---
_id: '594'
abstract:
- lang: eng
  text: Transcription of eukaryotic protein-coding genes commences with the assembly
    of a conserved initiation complex, which consists of RNA polymerase II (Pol II)
    and the general transcription factors, at promoter DNA. After two decades of research,
    the structural basis of transcription initiation is emerging. Crystal structures
    of many components of the initiation complex have been resolved, and structural
    information on Pol II complexes with general transcription factors has recently
    been obtained. Although mechanistic details await elucidation, available data
    outline how Pol II cooperates with the general transcription factors to bind to
    and open promoter DNA, and how Pol II directs RNA synthesis and escapes from the
    promoter.
article_processing_charge: No
author:
- first_name: Sarah
  full_name: Sainsbury, Sarah
  last_name: Sainsbury
- first_name: Carrie A
  full_name: Bernecky, Carrie A
  id: 2CB9DFE2-F248-11E8-B48F-1D18A9856A87
  last_name: Bernecky
  orcid: 0000-0003-0893-7036
- first_name: Patrick
  full_name: Cramer, Patrick
  last_name: Cramer
citation:
  ama: Sainsbury S, Bernecky C, Cramer P. Structural basis of transcription initiation
    by RNA polymerase II. <i>Nature Reviews Molecular Cell Biology</i>. 2015;16(3):129-143.
    doi:<a href="https://doi.org/10.1038/nrm3952">10.1038/nrm3952</a>
  apa: Sainsbury, S., Bernecky, C., &#38; Cramer, P. (2015). Structural basis of transcription
    initiation by RNA polymerase II. <i>Nature Reviews Molecular Cell Biology</i>.
    Nature Publishing Group. <a href="https://doi.org/10.1038/nrm3952">https://doi.org/10.1038/nrm3952</a>
  chicago: Sainsbury, Sarah, Carrie Bernecky, and Patrick Cramer. “Structural Basis
    of Transcription Initiation by RNA Polymerase II.” <i>Nature Reviews Molecular
    Cell Biology</i>. Nature Publishing Group, 2015. <a href="https://doi.org/10.1038/nrm3952">https://doi.org/10.1038/nrm3952</a>.
  ieee: S. Sainsbury, C. Bernecky, and P. Cramer, “Structural basis of transcription
    initiation by RNA polymerase II,” <i>Nature Reviews Molecular Cell Biology</i>,
    vol. 16, no. 3. Nature Publishing Group, pp. 129–143, 2015.
  ista: Sainsbury S, Bernecky C, Cramer P. 2015. Structural basis of transcription
    initiation by RNA polymerase II. Nature Reviews Molecular Cell Biology. 16(3),
    129–143.
  mla: Sainsbury, Sarah, et al. “Structural Basis of Transcription Initiation by RNA
    Polymerase II.” <i>Nature Reviews Molecular Cell Biology</i>, vol. 16, no. 3,
    Nature Publishing Group, 2015, pp. 129–43, doi:<a href="https://doi.org/10.1038/nrm3952">10.1038/nrm3952</a>.
  short: S. Sainsbury, C. Bernecky, P. Cramer, Nature Reviews Molecular Cell Biology
    16 (2015) 129–143.
date_created: 2018-12-11T11:47:23Z
date_published: 2015-03-26T00:00:00Z
date_updated: 2021-01-12T08:05:16Z
day: '26'
doi: 10.1038/nrm3952
extern: '1'
intvolume: '        16'
issue: '3'
language:
- iso: eng
month: '03'
oa_version: None
page: 129 - 143
publication: Nature Reviews Molecular Cell Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '7206'
status: public
title: Structural basis of transcription initiation by RNA polymerase II
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2015'
...
---
_id: '6118'
abstract:
- lang: eng
  text: 'Carbon dioxide (CO2) gradients are ubiquitous and provide animals with information
    about their environment, such as the potential presence of prey or predators.
    The nematode Caenorhabditis elegans avoids elevated CO2, and previous work identified
    three neuron pairs called “BAG,” “AFD,” and “ASE” that respond to CO2 stimuli.
    Using in vivo Ca2+ imaging and behavioral analysis, we show that C. elegans can
    detect CO2 independently of these sensory pathways. Many of the C. elegans sensory
    neurons we examined, including the AWC olfactory neurons, the ASJ and ASK gustatory
    neurons, and the ASH and ADL nociceptors, respond to a rise in CO2 with a rise
    in Ca2+. In contrast, glial sheath cells harboring the sensory endings of C. elegans’
    major chemosensory neurons exhibit strong and sustained decreases in Ca2+ in response
    to high CO2. Some of these CO2 responses appear to be cell intrinsic. Worms therefore
    may couple detection of CO2 to that of other cues at the earliest stages of sensory
    processing. We show that C. elegans persistently suppresses oviposition at high
    CO2. Hermaphrodite-specific neurons (HSNs), the executive neurons driving egg-laying,
    are tonically inhibited when CO2 is elevated. CO2 modulates the egg-laying system
    partly through the AWC olfactory neurons: High CO2 tonically activates AWC by
    a cGMP-dependent mechanism, and AWC output inhibits the HSNs. Our work shows that
    CO2 is a more complex sensory cue for C. elegans than previously thought, both
    in terms of behavior and neural circuitry.'
author:
- first_name: Lorenz A.
  full_name: Fenk, Lorenz A.
  last_name: Fenk
- first_name: Mario
  full_name: de Bono, Mario
  id: 4E3FF80E-F248-11E8-B48F-1D18A9856A87
  last_name: de Bono
  orcid: 0000-0001-8347-0443
citation:
  ama: Fenk LA, de Bono M. Environmental CO2 inhibits Caenorhabditis elegans egg-laying
    by modulating olfactory neurons and evokes widespread changes in neural activity.
    <i>Proceedings of the National Academy of Sciences</i>. 2015;112(27):E3525-E3534.
    doi:<a href="https://doi.org/10.1073/pnas.1423808112">10.1073/pnas.1423808112</a>
  apa: Fenk, L. A., &#38; de Bono, M. (2015). Environmental CO2 inhibits Caenorhabditis
    elegans egg-laying by modulating olfactory neurons and evokes widespread changes
    in neural activity. <i>Proceedings of the National Academy of Sciences</i>. National
    Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1423808112">https://doi.org/10.1073/pnas.1423808112</a>
  chicago: Fenk, Lorenz A., and Mario de Bono. “Environmental CO2 Inhibits Caenorhabditis
    Elegans Egg-Laying by Modulating Olfactory Neurons and Evokes Widespread Changes
    in Neural Activity.” <i>Proceedings of the National Academy of Sciences</i>. National
    Academy of Sciences, 2015. <a href="https://doi.org/10.1073/pnas.1423808112">https://doi.org/10.1073/pnas.1423808112</a>.
  ieee: L. A. Fenk and M. de Bono, “Environmental CO2 inhibits Caenorhabditis elegans
    egg-laying by modulating olfactory neurons and evokes widespread changes in neural
    activity,” <i>Proceedings of the National Academy of Sciences</i>, vol. 112, no.
    27. National Academy of Sciences, pp. E3525–E3534, 2015.
  ista: Fenk LA, de Bono M. 2015. Environmental CO2 inhibits Caenorhabditis elegans
    egg-laying by modulating olfactory neurons and evokes widespread changes in neural
    activity. Proceedings of the National Academy of Sciences. 112(27), E3525–E3534.
  mla: Fenk, Lorenz A., and Mario de Bono. “Environmental CO2 Inhibits Caenorhabditis
    Elegans Egg-Laying by Modulating Olfactory Neurons and Evokes Widespread Changes
    in Neural Activity.” <i>Proceedings of the National Academy of Sciences</i>, vol.
    112, no. 27, National Academy of Sciences, 2015, pp. E3525–34, doi:<a href="https://doi.org/10.1073/pnas.1423808112">10.1073/pnas.1423808112</a>.
  short: L.A. Fenk, M. de Bono, Proceedings of the National Academy of Sciences 112
    (2015) E3525–E3534.
date_created: 2019-03-19T14:15:50Z
date_published: 2015-07-07T00:00:00Z
date_updated: 2021-01-12T08:06:12Z
day: '07'
ddc:
- '570'
doi: 10.1073/pnas.1423808112
extern: '1'
external_id:
  pmid:
  - '26100886'
file:
- access_level: open_access
  checksum: 3d2da5af8d72467e382a565abc2e003d
  content_type: application/pdf
  creator: kschuh
  date_created: 2019-03-19T14:21:07Z
  date_updated: 2020-07-14T12:47:20Z
  file_id: '6119'
  file_name: 2015_PNAS_Fenk.pdf
  file_size: 2822681
  relation: main_file
file_date_updated: 2020-07-14T12:47:20Z
has_accepted_license: '1'
intvolume: '       112'
issue: '27'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: E3525-E3534
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  issn:
  - 0027-8424
  - 1091-6490
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
status: public
title: Environmental CO2 inhibits Caenorhabditis elegans egg-laying by modulating
  olfactory neurons and evokes widespread changes in neural activity
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 112
year: '2015'
...
---
_id: '6120'
abstract:
- lang: eng
  text: Brains organize behavior and physiology to optimize the response to threats
    or opportunities. We dissect how 21% O2, an indicator of surface exposure, reprograms
    C. elegans' global state, inducing sustained locomotory arousal and altering expression
    of neuropeptides, metabolic enzymes, and other non-neural genes. The URX O2-sensing
    neurons drive arousal at 21% O2 by tonically activating the RMG interneurons.
    Stimulating RMG is sufficient to switch behavioral state. Ablating the ASH, ADL,
    or ASK sensory neurons connected to RMG by gap junctions does not disrupt arousal.
    However, disrupting cation currents in these neurons curtails RMG neurosecretion
    and arousal. RMG signals high O2 by peptidergic secretion. Neuropeptide reporters
    reveal neural circuit state, as neurosecretion stimulates neuropeptide expression.
    Neural imaging in unrestrained animals shows that URX and RMG encode O2 concentration
    rather than behavior, while the activity of downstream interneurons such as AVB
    and AIY reflect both O2 levels and the behavior being executed.
article_number: e04241
author:
- first_name: Patrick
  full_name: Laurent, Patrick
  last_name: Laurent
- first_name: Zoltan
  full_name: Soltesz, Zoltan
  last_name: Soltesz
- first_name: Geoffrey M
  full_name: Nelson, Geoffrey M
  last_name: Nelson
- first_name: Changchun
  full_name: Chen, Changchun
  last_name: Chen
- first_name: Fausto
  full_name: Arellano-Carbajal, Fausto
  last_name: Arellano-Carbajal
- first_name: Emmanuel
  full_name: Levy, Emmanuel
  last_name: Levy
- first_name: Mario
  full_name: de Bono, Mario
  id: 4E3FF80E-F248-11E8-B48F-1D18A9856A87
  last_name: de Bono
  orcid: 0000-0001-8347-0443
citation:
  ama: Laurent P, Soltesz Z, Nelson GM, et al. Decoding a neural circuit controlling
    global animal state in C. elegans. <i>eLife</i>. 2015;4. doi:<a href="https://doi.org/10.7554/elife.04241">10.7554/elife.04241</a>
  apa: Laurent, P., Soltesz, Z., Nelson, G. M., Chen, C., Arellano-Carbajal, F., Levy,
    E., &#38; de Bono, M. (2015). Decoding a neural circuit controlling global animal
    state in C. elegans. <i>ELife</i>. eLife Sciences Publications. <a href="https://doi.org/10.7554/elife.04241">https://doi.org/10.7554/elife.04241</a>
  chicago: Laurent, Patrick, Zoltan Soltesz, Geoffrey M Nelson, Changchun Chen, Fausto
    Arellano-Carbajal, Emmanuel Levy, and Mario de Bono. “Decoding a Neural Circuit
    Controlling Global Animal State in C. Elegans.” <i>ELife</i>. eLife Sciences Publications,
    2015. <a href="https://doi.org/10.7554/elife.04241">https://doi.org/10.7554/elife.04241</a>.
  ieee: P. Laurent <i>et al.</i>, “Decoding a neural circuit controlling global animal
    state in C. elegans,” <i>eLife</i>, vol. 4. eLife Sciences Publications, 2015.
  ista: Laurent P, Soltesz Z, Nelson GM, Chen C, Arellano-Carbajal F, Levy E, de Bono
    M. 2015. Decoding a neural circuit controlling global animal state in C. elegans.
    eLife. 4, e04241.
  mla: Laurent, Patrick, et al. “Decoding a Neural Circuit Controlling Global Animal
    State in C. Elegans.” <i>ELife</i>, vol. 4, e04241, eLife Sciences Publications,
    2015, doi:<a href="https://doi.org/10.7554/elife.04241">10.7554/elife.04241</a>.
  short: P. Laurent, Z. Soltesz, G.M. Nelson, C. Chen, F. Arellano-Carbajal, E. Levy,
    M. de Bono, ELife 4 (2015).
date_created: 2019-03-19T14:23:51Z
date_published: 2015-03-11T00:00:00Z
date_updated: 2021-01-12T08:06:13Z
day: '11'
ddc:
- '570'
doi: 10.7554/elife.04241
extern: '1'
external_id:
  pmid:
  - '25760081'
file:
- access_level: open_access
  checksum: cf641b7a363aecd0a101755d23dee7e0
  content_type: application/pdf
  creator: kschuh
  date_created: 2019-03-19T14:29:43Z
  date_updated: 2020-07-14T12:47:20Z
  file_id: '6121'
  file_name: 2015_elife_Laurent.pdf
  file_size: 6723528
  relation: main_file
file_date_updated: 2020-07-14T12:47:20Z
has_accepted_license: '1'
intvolume: '         4'
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '03'
oa: 1
oa_version: Published Version
pmid: 1
publication: eLife
publication_identifier:
  issn:
  - 2050-084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
status: public
title: Decoding a neural circuit controlling global animal state in C. elegans
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: 4
year: '2015'
...
---
_id: '6507'
abstract:
- lang: eng
  text: The osteoclast-associated receptor (OSCAR) is a collagen-binding immune receptor
    with important roles in dendritic cell maturation and activation of inflammatory
    monocytes as well as in osteoclastogenesis. The crystal structure of the OSCAR
    ectodomain is presented, both free and in complex with a consensus triple-helical
    peptide (THP). The structures revealed a collagen-binding site in each immunoglobulin-like
    domain (D1 and D2). The THP binds near a predicted collagen-binding groove in
    D1, but a more extensive interaction with D2 is facilitated by the unusually wide
    D1-D2 interdomain angle in OSCAR. Direct binding assays, combined with site-directed
    mutagenesis, confirm that the primary collagen-binding site in OSCAR resides in
    D2, in marked contrast to the related collagen receptors, glycoprotein VI (GPVI)
    and leukocyte-associated immunoglobulin-like receptor-1 (LAIR-1). Monomeric OSCAR
    D1D2 binds to the consensus THP with a KD of 28 µM measured in solution, but shows
    a higher affinity (KD 1.5 μM) when binding to a solid-phase THP, most likely due
    to an avidity effect. These data suggest a 2-stage model for the interaction of
    OSCAR with a collagen fibril, with transient, low-affinity interactions initiated
    by the membrane-distal D1, followed by firm adhesion to the primary binding site
    in D2.
author:
- first_name: Long
  full_name: Zhou, Long
  id: 3E751364-F248-11E8-B48F-1D18A9856A87
  last_name: Zhou
  orcid: 0000-0002-1864-8951
- first_name: J. M.
  full_name: Hinerman, J. M.
  last_name: Hinerman
- first_name: M.
  full_name: Blaszczyk, M.
  last_name: Blaszczyk
- first_name: J. L. C.
  full_name: Miller, J. L. C.
  last_name: Miller
- first_name: D. G.
  full_name: Conrady, D. G.
  last_name: Conrady
- first_name: A. D.
  full_name: Barrow, A. D.
  last_name: Barrow
- first_name: D. Y.
  full_name: Chirgadze, D. Y.
  last_name: Chirgadze
- first_name: D.
  full_name: Bihan, D.
  last_name: Bihan
- first_name: R. W.
  full_name: Farndale, R. W.
  last_name: Farndale
- first_name: A. B.
  full_name: Herr, A. B.
  last_name: Herr
citation:
  ama: Zhou L, Hinerman JM, Blaszczyk M, et al. Structural basis for collagen recognition
    by the immune receptor OSCAR. <i>Blood</i>. 2015;127(5):529-537. doi:<a href="https://doi.org/10.1182/blood-2015-08-667055">10.1182/blood-2015-08-667055</a>
  apa: Zhou, L., Hinerman, J. M., Blaszczyk, M., Miller, J. L. C., Conrady, D. G.,
    Barrow, A. D., … Herr, A. B. (2015). Structural basis for collagen recognition
    by the immune receptor OSCAR. <i>Blood</i>. American Society of Hematology. <a
    href="https://doi.org/10.1182/blood-2015-08-667055">https://doi.org/10.1182/blood-2015-08-667055</a>
  chicago: Zhou, Long, J. M. Hinerman, M. Blaszczyk, J. L. C. Miller, D. G. Conrady,
    A. D. Barrow, D. Y. Chirgadze, D. Bihan, R. W. Farndale, and A. B. Herr. “Structural
    Basis for Collagen Recognition by the Immune Receptor OSCAR.” <i>Blood</i>. American
    Society of Hematology, 2015. <a href="https://doi.org/10.1182/blood-2015-08-667055">https://doi.org/10.1182/blood-2015-08-667055</a>.
  ieee: L. Zhou <i>et al.</i>, “Structural basis for collagen recognition by the immune
    receptor OSCAR,” <i>Blood</i>, vol. 127, no. 5. American Society of Hematology,
    pp. 529–537, 2015.
  ista: Zhou L, Hinerman JM, Blaszczyk M, Miller JLC, Conrady DG, Barrow AD, Chirgadze
    DY, Bihan D, Farndale RW, Herr AB. 2015. Structural basis for collagen recognition
    by the immune receptor OSCAR. Blood. 127(5), 529–537.
  mla: Zhou, Long, et al. “Structural Basis for Collagen Recognition by the Immune
    Receptor OSCAR.” <i>Blood</i>, vol. 127, no. 5, American Society of Hematology,
    2015, pp. 529–37, doi:<a href="https://doi.org/10.1182/blood-2015-08-667055">10.1182/blood-2015-08-667055</a>.
  short: L. Zhou, J.M. Hinerman, M. Blaszczyk, J.L.C. Miller, D.G. Conrady, A.D. Barrow,
    D.Y. Chirgadze, D. Bihan, R.W. Farndale, A.B. Herr, Blood 127 (2015) 529–537.
date_created: 2019-05-31T09:38:50Z
date_published: 2015-11-02T00:00:00Z
date_updated: 2021-01-12T08:07:47Z
day: '02'
doi: 10.1182/blood-2015-08-667055
extern: '1'
external_id:
  pmid:
  - '26552697'
intvolume: '       127'
issue: '5'
language:
- iso: eng
month: '11'
oa_version: None
page: 529-537
pmid: 1
publication: Blood
publication_identifier:
  issn:
  - 0006-4971
  - 1528-0020
publication_status: published
publisher: American Society of Hematology
quality_controlled: '1'
status: public
title: Structural basis for collagen recognition by the immune receptor OSCAR
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 127
year: '2015'
...
---
_id: '6736'
abstract:
- lang: eng
  text: Motivated by the significant performance gains which polar codes experience
    under successive cancellation list decoding, their scaling exponent is studied
    as a function of the list size. In particular, the error probability is fixed,
    and the tradeoff between the block length and back-off from capacity is analyzed.
    A lower bound is provided on the error probability under MAP decoding with list
    size L for any binary-input memoryless output-symmetric channel and for any class
    of linear codes such that their minimum distance is unbounded as the block length
    grows large. Then, it is shown that under MAP decoding, although the introduction
    of a list can significantly improve the involved constants, the scaling exponent
    itself, i.e., the speed at which capacity is approached, stays unaffected for
    any finite list size. In particular, this result applies to polar codes, since
    their minimum distance tends to infinity as the block length increases. A similar
    result is proved for genie-aided successive cancellation decoding when transmission
    takes place over the binary erasure channel, namely, the scaling exponent remains
    constant for any fixed number of helps from the genie. Note that since genie-aided
    successive cancellation decoding might be strictly worse than successive cancellation
    list decoding, the problem of establishing the scaling exponent of the latter
    remains open.
arxiv: 1
author:
- first_name: Marco
  full_name: Mondelli, Marco
  id: 27EB676C-8706-11E9-9510-7717E6697425
  last_name: Mondelli
  orcid: 0000-0002-3242-7020
- first_name: Hamed
  full_name: Hassani, Hamed
  last_name: Hassani
- first_name: Rudiger
  full_name: Urbanke, Rudiger
  last_name: Urbanke
citation:
  ama: Mondelli M, Hassani H, Urbanke R. Scaling exponent of list decoders with applications
    to polar codes. <i>IEEE Transactions on Information Theory</i>. 2015;61(9):4838-4851.
    doi:<a href="https://doi.org/10.1109/tit.2015.2453315">10.1109/tit.2015.2453315</a>
  apa: Mondelli, M., Hassani, H., &#38; Urbanke, R. (2015). Scaling exponent of list
    decoders with applications to polar codes. <i>IEEE Transactions on Information
    Theory</i>. IEEE. <a href="https://doi.org/10.1109/tit.2015.2453315">https://doi.org/10.1109/tit.2015.2453315</a>
  chicago: Mondelli, Marco, Hamed Hassani, and Rudiger Urbanke. “Scaling Exponent
    of List Decoders with Applications to Polar Codes.” <i>IEEE Transactions on Information
    Theory</i>. IEEE, 2015. <a href="https://doi.org/10.1109/tit.2015.2453315">https://doi.org/10.1109/tit.2015.2453315</a>.
  ieee: M. Mondelli, H. Hassani, and R. Urbanke, “Scaling exponent of list decoders
    with applications to polar codes,” <i>IEEE Transactions on Information Theory</i>,
    vol. 61, no. 9. IEEE, pp. 4838–4851, 2015.
  ista: Mondelli M, Hassani H, Urbanke R. 2015. Scaling exponent of list decoders
    with applications to polar codes. IEEE Transactions on Information Theory. 61(9),
    4838–4851.
  mla: Mondelli, Marco, et al. “Scaling Exponent of List Decoders with Applications
    to Polar Codes.” <i>IEEE Transactions on Information Theory</i>, vol. 61, no.
    9, IEEE, 2015, pp. 4838–51, doi:<a href="https://doi.org/10.1109/tit.2015.2453315">10.1109/tit.2015.2453315</a>.
  short: M. Mondelli, H. Hassani, R. Urbanke, IEEE Transactions on Information Theory
    61 (2015) 4838–4851.
date_created: 2019-07-31T06:50:34Z
date_published: 2015-09-01T00:00:00Z
date_updated: 2021-01-12T08:08:45Z
day: '01'
doi: 10.1109/tit.2015.2453315
extern: '1'
external_id:
  arxiv:
  - '1304.5220'
intvolume: '        61'
issue: '9'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1304.5220
month: '09'
oa: 1
oa_version: Preprint
page: 4838-4851
publication: IEEE Transactions on Information Theory
publication_status: published
publisher: IEEE
quality_controlled: '1'
status: public
title: Scaling exponent of list decoders with applications to polar codes
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 61
year: '2015'
...
---
_id: '6737'
abstract:
- lang: eng
  text: This paper presents polar coding schemes for the two-user discrete memoryless
    broadcast channel (DM-BC) which achieve Marton's region with both common and private
    messages. This is the best achievable rate region known to date, and it is tight
    for all classes of two-user DM-BCs whose capacity regions are known. To accomplish
    this task, we first construct polar codes for both the superposition as well as
    binning strategy. By combining these two schemes, we obtain Marton's region with
    private messages only. Finally, we show how to handle the case of common information.
    The proposed coding schemes possess the usual advantages of polar codes, i.e.,
    they have low encoding and decoding complexity and a superpolynomial decay rate
    of the error probability. We follow the lead of Goela, Abbe, and Gastpar, who
    recently introduced polar codes emulating the superposition and binning schemes.
    To align the polar indices, for both schemes, their solution involves some degradedness
    constraints that are assumed to hold between the auxiliary random variables and
    channel outputs. To remove these constraints, we consider the transmission of
    k blocks and employ a chaining construction that guarantees the proper alignment
    of the polarized indices. The techniques described in this paper are quite general,
    and they can be adopted to many other multiterminal scenarios whenever there polar
    indices need to be aligned.
arxiv: 1
author:
- first_name: Marco
  full_name: Mondelli, Marco
  id: 27EB676C-8706-11E9-9510-7717E6697425
  last_name: Mondelli
  orcid: 0000-0002-3242-7020
- first_name: Hamed
  full_name: Hassani, Hamed
  last_name: Hassani
- first_name: Igal
  full_name: Sason, Igal
  last_name: Sason
- first_name: Rudiger
  full_name: Urbanke, Rudiger
  last_name: Urbanke
citation:
  ama: Mondelli M, Hassani H, Sason I, Urbanke R. Achieving Marton’s region for broadcast
    channels using polar codes. <i>IEEE Transactions on Information Theory</i>. 2015;61(2):783-800.
    doi:<a href="https://doi.org/10.1109/tit.2014.2368555">10.1109/tit.2014.2368555</a>
  apa: Mondelli, M., Hassani, H., Sason, I., &#38; Urbanke, R. (2015). Achieving Marton’s
    region for broadcast channels using polar codes. <i>IEEE Transactions on Information
    Theory</i>. IEEE. <a href="https://doi.org/10.1109/tit.2014.2368555">https://doi.org/10.1109/tit.2014.2368555</a>
  chicago: Mondelli, Marco, Hamed Hassani, Igal Sason, and Rudiger Urbanke. “Achieving
    Marton’s Region for Broadcast Channels Using Polar Codes.” <i>IEEE Transactions
    on Information Theory</i>. IEEE, 2015. <a href="https://doi.org/10.1109/tit.2014.2368555">https://doi.org/10.1109/tit.2014.2368555</a>.
  ieee: M. Mondelli, H. Hassani, I. Sason, and R. Urbanke, “Achieving Marton’s region
    for broadcast channels using polar codes,” <i>IEEE Transactions on Information
    Theory</i>, vol. 61, no. 2. IEEE, pp. 783–800, 2015.
  ista: Mondelli M, Hassani H, Sason I, Urbanke R. 2015. Achieving Marton’s region
    for broadcast channels using polar codes. IEEE Transactions on Information Theory.
    61(2), 783–800.
  mla: Mondelli, Marco, et al. “Achieving Marton’s Region for Broadcast Channels Using
    Polar Codes.” <i>IEEE Transactions on Information Theory</i>, vol. 61, no. 2,
    IEEE, 2015, pp. 783–800, doi:<a href="https://doi.org/10.1109/tit.2014.2368555">10.1109/tit.2014.2368555</a>.
  short: M. Mondelli, H. Hassani, I. Sason, R. Urbanke, IEEE Transactions on Information
    Theory 61 (2015) 783–800.
date_created: 2019-07-31T07:03:38Z
date_published: 2015-02-01T00:00:00Z
date_updated: 2021-01-12T08:08:46Z
day: '01'
doi: 10.1109/tit.2014.2368555
extern: '1'
external_id:
  arxiv:
  - '1401.6060'
intvolume: '        61'
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1401.6060
month: '02'
oa: 1
oa_version: Preprint
page: 783-800
publication: IEEE Transactions on Information Theory
publication_status: published
publisher: IEEE
quality_controlled: '1'
status: public
title: Achieving Marton’s region for broadcast channels using polar codes
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 61
year: '2015'
...
---
_id: '7070'
abstract:
- lang: eng
  text: 'Torque magnetization measurements on YBa2Cu3Oy (YBCO) at doping y=6.67 (p=0.12),
    in dc fields (B) up to 33 T and temperatures down to 4.5 K, show that weak diamagnetism
    persists above the extrapolated irreversibility field Hirr(T=0)≈24 T. The differential
    susceptibility dM/dB, however, is more rapidly suppressed for B≳16 T than expected
    from the properties of the low field superconducting state, and saturates at a
    low value for fields B≳24 T. In addition, torque measurements on a p=0.11 YBCO
    crystal in pulsed field up to 65 T and temperatures down to 8 K show similar behavior,
    with no additional features at higher fields. We offer two candidate scenarios
    to explain these observations: (a) superconductivity survives but is heavily suppressed
    at high field by competition with charge-density-wave (CDW) order; (b) static
    superconductivity disappears near 24 T and is followed by a region of fluctuating
    superconductivity, which causes dM/dB to saturate at high field. The diamagnetic
    signal observed above 50 T for the p=0.11 crystal at 40 K and below may be caused
    by changes in the normal state susceptibility rather than bulk or fluctuating
    superconductivity. There will be orbital (Landau) diamagnetism from electron pockets
    and possibly a reduction in spin susceptibility caused by the stronger three-dimensional
    ordered CDW.'
article_number: '180509'
article_processing_charge: No
article_type: original
author:
- first_name: Jing Fei
  full_name: Yu, Jing Fei
  last_name: Yu
- first_name: B. J.
  full_name: Ramshaw, B. J.
  last_name: Ramshaw
- first_name: I.
  full_name: Kokanović, I.
  last_name: Kokanović
- first_name: Kimberly A
  full_name: Modic, Kimberly A
  id: 13C26AC0-EB69-11E9-87C6-5F3BE6697425
  last_name: Modic
  orcid: 0000-0001-9760-3147
- first_name: N.
  full_name: Harrison, N.
  last_name: Harrison
- first_name: James
  full_name: Day, James
  last_name: Day
- first_name: Ruixing
  full_name: Liang, Ruixing
  last_name: Liang
- first_name: W. N.
  full_name: Hardy, W. N.
  last_name: Hardy
- first_name: D. A.
  full_name: Bonn, D. A.
  last_name: Bonn
- first_name: A.
  full_name: McCollam, A.
  last_name: McCollam
- first_name: S. R.
  full_name: Julian, S. R.
  last_name: Julian
- first_name: J. R.
  full_name: Cooper, J. R.
  last_name: Cooper
citation:
  ama: Yu JF, Ramshaw BJ, Kokanović I, et al. Magnetization of underdoped YBa2Cu3Oy
    above the irreversibility field. <i>Physical Review B</i>. 2015;92(18). doi:<a
    href="https://doi.org/10.1103/physrevb.92.180509">10.1103/physrevb.92.180509</a>
  apa: Yu, J. F., Ramshaw, B. J., Kokanović, I., Modic, K. A., Harrison, N., Day,
    J., … Cooper, J. R. (2015). Magnetization of underdoped YBa2Cu3Oy above the irreversibility
    field. <i>Physical Review B</i>. APS. <a href="https://doi.org/10.1103/physrevb.92.180509">https://doi.org/10.1103/physrevb.92.180509</a>
  chicago: Yu, Jing Fei, B. J. Ramshaw, I. Kokanović, Kimberly A Modic, N. Harrison,
    James Day, Ruixing Liang, et al. “Magnetization of Underdoped YBa2Cu3Oy above
    the Irreversibility Field.” <i>Physical Review B</i>. APS, 2015. <a href="https://doi.org/10.1103/physrevb.92.180509">https://doi.org/10.1103/physrevb.92.180509</a>.
  ieee: J. F. Yu <i>et al.</i>, “Magnetization of underdoped YBa2Cu3Oy above the irreversibility
    field,” <i>Physical Review B</i>, vol. 92, no. 18. APS, 2015.
  ista: Yu JF, Ramshaw BJ, Kokanović I, Modic KA, Harrison N, Day J, Liang R, Hardy
    WN, Bonn DA, McCollam A, Julian SR, Cooper JR. 2015. Magnetization of underdoped
    YBa2Cu3Oy above the irreversibility field. Physical Review B. 92(18), 180509.
  mla: Yu, Jing Fei, et al. “Magnetization of Underdoped YBa2Cu3Oy above the Irreversibility
    Field.” <i>Physical Review B</i>, vol. 92, no. 18, 180509, APS, 2015, doi:<a href="https://doi.org/10.1103/physrevb.92.180509">10.1103/physrevb.92.180509</a>.
  short: J.F. Yu, B.J. Ramshaw, I. Kokanović, K.A. Modic, N. Harrison, J. Day, R.
    Liang, W.N. Hardy, D.A. Bonn, A. McCollam, S.R. Julian, J.R. Cooper, Physical
    Review B 92 (2015).
date_created: 2019-11-19T13:22:06Z
date_published: 2015-11-23T00:00:00Z
date_updated: 2021-01-12T08:11:42Z
day: '23'
doi: 10.1103/physrevb.92.180509
extern: '1'
intvolume: '        92'
issue: '18'
language:
- iso: eng
month: '11'
oa_version: None
publication: Physical Review B
publication_identifier:
  issn:
  - 1098-0121
  - 1550-235X
publication_status: published
publisher: APS
quality_controlled: '1'
status: public
title: Magnetization of underdoped YBa2Cu3Oy above the irreversibility field
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 92
year: '2015'
...
---
_id: '7456'
abstract:
- lang: eng
  text: The rational design of monodisperse ferroelectric nanocrystals with controlled
    size and shape and their organization into hierarchical structures has been a
    critical step for understanding the polar ordering in nanoscale ferroelectrics,
    as well as the design of nanocrystal-based functional materials which harness
    the properties of individual nanoparticles and the collective interactions between
    them. We report here on the synthesis and self-assembly of aggregate-free, single-crystalline
    titanium-based perovskite nanoparticles with controlled morphology and surface
    composition by using a simple, easily scalable and highly versatile colloidal
    route. Single-crystalline, non-aggregated BaTiO3 colloidal nanocrystals, used
    as a model system, have been prepared under solvothermal conditions at temperatures
    as low as 180 °C. The shape of the nanocrystals was tuned from spheroidal to cubic
    upon changing the polarity of the solvent, whereas their size was varied from
    16 to 30 nm for spheres and 5 to 78 nm for cubes by changing the concentration
    of the precursors and the reaction time, respectively. The hydrophobic, oleic
    acid-passivated nanoparticles exhibit very good solubility in non-polar solvents
    and can be rendered dispersible in polar solvents by a simple process involving
    the oxidative cleavage of the double bond upon treating the nanopowders with the
    Lemieux–von Rudloff reagent. Lattice dynamic analysis indicated that regardless
    of their size, BaTiO3 nanocrystals present local disorder within the perovskite
    unit cell, associated with the existence of polar ordering. We also demonstrate
    for the first time that, in addition to being used for fabricating large area,
    crack-free, highly uniform films, BaTiO3 nanocubes can serve as building blocks
    for the design of 2D and 3D mesoscale structures, such as superlattices and superparticles.
    Interestingly, the type of superlattice structure (simple cubic or face centered
    cubic) appears to be determined by the type of solvent in which the nanocrystals
    were dispersed. This approach provides an excellent platform for the synthesis
    of other titanium-based perovskite colloidal nanocrystals with controlled chemical
    composition, surface structure and morphology and for their assembly into complex
    architectures, therefore opening the door for the design of novel mesoscale functional
    materials/nanocomposites with potential applications in energy conversion, data
    storage and the biomedical field.
article_processing_charge: No
article_type: original
author:
- first_name: Daniela
  full_name: Caruntu, Daniela
  last_name: Caruntu
- first_name: Taha
  full_name: Rostamzadeh, Taha
  last_name: Rostamzadeh
- first_name: Tommaso
  full_name: Costanzo, Tommaso
  id: D93824F4-D9BA-11E9-BB12-F207E6697425
  last_name: Costanzo
  orcid: 0000-0001-9732-3815
- first_name: Saman
  full_name: Salemizadeh Parizi, Saman
  last_name: Salemizadeh Parizi
- first_name: Gabriel
  full_name: Caruntu, Gabriel
  last_name: Caruntu
citation:
  ama: Caruntu D, Rostamzadeh T, Costanzo T, Salemizadeh Parizi S, Caruntu G. Solvothermal
    synthesis and controlled self-assembly of monodisperse titanium-based perovskite
    colloidal nanocrystals. <i>Nanoscale</i>. 2015;7(30):12955-12969. doi:<a href="https://doi.org/10.1039/c5nr00737b">10.1039/c5nr00737b</a>
  apa: Caruntu, D., Rostamzadeh, T., Costanzo, T., Salemizadeh Parizi, S., &#38; Caruntu,
    G. (2015). Solvothermal synthesis and controlled self-assembly of monodisperse
    titanium-based perovskite colloidal nanocrystals. <i>Nanoscale</i>. RSC. <a href="https://doi.org/10.1039/c5nr00737b">https://doi.org/10.1039/c5nr00737b</a>
  chicago: Caruntu, Daniela, Taha Rostamzadeh, Tommaso Costanzo, Saman Salemizadeh
    Parizi, and Gabriel Caruntu. “Solvothermal Synthesis and Controlled Self-Assembly
    of Monodisperse Titanium-Based Perovskite Colloidal Nanocrystals.” <i>Nanoscale</i>.
    RSC, 2015. <a href="https://doi.org/10.1039/c5nr00737b">https://doi.org/10.1039/c5nr00737b</a>.
  ieee: D. Caruntu, T. Rostamzadeh, T. Costanzo, S. Salemizadeh Parizi, and G. Caruntu,
    “Solvothermal synthesis and controlled self-assembly of monodisperse titanium-based
    perovskite colloidal nanocrystals,” <i>Nanoscale</i>, vol. 7, no. 30. RSC, pp.
    12955–12969, 2015.
  ista: Caruntu D, Rostamzadeh T, Costanzo T, Salemizadeh Parizi S, Caruntu G. 2015.
    Solvothermal synthesis and controlled self-assembly of monodisperse titanium-based
    perovskite colloidal nanocrystals. Nanoscale. 7(30), 12955–12969.
  mla: Caruntu, Daniela, et al. “Solvothermal Synthesis and Controlled Self-Assembly
    of Monodisperse Titanium-Based Perovskite Colloidal Nanocrystals.” <i>Nanoscale</i>,
    vol. 7, no. 30, RSC, 2015, pp. 12955–69, doi:<a href="https://doi.org/10.1039/c5nr00737b">10.1039/c5nr00737b</a>.
  short: D. Caruntu, T. Rostamzadeh, T. Costanzo, S. Salemizadeh Parizi, G. Caruntu,
    Nanoscale 7 (2015) 12955–12969.
date_created: 2020-02-05T14:16:37Z
date_published: 2015-08-14T00:00:00Z
date_updated: 2023-02-23T13:08:24Z
day: '14'
doi: 10.1039/c5nr00737b
extern: '1'
external_id:
  pmid:
  - '26168304'
intvolume: '         7'
issue: '30'
language:
- iso: eng
month: '08'
oa_version: None
page: 12955-12969
pmid: 1
publication: Nanoscale
publication_identifier:
  issn:
  - 2040-3364
  - 2040-3372
publication_status: published
publisher: RSC
quality_controlled: '1'
status: public
title: Solvothermal synthesis and controlled self-assembly of monodisperse titanium-based
  perovskite colloidal nanocrystals
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2015'
...
---
_id: '7457'
abstract:
- lang: eng
  text: A new organic–inorganic ferroelectric hybrid capacitor designed by uniformly
    incorporating surface modified monodisperse 15 nm ferroelectric BaTiO3 nanocubes
    into non-polar polymer blends of poly(methyl methacrylate) (PMMA) polymer and
    acrylonitrile-butadiene-styrene (ABS) terpolymer is described. The investigation
    of spatial distribution of nanofillers via a non-distractive thermal pulse method
    illustrates that the surface functionalization of nanocubes plays a key role in
    the uniform distribution of charge polarization within the polymer matrix. The
    discharged energy density of the nanocomposite with 30 vol% BaTiO3 nanocubes is
    ∼44 × 10−3 J cm−3, which is almost six times higher than that of the neat polymer.
    The facile processing, along with the superior mechanical and electrical properties
    of the BaTiO3/PMMA–ABS nanocomposites make them suitable for implementation into
    capacitive electrical energy storage devices.
article_processing_charge: No
article_type: original
author:
- first_name: Saman Salemizadeh
  full_name: Parizi, Saman Salemizadeh
  last_name: Parizi
- first_name: Gavin
  full_name: Conley, Gavin
  last_name: Conley
- first_name: Tommaso
  full_name: Costanzo, Tommaso
  id: D93824F4-D9BA-11E9-BB12-F207E6697425
  last_name: Costanzo
  orcid: 0000-0001-9732-3815
- first_name: Bob
  full_name: Howell, Bob
  last_name: Howell
- first_name: Axel
  full_name: Mellinger, Axel
  last_name: Mellinger
- first_name: Gabriel
  full_name: Caruntu, Gabriel
  last_name: Caruntu
citation:
  ama: Parizi SS, Conley G, Costanzo T, Howell B, Mellinger A, Caruntu G. Fabrication
    of barium titanate/acrylonitrile-butadiene styrene/poly(methyl methacrylate) nanocomposite
    films for hybrid ferroelectric capacitors. <i>RSC Advances</i>. 2015;5(93):76356-76362.
    doi:<a href="https://doi.org/10.1039/c5ra11347d">10.1039/c5ra11347d</a>
  apa: Parizi, S. S., Conley, G., Costanzo, T., Howell, B., Mellinger, A., &#38; Caruntu,
    G. (2015). Fabrication of barium titanate/acrylonitrile-butadiene styrene/poly(methyl
    methacrylate) nanocomposite films for hybrid ferroelectric capacitors. <i>RSC
    Advances</i>. RSC. <a href="https://doi.org/10.1039/c5ra11347d">https://doi.org/10.1039/c5ra11347d</a>
  chicago: Parizi, Saman Salemizadeh, Gavin Conley, Tommaso Costanzo, Bob Howell,
    Axel Mellinger, and Gabriel Caruntu. “Fabrication of Barium Titanate/Acrylonitrile-Butadiene
    Styrene/Poly(Methyl Methacrylate) Nanocomposite Films for Hybrid Ferroelectric
    Capacitors.” <i>RSC Advances</i>. RSC, 2015. <a href="https://doi.org/10.1039/c5ra11347d">https://doi.org/10.1039/c5ra11347d</a>.
  ieee: S. S. Parizi, G. Conley, T. Costanzo, B. Howell, A. Mellinger, and G. Caruntu,
    “Fabrication of barium titanate/acrylonitrile-butadiene styrene/poly(methyl methacrylate)
    nanocomposite films for hybrid ferroelectric capacitors,” <i>RSC Advances</i>,
    vol. 5, no. 93. RSC, pp. 76356–76362, 2015.
  ista: Parizi SS, Conley G, Costanzo T, Howell B, Mellinger A, Caruntu G. 2015. Fabrication
    of barium titanate/acrylonitrile-butadiene styrene/poly(methyl methacrylate) nanocomposite
    films for hybrid ferroelectric capacitors. RSC Advances. 5(93), 76356–76362.
  mla: Parizi, Saman Salemizadeh, et al. “Fabrication of Barium Titanate/Acrylonitrile-Butadiene
    Styrene/Poly(Methyl Methacrylate) Nanocomposite Films for Hybrid Ferroelectric
    Capacitors.” <i>RSC Advances</i>, vol. 5, no. 93, RSC, 2015, pp. 76356–62, doi:<a
    href="https://doi.org/10.1039/c5ra11347d">10.1039/c5ra11347d</a>.
  short: S.S. Parizi, G. Conley, T. Costanzo, B. Howell, A. Mellinger, G. Caruntu,
    RSC Advances 5 (2015) 76356–76362.
date_created: 2020-02-05T14:17:26Z
date_published: 2015-09-01T00:00:00Z
date_updated: 2023-02-23T13:08:26Z
day: '01'
doi: 10.1039/c5ra11347d
extern: '1'
intvolume: '         5'
issue: '93'
language:
- iso: eng
month: '09'
oa_version: Submitted Version
page: 76356-76362
publication: RSC Advances
publication_identifier:
  issn:
  - 2046-2069
publication_status: published
publisher: RSC
quality_controlled: '1'
status: public
title: Fabrication of barium titanate/acrylonitrile-butadiene styrene/poly(methyl
  methacrylate) nanocomposite films for hybrid ferroelectric capacitors
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 5
year: '2015'
...
---
_id: '982'
abstract:
- lang: eng
  text: We propose a new approach to probing ergodicity and its breakdown in one-dimensional
    quantum manybody systems based on their response to a local perturbation. We study
    the distribution of matrix elements of a local operator between the system's eigenstates,
    finding a qualitatively different behavior in the manybody localized (MBL) and
    ergodic phases. To characterize how strongly a local perturbation modifies the
    eigenstates, we introduce the parameter g(L) = (In (Vnm/δ)) which represents the
    disorder-averaged ratio of a typical matrix element of a local operator V to energy
    level spacing δ this parameter is reminiscent of the Thouless conductance in the
    single-particle localization. We show that the parameter g(L) decreases with system
    size L in the MBL phase and grows in the ergodic phase. We surmise that the delocalization
    transition occurs when g(L) is independent of system size, g(L)=gc ~ 1. We illustrate
    our approach by studying the many-body localization transition and resolving the
    many-body mobility edge in a disordered one-dimensional XXZ spin-1=2 chain using
    exact diagonalization and time-evolving block-decimation methods. Our criterion
    for the MBL transition gives insights into microscopic details of transition.
    Its direct physical consequences, in particular, logarithmically slow transport
    at the transition and extensive entanglement entropy of the eigenstates, are consistent
    with recent renormalization-group predictions.
acknowledgement: We acknowledge helpful discussions with Sid Parameswaran, Andrew
  Potter, Antonello Scardicchio, Romain Vasseur, and especially with Ehud Altman and
  David Huse. We would like to thank Miles Stoudenmire for the assistance with ITensor
  library. Research at Perimeter Institute is supported by the Government of Canada
  through Industry Canada and by the Province of Ontario through the Ministry of Economic
  Development & Innovation. This research was supported by Gordon and Betty Moore
  Foundation EPiQS Initiative through Grant No. GBMF4307 (M. S.), Sloan Foundation,
  NSERC, and Early Researcher Award of Ontario (D. A.). This work made use of the
  facilities of N8 HPC Centre of Excellence, provided and funded by the N8 consortium
  and EPSRC (Grant No. EP/K000225/1). The Centre is coordinated by the Universities
  of Leeds and Manchester.
author:
- first_name: Maksym
  full_name: Maksym Serbyn
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
- first_name: Zlatko
  full_name: Papić, Zlatko
  last_name: Papić
- first_name: Dmitry
  full_name: Abanin, Dmitry A
  last_name: Abanin
citation:
  ama: Serbyn M, Papić Z, Abanin D. Criterion for many-body localization-delocalization
    phase transition. <i>Physical Review X</i>. 2015;5(4). doi:<a href="https://doi.org/10.1103/PhysRevX.5.041047">10.1103/PhysRevX.5.041047</a>
  apa: Serbyn, M., Papić, Z., &#38; Abanin, D. (2015). Criterion for many-body localization-delocalization
    phase transition. <i>Physical Review X</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevX.5.041047">https://doi.org/10.1103/PhysRevX.5.041047</a>
  chicago: Serbyn, Maksym, Zlatko Papić, and Dmitry Abanin. “Criterion for Many-Body
    Localization-Delocalization Phase Transition.” <i>Physical Review X</i>. American
    Physical Society, 2015. <a href="https://doi.org/10.1103/PhysRevX.5.041047">https://doi.org/10.1103/PhysRevX.5.041047</a>.
  ieee: M. Serbyn, Z. Papić, and D. Abanin, “Criterion for many-body localization-delocalization
    phase transition,” <i>Physical Review X</i>, vol. 5, no. 4. American Physical
    Society, 2015.
  ista: Serbyn M, Papić Z, Abanin D. 2015. Criterion for many-body localization-delocalization
    phase transition. Physical Review X. 5(4).
  mla: Serbyn, Maksym, et al. “Criterion for Many-Body Localization-Delocalization
    Phase Transition.” <i>Physical Review X</i>, vol. 5, no. 4, American Physical
    Society, 2015, doi:<a href="https://doi.org/10.1103/PhysRevX.5.041047">10.1103/PhysRevX.5.041047</a>.
  short: M. Serbyn, Z. Papić, D. Abanin, Physical Review X 5 (2015).
date_created: 2018-12-11T11:49:32Z
date_published: 2015-01-01T00:00:00Z
date_updated: 2021-01-12T08:22:25Z
day: '01'
doi: 10.1103/PhysRevX.5.041047
extern: 1
intvolume: '         5'
issue: '4'
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1507.01635
month: '01'
oa: 1
publication: Physical Review X
publication_status: published
publisher: American Physical Society
publist_id: '6418'
quality_controlled: 0
status: public
title: Criterion for many-body localization-delocalization phase transition
type: journal_article
volume: 5
year: '2015'
...
---
_id: '99'
abstract:
- lang: eng
  text: Quasiparticle excitations can compromise the performance of superconducting
    devices, causing high-frequency dissipation, decoherence in Josephson qubits,
    and braiding errors in proposed Majorana-based topological quantum computers.
    Quasiparticle dynamics have been studied in detail in metallic superconductors
    but remain relatively unexplored in semiconductor-superconductor structures, which
    are now being intensely pursued in the context of topological superconductivity.
    To this end, we use a system comprising a gate-confined semiconductor nanowire
    with an epitaxially grown superconductor layer, yielding an isolated, proximitized
    nanowire segment. We identify bound states in the semiconductor by means of bias
    spectroscopy, determine the characteristic temperatures and magnetic fields for
    quasiparticle excitations, and extract a parity lifetime (poisoning time) of the
    bound state in the semiconductor exceeding 10 ms.
acknowledgement: Research support by Microsoft Project Q, the Danish National Research
  Foundation, the Lundbeck Foundation, the Carlsberg Foundation, and the European
  Commission. A.P.H. acknowledges support from the US Department of Energy, C.M.M.
  acknowledges support from the Villum Foundation.
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: S M
  full_name: Albrecht, S M
  last_name: Albrecht
- first_name: Gediminas
  full_name: Kiršanskas, Gediminas
  last_name: Kiršanskas
- first_name: W
  full_name: Chang, W
  last_name: Chang
- first_name: Ferdinand
  full_name: Kuemmeth, Ferdinand
  last_name: Kuemmeth
- first_name: Peter
  full_name: Krogstrup, Peter
  last_name: Krogstrup
- first_name: Thomas
  full_name: Jespersen, Thomas
  last_name: Jespersen
- first_name: Jesper
  full_name: Nygård, Jesper
  last_name: Nygård
- first_name: Karsten
  full_name: Flensberg, Karsten
  last_name: Flensberg
- first_name: Charles
  full_name: Marcus, Charles
  last_name: Marcus
citation:
  ama: Higginbotham AP, Albrecht SM, Kiršanskas G, et al. Parity lifetime of bound
    states in a proximitized semiconductor nanowire. <i>Nature Physics</i>. 2015;11(12):1017-1021.
    doi:<a href="https://doi.org/10.1038/nphys3461">10.1038/nphys3461</a>
  apa: Higginbotham, A. P., Albrecht, S. M., Kiršanskas, G., Chang, W., Kuemmeth,
    F., Krogstrup, P., … Marcus, C. (2015). Parity lifetime of bound states in a proximitized
    semiconductor nanowire. <i>Nature Physics</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/nphys3461">https://doi.org/10.1038/nphys3461</a>
  chicago: Higginbotham, Andrew P, S M Albrecht, Gediminas Kiršanskas, W Chang, Ferdinand
    Kuemmeth, Peter Krogstrup, Thomas Jespersen, Jesper Nygård, Karsten Flensberg,
    and Charles Marcus. “Parity Lifetime of Bound States in a Proximitized Semiconductor
    Nanowire.” <i>Nature Physics</i>. Nature Publishing Group, 2015. <a href="https://doi.org/10.1038/nphys3461">https://doi.org/10.1038/nphys3461</a>.
  ieee: A. P. Higginbotham <i>et al.</i>, “Parity lifetime of bound states in a proximitized
    semiconductor nanowire,” <i>Nature Physics</i>, vol. 11, no. 12. Nature Publishing
    Group, pp. 1017–1021, 2015.
  ista: Higginbotham AP, Albrecht SM, Kiršanskas G, Chang W, Kuemmeth F, Krogstrup
    P, Jespersen T, Nygård J, Flensberg K, Marcus C. 2015. Parity lifetime of bound
    states in a proximitized semiconductor nanowire. Nature Physics. 11(12), 1017–1021.
  mla: Higginbotham, Andrew P., et al. “Parity Lifetime of Bound States in a Proximitized
    Semiconductor Nanowire.” <i>Nature Physics</i>, vol. 11, no. 12, Nature Publishing
    Group, 2015, pp. 1017–21, doi:<a href="https://doi.org/10.1038/nphys3461">10.1038/nphys3461</a>.
  short: A.P. Higginbotham, S.M. Albrecht, G. Kiršanskas, W. Chang, F. Kuemmeth, P.
    Krogstrup, T. Jespersen, J. Nygård, K. Flensberg, C. Marcus, Nature Physics 11
    (2015) 1017–1021.
date_created: 2018-12-11T11:44:37Z
date_published: 2015-09-14T00:00:00Z
date_updated: 2021-01-12T08:22:28Z
day: '14'
doi: 10.1038/nphys3461
extern: '1'
external_id:
  arxiv:
  - '1501.05155'
intvolume: '        11'
issue: '12'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1501.05155
month: '09'
oa: 1
oa_version: Preprint
page: 1017 - 1021
publication: Nature Physics
publication_status: published
publisher: Nature Publishing Group
publist_id: '7955'
quality_controlled: '1'
status: public
title: Parity lifetime of bound states in a proximitized semiconductor nanowire
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 11
year: '2015'
...
---
_id: '354'
abstract:
- lang: eng
  text: 'A simple and effective method to introduce precise amounts of doping in nanomaterials
    produced from the bottom-up assembly of colloidal nanoparticles (NPs) is described.
    The procedure takes advantage of a ligand displacement step to incorporate controlled
    concentrations of halide ions while removing carboxylic acids from the NP surface.
    Upon consolidation of the NPs into dense pellets, halide ions diffuse within the
    crystal structure, doping the anion sublattice and achieving n-type electrical
    doping. Through the characterization of the thermoelectric properties of nanocrystalline
    PbS, we demonstrate this strategy to be effective to control charge transport
    properties on thermoelectric nanomaterials assembled from NP building blocks.
    This approach is subsequently extended to PbTexSe1-x@PbS core-shell NPs, where
    a significant enhancement of the thermoelectric figure of merit is achieved. '
acknowledgement: At IREC, work was supported by European Regional Development Funds
  and the Framework 7 program under project UNION (FP7-NMP 310250). M.I. and S.O.
  thank AGAUR for their Beatriu i Pinós postdoctoral grant and the PhD grant, respectively.
  At Northwestern, work was supported by the Revolutionary Materials for Solid State
  Energy Conversion, an Energy Frontier Research Center funded by the U.S. Department
  of Energy, Office of Science, and Office of Basic Energy Sciences under Award Number
  DE-SC0001054.
article_processing_charge: No
article_type: original
author:
- first_name: Maria
  full_name: Ibáñez, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibáñez
  orcid: 0000-0001-5013-2843
- first_name: Rachel
  full_name: Korkosz, Rachel
  last_name: Korkosz
- first_name: Zhishan
  full_name: Luo, Zhishan
  last_name: Luo
- first_name: Pau
  full_name: Riba, Pau
  last_name: Riba
- first_name: Doris
  full_name: Cadavid, Doris
  last_name: Cadavid
- first_name: Silvia
  full_name: Ortega, Silvia
  last_name: Ortega
- first_name: Andreu
  full_name: Cabot, Andreu
  last_name: Cabot
- first_name: Mercouri
  full_name: Kanatzidis, Mercouri
  last_name: Kanatzidis
citation:
  ama: Ibáñez M, Korkosz R, Luo Z, et al. Electron doping in bottom up engineered
    thermoelectric nanomaterials through HCl mediated ligand displacement. <i>Journal
    of the American Chemical Society</i>. 2015;137(12):4046-4049. doi:<a href="https://doi.org/10.1021/jacs.5b00091">10.1021/jacs.5b00091</a>
  apa: Ibáñez, M., Korkosz, R., Luo, Z., Riba, P., Cadavid, D., Ortega, S., … Kanatzidis,
    M. (2015). Electron doping in bottom up engineered thermoelectric nanomaterials
    through HCl mediated ligand displacement. <i>Journal of the American Chemical
    Society</i>. American Chemical Society. <a href="https://doi.org/10.1021/jacs.5b00091">https://doi.org/10.1021/jacs.5b00091</a>
  chicago: Ibáñez, Maria, Rachel Korkosz, Zhishan Luo, Pau Riba, Doris Cadavid, Silvia
    Ortega, Andreu Cabot, and Mercouri Kanatzidis. “Electron Doping in Bottom up Engineered
    Thermoelectric Nanomaterials through HCl Mediated Ligand Displacement.” <i>Journal
    of the American Chemical Society</i>. American Chemical Society, 2015. <a href="https://doi.org/10.1021/jacs.5b00091">https://doi.org/10.1021/jacs.5b00091</a>.
  ieee: M. Ibáñez <i>et al.</i>, “Electron doping in bottom up engineered thermoelectric
    nanomaterials through HCl mediated ligand displacement,” <i>Journal of the American
    Chemical Society</i>, vol. 137, no. 12. American Chemical Society, pp. 4046–4049,
    2015.
  ista: Ibáñez M, Korkosz R, Luo Z, Riba P, Cadavid D, Ortega S, Cabot A, Kanatzidis
    M. 2015. Electron doping in bottom up engineered thermoelectric nanomaterials
    through HCl mediated ligand displacement. Journal of the American Chemical Society.
    137(12), 4046–4049.
  mla: Ibáñez, Maria, et al. “Electron Doping in Bottom up Engineered Thermoelectric
    Nanomaterials through HCl Mediated Ligand Displacement.” <i>Journal of the American
    Chemical Society</i>, vol. 137, no. 12, American Chemical Society, 2015, pp. 4046–49,
    doi:<a href="https://doi.org/10.1021/jacs.5b00091">10.1021/jacs.5b00091</a>.
  short: M. Ibáñez, R. Korkosz, Z. Luo, P. Riba, D. Cadavid, S. Ortega, A. Cabot,
    M. Kanatzidis, Journal of the American Chemical Society 137 (2015) 4046–4049.
date_created: 2018-12-11T11:45:59Z
date_published: 2015-03-11T00:00:00Z
date_updated: 2021-01-12T07:44:10Z
day: '11'
doi: 10.1021/jacs.5b00091
extern: '1'
intvolume: '       137'
issue: '12'
language:
- iso: eng
month: '03'
oa_version: None
page: 4046 - 4049
publication: Journal of the American Chemical Society
publication_status: published
publisher: American Chemical Society
publist_id: '7470'
quality_controlled: '1'
status: public
title: Electron doping in bottom up engineered thermoelectric nanomaterials through
  HCl mediated ligand displacement
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 137
year: '2015'
...
---
_id: '361'
abstract:
- lang: eng
  text: We report the synthesis and photocatalytic and magnetic characterization of
    colloidal nanoheterostructures formed by combining a Pt-based magnetic metal alloy
    (PtCo, PtNi) with Cu2ZnSnS4 (CZTS). While CZTS is one of the main candidate materials
    for solar energy conversion, the introduction of a Pt-based alloy on its surface
    strongly influences its chemical and electronic properties, ultimately determining
    its functionality. In this regard, up to a 15-fold increase of the photocatalytic
    hydrogen evolution activity was obtained with CZTS–PtCo when compared with CZTS.
    Furthermore, two times higher hydrogen evolution rates were obtained for CZTS–PtCo
    when compared with CZTS–Pt, in spite of the lower precious metal loading of the
    former. Besides, the magnetic properties of the PtCo nanoparticles attached to
    the CZTS nanocrystals were retained in the heterostructures, which could facilitate
    catalyst purification and recovery for its posterior recycling and/or reutilization.
acknowledgement: This work was supported by the National Natural Science Foundation
  of China (Grant 21401212), Fundamental Research Funds for the Central Universities
  (2652015086), the Framework 7 program under project SCALENANO (FP7-NMP-ENERGY-2011-284486),
  and the MICINN project ENE2013-46624-C4-3-R. Authors acknowledge the funding from
  Generalitat de Catalunya 2014 SGR 1638.
article_processing_charge: No
author:
- first_name: Xuelian
  full_name: Yu, Xuelian
  last_name: Yu
- first_name: Xiaoqiang
  full_name: An, Xiaoqiang
  last_name: An
- first_name: Aziz
  full_name: Genç, Aziz
  last_name: Genç
- first_name: Maria
  full_name: Ibáñez, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibáñez
  orcid: 0000-0001-5013-2843
- first_name: Jordi
  full_name: Arbiol, Jordi
  last_name: Arbiol
- first_name: Yihe
  full_name: Zhang, Yihe
  last_name: Zhang
- first_name: Andreu
  full_name: Cabot, Andreu
  last_name: Cabot
citation:
  ama: Yu X, An X, Genç A, et al. Cu2ZnSnS4–PtM (M = Co, Ni) nanoheterostructures
    for photocatalytic hydrogen evolution. <i>Journal of Physical Chemistry C</i>.
    2015;119(38):21882-21888. doi:<a href="https://doi.org/10.1021/acs.jpcc.5b06199">10.1021/acs.jpcc.5b06199</a>
  apa: Yu, X., An, X., Genç, A., Ibáñez, M., Arbiol, J., Zhang, Y., &#38; Cabot, A.
    (2015). Cu2ZnSnS4–PtM (M = Co, Ni) nanoheterostructures for photocatalytic hydrogen
    evolution. <i>Journal of Physical Chemistry C</i>. American Chemical Society.
    <a href="https://doi.org/10.1021/acs.jpcc.5b06199">https://doi.org/10.1021/acs.jpcc.5b06199</a>
  chicago: Yu, Xuelian, Xiaoqiang An, Aziz Genç, Maria Ibáñez, Jordi Arbiol, Yihe
    Zhang, and Andreu Cabot. “Cu2ZnSnS4–PtM (M = Co, Ni) Nanoheterostructures for
    Photocatalytic Hydrogen Evolution.” <i>Journal of Physical Chemistry C</i>. American
    Chemical Society, 2015. <a href="https://doi.org/10.1021/acs.jpcc.5b06199">https://doi.org/10.1021/acs.jpcc.5b06199</a>.
  ieee: X. Yu <i>et al.</i>, “Cu2ZnSnS4–PtM (M = Co, Ni) nanoheterostructures for
    photocatalytic hydrogen evolution,” <i>Journal of Physical Chemistry C</i>, vol.
    119, no. 38. American Chemical Society, pp. 21882–21888, 2015.
  ista: Yu X, An X, Genç A, Ibáñez M, Arbiol J, Zhang Y, Cabot A. 2015. Cu2ZnSnS4–PtM
    (M = Co, Ni) nanoheterostructures for photocatalytic hydrogen evolution. Journal
    of Physical Chemistry C. 119(38), 21882–21888.
  mla: Yu, Xuelian, et al. “Cu2ZnSnS4–PtM (M = Co, Ni) Nanoheterostructures for Photocatalytic
    Hydrogen Evolution.” <i>Journal of Physical Chemistry C</i>, vol. 119, no. 38,
    American Chemical Society, 2015, pp. 21882–88, doi:<a href="https://doi.org/10.1021/acs.jpcc.5b06199">10.1021/acs.jpcc.5b06199</a>.
  short: X. Yu, X. An, A. Genç, M. Ibáñez, J. Arbiol, Y. Zhang, A. Cabot, Journal
    of Physical Chemistry C 119 (2015) 21882–21888.
date_created: 2018-12-11T11:46:01Z
date_published: 2015-08-26T00:00:00Z
date_updated: 2021-01-12T07:44:38Z
day: '26'
doi: 10.1021/acs.jpcc.5b06199
extern: '1'
intvolume: '       119'
issue: '38'
language:
- iso: eng
month: '08'
oa_version: None
page: 21882 - 21888
publication: Journal of Physical Chemistry C
publication_status: published
publisher: American Chemical Society
publist_id: '7468'
status: public
title: Cu2ZnSnS4–PtM (M = Co, Ni) nanoheterostructures for photocatalytic hydrogen
  evolution
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 119
year: '2015'
...
---
_id: '362'
abstract:
- lang: eng
  text: 'Monodisperse Pd2Sn nanorods with tuned size and aspect ratio were prepared
    by co-reduction of metal salts in the presence of trioctylphosphine, amine, and
    chloride ions. Asymmetric Pd2Sn nanostructures were achieved by the selective
    desorption of a surfactant mediated by chlorine ions. A preliminary evaluation
    of the geometry influence on catalytic properties evidenced Pd2Sn nanorods to
    have improved catalytic performance. In view of these results, Pd2Sn nanorods
    were also evaluated for water denitration. '
article_processing_charge: No
author:
- first_name: Zhishan
  full_name: Lu, Zhishan
  last_name: Lu
- first_name: Maria
  full_name: Ibáñez, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibáñez
  orcid: 0000-0001-5013-2843
- first_name: Ana
  full_name: Antolín, Ana
  last_name: Antolín
- first_name: Aziz
  full_name: Genç, Aziz
  last_name: Genç
- first_name: Alexey
  full_name: Shavel, Alexey
  last_name: Shavel
- first_name: Sandra
  full_name: Contreras, Sandra
  last_name: Contreras
- first_name: Francesc
  full_name: Medina, Francesc
  last_name: Medina
- first_name: Jordi
  full_name: Arbiol, Jordi
  last_name: Arbiol
- first_name: Andreu
  full_name: Cabot, Andreu
  last_name: Cabot
citation:
  ama: Lu Z, Ibáñez M, Antolín A, et al. Size and aspect ratio control of Pd inf 2
    inf Sn nanorods and their water denitration properties. <i>Langmuir</i>. 2015;31(13):3952-3957.
    doi:<a href="https://doi.org/10.1021/la504906q">10.1021/la504906q</a>
  apa: Lu, Z., Ibáñez, M., Antolín, A., Genç, A., Shavel, A., Contreras, S., … Cabot,
    A. (2015). Size and aspect ratio control of Pd inf 2 inf Sn nanorods and their
    water denitration properties. <i>Langmuir</i>. American Chemical Society. <a href="https://doi.org/10.1021/la504906q">https://doi.org/10.1021/la504906q</a>
  chicago: Lu, Zhishan, Maria Ibáñez, Ana Antolín, Aziz Genç, Alexey Shavel, Sandra
    Contreras, Francesc Medina, Jordi Arbiol, and Andreu Cabot. “Size and Aspect Ratio
    Control of Pd Inf 2 Inf Sn Nanorods and Their Water Denitration Properties.” <i>Langmuir</i>.
    American Chemical Society, 2015. <a href="https://doi.org/10.1021/la504906q">https://doi.org/10.1021/la504906q</a>.
  ieee: Z. Lu <i>et al.</i>, “Size and aspect ratio control of Pd inf 2 inf Sn nanorods
    and their water denitration properties,” <i>Langmuir</i>, vol. 31, no. 13. American
    Chemical Society, pp. 3952–3957, 2015.
  ista: Lu Z, Ibáñez M, Antolín A, Genç A, Shavel A, Contreras S, Medina F, Arbiol
    J, Cabot A. 2015. Size and aspect ratio control of Pd inf 2 inf Sn nanorods and
    their water denitration properties. Langmuir. 31(13), 3952–3957.
  mla: Lu, Zhishan, et al. “Size and Aspect Ratio Control of Pd Inf 2 Inf Sn Nanorods
    and Their Water Denitration Properties.” <i>Langmuir</i>, vol. 31, no. 13, American
    Chemical Society, 2015, pp. 3952–57, doi:<a href="https://doi.org/10.1021/la504906q">10.1021/la504906q</a>.
  short: Z. Lu, M. Ibáñez, A. Antolín, A. Genç, A. Shavel, S. Contreras, F. Medina,
    J. Arbiol, A. Cabot, Langmuir 31 (2015) 3952–3957.
date_created: 2018-12-11T11:46:02Z
date_published: 2015-04-07T00:00:00Z
date_updated: 2021-01-12T07:44:42Z
day: '07'
doi: 10.1021/la504906q
extern: '1'
intvolume: '        31'
issue: '13'
language:
- iso: eng
month: '04'
oa_version: None
page: 3952 - 3957
publication: Langmuir
publication_status: published
publisher: American Chemical Society
publist_id: '7469'
status: public
title: Size and aspect ratio control of Pd inf 2 inf Sn nanorods and their water denitration
  properties
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 31
year: '2015'
...
---
_id: '388'
abstract:
- lang: eng
  text: We use ultrafast optical spectroscopy to observe binding of charged single-particle
    excitations (SE) in the magnetically frustrated Mott insulator Na2IrO3. Above
    the antiferromagnetic ordering temperature (TN) the system response is due to
    both Hubbard excitons (HE) and their constituent unpaired SE. The SE response
    becomes strongly suppressed immediately below TN. We argue that this increase
    in binding energy is due to a unique interplay between the frustrated Kitaev and
    the weak Heisenberg-type ordering term in the Hamiltonian, mediating an effective
    interaction between the spin-singlet SE. This interaction grows with distance
    causing the SE to become trapped in the HE, similar to quark confinement inside
    hadrons. This binding of charged particles, induced by magnetic ordering, is a
    result of a confinement-deconfinement transition of spin excitations. This observation
    provides evidence for spin liquid type behavior which is expected in Na2IrO3.
article_processing_charge: No
article_type: original
author:
- first_name: Zhanybek
  full_name: Alpichshev, Zhanybek
  id: 45E67A2A-F248-11E8-B48F-1D18A9856A87
  last_name: Alpichshev
  orcid: 0000-0002-7183-5203
- first_name: Fahad
  full_name: Mahmood, Fahad
  last_name: Mahmood
- first_name: Gang
  full_name: Cao, Gang
  last_name: Cao
- first_name: Nuh
  full_name: Gedik, Nuh
  last_name: Gedik
citation:
  ama: Alpichshev Z, Mahmood F, Cao G, Gedik N. Confinement deconfinement transition
    as an indication of spin liquid type behavior in Na2IrO3. <i>Physical Review Letters</i>.
    2015;114(1). doi:<a href="https://doi.org/10.1103/PhysRevLett.114.017203">10.1103/PhysRevLett.114.017203</a>
  apa: Alpichshev, Z., Mahmood, F., Cao, G., &#38; Gedik, N. (2015). Confinement deconfinement
    transition as an indication of spin liquid type behavior in Na2IrO3. <i>Physical
    Review Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevLett.114.017203">https://doi.org/10.1103/PhysRevLett.114.017203</a>
  chicago: Alpichshev, Zhanybek, Fahad Mahmood, Gang Cao, and Nuh Gedik. “Confinement
    Deconfinement Transition as an Indication of Spin Liquid Type Behavior in Na2IrO3.”
    <i>Physical Review Letters</i>. American Physical Society, 2015. <a href="https://doi.org/10.1103/PhysRevLett.114.017203">https://doi.org/10.1103/PhysRevLett.114.017203</a>.
  ieee: Z. Alpichshev, F. Mahmood, G. Cao, and N. Gedik, “Confinement deconfinement
    transition as an indication of spin liquid type behavior in Na2IrO3,” <i>Physical
    Review Letters</i>, vol. 114, no. 1. American Physical Society, 2015.
  ista: Alpichshev Z, Mahmood F, Cao G, Gedik N. 2015. Confinement deconfinement transition
    as an indication of spin liquid type behavior in Na2IrO3. Physical Review Letters.
    114(1).
  mla: Alpichshev, Zhanybek, et al. “Confinement Deconfinement Transition as an Indication
    of Spin Liquid Type Behavior in Na2IrO3.” <i>Physical Review Letters</i>, vol.
    114, no. 1, American Physical Society, 2015, doi:<a href="https://doi.org/10.1103/PhysRevLett.114.017203">10.1103/PhysRevLett.114.017203</a>.
  short: Z. Alpichshev, F. Mahmood, G. Cao, N. Gedik, Physical Review Letters 114
    (2015).
date_created: 2018-12-11T11:46:11Z
date_published: 2015-07-07T00:00:00Z
date_updated: 2021-01-12T07:52:54Z
day: '07'
doi: 10.1103/PhysRevLett.114.017203
extern: '1'
intvolume: '       114'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://dspace.mit.edu/handle/1721.1/92979
month: '07'
oa: 1
oa_version: Published Version
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '7441'
quality_controlled: '1'
status: public
title: Confinement deconfinement transition as an indication of spin liquid type behavior
  in Na2IrO3
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 114
year: '2015'
...
---
_id: '8183'
abstract:
- lang: eng
  text: "We study conditions under which a finite simplicial complex $K$ can be mapped
    to $\\mathbb R^d$ without higher-multiplicity intersections. An almost $r$-embedding
    is a map $f: K\\to \\mathbb R^d$ such that the images of any $r$\r\npairwise disjoint
    simplices of $K$ do not have a common point. We show that if $r$ is not a prime
    power and $d\\geq 2r+1$, then there is a counterexample to the topological Tverberg
    conjecture, i.e., there is an almost $r$-embedding of\r\nthe $(d+1)(r-1)$-simplex
    in $\\mathbb R^d$. This improves on previous constructions of counterexamples
    (for $d\\geq 3r$) based on a series of papers by M. \\\"Ozaydin, M. Gromov, P.
    Blagojevi\\'c, F. Frick, G. Ziegler, and the second and fourth present authors.
    The counterexamples are obtained by proving the following algebraic criterion
    in codimension 2: If $r\\ge3$ and if $K$ is a finite $2(r-1)$-complex then there
    exists an almost $r$-embedding $K\\to \\mathbb R^{2r}$ if and only if there exists
    a general position PL map $f:K\\to \\mathbb R^{2r}$ such that the algebraic intersection
    number of the $f$-images of any $r$ pairwise disjoint simplices of $K$ is zero.
    This result can be restated in terms of cohomological obstructions or equivariant
    maps, and extends an analogous codimension 3 criterion by the second and fourth
    authors. As another application we classify ornaments $f:S^3 \\sqcup S^3\\sqcup
    S^3\\to \\mathbb R^5$ up to ornament\r\nconcordance. It follows from work of M.
    Freedman, V. Krushkal and P. Teichner that the analogous criterion for $r=2$ is
    false. We prove a lemma on singular higher-dimensional Borromean rings, yielding
    an elementary proof of the counterexample."
acknowledgement: We would like to thank A. Klyachko, V. Krushkal, S. Melikhov, M.
  Tancer, P. Teichner and anonymous referees for helpful discussions.
article_number: '1511.03501'
article_processing_charge: No
arxiv: 1
author:
- first_name: Sergey
  full_name: Avvakumov, Sergey
  id: 3827DAC8-F248-11E8-B48F-1D18A9856A87
  last_name: Avvakumov
  orcid: 0000-0002-7840-5062
- first_name: Isaac
  full_name: Mabillard, Isaac
  id: 32BF9DAA-F248-11E8-B48F-1D18A9856A87
  last_name: Mabillard
- first_name: A.
  full_name: Skopenkov, A.
  last_name: Skopenkov
- first_name: Uli
  full_name: Wagner, Uli
  id: 36690CA2-F248-11E8-B48F-1D18A9856A87
  last_name: Wagner
  orcid: 0000-0002-1494-0568
citation:
  ama: Avvakumov S, Mabillard I, Skopenkov A, Wagner U. Eliminating higher-multiplicity
    intersections, III. Codimension 2. <i>arXiv</i>. doi:<a href="https://doi.org/10.48550/arXiv.1511.03501">10.48550/arXiv.1511.03501</a>
  apa: Avvakumov, S., Mabillard, I., Skopenkov, A., &#38; Wagner, U. (n.d.). Eliminating
    higher-multiplicity intersections, III. Codimension 2. <i>arXiv</i>. <a href="https://doi.org/10.48550/arXiv.1511.03501">https://doi.org/10.48550/arXiv.1511.03501</a>
  chicago: Avvakumov, Sergey, Isaac Mabillard, A. Skopenkov, and Uli Wagner. “Eliminating
    Higher-Multiplicity Intersections, III. Codimension 2.” <i>ArXiv</i>, n.d. <a
    href="https://doi.org/10.48550/arXiv.1511.03501">https://doi.org/10.48550/arXiv.1511.03501</a>.
  ieee: S. Avvakumov, I. Mabillard, A. Skopenkov, and U. Wagner, “Eliminating higher-multiplicity
    intersections, III. Codimension 2,” <i>arXiv</i>. .
  ista: Avvakumov S, Mabillard I, Skopenkov A, Wagner U. Eliminating higher-multiplicity
    intersections, III. Codimension 2. arXiv, 1511.03501.
  mla: Avvakumov, Sergey, et al. “Eliminating Higher-Multiplicity Intersections, III.
    Codimension 2.” <i>ArXiv</i>, 1511.03501, doi:<a href="https://doi.org/10.48550/arXiv.1511.03501">10.48550/arXiv.1511.03501</a>.
  short: S. Avvakumov, I. Mabillard, A. Skopenkov, U. Wagner, ArXiv (n.d.).
corr_author: '1'
date_created: 2020-07-30T10:45:19Z
date_published: 2015-11-15T00:00:00Z
date_updated: 2026-04-08T07:25:54Z
day: '15'
department:
- _id: UlWa
doi: 10.48550/arXiv.1511.03501
external_id:
  arxiv:
  - '1511.03501'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1511.03501
month: '11'
oa: 1
oa_version: Preprint
publication: arXiv
publication_status: draft
related_material:
  record:
  - id: '9308'
    relation: later_version
    status: public
  - id: '10220'
    relation: later_version
    status: public
  - id: '8156'
    relation: dissertation_contains
    status: public
status: public
title: Eliminating higher-multiplicity intersections, III. Codimension 2
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2015'
...
---
_id: '1576'
abstract:
- lang: eng
  text: 'Gene expression is controlled primarily by interactions between transcription
    factor proteins (TFs) and the regulatory DNA sequence, a process that can be captured
    well by thermodynamic models of regulation. These models, however, neglect regulatory
    crosstalk: the possibility that noncognate TFs could initiate transcription, with
    potentially disastrous effects for the cell. Here, we estimate the importance
    of crosstalk, suggest that its avoidance strongly constrains equilibrium models
    of TF binding, and propose an alternative nonequilibrium scheme that implements
    kinetic proofreading to suppress erroneous initiation. This proposal is consistent
    with the observed covalent modifications of the transcriptional apparatus and
    predicts increased noise in gene expression as a trade-off for improved specificity.
    Using information theory, we quantify this trade-off to find when optimal proofreading
    architectures are favored over their equilibrium counterparts. Such architectures
    exhibit significant super-Poisson noise at low expression in steady state.'
article_number: '248101'
article_processing_charge: No
arxiv: 1
author:
- first_name: Sarah A
  full_name: Cepeda Humerez, Sarah A
  id: 3DEE19A4-F248-11E8-B48F-1D18A9856A87
  last_name: Cepeda Humerez
- first_name: Georg
  full_name: Rieckh, Georg
  id: 34DA8BD6-F248-11E8-B48F-1D18A9856A87
  last_name: Rieckh
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
citation:
  ama: Cepeda Humerez SA, Rieckh G, Tkačik G. Stochastic proofreading mechanism alleviates
    crosstalk in transcriptional regulation. <i>Physical Review Letters</i>. 2015;115(24).
    doi:<a href="https://doi.org/10.1103/PhysRevLett.115.248101">10.1103/PhysRevLett.115.248101</a>
  apa: Cepeda Humerez, S. A., Rieckh, G., &#38; Tkačik, G. (2015). Stochastic proofreading
    mechanism alleviates crosstalk in transcriptional regulation. <i>Physical Review
    Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevLett.115.248101">https://doi.org/10.1103/PhysRevLett.115.248101</a>
  chicago: Cepeda Humerez, Sarah A, Georg Rieckh, and Gašper Tkačik. “Stochastic Proofreading
    Mechanism Alleviates Crosstalk in Transcriptional Regulation.” <i>Physical Review
    Letters</i>. American Physical Society, 2015. <a href="https://doi.org/10.1103/PhysRevLett.115.248101">https://doi.org/10.1103/PhysRevLett.115.248101</a>.
  ieee: S. A. Cepeda Humerez, G. Rieckh, and G. Tkačik, “Stochastic proofreading mechanism
    alleviates crosstalk in transcriptional regulation,” <i>Physical Review Letters</i>,
    vol. 115, no. 24. American Physical Society, 2015.
  ista: Cepeda Humerez SA, Rieckh G, Tkačik G. 2015. Stochastic proofreading mechanism
    alleviates crosstalk in transcriptional regulation. Physical Review Letters. 115(24),
    248101.
  mla: Cepeda Humerez, Sarah A., et al. “Stochastic Proofreading Mechanism Alleviates
    Crosstalk in Transcriptional Regulation.” <i>Physical Review Letters</i>, vol.
    115, no. 24, 248101, American Physical Society, 2015, doi:<a href="https://doi.org/10.1103/PhysRevLett.115.248101">10.1103/PhysRevLett.115.248101</a>.
  short: S.A. Cepeda Humerez, G. Rieckh, G. Tkačik, Physical Review Letters 115 (2015).
corr_author: '1'
date_created: 2018-12-11T11:52:49Z
date_published: 2015-12-08T00:00:00Z
date_updated: 2026-04-08T13:55:46Z
day: '08'
department:
- _id: GaTk
doi: 10.1103/PhysRevLett.115.248101
ec_funded: 1
external_id:
  arxiv:
  - '1504.05716'
  isi:
  - '000366106700014'
intvolume: '       115'
isi: 1
issue: '24'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1504.05716
month: '12'
oa: 1
oa_version: Preprint
project:
- _id: 25B07788-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '250152'
  name: Limits to selection in biology and in evolutionary computation
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '5595'
quality_controlled: '1'
related_material:
  record:
  - id: '6473'
    relation: part_of_dissertation
    status: public
scopus_import: '1'
status: public
title: Stochastic proofreading mechanism alleviates crosstalk in transcriptional regulation
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 115
year: '2015'
...
---
_id: '1677'
abstract:
- lang: eng
  text: We consider real symmetric and complex Hermitian random matrices with the
    additional symmetry hxy = hN-y,N-x. The matrix elements are independent (up to
    the fourfold symmetry) and not necessarily identically distributed. This ensemble
    naturally arises as the Fourier transform of a Gaussian orthogonal ensemble. Italso
    occurs as the flip matrix model - an approximation of the two-dimensional Anderson
    model at small disorder. We show that the density of states converges to the Wigner
    semicircle law despite the new symmetry type. We also prove the local version
    of the semicircle law on the optimal scale.
article_number: '103301'
article_processing_charge: No
arxiv: 1
author:
- first_name: Johannes
  full_name: Alt, Johannes
  id: 36D3D8B6-F248-11E8-B48F-1D18A9856A87
  last_name: Alt
citation:
  ama: Alt J. The local semicircle law for random matrices with a fourfold symmetry.
    <i>Journal of Mathematical Physics</i>. 2015;56(10). doi:<a href="https://doi.org/10.1063/1.4932606">10.1063/1.4932606</a>
  apa: Alt, J. (2015). The local semicircle law for random matrices with a fourfold
    symmetry. <i>Journal of Mathematical Physics</i>. American Institute of Physics.
    <a href="https://doi.org/10.1063/1.4932606">https://doi.org/10.1063/1.4932606</a>
  chicago: Alt, Johannes. “The Local Semicircle Law for Random Matrices with a Fourfold
    Symmetry.” <i>Journal of Mathematical Physics</i>. American Institute of Physics,
    2015. <a href="https://doi.org/10.1063/1.4932606">https://doi.org/10.1063/1.4932606</a>.
  ieee: J. Alt, “The local semicircle law for random matrices with a fourfold symmetry,”
    <i>Journal of Mathematical Physics</i>, vol. 56, no. 10. American Institute of
    Physics, 2015.
  ista: Alt J. 2015. The local semicircle law for random matrices with a fourfold
    symmetry. Journal of Mathematical Physics. 56(10), 103301.
  mla: Alt, Johannes. “The Local Semicircle Law for Random Matrices with a Fourfold
    Symmetry.” <i>Journal of Mathematical Physics</i>, vol. 56, no. 10, 103301, American
    Institute of Physics, 2015, doi:<a href="https://doi.org/10.1063/1.4932606">10.1063/1.4932606</a>.
  short: J. Alt, Journal of Mathematical Physics 56 (2015).
corr_author: '1'
date_created: 2018-12-11T11:53:25Z
date_published: 2015-10-09T00:00:00Z
date_updated: 2026-04-08T14:11:36Z
day: '09'
department:
- _id: LaEr
doi: 10.1063/1.4932606
ec_funded: 1
external_id:
  arxiv:
  - '1506.04683'
  isi:
  - '000364237000026'
intvolume: '        56'
isi: 1
issue: '10'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/1506.04683
month: '10'
oa: 1
oa_version: Preprint
project:
- _id: 258DCDE6-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '338804'
  name: Random matrices, universality and disordered quantum systems
publication: Journal of Mathematical Physics
publication_status: published
publisher: American Institute of Physics
publist_id: '5472'
quality_controlled: '1'
related_material:
  record:
  - id: '149'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: The local semicircle law for random matrices with a fourfold symmetry
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 56
year: '2015'
...
---
_id: '1678'
abstract:
- lang: eng
  text: High-throughput live-cell screens are intricate elements of systems biology
    studies and drug discovery pipelines. Here, we demonstrate an optogenetics-assisted
    method that avoids the need for chemical activators and reporters, reduces the
    number of operational steps and increases information content in a cell-based
    small-molecule screen against human protein kinases, including an orphan receptor
    tyrosine kinase. This blueprint for all-optical screening can be adapted to many
    drug targets and cellular processes.
acknowledgement: 'This work was supported by grants from the European Union Seventh
  Framework Programme (CIG-303564 to H.J. and ERC-StG-311166 to S.M.B.N.), the Human
  Frontier Science Program (RGY0084_2012 to H.J.) and the Herzfelder Foundation (to
  M.G.). A.I.-P. was supported by a Ramon Areces fellowship, and E.R. by the graduate
  program MolecularDrugTargets (Austrian Science Fund (FWF): W 1232) and a FemTech
  fellowship (3580812 Austrian Research Promotion Agency).'
author:
- 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: Eva
  full_name: Gschaider-Reichhart, Eva
  id: 3FEE232A-F248-11E8-B48F-1D18A9856A87
  last_name: Gschaider-Reichhart
  orcid: 0000-0002-7218-7738
- first_name: Markus
  full_name: Muellner, Markus
  last_name: Muellner
- first_name: Matthias
  full_name: Nowak, Matthias
  id: 30845DAA-F248-11E8-B48F-1D18A9856A87
  last_name: Nowak
- first_name: Sebastian
  full_name: Nijman, Sebastian
  last_name: Nijman
- first_name: Michael
  full_name: Grusch, Michael
  last_name: Grusch
- first_name: Harald L
  full_name: Janovjak, Harald L
  id: 33BA6C30-F248-11E8-B48F-1D18A9856A87
  last_name: Janovjak
  orcid: 0000-0002-8023-9315
citation:
  ama: Inglés Prieto Á, Gschaider-Reichhart E, Muellner M, et al. Light-assisted small-molecule
    screening against protein kinases. <i>Nature Chemical Biology</i>. 2015;11(12):952-954.
    doi:<a href="https://doi.org/10.1038/nchembio.1933">10.1038/nchembio.1933</a>
  apa: Inglés Prieto, Á., Gschaider-Reichhart, E., Muellner, M., Nowak, M., Nijman,
    S., Grusch, M., &#38; Janovjak, H. L. (2015). Light-assisted small-molecule screening
    against protein kinases. <i>Nature Chemical Biology</i>. Nature Publishing Group.
    <a href="https://doi.org/10.1038/nchembio.1933">https://doi.org/10.1038/nchembio.1933</a>
  chicago: Inglés Prieto, Álvaro, Eva Gschaider-Reichhart, Markus Muellner, Matthias
    Nowak, Sebastian Nijman, Michael Grusch, and Harald L Janovjak. “Light-Assisted
    Small-Molecule Screening against Protein Kinases.” <i>Nature Chemical Biology</i>.
    Nature Publishing Group, 2015. <a href="https://doi.org/10.1038/nchembio.1933">https://doi.org/10.1038/nchembio.1933</a>.
  ieee: Á. Inglés Prieto <i>et al.</i>, “Light-assisted small-molecule screening against
    protein kinases,” <i>Nature Chemical Biology</i>, vol. 11, no. 12. Nature Publishing
    Group, pp. 952–954, 2015.
  ista: Inglés Prieto Á, Gschaider-Reichhart E, Muellner M, Nowak M, Nijman S, Grusch
    M, Janovjak HL. 2015. Light-assisted small-molecule screening against protein
    kinases. Nature Chemical Biology. 11(12), 952–954.
  mla: Inglés Prieto, Álvaro, et al. “Light-Assisted Small-Molecule Screening against
    Protein Kinases.” <i>Nature Chemical Biology</i>, vol. 11, no. 12, Nature Publishing
    Group, 2015, pp. 952–54, doi:<a href="https://doi.org/10.1038/nchembio.1933">10.1038/nchembio.1933</a>.
  short: Á. Inglés Prieto, E. Gschaider-Reichhart, M. Muellner, M. Nowak, S. Nijman,
    M. Grusch, H.L. Janovjak, Nature Chemical Biology 11 (2015) 952–954.
corr_author: '1'
date_created: 2018-12-11T11:53:25Z
date_published: 2015-10-12T00:00:00Z
date_updated: 2026-04-08T14:11:53Z
day: '12'
ddc:
- '571'
department:
- _id: HaJa
- _id: LifeSc
doi: 10.1038/nchembio.1933
ec_funded: 1
file:
- access_level: open_access
  checksum: e9fb251dfcb7cd209b83f17867e61321
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:10:51Z
  date_updated: 2020-07-14T12:45:12Z
  file_id: '4842'
  file_name: IST-2017-837-v1+1_ingles-prieto.pdf
  file_size: 1308364
  relation: main_file
file_date_updated: 2020-07-14T12:45:12Z
has_accepted_license: '1'
intvolume: '        11'
issue: '12'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Submitted Version
page: 952 - 954
project:
- _id: 25548C20-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '303564'
  name: Microbial Ion Channels for Synthetic Neurobiology
- _id: 255BFFFA-B435-11E9-9278-68D0E5697425
  grant_number: RGY0084/2012
  name: In situ real-time imaging of neurotransmitter signaling using designer optical
    sensors
- _id: 255A6082-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W1232-B24
  name: Molecular Drug Targets
publication: Nature Chemical Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '5471'
pubrep_id: '837'
quality_controlled: '1'
related_material:
  record:
  - id: '418'
    relation: dissertation_contains
    status: public
scopus_import: 1
status: public
title: Light-assisted small-molecule screening against protein kinases
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 11
year: '2015'
...
---
_id: '1633'
abstract:
- lang: eng
  text: "We present a method for simulating brittle fracture under the assumptions
    of quasi-static linear elastic fracture mechanics (LEFM). Using the boundary element
    method (BEM) and Lagrangian crack-fronts, we produce highly detailed fracture
    surfaces. The computational cost of the BEM is alleviated by using a low-resolution
    mesh and interpolating the resulting stress intensity factors when propagating
    the high-resolution crack-front.\r\n\r\nOur system produces physics-based fracture
    surfaces with high spatial and temporal resolution, taking spatial variation of
    material toughness and/or strength into account. It also allows for crack initiation
    to be handled separately from crack propagation, which is not only more reasonable
    from a physics perspective, but can also be used to control the simulation.\r\n\r\nSeparating
    the resolution of the crack-front from the resolution of the computational mesh
    increases the efficiency and therefore the amount of visual detail on the resulting
    fracture surfaces. The BEM also allows us to re-use previously computed blocks
    of the system matrix."
article_number: '151'
article_processing_charge: No
author:
- first_name: David
  full_name: Hahn, David
  id: 357A6A66-F248-11E8-B48F-1D18A9856A87
  last_name: Hahn
- first_name: Christopher J
  full_name: Wojtan, Christopher J
  id: 3C61F1D2-F248-11E8-B48F-1D18A9856A87
  last_name: Wojtan
  orcid: 0000-0001-6646-5546
citation:
  ama: 'Hahn D, Wojtan C. High-resolution brittle fracture simulation with boundary
    elements. In: Vol 34. ACM; 2015. doi:<a href="https://doi.org/10.1145/2766896">10.1145/2766896</a>'
  apa: 'Hahn, D., &#38; Wojtan, C. (2015). High-resolution brittle fracture simulation
    with boundary elements (Vol. 34). Presented at the SIGGRAPH: Special Interest
    Group on Computer Graphics and Interactive Techniques, Los Angeles, CA, United
    States: ACM. <a href="https://doi.org/10.1145/2766896">https://doi.org/10.1145/2766896</a>'
  chicago: Hahn, David, and Chris Wojtan. “High-Resolution Brittle Fracture Simulation
    with Boundary Elements,” Vol. 34. ACM, 2015. <a href="https://doi.org/10.1145/2766896">https://doi.org/10.1145/2766896</a>.
  ieee: 'D. Hahn and C. Wojtan, “High-resolution brittle fracture simulation with
    boundary elements,” presented at the SIGGRAPH: Special Interest Group on Computer
    Graphics and Interactive Techniques, Los Angeles, CA, United States, 2015, vol.
    34, no. 4.'
  ista: 'Hahn D, Wojtan C. 2015. High-resolution brittle fracture simulation with
    boundary elements. SIGGRAPH: Special Interest Group on Computer Graphics and Interactive
    Techniques vol. 34, 151.'
  mla: Hahn, David, and Chris Wojtan. <i>High-Resolution Brittle Fracture Simulation
    with Boundary Elements</i>. Vol. 34, no. 4, 151, ACM, 2015, doi:<a href="https://doi.org/10.1145/2766896">10.1145/2766896</a>.
  short: D. Hahn, C. Wojtan, in:, ACM, 2015.
conference:
  end_date: 2015-08-13
  location: Los Angeles, CA, United States
  name: 'SIGGRAPH: Special Interest Group on Computer Graphics and Interactive Techniques'
  start_date: 2015-08-09
corr_author: '1'
date_created: 2018-12-11T11:53:09Z
date_published: 2015-07-27T00:00:00Z
date_updated: 2026-04-08T14:20:15Z
day: '27'
ddc:
- '000'
department:
- _id: ChWo
doi: 10.1145/2766896
ec_funded: 1
external_id:
  isi:
  - '000358786600117'
file:
- access_level: open_access
  checksum: 955aee971983f6b6152bcc1c9b4a7c20
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:15:13Z
  date_updated: 2020-07-14T12:45:07Z
  file_id: '5131'
  file_name: IST-2016-609-v1+1_FractureBEM.pdf
  file_size: 20154270
  relation: main_file
file_date_updated: 2020-07-14T12:45:07Z
has_accepted_license: '1'
intvolume: '        34'
isi: 1
issue: '4'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Submitted Version
project:
- _id: 2533E772-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '638176'
  name: 'Big Splash: Efficient Simulation of Natural Phenomena at Extremely Large
    Scales'
publication_status: published
publisher: ACM
publist_id: '5522'
pubrep_id: '609'
quality_controlled: '1'
related_material:
  record:
  - id: '839'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: High-resolution brittle fracture simulation with boundary elements
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 34
year: '2015'
...
