award DE-SC0010526.
author:
- first_name: Maksym
  full_name: Maksym Serbyn
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
- first_name: Liang
  full_name: Fu, Liang
  last_name: Fu
citation:
  ama: Serbyn M, Fu L. Symmetry breaking and Landau quantization in topological crystalline
    insulators. <i>Physical Review B - Condensed Matter and Materials Physics</i>.
    2014;90(3). doi:<a href="https://doi.org/10.1103/PhysRevB.90.035402">10.1103/PhysRevB.90.035402</a>
  apa: Serbyn, M., &#38; Fu, L. (2014). Symmetry breaking and Landau quantization
    in topological crystalline insulators. <i>Physical Review B - Condensed Matter
    and Materials Physics</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevB.90.035402">https://doi.org/10.1103/PhysRevB.90.035402</a>
  chicago: Serbyn, Maksym, and Liang Fu. “Symmetry Breaking and Landau Quantization
    in Topological Crystalline Insulators.” <i>Physical Review B - Condensed Matter
    and Materials Physics</i>. American Physical Society, 2014. <a href="https://doi.org/10.1103/PhysRevB.90.035402">https://doi.org/10.1103/PhysRevB.90.035402</a>.
  ieee: M. Serbyn and L. Fu, “Symmetry breaking and Landau quantization in topological
    crystalline insulators,” <i>Physical Review B - Condensed Matter and Materials
    Physics</i>, vol. 90, no. 3. American Physical Society, 2014.
  ista: Serbyn M, Fu L. 2014. Symmetry breaking and Landau quantization in topological
    crystalline insulators. Physical Review B - Condensed Matter and Materials Physics.
    90(3).
  mla: Serbyn, Maksym, and Liang Fu. “Symmetry Breaking and Landau Quantization in
    Topological Crystalline Insulators.” <i>Physical Review B - Condensed Matter and
    Materials Physics</i>, vol. 90, no. 3, American Physical Society, 2014, doi:<a
    href="https://doi.org/10.1103/PhysRevB.90.035402">10.1103/PhysRevB.90.035402</a>.
  short: M. Serbyn, L. Fu, Physical Review B - Condensed Matter and Materials Physics
    90 (2014).
date_created: 2018-12-11T11:49:31Z
date_published: 2014-07-03T00:00:00Z
date_updated: 2021-01-12T08:22:23Z
day: '03'
doi: 10.1103/PhysRevB.90.035402
extern: 1
intvolume: '        90'
issue: '3'
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1403.8153
month: '07'
oa: 1
publication: Physical Review B - Condensed Matter and Materials Physics
publication_status: published
publisher: American Physical Society
publist_id: '6422'
quality_controlled: 0
status: public
title: Symmetry breaking and Landau quantization in topological crystalline insulators
type: journal_article
volume: 90
year: '2014'
...
