---
_id: '14363'
abstract:
- lang: eng
  text: Mitochondrial networks remodel their connectivity, content, and subcellular
    localization to support optimized energy production in conditions of increased
    environmental or cellular stress. Microglia rely on mitochondria to respond to
    these stressors, however our knowledge about mitochondrial networks and their
    adaptations in microglia in vivo is limited. Here, we generate a mouse model that
    selectively labels mitochondria in microglia. We identify that mitochondrial networks
    are more fragmented with increased content and perinuclear localization in vitro
    vs. in vivo. Mitochondrial networks adapt similarly in microglia closest to the
    injury site after optic nerve crush. Preventing microglial UCP2 increase after
    injury by selective knockout induces cellular stress. This results in mitochondrial
    hyperfusion in male microglia, a phenotype absent in females due to circulating
    estrogens. Our results establish the foundation for mitochondrial network analysis
    of microglia in vivo, emphasizing the importance of mitochondrial-based sex effects
    of microglia in other pathologies.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: PreCl
acknowledgement: We thank the Scientific Service Units (SSU) of ISTA through resources
  provided by the Imaging and Optics Facility (IOF), the Lab Support Facility (LSF),
  and the Pre-Clinical Facility (PCF) team, specifically Sonja Haslinger and Michael
  Schunn for excellent mouse colony management and support. This research was supported
  by the FWF Sonderforschungsbereich F83 (to E.E.P). We thank Bálint Nagy, Ryan John
  A. Cubero, Marco Benevento and all members of the Siegert group for constant feedback
  on the project and article.
article_number: '107780'
article_processing_charge: Yes
article_type: original
author:
- first_name: Margaret E
  full_name: Maes, Margaret E
  id: 3838F452-F248-11E8-B48F-1D18A9856A87
  last_name: Maes
  orcid: 0000-0001-9642-1085
- first_name: Gloria
  full_name: Colombo, Gloria
  id: 3483CF6C-F248-11E8-B48F-1D18A9856A87
  last_name: Colombo
  orcid: 0000-0001-9434-8902
- first_name: Florianne E
  full_name: Schoot Uiterkamp, Florianne E
  id: 3526230C-F248-11E8-B48F-1D18A9856A87
  last_name: Schoot Uiterkamp
- first_name: Felix
  full_name: Sternberg, Felix
  last_name: Sternberg
- first_name: Alessandro
  full_name: Venturino, Alessandro
  id: 41CB84B2-F248-11E8-B48F-1D18A9856A87
  last_name: Venturino
  orcid: 0000-0003-2356-9403
- first_name: Elena E.
  full_name: Pohl, Elena E.
  last_name: Pohl
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
citation:
  ama: Maes ME, Colombo G, Schoot Uiterkamp FE, et al. Mitochondrial network adaptations
    of microglia reveal sex-specific stress response after injury and UCP2 knockout.
    <i>iScience</i>. 2023;26(10). doi:<a href="https://doi.org/10.1016/j.isci.2023.107780">10.1016/j.isci.2023.107780</a>
  apa: Maes, M. E., Colombo, G., Schoot Uiterkamp, F. E., Sternberg, F., Venturino,
    A., Pohl, E. E., &#38; Siegert, S. (2023). Mitochondrial network adaptations of
    microglia reveal sex-specific stress response after injury and UCP2 knockout.
    <i>IScience</i>. Elsevier. <a href="https://doi.org/10.1016/j.isci.2023.107780">https://doi.org/10.1016/j.isci.2023.107780</a>
  chicago: Maes, Margaret E, Gloria Colombo, Florianne E Schoot Uiterkamp, Felix Sternberg,
    Alessandro Venturino, Elena E. Pohl, and Sandra Siegert. “Mitochondrial Network
    Adaptations of Microglia Reveal Sex-Specific Stress Response after Injury and
    UCP2 Knockout.” <i>IScience</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.isci.2023.107780">https://doi.org/10.1016/j.isci.2023.107780</a>.
  ieee: M. E. Maes <i>et al.</i>, “Mitochondrial network adaptations of microglia
    reveal sex-specific stress response after injury and UCP2 knockout,” <i>iScience</i>,
    vol. 26, no. 10. Elsevier, 2023.
  ista: Maes ME, Colombo G, Schoot Uiterkamp FE, Sternberg F, Venturino A, Pohl EE,
    Siegert S. 2023. Mitochondrial network adaptations of microglia reveal sex-specific
    stress response after injury and UCP2 knockout. iScience. 26(10), 107780.
  mla: Maes, Margaret E., et al. “Mitochondrial Network Adaptations of Microglia Reveal
    Sex-Specific Stress Response after Injury and UCP2 Knockout.” <i>IScience</i>,
    vol. 26, no. 10, 107780, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.isci.2023.107780">10.1016/j.isci.2023.107780</a>.
  short: M.E. Maes, G. Colombo, F.E. Schoot Uiterkamp, F. Sternberg, A. Venturino,
    E.E. Pohl, S. Siegert, IScience 26 (2023).
date_created: 2023-09-24T22:01:11Z
date_published: 2023-10-20T00:00:00Z
date_updated: 2023-12-13T12:27:30Z
day: '20'
ddc:
- '570'
department:
- _id: SaSi
doi: 10.1016/j.isci.2023.107780
external_id:
  isi:
  - '001080403500001'
  pmid:
  - '37731609'
file:
- access_level: open_access
  checksum: be1a560efdd96d20712311f4fc54aac2
  content_type: application/pdf
  creator: dernst
  date_created: 2023-11-07T08:53:21Z
  date_updated: 2023-11-07T08:53:21Z
  file_id: '14497'
  file_name: 2023_iScience_Maes.pdf
  file_size: 8197935
  relation: main_file
  success: 1
file_date_updated: 2023-11-07T08:53:21Z
has_accepted_license: '1'
intvolume: '        26'
isi: 1
issue: '10'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
pmid: 1
publication: iScience
publication_identifier:
  eissn:
  - 2589-0042
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mitochondrial network adaptations of microglia reveal sex-specific stress response
  after injury and UCP2 knockout
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 26
year: '2023'
...
---
_id: '14364'
abstract:
- lang: eng
  text: We introduce extension-based proofs, a class of impossibility proofs that
    includes valency arguments. They are modelled as an interaction between a prover
    and a protocol. Using proofs based on combinatorial topology, it has been shown
    that it is impossible to deterministically solve -set agreement among  processes
    or approximate agreement on a cycle of length 4 among  processes in a wait-free
    manner in asynchronous models where processes communicate using objects that can
    be constructed from shared registers. However, it was unknown whether proofs based
    on simpler techniques were possible. We show that these impossibility results
    cannot be obtained by extension-based proofs in the iterated snapshot model and,
    hence, extension-based proofs are limited in power.
acknowledgement: "We would like to thank Valerie King, Toniann Pitassi, and Michael
  Saks for helpful discussions and Shi Hao Liu for his useful feedback.\r\nThis research
  was supported by the Natural Science and Engineering Research Council of Canada
  under grants RGPIN-2015-05080 and RGPIN-2020-04178, a postgraduate scholarship,
  and a postdoctoral fellowship; a University of Toronto postdoctoral fellowship;
  the National Science Foundation under grants CCF-1217921, CCF-1301926, CCF-1637385,
  CCF-1650596, and IIS-1447786; the U.S. Department of Energy under grant ER26116/DE-SC0008923;
  the European Research Council (ERC) under the European Union’s Horizon 2020 research
  and innovation programme grant agreement 805223 ScaleML; and the Oracle and Intel
  corporations. Some of the work on this paper was done while Faith Ellen was visiting
  IST Austria."
article_processing_charge: No
article_type: original
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: James
  full_name: Aspnes, James
  last_name: Aspnes
- first_name: Faith
  full_name: Ellen, Faith
  last_name: Ellen
- first_name: Rati
  full_name: Gelashvili, Rati
  last_name: Gelashvili
- first_name: Leqi
  full_name: Zhu, Leqi
  id: a2117c59-cee4-11ed-b9d0-874ecf0f8ac5
  last_name: Zhu
citation:
  ama: Alistarh D-A, Aspnes J, Ellen F, Gelashvili R, Zhu L. Why extension-based proofs
    fail. <i>SIAM Journal on Computing</i>. 2023;52(4):913-944. doi:<a href="https://doi.org/10.1137/20M1375851">10.1137/20M1375851</a>
  apa: Alistarh, D.-A., Aspnes, J., Ellen, F., Gelashvili, R., &#38; Zhu, L. (2023).
    Why extension-based proofs fail. <i>SIAM Journal on Computing</i>. Society for
    Industrial and Applied Mathematics. <a href="https://doi.org/10.1137/20M1375851">https://doi.org/10.1137/20M1375851</a>
  chicago: Alistarh, Dan-Adrian, James Aspnes, Faith Ellen, Rati Gelashvili, and Leqi
    Zhu. “Why Extension-Based Proofs Fail.” <i>SIAM Journal on Computing</i>. Society
    for Industrial and Applied Mathematics, 2023. <a href="https://doi.org/10.1137/20M1375851">https://doi.org/10.1137/20M1375851</a>.
  ieee: D.-A. Alistarh, J. Aspnes, F. Ellen, R. Gelashvili, and L. Zhu, “Why extension-based
    proofs fail,” <i>SIAM Journal on Computing</i>, vol. 52, no. 4. Society for Industrial
    and Applied Mathematics, pp. 913–944, 2023.
  ista: Alistarh D-A, Aspnes J, Ellen F, Gelashvili R, Zhu L. 2023. Why extension-based
    proofs fail. SIAM Journal on Computing. 52(4), 913–944.
  mla: Alistarh, Dan-Adrian, et al. “Why Extension-Based Proofs Fail.” <i>SIAM Journal
    on Computing</i>, vol. 52, no. 4, Society for Industrial and Applied Mathematics,
    2023, pp. 913–44, doi:<a href="https://doi.org/10.1137/20M1375851">10.1137/20M1375851</a>.
  short: D.-A. Alistarh, J. Aspnes, F. Ellen, R. Gelashvili, L. Zhu, SIAM Journal
    on Computing 52 (2023) 913–944.
date_created: 2023-09-24T22:01:11Z
date_published: 2023-07-25T00:00:00Z
date_updated: 2023-12-13T12:28:29Z
day: '25'
department:
- _id: DaAl
doi: 10.1137/20M1375851
ec_funded: 1
external_id:
  arxiv:
  - '1811.01421'
  isi:
  - '001082972300004'
intvolume: '        52'
isi: 1
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1811.01421
month: '07'
oa: 1
oa_version: Preprint
page: 913-944
project:
- _id: 268A44D6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '805223'
  name: Elastic Coordination for Scalable Machine Learning
publication: SIAM Journal on Computing
publication_identifier:
  eissn:
  - 1095-7111
  issn:
  - 0097-5397
publication_status: published
publisher: Society for Industrial and Applied Mathematics
quality_controlled: '1'
related_material:
  record:
  - id: '6676'
    relation: earlier_version
    status: public
scopus_import: '1'
status: public
title: Why extension-based proofs fail
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 52
year: '2023'
...
---
_id: '14368'
abstract:
- lang: eng
  text: "Purpose: \r\nBiallelic variants in TARS2, encoding the mitochondrial threonyl-tRNA-synthetase,
    have been reported in a small group of individuals displaying a neurodevelopmental
    phenotype but with limited neuroradiological data and insufficient evidence for
    causality of the variants.\r\nMethods:\r\nExome or genome sequencing was carried
    out in 15 families. Clinical and neuroradiological evaluation was performed for
    all affected individuals, including review of 10 previously reported individuals.
    The pathogenicity of TARS2 variants was evaluated using in vitro assays and a
    zebrafish model.\r\nResults:\r\nWe report 18 new individuals harboring biallelic
    TARS2 variants. Phenotypically, these individuals show developmental delay/intellectual
    disability, regression, cerebellar and cerebral atrophy, basal ganglia signal
    alterations, hypotonia, cerebellar signs, and increased blood lactate. In vitro
    studies showed that variants within the TARS2301-381 region had decreased binding
    to Rag GTPases, likely impairing mTORC1 activity. The zebrafish model recapitulated
    key features of the human phenotype and unraveled dysregulation of downstream
    targets of mTORC1 signaling. Functional testing of the variants confirmed the
    pathogenicity in a zebrafish model.\r\nConclusion:\r\nWe define the clinico-radiological
    spectrum of TARS2-related mitochondrial disease, unveil the likely involvement
    of the mTORC1 signaling pathway as a distinct molecular mechanism, and establish
    a TARS2 zebrafish model as an important tool to study variant pathogenicity."
article_number: '100938'
article_processing_charge: No
article_type: original
author:
- first_name: Andrea
  full_name: Accogli, Andrea
  last_name: Accogli
- first_name: Sheng-Jia
  full_name: Lin, Sheng-Jia
  last_name: Lin
- first_name: Mariasavina
  full_name: Severino, Mariasavina
  last_name: Severino
- first_name: Sung-Hoon
  full_name: Kim, Sung-Hoon
  last_name: Kim
- first_name: Kevin
  full_name: Huang, Kevin
  id: 3b3d2888-1ff6-11ee-9fa6-8f209ca91fe3
  last_name: Huang
  orcid: 0000-0002-2512-7812
- first_name: Clarissa
  full_name: Rocca, Clarissa
  last_name: Rocca
- first_name: Megan
  full_name: Landsverk, Megan
  last_name: Landsverk
- first_name: Maha S.
  full_name: Zaki, Maha S.
  last_name: Zaki
- first_name: Almundher
  full_name: Al-Maawali, Almundher
  last_name: Al-Maawali
- first_name: Varunvenkat M.
  full_name: Srinivasan, Varunvenkat M.
  last_name: Srinivasan
- first_name: Khalid
  full_name: Al-Thihli, Khalid
  last_name: Al-Thihli
- first_name: G. Bradly
  full_name: Schaefer, G. Bradly
  last_name: Schaefer
- first_name: Monica
  full_name: Davis, Monica
  last_name: Davis
- first_name: Davide
  full_name: Tonduti, Davide
  last_name: Tonduti
- first_name: Chiara
  full_name: Doneda, Chiara
  last_name: Doneda
- first_name: Lara M.
  full_name: Marten, Lara M.
  last_name: Marten
- first_name: Chris
  full_name: Mühlhausen, Chris
  last_name: Mühlhausen
- first_name: Maria
  full_name: Gomez, Maria
  last_name: Gomez
- first_name: Eleonora
  full_name: Lamantea, Eleonora
  last_name: Lamantea
- first_name: Rafael
  full_name: Mena, Rafael
  last_name: Mena
- first_name: Mathilde
  full_name: Nizon, Mathilde
  last_name: Nizon
- first_name: Vincent
  full_name: Procaccio, Vincent
  last_name: Procaccio
- first_name: Amber
  full_name: Begtrup, Amber
  last_name: Begtrup
- first_name: Aida
  full_name: Telegrafi, Aida
  last_name: Telegrafi
- first_name: Hong
  full_name: Cui, Hong
  last_name: Cui
- first_name: Heidi L.
  full_name: Schulz, Heidi L.
  last_name: Schulz
- first_name: Julia
  full_name: Mohr, Julia
  last_name: Mohr
- first_name: Saskia
  full_name: Biskup, Saskia
  last_name: Biskup
- first_name: Mariana Amina
  full_name: Loos, Mariana Amina
  last_name: Loos
- first_name: Hilda Verónica
  full_name: Aráoz, Hilda Verónica
  last_name: Aráoz
- first_name: Vincenzo
  full_name: Salpietro, Vincenzo
  last_name: Salpietro
- first_name: Laura Davis
  full_name: Keppen, Laura Davis
  last_name: Keppen
- first_name: Manali
  full_name: Chitre, Manali
  last_name: Chitre
- first_name: Cassidy
  full_name: Petree, Cassidy
  last_name: Petree
- first_name: Lucy
  full_name: Raymond, Lucy
  last_name: Raymond
- first_name: Julie
  full_name: Vogt, Julie
  last_name: Vogt
- first_name: Lindsey B.
  full_name: Sawyer, Lindsey B.
  last_name: Sawyer
- first_name: Alice A.
  full_name: Basinger, Alice A.
  last_name: Basinger
- first_name: Signe Vandal
  full_name: Pedersen, Signe Vandal
  last_name: Pedersen
- first_name: Toni S.
  full_name: Pearson, Toni S.
  last_name: Pearson
- first_name: Dorothy K.
  full_name: Grange, Dorothy K.
  last_name: Grange
- first_name: Lokesh
  full_name: Lingappa, Lokesh
  last_name: Lingappa
- first_name: Paige
  full_name: McDunnah, Paige
  last_name: McDunnah
- first_name: Rita
  full_name: Horvath, Rita
  last_name: Horvath
- first_name: Benjamin
  full_name: Cognè, Benjamin
  last_name: Cognè
- first_name: Bertrand
  full_name: Isidor, Bertrand
  last_name: Isidor
- first_name: Andreas
  full_name: Hahn, Andreas
  last_name: Hahn
- first_name: Karen W.
  full_name: Gripp, Karen W.
  last_name: Gripp
- first_name: Seyed Mehdi
  full_name: Jafarnejad, Seyed Mehdi
  last_name: Jafarnejad
- first_name: Elsebet
  full_name: Østergaard, Elsebet
  last_name: Østergaard
- first_name: Carlos E.
  full_name: Prada, Carlos E.
  last_name: Prada
- first_name: Daniele
  full_name: Ghezzi, Daniele
  last_name: Ghezzi
- first_name: Vykuntaraju K.
  full_name: Gowda, Vykuntaraju K.
  last_name: Gowda
- first_name: Robert W.
  full_name: Taylor, Robert W.
  last_name: Taylor
- first_name: Nahum
  full_name: Sonenberg, Nahum
  last_name: Sonenberg
- first_name: Henry
  full_name: Houlden, Henry
  last_name: Houlden
- first_name: Marie
  full_name: Sissler, Marie
  last_name: Sissler
- first_name: Gaurav K.
  full_name: Varshney, Gaurav K.
  last_name: Varshney
- first_name: Reza
  full_name: Maroofian, Reza
  last_name: Maroofian
citation:
  ama: Accogli A, Lin S-J, Severino M, et al. Clinical, neuroradiological, and molecular
    characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder.
    <i>Genetics in Medicine</i>. 2023;25(11). doi:<a href="https://doi.org/10.1016/j.gim.2023.100938">10.1016/j.gim.2023.100938</a>
  apa: Accogli, A., Lin, S.-J., Severino, M., Kim, S.-H., Huang, K., Rocca, C., …
    Maroofian, R. (2023). Clinical, neuroradiological, and molecular characterization
    of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder. <i>Genetics
    in Medicine</i>. Elsevier. <a href="https://doi.org/10.1016/j.gim.2023.100938">https://doi.org/10.1016/j.gim.2023.100938</a>
  chicago: Accogli, Andrea, Sheng-Jia Lin, Mariasavina Severino, Sung-Hoon Kim, Kevin
    Huang, Clarissa Rocca, Megan Landsverk, et al. “Clinical, Neuroradiological, and
    Molecular Characterization of Mitochondrial Threonyl-TRNA-Synthetase (TARS2)-Related
    Disorder.” <i>Genetics in Medicine</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.gim.2023.100938">https://doi.org/10.1016/j.gim.2023.100938</a>.
  ieee: A. Accogli <i>et al.</i>, “Clinical, neuroradiological, and molecular characterization
    of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder,” <i>Genetics
    in Medicine</i>, vol. 25, no. 11. Elsevier, 2023.
  ista: Accogli A, Lin S-J, Severino M, Kim S-H, Huang K, Rocca C, Landsverk M, Zaki
    MS, Al-Maawali A, Srinivasan VM, Al-Thihli K, Schaefer GB, Davis M, Tonduti D,
    Doneda C, Marten LM, Mühlhausen C, Gomez M, Lamantea E, Mena R, Nizon M, Procaccio
    V, Begtrup A, Telegrafi A, Cui H, Schulz HL, Mohr J, Biskup S, Loos MA, Aráoz
    HV, Salpietro V, Keppen LD, Chitre M, Petree C, Raymond L, Vogt J, Sawyer LB,
    Basinger AA, Pedersen SV, Pearson TS, Grange DK, Lingappa L, McDunnah P, Horvath
    R, Cognè B, Isidor B, Hahn A, Gripp KW, Jafarnejad SM, Østergaard E, Prada CE,
    Ghezzi D, Gowda VK, Taylor RW, Sonenberg N, Houlden H, Sissler M, Varshney GK,
    Maroofian R. 2023. Clinical, neuroradiological, and molecular characterization
    of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder. Genetics in
    Medicine. 25(11), 100938.
  mla: Accogli, Andrea, et al. “Clinical, Neuroradiological, and Molecular Characterization
    of Mitochondrial Threonyl-TRNA-Synthetase (TARS2)-Related Disorder.” <i>Genetics
    in Medicine</i>, vol. 25, no. 11, 100938, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.gim.2023.100938">10.1016/j.gim.2023.100938</a>.
  short: A. Accogli, S.-J. Lin, M. Severino, S.-H. Kim, K. Huang, C. Rocca, M. Landsverk,
    M.S. Zaki, A. Al-Maawali, V.M. Srinivasan, K. Al-Thihli, G.B. Schaefer, M. Davis,
    D. Tonduti, C. Doneda, L.M. Marten, C. Mühlhausen, M. Gomez, E. Lamantea, R. Mena,
    M. Nizon, V. Procaccio, A. Begtrup, A. Telegrafi, H. Cui, H.L. Schulz, J. Mohr,
    S. Biskup, M.A. Loos, H.V. Aráoz, V. Salpietro, L.D. Keppen, M. Chitre, C. Petree,
    L. Raymond, J. Vogt, L.B. Sawyer, A.A. Basinger, S.V. Pedersen, T.S. Pearson,
    D.K. Grange, L. Lingappa, P. McDunnah, R. Horvath, B. Cognè, B. Isidor, A. Hahn,
    K.W. Gripp, S.M. Jafarnejad, E. Østergaard, C.E. Prada, D. Ghezzi, V.K. Gowda,
    R.W. Taylor, N. Sonenberg, H. Houlden, M. Sissler, G.K. Varshney, R. Maroofian,
    Genetics in Medicine 25 (2023).
date_created: 2023-09-25T08:44:29Z
date_published: 2023-11-01T00:00:00Z
date_updated: 2023-09-25T08:50:10Z
day: '01'
ddc:
- '570'
doi: 10.1016/j.gim.2023.100938
extern: '1'
file:
- access_level: open_access
  checksum: 440f0cd8a2ffcbe03c015c1746728387
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-25T08:48:54Z
  date_updated: 2023-09-25T08:48:54Z
  file_id: '14369'
  file_name: 2023_GeneticsMedicine_Accogli.pdf
  file_size: 4105513
  relation: main_file
  success: 1
file_date_updated: 2023-09-25T08:48:54Z
has_accepted_license: '1'
intvolume: '        25'
issue: '11'
keyword:
- Genetics (clinical)
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
publication: Genetics in Medicine
publication_identifier:
  issn:
  - 1098-3600
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Clinical, neuroradiological, and molecular characterization of mitochondrial
  threonyl-tRNA-synthetase (TARS2)-related disorder
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 25
year: '2023'
...
---
_id: '14374'
abstract:
- lang: eng
  text: "Superconductivity has many important applications ranging from levitating
    trains over qubits to MRI scanners. The phenomenon is successfully modeled by
    Bardeen-Cooper-Schrieffer (BCS) theory. From a mathematical perspective, BCS theory
    has been studied extensively for systems without boundary. However, little is
    known in the presence of boundaries. With the help of numerical methods physicists
    observed that the critical temperature may increase in the presence of a boundary.
    The goal of this thesis is to understand the influence of boundaries on the critical
    temperature in BCS theory and to give a first rigorous justification of these
    observations. On the way, we also study two-body Schrödinger operators on domains
    with boundaries and prove additional results for superconductors without boundary.\r\n\r\nBCS
    theory is based on a non-linear functional, where the minimizer indicates whether
    the system is superconducting or in the normal, non-superconducting state. By
    considering the Hessian of the BCS functional at the normal state, one can analyze
    whether the normal state is possibly a minimum of the BCS functional and estimate
    the critical temperature. The Hessian turns out to be a linear operator resembling
    a Schrödinger operator for two interacting particles, but with more complicated
    kinetic energy. As a first step, we study the two-body Schrödinger operator in
    the presence of boundaries.\r\nFor Neumann boundary conditions, we prove that
    the addition of a boundary can create new eigenvalues, which correspond to the
    two particles forming a bound state close to the boundary.\r\n\r\nSecond, we need
    to understand superconductivity in the translation invariant setting. While in
    three dimensions this has been extensively studied, there is no mathematical literature
    for the one and two dimensional cases. In dimensions one and two, we compute the
    weak coupling asymptotics of the critical temperature and the energy gap  in the
    translation invariant setting. We also prove that their ratio is independent of
    the microscopic details of the model in the weak coupling limit; this property
    is referred to as universality.\r\n\r\nIn the third part, we study the critical
    temperature of superconductors in the presence of boundaries. We start by considering
    the one-dimensional case of a half-line with contact interaction. Then, we generalize
    the results to generic interactions and half-spaces in one, two and three dimensions.
    Finally, we compare the critical temperature of a quarter space in two dimensions
    to the critical temperatures of a half-space and of the full space."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Barbara
  full_name: Roos, Barbara
  id: 5DA90512-D80F-11E9-8994-2E2EE6697425
  last_name: Roos
  orcid: 0000-0002-9071-5880
citation:
  ama: Roos B. Boundary superconductivity in BCS theory. 2023. doi:<a href="https://doi.org/10.15479/at:ista:14374">10.15479/at:ista:14374</a>
  apa: Roos, B. (2023). <i>Boundary superconductivity in BCS theory</i>. Institute
    of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:14374">https://doi.org/10.15479/at:ista:14374</a>
  chicago: Roos, Barbara. “Boundary Superconductivity in BCS Theory.” Institute of
    Science and Technology Austria, 2023. <a href="https://doi.org/10.15479/at:ista:14374">https://doi.org/10.15479/at:ista:14374</a>.
  ieee: B. Roos, “Boundary superconductivity in BCS theory,” Institute of Science
    and Technology Austria, 2023.
  ista: Roos B. 2023. Boundary superconductivity in BCS theory. Institute of Science
    and Technology Austria.
  mla: Roos, Barbara. <i>Boundary Superconductivity in BCS Theory</i>. Institute of
    Science and Technology Austria, 2023, doi:<a href="https://doi.org/10.15479/at:ista:14374">10.15479/at:ista:14374</a>.
  short: B. Roos, Boundary Superconductivity in BCS Theory, Institute of Science and
    Technology Austria, 2023.
date_created: 2023-09-28T14:23:04Z
date_published: 2023-09-30T00:00:00Z
date_updated: 2023-10-27T10:37:30Z
day: '30'
ddc:
- '515'
- '539'
degree_awarded: PhD
department:
- _id: GradSch
- _id: RoSe
doi: 10.15479/at:ista:14374
ec_funded: 1
file:
- access_level: open_access
  checksum: ef039ffc3de2cb8dee5b14110938e9b6
  content_type: application/pdf
  creator: broos
  date_created: 2023-10-06T11:35:56Z
  date_updated: 2023-10-06T11:35:56Z
  file_id: '14398'
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  file_size: 2365702
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  checksum: 81dcac33daeefaf0111db52f41bb1fd0
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  creator: broos
  date_created: 2023-10-06T11:38:01Z
  date_updated: 2023-10-06T11:38:01Z
  file_id: '14399'
  file_name: Version5.zip
  file_size: 4691734
  relation: source_file
file_date_updated: 2023-10-06T11:38:01Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '206'
project:
- _id: 25C6DC12-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '694227'
  name: Analysis of quantum many-body systems
- _id: bda63fe5-d553-11ed-ba76-a16e3d2f256b
  grant_number: I06427
  name: Mathematical Challenges in BCS Theory of Superconductivity
publication_identifier:
  issn:
  - 2663 - 337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '13207'
    relation: part_of_dissertation
    status: public
  - id: '10850'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
title: Boundary superconductivity in BCS theory
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: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2023'
...
---
_id: '14377'
abstract:
- lang: eng
  text: Coherent flows of self-propelled particles are characterized by vortices and
    jets that sustain chaotic flows, referred to as active turbulence. Here, we reveal
    a crossover between defect-free active turbulence and active turbulence laden
    with topological defects. Interestingly, we show that concurrent to the crossover
    from defect-free to defect-laden active turbulence is the restoration of the previously
    broken SO(2) symmetry signaled by the fast decay of the two-point correlations.
    By stability analyses of the topological charge density field, we provide theoretical
    insights on the criterion for the crossover to the defect-laden active turbulent
    state. Despite the distinct symmetry features between these two active turbulence
    regimes, the flow fluctuations exhibit universal statistical scaling behaviors
    at large scales, while the spectrum of polarity fluctuations decays exponentially
    at small length scales compared to the active energy injection length. These findings
    reveal a dynamical crossover between distinct spatiotemporal organization patterns
    in polar active matter.
article_number: '063101'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Benjamin H.
  full_name: Andersen, Benjamin H.
  last_name: Andersen
- first_name: Julian B
  full_name: Renaud, Julian B
  id: 7af6767d-14eb-11ed-b536-a32449ae867c
  last_name: Renaud
- first_name: Jonas
  full_name: Rønning, Jonas
  last_name: Rønning
- first_name: Luiza
  full_name: Angheluta, Luiza
  last_name: Angheluta
- first_name: Amin
  full_name: Doostmohammadi, Amin
  last_name: Doostmohammadi
citation:
  ama: Andersen BH, Renaud JB, Rønning J, Angheluta L, Doostmohammadi A. Symmetry-restoring
    crossover from defect-free to defect-laden turbulence in polar active matter.
    <i>Physical Review Fluids</i>. 2023;8(6). doi:<a href="https://doi.org/10.1103/physrevfluids.8.063101">10.1103/physrevfluids.8.063101</a>
  apa: Andersen, B. H., Renaud, J. B., Rønning, J., Angheluta, L., &#38; Doostmohammadi,
    A. (2023). Symmetry-restoring crossover from defect-free to defect-laden turbulence
    in polar active matter. <i>Physical Review Fluids</i>. American Physical Society.
    <a href="https://doi.org/10.1103/physrevfluids.8.063101">https://doi.org/10.1103/physrevfluids.8.063101</a>
  chicago: Andersen, Benjamin H., Julian B Renaud, Jonas Rønning, Luiza Angheluta,
    and Amin Doostmohammadi. “Symmetry-Restoring Crossover from Defect-Free to Defect-Laden
    Turbulence in Polar Active Matter.” <i>Physical Review Fluids</i>. American Physical
    Society, 2023. <a href="https://doi.org/10.1103/physrevfluids.8.063101">https://doi.org/10.1103/physrevfluids.8.063101</a>.
  ieee: B. H. Andersen, J. B. Renaud, J. Rønning, L. Angheluta, and A. Doostmohammadi,
    “Symmetry-restoring crossover from defect-free to defect-laden turbulence in polar
    active matter,” <i>Physical Review Fluids</i>, vol. 8, no. 6. American Physical
    Society, 2023.
  ista: Andersen BH, Renaud JB, Rønning J, Angheluta L, Doostmohammadi A. 2023. Symmetry-restoring
    crossover from defect-free to defect-laden turbulence in polar active matter.
    Physical Review Fluids. 8(6), 063101.
  mla: Andersen, Benjamin H., et al. “Symmetry-Restoring Crossover from Defect-Free
    to Defect-Laden Turbulence in Polar Active Matter.” <i>Physical Review Fluids</i>,
    vol. 8, no. 6, 063101, American Physical Society, 2023, doi:<a href="https://doi.org/10.1103/physrevfluids.8.063101">10.1103/physrevfluids.8.063101</a>.
  short: B.H. Andersen, J.B. Renaud, J. Rønning, L. Angheluta, A. Doostmohammadi,
    Physical Review Fluids 8 (2023).
date_created: 2023-09-29T08:46:47Z
date_published: 2023-06-14T00:00:00Z
date_updated: 2023-10-03T07:25:39Z
day: '14'
doi: 10.1103/physrevfluids.8.063101
extern: '1'
external_id:
  arxiv:
  - '2209.10916'
intvolume: '         8'
issue: '6'
keyword:
- Fluid Flow and Transfer Processes
- Modeling and Simulation
- Computational Mechanics
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/2209.10916
month: '06'
oa: 1
oa_version: Preprint
publication: Physical Review Fluids
publication_identifier:
  issn:
  - 2469-990X
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Symmetry-restoring crossover from defect-free to defect-laden turbulence in
  polar active matter
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2023'
...
---
_id: '14378'
abstract:
- lang: eng
  text: 'Branching morphogenesis is a ubiquitous process that gives rise to high exchange
    surfaces in the vasculature and epithelial organs. Lymphatic capillaries form
    branched networks, which play a key role in the circulation of tissue fluid and
    immune cells. Although mouse models and correlative patient data indicate that
    the lymphatic capillary density directly correlates with functional output, i.e.,
    tissue fluid drainage and trafficking efficiency of dendritic cells, the mechanisms
    ensuring efficient tissue coverage remain poorly understood. Here, we use the
    mouse ear pinna lymphatic vessel network as a model system and combine lineage-tracing,
    genetic perturbations, whole-organ reconstructions and theoretical modeling to
    show that the dermal lymphatic capillaries tile space in an optimal, space-filling
    manner. This coverage is achieved by two complementary mechanisms: initial tissue
    invasion provides a non-optimal global scaffold via self-organized branching morphogenesis,
    while VEGF-C dependent side-branching from existing capillaries rapidly optimizes
    local coverage by directionally targeting low-density regions. With these two
    ingredients, we show that a minimal biophysical model can reproduce quantitatively
    whole-network reconstructions, across development and perturbations. Our results
    show that lymphatic capillary networks can exploit local self-organizing mechanisms
    to achieve tissue-scale optimization.'
acknowledgement: "We thank Dr. Kari Alitalo (University of Helsinki and Wihuri Research
  Institute) for critical reading of the manuscript, providing Vegfc+/− and Clp24ΔEC
  mouse strains and for hosting K.V.’s Academy of Finland postdoctoral researcher
  period (2015–2018). We thank Dr. Sara Wickström (University of Helsinki and Wihuri
  Research Institute) for providing Sox9:Egfp mouse\r\nstrain and the discussions.
  We thank Maija Atuegwu and Tapio Tainola for technical assistance. This work received
  funding from the Academy of Finland (K.V., 315710), Sigrid Juselius Foundation (K.V.),
  University of Helsinki (K.V.), Wihuri Research Institute (K.V.), the ERC under the
  European Union’s Horizon 2020 research and innovation program (grant agreement\r\nNo.
  851288 to E.H.) and under the Marie Skłodowska-Curie grant agreement No. 754411
  (to M.C.U.). Part of the work was carried out with the support of HiLIFE Laboratory
  Animal Centre Core Facility, University of Helsinki, Finland. Imaging was performed
  at the Biomedicum Imaging Unit, Helsinki University, Helsinki, Finland, with the
  support of Biocenter Finland. The AAVpreparations were produced at the Helsinki
  Virus (HelVi) Core."
article_number: '5878'
article_processing_charge: Yes
article_type: original
author:
- first_name: Mehmet C
  full_name: Ucar, Mehmet C
  id: 50B2A802-6007-11E9-A42B-EB23E6697425
  last_name: Ucar
  orcid: 0000-0003-0506-4217
- first_name: Edouard B
  full_name: Hannezo, Edouard B
  id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
  last_name: Hannezo
  orcid: 0000-0001-6005-1561
- first_name: Emmi
  full_name: Tiilikainen, Emmi
  last_name: Tiilikainen
- first_name: Inam
  full_name: Liaqat, Inam
  last_name: Liaqat
- first_name: Emma
  full_name: Jakobsson, Emma
  last_name: Jakobsson
- first_name: Harri
  full_name: Nurmi, Harri
  last_name: Nurmi
- first_name: Kari
  full_name: Vaahtomeri, Kari
  id: 368EE576-F248-11E8-B48F-1D18A9856A87
  last_name: Vaahtomeri
  orcid: 0000-0001-7829-3518
citation:
  ama: Ucar MC, Hannezo EB, Tiilikainen E, et al. Self-organized and directed branching
    results in optimal coverage in developing dermal lymphatic networks. <i>Nature
    Communications</i>. 2023;14. doi:<a href="https://doi.org/10.1038/s41467-023-41456-7">10.1038/s41467-023-41456-7</a>
  apa: Ucar, M. C., Hannezo, E. B., Tiilikainen, E., Liaqat, I., Jakobsson, E., Nurmi,
    H., &#38; Vaahtomeri, K. (2023). Self-organized and directed branching results
    in optimal coverage in developing dermal lymphatic networks. <i>Nature Communications</i>.
    Springer Nature. <a href="https://doi.org/10.1038/s41467-023-41456-7">https://doi.org/10.1038/s41467-023-41456-7</a>
  chicago: Ucar, Mehmet C, Edouard B Hannezo, Emmi Tiilikainen, Inam Liaqat, Emma
    Jakobsson, Harri Nurmi, and Kari Vaahtomeri. “Self-Organized and Directed Branching
    Results in Optimal Coverage in Developing Dermal Lymphatic Networks.” <i>Nature
    Communications</i>. Springer Nature, 2023. <a href="https://doi.org/10.1038/s41467-023-41456-7">https://doi.org/10.1038/s41467-023-41456-7</a>.
  ieee: M. C. Ucar <i>et al.</i>, “Self-organized and directed branching results in
    optimal coverage in developing dermal lymphatic networks,” <i>Nature Communications</i>,
    vol. 14. Springer Nature, 2023.
  ista: Ucar MC, Hannezo EB, Tiilikainen E, Liaqat I, Jakobsson E, Nurmi H, Vaahtomeri
    K. 2023. Self-organized and directed branching results in optimal coverage in
    developing dermal lymphatic networks. Nature Communications. 14, 5878.
  mla: Ucar, Mehmet C., et al. “Self-Organized and Directed Branching Results in Optimal
    Coverage in Developing Dermal Lymphatic Networks.” <i>Nature Communications</i>,
    vol. 14, 5878, Springer Nature, 2023, doi:<a href="https://doi.org/10.1038/s41467-023-41456-7">10.1038/s41467-023-41456-7</a>.
  short: M.C. Ucar, E.B. Hannezo, E. Tiilikainen, I. Liaqat, E. Jakobsson, H. Nurmi,
    K. Vaahtomeri, Nature Communications 14 (2023).
date_created: 2023-10-01T22:01:13Z
date_published: 2023-09-21T00:00:00Z
date_updated: 2023-12-13T12:31:05Z
day: '21'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.1038/s41467-023-41456-7
ec_funded: 1
external_id:
  isi:
  - '001075884500007'
  pmid:
  - '37735168'
file:
- access_level: open_access
  checksum: 4fe5423403f2531753bcd9e0fea48e05
  content_type: application/pdf
  creator: dernst
  date_created: 2023-10-03T07:46:36Z
  date_updated: 2023-10-03T07:46:36Z
  file_id: '14384'
  file_name: 2023_NatureComm_Ucar.pdf
  file_size: 8143264
  relation: main_file
  success: 1
file_date_updated: 2023-10-03T07:46:36Z
has_accepted_license: '1'
intvolume: '        14'
isi: 1
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '851288'
  name: Design Principles of Branching Morphogenesis
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Nature Communications
publication_identifier:
  eissn:
  - 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Self-organized and directed branching results in optimal coverage in developing
  dermal lymphatic networks
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 14
year: '2023'
...
---
_id: '14379'
abstract:
- lang: eng
  text: We report on a simple surfactant/template free chemical route for the synthesis
    of semi-polycrystalline polyaniline-graphite (SPani-graphite) composite and its
    application as an electroactive material in electrochemical charge storage. The
    synthesized material exhibits well-defined poly-crystallographic lattices in high
    resolution transmission electron micrographs and sharp peaks in x-ray diffraction
    spectra suggesting crystalline nature of the material. The specific capacitance
    computed from the galvanostatic charge-discharge (GCD) data obtained from 3-electrode
    cell configuration using 1 M aq. Na2SO4 as an electrolyte was 111.4 F g−1 at a
    current density of 0.1 A g−1 which rises to 269 F g−1 at an elevated current density
    of 1.0 A g−1. A similar pattern of increase in the specific capacitance values
    with an increase in the current density was observed in the results obtained from
    2-electrode symmetric device configuration using polymer gel electrolyte (xanthan
    gum in 1 M aq. Na2SO4). The specific capacitance computed from the GCD data obtained
    from the device configuration was 20 F g−1 at the current density of 1.0 A g−1.
    The device delivers an energy density of 1.7 Wh kg−1 and a power density of 2.48
    kWh kg−1 at an applied current density of 0.5 A g−1 suggesting an excellent rate
    capability and power management. In addition, the device exhibits ⁓92 % specific
    capacitance retention up to 8000 continuous GCD cycles and ⁓80 % coulombic efficiency
    up to 10,000 continuous GCD cycles indicating excellent cycling stability. The
    unique feature of increasing specific capacitance with respect to applied current
    density is attributed to the presence of semi-polycrystalline phases in the SPani-graphite
    matrix. The material behaves as a surface redox supercapacitor and its unique
    mechanism of charge storage is discussed in detail in the article.
acknowledgement: This work was supported by 2023 Yeungnam University Research Grant.
article_number: '117463'
article_processing_charge: No
article_type: original
author:
- first_name: Neelima
  full_name: Mahato, Neelima
  last_name: Mahato
- first_name: Saurabh
  full_name: Singh, Saurabh
  id: 12d625da-9cb3-11ed-9667-af09d37d3f0a
  last_name: Singh
  orcid: 0000-0003-2209-5269
- first_name: Mohammad
  full_name: Faisal, Mohammad
  last_name: Faisal
- first_name: T. V.M.
  full_name: Sreekanth, T. V.M.
  last_name: Sreekanth
- first_name: Sutripto
  full_name: Majumder, Sutripto
  last_name: Majumder
- first_name: Kisoo
  full_name: Yoo, Kisoo
  last_name: Yoo
- first_name: Jonghoon
  full_name: Kim, Jonghoon
  last_name: Kim
citation:
  ama: Mahato N, Singh S, Faisal M, et al. Polycrystalline phases grown in-situ engendering
    unique mechanism of charge storage in polyaniline-graphite composite. <i>Synthetic
    Metals</i>. 2023;299. doi:<a href="https://doi.org/10.1016/j.synthmet.2023.117463">10.1016/j.synthmet.2023.117463</a>
  apa: Mahato, N., Singh, S., Faisal, M., Sreekanth, T. V. M., Majumder, S., Yoo,
    K., &#38; Kim, J. (2023). Polycrystalline phases grown in-situ engendering unique
    mechanism of charge storage in polyaniline-graphite composite. <i>Synthetic Metals</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.synthmet.2023.117463">https://doi.org/10.1016/j.synthmet.2023.117463</a>
  chicago: Mahato, Neelima, Saurabh Singh, Mohammad Faisal, T. V.M. Sreekanth, Sutripto
    Majumder, Kisoo Yoo, and Jonghoon Kim. “Polycrystalline Phases Grown In-Situ Engendering
    Unique Mechanism of Charge Storage in Polyaniline-Graphite Composite.” <i>Synthetic
    Metals</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.synthmet.2023.117463">https://doi.org/10.1016/j.synthmet.2023.117463</a>.
  ieee: N. Mahato <i>et al.</i>, “Polycrystalline phases grown in-situ engendering
    unique mechanism of charge storage in polyaniline-graphite composite,” <i>Synthetic
    Metals</i>, vol. 299. Elsevier, 2023.
  ista: Mahato N, Singh S, Faisal M, Sreekanth TVM, Majumder S, Yoo K, Kim J. 2023.
    Polycrystalline phases grown in-situ engendering unique mechanism of charge storage
    in polyaniline-graphite composite. Synthetic Metals. 299, 117463.
  mla: Mahato, Neelima, et al. “Polycrystalline Phases Grown In-Situ Engendering Unique
    Mechanism of Charge Storage in Polyaniline-Graphite Composite.” <i>Synthetic Metals</i>,
    vol. 299, 117463, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.synthmet.2023.117463">10.1016/j.synthmet.2023.117463</a>.
  short: N. Mahato, S. Singh, M. Faisal, T.V.M. Sreekanth, S. Majumder, K. Yoo, J.
    Kim, Synthetic Metals 299 (2023).
date_created: 2023-10-01T22:01:13Z
date_published: 2023-11-01T00:00:00Z
date_updated: 2024-01-30T13:55:50Z
day: '01'
department:
- _id: MaIb
doi: 10.1016/j.synthmet.2023.117463
external_id:
  isi:
  - '001083568900001'
intvolume: '       299'
isi: 1
language:
- iso: eng
month: '11'
oa_version: None
publication: Synthetic Metals
publication_identifier:
  issn:
  - 0379-6779
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Polycrystalline phases grown in-situ engendering unique mechanism of charge
  storage in polyaniline-graphite composite
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 299
year: '2023'
...
---
_id: '14400'
abstract:
- lang: eng
  text: "We consider the problem of computing the maximal probability of satisfying
    an \r\n-regular specification for stochastic, continuous-state, nonlinear systems
    evolving in discrete time. The problem reduces, after automata-theoretic constructions,
    to finding the maximal probability of satisfying a parity condition on a (possibly
    hybrid) state space. While characterizing the exact satisfaction probability is
    open, we show that a lower bound on this probability can be obtained by (I) computing
    an under-approximation of the qualitative winning region, i.e., states from which
    the parity condition can be enforced almost surely, and (II) computing the maximal
    probability of reaching this qualitative winning region.\r\nThe heart of our approach
    is a technique to symbolically compute the under-approximation of the qualitative
    winning region in step (I) via a finite-state abstraction of the original system
    as a \r\n-player parity game. Our abstraction procedure uses only the support
    of the probabilistic evolution; it does not use precise numerical transition probabilities.
    We prove that the winning set in the abstract -player game induces an under-approximation
    of the qualitative winning region in the original synthesis problem, along with
    a policy to solve it. By combining these contributions with (a) a symbolic fixpoint
    algorithm to solve \r\n-player games and (b) existing techniques for reachability
    policy synthesis in stochastic nonlinear systems, we get an abstraction-based
    algorithm for finding a lower bound on the maximal satisfaction probability.\r\nWe
    have implemented the abstraction-based algorithm in Mascot-SDS, where we combined
    the outlined abstraction step with our tool Genie (Majumdar et al., 2023) that
    solves \r\n-player parity games (through a reduction to Rabin games) more efficiently
    than existing algorithms. We evaluated our implementation on the nonlinear model
    of a perturbed bistable switch from the literature. We show empirically that the
    lower bound on the winning region computed by our approach is precise, by comparing
    against an over-approximation of the qualitative winning region. Moreover, our
    implementation outperforms a recently proposed tool for solving this problem by
    a large margin."
acknowledgement: "We thank Daniel Hausmann and Nir Piterman for their valuable comments
  on an earlier version of the manuscript of our other paper [22] where we present,
  among other things, the parity fixpoint for 2 1/2-player games (for a slightly more
  general class of games) with a different and indirect proof of correctness. Based
  on their comments we observed that, unlike the other fixpoints that we present in
  [22], the parity fixpoint does not follow the exact same structure as its counterpart
  for 2-player games, which we also use int his paper.\r\nWe also thank Thejaswini
  Raghavan for observing that our symbolic parity fixpoint algorithm can be solved
  in quasi-polynomial time using recent improved algorithms for solving \r\n-calculus
  expressions. This significantly improved the complexity bounds of our algorithm
  in this paper.\r\nThe work of R. Majumdar and A.-K. Schmuck are partially supported
  by DFG, Germany project 389792660 TRR 248–CPEC. A.-K. Schmuck is additionally funded
  through DFG, Germany project (SCHM 3541/1-1). K. Mallik is supported by the ERC
  project ERC-2020-AdG 101020093. S. Soudjani is supported by the following projects:
  EPSRC EP/V043676/1, EIC 101070802, and ERC 101089047."
article_number: '101430'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Rupak
  full_name: Majumdar, Rupak
  last_name: Majumdar
- first_name: Kaushik
  full_name: Mallik, Kaushik
  id: 0834ff3c-6d72-11ec-94e0-b5b0a4fb8598
  last_name: Mallik
  orcid: 0000-0001-9864-7475
- first_name: Anne Kathrin
  full_name: Schmuck, Anne Kathrin
  last_name: Schmuck
- first_name: Sadegh
  full_name: Soudjani, Sadegh
  last_name: Soudjani
citation:
  ama: 'Majumdar R, Mallik K, Schmuck AK, Soudjani S. Symbolic control for stochastic
    systems via finite parity games. <i>Nonlinear Analysis: Hybrid Systems</i>. 2023;51.
    doi:<a href="https://doi.org/10.1016/j.nahs.2023.101430">10.1016/j.nahs.2023.101430</a>'
  apa: 'Majumdar, R., Mallik, K., Schmuck, A. K., &#38; Soudjani, S. (2023). Symbolic
    control for stochastic systems via finite parity games. <i>Nonlinear Analysis:
    Hybrid Systems</i>. Elsevier. <a href="https://doi.org/10.1016/j.nahs.2023.101430">https://doi.org/10.1016/j.nahs.2023.101430</a>'
  chicago: 'Majumdar, Rupak, Kaushik Mallik, Anne Kathrin Schmuck, and Sadegh Soudjani.
    “Symbolic Control for Stochastic Systems via Finite Parity Games.” <i>Nonlinear
    Analysis: Hybrid Systems</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.nahs.2023.101430">https://doi.org/10.1016/j.nahs.2023.101430</a>.'
  ieee: 'R. Majumdar, K. Mallik, A. K. Schmuck, and S. Soudjani, “Symbolic control
    for stochastic systems via finite parity games,” <i>Nonlinear Analysis: Hybrid
    Systems</i>, vol. 51. Elsevier, 2023.'
  ista: 'Majumdar R, Mallik K, Schmuck AK, Soudjani S. 2023. Symbolic control for
    stochastic systems via finite parity games. Nonlinear Analysis: Hybrid Systems.
    51, 101430.'
  mla: 'Majumdar, Rupak, et al. “Symbolic Control for Stochastic Systems via Finite
    Parity Games.” <i>Nonlinear Analysis: Hybrid Systems</i>, vol. 51, 101430, Elsevier,
    2023, doi:<a href="https://doi.org/10.1016/j.nahs.2023.101430">10.1016/j.nahs.2023.101430</a>.'
  short: 'R. Majumdar, K. Mallik, A.K. Schmuck, S. Soudjani, Nonlinear Analysis: Hybrid
    Systems 51 (2023).'
date_created: 2023-10-08T22:01:15Z
date_published: 2023-09-27T00:00:00Z
date_updated: 2023-12-13T12:58:56Z
day: '27'
department:
- _id: ToHe
doi: 10.1016/j.nahs.2023.101430
ec_funded: 1
external_id:
  arxiv:
  - '2101.00834'
  isi:
  - '001093188100001'
intvolume: '        51'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.nahs.2023.101430
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 62781420-2b32-11ec-9570-8d9b63373d4d
  call_identifier: H2020
  grant_number: '101020093'
  name: Vigilant Algorithmic Monitoring of Software
publication: 'Nonlinear Analysis: Hybrid Systems'
publication_identifier:
  issn:
  - 1751-570X
publication_status: epub_ahead
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Symbolic control for stochastic systems via finite parity games
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 51
year: '2023'
...
---
_id: '14401'
abstract:
- lang: eng
  text: "Background: \r\nPro-apoptotic BAX is a central mediator of retinal ganglion
    cell (RGC) death after optic nerve damage. BAX activation occurs in two stages
    including translocation of latent BAX to the mitochondrial outer membrane (MOM)
    and then permeabilization of the MOM to facilitate the release of apoptotic signaling
    molecules. As a critical component of RGC death, BAX is an attractive target for
    neuroprotective therapies and an understanding of the kinetics of BAX activation
    and the mechanisms controlling the two stages of this process in RGCs is potentially
    valuable in informing the development of a neuroprotective strategy.\r\nMethods:\r\nThe
    kinetics of BAX translocation were assessed by both static and live-cell imaging
    of a GFP-BAX fusion protein introduced into RGCs using AAV2-mediated gene transfer
    in mice. Activation of BAX was achieved using an acute optic nerve crush (ONC)
    protocol. Live-cell imaging of GFP-BAX was achieved using explants of mouse retina
    harvested 7 days after ONC. Kinetics of translocation in RGCs were compared to
    GFP-BAX translocation in 661W tissue culture cells. Permeabilization of GFP-BAX
    was assessed by staining with the 6A7 monoclonal antibody, which recognizes a
    conformational change in this protein after MOM insertion. Assessment of individual
    kinases associated with both stages of activation was made using small molecule
    inhibitors injected into the vitreous either independently or in concert with
    ONC surgery. The contribution of the Dual Leucine Zipper-JUN-N-Terminal Kinase
    cascade was evaluated using mice with a double conditional knock-out of both Mkk4
    and Mkk7.\r\nResults:\r\nONC induces the translocation of GFP-BAX in RGCs at a
    slower rate and with less intracellular synchronicity than 661W cells, but exhibits
    less variability among mitochondrial foci within a single cell. GFP-BAX was also
    found to translocate in all compartments of an RGC including the dendritic arbor
    and axon. Approximately 6% of translocating RGCs exhibited retrotranslocation
    of BAX immediately following translocation. Unlike tissue culture cells, which
    exhibit simultaneous translocation and permeabilization, RGCs exhibited a significant
    delay between these two stages, similar to detached cells undergoing anoikis.
    Translocation, with minimal permeabilization could be induced in a subset of RGCs
    using an inhibitor of Focal Adhesion Kinase (PF573228). Permeabilization after
    ONC, in a majority of RGCs, could be inhibited with a broad spectrum kinase inhibitor
    (sunitinib) or a selective inhibitor for p38/MAPK14 (SB203580). Intervention of
    DLK-JNK axis signaling abrogated GFP-BAX translocation after ONC.\r\nConclusions:\r\nA
    comparison between BAX activation kinetics in tissue culture cells and in cells
    of a complex tissue environment shows distinct differences indicating that caution
    should be used when translating findings from one condition to the other. RGCs
    exhibit both a delay between translocation and permeabilization and the ability
    for translocated BAX to be retrotranslocated, suggesting several stages at which
    intervention of the activation process could be exploited in the design of a therapeutic
    strategy."
acknowledgement: "The authors would like to thank Mr. Joel Dietz for management of
  the mouse colony and helpful advice for conducting quantitative PCR studies and
  Mr. Santoshi Kinoshita at the Translational Research Initiative in Pathology laboratory
  at the University of Wisconsin-Madison for cutting sections analyzed in this study.\r\nThis
  work was supported by National Eye Institute grants R01 EY030123 (RWN), R01 EY018606
  (RTL), P30 EY016665 (Department of Ophthalmology and Visual Sciences, University
  of Wisconsin-Madison), T32 EY027721 (RJD) and F31 EY030739 (OJM). Additional funding
  was provided by the BrightFocus Foundation (RWN) and unrestricted grants from Research
  to Prevent Blindness, Inc to the Department of Ophthalmology and Visual Sciences
  (University of Wisconsin-Madison) and to the Department of Ophthalmology (University
  of Rochester)."
article_number: '67'
article_processing_charge: Yes
article_type: original
author:
- first_name: Margaret E
  full_name: Maes, Margaret E
  id: 3838F452-F248-11E8-B48F-1D18A9856A87
  last_name: Maes
  orcid: 0000-0001-9642-1085
- first_name: Ryan J.
  full_name: Donahue, Ryan J.
  last_name: Donahue
- first_name: Cassandra L.
  full_name: Schlamp, Cassandra L.
  last_name: Schlamp
- first_name: Olivia J.
  full_name: Marola, Olivia J.
  last_name: Marola
- first_name: Richard T.
  full_name: Libby, Richard T.
  last_name: Libby
- first_name: Robert W.
  full_name: Nickells, Robert W.
  last_name: Nickells
citation:
  ama: Maes ME, Donahue RJ, Schlamp CL, Marola OJ, Libby RT, Nickells RW. BAX activation
    in mouse retinal ganglion cells occurs in two temporally and mechanistically distinct
    steps. <i>Molecular Neurodegeneration</i>. 2023;18. doi:<a href="https://doi.org/10.1186/s13024-023-00659-8">10.1186/s13024-023-00659-8</a>
  apa: Maes, M. E., Donahue, R. J., Schlamp, C. L., Marola, O. J., Libby, R. T., &#38;
    Nickells, R. W. (2023). BAX activation in mouse retinal ganglion cells occurs
    in two temporally and mechanistically distinct steps. <i>Molecular Neurodegeneration</i>.
    Springer Nature. <a href="https://doi.org/10.1186/s13024-023-00659-8">https://doi.org/10.1186/s13024-023-00659-8</a>
  chicago: Maes, Margaret E, Ryan J. Donahue, Cassandra L. Schlamp, Olivia J. Marola,
    Richard T. Libby, and Robert W. Nickells. “BAX Activation in Mouse Retinal Ganglion
    Cells Occurs in Two Temporally and Mechanistically Distinct Steps.” <i>Molecular
    Neurodegeneration</i>. Springer Nature, 2023. <a href="https://doi.org/10.1186/s13024-023-00659-8">https://doi.org/10.1186/s13024-023-00659-8</a>.
  ieee: M. E. Maes, R. J. Donahue, C. L. Schlamp, O. J. Marola, R. T. Libby, and R.
    W. Nickells, “BAX activation in mouse retinal ganglion cells occurs in two temporally
    and mechanistically distinct steps,” <i>Molecular Neurodegeneration</i>, vol.
    18. Springer Nature, 2023.
  ista: Maes ME, Donahue RJ, Schlamp CL, Marola OJ, Libby RT, Nickells RW. 2023. BAX
    activation in mouse retinal ganglion cells occurs in two temporally and mechanistically
    distinct steps. Molecular Neurodegeneration. 18, 67.
  mla: Maes, Margaret E., et al. “BAX Activation in Mouse Retinal Ganglion Cells Occurs
    in Two Temporally and Mechanistically Distinct Steps.” <i>Molecular Neurodegeneration</i>,
    vol. 18, 67, Springer Nature, 2023, doi:<a href="https://doi.org/10.1186/s13024-023-00659-8">10.1186/s13024-023-00659-8</a>.
  short: M.E. Maes, R.J. Donahue, C.L. Schlamp, O.J. Marola, R.T. Libby, R.W. Nickells,
    Molecular Neurodegeneration 18 (2023).
date_created: 2023-10-08T22:01:15Z
date_published: 2023-09-26T00:00:00Z
date_updated: 2024-01-30T14:34:21Z
day: '26'
ddc:
- '570'
department:
- _id: SaSi
doi: 10.1186/s13024-023-00659-8
external_id:
  isi:
  - '001071403800001'
  pmid:
  - '37292963'
file:
- access_level: open_access
  checksum: 3aa218ddea4a082d8fd5e196ae55ca06
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-30T14:33:31Z
  date_updated: 2024-01-30T14:33:31Z
  file_id: '14917'
  file_name: 2023_MolecularNeurodegeneration_Maes.pdf
  file_size: 11568350
  relation: main_file
  success: 1
file_date_updated: 2024-01-30T14:33:31Z
has_accepted_license: '1'
intvolume: '        18'
isi: 1
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
publication: Molecular Neurodegeneration
publication_identifier:
  eissn:
  - 1750-1326
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: BAX activation in mouse retinal ganglion cells occurs in two temporally and
  mechanistically distinct steps
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 18
year: '2023'
...
---
_id: '14402'
abstract:
- lang: eng
  text: Alpha oscillations are a distinctive feature of the awake resting state of
    the human brain. However, their functional role in resting-state neuronal dynamics
    remains poorly understood. Here we show that, during resting wakefulness, alpha
    oscillations drive an alternation of attenuation and amplification bouts in neural
    activity. Our analysis indicates that inhibition is activated in pulses that last
    for a single alpha cycle and gradually suppress neural activity, while excitation
    is successively enhanced over a few alpha cycles to amplify neural activity. Furthermore,
    we show that long-term alpha amplitude fluctuations—the “waxing and waning” phenomenon—are
    an attenuation-amplification mechanism described by a power-law decay of the activity
    rate in the “waning” phase. Importantly, we do not observe such dynamics during
    non-rapid eye movement (NREM) sleep with marginal alpha oscillations. The results
    suggest that alpha oscillations modulate neural activity not only through pulses
    of inhibition (pulsed inhibition hypothesis) but also by timely enhancement of
    excitation (or disinhibition).
acknowledgement: This research was funded in whole or in part by the Austrian Science
  Fund (FWF) (grant PT1013M03318 to F.L.). For the purpose of open access, the author
  has applied a CC BY public copyright license to any Author Accepted Manuscript version
  arising from this submission. The study was supported by the European Union Horizon
  2020 Research and Innovation Program under the Marie Sklodowska-Curie action (grant
  agreement 754411 to F.L.) and in part by the NextGenerationEU through the grant
  TAlent in ReSearch@University of Padua – STARS@UNIPD (to F.L.) (project BRAINCIP
  [brain criticality and information processing]). L.d.A. acknowledges support from
  the Italian MIUR project PRIN2017WZFTZP and partial support from NEXTGENERATIONEU
  (NGEU) funded by the Ministry of University and Research (MUR), National Recovery
  and Resilience Plan (NRRP), and project MNESYS (PE0000006)—a multiscale integrated
  approach to the study of the nervous system in health and disease (DN. 1553 11.10.2022).
  O.S. acknowledges support from the Israel Science Foundation, grant 504/17. The
  work was supported in part by DIRP ZIAMH02797 (to D.P.).
article_number: '113162'
article_processing_charge: Yes
article_type: original
author:
- first_name: Fabrizio
  full_name: Lombardi, Fabrizio
  id: A057D288-3E88-11E9-986D-0CF4E5697425
  last_name: Lombardi
  orcid: 0000-0003-2623-5249
- first_name: Hans J.
  full_name: Herrmann, Hans J.
  last_name: Herrmann
- first_name: Liborio
  full_name: Parrino, Liborio
  last_name: Parrino
- first_name: Dietmar
  full_name: Plenz, Dietmar
  last_name: Plenz
- first_name: Silvia
  full_name: Scarpetta, Silvia
  last_name: Scarpetta
- first_name: Anna Elisabetta
  full_name: Vaudano, Anna Elisabetta
  last_name: Vaudano
- first_name: Lucilla
  full_name: De Arcangelis, Lucilla
  last_name: De Arcangelis
- first_name: Oren
  full_name: Shriki, Oren
  last_name: Shriki
citation:
  ama: 'Lombardi F, Herrmann HJ, Parrino L, et al. Beyond pulsed inhibition: Alpha
    oscillations modulate attenuation and amplification of neural activity in the
    awake resting state. <i>Cell Reports</i>. 2023;42(10). doi:<a href="https://doi.org/10.1016/j.celrep.2023.113162">10.1016/j.celrep.2023.113162</a>'
  apa: 'Lombardi, F., Herrmann, H. J., Parrino, L., Plenz, D., Scarpetta, S., Vaudano,
    A. E., … Shriki, O. (2023). Beyond pulsed inhibition: Alpha oscillations modulate
    attenuation and amplification of neural activity in the awake resting state. <i>Cell
    Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2023.113162">https://doi.org/10.1016/j.celrep.2023.113162</a>'
  chicago: 'Lombardi, Fabrizio, Hans J. Herrmann, Liborio Parrino, Dietmar Plenz,
    Silvia Scarpetta, Anna Elisabetta Vaudano, Lucilla De Arcangelis, and Oren Shriki.
    “Beyond Pulsed Inhibition: Alpha Oscillations Modulate Attenuation and Amplification
    of Neural Activity in the Awake Resting State.” <i>Cell Reports</i>. Elsevier,
    2023. <a href="https://doi.org/10.1016/j.celrep.2023.113162">https://doi.org/10.1016/j.celrep.2023.113162</a>.'
  ieee: 'F. Lombardi <i>et al.</i>, “Beyond pulsed inhibition: Alpha oscillations
    modulate attenuation and amplification of neural activity in the awake resting
    state,” <i>Cell Reports</i>, vol. 42, no. 10. Elsevier, 2023.'
  ista: 'Lombardi F, Herrmann HJ, Parrino L, Plenz D, Scarpetta S, Vaudano AE, De
    Arcangelis L, Shriki O. 2023. Beyond pulsed inhibition: Alpha oscillations modulate
    attenuation and amplification of neural activity in the awake resting state. Cell
    Reports. 42(10), 113162.'
  mla: 'Lombardi, Fabrizio, et al. “Beyond Pulsed Inhibition: Alpha Oscillations Modulate
    Attenuation and Amplification of Neural Activity in the Awake Resting State.”
    <i>Cell Reports</i>, vol. 42, no. 10, 113162, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.celrep.2023.113162">10.1016/j.celrep.2023.113162</a>.'
  short: F. Lombardi, H.J. Herrmann, L. Parrino, D. Plenz, S. Scarpetta, A.E. Vaudano,
    L. De Arcangelis, O. Shriki, Cell Reports 42 (2023).
date_created: 2023-10-08T22:01:15Z
date_published: 2023-10-31T00:00:00Z
date_updated: 2024-01-30T14:07:40Z
day: '31'
ddc:
- '570'
department:
- _id: GaTk
doi: 10.1016/j.celrep.2023.113162
ec_funded: 1
external_id:
  isi:
  - '001086695500001'
  pmid:
  - '37777965'
file:
- access_level: open_access
  checksum: 9c71eb2a03aa160415f01ad95f49ceb5
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-30T14:07:08Z
  date_updated: 2024-01-30T14:07:08Z
  file_id: '14914'
  file_name: 2023_CellReports_Lombardi.pdf
  file_size: 5599007
  relation: main_file
  success: 1
file_date_updated: 2024-01-30T14:07:08Z
has_accepted_license: '1'
intvolume: '        42'
isi: 1
issue: '10'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: eb943429-77a9-11ec-83b8-9f471cdf5c67
  grant_number: M03318
  name: Functional Advantages of Critical Brain Dynamics
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Beyond pulsed inhibition: Alpha oscillations modulate attenuation and amplification
  of neural activity in the awake resting state'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 42
year: '2023'
...
---
_id: '14404'
abstract:
- lang: eng
  text: A light-triggered fabrication method extends the functionality of printable
    nanomaterials
acknowledgement: The authors thank the Werner-Siemens-Stiftung and the Institute of
  Science and Technology Austria for financial support.
article_processing_charge: No
article_type: letter_note
author:
- first_name: Daniel
  full_name: Balazs, Daniel
  id: 302BADF6-85FC-11EA-9E3B-B9493DDC885E
  last_name: Balazs
  orcid: 0000-0001-7597-043X
- first_name: Maria
  full_name: Ibáñez, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibáñez
  orcid: 0000-0001-5013-2843
citation:
  ama: Balazs D, Ibáñez M. Widening the use of 3D printing. <i>Science</i>. 2023;381(6665):1413-1414.
    doi:<a href="https://doi.org/10.1126/science.adk3070">10.1126/science.adk3070</a>
  apa: Balazs, D., &#38; Ibáñez, M. (2023). Widening the use of 3D printing. <i>Science</i>.
    AAAS. <a href="https://doi.org/10.1126/science.adk3070">https://doi.org/10.1126/science.adk3070</a>
  chicago: Balazs, Daniel, and Maria Ibáñez. “Widening the Use of 3D Printing.” <i>Science</i>.
    AAAS, 2023. <a href="https://doi.org/10.1126/science.adk3070">https://doi.org/10.1126/science.adk3070</a>.
  ieee: D. Balazs and M. Ibáñez, “Widening the use of 3D printing,” <i>Science</i>,
    vol. 381, no. 6665. AAAS, pp. 1413–1414, 2023.
  ista: Balazs D, Ibáñez M. 2023. Widening the use of 3D printing. Science. 381(6665),
    1413–1414.
  mla: Balazs, Daniel, and Maria Ibáñez. “Widening the Use of 3D Printing.” <i>Science</i>,
    vol. 381, no. 6665, AAAS, 2023, pp. 1413–14, doi:<a href="https://doi.org/10.1126/science.adk3070">10.1126/science.adk3070</a>.
  short: D. Balazs, M. Ibáñez, Science 381 (2023) 1413–1414.
date_created: 2023-10-08T22:01:16Z
date_published: 2023-09-29T00:00:00Z
date_updated: 2023-10-09T07:32:58Z
day: '29'
department:
- _id: MaIb
- _id: LifeSc
doi: 10.1126/science.adk3070
external_id:
  pmid:
  - '37769110'
intvolume: '       381'
issue: '6665'
language:
- iso: eng
month: '09'
oa_version: None
page: 1413-1414
pmid: 1
project:
- _id: 9B8F7476-BA93-11EA-9121-9846C619BF3A
  name: 'HighTE: The Werner Siemens Laboratory for the High Throughput Discovery of
    Semiconductors for Waste Heat Recovery'
publication: Science
publication_identifier:
  eissn:
  - 1095-9203
publication_status: published
publisher: AAAS
quality_controlled: '1'
scopus_import: '1'
status: public
title: Widening the use of 3D printing
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 381
year: '2023'
...
---
_id: '14405'
abstract:
- lang: eng
  text: We introduce hypernode automata as a new specification formalism for hyperproperties
    of concurrent systems. They are finite automata with nodes labeled with hypernode
    logic formulas and transitions labeled with actions. A hypernode logic formula
    specifies relations between sequences of variable values in different system executions.
    Unlike HyperLTL, hypernode logic takes an asynchronous view on execution traces
    by constraining the values and the order of value changes of each variable without
    correlating the timing of the changes. Different execution traces are synchronized
    solely through the transitions of hypernode automata. Hypernode automata naturally
    combine asynchronicity at the node level with synchronicity at the transition
    level. We show that the model-checking problem for hypernode automata is decidable
    over action-labeled Kripke structures, whose actions induce transitions of the
    specification automata. For this reason, hypernode automaton is a suitable formalism
    for specifying and verifying asynchronous hyperproperties, such as declassifying
    observational determinism in multi-threaded programs.
acknowledgement: "This work was supported in part by the Austrian Science Fund (FWF)
  SFB project\r\nSpyCoDe F8502, by the FWF projects ZK-35 and W1255-N23, and by the
  ERC Advanced Grant\r\nVAMOS 101020093."
alternative_title:
- LIPIcs
article_number: '21'
article_processing_charge: Yes
arxiv: 1
author:
- first_name: Ezio
  full_name: Bartocci, Ezio
  last_name: Bartocci
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000-0002-2985-7724
- first_name: Dejan
  full_name: Nickovic, Dejan
  id: 41BCEE5C-F248-11E8-B48F-1D18A9856A87
  last_name: Nickovic
- first_name: Ana
  full_name: Oliveira da Costa, Ana
  id: f347ec37-6676-11ee-b395-a888cb7b4fb4
  last_name: Oliveira da Costa
  orcid: 0000-0002-8741-5799
citation:
  ama: 'Bartocci E, Henzinger TA, Nickovic D, Oliveira da Costa A. Hypernode automata.
    In: <i>34th International Conference on Concurrency Theory</i>. Vol 279. Schloss
    Dagstuhl - Leibniz-Zentrum für Informatik; 2023. doi:<a href="https://doi.org/10.4230/LIPIcs.CONCUR.2023.21">10.4230/LIPIcs.CONCUR.2023.21</a>'
  apa: 'Bartocci, E., Henzinger, T. A., Nickovic, D., &#38; Oliveira da Costa, A.
    (2023). Hypernode automata. In <i>34th International Conference on Concurrency
    Theory</i> (Vol. 279). Antwerp, Belgium: Schloss Dagstuhl - Leibniz-Zentrum für
    Informatik. <a href="https://doi.org/10.4230/LIPIcs.CONCUR.2023.21">https://doi.org/10.4230/LIPIcs.CONCUR.2023.21</a>'
  chicago: Bartocci, Ezio, Thomas A Henzinger, Dejan Nickovic, and Ana Oliveira da
    Costa. “Hypernode Automata.” In <i>34th International Conference on Concurrency
    Theory</i>, Vol. 279. Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2023.
    <a href="https://doi.org/10.4230/LIPIcs.CONCUR.2023.21">https://doi.org/10.4230/LIPIcs.CONCUR.2023.21</a>.
  ieee: E. Bartocci, T. A. Henzinger, D. Nickovic, and A. Oliveira da Costa, “Hypernode
    automata,” in <i>34th International Conference on Concurrency Theory</i>, Antwerp,
    Belgium, 2023, vol. 279.
  ista: 'Bartocci E, Henzinger TA, Nickovic D, Oliveira da Costa A. 2023. Hypernode
    automata. 34th International Conference on Concurrency Theory. CONCUR: Conference
    on Concurrency Theory, LIPIcs, vol. 279, 21.'
  mla: Bartocci, Ezio, et al. “Hypernode Automata.” <i>34th International Conference
    on Concurrency Theory</i>, vol. 279, 21, Schloss Dagstuhl - Leibniz-Zentrum für
    Informatik, 2023, doi:<a href="https://doi.org/10.4230/LIPIcs.CONCUR.2023.21">10.4230/LIPIcs.CONCUR.2023.21</a>.
  short: E. Bartocci, T.A. Henzinger, D. Nickovic, A. Oliveira da Costa, in:, 34th
    International Conference on Concurrency Theory, Schloss Dagstuhl - Leibniz-Zentrum
    für Informatik, 2023.
conference:
  end_date: 2023-09-22
  location: Antwerp, Belgium
  name: 'CONCUR: Conference on Concurrency Theory'
  start_date: 2023-09-19
date_created: 2023-10-08T22:01:16Z
date_published: 2023-09-01T00:00:00Z
date_updated: 2023-10-09T07:43:44Z
day: '01'
ddc:
- '000'
department:
- _id: ToHe
doi: 10.4230/LIPIcs.CONCUR.2023.21
ec_funded: 1
external_id:
  arxiv:
  - '2305.02836'
file:
- access_level: open_access
  checksum: 215765e40454d806174ac0a223e8d6fa
  content_type: application/pdf
  creator: dernst
  date_created: 2023-10-09T07:42:45Z
  date_updated: 2023-10-09T07:42:45Z
  file_id: '14413'
  file_name: 2023_LIPcs_Bartocci.pdf
  file_size: 795790
  relation: main_file
  success: 1
file_date_updated: 2023-10-09T07:42:45Z
has_accepted_license: '1'
intvolume: '       279'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: 62781420-2b32-11ec-9570-8d9b63373d4d
  call_identifier: H2020
  grant_number: '101020093'
  name: Vigilant Algorithmic Monitoring of Software
publication: 34th International Conference on Concurrency Theory
publication_identifier:
  isbn:
  - '9783959772990'
  issn:
  - '18688969'
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
quality_controlled: '1'
scopus_import: '1'
status: public
title: Hypernode automata
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: 279
year: '2023'
...
---
_id: '14406'
abstract:
- lang: eng
  text: "Recently, a concept of generalized multifractality, which characterizes fluctuations
    and correlations of critical eigenstates, was introduced and explored for all
    10 symmetry classes of disordered systems. Here, by using the nonlinear sigma-model
    (\r\nNL\r\nσ\r\nM\r\n) field theory, we extend the theory of generalized multifractality
    to boundaries of systems at criticality. Our numerical simulations on two-dimensional
    systems of symmetry classes A, C, and AII fully confirm the analytical predictions
    of pure-scaling observables and Weyl symmetry relations between critical exponents
    of surface generalized multifractality. This demonstrates the validity of the
    \r\nNL\r\nσ\r\nM\r\n for the description of Anderson-localization critical phenomena,
    not only in the bulk but also on the boundary. The critical exponents strongly
    violate generalized parabolicity, in analogy with earlier results for the bulk,
    corroborating the conclusion that the considered Anderson-localization critical
    points are not described by conformal field theories. We further derive relations
    between generalized surface multifractal spectra and linear combinations of Lyapunov
    exponents of a strip in quasi-one-dimensional geometry, which hold under the assumption
    of invariance with respect to a logarithmic conformal map. Our numerics demonstrate
    that these relations hold with an excellent accuracy. Taken together, our results
    indicate an intriguing situation: the conformal invariance is broken but holds
    partially at critical points of Anderson localization."
acknowledgement: "We thank Ilya Gruzberg for many illuminating discussions. S.S.B.,
  J.F.K., and A.D.M. acknowledge support by the Deutsche Forschungsgemeinschaft (DFG)
  via the Grant\r\nNo. MI 658/14-1. I.S.B. acknowledges support from Russian Science
  Foundation (Grant No. 22-42-04416)."
article_number: '104205'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Serafim
  full_name: Babkin, Serafim
  id: 41e64307-6672-11ee-b9ad-cc7a0075a479
  last_name: Babkin
  orcid: 0009-0003-7382-8036
- first_name: Jonas F.
  full_name: Karcher, Jonas F.
  last_name: Karcher
- first_name: Igor S.
  full_name: Burmistrov, Igor S.
  last_name: Burmistrov
- first_name: Alexander D.
  full_name: Mirlin, Alexander D.
  last_name: Mirlin
citation:
  ama: Babkin S, Karcher JF, Burmistrov IS, Mirlin AD. Generalized surface multifractality
    in two-dimensional disordered systems. <i>Physical Review B</i>. 2023;108(10).
    doi:<a href="https://doi.org/10.1103/PhysRevB.108.104205">10.1103/PhysRevB.108.104205</a>
  apa: Babkin, S., Karcher, J. F., Burmistrov, I. S., &#38; Mirlin, A. D. (2023).
    Generalized surface multifractality in two-dimensional disordered systems. <i>Physical
    Review B</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevB.108.104205">https://doi.org/10.1103/PhysRevB.108.104205</a>
  chicago: Babkin, Serafim, Jonas F. Karcher, Igor S. Burmistrov, and Alexander D.
    Mirlin. “Generalized Surface Multifractality in Two-Dimensional Disordered Systems.”
    <i>Physical Review B</i>. American Physical Society, 2023. <a href="https://doi.org/10.1103/PhysRevB.108.104205">https://doi.org/10.1103/PhysRevB.108.104205</a>.
  ieee: S. Babkin, J. F. Karcher, I. S. Burmistrov, and A. D. Mirlin, “Generalized
    surface multifractality in two-dimensional disordered systems,” <i>Physical Review
    B</i>, vol. 108, no. 10. American Physical Society, 2023.
  ista: Babkin S, Karcher JF, Burmistrov IS, Mirlin AD. 2023. Generalized surface
    multifractality in two-dimensional disordered systems. Physical Review B. 108(10),
    104205.
  mla: Babkin, Serafim, et al. “Generalized Surface Multifractality in Two-Dimensional
    Disordered Systems.” <i>Physical Review B</i>, vol. 108, no. 10, 104205, American
    Physical Society, 2023, doi:<a href="https://doi.org/10.1103/PhysRevB.108.104205">10.1103/PhysRevB.108.104205</a>.
  short: S. Babkin, J.F. Karcher, I.S. Burmistrov, A.D. Mirlin, Physical Review B
    108 (2023).
date_created: 2023-10-08T22:01:17Z
date_published: 2023-09-01T00:00:00Z
date_updated: 2023-10-09T07:09:30Z
day: '01'
department:
- _id: MaSe
doi: 10.1103/PhysRevB.108.104205
external_id:
  arxiv:
  - '2306.09455'
intvolume: '       108'
issue: '10'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.2306.09455
month: '09'
oa: 1
oa_version: Preprint
publication: Physical Review B
publication_identifier:
  eissn:
  - 2469-9969
  issn:
  - 2469-9950
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Generalized surface multifractality in two-dimensional disordered systems
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 108
year: '2023'
...
---
_id: '14408'
abstract:
- lang: eng
  text: "We prove that the mesoscopic linear statistics ∑if(na(σi−z0)) of the eigenvalues
    {σi}i of large n×n non-Hermitian random matrices with complex centred i.i.d. entries
    are asymptotically Gaussian for any H20-functions f around any point z0 in the
    bulk of the spectrum on any mesoscopic scale 0<a<1/2. This extends our previous
    result (Cipolloni et al. in Commun Pure Appl Math, 2019. arXiv:1912.04100), that
    was valid on the macroscopic scale, a=0\r\n, to cover the entire mesoscopic regime.
    The main novelty is a local law for the product of resolvents for the Hermitization
    of X at spectral parameters z1,z2 with an improved error term in the entire mesoscopic
    regime |z1−z2|≫n−1/2. The proof is dynamical; it relies on a recursive tandem
    of the characteristic flow method and the Green function comparison idea combined
    with a separation of the unstable mode of the underlying stability operator."
acknowledgement: The authors are grateful to Joscha Henheik for his help with the
  formulas in Appendix B.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Giorgio
  full_name: Cipolloni, Giorgio
  id: 42198EFA-F248-11E8-B48F-1D18A9856A87
  last_name: Cipolloni
  orcid: 0000-0002-4901-7992
- first_name: László
  full_name: Erdös, László
  id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
  last_name: Erdös
  orcid: 0000-0001-5366-9603
- first_name: Dominik J
  full_name: Schröder, Dominik J
  id: 408ED176-F248-11E8-B48F-1D18A9856A87
  last_name: Schröder
  orcid: 0000-0002-2904-1856
citation:
  ama: Cipolloni G, Erdös L, Schröder DJ. Mesoscopic central limit theorem for non-Hermitian
    random matrices. <i>Probability Theory and Related Fields</i>. 2023. doi:<a href="https://doi.org/10.1007/s00440-023-01229-1">10.1007/s00440-023-01229-1</a>
  apa: Cipolloni, G., Erdös, L., &#38; Schröder, D. J. (2023). Mesoscopic central
    limit theorem for non-Hermitian random matrices. <i>Probability Theory and Related
    Fields</i>. Springer Nature. <a href="https://doi.org/10.1007/s00440-023-01229-1">https://doi.org/10.1007/s00440-023-01229-1</a>
  chicago: Cipolloni, Giorgio, László Erdös, and Dominik J Schröder. “Mesoscopic Central
    Limit Theorem for Non-Hermitian Random Matrices.” <i>Probability Theory and Related
    Fields</i>. Springer Nature, 2023. <a href="https://doi.org/10.1007/s00440-023-01229-1">https://doi.org/10.1007/s00440-023-01229-1</a>.
  ieee: G. Cipolloni, L. Erdös, and D. J. Schröder, “Mesoscopic central limit theorem
    for non-Hermitian random matrices,” <i>Probability Theory and Related Fields</i>.
    Springer Nature, 2023.
  ista: Cipolloni G, Erdös L, Schröder DJ. 2023. Mesoscopic central limit theorem
    for non-Hermitian random matrices. Probability Theory and Related Fields.
  mla: Cipolloni, Giorgio, et al. “Mesoscopic Central Limit Theorem for Non-Hermitian
    Random Matrices.” <i>Probability Theory and Related Fields</i>, Springer Nature,
    2023, doi:<a href="https://doi.org/10.1007/s00440-023-01229-1">10.1007/s00440-023-01229-1</a>.
  short: G. Cipolloni, L. Erdös, D.J. Schröder, Probability Theory and Related Fields
    (2023).
date_created: 2023-10-08T22:01:17Z
date_published: 2023-09-28T00:00:00Z
date_updated: 2023-10-09T07:19:01Z
day: '28'
department:
- _id: LaEr
doi: 10.1007/s00440-023-01229-1
external_id:
  arxiv:
  - '2210.12060'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.2210.12060
month: '09'
oa: 1
oa_version: Preprint
publication: Probability Theory and Related Fields
publication_identifier:
  eissn:
  - 1432-2064
  issn:
  - 0178-8051
publication_status: epub_ahead
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mesoscopic central limit theorem for non-Hermitian random matrices
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '14409'
abstract:
- lang: eng
  text: We present a photon- and metal-free approach for the radical fluorination
    of aliphatic oxalate-activated alcohols. The method relies on the spontaneous
    generation of the N-(chloromethyl)triethylenediamine radical dication, a potent
    single electron oxidant, from Selectfluor and 4-(dimethylamino)pyridine. The protocol
    is easily scalable and provides the desired fluorinated products within only a
    few minutes reaction time.
acknowledgement: We gratefully acknowledge the Max-Planck Society and the Institute
  of Science and Technology Austria (ISTA) for generous financial support. We also
  thank the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under
  Germany's Excellence Strategy – EXC 2008 – 390540038 – UniSysCat for funding. B.P.
  thanks the Boehringer Ingelheim Foundation for funding through the Plus 3 Perspectives
  Programme.
article_number: e202300769
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Haralds
  full_name: Baunis, Haralds
  id: 2eea55ec-e8ec-11ed-86cb-d9c76787acfe
  last_name: Baunis
- first_name: Bartholomäus
  full_name: Pieber, Bartholomäus
  id: 93e5e5b2-0da6-11ed-8a41-af589a024726
  last_name: Pieber
  orcid: 0000-0001-8689-388X
citation:
  ama: Baunis H, Pieber B. Formal radical deoxyfluorination of oxalate-activated alcohols
    triggered by the selectfluor-DMAP charge-transfer complex. <i>European Journal
    of Organic Chemistry</i>. 2023;26(42). doi:<a href="https://doi.org/10.1002/ejoc.202300769">10.1002/ejoc.202300769</a>
  apa: Baunis, H., &#38; Pieber, B. (2023). Formal radical deoxyfluorination of oxalate-activated
    alcohols triggered by the selectfluor-DMAP charge-transfer complex. <i>European
    Journal of Organic Chemistry</i>. Wiley. <a href="https://doi.org/10.1002/ejoc.202300769">https://doi.org/10.1002/ejoc.202300769</a>
  chicago: Baunis, Haralds, and Bartholomäus Pieber. “Formal Radical Deoxyfluorination
    of Oxalate-Activated Alcohols Triggered by the Selectfluor-DMAP Charge-Transfer
    Complex.” <i>European Journal of Organic Chemistry</i>. Wiley, 2023. <a href="https://doi.org/10.1002/ejoc.202300769">https://doi.org/10.1002/ejoc.202300769</a>.
  ieee: H. Baunis and B. Pieber, “Formal radical deoxyfluorination of oxalate-activated
    alcohols triggered by the selectfluor-DMAP charge-transfer complex,” <i>European
    Journal of Organic Chemistry</i>, vol. 26, no. 42. Wiley, 2023.
  ista: Baunis H, Pieber B. 2023. Formal radical deoxyfluorination of oxalate-activated
    alcohols triggered by the selectfluor-DMAP charge-transfer complex. European Journal
    of Organic Chemistry. 26(42), e202300769.
  mla: Baunis, Haralds, and Bartholomäus Pieber. “Formal Radical Deoxyfluorination
    of Oxalate-Activated Alcohols Triggered by the Selectfluor-DMAP Charge-Transfer
    Complex.” <i>European Journal of Organic Chemistry</i>, vol. 26, no. 42, e202300769,
    Wiley, 2023, doi:<a href="https://doi.org/10.1002/ejoc.202300769">10.1002/ejoc.202300769</a>.
  short: H. Baunis, B. Pieber, European Journal of Organic Chemistry 26 (2023).
date_created: 2023-10-08T22:01:18Z
date_published: 2023-11-07T00:00:00Z
date_updated: 2024-01-30T14:05:14Z
day: '07'
ddc:
- '540'
department:
- _id: BaPi
doi: 10.1002/ejoc.202300769
external_id:
  isi:
  - '001072666500001'
file:
- access_level: open_access
  checksum: e8ad7865acd94672e476f273ccf3d542
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-30T14:04:44Z
  date_updated: 2024-01-30T14:04:44Z
  file_id: '14913'
  file_name: 2023_EurJOrgChem_Baunis.pdf
  file_size: 3277622
  relation: main_file
  success: 1
file_date_updated: 2024-01-30T14:04:44Z
has_accepted_license: '1'
intvolume: '        26'
isi: 1
issue: '42'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc/4.0/
month: '11'
oa: 1
oa_version: Published Version
publication: European Journal of Organic Chemistry
publication_identifier:
  eissn:
  - 1099-0690
  issn:
  - 1434-193X
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Formal radical deoxyfluorination of oxalate-activated alcohols triggered by
  the selectfluor-DMAP charge-transfer complex
tmp:
  image: /images/cc_by_nc.png
  legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
  short: CC BY-NC (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 26
year: '2023'
...
---
_id: '14410'
abstract:
- lang: eng
  text: This paper focuses on the implementation details of the baseline methods and
    a recent lightweight conditional model extrapolation algorithm LIMES [5] for streaming
    data under class-prior shift. LIMES achieves superior performance over the baseline
    methods, especially concerning the minimum-across-day accuracy, which is important
    for the users of the system. In this work, the key measures to facilitate reproducibility
    and enhance the credibility of the results are described.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Paulina
  full_name: Tomaszewska, Paulina
  last_name: Tomaszewska
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
citation:
  ama: 'Tomaszewska P, Lampert C. On the implementation of baselines and lightweight
    conditional model extrapolation (LIMES) under class-prior shift. In: <i>International
    Workshop on Reproducible Research in Pattern Recognition</i>. Vol 14068. Springer
    Nature; 2023:67-73. doi:<a href="https://doi.org/10.1007/978-3-031-40773-4_6">10.1007/978-3-031-40773-4_6</a>'
  apa: 'Tomaszewska, P., &#38; Lampert, C. (2023). On the implementation of baselines
    and lightweight conditional model extrapolation (LIMES) under class-prior shift.
    In <i>International Workshop on Reproducible Research in Pattern Recognition</i>
    (Vol. 14068, pp. 67–73). Montreal, Canada: Springer Nature. <a href="https://doi.org/10.1007/978-3-031-40773-4_6">https://doi.org/10.1007/978-3-031-40773-4_6</a>'
  chicago: Tomaszewska, Paulina, and Christoph Lampert. “On the Implementation of Baselines
    and Lightweight Conditional Model Extrapolation (LIMES) under Class-Prior Shift.”
    In <i>International Workshop on Reproducible Research in Pattern Recognition</i>,
    14068:67–73. Springer Nature, 2023. <a href="https://doi.org/10.1007/978-3-031-40773-4_6">https://doi.org/10.1007/978-3-031-40773-4_6</a>.
  ieee: P. Tomaszewska and C. Lampert, “On the implementation of baselines and lightweight
    conditional model extrapolation (LIMES) under class-prior shift,” in <i>International
    Workshop on Reproducible Research in Pattern Recognition</i>, Montreal, Canada,
    2023, vol. 14068, pp. 67–73.
  ista: 'Tomaszewska P, Lampert C. 2023. On the implementation of baselines and lightweight
    conditional model extrapolation (LIMES) under class-prior shift. International
    Workshop on Reproducible Research in Pattern Recognition. RRPR: Reproducible Research
    in Pattern Recognition, LNCS, vol. 14068, 67–73.'
  mla: Tomaszewska, Paulina, and Christoph Lampert. “On the Implementation of Baselines
    and Lightweight Conditional Model Extrapolation (LIMES) under Class-Prior Shift.”
    <i>International Workshop on Reproducible Research in Pattern Recognition</i>,
    vol. 14068, Springer Nature, 2023, pp. 67–73, doi:<a href="https://doi.org/10.1007/978-3-031-40773-4_6">10.1007/978-3-031-40773-4_6</a>.
  short: P. Tomaszewska, C. Lampert, in:, International Workshop on Reproducible Research
    in Pattern Recognition, Springer Nature, 2023, pp. 67–73.
conference:
  end_date: 2022-08-21
  location: Montreal, Canada
  name: 'RRPR: Reproducible Research in Pattern Recognition'
  start_date: 2022-08-21
date_created: 2023-10-08T22:01:18Z
date_published: 2023-08-20T00:00:00Z
date_updated: 2023-10-09T06:48:02Z
day: '20'
department:
- _id: ChLa
doi: 10.1007/978-3-031-40773-4_6
intvolume: '     14068'
language:
- iso: eng
month: '08'
oa_version: None
page: 67-73
publication: International Workshop on Reproducible Research in Pattern Recognition
publication_identifier:
  eissn:
  - 1611-3349
  isbn:
  - '9783031407727'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: On the implementation of baselines and lightweight conditional model extrapolation
  (LIMES) under class-prior shift
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 14068
year: '2023'
...
---
_id: '14411'
abstract:
- lang: eng
  text: "Partially specified Boolean networks (PSBNs) represent a promising framework
    for the qualitative modelling of biological systems in which the logic of interactions
    is not completely known. Phenotype control aims to stabilise the network in states
    exhibiting specific traits.\r\nIn this paper, we define the phenotype control
    problem in the context of asynchronous PSBNs and propose a novel semi-symbolic
    algorithm for solving this problem with permanent variable perturbations."
acknowledgement: This work was supported by the Czech Foundation grant No. GA22-10845S,
  Grant Agency of Masaryk University grant No. MUNI/G/1771/2020, and the European
  Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie
  Grant Agreement No. 101034413.
alternative_title:
- LNBI
article_processing_charge: No
author:
- first_name: Nikola
  full_name: Beneš, Nikola
  last_name: Beneš
- first_name: Luboš
  full_name: Brim, Luboš
  last_name: Brim
- first_name: Samuel
  full_name: Pastva, Samuel
  id: 07c5ea74-f61c-11ec-a664-aa7c5d957b2b
  last_name: Pastva
  orcid: 0000-0003-1993-0331
- first_name: David
  full_name: Šafránek, David
  last_name: Šafránek
- first_name: Eva
  full_name: Šmijáková, Eva
  last_name: Šmijáková
citation:
  ama: 'Beneš N, Brim L, Pastva S, Šafránek D, Šmijáková E. Phenotype control of partially
    specified boolean networks. In: <i>21st International Conference on Computational
    Methods in Systems Biology</i>. Vol 14137. Springer Nature; 2023:18-35. doi:<a
    href="https://doi.org/10.1007/978-3-031-42697-1_2">10.1007/978-3-031-42697-1_2</a>'
  apa: 'Beneš, N., Brim, L., Pastva, S., Šafránek, D., &#38; Šmijáková, E. (2023).
    Phenotype control of partially specified boolean networks. In <i>21st International
    Conference on Computational Methods in Systems Biology</i> (Vol. 14137, pp. 18–35).
    Luxembourg City, Luxembourg: Springer Nature. <a href="https://doi.org/10.1007/978-3-031-42697-1_2">https://doi.org/10.1007/978-3-031-42697-1_2</a>'
  chicago: Beneš, Nikola, Luboš Brim, Samuel Pastva, David Šafránek, and Eva Šmijáková.
    “Phenotype Control of Partially Specified Boolean Networks.” In <i>21st International
    Conference on Computational Methods in Systems Biology</i>, 14137:18–35. Springer
    Nature, 2023. <a href="https://doi.org/10.1007/978-3-031-42697-1_2">https://doi.org/10.1007/978-3-031-42697-1_2</a>.
  ieee: N. Beneš, L. Brim, S. Pastva, D. Šafránek, and E. Šmijáková, “Phenotype control
    of partially specified boolean networks,” in <i>21st International Conference
    on Computational Methods in Systems Biology</i>, Luxembourg City, Luxembourg,
    2023, vol. 14137, pp. 18–35.
  ista: 'Beneš N, Brim L, Pastva S, Šafránek D, Šmijáková E. 2023. Phenotype control
    of partially specified boolean networks. 21st International Conference on Computational
    Methods in Systems Biology. CMSB: Computational Methods in Systems Biology, LNBI,
    vol. 14137, 18–35.'
  mla: Beneš, Nikola, et al. “Phenotype Control of Partially Specified Boolean Networks.”
    <i>21st International Conference on Computational Methods in Systems Biology</i>,
    vol. 14137, Springer Nature, 2023, pp. 18–35, doi:<a href="https://doi.org/10.1007/978-3-031-42697-1_2">10.1007/978-3-031-42697-1_2</a>.
  short: N. Beneš, L. Brim, S. Pastva, D. Šafránek, E. Šmijáková, in:, 21st International
    Conference on Computational Methods in Systems Biology, Springer Nature, 2023,
    pp. 18–35.
conference:
  end_date: 2023-09-15
  location: Luxembourg City, Luxembourg
  name: 'CMSB: Computational Methods in Systems Biology'
  start_date: 2023-09-13
date_created: 2023-10-08T22:01:18Z
date_published: 2023-09-09T00:00:00Z
date_updated: 2024-02-20T09:02:04Z
day: '09'
ddc:
- '000'
department:
- _id: ToHe
doi: 10.1007/978-3-031-42697-1_2
ec_funded: 1
file:
- access_level: open_access
  checksum: 6f71bdaedb770b52380222fd9f4d7937
  content_type: application/pdf
  creator: spastva
  date_created: 2024-02-16T08:26:32Z
  date_updated: 2024-02-16T08:26:32Z
  file_id: '14997'
  file_name: cmsb2023.pdf
  file_size: 691582
  relation: main_file
  success: 1
file_date_updated: 2024-02-16T08:26:32Z
has_accepted_license: '1'
intvolume: '     14137'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Submitted Version
page: 18-35
project:
- _id: fc2ed2f7-9c52-11eb-aca3-c01059dda49c
  call_identifier: H2020
  grant_number: '101034413'
  name: 'IST-BRIDGE: International postdoctoral program'
publication: 21st International Conference on Computational Methods in Systems Biology
publication_identifier:
  eissn:
  - 1611-3349
  isbn:
  - '9783031426964'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Phenotype control of partially specified boolean networks
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: 14137
year: '2023'
...
---
_id: '14417'
abstract:
- lang: eng
  text: Entropic risk (ERisk) is an established risk measure in finance, quantifying
    risk by an exponential re-weighting of rewards. We study ERisk for the first time
    in the context of turn-based stochastic games with the total reward objective.
    This gives rise to an objective function that demands the control of systems in
    a risk-averse manner. We show that the resulting games are determined and, in
    particular, admit optimal memoryless deterministic strategies. This contrasts
    risk measures that previously have been considered in the special case of Markov
    decision processes and that require randomization and/or memory. We provide several
    results on the decidability and the computational complexity of the threshold
    problem, i.e. whether the optimal value of ERisk exceeds a given threshold. In
    the most general case, the problem is decidable subject to Shanuel’s conjecture.
    If all inputs are rational, the resulting threshold problem can be solved using
    algebraic numbers, leading to decidability via a polynomial-time reduction to
    the existential theory of the reals. Further restrictions on the encoding of the
    input allow the solution of the threshold problem in NP∩coNP. Finally, an approximation
    algorithm for the optimal value of ERisk is provided.
acknowledgement: "This work was partly funded by the ERC CoG 863818 (ForM-SMArt),
  the DFG Grant\r\n389792660 as part of TRR 248 (Foundations of Perspicuous Software
  Systems), the Cluster of\r\nExcellence EXC 2050/1 (CeTI, project ID 390696704, as
  part of Germany’s Excellence Strategy), and the DFG projects BA-1679/11-1 and BA-1679/12-1."
alternative_title:
- LIPIcs
article_number: '15'
article_processing_charge: Yes
arxiv: 1
author:
- first_name: Christel
  full_name: Baier, Christel
  last_name: Baier
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Tobias
  full_name: Meggendorfer, Tobias
  id: b21b0c15-30a2-11eb-80dc-f13ca25802e1
  last_name: Meggendorfer
  orcid: 0000-0002-1712-2165
- first_name: Jakob
  full_name: Piribauer, Jakob
  last_name: Piribauer
citation:
  ama: 'Baier C, Chatterjee K, Meggendorfer T, Piribauer J. Entropic risk for turn-based
    stochastic games. In: <i>48th International Symposium on Mathematical Foundations
    of Computer Science</i>. Vol 272. Schloss Dagstuhl - Leibniz-Zentrum für Informatik;
    2023. doi:<a href="https://doi.org/10.4230/LIPIcs.MFCS.2023.15">10.4230/LIPIcs.MFCS.2023.15</a>'
  apa: 'Baier, C., Chatterjee, K., Meggendorfer, T., &#38; Piribauer, J. (2023). Entropic
    risk for turn-based stochastic games. In <i>48th International Symposium on Mathematical
    Foundations of Computer Science</i> (Vol. 272). Bordeaux, France: Schloss Dagstuhl
    - Leibniz-Zentrum für Informatik. <a href="https://doi.org/10.4230/LIPIcs.MFCS.2023.15">https://doi.org/10.4230/LIPIcs.MFCS.2023.15</a>'
  chicago: Baier, Christel, Krishnendu Chatterjee, Tobias Meggendorfer, and Jakob
    Piribauer. “Entropic Risk for Turn-Based Stochastic Games.” In <i>48th International
    Symposium on Mathematical Foundations of Computer Science</i>, Vol. 272. Schloss
    Dagstuhl - Leibniz-Zentrum für Informatik, 2023. <a href="https://doi.org/10.4230/LIPIcs.MFCS.2023.15">https://doi.org/10.4230/LIPIcs.MFCS.2023.15</a>.
  ieee: C. Baier, K. Chatterjee, T. Meggendorfer, and J. Piribauer, “Entropic risk
    for turn-based stochastic games,” in <i>48th International Symposium on Mathematical
    Foundations of Computer Science</i>, Bordeaux, France, 2023, vol. 272.
  ista: 'Baier C, Chatterjee K, Meggendorfer T, Piribauer J. 2023. Entropic risk for
    turn-based stochastic games. 48th International Symposium on Mathematical Foundations
    of Computer Science. MFCS: Symposium on Mathematical Foundations of Computer Science,
    LIPIcs, vol. 272, 15.'
  mla: Baier, Christel, et al. “Entropic Risk for Turn-Based Stochastic Games.” <i>48th
    International Symposium on Mathematical Foundations of Computer Science</i>, vol.
    272, 15, Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2023, doi:<a href="https://doi.org/10.4230/LIPIcs.MFCS.2023.15">10.4230/LIPIcs.MFCS.2023.15</a>.
  short: C. Baier, K. Chatterjee, T. Meggendorfer, J. Piribauer, in:, 48th International
    Symposium on Mathematical Foundations of Computer Science, Schloss Dagstuhl -
    Leibniz-Zentrum für Informatik, 2023.
conference:
  end_date: 2023-09-01
  location: Bordeaux, France
  name: 'MFCS: Symposium on Mathematical Foundations of Computer Science'
  start_date: 2023-08-28
date_created: 2023-10-09T09:21:05Z
date_published: 2023-08-21T00:00:00Z
date_updated: 2025-07-14T09:09:57Z
day: '21'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.4230/LIPIcs.MFCS.2023.15
ec_funded: 1
external_id:
  arxiv:
  - '2307.06611'
file:
- access_level: open_access
  checksum: 402281b17ed669bbf149d0fdf68ac201
  content_type: application/pdf
  creator: dernst
  date_created: 2023-10-09T09:19:11Z
  date_updated: 2023-10-09T09:19:11Z
  file_id: '14418'
  file_name: 2023_LIPIcsMFCS_Baier.pdf
  file_size: 826843
  relation: main_file
  success: 1
file_date_updated: 2023-10-09T09:19:11Z
has_accepted_license: '1'
intvolume: '       272'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
project:
- _id: 0599E47C-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '863818'
  name: 'Formal Methods for Stochastic Models: Algorithms and Applications'
publication: 48th International Symposium on Mathematical Foundations of Computer
  Science
publication_identifier:
  eissn:
  - 1868-8969
  isbn:
  - '9783959772921'
publication_status: published
publisher: Schloss Dagstuhl - Leibniz-Zentrum für Informatik
quality_controlled: '1'
scopus_import: '1'
status: public
title: Entropic risk for turn-based stochastic games
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: 272
year: '2023'
...
---
_id: '14421'
abstract:
- lang: eng
  text: Only recently has it been possible to construct a self-adjoint Hamiltonian
    that involves the creation of Dirac particles at a point source in 3d space. Its
    definition makes use of an interior-boundary condition. Here, we develop for this
    Hamiltonian a corresponding theory of the Bohmian configuration. That is, we (non-rigorously)
    construct a Markov jump process $(Q_t)_{t\in\mathbb{R}}$ in the configuration
    space of a variable number of particles that is $|\psi_t|^2$-distributed at every
    time t and follows Bohmian trajectories between the jumps. The jumps correspond
    to particle creation or annihilation events and occur either to or from a configuration
    with a particle located at the source. The process is the natural analog of Bell's
    jump process, and a central piece in its construction is the determination of
    the rate of particle creation. The construction requires an analysis of the asymptotic
    behavior of the Bohmian trajectories near the source. We find that the particle
    reaches the source with radial speed 0, but orbits around the source infinitely
    many times in finite time before absorption (or after emission).
acknowledgement: J H gratefully acknowledges partial financial support by the ERC
  Advanced Grant 'RMTBeyond' No. 101020331.
article_number: '445201'
article_processing_charge: Yes (via OA deal)
article_type: original
arxiv: 1
author:
- first_name: Sven Joscha
  full_name: Henheik, Sven Joscha
  id: 31d731d7-d235-11ea-ad11-b50331c8d7fb
  last_name: Henheik
  orcid: 0000-0003-1106-327X
- first_name: Roderich
  full_name: Tumulka, Roderich
  last_name: Tumulka
citation:
  ama: 'Henheik SJ, Tumulka R. Creation rate of Dirac particles at a point source.
    <i>Journal of Physics A: Mathematical and Theoretical</i>. 2023;56(44). doi:<a
    href="https://doi.org/10.1088/1751-8121/acfe62">10.1088/1751-8121/acfe62</a>'
  apa: 'Henheik, S. J., &#38; Tumulka, R. (2023). Creation rate of Dirac particles
    at a point source. <i>Journal of Physics A: Mathematical and Theoretical</i>.
    IOP Publishing. <a href="https://doi.org/10.1088/1751-8121/acfe62">https://doi.org/10.1088/1751-8121/acfe62</a>'
  chicago: 'Henheik, Sven Joscha, and Roderich Tumulka. “Creation Rate of Dirac Particles
    at a Point Source.” <i>Journal of Physics A: Mathematical and Theoretical</i>.
    IOP Publishing, 2023. <a href="https://doi.org/10.1088/1751-8121/acfe62">https://doi.org/10.1088/1751-8121/acfe62</a>.'
  ieee: 'S. J. Henheik and R. Tumulka, “Creation rate of Dirac particles at a point
    source,” <i>Journal of Physics A: Mathematical and Theoretical</i>, vol. 56, no.
    44. IOP Publishing, 2023.'
  ista: 'Henheik SJ, Tumulka R. 2023. Creation rate of Dirac particles at a point
    source. Journal of Physics A: Mathematical and Theoretical. 56(44), 445201.'
  mla: 'Henheik, Sven Joscha, and Roderich Tumulka. “Creation Rate of Dirac Particles
    at a Point Source.” <i>Journal of Physics A: Mathematical and Theoretical</i>,
    vol. 56, no. 44, 445201, IOP Publishing, 2023, doi:<a href="https://doi.org/10.1088/1751-8121/acfe62">10.1088/1751-8121/acfe62</a>.'
  short: 'S.J. Henheik, R. Tumulka, Journal of Physics A: Mathematical and Theoretical
    56 (2023).'
date_created: 2023-10-12T12:42:53Z
date_published: 2023-10-11T00:00:00Z
date_updated: 2023-12-13T13:01:25Z
day: '11'
ddc:
- '510'
department:
- _id: GradSch
- _id: LaEr
doi: 10.1088/1751-8121/acfe62
ec_funded: 1
external_id:
  arxiv:
  - '2211.16606'
  isi:
  - '001080908000001'
file:
- access_level: open_access
  checksum: 5b68de147dd4c608b71a6e0e844d2ce9
  content_type: application/pdf
  creator: dernst
  date_created: 2023-10-16T07:07:24Z
  date_updated: 2023-10-16T07:07:24Z
  file_id: '14429'
  file_name: 2023_JourPhysics_Henheik.pdf
  file_size: 721399
  relation: main_file
  success: 1
file_date_updated: 2023-10-16T07:07:24Z
has_accepted_license: '1'
intvolume: '        56'
isi: 1
issue: '44'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
project:
- _id: 62796744-2b32-11ec-9570-940b20777f1d
  call_identifier: H2020
  grant_number: '101020331'
  name: Random matrices beyond Wigner-Dyson-Mehta
publication: 'Journal of Physics A: Mathematical and Theoretical'
publication_identifier:
  eissn:
  - 1751-8121
  issn:
  - 1751-8113
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Creation rate of Dirac particles at a point source
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 56
year: '2023'
...
---
_id: '14422'
abstract:
- lang: eng
  text: "Animals exhibit a remarkable ability to learn and remember new behaviors,
    skills, and associations throughout their lifetime. These capabilities are made
    possible thanks to a variety of\r\nchanges in the brain throughout adulthood,
    regrouped under the term \"plasticity\". Some cells\r\nin the brain —neurons—
    and specifically changes in the connections between neurons, the\r\nsynapses,
    were shown to be crucial for the formation, selection, and consolidation of memories\r\nfrom
    past experiences. These ongoing changes of synapses across time are called synaptic\r\nplasticity.
    Understanding how a myriad of biochemical processes operating at individual\r\nsynapses
    can somehow work in concert to give rise to meaningful changes in behavior is
    a\r\nfascinating problem and an active area of research.\r\nHowever, the experimental
    search for the precise plasticity mechanisms at play in the brain\r\nis daunting,
    as it is difficult to control and observe synapses during learning. Theoretical\r\napproaches
    have thus been the default method to probe the plasticity-behavior connection.
    Such\r\nstudies attempt to extract unifying principles across synapses and model
    all observed synaptic\r\nchanges using plasticity rules: equations that govern
    the evolution of synaptic strengths across\r\ntime in neuronal network models.
    These rules can use many relevant quantities to determine\r\nthe magnitude of
    synaptic changes, such as the precise timings of pre- and postsynaptic\r\naction
    potentials, the recent neuronal activity levels, the state of neighboring synapses,
    etc.\r\nHowever, analytical studies rely heavily on human intuition and are forced
    to make simplifying\r\nassumptions about plasticity rules.\r\nIn this thesis,
    we aim to assist and augment human intuition in this search for plasticity rules.\r\nWe
    explore whether a numerical approach could automatically discover the plasticity
    rules\r\nthat elicit desired behaviors in large networks of interconnected neurons.
    This approach is\r\ndubbed meta-learning synaptic plasticity: learning plasticity
    rules which themselves will make\r\nneuronal networks learn how to solve a desired
    task. We first write all the potential plasticity\r\nmechanisms to consider using
    a single expression with adjustable parameters. We then optimize\r\nthese plasticity
    parameters using evolutionary strategies or Bayesian inference on tasks known\r\nto
    involve synaptic plasticity, such as familiarity detection and network stabilization.\r\nWe
    show that these automated approaches are powerful tools, able to complement established\r\nanalytical
    methods. By comprehensively screening plasticity rules at all synapse types in\r\nrealistic,
    spiking neuronal network models, we discover entire sets of degenerate plausible\r\nplasticity
    rules that reliably elicit memory-related behaviors. Our approaches allow for
    more\r\nrobust experimental predictions, by abstracting out the idiosyncrasies
    of individual plasticity\r\nrules, and provide fresh insights on synaptic plasticity
    in spiking network models.\r\n"
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Basile J
  full_name: Confavreux, Basile J
  id: C7610134-B532-11EA-BD9F-F5753DDC885E
  last_name: Confavreux
citation:
  ama: 'Confavreux BJ. Synapseek: Meta-learning synaptic plasticity rules. 2023. doi:<a
    href="https://doi.org/10.15479/at:ista:14422">10.15479/at:ista:14422</a>'
  apa: 'Confavreux, B. J. (2023). <i>Synapseek: Meta-learning synaptic plasticity
    rules</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:14422">https://doi.org/10.15479/at:ista:14422</a>'
  chicago: 'Confavreux, Basile J. “Synapseek: Meta-Learning Synaptic Plasticity Rules.”
    Institute of Science and Technology Austria, 2023. <a href="https://doi.org/10.15479/at:ista:14422">https://doi.org/10.15479/at:ista:14422</a>.'
  ieee: 'B. J. Confavreux, “Synapseek: Meta-learning synaptic plasticity rules,” Institute
    of Science and Technology Austria, 2023.'
  ista: 'Confavreux BJ. 2023. Synapseek: Meta-learning synaptic plasticity rules.
    Institute of Science and Technology Austria.'
  mla: 'Confavreux, Basile J. <i>Synapseek: Meta-Learning Synaptic Plasticity Rules</i>.
    Institute of Science and Technology Austria, 2023, doi:<a href="https://doi.org/10.15479/at:ista:14422">10.15479/at:ista:14422</a>.'
  short: 'B.J. Confavreux, Synapseek: Meta-Learning Synaptic Plasticity Rules, Institute
    of Science and Technology Austria, 2023.'
date_created: 2023-10-12T14:13:25Z
date_published: 2023-10-12T00:00:00Z
date_updated: 2023-10-18T09:20:56Z
day: '12'
ddc:
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degree_awarded: PhD
department:
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- _id: TiVo
doi: 10.15479/at:ista:14422
ec_funded: 1
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language:
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month: '10'
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page: '148'
project:
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  call_identifier: H2020
  grant_number: '819603'
  name: Learning the shape of synaptic plasticity rules for neuronal architectures
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publication_identifier:
  issn:
  - 2663 - 337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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  - id: '9633'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
title: 'Synapseek: Meta-learning synaptic plasticity rules'
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  short: CC BY-NC-SA (4.0)
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2023'
...
