---
_id: '6183'
abstract:
- lang: eng
  text: "We study the unique solution $m$ of the Dyson equation \\[ -m(z)^{-1} = z
    - a\r\n+ S[m(z)] \\] on a von Neumann algebra $\\mathcal{A}$ with the constraint\r\n$\\mathrm{Im}\\,m\\geq
    0$. Here, $z$ lies in the complex upper half-plane, $a$ is\r\na self-adjoint element
    of $\\mathcal{A}$ and $S$ is a positivity-preserving\r\nlinear operator on $\\mathcal{A}$.
    We show that $m$ is the Stieltjes transform\r\nof a compactly supported $\\mathcal{A}$-valued
    measure on $\\mathbb{R}$. Under\r\nsuitable assumptions, we establish that this
    measure has a uniformly\r\n$1/3$-H\\\"{o}lder continuous density with respect
    to the Lebesgue measure, which\r\nis supported on finitely many intervals, called
    bands. In fact, the density is\r\nanalytic inside the bands with a square-root
    growth at the edges and internal\r\ncubic root cusps whenever the gap between
    two bands vanishes. The shape of\r\nthese singularities is universal and no other
    singularity may occur. We give a\r\nprecise asymptotic description of $m$ near
    the singular points. These\r\nasymptotics generalize the analysis at the regular
    edges given in the companion\r\npaper on the Tracy-Widom universality for the
    edge eigenvalue statistics for\r\ncorrelated random matrices [arXiv:1804.07744]
    and they play a key role in the\r\nproof of the Pearcey universality at the cusp
    for Wigner-type matrices\r\n[arXiv:1809.03971,arXiv:1811.04055]. We also extend
    the finite dimensional band\r\nmass formula from [arXiv:1804.07744] to the von
    Neumann algebra setting by\r\nshowing that the spectral mass of the bands is topologically
    rigid under\r\ndeformations and we conclude that these masses are quantized in
    some important\r\ncases."
article_number: '1804.07752'
article_processing_charge: No
arxiv: 1
author:
- first_name: Johannes
  full_name: Alt, Johannes
  id: 36D3D8B6-F248-11E8-B48F-1D18A9856A87
  last_name: Alt
- first_name: László
  full_name: Erdös, László
  id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
  last_name: Erdös
  orcid: 0000-0001-5366-9603
- first_name: Torben H
  full_name: Krüger, Torben H
  id: 3020C786-F248-11E8-B48F-1D18A9856A87
  last_name: Krüger
  orcid: 0000-0002-4821-3297
citation:
  ama: 'Alt J, Erdös L, Krüger TH. The Dyson equation with linear self-energy: Spectral
    bands, edges and  cusps. <i>arXiv</i>.'
  apa: 'Alt, J., Erdös, L., &#38; Krüger, T. H. (n.d.). The Dyson equation with linear
    self-energy: Spectral bands, edges and  cusps. <i>arXiv</i>.'
  chicago: 'Alt, Johannes, László Erdös, and Torben H Krüger. “The Dyson Equation
    with Linear Self-Energy: Spectral Bands, Edges and  Cusps.” <i>ArXiv</i>, n.d.'
  ieee: 'J. Alt, L. Erdös, and T. H. Krüger, “The Dyson equation with linear self-energy:
    Spectral bands, edges and  cusps,” <i>arXiv</i>. .'
  ista: 'Alt J, Erdös L, Krüger TH. The Dyson equation with linear self-energy: Spectral
    bands, edges and  cusps. arXiv, 1804.07752.'
  mla: 'Alt, Johannes, et al. “The Dyson Equation with Linear Self-Energy: Spectral
    Bands, Edges and  Cusps.” <i>ArXiv</i>, 1804.07752.'
  short: J. Alt, L. Erdös, T.H. Krüger, ArXiv (n.d.).
date_created: 2019-03-28T09:20:06Z
date_published: 2018-04-20T00:00:00Z
date_updated: 2023-12-18T10:46:08Z
day: '20'
department:
- _id: LaEr
external_id:
  arxiv:
  - '1804.07752'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1804.07752
month: '04'
oa: 1
oa_version: Preprint
publication: arXiv
publication_status: submitted
related_material:
  record:
  - id: '149'
    relation: dissertation_contains
    status: public
  - id: '14694'
    relation: later_version
    status: public
status: public
title: 'The Dyson equation with linear self-energy: Spectral bands, edges and  cusps'
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '6195'
abstract:
- lang: eng
  text: In the context of robotic manipulation and grasping, the shift from a view
    that is static (force closure of a single posture) and contact-deprived (only
    contact for force closure is allowed, everything else is obstacle) towards a view
    that is dynamic and contact-rich (soft manipulation) has led to an increased interest
    in soft hands. These hands can easily exploit environmental constraints and object
    surfaces without risk, and safely interact with humans, but present also some
    challenges. Designing them is difficult, as well as predicting, modelling, and
    “programming” their interactions with the objects and the environment. This paper
    tackles the problem of simulating them in a fast and effective way, leveraging
    on novel and existing simulation technologies. We present a triple-layered simulation
    framework where dynamic properties such as stiffness are determined from slow
    but accurate FEM simulation data once, and then condensed into a lumped parameter
    model that can be used to fast simulate soft fingers and soft hands. We apply
    our approach to the simulation of soft pneumatic fingers.
article_number: '8461106'
article_processing_charge: No
author:
- first_name: Maria
  full_name: Pozzi, Maria
  last_name: Pozzi
- first_name: Eder
  full_name: Miguel Villalba, Eder
  id: 3FB91342-F248-11E8-B48F-1D18A9856A87
  last_name: Miguel Villalba
  orcid: 0000-0001-5665-0430
- first_name: Raphael
  full_name: Deimel, Raphael
  last_name: Deimel
- first_name: Monica
  full_name: Malvezzi, Monica
  last_name: Malvezzi
- first_name: Bernd
  full_name: Bickel, Bernd
  id: 49876194-F248-11E8-B48F-1D18A9856A87
  last_name: Bickel
  orcid: 0000-0001-6511-9385
- first_name: Oliver
  full_name: Brock, Oliver
  last_name: Brock
- first_name: Domenico
  full_name: Prattichizzo, Domenico
  last_name: Prattichizzo
citation:
  ama: 'Pozzi M, Miguel Villalba E, Deimel R, et al. Efficient FEM-based simulation
    of soft robots modeled as kinematic chains. In: IEEE; 2018. doi:<a href="https://doi.org/10.1109/icra.2018.8461106">10.1109/icra.2018.8461106</a>'
  apa: 'Pozzi, M., Miguel Villalba, E., Deimel, R., Malvezzi, M., Bickel, B., Brock,
    O., &#38; Prattichizzo, D. (2018). Efficient FEM-based simulation of soft robots
    modeled as kinematic chains. Presented at the ICRA: International Conference on
    Robotics and Automation, Brisbane, Australia: IEEE. <a href="https://doi.org/10.1109/icra.2018.8461106">https://doi.org/10.1109/icra.2018.8461106</a>'
  chicago: Pozzi, Maria, Eder Miguel Villalba, Raphael Deimel, Monica Malvezzi, Bernd
    Bickel, Oliver Brock, and Domenico Prattichizzo. “Efficient FEM-Based Simulation
    of Soft Robots Modeled as Kinematic Chains.” IEEE, 2018. <a href="https://doi.org/10.1109/icra.2018.8461106">https://doi.org/10.1109/icra.2018.8461106</a>.
  ieee: 'M. Pozzi <i>et al.</i>, “Efficient FEM-based simulation of soft robots modeled
    as kinematic chains,” presented at the ICRA: International Conference on Robotics
    and Automation, Brisbane, Australia, 2018.'
  ista: 'Pozzi M, Miguel Villalba E, Deimel R, Malvezzi M, Bickel B, Brock O, Prattichizzo
    D. 2018. Efficient FEM-based simulation of soft robots modeled as kinematic chains.
    ICRA: International Conference on Robotics and Automation, 8461106.'
  mla: Pozzi, Maria, et al. <i>Efficient FEM-Based Simulation of Soft Robots Modeled
    as Kinematic Chains</i>. 8461106, IEEE, 2018, doi:<a href="https://doi.org/10.1109/icra.2018.8461106">10.1109/icra.2018.8461106</a>.
  short: M. Pozzi, E. Miguel Villalba, R. Deimel, M. Malvezzi, B. Bickel, O. Brock,
    D. Prattichizzo, in:, IEEE, 2018.
conference:
  end_date: 2018-05-25
  location: Brisbane, Australia
  name: 'ICRA: International Conference on Robotics and Automation'
  start_date: 2018-05-21
date_created: 2019-04-04T09:50:38Z
date_published: 2018-09-10T00:00:00Z
date_updated: 2023-09-19T14:49:03Z
day: '10'
department:
- _id: BeBi
doi: 10.1109/icra.2018.8461106
external_id:
  isi:
  - '000446394503031'
isi: 1
language:
- iso: eng
month: '09'
oa_version: None
publication_identifier:
  isbn:
  - '9781538630815'
publication_status: published
publisher: IEEE
quality_controlled: '1'
scopus_import: '1'
status: public
title: Efficient FEM-based simulation of soft robots modeled as kinematic chains
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '62'
abstract:
- lang: eng
  text: Imaging is a dominant strategy for data collection in neuroscience, yielding
    stacks of images that often scale to gigabytes of data for a single experiment.
    Machine learning algorithms from computer vision can serve as a pair of virtual
    eyes that tirelessly processes these images, automatically detecting and identifying
    microstructures. Unlike learning methods, our Flexible Learning-free Reconstruction
    of Imaged Neural volumes (FLoRIN) pipeline exploits structure-specific contextual
    clues and requires no training. This approach generalizes across different modalities,
    including serially-sectioned scanning electron microscopy (sSEM) of genetically
    labeled and contrast enhanced processes, spectral confocal reflectance (SCoRe)
    microscopy, and high-energy synchrotron X-ray microtomography (μCT) of large tissue
    volumes. We deploy the FLoRIN pipeline on newly published and novel mouse datasets,
    demonstrating the high biological fidelity of the pipeline’s reconstructions.
    FLoRIN reconstructions are of sufficient quality for preliminary biological study,
    for example examining the distribution and morphology of cells or extracting single
    axons from functional data. Compared to existing supervised learning methods,
    FLoRIN is one to two orders of magnitude faster and produces high-quality reconstructions
    that are tolerant to noise and artifacts, as is shown qualitatively and quantitatively.
acknowledgement: 'Equipment was generously donated by the NVIDIA Corporation, and
  made available by the National Science Foundation (NSF) through grant #CNS-1629914.
  This research used resources of the Argonne Leadership Computing Facility, which
  is a DOE Office of Science User Facility supported under Contract DE-AC02-06CH11357.'
article_number: '14247'
article_processing_charge: No
article_type: original
author:
- first_name: Ali
  full_name: Shabazi, Ali
  last_name: Shabazi
- first_name: Jeffery
  full_name: Kinnison, Jeffery
  last_name: Kinnison
- first_name: Rafael
  full_name: Vescovi, Rafael
  last_name: Vescovi
- first_name: Ming
  full_name: Du, Ming
  last_name: Du
- first_name: Robert
  full_name: Hill, Robert
  last_name: Hill
- first_name: Maximilian A
  full_name: Jösch, Maximilian A
  id: 2BD278E6-F248-11E8-B48F-1D18A9856A87
  last_name: Jösch
  orcid: 0000-0002-3937-1330
- first_name: Marc
  full_name: Takeno, Marc
  last_name: Takeno
- first_name: Hongkui
  full_name: Zeng, Hongkui
  last_name: Zeng
- first_name: Nuno
  full_name: Da Costa, Nuno
  last_name: Da Costa
- first_name: Jaime
  full_name: Grutzendler, Jaime
  last_name: Grutzendler
- first_name: Narayanan
  full_name: Kasthuri, Narayanan
  last_name: Kasthuri
- first_name: Walter
  full_name: Scheirer, Walter
  last_name: Scheirer
citation:
  ama: Shabazi A, Kinnison J, Vescovi R, et al. Flexible learning-free segmentation
    and reconstruction of neural volumes. <i>Scientific Reports</i>. 2018;8(1). doi:<a
    href="https://doi.org/10.1038/s41598-018-32628-3">10.1038/s41598-018-32628-3</a>
  apa: Shabazi, A., Kinnison, J., Vescovi, R., Du, M., Hill, R., Jösch, M. A., … Scheirer,
    W. (2018). Flexible learning-free segmentation and reconstruction of neural volumes.
    <i>Scientific Reports</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/s41598-018-32628-3">https://doi.org/10.1038/s41598-018-32628-3</a>
  chicago: Shabazi, Ali, Jeffery Kinnison, Rafael Vescovi, Ming Du, Robert Hill, Maximilian
    A Jösch, Marc Takeno, et al. “Flexible Learning-Free Segmentation and Reconstruction
    of Neural Volumes.” <i>Scientific Reports</i>. Nature Publishing Group, 2018.
    <a href="https://doi.org/10.1038/s41598-018-32628-3">https://doi.org/10.1038/s41598-018-32628-3</a>.
  ieee: A. Shabazi <i>et al.</i>, “Flexible learning-free segmentation and reconstruction
    of neural volumes,” <i>Scientific Reports</i>, vol. 8, no. 1. Nature Publishing
    Group, 2018.
  ista: Shabazi A, Kinnison J, Vescovi R, Du M, Hill R, Jösch MA, Takeno M, Zeng H,
    Da Costa N, Grutzendler J, Kasthuri N, Scheirer W. 2018. Flexible learning-free
    segmentation and reconstruction of neural volumes. Scientific Reports. 8(1), 14247.
  mla: Shabazi, Ali, et al. “Flexible Learning-Free Segmentation and Reconstruction
    of Neural Volumes.” <i>Scientific Reports</i>, vol. 8, no. 1, 14247, Nature Publishing
    Group, 2018, doi:<a href="https://doi.org/10.1038/s41598-018-32628-3">10.1038/s41598-018-32628-3</a>.
  short: A. Shabazi, J. Kinnison, R. Vescovi, M. Du, R. Hill, M.A. Jösch, M. Takeno,
    H. Zeng, N. Da Costa, J. Grutzendler, N. Kasthuri, W. Scheirer, Scientific Reports
    8 (2018).
date_created: 2018-12-11T11:44:25Z
date_published: 2018-09-24T00:00:00Z
date_updated: 2023-09-11T14:02:55Z
day: '24'
ddc:
- '570'
department:
- _id: MaJö
doi: 10.1038/s41598-018-32628-3
external_id:
  isi:
  - '000445336600015'
file:
- access_level: open_access
  checksum: 1a14ae0666b82fbaa04bef110e3f6bf2
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T12:22:24Z
  date_updated: 2020-07-14T12:47:24Z
  file_id: '5699'
  file_name: 2018_ScientificReports_Shahbazi.pdf
  file_size: 4141645
  relation: main_file
file_date_updated: 2020-07-14T12:47:24Z
has_accepted_license: '1'
intvolume: '         8'
isi: 1
issue: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '09'
oa: 1
oa_version: Published Version
publication: Scientific Reports
publication_status: published
publisher: Nature Publishing Group
publist_id: '7992'
quality_controlled: '1'
related_material:
  link:
  - relation: erratum
    url: http://doi.org/10.1038/s41598-018-36220-7
scopus_import: '1'
status: public
title: Flexible learning-free segmentation and reconstruction of neural volumes
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 8
year: '2018'
...
---
_id: '620'
abstract:
- lang: eng
  text: Clathrin-mediated endocytosis requires the coordinated assembly of various
    endocytic proteins and lipids at the plasma membrane. Accumulating evidence demonstrates
    a crucial role for phosphatidylinositol-4,5-bisphosphate (PtdIns(4,5)P2) in endocytosis,
    but specific roles for PtdIns(4)P other than as the biosynthetic precursor of
    PtdIns(4,5)P2 have not been clarified. In this study we investigated the role
    of PtdIns(4)P or PtdIns(4,5)P2 in receptor-mediated endocytosis through the construction
    of temperature-sensitive (ts) mutants for the PI 4-kinases Stt4p and Pik1p and
    the PtdIns(4) 5-kinase Mss4p. Quantitative analyses of endocytosis revealed that
    both the stt4(ts)pik1(ts) and mss4(ts) mutants have a severe defect in endocytic
    internalization. Live-cell imaging of endocytic protein dynamics in stt4(ts)pik1(ts)
    and mss4(ts) mutants revealed that PtdIns(4)P is required for the recruitment
    of the alpha-factor receptor Ste2p to clathrin-coated pits whereas PtdIns(4,5)P2
    is required for membrane internalization. We also found that the localization
    to endocytic sites of the ENTH/ANTH domain-bearing clathrin adaptors, Ent1p/Ent2p
    and Yap1801p/Yap1802p, is significantly impaired in the stt4(ts)pik1(ts) mutant,
    but not in the mss4(ts) mutant. These results suggest distinct roles in successive
    steps for PtdIns(4)P and PtdIns(4,5)P2 during receptor-mediated endocytosis.
article_number: jcs207696
article_processing_charge: No
author:
- first_name: Wataru
  full_name: Yamamoto, Wataru
  last_name: Yamamoto
- first_name: Suguru
  full_name: Wada, Suguru
  last_name: Wada
- first_name: Makoto
  full_name: Nagano, Makoto
  last_name: Nagano
- first_name: Kaito
  full_name: Aoshima, Kaito
  last_name: Aoshima
- first_name: Daria E
  full_name: Siekhaus, Daria E
  id: 3D224B9E-F248-11E8-B48F-1D18A9856A87
  last_name: Siekhaus
  orcid: 0000-0001-8323-8353
- first_name: Junko
  full_name: Toshima, Junko
  last_name: Toshima
- first_name: Jiro
  full_name: Toshima, Jiro
  last_name: Toshima
citation:
  ama: Yamamoto W, Wada S, Nagano M, et al. Distinct roles for plasma membrane PtdIns
    4 P and PtdIns 4 5 P2 during yeast receptor mediated endocytosis. <i>Journal of
    Cell Science</i>. 2018;131(1). doi:<a href="https://doi.org/10.1242/jcs.207696">10.1242/jcs.207696</a>
  apa: Yamamoto, W., Wada, S., Nagano, M., Aoshima, K., Siekhaus, D. E., Toshima,
    J., &#38; Toshima, J. (2018). Distinct roles for plasma membrane PtdIns 4 P and
    PtdIns 4 5 P2 during yeast receptor mediated endocytosis. <i>Journal of Cell Science</i>.
    Company of Biologists. <a href="https://doi.org/10.1242/jcs.207696">https://doi.org/10.1242/jcs.207696</a>
  chicago: Yamamoto, Wataru, Suguru Wada, Makoto Nagano, Kaito Aoshima, Daria E Siekhaus,
    Junko Toshima, and Jiro Toshima. “Distinct Roles for Plasma Membrane PtdIns 4
    P and PtdIns 4 5 P2 during Yeast Receptor Mediated Endocytosis.” <i>Journal of
    Cell Science</i>. Company of Biologists, 2018. <a href="https://doi.org/10.1242/jcs.207696">https://doi.org/10.1242/jcs.207696</a>.
  ieee: W. Yamamoto <i>et al.</i>, “Distinct roles for plasma membrane PtdIns 4 P
    and PtdIns 4 5 P2 during yeast receptor mediated endocytosis,” <i>Journal of Cell
    Science</i>, vol. 131, no. 1. Company of Biologists, 2018.
  ista: Yamamoto W, Wada S, Nagano M, Aoshima K, Siekhaus DE, Toshima J, Toshima J.
    2018. Distinct roles for plasma membrane PtdIns 4 P and PtdIns 4 5 P2 during yeast
    receptor mediated endocytosis. Journal of Cell Science. 131(1), jcs207696.
  mla: Yamamoto, Wataru, et al. “Distinct Roles for Plasma Membrane PtdIns 4 P and
    PtdIns 4 5 P2 during Yeast Receptor Mediated Endocytosis.” <i>Journal of Cell
    Science</i>, vol. 131, no. 1, jcs207696, Company of Biologists, 2018, doi:<a href="https://doi.org/10.1242/jcs.207696">10.1242/jcs.207696</a>.
  short: W. Yamamoto, S. Wada, M. Nagano, K. Aoshima, D.E. Siekhaus, J. Toshima, J.
    Toshima, Journal of Cell Science 131 (2018).
date_created: 2018-12-11T11:47:32Z
date_published: 2018-01-04T00:00:00Z
date_updated: 2023-09-11T12:57:13Z
day: '04'
department:
- _id: DaSi
doi: 10.1242/jcs.207696
external_id:
  isi:
  - '000424786900012'
  pmid:
  - '29192062'
intvolume: '       131'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pubmed/29192062
month: '01'
oa: 1
oa_version: Published Version
pmid: 1
publication: Journal of Cell Science
publication_status: published
publisher: Company of Biologists
publist_id: '7184'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Distinct roles for plasma membrane PtdIns 4 P and PtdIns 4 5 P2 during yeast
  receptor mediated endocytosis
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 131
year: '2018'
...
---
_id: '6263'
abstract:
- lang: eng
  text: 'Antibiotic  resistance  can  emerge  spontaneously  through  genomic  mutation  and  render
    treatment   ineffective.   To   counteract   this process, in   addition   to   the   discovery   and
    description of resistance mechanisms,a deeper understanding of resistanceevolvabilityand
    its  determinantsis  needed. To address  this challenge,  this  thesisuncoversnew  genetic
    determinants   of   resistance   evolvability   using   a   customized   robotic   setup,
    exploressystematic   ways   in   which   resistance   evolution   is   perturbed   due   to
    dose-responsecharacteristics  of  drugs and  mutation  rate  differences,and  mathematically  investigates
    the evolutionary fate of one specific type of evolvability modifier -a stress-induced
    mutagenesis allele.We  find  severalgenes  which  strongly  inhibit  or  potentiate  resistance  evolution.  In  order
    to identify   them,   we   first developedan   automated   high-throughput   feedback-controlled
    protocol whichkeeps the population size and selection pressure approximately constant
    for hundreds  of  cultures  by  dynamically  re-diluting  the  cultures  and  adjusting  the  antibiotic
    concentration.  We  implementedthis  protocol  on  a  customized  liquid  handling  robot  and
    propagated  100  different  gene  deletion  strains  of Escherichia  coliin  triplicate  for  over  100
    generations  in  tetracycline  and  in  chloramphenicol,  and  comparedtheir  adaptation  rates.We  find  a  diminishing  returns  pattern,  where  initially  sensitive  strains  adapted  more
    compared to less sensitive ones.  Our data uncover that deletions of certain genes
    which do not  affect  mutation  rate,including  efflux  pump  components,  a  chaperone  and
    severalstructural  and regulatory  genes  can strongly  and  reproducibly  alterresistance  evolution.
    Sequencing   analysis of   evolved   populations   indicates   that   epistasis   with   resistance
    mutations  is  the  most  likelyexplanation. This  work  could  inspire  treatment  strategies  in
    which  targeted  inhibitors  of  evolvability  mechanisms  will  be  given  alongside  antibiotics  to
    slow down resistance evolution and extend theefficacy of antibiotics.We implemented  astochasticpopulation  genetics  model,
    toverifyways  in  which  general properties,  namely,  dose-response  characteristics  of  drugs  and  mutation  rates,  influence
    evolutionary  dynamics.  In  particular,  under  the  exposure  to  antibiotics  with  shallow  dose-response  curves,bacteria  have  narrower  distributions  of  fitness  effects  of  new  mutations.
    We  show  that in  silicothis  also  leads  to  slower  resistance  evolution.  We
    see and  confirm with experiments that increased mutation rates, apart from speeding
    up evolution, also leadto high reproducibility of phenotypic adaptation in a context
    of continually strong selection pressure.Knowledge  of  these  patterns  can  aid  in  predicting  the  dynamics  of  antibiotic
    resistance evolutionand adapting treatment schemes accordingly.Focusing on   a   previously   described   type   of   evolvability   modifier
    –a   stress-induced mutagenesis  allele –we  find  conditions  under  which  it  can  persist  in  a  population  under
    periodic  selectionakin  to  clinical  treatment. We  set  up  a  deterministic
    infinite  populationcontinuous  time  model  tracking  the  frequencies  of  a  mutator  and  resistance  allele  and
    evaluate  various  treatment  schemes  in  how  well  they  maintain  a stress-induced
    mutator allele. In particular,a high diversity  of stresses  is  crucial  for  the  persistence
    of the  mutator allele. This leads to a general trade-off where exactly those
    diversifying treatment schemes which  are  likely  to  decrease  levels  of  resistance  could  lead  to  stronger  selection  of  highly
    evolvable genotypes.In  the  long  run,  this  work  will  lead  to  a  deeper  understanding  of  the  genetic  and  cellular
    mechanisms involved in antibiotic resistance evolution and could inspire new strategies
    for slowing down its rate. '
acknowledged_ssus:
- _id: M-Shop
- _id: LifeSc
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Marta
  full_name: Lukacisinova, Marta
  id: 4342E402-F248-11E8-B48F-1D18A9856A87
  last_name: Lukacisinova
  orcid: 0000-0002-2519-8004
citation:
  ama: Lukacisinova M. Genetic determinants of antibiotic resistance evolution. 2018.
    doi:<a href="https://doi.org/10.15479/AT:ISTA:th1072">10.15479/AT:ISTA:th1072</a>
  apa: Lukacisinova, M. (2018). <i>Genetic determinants of antibiotic resistance evolution</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:th1072">https://doi.org/10.15479/AT:ISTA:th1072</a>
  chicago: Lukacisinova, Marta. “Genetic Determinants of Antibiotic Resistance Evolution.”
    Institute of Science and Technology Austria, 2018. <a href="https://doi.org/10.15479/AT:ISTA:th1072">https://doi.org/10.15479/AT:ISTA:th1072</a>.
  ieee: M. Lukacisinova, “Genetic determinants of antibiotic resistance evolution,”
    Institute of Science and Technology Austria, 2018.
  ista: Lukacisinova M. 2018. Genetic determinants of antibiotic resistance evolution.
    Institute of Science and Technology Austria.
  mla: Lukacisinova, Marta. <i>Genetic Determinants of Antibiotic Resistance Evolution</i>.
    Institute of Science and Technology Austria, 2018, doi:<a href="https://doi.org/10.15479/AT:ISTA:th1072">10.15479/AT:ISTA:th1072</a>.
  short: M. Lukacisinova, Genetic Determinants of Antibiotic Resistance Evolution,
    Institute of Science and Technology Austria, 2018.
date_created: 2019-04-09T13:57:15Z
date_published: 2018-12-28T00:00:00Z
date_updated: 2023-09-22T09:20:37Z
day: '28'
ddc:
- '570'
- '576'
- '579'
degree_awarded: PhD
department:
- _id: ToBo
doi: 10.15479/AT:ISTA:th1072
file:
- access_level: open_access
  checksum: fc60585c9eaad868ac007004ef130908
  content_type: application/pdf
  creator: dernst
  date_created: 2019-04-09T13:49:24Z
  date_updated: 2021-02-11T11:17:17Z
  embargo: 2020-01-25
  file_id: '6264'
  file_name: 2018_Thesis_Lukacisinova.pdf
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  relation: main_file
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  creator: dernst
  date_created: 2019-04-09T13:49:23Z
  date_updated: 2020-07-14T12:47:25Z
  embargo_to: open_access
  file_id: '6265'
  file_name: 2018_Thesis_Lukacisinova_source.docx
  file_size: 5168054
  relation: source_file
file_date_updated: 2021-02-11T11:17:17Z
has_accepted_license: '1'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: '91'
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '1619'
    relation: part_of_dissertation
    status: public
  - id: '696'
    relation: part_of_dissertation
    status: public
  - id: '1027'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Tobias
  full_name: Bollenbach, Tobias
  id: 3E6DB97A-F248-11E8-B48F-1D18A9856A87
  last_name: Bollenbach
  orcid: 0000-0003-4398-476X
title: Genetic determinants of antibiotic resistance evolution
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '6266'
abstract:
- lang: eng
  text: 'A major challenge in neuroscience research is to dissect the circuits that
    orchestrate behavior in health and disease. Proteins from a wide range of non-mammalian
    species, such as microbial opsins, have been successfully transplanted to specific
    neuronal targets to override their natural communication patterns. The goal of
    our work is to manipulate synaptic communication in a manner that closely incorporates
    the functional intricacies of synapses by preserving temporal encoding (i.e. the
    firing pattern of the presynaptic neuron) and connectivity (i.e. target specific
    synapses rather than specific neurons). Our strategy to achieve this goal builds
    on the use of non-mammalian transplants to create a synthetic synapse. The mode
    of modulation comes from pre-synaptic uptake of a synthetic neurotransmitter (SN)
    into synaptic vesicles by means of a genetically targeted transporter selective
    for the SN. Upon natural vesicular release, exposure of the SN to the synaptic
    cleft will modify the post-synaptic potential through an orthogonal ligand gated
    ion channel. To achieve this goal we have functionally characterized a mixed cationic
    methionine-gated ion channel from Arabidopsis thaliana, designed a method to functionally
    characterize a synthetic transporter in isolated synaptic vesicles without the
    need for transgenic animals, identified and extracted multiple prokaryotic uptake
    systems that are substrate specific for methionine (Met), and established a primary/cell
    line co-culture system that would allow future combinatorial testing of this orthogonal
    transmitter-transporter-channel trifecta. Synthetic synapses will provide a unique
    opportunity to manipulate synaptic communication while maintaining the electrophysiological
    integrity of the pre-synaptic cell. In this way, information may be preserved
    that was generated in upstream circuits and that could be essential for concerted
    function and information processing. '
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Catherine
  full_name: Mckenzie, Catherine
  id: 3EEDE19A-F248-11E8-B48F-1D18A9856A87
  last_name: Mckenzie
citation:
  ama: Mckenzie C. Design and characterization of methods and biological components
    to realize synthetic neurotransmission . 2018. doi:<a href="https://doi.org/10.15479/at:ista:th_1055">10.15479/at:ista:th_1055</a>
  apa: Mckenzie, C. (2018). <i>Design and characterization of methods and biological
    components to realize synthetic neurotransmission </i>. Institute of Science and
    Technology Austria. <a href="https://doi.org/10.15479/at:ista:th_1055">https://doi.org/10.15479/at:ista:th_1055</a>
  chicago: Mckenzie, Catherine. “Design and Characterization of Methods and Biological
    Components to Realize Synthetic Neurotransmission .” Institute of Science and
    Technology Austria, 2018. <a href="https://doi.org/10.15479/at:ista:th_1055">https://doi.org/10.15479/at:ista:th_1055</a>.
  ieee: C. Mckenzie, “Design and characterization of methods and biological components
    to realize synthetic neurotransmission ,” Institute of Science and Technology
    Austria, 2018.
  ista: Mckenzie C. 2018. Design and characterization of methods and biological components
    to realize synthetic neurotransmission . Institute of Science and Technology Austria.
  mla: Mckenzie, Catherine. <i>Design and Characterization of Methods and Biological
    Components to Realize Synthetic Neurotransmission </i>. Institute of Science and
    Technology Austria, 2018, doi:<a href="https://doi.org/10.15479/at:ista:th_1055">10.15479/at:ista:th_1055</a>.
  short: C. Mckenzie, Design and Characterization of Methods and Biological Components
    to Realize Synthetic Neurotransmission , Institute of Science and Technology Austria,
    2018.
date_created: 2019-04-09T14:13:39Z
date_published: 2018-10-31T00:00:00Z
date_updated: 2023-09-07T13:02:37Z
day: '31'
ddc:
- '571'
- '573'
degree_awarded: PhD
department:
- _id: HaJa
doi: 10.15479/at:ista:th_1055
file:
- access_level: open_access
  checksum: 9d2c2dca04b00e485470c28b262af59a
  content_type: application/pdf
  creator: dernst
  date_created: 2019-04-09T14:12:40Z
  date_updated: 2021-02-11T11:17:16Z
  embargo: 2019-11-24
  file_id: '6267'
  file_name: 2018_Thesis_McKenzie.pdf
  file_size: 4906420
  relation: main_file
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  checksum: 50b58c272899601bc6fd9642c4dc97f1
  content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
  creator: dernst
  date_created: 2019-04-09T14:12:40Z
  date_updated: 2020-07-14T12:47:25Z
  embargo_to: open_access
  file_id: '6268'
  file_name: 2018_Thesis_McKenzie_source.docx
  file_size: 5053545
  relation: source_file
file_date_updated: 2021-02-11T11:17:16Z
has_accepted_license: '1'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: '95'
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
pubrep_id: '1055'
related_material:
  record:
  - id: '7132'
    relation: new_edition
    status: public
status: public
supervisor:
- first_name: Harald L
  full_name: Janovjak, Harald L
  id: 33BA6C30-F248-11E8-B48F-1D18A9856A87
  last_name: Janovjak
  orcid: 0000-0002-8023-9315
title: 'Design and characterization of methods and biological components to realize
  synthetic neurotransmission '
type: dissertation
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '63'
abstract:
- lang: eng
  text: African cichlids display a remarkable assortment of jaw morphologies, pigmentation
    patterns, and mating behaviors. In addition to this previously documented diversity,
    recent studies have documented a rich diversity of sex chromosomes within these
    fishes. Here we review the known sex-determination network within vertebrates,
    and the extraordinary number of sex chromosomes systems segregating in African
    cichlids. We also propose a model for understanding the unusual number of sex
    chromosome systems within this clade.
acknowledgement: NSF DEB-1830753 and ISTPlus Fellowship
article_number: '480'
article_processing_charge: No
author:
- first_name: William J
  full_name: Gammerdinger, William J
  id: 3A7E01BC-F248-11E8-B48F-1D18A9856A87
  last_name: Gammerdinger
  orcid: 0000-0001-9638-1220
- first_name: Thomas
  full_name: Kocher, Thomas
  last_name: Kocher
citation:
  ama: Gammerdinger WJ, Kocher T. Unusual diversity of sex chromosomes in African
    cichlid fishes. <i>Genes</i>. 2018;9(10). doi:<a href="https://doi.org/10.3390/genes9100480">10.3390/genes9100480</a>
  apa: Gammerdinger, W. J., &#38; Kocher, T. (2018). Unusual diversity of sex chromosomes
    in African cichlid fishes. <i>Genes</i>. MDPI AG. <a href="https://doi.org/10.3390/genes9100480">https://doi.org/10.3390/genes9100480</a>
  chicago: Gammerdinger, William J, and Thomas Kocher. “Unusual Diversity of Sex Chromosomes
    in African Cichlid Fishes.” <i>Genes</i>. MDPI AG, 2018. <a href="https://doi.org/10.3390/genes9100480">https://doi.org/10.3390/genes9100480</a>.
  ieee: W. J. Gammerdinger and T. Kocher, “Unusual diversity of sex chromosomes in
    African cichlid fishes,” <i>Genes</i>, vol. 9, no. 10. MDPI AG, 2018.
  ista: Gammerdinger WJ, Kocher T. 2018. Unusual diversity of sex chromosomes in African
    cichlid fishes. Genes. 9(10), 480.
  mla: Gammerdinger, William J., and Thomas Kocher. “Unusual Diversity of Sex Chromosomes
    in African Cichlid Fishes.” <i>Genes</i>, vol. 9, no. 10, 480, MDPI AG, 2018,
    doi:<a href="https://doi.org/10.3390/genes9100480">10.3390/genes9100480</a>.
  short: W.J. Gammerdinger, T. Kocher, Genes 9 (2018).
date_created: 2018-12-11T11:44:26Z
date_published: 2018-10-04T00:00:00Z
date_updated: 2023-09-19T10:37:03Z
day: '04'
ddc:
- '570'
department:
- _id: BeVi
doi: 10.3390/genes9100480
ec_funded: 1
external_id:
  isi:
  - '000448656700018'
file:
- access_level: open_access
  checksum: bec527692e2c9b56919c0429634ff337
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-18T09:54:46Z
  date_updated: 2020-07-14T12:47:27Z
  file_id: '5743'
  file_name: 2018_Genes_Gammerdinger.pdf
  file_size: 1415791
  relation: main_file
file_date_updated: 2020-07-14T12:47:27Z
has_accepted_license: '1'
intvolume: '         9'
isi: 1
issue: '10'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: Genes
publication_status: published
publisher: MDPI AG
publist_id: '7991'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Unusual diversity of sex chromosomes in African cichlid fishes
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 9
year: '2018'
...
---
_id: '6339'
abstract:
- lang: eng
  text: We introduce a diagrammatic Monte Carlo approach to angular momentum properties
    of quantum many-particle systems possessing a macroscopic number of degrees of
    freedom. The treatment is based on a diagrammatic expansion that merges the usual
    Feynman diagrams with the angular momentum diagrams known from atomic and nuclear
    structure theory, thereby incorporating the non-Abelian algebra inherent to quantum
    rotations. Our approach is applicable at arbitrary coupling, is free of systematic
    errors and of finite-size effects, and naturally provides access to the impurity
    Green function. We exemplify the technique by obtaining an all-coupling solution
    of the angulon model; however, the method is quite general and can be applied
    to a broad variety of systems in which particles exchange quantum angular momentum
    with their many-body environment.
article_number: '165301'
article_processing_charge: No
arxiv: 1
author:
- first_name: Giacomo
  full_name: Bighin, Giacomo
  id: 4CA96FD4-F248-11E8-B48F-1D18A9856A87
  last_name: Bighin
  orcid: 0000-0001-8823-9777
- first_name: Timur
  full_name: Tscherbul, Timur
  last_name: Tscherbul
- first_name: Mikhail
  full_name: Lemeshko, Mikhail
  id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
  last_name: Lemeshko
  orcid: 0000-0002-6990-7802
citation:
  ama: Bighin G, Tscherbul T, Lemeshko M. Diagrammatic Monte Carlo approach to angular
    momentum in quantum many-particle systems. <i>Physical Review Letters</i>. 2018;121(16).
    doi:<a href="https://doi.org/10.1103/physrevlett.121.165301">10.1103/physrevlett.121.165301</a>
  apa: Bighin, G., Tscherbul, T., &#38; Lemeshko, M. (2018). Diagrammatic Monte Carlo
    approach to angular momentum in quantum many-particle systems. <i>Physical Review
    Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/physrevlett.121.165301">https://doi.org/10.1103/physrevlett.121.165301</a>
  chicago: Bighin, Giacomo, Timur Tscherbul, and Mikhail Lemeshko. “Diagrammatic Monte Carlo
    Approach to Angular Momentum in Quantum Many-Particle Systems.” <i>Physical Review
    Letters</i>. American Physical Society, 2018. <a href="https://doi.org/10.1103/physrevlett.121.165301">https://doi.org/10.1103/physrevlett.121.165301</a>.
  ieee: G. Bighin, T. Tscherbul, and M. Lemeshko, “Diagrammatic Monte Carlo approach
    to angular momentum in quantum many-particle systems,” <i>Physical Review Letters</i>,
    vol. 121, no. 16. American Physical Society, 2018.
  ista: Bighin G, Tscherbul T, Lemeshko M. 2018. Diagrammatic Monte Carlo approach
    to angular momentum in quantum many-particle systems. Physical Review Letters.
    121(16), 165301.
  mla: Bighin, Giacomo, et al. “Diagrammatic Monte Carlo Approach to Angular Momentum
    in Quantum Many-Particle Systems.” <i>Physical Review Letters</i>, vol. 121, no.
    16, 165301, American Physical Society, 2018, doi:<a href="https://doi.org/10.1103/physrevlett.121.165301">10.1103/physrevlett.121.165301</a>.
  short: G. Bighin, T. Tscherbul, M. Lemeshko, Physical Review Letters 121 (2018).
date_created: 2019-04-17T10:53:38Z
date_published: 2018-10-16T00:00:00Z
date_updated: 2024-02-28T13:15:09Z
day: '16'
department:
- _id: MiLe
doi: 10.1103/physrevlett.121.165301
external_id:
  arxiv:
  - '1803.07990'
  isi:
  - '000447468400008'
intvolume: '       121'
isi: 1
issue: '16'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1803.07990
month: '10'
oa: 1
oa_version: Preprint
project:
- _id: 26031614-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P29902
  name: Quantum rotations in the presence of a many-body environment
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
related_material:
  link:
  - description: News on IST Homepage
    relation: press_release
    url: https://ist.ac.at/en/news/description-of-rotating-molecules-made-easy/
scopus_import: '1'
status: public
title: Diagrammatic Monte Carlo approach to angular momentum in quantum many-particle
  systems
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 121
year: '2018'
...
---
_id: '6340'
abstract:
- lang: eng
  text: We  present  a  secure  approach  for  maintaining  andreporting  credit  history  records  on  the  Blockchain.  Our  ap-proach  removes  third-parties  such  as  credit  reporting  agen-cies  from  the  lending  process  and  replaces  them  with  smartcontracts.  This  allows  customers  to  interact  directly  with  thelenders  or  banks  while  ensuring  the  integrity,  unmalleabilityand  privacy  of  their  credit  data.  Additionally,  each  customerhas  full  control  over  complete  or  selective  disclosure  of  hercredit
    records, eliminating the risk of privacy violations or databreaches. Moreover,
    our approach provides strong guaranteesfor the lenders as well. A lender can check
    both correctness andcompleteness of the credit data disclosed to her. This is
    the firstapproach  that  can  perform  all  credit  reporting  tasks  withouta  central  authority  or  changing  the  financial  mechanisms*.
article_processing_charge: No
arxiv: 1
author:
- first_name: Amir Kafshdar
  full_name: Goharshady, Amir Kafshdar
  id: 391365CE-F248-11E8-B48F-1D18A9856A87
  last_name: Goharshady
  orcid: 0000-0003-1702-6584
- first_name: Ali
  full_name: Behrouz, Ali
  last_name: Behrouz
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
citation:
  ama: 'Goharshady AK, Behrouz A, Chatterjee K. Secure Credit Reporting on the Blockchain.
    In: <i>Proceedings of the IEEE International Conference on Blockchain</i>. IEEE;
    2018:1343-1348. doi:<a href="https://doi.org/10.1109/Cybermatics_2018.2018.00231">10.1109/Cybermatics_2018.2018.00231</a>'
  apa: 'Goharshady, A. K., Behrouz, A., &#38; Chatterjee, K. (2018). Secure Credit
    Reporting on the Blockchain. In <i>Proceedings of the IEEE International Conference
    on Blockchain</i> (pp. 1343–1348). Halifax, Canada: IEEE. <a href="https://doi.org/10.1109/Cybermatics_2018.2018.00231">https://doi.org/10.1109/Cybermatics_2018.2018.00231</a>'
  chicago: Goharshady, Amir Kafshdar, Ali Behrouz, and Krishnendu Chatterjee. “Secure
    Credit Reporting on the Blockchain.” In <i>Proceedings of the IEEE International
    Conference on Blockchain</i>, 1343–48. IEEE, 2018. <a href="https://doi.org/10.1109/Cybermatics_2018.2018.00231">https://doi.org/10.1109/Cybermatics_2018.2018.00231</a>.
  ieee: A. K. Goharshady, A. Behrouz, and K. Chatterjee, “Secure Credit Reporting
    on the Blockchain,” in <i>Proceedings of the IEEE International Conference on
    Blockchain</i>, Halifax, Canada, 2018, pp. 1343–1348.
  ista: Goharshady AK, Behrouz A, Chatterjee K. 2018. Secure Credit Reporting on the
    Blockchain. Proceedings of the IEEE International Conference on Blockchain. IEEE
    International Conference on Blockchain, 1343–1348.
  mla: Goharshady, Amir Kafshdar, et al. “Secure Credit Reporting on the Blockchain.”
    <i>Proceedings of the IEEE International Conference on Blockchain</i>, IEEE, 2018,
    pp. 1343–48, doi:<a href="https://doi.org/10.1109/Cybermatics_2018.2018.00231">10.1109/Cybermatics_2018.2018.00231</a>.
  short: A.K. Goharshady, A. Behrouz, K. Chatterjee, in:, Proceedings of the IEEE
    International Conference on Blockchain, IEEE, 2018, pp. 1343–1348.
conference:
  end_date: 2018-08-03
  location: Halifax, Canada
  name: IEEE International Conference on Blockchain
  start_date: 2018-07-30
date_created: 2019-04-18T10:37:35Z
date_published: 2018-09-01T00:00:00Z
date_updated: 2025-06-02T08:53:45Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1109/Cybermatics_2018.2018.00231
ec_funded: 1
external_id:
  arxiv:
  - '1805.09104'
  isi:
  - '000481634500196'
file:
- access_level: open_access
  checksum: b25c9bb7cf6e7e6634e692d26d41ead8
  content_type: application/pdf
  creator: akafshda
  date_created: 2019-04-18T10:36:39Z
  date_updated: 2020-07-14T12:47:27Z
  file_id: '6341'
  file_name: blockchain2018.pdf
  file_size: 624338
  relation: main_file
file_date_updated: 2020-07-14T12:47:27Z
has_accepted_license: '1'
isi: 1
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '09'
oa: 1
oa_version: Submitted Version
page: 1343-1348
project:
- _id: 25892FC0-B435-11E9-9278-68D0E5697425
  grant_number: ICT15-003
  name: Efficient Algorithms for Computer Aided Verification
- _id: 266EEEC0-B435-11E9-9278-68D0E5697425
  name: Quantitative Game-theoretic Analysis of Blockchain Applications and Smart
    Contracts
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
publication: Proceedings of the IEEE International Conference on Blockchain
publication_identifier:
  isbn:
  - '978-1-5386-7975-3 '
publication_status: published
publisher: IEEE
quality_controlled: '1'
related_material:
  record:
  - id: '8934'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Secure Credit Reporting on the Blockchain
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2018'
...
---
_id: '6354'
abstract:
- lang: eng
  text: Blood platelets are critical for hemostasis and thrombosis, but also play
    diverse roles during immune responses. We have recently reported that platelets
    migrate at sites of infection in vitro and in vivo. Importantly, platelets use
    their ability to migrate to collect and bundle fibrin (ogen)-bound bacteria accomplishing
    efficient intravascular bacterial trapping. Here, we describe a method that allows
    analyzing platelet migration in vitro, focusing on their ability to collect bacteria
    and trap bacteria under flow.
acknowledgement: ' FöFoLe project 947 (F.G.), the Friedrich-Baur-Stiftung project
  41/16 (F.G.)'
article_number: e3018
author:
- first_name: Shuxia
  full_name: Fan, Shuxia
  last_name: Fan
- first_name: Michael
  full_name: Lorenz, Michael
  last_name: Lorenz
- first_name: Steffen
  full_name: Massberg, Steffen
  last_name: Massberg
- first_name: Florian R
  full_name: Gärtner, Florian R
  id: 397A88EE-F248-11E8-B48F-1D18A9856A87
  last_name: Gärtner
  orcid: 0000-0001-6120-3723
citation:
  ama: Fan S, Lorenz M, Massberg S, Gärtner FR. Platelet migration and bacterial trapping
    assay under flow. <i>Bio-Protocol</i>. 2018;8(18). doi:<a href="https://doi.org/10.21769/bioprotoc.3018">10.21769/bioprotoc.3018</a>
  apa: Fan, S., Lorenz, M., Massberg, S., &#38; Gärtner, F. R. (2018). Platelet migration
    and bacterial trapping assay under flow. <i>Bio-Protocol</i>. Bio-Protocol. <a
    href="https://doi.org/10.21769/bioprotoc.3018">https://doi.org/10.21769/bioprotoc.3018</a>
  chicago: Fan, Shuxia, Michael Lorenz, Steffen Massberg, and Florian R Gärtner. “Platelet
    Migration and Bacterial Trapping Assay under Flow.” <i>Bio-Protocol</i>. Bio-Protocol,
    2018. <a href="https://doi.org/10.21769/bioprotoc.3018">https://doi.org/10.21769/bioprotoc.3018</a>.
  ieee: S. Fan, M. Lorenz, S. Massberg, and F. R. Gärtner, “Platelet migration and
    bacterial trapping assay under flow,” <i>Bio-Protocol</i>, vol. 8, no. 18. Bio-Protocol,
    2018.
  ista: Fan S, Lorenz M, Massberg S, Gärtner FR. 2018. Platelet migration and bacterial
    trapping assay under flow. Bio-Protocol. 8(18), e3018.
  mla: Fan, Shuxia, et al. “Platelet Migration and Bacterial Trapping Assay under
    Flow.” <i>Bio-Protocol</i>, vol. 8, no. 18, e3018, Bio-Protocol, 2018, doi:<a
    href="https://doi.org/10.21769/bioprotoc.3018">10.21769/bioprotoc.3018</a>.
  short: S. Fan, M. Lorenz, S. Massberg, F.R. Gärtner, Bio-Protocol 8 (2018).
date_created: 2019-04-29T09:40:33Z
date_published: 2018-09-20T00:00:00Z
date_updated: 2021-01-12T08:07:12Z
day: '20'
ddc:
- '570'
department:
- _id: MiSi
doi: 10.21769/bioprotoc.3018
ec_funded: 1
file:
- access_level: open_access
  checksum: d4588377e789da7f360b553ae02c5119
  content_type: application/pdf
  creator: dernst
  date_created: 2019-04-30T08:04:33Z
  date_updated: 2020-07-14T12:47:28Z
  file_id: '6360'
  file_name: 2018_BioProtocol_Fan.pdf
  file_size: 2928337
  relation: main_file
file_date_updated: 2020-07-14T12:47:28Z
has_accepted_license: '1'
intvolume: '         8'
issue: '18'
keyword:
- Platelets
- Cell migration
- Bacteria
- Shear flow
- Fibrinogen
- E. coli
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 260AA4E2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '747687'
  name: Mechanical Adaptation of Lamellipodial Actin Networks in Migrating Cells
publication: Bio-Protocol
publication_identifier:
  issn:
  - 2331-8325
publication_status: published
publisher: Bio-Protocol
quality_controlled: '1'
status: public
title: Platelet migration and bacterial trapping assay under flow
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: 8
year: '2018'
...
---
_id: '6355'
abstract:
- lang: eng
  text: We  prove  that  any  cyclic  quadrilateral  can  be  inscribed  in  any  closed  convex
    C1-curve.  The smoothness condition is not required if the quadrilateral is a
    rectangle.
article_number: e7
article_processing_charge: No
arxiv: 1
author:
- first_name: Arseniy
  full_name: Akopyan, Arseniy
  id: 430D2C90-F248-11E8-B48F-1D18A9856A87
  last_name: Akopyan
  orcid: 0000-0002-2548-617X
- first_name: Sergey
  full_name: Avvakumov, Sergey
  id: 3827DAC8-F248-11E8-B48F-1D18A9856A87
  last_name: Avvakumov
citation:
  ama: Akopyan A, Avvakumov S. Any cyclic quadrilateral can be inscribed in any closed
    convex smooth curve. <i>Forum of Mathematics, Sigma</i>. 2018;6. doi:<a href="https://doi.org/10.1017/fms.2018.7">10.1017/fms.2018.7</a>
  apa: Akopyan, A., &#38; Avvakumov, S. (2018). Any cyclic quadrilateral can be inscribed
    in any closed convex smooth curve. <i>Forum of Mathematics, Sigma</i>. Cambridge
    University Press. <a href="https://doi.org/10.1017/fms.2018.7">https://doi.org/10.1017/fms.2018.7</a>
  chicago: Akopyan, Arseniy, and Sergey Avvakumov. “Any Cyclic Quadrilateral Can Be
    Inscribed in Any Closed Convex Smooth Curve.” <i>Forum of Mathematics, Sigma</i>.
    Cambridge University Press, 2018. <a href="https://doi.org/10.1017/fms.2018.7">https://doi.org/10.1017/fms.2018.7</a>.
  ieee: A. Akopyan and S. Avvakumov, “Any cyclic quadrilateral can be inscribed in
    any closed convex smooth curve,” <i>Forum of Mathematics, Sigma</i>, vol. 6. Cambridge
    University Press, 2018.
  ista: Akopyan A, Avvakumov S. 2018. Any cyclic quadrilateral can be inscribed in
    any closed convex smooth curve. Forum of Mathematics, Sigma. 6, e7.
  mla: Akopyan, Arseniy, and Sergey Avvakumov. “Any Cyclic Quadrilateral Can Be Inscribed
    in Any Closed Convex Smooth Curve.” <i>Forum of Mathematics, Sigma</i>, vol. 6,
    e7, Cambridge University Press, 2018, doi:<a href="https://doi.org/10.1017/fms.2018.7">10.1017/fms.2018.7</a>.
  short: A. Akopyan, S. Avvakumov, Forum of Mathematics, Sigma 6 (2018).
date_created: 2019-04-30T06:09:57Z
date_published: 2018-05-31T00:00:00Z
date_updated: 2023-09-19T14:50:12Z
day: '31'
ddc:
- '510'
department:
- _id: UlWa
- _id: HeEd
- _id: JaMa
doi: 10.1017/fms.2018.7
ec_funded: 1
external_id:
  arxiv:
  - '1712.10205'
  isi:
  - '000433915500001'
file:
- access_level: open_access
  checksum: 5a71b24ba712a3eb2e46165a38fbc30a
  content_type: application/pdf
  creator: dernst
  date_created: 2019-04-30T06:14:58Z
  date_updated: 2020-07-14T12:47:28Z
  file_id: '6356'
  file_name: 2018_ForumMahtematics_Akopyan.pdf
  file_size: 249246
  relation: main_file
file_date_updated: 2020-07-14T12:47:28Z
has_accepted_license: '1'
intvolume: '         6'
isi: 1
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
project:
- _id: 256E75B8-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '716117'
  name: Optimal Transport and Stochastic Dynamics
publication: Forum of Mathematics, Sigma
publication_identifier:
  issn:
  - 2050-5094
publication_status: published
publisher: Cambridge University Press
quality_controlled: '1'
related_material:
  record:
  - id: '8156'
    relation: dissertation_contains
    status: public
status: public
title: Any cyclic quadrilateral can be inscribed in any closed convex smooth curve
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 6
year: '2018'
...
---
_id: '64'
abstract:
- lang: eng
  text: Tropical geometry, an established field in pure mathematics, is a place where
    string theory, mirror symmetry, computational algebra, auction theory, and so
    forth meet and influence one another. In this paper, we report on our discovery
    of a tropical model with self-organized criticality (SOC) behavior. Our model
    is continuous, in contrast to all known models of SOC, and is a certain scaling
    limit of the sandpile model, the first and archetypical model of SOC. We describe
    how our model is related to pattern formation and proportional growth phenomena
    and discuss the dichotomy between continuous and discrete models in several contexts.
    Our aim in this context is to present an idealized tropical toy model (cf. Turing
    reaction-diffusion model), requiring further investigation.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Nikita
  full_name: Kalinin, Nikita
  last_name: Kalinin
- first_name: Aldo
  full_name: Guzmán Sáenz, Aldo
  last_name: Guzmán Sáenz
- first_name: Y
  full_name: Prieto, Y
  last_name: Prieto
- first_name: Mikhail
  full_name: Shkolnikov, Mikhail
  id: 35084A62-F248-11E8-B48F-1D18A9856A87
  last_name: Shkolnikov
  orcid: 0000-0002-4310-178X
- first_name: V
  full_name: Kalinina, V
  last_name: Kalinina
- first_name: Ernesto
  full_name: Lupercio, Ernesto
  last_name: Lupercio
citation:
  ama: 'Kalinin N, Guzmán Sáenz A, Prieto Y, Shkolnikov M, Kalinina V, Lupercio E.
    Self-organized criticality and pattern emergence through the lens of tropical
    geometry. <i>PNAS: Proceedings of the National Academy of Sciences of the United
    States of America</i>. 2018;115(35):E8135-E8142. doi:<a href="https://doi.org/10.1073/pnas.1805847115">10.1073/pnas.1805847115</a>'
  apa: 'Kalinin, N., Guzmán Sáenz, A., Prieto, Y., Shkolnikov, M., Kalinina, V., &#38;
    Lupercio, E. (2018). Self-organized criticality and pattern emergence through
    the lens of tropical geometry. <i>PNAS: Proceedings of the National Academy of
    Sciences of the United States of America</i>. National Academy of Sciences. <a
    href="https://doi.org/10.1073/pnas.1805847115">https://doi.org/10.1073/pnas.1805847115</a>'
  chicago: 'Kalinin, Nikita, Aldo Guzmán Sáenz, Y Prieto, Mikhail Shkolnikov, V Kalinina,
    and Ernesto Lupercio. “Self-Organized Criticality and Pattern Emergence through
    the Lens of Tropical Geometry.” <i>PNAS: Proceedings of the National Academy of
    Sciences of the United States of America</i>. National Academy of Sciences, 2018.
    <a href="https://doi.org/10.1073/pnas.1805847115">https://doi.org/10.1073/pnas.1805847115</a>.'
  ieee: 'N. Kalinin, A. Guzmán Sáenz, Y. Prieto, M. Shkolnikov, V. Kalinina, and E.
    Lupercio, “Self-organized criticality and pattern emergence through the lens of
    tropical geometry,” <i>PNAS: Proceedings of the National Academy of Sciences of
    the United States of America</i>, vol. 115, no. 35. National Academy of Sciences,
    pp. E8135–E8142, 2018.'
  ista: 'Kalinin N, Guzmán Sáenz A, Prieto Y, Shkolnikov M, Kalinina V, Lupercio E.
    2018. Self-organized criticality and pattern emergence through the lens of tropical
    geometry. PNAS: Proceedings of the National Academy of Sciences of the United
    States of America. 115(35), E8135–E8142.'
  mla: 'Kalinin, Nikita, et al. “Self-Organized Criticality and Pattern Emergence
    through the Lens of Tropical Geometry.” <i>PNAS: Proceedings of the National Academy
    of Sciences of the United States of America</i>, vol. 115, no. 35, National Academy
    of Sciences, 2018, pp. E8135–42, doi:<a href="https://doi.org/10.1073/pnas.1805847115">10.1073/pnas.1805847115</a>.'
  short: 'N. Kalinin, A. Guzmán Sáenz, Y. Prieto, M. Shkolnikov, V. Kalinina, E. Lupercio,
    PNAS: Proceedings of the National Academy of Sciences of the United States of
    America 115 (2018) E8135–E8142.'
date_created: 2018-12-11T11:44:26Z
date_published: 2018-08-28T00:00:00Z
date_updated: 2023-09-18T08:41:16Z
day: '28'
department:
- _id: TaHa
doi: 10.1073/pnas.1805847115
ec_funded: 1
external_id:
  arxiv:
  - '1806.09153'
  isi:
  - '000442861600009'
intvolume: '       115'
isi: 1
issue: '35'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1806.09153
month: '08'
oa: 1
oa_version: Preprint
page: E8135 - E8142
project:
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: 'PNAS: Proceedings of the National Academy of Sciences of the United
  States of America'
publication_identifier:
  issn:
  - '00278424'
publication_status: published
publisher: National Academy of Sciences
publist_id: '7990'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Self-organized criticality and pattern emergence through the lens of tropical
  geometry
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 115
year: '2018'
...
---
_id: '6459'
author:
- first_name: Barbara
  full_name: Petritsch, Barbara
  id: 406048EC-F248-11E8-B48F-1D18A9856A87
  last_name: Petritsch
  orcid: 0000-0003-2724-4614
citation:
  ama: Petritsch B. <i>Open Access at IST Austria 2009-2017</i>. IST Austria; 2018.
    doi:<a href="https://doi.org/10.5281/zenodo.1410279">10.5281/zenodo.1410279</a>
  apa: 'Petritsch, B. (2018). <i>Open Access at IST Austria 2009-2017</i>. Presented
    at the Open-Access-Tage, Graz, Austria: IST Austria. <a href="https://doi.org/10.5281/zenodo.1410279">https://doi.org/10.5281/zenodo.1410279</a>'
  chicago: Petritsch, Barbara. <i>Open Access at IST Austria 2009-2017</i>. IST Austria,
    2018. <a href="https://doi.org/10.5281/zenodo.1410279">https://doi.org/10.5281/zenodo.1410279</a>.
  ieee: B. Petritsch, <i>Open Access at IST Austria 2009-2017</i>. IST Austria, 2018.
  ista: Petritsch B. 2018. Open Access at IST Austria 2009-2017, IST Austria,p.
  mla: Petritsch, Barbara. <i>Open Access at IST Austria 2009-2017</i>. IST Austria,
    2018, doi:<a href="https://doi.org/10.5281/zenodo.1410279">10.5281/zenodo.1410279</a>.
  short: B. Petritsch, Open Access at IST Austria 2009-2017, IST Austria, 2018.
conference:
  end_date: 2018-09-26
  location: Graz, Austria
  name: Open-Access-Tage
  start_date: 2018-09-24
date_created: 2019-05-16T07:27:14Z
date_published: 2018-09-24T00:00:00Z
date_updated: 2020-07-14T23:06:21Z
day: '24'
ddc:
- '020'
department:
- _id: E-Lib
doi: 10.5281/zenodo.1410279
file:
- access_level: open_access
  checksum: 9063ab4d10ea93353c3a03bbf53fbcf1
  content_type: application/pdf
  creator: dernst
  date_created: 2019-05-16T07:26:25Z
  date_updated: 2020-07-14T12:47:30Z
  file_id: '6460'
  file_name: Poster_Beitrag_125_Petritsch.pdf
  file_size: 1967778
  relation: main_file
file_date_updated: 2020-07-14T12:47:30Z
has_accepted_license: '1'
keyword:
- Open Access
- Publication Analysis
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
publication_status: published
publisher: IST Austria
status: public
title: Open Access at IST Austria 2009-2017
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: conference_poster
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '6497'
abstract:
- lang: eng
  text: T cells are actively scanning pMHC-presenting cells in lymphoid organs and
    nonlymphoid tissues (NLTs) with divergent topologies and confinement. How the
    T cell actomyosin cytoskeleton facilitates this task in distinct environments
    is incompletely understood. Here, we show that lack of Myosin IXb (Myo9b), a negative
    regulator of the small GTPase Rho, led to increased Rho-GTP levels and cell surface
    stiffness in primary T cells. Nonetheless, intravital imaging revealed robust
    motility of Myo9b−/− CD8+ T cells in lymphoid tissue and similar expansion and
    differentiation during immune responses. In contrast, accumulation of Myo9b−/−
    CD8+ T cells in NLTs was strongly impaired. Specifically, Myo9b was required for
    T cell crossing of basement membranes, such as those which are present between
    dermis and epidermis. As consequence, Myo9b−/− CD8+ T cells showed impaired control
    of skin infections. In sum, we show that Myo9b is critical for the CD8+ T cell
    adaptation from lymphoid to NLT surveillance and the establishment of protective
    tissue–resident T cell populations.
article_processing_charge: No
author:
- first_name: Federica
  full_name: Moalli, Federica
  last_name: Moalli
- first_name: Xenia
  full_name: Ficht, Xenia
  last_name: Ficht
- first_name: Philipp
  full_name: Germann, Philipp
  last_name: Germann
- first_name: Mykhailo
  full_name: Vladymyrov, Mykhailo
  last_name: Vladymyrov
- first_name: Bettina
  full_name: Stolp, Bettina
  last_name: Stolp
- first_name: Ingrid
  full_name: de Vries, Ingrid
  id: 4C7D837E-F248-11E8-B48F-1D18A9856A87
  last_name: de Vries
- first_name: Ruth
  full_name: Lyck, Ruth
  last_name: Lyck
- first_name: Jasmin
  full_name: Balmer, Jasmin
  last_name: Balmer
- first_name: Amleto
  full_name: Fiocchi, Amleto
  last_name: Fiocchi
- first_name: Mario
  full_name: Kreutzfeldt, Mario
  last_name: Kreutzfeldt
- first_name: Doron
  full_name: Merkler, Doron
  last_name: Merkler
- first_name: Matteo
  full_name: Iannacone, Matteo
  last_name: Iannacone
- first_name: Akitaka
  full_name: Ariga, Akitaka
  last_name: Ariga
- first_name: Michael H.
  full_name: Stoffel, Michael H.
  last_name: Stoffel
- first_name: James
  full_name: Sharpe, James
  last_name: Sharpe
- first_name: Martin
  full_name: Bähler, Martin
  last_name: Bähler
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
- first_name: Alba
  full_name: Diz-Muñoz, Alba
  last_name: Diz-Muñoz
- first_name: Jens V.
  full_name: Stein, Jens V.
  last_name: Stein
citation:
  ama: Moalli F, Ficht X, Germann P, et al. The Rho regulator Myosin IXb enables nonlymphoid
    tissue seeding of protective CD8+T cells. <i>The Journal of Experimental Medicine</i>.
    2018;2015(7):1869–1890. doi:<a href="https://doi.org/10.1084/jem.20170896">10.1084/jem.20170896</a>
  apa: Moalli, F., Ficht, X., Germann, P., Vladymyrov, M., Stolp, B., de Vries, I.,
    … Stein, J. V. (2018). The Rho regulator Myosin IXb enables nonlymphoid tissue
    seeding of protective CD8+T cells. <i>The Journal of Experimental Medicine</i>.
    Rockefeller University Press. <a href="https://doi.org/10.1084/jem.20170896">https://doi.org/10.1084/jem.20170896</a>
  chicago: Moalli, Federica, Xenia Ficht, Philipp Germann, Mykhailo Vladymyrov, Bettina
    Stolp, Ingrid de Vries, Ruth Lyck, et al. “The Rho Regulator Myosin IXb Enables
    Nonlymphoid Tissue Seeding of Protective CD8+T Cells.” <i>The Journal of Experimental
    Medicine</i>. Rockefeller University Press, 2018. <a href="https://doi.org/10.1084/jem.20170896">https://doi.org/10.1084/jem.20170896</a>.
  ieee: F. Moalli <i>et al.</i>, “The Rho regulator Myosin IXb enables nonlymphoid
    tissue seeding of protective CD8+T cells,” <i>The Journal of Experimental Medicine</i>,
    vol. 2015, no. 7. Rockefeller University Press, pp. 1869–1890, 2018.
  ista: Moalli F, Ficht X, Germann P, Vladymyrov M, Stolp B, de Vries I, Lyck R, Balmer
    J, Fiocchi A, Kreutzfeldt M, Merkler D, Iannacone M, Ariga A, Stoffel MH, Sharpe
    J, Bähler M, Sixt MK, Diz-Muñoz A, Stein JV. 2018. The Rho regulator Myosin IXb
    enables nonlymphoid tissue seeding of protective CD8+T cells. The Journal of Experimental
    Medicine. 2015(7), 1869–1890.
  mla: Moalli, Federica, et al. “The Rho Regulator Myosin IXb Enables Nonlymphoid
    Tissue Seeding of Protective CD8+T Cells.” <i>The Journal of Experimental Medicine</i>,
    vol. 2015, no. 7, Rockefeller University Press, 2018, pp. 1869–1890, doi:<a href="https://doi.org/10.1084/jem.20170896">10.1084/jem.20170896</a>.
  short: F. Moalli, X. Ficht, P. Germann, M. Vladymyrov, B. Stolp, I. de Vries, R.
    Lyck, J. Balmer, A. Fiocchi, M. Kreutzfeldt, D. Merkler, M. Iannacone, A. Ariga,
    M.H. Stoffel, J. Sharpe, M. Bähler, M.K. Sixt, A. Diz-Muñoz, J.V. Stein, The Journal
    of Experimental Medicine 2015 (2018) 1869–1890.
date_created: 2019-05-28T12:36:47Z
date_published: 2018-06-06T00:00:00Z
date_updated: 2023-09-19T14:52:08Z
day: '06'
ddc:
- '570'
department:
- _id: MiSi
doi: 10.1084/jem.20170896
external_id:
  isi:
  - '000440822900011'
file:
- access_level: open_access
  checksum: 86ae5331f9bfced9a6358a790a04bef4
  content_type: application/pdf
  creator: kschuh
  date_created: 2019-05-28T12:40:05Z
  date_updated: 2020-07-14T12:47:32Z
  file_id: '6498'
  file_name: 2018_rupress_Moalli.pdf
  file_size: 3841660
  relation: main_file
file_date_updated: 2020-07-14T12:47:32Z
has_accepted_license: '1'
intvolume: '      2015'
isi: 1
issue: '7'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-sa/4.0/
month: '06'
oa: 1
oa_version: Published Version
page: 1869–1890
publication: The Journal of Experimental Medicine
publication_identifier:
  eissn:
  - 1540-9538
  issn:
  - 0022-1007
publication_status: published
publisher: Rockefeller University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: The Rho regulator Myosin IXb enables nonlymphoid tissue seeding of protective
  CD8+T cells
tmp:
  image: /images/cc_by_nc_sa.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC
    BY-NC-SA 4.0)
  short: CC BY-NC-SA (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 2015
year: '2018'
...
---
_id: '6499'
abstract:
- lang: eng
  text: Expansion microscopy is a recently introduced imaging technique that achieves
    super‐resolution through physically expanding the specimen by ~4×, after embedding
    into a swellable gel. The resolution attained is, correspondingly, approximately
    fourfold better than the diffraction limit, or ~70 nm. This is a major improvement
    over conventional microscopy, but still lags behind modern STED or STORM setups,
    whose resolution can reach 20–30 nm. We addressed this issue here by introducing
    an improved gel recipe that enables an expansion factor of ~10× in each dimension,
    which corresponds to an expansion of the sample volume by more than 1,000‐fold.
    Our protocol, which we termed X10 microscopy, achieves a resolution of 25–30 nm
    on conventional epifluorescence microscopes. X10 provides multi‐color images similar
    or even superior to those produced with more challenging methods, such as STED,
    STORM, and iterative expansion microscopy (iExM). X10 is therefore the cheapest
    and easiest option for high‐quality super‐resolution imaging currently available.
    X10 should be usable in any laboratory, irrespective of the machinery owned or
    of the technical knowledge.
article_number: e45836
article_processing_charge: No
author:
- first_name: Sven M
  full_name: Truckenbrodt, Sven M
  id: 45812BD4-F248-11E8-B48F-1D18A9856A87
  last_name: Truckenbrodt
- first_name: Manuel
  full_name: Maidorn, Manuel
  last_name: Maidorn
- first_name: Dagmar
  full_name: Crzan, Dagmar
  last_name: Crzan
- first_name: Hanna
  full_name: Wildhagen, Hanna
  last_name: Wildhagen
- first_name: Selda
  full_name: Kabatas, Selda
  last_name: Kabatas
- first_name: Silvio O
  full_name: Rizzoli, Silvio O
  last_name: Rizzoli
citation:
  ama: Truckenbrodt SM, Maidorn M, Crzan D, Wildhagen H, Kabatas S, Rizzoli SO. X10
    expansion microscopy enables 25‐nm resolution on conventional microscopes. <i>EMBO
    reports</i>. 2018;19(9). doi:<a href="https://doi.org/10.15252/embr.201845836">10.15252/embr.201845836</a>
  apa: Truckenbrodt, S. M., Maidorn, M., Crzan, D., Wildhagen, H., Kabatas, S., &#38;
    Rizzoli, S. O. (2018). X10 expansion microscopy enables 25‐nm resolution on conventional
    microscopes. <i>EMBO Reports</i>. EMBO. <a href="https://doi.org/10.15252/embr.201845836">https://doi.org/10.15252/embr.201845836</a>
  chicago: Truckenbrodt, Sven M, Manuel Maidorn, Dagmar Crzan, Hanna Wildhagen, Selda
    Kabatas, and Silvio O Rizzoli. “X10 Expansion Microscopy Enables 25‐nm Resolution
    on Conventional Microscopes.” <i>EMBO Reports</i>. EMBO, 2018. <a href="https://doi.org/10.15252/embr.201845836">https://doi.org/10.15252/embr.201845836</a>.
  ieee: S. M. Truckenbrodt, M. Maidorn, D. Crzan, H. Wildhagen, S. Kabatas, and S.
    O. Rizzoli, “X10 expansion microscopy enables 25‐nm resolution on conventional
    microscopes,” <i>EMBO reports</i>, vol. 19, no. 9. EMBO, 2018.
  ista: Truckenbrodt SM, Maidorn M, Crzan D, Wildhagen H, Kabatas S, Rizzoli SO. 2018.
    X10 expansion microscopy enables 25‐nm resolution on conventional microscopes.
    EMBO reports. 19(9), e45836.
  mla: Truckenbrodt, Sven M., et al. “X10 Expansion Microscopy Enables 25‐nm Resolution
    on Conventional Microscopes.” <i>EMBO Reports</i>, vol. 19, no. 9, e45836, EMBO,
    2018, doi:<a href="https://doi.org/10.15252/embr.201845836">10.15252/embr.201845836</a>.
  short: S.M. Truckenbrodt, M. Maidorn, D. Crzan, H. Wildhagen, S. Kabatas, S.O. Rizzoli,
    EMBO Reports 19 (2018).
date_created: 2019-05-28T13:16:08Z
date_published: 2018-09-01T00:00:00Z
date_updated: 2023-09-19T14:52:32Z
day: '01'
ddc:
- '580'
department:
- _id: JoDa
doi: 10.15252/embr.201845836
external_id:
  isi:
  - '000443682200009'
file:
- access_level: open_access
  checksum: 6ec90abc637f09cca3a7b6424d7e7a26
  content_type: application/pdf
  creator: kschuh
  date_created: 2019-05-28T13:17:19Z
  date_updated: 2020-07-14T12:47:32Z
  file_id: '6500'
  file_name: 2018_embo_Truckenbrodt.pdf
  file_size: 2005572
  relation: main_file
file_date_updated: 2020-07-14T12:47:32Z
has_accepted_license: '1'
intvolume: '        19'
isi: 1
issue: '9'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
publication: EMBO reports
publication_identifier:
  eissn:
  - 1469-3178
  issn:
  - 1469-221X
publication_status: published
publisher: EMBO
quality_controlled: '1'
scopus_import: '1'
status: public
title: X10 expansion microscopy enables 25‐nm resolution on conventional microscopes
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 19
year: '2018'
...
---
_id: '6525'
abstract:
- lang: eng
  text: This chapter finds an agreement of equivariant indices of semi-classical homomorphisms
    between pairwise mirror branes in the GL2 Higgs moduli space on a Riemann surface.
    On one side of the agreement, components of the Lagrangian brane of U(1,1) Higgs
    bundles, whose mirror was proposed by Hitchin to be certain even exterior powers
    of the hyperholomorphic Dirac bundle on the SL2 Higgs moduli space, are present.
    The agreement arises from a mysterious functional equation. This gives strong
    computational evidence for Hitchin’s proposal.
author:
- first_name: Tamás
  full_name: Hausel, Tamás
  id: 4A0666D8-F248-11E8-B48F-1D18A9856A87
  last_name: Hausel
- first_name: Anton
  full_name: Mellit, Anton
  id: 388D3134-F248-11E8-B48F-1D18A9856A87
  last_name: Mellit
- first_name: Du
  full_name: Pei, Du
  last_name: Pei
citation:
  ama: 'Hausel T, Mellit A, Pei D. Mirror symmetry with branes by equivariant verlinde
    formulas. In: <i>Geometry and Physics: Volume I</i>. Oxford University Press;
    2018:189-218. doi:<a href="https://doi.org/10.1093/oso/9780198802013.003.0009">10.1093/oso/9780198802013.003.0009</a>'
  apa: 'Hausel, T., Mellit, A., &#38; Pei, D. (2018). Mirror symmetry with branes
    by equivariant verlinde formulas. In <i>Geometry and Physics: Volume I</i> (pp.
    189–218). Oxford University Press. <a href="https://doi.org/10.1093/oso/9780198802013.003.0009">https://doi.org/10.1093/oso/9780198802013.003.0009</a>'
  chicago: 'Hausel, Tamás, Anton Mellit, and Du Pei. “Mirror Symmetry with Branes
    by Equivariant Verlinde Formulas.” In <i>Geometry and Physics: Volume I</i>, 189–218.
    Oxford University Press, 2018. <a href="https://doi.org/10.1093/oso/9780198802013.003.0009">https://doi.org/10.1093/oso/9780198802013.003.0009</a>.'
  ieee: 'T. Hausel, A. Mellit, and D. Pei, “Mirror symmetry with branes by equivariant
    verlinde formulas,” in <i>Geometry and Physics: Volume I</i>, Oxford University
    Press, 2018, pp. 189–218.'
  ista: 'Hausel T, Mellit A, Pei D. 2018.Mirror symmetry with branes by equivariant
    verlinde formulas. In: Geometry and Physics: Volume I. , 189–218.'
  mla: 'Hausel, Tamás, et al. “Mirror Symmetry with Branes by Equivariant Verlinde
    Formulas.” <i>Geometry and Physics: Volume I</i>, Oxford University Press, 2018,
    pp. 189–218, doi:<a href="https://doi.org/10.1093/oso/9780198802013.003.0009">10.1093/oso/9780198802013.003.0009</a>.'
  short: 'T. Hausel, A. Mellit, D. Pei, in:, Geometry and Physics: Volume I, Oxford
    University Press, 2018, pp. 189–218.'
date_created: 2019-06-06T12:42:01Z
date_published: 2018-01-01T00:00:00Z
date_updated: 2021-01-12T08:07:52Z
day: '01'
department:
- _id: TaHa
doi: 10.1093/oso/9780198802013.003.0009
language:
- iso: eng
month: '01'
oa_version: None
page: 189-218
publication: 'Geometry and Physics: Volume I'
publication_identifier:
  isbn:
  - '9780198802013'
  - '9780191840500'
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: 1
status: public
title: Mirror symmetry with branes by equivariant verlinde formulas
type: book_chapter
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '6558'
abstract:
- lang: eng
  text: This paper studies the problem of distributed stochastic optimization in an
    adversarial setting where, out of m machines which allegedly compute stochastic
    gradients every iteration, an α-fraction are Byzantine, and may behave adversarially.
    Our main result is a variant of stochastic gradient descent (SGD) which finds
    ε-approximate minimizers of convex functions in T=O~(1/ε²m+α²/ε²) iterations.
    In contrast, traditional mini-batch SGD needs T=O(1/ε²m) iterations, but cannot
    tolerate Byzantine failures. Further, we provide a lower bound showing that, up
    to logarithmic factors, our algorithm is information-theoretically optimal both
    in terms of sample complexity and time complexity.
article_processing_charge: No
arxiv: 1
author:
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
- first_name: Zeyuan
  full_name: Allen-Zhu, Zeyuan
  last_name: Allen-Zhu
- first_name: Jerry
  full_name: Li, Jerry
  last_name: Li
citation:
  ama: 'Alistarh D-A, Allen-Zhu Z, Li J. Byzantine stochastic gradient descent. In:
    <i>Advances in Neural Information Processing Systems</i>. Vol 2018. Neural Information
    Processing Systems Foundation; 2018:4613-4623.'
  apa: 'Alistarh, D.-A., Allen-Zhu, Z., &#38; Li, J. (2018). Byzantine stochastic
    gradient descent. In <i>Advances in Neural Information Processing Systems</i>
    (Vol. 2018, pp. 4613–4623). Montreal, Canada: Neural Information Processing Systems
    Foundation.'
  chicago: Alistarh, Dan-Adrian, Zeyuan Allen-Zhu, and Jerry Li. “Byzantine Stochastic
    Gradient Descent.” In <i>Advances in Neural Information Processing Systems</i>,
    2018:4613–23. Neural Information Processing Systems Foundation, 2018.
  ieee: D.-A. Alistarh, Z. Allen-Zhu, and J. Li, “Byzantine stochastic gradient descent,”
    in <i>Advances in Neural Information Processing Systems</i>, Montreal, Canada,
    2018, vol. 2018, pp. 4613–4623.
  ista: 'Alistarh D-A, Allen-Zhu Z, Li J. 2018. Byzantine stochastic gradient descent.
    Advances in Neural Information Processing Systems. NeurIPS: Conference on Neural
    Information Processing Systems vol. 2018, 4613–4623.'
  mla: Alistarh, Dan-Adrian, et al. “Byzantine Stochastic Gradient Descent.” <i>Advances
    in Neural Information Processing Systems</i>, vol. 2018, Neural Information Processing
    Systems Foundation, 2018, pp. 4613–23.
  short: D.-A. Alistarh, Z. Allen-Zhu, J. Li, in:, Advances in Neural Information
    Processing Systems, Neural Information Processing Systems Foundation, 2018, pp.
    4613–4623.
conference:
  end_date: 2018-12-08
  location: Montreal, Canada
  name: 'NeurIPS: Conference on Neural Information Processing Systems'
  start_date: 2018-12-02
date_created: 2019-06-13T08:22:37Z
date_published: 2018-12-01T00:00:00Z
date_updated: 2023-09-19T15:12:45Z
day: '01'
department:
- _id: DaAl
external_id:
  arxiv:
  - '1803.08917'
  isi:
  - '000461823304061'
intvolume: '      2018'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1803.08917
month: '12'
oa: 1
oa_version: Published Version
page: 4613-4623
publication: Advances in Neural Information Processing Systems
publication_status: published
publisher: Neural Information Processing Systems Foundation
quality_controlled: '1'
scopus_import: '1'
status: public
title: Byzantine stochastic gradient descent
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 2018
year: '2018'
...
---
_id: '6589'
abstract:
- lang: eng
  text: Distributed training of massive machine learning models, in particular deep
    neural networks, via Stochastic Gradient Descent (SGD) is becoming commonplace.
    Several families of communication-reduction methods, such as quantization, large-batch
    methods, and gradient sparsification, have been proposed. To date, gradient sparsification
    methods--where each node sorts gradients by magnitude, and only communicates a
    subset of the components, accumulating the rest locally--are known to yield some
    of the largest practical gains. Such methods can reduce the amount of communication
    per step by up to \emph{three orders of magnitude}, while preserving model accuracy.
    Yet, this family of methods currently has no theoretical justification. This is
    the question we address in this paper. We prove that, under analytic assumptions,
    sparsifying gradients by magnitude with local error correction provides convergence
    guarantees, for both convex and non-convex smooth objectives, for data-parallel
    SGD. The main insight is that sparsification methods implicitly maintain bounds
    on the maximum impact of stale updates, thanks to selection by magnitude. Our
    analysis and empirical validation also reveal that these methods do require analytical
    conditions to converge well, justifying existing heuristics.
article_processing_charge: No
arxiv: 1
author:
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
- first_name: Torsten
  full_name: Hoefler, Torsten
  last_name: Hoefler
- first_name: Mikael
  full_name: Johansson, Mikael
  last_name: Johansson
- first_name: Nikola H
  full_name: Konstantinov, Nikola H
  id: 4B9D76E4-F248-11E8-B48F-1D18A9856A87
  last_name: Konstantinov
- first_name: Sarit
  full_name: Khirirat, Sarit
  last_name: Khirirat
- first_name: Cedric
  full_name: Renggli, Cedric
  last_name: Renggli
citation:
  ama: 'Alistarh D-A, Hoefler T, Johansson M, Konstantinov NH, Khirirat S, Renggli
    C. The convergence of sparsified gradient methods. In: <i>Advances in Neural Information
    Processing Systems 31</i>. Vol Volume 2018. Neural Information Processing Systems
    Foundation; 2018:5973-5983.'
  apa: 'Alistarh, D.-A., Hoefler, T., Johansson, M., Konstantinov, N. H., Khirirat,
    S., &#38; Renggli, C. (2018). The convergence of sparsified gradient methods.
    In <i>Advances in Neural Information Processing Systems 31</i> (Vol. Volume 2018,
    pp. 5973–5983). Montreal, Canada: Neural Information Processing Systems Foundation.'
  chicago: Alistarh, Dan-Adrian, Torsten Hoefler, Mikael Johansson, Nikola H Konstantinov,
    Sarit Khirirat, and Cedric Renggli. “The Convergence of Sparsified Gradient Methods.”
    In <i>Advances in Neural Information Processing Systems 31</i>, Volume 2018:5973–83.
    Neural Information Processing Systems Foundation, 2018.
  ieee: D.-A. Alistarh, T. Hoefler, M. Johansson, N. H. Konstantinov, S. Khirirat,
    and C. Renggli, “The convergence of sparsified gradient methods,” in <i>Advances
    in Neural Information Processing Systems 31</i>, Montreal, Canada, 2018, vol.
    Volume 2018, pp. 5973–5983.
  ista: 'Alistarh D-A, Hoefler T, Johansson M, Konstantinov NH, Khirirat S, Renggli
    C. 2018. The convergence of sparsified gradient methods. Advances in Neural Information
    Processing Systems 31. NeurIPS: Conference on Neural Information Processing Systems
    vol. Volume 2018, 5973–5983.'
  mla: Alistarh, Dan-Adrian, et al. “The Convergence of Sparsified Gradient Methods.”
    <i>Advances in Neural Information Processing Systems 31</i>, vol. Volume 2018,
    Neural Information Processing Systems Foundation, 2018, pp. 5973–83.
  short: D.-A. Alistarh, T. Hoefler, M. Johansson, N.H. Konstantinov, S. Khirirat,
    C. Renggli, in:, Advances in Neural Information Processing Systems 31, Neural
    Information Processing Systems Foundation, 2018, pp. 5973–5983.
conference:
  end_date: 2018-12-08
  location: Montreal, Canada
  name: 'NeurIPS: Conference on Neural Information Processing Systems'
  start_date: 2018-12-02
date_created: 2019-06-27T09:32:55Z
date_published: 2018-12-01T00:00:00Z
date_updated: 2023-10-17T11:47:20Z
day: '01'
department:
- _id: DaAl
- _id: ChLa
ec_funded: 1
external_id:
  arxiv:
  - '1809.10505'
  isi:
  - '000461852000047'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1809.10505
month: '12'
oa: 1
oa_version: Preprint
page: 5973-5983
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication: Advances in Neural Information Processing Systems 31
publication_status: published
publisher: Neural Information Processing Systems Foundation
quality_controlled: '1'
scopus_import: '1'
status: public
title: The convergence of sparsified gradient methods
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: Volume 2018
year: '2018'
...
---
_id: '66'
abstract:
- lang: eng
  text: 'Crypto-currencies are digital assets designed to work as a medium of exchange,
    e.g., Bitcoin, but they are susceptible to attacks (dishonest behavior of participants).
    A framework for the analysis of attacks in crypto-currencies requires (a) modeling
    of game-theoretic aspects to analyze incentives for deviation from honest behavior;
    (b) concurrent interactions between participants; and (c) analysis of long-term
    monetary gains. Traditional game-theoretic approaches for the analysis of security
    protocols consider either qualitative temporal properties such as safety and termination,
    or the very special class of one-shot (stateless) games. However, to analyze general
    attacks on protocols for crypto-currencies, both stateful analysis and quantitative
    objectives are necessary. In this work our main contributions are as follows:
    (a) we show how a class of concurrent mean-payo games, namely ergodic games, can
    model various attacks that arise naturally in crypto-currencies; (b) we present
    the first practical implementation of algorithms for ergodic games that scales
    to model realistic problems for crypto-currencies; and (c) we present experimental
    results showing that our framework can handle games with thousands of states and
    millions of transitions.'
alternative_title:
- LIPIcs
article_number: '11'
article_processing_charge: No
arxiv: 1
author:
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Amir
  full_name: Goharshady, Amir
  id: 391365CE-F248-11E8-B48F-1D18A9856A87
  last_name: Goharshady
  orcid: 0000-0003-1702-6584
- first_name: Rasmus
  full_name: Ibsen-Jensen, Rasmus
  id: 3B699956-F248-11E8-B48F-1D18A9856A87
  last_name: Ibsen-Jensen
  orcid: 0000-0003-4783-0389
- first_name: Yaron
  full_name: Velner, Yaron
  last_name: Velner
citation:
  ama: 'Chatterjee K, Goharshady AK, Ibsen-Jensen R, Velner Y. Ergodic mean-payoff
    games for the analysis of attacks in crypto-currencies. In: Vol 118. Schloss Dagstuhl
    - Leibniz-Zentrum für Informatik; 2018. doi:<a href="https://doi.org/10.4230/LIPIcs.CONCUR.2018.11">10.4230/LIPIcs.CONCUR.2018.11</a>'
  apa: 'Chatterjee, K., Goharshady, A. K., Ibsen-Jensen, R., &#38; Velner, Y. (2018).
    Ergodic mean-payoff games for the analysis of attacks in crypto-currencies (Vol.
    118). Presented at the CONCUR: Conference on Concurrency Theory, Beijing, China:
    Schloss Dagstuhl - Leibniz-Zentrum für Informatik. <a href="https://doi.org/10.4230/LIPIcs.CONCUR.2018.11">https://doi.org/10.4230/LIPIcs.CONCUR.2018.11</a>'
  chicago: Chatterjee, Krishnendu, Amir Kafshdar Goharshady, Rasmus Ibsen-Jensen,
    and Yaron Velner. “Ergodic Mean-Payoff Games for the Analysis of Attacks in Crypto-Currencies,”
    Vol. 118. Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2018. <a href="https://doi.org/10.4230/LIPIcs.CONCUR.2018.11">https://doi.org/10.4230/LIPIcs.CONCUR.2018.11</a>.
  ieee: 'K. Chatterjee, A. K. Goharshady, R. Ibsen-Jensen, and Y. Velner, “Ergodic
    mean-payoff games for the analysis of attacks in crypto-currencies,” presented
    at the CONCUR: Conference on Concurrency Theory, Beijing, China, 2018, vol. 118.'
  ista: 'Chatterjee K, Goharshady AK, Ibsen-Jensen R, Velner Y. 2018. Ergodic mean-payoff
    games for the analysis of attacks in crypto-currencies. CONCUR: Conference on
    Concurrency Theory, LIPIcs, vol. 118, 11.'
  mla: Chatterjee, Krishnendu, et al. <i>Ergodic Mean-Payoff Games for the Analysis
    of Attacks in Crypto-Currencies</i>. Vol. 118, 11, Schloss Dagstuhl - Leibniz-Zentrum
    für Informatik, 2018, doi:<a href="https://doi.org/10.4230/LIPIcs.CONCUR.2018.11">10.4230/LIPIcs.CONCUR.2018.11</a>.
  short: K. Chatterjee, A.K. Goharshady, R. Ibsen-Jensen, Y. Velner, in:, Schloss
    Dagstuhl - Leibniz-Zentrum für Informatik, 2018.
conference:
  end_date: 2018-09-07
  location: Beijing, China
  name: 'CONCUR: Conference on Concurrency Theory'
  start_date: 2018-09-04
date_created: 2018-12-11T11:44:27Z
date_published: 2018-09-01T00:00:00Z
date_updated: 2025-06-02T08:53:46Z
day: '01'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.4230/LIPIcs.CONCUR.2018.11
ec_funded: 1
external_id:
  arxiv:
  - '1806.03108'
file:
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  date_created: 2018-12-17T12:08:00Z
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  file_name: 2018_CONCUR_Chatterjee.pdf
  file_size: 1078309
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file_date_updated: 2020-07-14T12:47:34Z
has_accepted_license: '1'
intvolume: '       118'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 25892FC0-B435-11E9-9278-68D0E5697425
  grant_number: ICT15-003
  name: Efficient Algorithms for Computer Aided Verification
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 266EEEC0-B435-11E9-9278-68D0E5697425
  name: Quantitative Game-theoretic Analysis of Blockchain Applications and Smart
    Contracts
publication_identifier:
  isbn:
  - 978-3-95977-087-3
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
publist_id: '7988'
quality_controlled: '1'
related_material:
  record:
  - id: '8934'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Ergodic mean-payoff games for the analysis of attacks in crypto-currencies
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: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 118
year: '2018'
...
---
_id: '14327'
abstract:
- lang: eng
  text: "A common assumption in causal modeling posits that the data is generated
    by a\r\nset of independent mechanisms, and algorithms should aim to recover this\r\nstructure.
    Standard unsupervised learning, however, is often concerned with\r\ntraining a
    single model to capture the overall distribution or aspects thereof.\r\nInspired
    by clustering approaches, we consider mixtures of implicit generative\r\nmodels
    that ``disentangle'' the independent generative mechanisms underlying\r\nthe data.
    Relying on an additional set of discriminators, we propose a\r\ncompetitive training
    procedure in which the models only need to capture the\r\nportion of the data
    distribution from which they can produce realistic samples.\r\nAs a by-product,
    each model is simpler and faster to train. We empirically show\r\nthat our approach
    splits the training distribution in a sensible way and\r\nincreases the quality
    of the generated samples."
article_number: '1804.11130'
article_processing_charge: No
arxiv: 1
author:
- first_name: Francesco
  full_name: Locatello, Francesco
  id: 26cfd52f-2483-11ee-8040-88983bcc06d4
  last_name: Locatello
  orcid: 0000-0002-4850-0683
- first_name: Damien
  full_name: Vincent, Damien
  last_name: Vincent
- first_name: Ilya
  full_name: Tolstikhin, Ilya
  last_name: Tolstikhin
- first_name: Gunnar
  full_name: Rätsch, Gunnar
  last_name: Rätsch
- first_name: Sylvain
  full_name: Gelly, Sylvain
  last_name: Gelly
- first_name: Bernhard
  full_name: Schölkopf, Bernhard
  last_name: Schölkopf
citation:
  ama: Locatello F, Vincent D, Tolstikhin I, Rätsch G, Gelly S, Schölkopf B. Competitive
    training of mixtures of independent deep generative models. <i>arXiv</i>. doi:<a
    href="https://doi.org/10.48550/arXiv.1804.11130">10.48550/arXiv.1804.11130</a>
  apa: Locatello, F., Vincent, D., Tolstikhin, I., Rätsch, G., Gelly, S., &#38; Schölkopf,
    B. (n.d.). Competitive training of mixtures of independent deep generative models.
    <i>arXiv</i>. <a href="https://doi.org/10.48550/arXiv.1804.11130">https://doi.org/10.48550/arXiv.1804.11130</a>
  chicago: Locatello, Francesco, Damien Vincent, Ilya Tolstikhin, Gunnar Rätsch, Sylvain
    Gelly, and Bernhard Schölkopf. “Competitive Training of Mixtures of Independent
    Deep Generative Models.” <i>ArXiv</i>, n.d. <a href="https://doi.org/10.48550/arXiv.1804.11130">https://doi.org/10.48550/arXiv.1804.11130</a>.
  ieee: F. Locatello, D. Vincent, I. Tolstikhin, G. Rätsch, S. Gelly, and B. Schölkopf,
    “Competitive training of mixtures of independent deep generative models,” <i>arXiv</i>.
    .
  ista: Locatello F, Vincent D, Tolstikhin I, Rätsch G, Gelly S, Schölkopf B. Competitive
    training of mixtures of independent deep generative models. arXiv, 1804.11130.
  mla: Locatello, Francesco, et al. “Competitive Training of Mixtures of Independent
    Deep Generative Models.” <i>ArXiv</i>, 1804.11130, doi:<a href="https://doi.org/10.48550/arXiv.1804.11130">10.48550/arXiv.1804.11130</a>.
  short: F. Locatello, D. Vincent, I. Tolstikhin, G. Rätsch, S. Gelly, B. Schölkopf,
    ArXiv (n.d.).
date_created: 2023-09-13T12:20:49Z
date_published: 2018-04-30T00:00:00Z
date_updated: 2023-09-13T12:23:03Z
day: '30'
department:
- _id: FrLo
doi: 10.48550/arXiv.1804.11130
extern: '1'
external_id:
  arxiv:
  - '1804.11130'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.1804.11130
month: '04'
oa: 1
oa_version: Preprint
publication: arXiv
publication_status: submitted
status: public
title: Competitive training of mixtures of independent deep generative models
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
