---
_id: '14244'
abstract:
- lang: eng
  text: "In this paper, we determine the motivic class — in particular, the weight
    polynomial and conjecturally the Poincaré polynomial — of the open de Rham space,
    defined and studied by Boalch, of certain moduli spaces of irregular meromorphic
    connections on the trivial rank \r\n bundle on P1. The computation is by motivic
    Fourier transform. We show that the result satisfies the purity conjecture, that
    is, it agrees with the pure part of the conjectured mixed Hodge polynomial of
    the corresponding wild character variety. We also identify the open de Rham spaces
    with quiver varieties with multiplicities of Yamakawa and Geiss–Leclerc–Schröer.
    We finish with constructing natural complete hyperkähler metrics on them, which
    in the four-dimensional cases are expected to be of type ALF."
acknowledgement: We would like to thank Gergely Bérczy, Roger Bielawski, Philip Boalch,
  Sergey Cherkis, Andrew Dancer, Brent Doran, Eloïse Hamilton, Frances Kirwan, Bernard
  Leclerc, Emmanuel Letellier, Alessia Mandini, Maxence Mayrand, András Némethi, Szilárd
  Szabó, and Daisuke Yamakawa for discussions related to the paper. We especially
  thank the referee for an extensive list of very careful comments. At various stages
  of this project, the authors were supported by the Advanced Grant “Arithmetic and
  physics of Higgs moduli spaces” no. 320593 of the European Research Council, by
  grant no. 153627 and NCCR SwissMAP, both funded by the Swiss National Science Foundation
  as well as by EPF Lausanne and IST Austria. In the final stages of this project,
  MLW was supported by SFB/TR 45 “Periods, moduli and arithmetic of algebraic varieties,”
  subproject M08-10 “Moduli of vector bundles on higher-dimensional varieties.” DW
  was also supported by the Fondation Sciences Mathématiques de Paris, as well as
  public grants overseen by the Agence national de la recherche (ANR) of France as
  part of the Investissements d'avenir program, under reference numbers ANR-10-LABX-0098
  and ANR-15-CE40-0008 (Défigéo).
article_processing_charge: Yes (via OA deal)
article_type: original
arxiv: 1
author:
- first_name: Tamás
  full_name: Hausel, Tamás
  id: 4A0666D8-F248-11E8-B48F-1D18A9856A87
  last_name: Hausel
- first_name: Michael Lennox
  full_name: Wong, Michael Lennox
  last_name: Wong
- first_name: Dimitri
  full_name: Wyss, Dimitri
  last_name: Wyss
citation:
  ama: Hausel T, Wong ML, Wyss D. Arithmetic and metric aspects of open de Rham spaces.
    <i>Proceedings of the London Mathematical Society</i>. 2023;127(4):958-1027. doi:<a
    href="https://doi.org/10.1112/plms.12555">10.1112/plms.12555</a>
  apa: Hausel, T., Wong, M. L., &#38; Wyss, D. (2023). Arithmetic and metric aspects
    of open de Rham spaces. <i>Proceedings of the London Mathematical Society</i>.
    Wiley. <a href="https://doi.org/10.1112/plms.12555">https://doi.org/10.1112/plms.12555</a>
  chicago: Hausel, Tamás, Michael Lennox Wong, and Dimitri Wyss. “Arithmetic and Metric
    Aspects of Open de Rham Spaces.” <i>Proceedings of the London Mathematical Society</i>.
    Wiley, 2023. <a href="https://doi.org/10.1112/plms.12555">https://doi.org/10.1112/plms.12555</a>.
  ieee: T. Hausel, M. L. Wong, and D. Wyss, “Arithmetic and metric aspects of open
    de Rham spaces,” <i>Proceedings of the London Mathematical Society</i>, vol. 127,
    no. 4. Wiley, pp. 958–1027, 2023.
  ista: Hausel T, Wong ML, Wyss D. 2023. Arithmetic and metric aspects of open de
    Rham spaces. Proceedings of the London Mathematical Society. 127(4), 958–1027.
  mla: Hausel, Tamás, et al. “Arithmetic and Metric Aspects of Open de Rham Spaces.”
    <i>Proceedings of the London Mathematical Society</i>, vol. 127, no. 4, Wiley,
    2023, pp. 958–1027, doi:<a href="https://doi.org/10.1112/plms.12555">10.1112/plms.12555</a>.
  short: T. Hausel, M.L. Wong, D. Wyss, Proceedings of the London Mathematical Society
    127 (2023) 958–1027.
date_created: 2023-08-27T22:01:18Z
date_published: 2023-10-01T00:00:00Z
date_updated: 2024-01-30T12:56:10Z
day: '01'
ddc:
- '510'
department:
- _id: TaHa
doi: 10.1112/plms.12555
ec_funded: 1
external_id:
  arxiv:
  - '1807.04057'
  isi:
  - '001049312700001'
file:
- access_level: open_access
  checksum: 2af4d2d6a8ae42f7d3fba0188e79ae82
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-30T12:56:00Z
  date_updated: 2024-01-30T12:56:00Z
  file_id: '14910'
  file_name: 2023_ProcLondonMathSoc_Hausel.pdf
  file_size: 651335
  relation: main_file
  success: 1
file_date_updated: 2024-01-30T12:56:00Z
has_accepted_license: '1'
intvolume: '       127'
isi: 1
issue: '4'
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '10'
oa: 1
oa_version: Published Version
page: 958-1027
project:
- _id: 25E549F4-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '320593'
  name: Arithmetic and physics of Higgs moduli spaces
- _id: 25E6C798-B435-11E9-9278-68D0E5697425
  grant_number: '153627'
  name: Arithmetic quantization of character and quiver varities
publication: Proceedings of the London Mathematical Society
publication_identifier:
  eissn:
  - 1460-244X
  issn:
  - 0024-6115
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Arithmetic and metric aspects of open de Rham spaces
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: 127
year: '2023'
...
---
_id: '14245'
abstract:
- lang: eng
  text: We establish effective counting results for lattice points in families of
    domains in real, complex and quaternionic hyperbolic spaces of any dimension.
    The domains we focus on are defined as product sets with respect to an Iwasawa
    decomposition. Several natural diophantine problems can be reduced to counting
    lattice points in such domains. These include equidistribution of the ratio of
    the length of the shortest solution (x,y) to the gcd equation bx−ay=1 relative
    to the length of (a,b), where (a,b) ranges over primitive vectors in a disc whose
    radius increases, the natural analog of this problem in imaginary quadratic number
    fields, as well as equidistribution of integral solutions to the diophantine equation
    defined by an integral Lorentz form in three or more variables. We establish an
    effective rate of convergence for these equidistribution problems, depending on
    the size of the spectral gap associated with a suitable lattice subgroup in the
    isometry group of the relevant hyperbolic space. The main result underlying our
    discussion amounts to establishing effective joint equidistribution for the horospherical
    component and the radial component in the Iwasawa decomposition of lattice elements.
acknowledgement: The authors thank the referee for important comments which led to
  significant improvements is the presentation of several results in the paper. They
  also thank Ami Paz for preparing the figures for this paper. Horesh thanks Ami Paz
  and Yakov Karasik for helpful discussions. Nevo thanks John Parker and Rene Rühr
  for providing some very useful references. Nevo is supported by ISF Grant No. 2095/15.
article_processing_charge: Yes
article_type: original
arxiv: 1
author:
- first_name: Tal
  full_name: Horesh, Tal
  id: C8B7BF48-8D81-11E9-BCA9-F536E6697425
  last_name: Horesh
- first_name: Amos
  full_name: Nevo, Amos
  last_name: Nevo
citation:
  ama: 'Horesh T, Nevo A. Horospherical coordinates of lattice points in hyperbolic
    spaces: Effective counting and equidistribution. <i>Pacific Journal of Mathematics</i>.
    2023;324(2):265-294. doi:<a href="https://doi.org/10.2140/pjm.2023.324.265">10.2140/pjm.2023.324.265</a>'
  apa: 'Horesh, T., &#38; Nevo, A. (2023). Horospherical coordinates of lattice points
    in hyperbolic spaces: Effective counting and equidistribution. <i>Pacific Journal
    of Mathematics</i>. Mathematical Sciences Publishers. <a href="https://doi.org/10.2140/pjm.2023.324.265">https://doi.org/10.2140/pjm.2023.324.265</a>'
  chicago: 'Horesh, Tal, and Amos Nevo. “Horospherical Coordinates of Lattice Points
    in Hyperbolic Spaces: Effective Counting and Equidistribution.” <i>Pacific Journal
    of Mathematics</i>. Mathematical Sciences Publishers, 2023. <a href="https://doi.org/10.2140/pjm.2023.324.265">https://doi.org/10.2140/pjm.2023.324.265</a>.'
  ieee: 'T. Horesh and A. Nevo, “Horospherical coordinates of lattice points in hyperbolic
    spaces: Effective counting and equidistribution,” <i>Pacific Journal of Mathematics</i>,
    vol. 324, no. 2. Mathematical Sciences Publishers, pp. 265–294, 2023.'
  ista: 'Horesh T, Nevo A. 2023. Horospherical coordinates of lattice points in hyperbolic
    spaces: Effective counting and equidistribution. Pacific Journal of Mathematics.
    324(2), 265–294.'
  mla: 'Horesh, Tal, and Amos Nevo. “Horospherical Coordinates of Lattice Points in
    Hyperbolic Spaces: Effective Counting and Equidistribution.” <i>Pacific Journal
    of Mathematics</i>, vol. 324, no. 2, Mathematical Sciences Publishers, 2023, pp.
    265–94, doi:<a href="https://doi.org/10.2140/pjm.2023.324.265">10.2140/pjm.2023.324.265</a>.'
  short: T. Horesh, A. Nevo, Pacific Journal of Mathematics 324 (2023) 265–294.
date_created: 2023-08-27T22:01:18Z
date_published: 2023-07-26T00:00:00Z
date_updated: 2023-12-13T12:19:42Z
day: '26'
ddc:
- '510'
department:
- _id: TiBr
doi: 10.2140/pjm.2023.324.265
external_id:
  arxiv:
  - '1612.08215'
  isi:
  - '001047690500001'
file:
- access_level: open_access
  checksum: a675b53cfb31fa46be1e879b7e77fe8c
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-05T07:26:17Z
  date_updated: 2023-09-05T07:26:17Z
  file_id: '14267'
  file_name: 2023_PacificJourMaths_Horesh.pdf
  file_size: 654895
  relation: main_file
  success: 1
file_date_updated: 2023-09-05T07:26:17Z
has_accepted_license: '1'
intvolume: '       324'
isi: 1
issue: '2'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 265-294
publication: Pacific Journal of Mathematics
publication_identifier:
  eissn:
  - 1945-5844
  issn:
  - 0030-8730
publication_status: published
publisher: Mathematical Sciences Publishers
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Horospherical coordinates of lattice points in hyperbolic spaces: Effective
  counting and equidistribution'
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: 324
year: '2023'
...
---
_id: '14246'
abstract:
- lang: eng
  text: The model of a ring threaded by the Aharonov-Bohm flux underlies our understanding
    of a coupling between gauge potentials and matter. The typical formulation of
    the model is based upon a single particle picture, and should be extended when
    interactions with other particles become relevant. Here, we illustrate such an
    extension for a particle in an Aharonov-Bohm ring subject to interactions with
    a weakly interacting Bose gas. We show that the ground state of the system can
    be described using the Bose-polaron concept—a particle dressed by interactions
    with a bosonic environment. We connect the energy spectrum to the effective mass
    of the polaron, and demonstrate how to change currents in the system by tuning
    boson-particle interactions. Our results suggest the Aharonov-Bohm ring as a platform
    for studying coherence and few- to many-body crossover of quasi-particles that
    arise from an impurity immersed in a medium.
acknowledgement: "Open Access funding enabled and organized by Projekt DEAL.\r\nWe
  would like to thank Jonas Jager for sharing his data with us in the early stages
  of this project. We thank Joachim Brand and Ray Yang for sharing with us data from
  Yang et al.46. This work has received funding from the DFG Project no. 413495248
  [VO 2437/1-1] (F.B., H.-W.H., A.G.V.). We acknowledge support from the Deutsche
  Forschungsgemeinschaft (DFG - German Research Foundation) and the Open Access Publishing
  Fund of the Technical University of Darmstadt."
article_number: '224'
article_processing_charge: Yes (via OA deal)
article_type: original
arxiv: 1
author:
- first_name: Fabian
  full_name: Brauneis, Fabian
  last_name: Brauneis
- first_name: Areg
  full_name: Ghazaryan, Areg
  id: 4AF46FD6-F248-11E8-B48F-1D18A9856A87
  last_name: Ghazaryan
  orcid: 0000-0001-9666-3543
- first_name: Hans-Werner
  full_name: Hammer, Hans-Werner
  last_name: Hammer
- first_name: Artem
  full_name: Volosniev, Artem
  id: 37D278BC-F248-11E8-B48F-1D18A9856A87
  last_name: Volosniev
  orcid: 0000-0003-0393-5525
citation:
  ama: Brauneis F, Ghazaryan A, Hammer H-W, Volosniev A. Emergence of a Bose polaron
    in a small ring threaded by the Aharonov-Bohm flux. <i>Communications Physics</i>.
    2023;6. doi:<a href="https://doi.org/10.1038/s42005-023-01281-2">10.1038/s42005-023-01281-2</a>
  apa: Brauneis, F., Ghazaryan, A., Hammer, H.-W., &#38; Volosniev, A. (2023). Emergence
    of a Bose polaron in a small ring threaded by the Aharonov-Bohm flux. <i>Communications
    Physics</i>. Springer Nature. <a href="https://doi.org/10.1038/s42005-023-01281-2">https://doi.org/10.1038/s42005-023-01281-2</a>
  chicago: Brauneis, Fabian, Areg Ghazaryan, Hans-Werner Hammer, and Artem Volosniev.
    “Emergence of a Bose Polaron in a Small Ring Threaded by the Aharonov-Bohm Flux.”
    <i>Communications Physics</i>. Springer Nature, 2023. <a href="https://doi.org/10.1038/s42005-023-01281-2">https://doi.org/10.1038/s42005-023-01281-2</a>.
  ieee: F. Brauneis, A. Ghazaryan, H.-W. Hammer, and A. Volosniev, “Emergence of a
    Bose polaron in a small ring threaded by the Aharonov-Bohm flux,” <i>Communications
    Physics</i>, vol. 6. Springer Nature, 2023.
  ista: Brauneis F, Ghazaryan A, Hammer H-W, Volosniev A. 2023. Emergence of a Bose
    polaron in a small ring threaded by the Aharonov-Bohm flux. Communications Physics.
    6, 224.
  mla: Brauneis, Fabian, et al. “Emergence of a Bose Polaron in a Small Ring Threaded
    by the Aharonov-Bohm Flux.” <i>Communications Physics</i>, vol. 6, 224, Springer
    Nature, 2023, doi:<a href="https://doi.org/10.1038/s42005-023-01281-2">10.1038/s42005-023-01281-2</a>.
  short: F. Brauneis, A. Ghazaryan, H.-W. Hammer, A. Volosniev, Communications Physics
    6 (2023).
date_created: 2023-08-28T12:36:49Z
date_published: 2023-08-22T00:00:00Z
date_updated: 2023-12-13T12:21:09Z
day: '22'
ddc:
- '530'
department:
- _id: MiLe
doi: 10.1038/s42005-023-01281-2
external_id:
  arxiv:
  - '2301.10488'
  isi:
  - '001052577500002'
file:
- access_level: open_access
  checksum: 6edfc59b0ee7dc406d0968b05236e83d
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-05T08:45:49Z
  date_updated: 2023-09-05T08:45:49Z
  file_id: '14268'
  file_name: 2023_CommPhysics_Brauneis.pdf
  file_size: 855960
  relation: main_file
  success: 1
file_date_updated: 2023-09-05T08:45:49Z
has_accepted_license: '1'
intvolume: '         6'
isi: 1
keyword:
- General Physics and Astronomy
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
publication: Communications Physics
publication_identifier:
  issn:
  - 2399-3650
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Emergence of a Bose polaron in a small ring threaded by the Aharonov-Bohm flux
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: 6
year: '2023'
...
---
_id: '14253'
abstract:
- lang: eng
  text: Junctions between the endoplasmic reticulum (ER) and the plasma membrane (PM)
    are specialized membrane contacts ubiquitous in eukaryotic cells. Concentration
    of intracellular signaling machinery near ER-PM junctions allows these domains
    to serve critical roles in lipid and Ca2+ signaling and homeostasis. Subcellular
    compartmentalization of protein kinase A (PKA) signaling also regulates essential
    cellular functions, however, no specific association between PKA and ER-PM junctional
    domains is known. Here, we show that in brain neurons type I PKA is directed to
    Kv2.1 channel-dependent ER-PM junctional domains via SPHKAP, a type I PKA-specific
    anchoring protein. SPHKAP association with type I PKA regulatory subunit RI and
    ER-resident VAP proteins results in the concentration of type I PKA between stacked
    ER cisternae associated with ER-PM junctions. This ER-associated PKA signalosome
    enables reciprocal regulation between PKA and Ca2+ signaling machinery to support
    Ca2+ influx and excitation-transcription coupling. These data reveal that neuronal
    ER-PM junctions support a receptor-independent form of PKA signaling driven by
    membrane depolarization and intracellular Ca2+, allowing conversion of information
    encoded in electrical signals into biochemical changes universally recognized
    throughout the cell.
acknowledgement: We thank Kayla Templeton and Peter Turcanu for technical assistance,
  Michelle Salemi for assistance with LC-MS data acquisition and analysis, Dr. Belvin
  Gong for advice on monoclonal antibody generation, Drs. Maria Casas Prat and Eamonn
  Dickson for assistance with super-resolution TIRF microscopy, Dr. Oscar Cerda for
  assistance with the design of TAT-FFAT peptides, Dr. Fernando Santana for helpful
  discussions, and Dr. Jodi Nunnari for a careful reading of our manuscript. We also
  thank Dr. Alan Howe, Dr. Sohum Mehta, and Dr. Jin Zhang for providing plasmids used
  in this study. This project was funded by NIH Grants R01NS114210 and R21NS101648
  (J.S.T.), and F32NS108519 (N.C.V.).
article_number: '5231'
article_processing_charge: Yes
article_type: original
author:
- first_name: Nicholas C.
  full_name: Vierra, Nicholas C.
  last_name: Vierra
- first_name: Luisa
  full_name: Ribeiro-Silva, Luisa
  last_name: Ribeiro-Silva
- first_name: Michael
  full_name: Kirmiz, Michael
  last_name: Kirmiz
- first_name: Deborah
  full_name: Van Der List, Deborah
  last_name: Van Der List
- first_name: Pradeep
  full_name: Bhandari, Pradeep
  id: 45EDD1BC-F248-11E8-B48F-1D18A9856A87
  last_name: Bhandari
  orcid: 0000-0003-0863-4481
- first_name: Olivia A.
  full_name: Mack, Olivia A.
  last_name: Mack
- first_name: James
  full_name: Carroll, James
  last_name: Carroll
- first_name: Elodie
  full_name: Le Monnier, Elodie
  id: 3B59276A-F248-11E8-B48F-1D18A9856A87
  last_name: Le Monnier
- first_name: Sue A.
  full_name: Aicher, Sue A.
  last_name: Aicher
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: James S.
  full_name: Trimmer, James S.
  last_name: Trimmer
citation:
  ama: Vierra NC, Ribeiro-Silva L, Kirmiz M, et al. Neuronal ER-plasma membrane junctions
    couple excitation to Ca2+-activated PKA signaling. <i>Nature Communications</i>.
    2023;14. doi:<a href="https://doi.org/10.1038/s41467-023-40930-6">10.1038/s41467-023-40930-6</a>
  apa: Vierra, N. C., Ribeiro-Silva, L., Kirmiz, M., Van Der List, D., Bhandari, P.,
    Mack, O. A., … Trimmer, J. S. (2023). Neuronal ER-plasma membrane junctions couple
    excitation to Ca2+-activated PKA signaling. <i>Nature Communications</i>. Springer
    Nature. <a href="https://doi.org/10.1038/s41467-023-40930-6">https://doi.org/10.1038/s41467-023-40930-6</a>
  chicago: Vierra, Nicholas C., Luisa Ribeiro-Silva, Michael Kirmiz, Deborah Van Der
    List, Pradeep Bhandari, Olivia A. Mack, James Carroll, et al. “Neuronal ER-Plasma
    Membrane Junctions Couple Excitation to Ca2+-Activated PKA Signaling.” <i>Nature
    Communications</i>. Springer Nature, 2023. <a href="https://doi.org/10.1038/s41467-023-40930-6">https://doi.org/10.1038/s41467-023-40930-6</a>.
  ieee: N. C. Vierra <i>et al.</i>, “Neuronal ER-plasma membrane junctions couple
    excitation to Ca2+-activated PKA signaling,” <i>Nature Communications</i>, vol.
    14. Springer Nature, 2023.
  ista: Vierra NC, Ribeiro-Silva L, Kirmiz M, Van Der List D, Bhandari P, Mack OA,
    Carroll J, Le Monnier E, Aicher SA, Shigemoto R, Trimmer JS. 2023. Neuronal ER-plasma
    membrane junctions couple excitation to Ca2+-activated PKA signaling. Nature Communications.
    14, 5231.
  mla: Vierra, Nicholas C., et al. “Neuronal ER-Plasma Membrane Junctions Couple Excitation
    to Ca2+-Activated PKA Signaling.” <i>Nature Communications</i>, vol. 14, 5231,
    Springer Nature, 2023, doi:<a href="https://doi.org/10.1038/s41467-023-40930-6">10.1038/s41467-023-40930-6</a>.
  short: N.C. Vierra, L. Ribeiro-Silva, M. Kirmiz, D. Van Der List, P. Bhandari, O.A.
    Mack, J. Carroll, E. Le Monnier, S.A. Aicher, R. Shigemoto, J.S. Trimmer, Nature
    Communications 14 (2023).
date_created: 2023-09-03T22:01:14Z
date_published: 2023-08-26T00:00:00Z
date_updated: 2023-09-06T06:53:32Z
day: '26'
ddc:
- '570'
department:
- _id: RySh
doi: 10.1038/s41467-023-40930-6
external_id:
  pmid:
  - '37633939'
file:
- access_level: open_access
  checksum: 6ab8aab4e957f626a09a1c73db3388fb
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T06:50:07Z
  date_updated: 2023-09-06T06:50:07Z
  file_id: '14270'
  file_name: 2023_NatureComm_Vierra.pdf
  file_size: 9412549
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T06:50:07Z
has_accepted_license: '1'
intvolume: '        14'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
  eissn:
  - 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Neuronal ER-plasma membrane junctions couple excitation to Ca2+-activated PKA
  signaling
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: '14254'
abstract:
- lang: eng
  text: In [10] Nam proved a Lieb–Thirring Inequality for the kinetic energy of a
    fermionic quantum system, with almost optimal (semi-classical) constant and a
    gradient correction term. We present a stronger version of this inequality, with
    a much simplified proof. As a corollary we obtain a simple proof of the original
    Lieb–Thirring inequality.
acknowledgement: J.P.S. thanks the Institute of Science and Technology Austria for
  the hospitality and support during a visit where this work was done. J.P.S. was
  also partially supported by the VILLUM Centre of Excellence for the Mathematics
  of Quantum Theory (QMATH) (grant No. 10059).
article_number: '110129'
article_processing_charge: Yes (via OA deal)
article_type: original
arxiv: 1
author:
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
- first_name: Jan Philip
  full_name: Solovej, Jan Philip
  last_name: Solovej
citation:
  ama: Seiringer R, Solovej JP. A simple approach to Lieb-Thirring type inequalities.
    <i>Journal of Functional Analysis</i>. 2023;285(10). doi:<a href="https://doi.org/10.1016/j.jfa.2023.110129">10.1016/j.jfa.2023.110129</a>
  apa: Seiringer, R., &#38; Solovej, J. P. (2023). A simple approach to Lieb-Thirring
    type inequalities. <i>Journal of Functional Analysis</i>. Elsevier. <a href="https://doi.org/10.1016/j.jfa.2023.110129">https://doi.org/10.1016/j.jfa.2023.110129</a>
  chicago: Seiringer, Robert, and Jan Philip Solovej. “A Simple Approach to Lieb-Thirring
    Type Inequalities.” <i>Journal of Functional Analysis</i>. Elsevier, 2023. <a
    href="https://doi.org/10.1016/j.jfa.2023.110129">https://doi.org/10.1016/j.jfa.2023.110129</a>.
  ieee: R. Seiringer and J. P. Solovej, “A simple approach to Lieb-Thirring type inequalities,”
    <i>Journal of Functional Analysis</i>, vol. 285, no. 10. Elsevier, 2023.
  ista: Seiringer R, Solovej JP. 2023. A simple approach to Lieb-Thirring type inequalities.
    Journal of Functional Analysis. 285(10), 110129.
  mla: Seiringer, Robert, and Jan Philip Solovej. “A Simple Approach to Lieb-Thirring
    Type Inequalities.” <i>Journal of Functional Analysis</i>, vol. 285, no. 10, 110129,
    Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.jfa.2023.110129">10.1016/j.jfa.2023.110129</a>.
  short: R. Seiringer, J.P. Solovej, Journal of Functional Analysis 285 (2023).
date_created: 2023-09-03T22:01:14Z
date_published: 2023-11-15T00:00:00Z
date_updated: 2024-01-30T14:17:23Z
day: '15'
ddc:
- '510'
department:
- _id: RoSe
doi: 10.1016/j.jfa.2023.110129
external_id:
  arxiv:
  - '2303.04504'
  isi:
  - '001071552300001'
file:
- access_level: open_access
  checksum: 28e424ad91be6219e9d321054ce3a412
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-30T14:15:16Z
  date_updated: 2024-01-30T14:15:16Z
  file_id: '14915'
  file_name: 2023_JourFunctionalAnalysis_Seiringer.pdf
  file_size: 232934
  relation: main_file
  success: 1
file_date_updated: 2024-01-30T14:15:16Z
has_accepted_license: '1'
intvolume: '       285'
isi: 1
issue: '10'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
publication: Journal of Functional Analysis
publication_identifier:
  eissn:
  - 1096-0783
  issn:
  - 0022-1236
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: A simple approach to Lieb-Thirring type inequalities
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: 285
year: '2023'
...
---
_id: '14255'
abstract:
- lang: eng
  text: Toscana virus is a major cause of arboviral disease in humans in the Mediterranean
    basin during summer. However, early virus-host cell interactions and entry mechanisms
    remain poorly characterized. Investigating iPSC-derived human neurons and cell
    lines, we found that virus binding to the cell surface was specific, and 50% of
    bound virions were endocytosed within 10 min. Virions entered Rab5a+ early endosomes
    and, subsequently, Rab7a+ and LAMP-1+ late endosomal compartments. Penetration
    required intact late endosomes and occurred within 30 min following internalization.
    Virus entry relied on vacuolar acidification, with an optimal pH for viral membrane
    fusion at pH 5.5. The pH threshold increased to 5.8 with longer pre-exposure of
    virions to the slightly acidic pH in early endosomes. Strikingly, the particles
    remained infectious after entering late endosomes with a pH below the fusion threshold.
    Overall, our study establishes Toscana virus as a late-penetrating virus and reveals
    an atypical use of vacuolar acidity by this virus to enter host cells.
acknowledged_ssus:
- _id: EM-Fac
acknowledgement: "We acknowledge Elodie Chatre and the Imaging Platform Platim, SFR
  Biosciences, Lyon, as well as Vibor Laketa and the Infectious Diseases Imaging Platform
  (IDIP) at the Center for Integrative Infectious Disease Research (CIID) Heidelberg.
  The sand fly cell lines were supplied by the Tick Cell Biobank at the University
  of Liverpool. F.K.M.S. acknowledges support from the Scientific Service Units (SSUs)
  of ISTA through resources provided by the Electron Microscopy Facility (EMF).\r\nThis
  work was supported by CellNetworks Research Group funds and Deutsche Forschungsgemeinschaft
  (DFG) funding (LO-2338/3-1) and the Agence Nationale de la Recherche (ANR) funding
  (grant numbers ANR-21-CE11-0012 and ANR-22-CE15-0034), all awarded to P.-Y.L. This
  work was also supported by the LABEX ECOFECT (ANR-11-LABX-0048) of Université de
  Lyon (UDL), within the program “Investissements d’Avenir” (ANR-11-IDEX-0007) operated
  by the ANR and by the RESPOND program of the UDL (awarded to P.-Y.L) . C.A. was
  supported by the Chica and Heinz Schaller Research Group funds, NARSAD 2019 award,
  a Fritz Thyssen Research Grant, and the SFB1158-S02 grant. L.B-S. is supported by
  a United Kingdom Biotechnology and Biological Sciences Research Council grant (BB/P024270/1)
  and a Wellcome Trust grant (223743/Z/21/Z). F.K.M.S acknowledges support from the
  Austrian Science Fund (FWF, P31445). J.K. received a salary from the DFG (LO-2338/3-1)
  and then from the ANR (ANR-11-LABX-0048). The salary of Z.M.U. was partially covered
  by the DFG (LO-2338/3-1). S.K. received a salary from the DFG (SFB1129). We are
  grateful to the Chinese Scholarship Council (CSC; 201904910701), DAAD/ANID (57451854/62180003),
  the Rufus A. Kellogg fellowship program (Amherst College, Massachusetts, USA) for
  awarding fellowships to Q.X., J.C., and H.A.A., respectively."
article_number: e1011562
article_processing_charge: Yes
article_type: original
author:
- first_name: Jana
  full_name: Koch, Jana
  last_name: Koch
- first_name: Qilin
  full_name: Xin, Qilin
  last_name: Xin
- first_name: Martin
  full_name: Obr, Martin
  id: 4741CA5A-F248-11E8-B48F-1D18A9856A87
  last_name: Obr
  orcid: 0000-0003-1756-6564
- first_name: Alicia
  full_name: Schäfer, Alicia
  last_name: Schäfer
- first_name: Nina
  full_name: Rolfs, Nina
  last_name: Rolfs
- first_name: Holda A.
  full_name: Anagho, Holda A.
  last_name: Anagho
- first_name: Aiste
  full_name: Kudulyte, Aiste
  last_name: Kudulyte
- first_name: Lea
  full_name: Woltereck, Lea
  last_name: Woltereck
- first_name: Susann
  full_name: Kummer, Susann
  last_name: Kummer
- first_name: Joaquin
  full_name: Campos, Joaquin
  last_name: Campos
- first_name: Zina M.
  full_name: Uckeley, Zina M.
  last_name: Uckeley
- first_name: Lesley
  full_name: Bell-Sakyi, Lesley
  last_name: Bell-Sakyi
- first_name: Hans Georg
  full_name: Kräusslich, Hans Georg
  last_name: Kräusslich
- first_name: Florian Km
  full_name: Schur, Florian Km
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
- first_name: Claudio
  full_name: Acuna, Claudio
  last_name: Acuna
- first_name: Pierre Yves
  full_name: Lozach, Pierre Yves
  last_name: Lozach
citation:
  ama: Koch J, Xin Q, Obr M, et al. The phenuivirus Toscana virus makes an atypical
    use of vacuolar acidity to enter host cells. <i>PLoS Pathogens</i>. 2023;19(8).
    doi:<a href="https://doi.org/10.1371/journal.ppat.1011562">10.1371/journal.ppat.1011562</a>
  apa: Koch, J., Xin, Q., Obr, M., Schäfer, A., Rolfs, N., Anagho, H. A., … Lozach,
    P. Y. (2023). The phenuivirus Toscana virus makes an atypical use of vacuolar
    acidity to enter host cells. <i>PLoS Pathogens</i>. Public Library of Science.
    <a href="https://doi.org/10.1371/journal.ppat.1011562">https://doi.org/10.1371/journal.ppat.1011562</a>
  chicago: Koch, Jana, Qilin Xin, Martin Obr, Alicia Schäfer, Nina Rolfs, Holda A.
    Anagho, Aiste Kudulyte, et al. “The Phenuivirus Toscana Virus Makes an Atypical
    Use of Vacuolar Acidity to Enter Host Cells.” <i>PLoS Pathogens</i>. Public Library
    of Science, 2023. <a href="https://doi.org/10.1371/journal.ppat.1011562">https://doi.org/10.1371/journal.ppat.1011562</a>.
  ieee: J. Koch <i>et al.</i>, “The phenuivirus Toscana virus makes an atypical use
    of vacuolar acidity to enter host cells,” <i>PLoS Pathogens</i>, vol. 19, no.
    8. Public Library of Science, 2023.
  ista: Koch J, Xin Q, Obr M, Schäfer A, Rolfs N, Anagho HA, Kudulyte A, Woltereck
    L, Kummer S, Campos J, Uckeley ZM, Bell-Sakyi L, Kräusslich HG, Schur FK, Acuna
    C, Lozach PY. 2023. The phenuivirus Toscana virus makes an atypical use of vacuolar
    acidity to enter host cells. PLoS Pathogens. 19(8), e1011562.
  mla: Koch, Jana, et al. “The Phenuivirus Toscana Virus Makes an Atypical Use of
    Vacuolar Acidity to Enter Host Cells.” <i>PLoS Pathogens</i>, vol. 19, no. 8,
    e1011562, Public Library of Science, 2023, doi:<a href="https://doi.org/10.1371/journal.ppat.1011562">10.1371/journal.ppat.1011562</a>.
  short: J. Koch, Q. Xin, M. Obr, A. Schäfer, N. Rolfs, H.A. Anagho, A. Kudulyte,
    L. Woltereck, S. Kummer, J. Campos, Z.M. Uckeley, L. Bell-Sakyi, H.G. Kräusslich,
    F.K. Schur, C. Acuna, P.Y. Lozach, PLoS Pathogens 19 (2023).
date_created: 2023-09-03T22:01:14Z
date_published: 2023-08-14T00:00:00Z
date_updated: 2023-12-13T12:22:22Z
day: '14'
ddc:
- '570'
department:
- _id: FlSc
doi: 10.1371/journal.ppat.1011562
external_id:
  isi:
  - '001050846300004'
  pmid:
  - '37578957'
file:
- access_level: open_access
  checksum: 47ca3bb54b27f28b05644be0ad064bc6
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T06:41:52Z
  date_updated: 2023-09-06T06:41:52Z
  file_id: '14269'
  file_name: 2023_PloSPathogens_Koch.pdf
  file_size: 4458336
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T06:41:52Z
has_accepted_license: '1'
intvolume: '        19'
isi: 1
issue: '8'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 26736D6A-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P31445
  name: Structural conservation and diversity in retroviral capsid
publication: PLoS Pathogens
publication_identifier:
  eissn:
  - 1553-7374
  issn:
  - 1553-7366
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: The phenuivirus Toscana virus makes an atypical use of vacuolar acidity to
  enter host cells
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: 19
year: '2023'
...
---
_id: '14256'
abstract:
- lang: eng
  text: "Context. Space asteroseismology is revolutionizing our knowledge of the internal
    structure and dynamics of stars. A breakthrough is ongoing with the recent discoveries
    of signatures of strong magnetic fields in the core of red giant stars. The key
    signature for such a detection is the asymmetry these fields induce in the frequency
    splittings of observed dipolar mixed gravito-acoustic modes.\r\nAims. We investigate
    the ability of the observed asymmetries of the frequency splittings of dipolar
    mixed modes to constrain the geometrical properties of deep magnetic fields.\r\nMethods.
    We used the powerful analytical Racah-Wigner algebra used in quantum mechanics
    to characterize the geometrical couplings of dipolar mixed oscillation modes with
    various realistically plausible topologies of fossil magnetic fields. We also
    computed the induced perturbation of their frequencies.\r\nResults. First, in
    the case of an oblique magnetic dipole, we provide the exact analytical expression
    of the asymmetry as a function of the angle between the rotation and magnetic
    axes. Its value provides a direct measure of this angle. Second, considering a
    combination of axisymmetric dipolar and quadrupolar fields, we show how the asymmetry
    is blind to the unraveling of the relative strength and sign of each component.
    Finally, in the case of a given multipole, we show that a negative asymmetry is
    a signature of non-axisymmetric topologies.\r\nConclusions. Asymmetries of dipolar
    mixed modes provide a key bit of information on the geometrical topology of deep
    fossil magnetic fields, but this is insufficient on its own. Asteroseismic constraints
    should therefore be combined with spectropolarimetric observations and numerical
    simulations, which aim to predict the more probable stable large-scale geometries."
acknowledgement: The authors are grateful to the referee for her/his detailed and
  constructive report, which has allowed us to improve our article. S. M. acknowledges
  support from the CNES GOLF-SOHO and PLATO grants at CEA/DAp and PNPS (CNRS/INSU).
  We thank R. A. Garcia for fruitful discussions and suggestions.
article_number: L9
article_processing_charge: Yes (in subscription journal)
article_type: letter_note
arxiv: 1
author:
- first_name: S.
  full_name: Mathis, S.
  last_name: Mathis
- first_name: Lisa Annabelle
  full_name: Bugnet, Lisa Annabelle
  id: d9edb345-f866-11ec-9b37-d119b5234501
  last_name: Bugnet
  orcid: 0000-0003-0142-4000
citation:
  ama: 'Mathis S, Bugnet LA. Asymmetries of frequency splittings of dipolar mixed
    modes: A window on the topology of deep magnetic fields. <i>Astronomy and Astrophysics</i>.
    2023;676. doi:<a href="https://doi.org/10.1051/0004-6361/202346832">10.1051/0004-6361/202346832</a>'
  apa: 'Mathis, S., &#38; Bugnet, L. A. (2023). Asymmetries of frequency splittings
    of dipolar mixed modes: A window on the topology of deep magnetic fields. <i>Astronomy
    and Astrophysics</i>. EDP Sciences. <a href="https://doi.org/10.1051/0004-6361/202346832">https://doi.org/10.1051/0004-6361/202346832</a>'
  chicago: 'Mathis, S., and Lisa Annabelle Bugnet. “Asymmetries of Frequency Splittings
    of Dipolar Mixed Modes: A Window on the Topology of Deep Magnetic Fields.” <i>Astronomy
    and Astrophysics</i>. EDP Sciences, 2023. <a href="https://doi.org/10.1051/0004-6361/202346832">https://doi.org/10.1051/0004-6361/202346832</a>.'
  ieee: 'S. Mathis and L. A. Bugnet, “Asymmetries of frequency splittings of dipolar
    mixed modes: A window on the topology of deep magnetic fields,” <i>Astronomy and
    Astrophysics</i>, vol. 676. EDP Sciences, 2023.'
  ista: 'Mathis S, Bugnet LA. 2023. Asymmetries of frequency splittings of dipolar
    mixed modes: A window on the topology of deep magnetic fields. Astronomy and Astrophysics.
    676, L9.'
  mla: 'Mathis, S., and Lisa Annabelle Bugnet. “Asymmetries of Frequency Splittings
    of Dipolar Mixed Modes: A Window on the Topology of Deep Magnetic Fields.” <i>Astronomy
    and Astrophysics</i>, vol. 676, L9, EDP Sciences, 2023, doi:<a href="https://doi.org/10.1051/0004-6361/202346832">10.1051/0004-6361/202346832</a>.'
  short: S. Mathis, L.A. Bugnet, Astronomy and Astrophysics 676 (2023).
date_created: 2023-09-03T22:01:15Z
date_published: 2023-08-01T00:00:00Z
date_updated: 2023-09-06T11:05:58Z
day: '01'
ddc:
- '520'
department:
- _id: LiBu
doi: 10.1051/0004-6361/202346832
external_id:
  arxiv:
  - '2306.11587'
  isi:
  - '001046037700007'
file:
- access_level: open_access
  checksum: 7b30d26fb2b7bcb5b5be1414950615f9
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T07:13:19Z
  date_updated: 2023-09-06T07:13:19Z
  file_id: '14271'
  file_name: 2023_AstronomyAstrophysics_Mathis.pdf
  file_size: 458120
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T07:13:19Z
has_accepted_license: '1'
intvolume: '       676'
isi: 1
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
publication: Astronomy and Astrophysics
publication_identifier:
  eissn:
  - 1432-0746
  issn:
  - 0004-6361
publication_status: published
publisher: EDP Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Asymmetries of frequency splittings of dipolar mixed modes: A window on the
  topology of deep magnetic fields'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 676
year: '2023'
...
---
_id: '14257'
abstract:
- lang: eng
  text: Mapping the complex and dense arrangement of cells and their connectivity
    in brain tissue demands nanoscale spatial resolution imaging. Super-resolution
    optical microscopy excels at visualizing specific molecules and individual cells
    but fails to provide tissue context. Here we developed Comprehensive Analysis
    of Tissues across Scales (CATS), a technology to densely map brain tissue architecture
    from millimeter regional to nanometer synaptic scales in diverse chemically fixed
    brain preparations, including rodent and human. CATS uses fixation-compatible
    extracellular labeling and optical imaging, including stimulated emission depletion
    or expansion microscopy, to comprehensively delineate cellular structures. It
    enables three-dimensional reconstruction of single synapses and mapping of synaptic
    connectivity by identification and analysis of putative synaptic cleft regions.
    Applying CATS to the mouse hippocampal mossy fiber circuitry, we reconstructed
    and quantified the synaptic input and output structure of identified neurons.
    We furthermore demonstrate applicability to clinically derived human tissue samples,
    including formalin-fixed paraffin-embedded routine diagnostic specimens, for visualizing
    the cellular architecture of brain tissue in health and disease.
acknowledged_ssus:
- _id: ScienComp
- _id: Bio
- _id: PreCl
- _id: LifeSc
- _id: M-Shop
- _id: E-Lib
acknowledgement: 'We thank J. Vorlaufer, N. Agudelo-Dueñas, W. Jahr and A. Wartak
  for microscope maintenance and troubleshooting; C. Kreuzinger, A. Freeman and I.
  Erber for technical assistance; and M. Tomschik for support with obtaining human
  samples. We gratefully acknowledge E. Miguel for setting up webKnossos and M. Šuplata
  for computational support and hardware control. We are grateful to R. Shigemoto
  and B. Bickel for generous support and M. Sixt and S. Boyd (Stanford University)
  for discussions and critical reading of the paper. PSD95-HaloTag mice were kindly
  provided by S. Grant (University of Edinburgh). We acknowledge expert support by
  Institute of Science and Technology Austria’s scientific computing, imaging and
  optics, preclinical and lab support facilities and by the Miba machine shop and
  library. We gratefully acknowledge funding by the following sources: Austrian Science
  Fund (FWF) grant I3600-B27 (J.G.D.); Austrian Science Fund (FWF) grant DK W1232
  (J.G.D. and J.M.M.); Austrian Science Fund (FWF) grant Z 312-B27, Wittgenstein award
  (P.J.); Austrian Science Fund (FWF) projects I4685-B, I6565-B (SYNABS) and DOC 33-B27
  (R.H.); Gesellschaft für Forschungsförderung NÖ (NFB) grant LSC18-022 (J.G.D.);
  European Union’s Horizon 2020 research and innovation programme, European Research
  Council (ERC) grant 715508 – REVERSEAUTISM (G.N.); European Union’s Horizon 2020
  research and innovation programme, European Research Council (ERC) grant 692692
  – GIANTSYN (P.J.); Marie Skłodowska-Curie Actions Fellowship GA no. 665385 under
  the EU Horizon 2020 program (J.M.M. and J.L.); and Marie Skłodowska-Curie Actions
  Individual Fellowship no. 101026635 under the EU Horizon 2020 program (J.F.W.).'
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Julia M
  full_name: Michalska, Julia M
  id: 443DB6DE-F248-11E8-B48F-1D18A9856A87
  last_name: Michalska
  orcid: 0000-0003-3862-1235
- first_name: Julia
  full_name: Lyudchik, Julia
  id: 46E28B80-F248-11E8-B48F-1D18A9856A87
  last_name: Lyudchik
- first_name: Philipp
  full_name: Velicky, Philipp
  id: 39BDC62C-F248-11E8-B48F-1D18A9856A87
  last_name: Velicky
  orcid: 0000-0002-2340-7431
- first_name: Hana
  full_name: Korinkova, Hana
  id: ee3cb6ca-ec98-11ea-ae11-ff703e2254ed
  last_name: Korinkova
- first_name: Jake
  full_name: Watson, Jake
  id: 63836096-4690-11EA-BD4E-32803DDC885E
  last_name: Watson
  orcid: 0000-0002-8698-3823
- first_name: Alban
  full_name: Cenameri, Alban
  id: 9ac8f577-2357-11eb-997a-e566c5550886
  last_name: Cenameri
- first_name: Christoph M
  full_name: Sommer, Christoph M
  id: 4DF26D8C-F248-11E8-B48F-1D18A9856A87
  last_name: Sommer
  orcid: 0000-0003-1216-9105
- first_name: Nicole
  full_name: Amberg, Nicole
  id: 4CD6AAC6-F248-11E8-B48F-1D18A9856A87
  last_name: Amberg
  orcid: 0000-0002-3183-8207
- first_name: Alessandro
  full_name: Venturino, Alessandro
  id: 41CB84B2-F248-11E8-B48F-1D18A9856A87
  last_name: Venturino
  orcid: 0000-0003-2356-9403
- first_name: Karl
  full_name: Roessler, Karl
  last_name: Roessler
- first_name: Thomas
  full_name: Czech, Thomas
  last_name: Czech
- first_name: Romana
  full_name: Höftberger, Romana
  last_name: Höftberger
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
- first_name: Gaia
  full_name: Novarino, Gaia
  id: 3E57A680-F248-11E8-B48F-1D18A9856A87
  last_name: Novarino
  orcid: 0000-0002-7673-7178
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
- first_name: Johann G
  full_name: Danzl, Johann G
  id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87
  last_name: Danzl
  orcid: 0000-0001-8559-3973
citation:
  ama: Michalska JM, Lyudchik J, Velicky P, et al. Imaging brain tissue architecture
    across millimeter to nanometer scales. <i>Nature Biotechnology</i>. 2023. doi:<a
    href="https://doi.org/10.1038/s41587-023-01911-8">10.1038/s41587-023-01911-8</a>
  apa: Michalska, J. M., Lyudchik, J., Velicky, P., Korinkova, H., Watson, J., Cenameri,
    A., … Danzl, J. G. (2023). Imaging brain tissue architecture across millimeter
    to nanometer scales. <i>Nature Biotechnology</i>. Springer Nature. <a href="https://doi.org/10.1038/s41587-023-01911-8">https://doi.org/10.1038/s41587-023-01911-8</a>
  chicago: Michalska, Julia M, Julia Lyudchik, Philipp Velicky, Hana Korinkova, Jake
    Watson, Alban Cenameri, Christoph M Sommer, et al. “Imaging Brain Tissue Architecture
    across Millimeter to Nanometer Scales.” <i>Nature Biotechnology</i>. Springer
    Nature, 2023. <a href="https://doi.org/10.1038/s41587-023-01911-8">https://doi.org/10.1038/s41587-023-01911-8</a>.
  ieee: J. M. Michalska <i>et al.</i>, “Imaging brain tissue architecture across millimeter
    to nanometer scales,” <i>Nature Biotechnology</i>. Springer Nature, 2023.
  ista: Michalska JM, Lyudchik J, Velicky P, Korinkova H, Watson J, Cenameri A, Sommer
    CM, Amberg N, Venturino A, Roessler K, Czech T, Höftberger R, Siegert S, Novarino
    G, Jonas PM, Danzl JG. 2023. Imaging brain tissue architecture across millimeter
    to nanometer scales. Nature Biotechnology.
  mla: Michalska, Julia M., et al. “Imaging Brain Tissue Architecture across Millimeter
    to Nanometer Scales.” <i>Nature Biotechnology</i>, Springer Nature, 2023, doi:<a
    href="https://doi.org/10.1038/s41587-023-01911-8">10.1038/s41587-023-01911-8</a>.
  short: J.M. Michalska, J. Lyudchik, P. Velicky, H. Korinkova, J. Watson, A. Cenameri,
    C.M. Sommer, N. Amberg, A. Venturino, K. Roessler, T. Czech, R. Höftberger, S.
    Siegert, G. Novarino, P.M. Jonas, J.G. Danzl, Nature Biotechnology (2023).
date_created: 2023-09-03T22:01:15Z
date_published: 2023-08-31T00:00:00Z
date_updated: 2024-02-21T12:18:18Z
day: '31'
department:
- _id: SaSi
- _id: GaNo
- _id: PeJo
- _id: JoDa
- _id: Bio
- _id: RySh
doi: 10.1038/s41587-023-01911-8
ec_funded: 1
external_id:
  isi:
  - '001065254200001'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1038/s41587-023-01911-8
month: '08'
oa: 1
oa_version: Published Version
project:
- _id: 265CB4D0-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I03600
  name: Optical control of synaptic function via adhesion molecules
- _id: 2548AE96-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W1232-B24
  name: Molecular Drug Targets
- _id: 25C5A090-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z00312
  name: The Wittgenstein Prize
- _id: 23889792-32DE-11EA-91FC-C7463DDC885E
  name: High content imaging to decode human immune cell interactions in health and
    allergic disease
- _id: 25444568-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715508'
  name: Probing the Reversibility of Autism Spectrum Disorders by Employing in vivo
    and in vitro Models
- _id: 25B7EB9E-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '692692'
  name: Biophysics and circuit function of a giant cortical glumatergic synapse
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: fc2be41b-9c52-11eb-aca3-faa90aa144e9
  call_identifier: H2020
  grant_number: '101026635'
  name: Synaptic computations of the hippocampal CA3 circuitry
publication: Nature Biotechnology
publication_identifier:
  eissn:
  - 1546-1696
  issn:
  - 1087-0156
publication_status: epub_ahead
publisher: Springer Nature
quality_controlled: '1'
related_material:
  link:
  - relation: software
    url: https://github.com/danzllab/CATS
  record:
  - id: '13126'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Imaging brain tissue architecture across millimeter to nanometer scales
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '14258'
abstract:
- lang: eng
  text: There is currently little evidence that the genetic basis of human phenotype
    varies significantly across the lifespan. However, time-to-event phenotypes are
    understudied and can be thought of as reflecting an underlying hazard, which is
    unlikely to be constant through life when values take a broad range. Here, we
    find that 74% of 245 genome-wide significant genetic associations with age at
    natural menopause (ANM) in the UK Biobank show a form of age-specific effect.
    Nineteen of these replicated discoveries are identified only by our modeling framework,
    which determines the time dependency of DNA-variant age-at-onset associations
    without a significant multiple-testing burden. Across the range of early to late
    menopause, we find evidence for significantly different underlying biological
    pathways, changes in the signs of genetic correlations of ANM to health indicators
    and outcomes, and differences in inferred causal relationships. We find that DNA
    damage response processes only act to shape ovarian reserve and depletion for
    women of early ANM. Genetically mediated delays in ANM were associated with increased
    relative risk of breast cancer and leiomyoma at all ages and with high cholesterol
    and heart failure for late-ANM women. These findings suggest that a better understanding
    of the age dependency of genetic risk factor relationships among health indicators
    and outcomes is achievable through appropriate statistical modeling of large-scale
    biobank data.
acknowledgement: This project was funded by an SNSF Eccellenza grant to M.R.R. (PCEGP3-181181)
  and by core funding from the Institute of Science and Technology Austria. K.L. and
  R.M. were supported by the Estonian Research Council grant 1911. Estonian Biobank
  computations were performed in the High-Performance Computing Center, University
  of Tartu. We thank Triin Laisk for her valuable insights and comments that helped
  greatly. We would like to acknowledge the participants and investigators of UK Biobank
  and Estonian Biobank studies. This project uses UK Biobank data under project number
  35520.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Sven E.
  full_name: Ojavee, Sven E.
  last_name: Ojavee
- first_name: Liza
  full_name: Darrous, Liza
  last_name: Darrous
- first_name: Marion
  full_name: Patxot, Marion
  last_name: Patxot
- first_name: Kristi
  full_name: Läll, Kristi
  last_name: Läll
- first_name: Krista
  full_name: Fischer, Krista
  last_name: Fischer
- first_name: Reedik
  full_name: Mägi, Reedik
  last_name: Mägi
- first_name: Zoltan
  full_name: Kutalik, Zoltan
  last_name: Kutalik
- first_name: Matthew Richard
  full_name: Robinson, Matthew Richard
  id: E5D42276-F5DA-11E9-8E24-6303E6697425
  last_name: Robinson
  orcid: 0000-0001-8982-8813
citation:
  ama: Ojavee SE, Darrous L, Patxot M, et al. Genetic insights into the age-specific
    biological mechanisms governing human ovarian aging. <i>American Journal of Human
    Genetics</i>. 2023;110(9):1549-1563. doi:<a href="https://doi.org/10.1016/j.ajhg.2023.07.006">10.1016/j.ajhg.2023.07.006</a>
  apa: Ojavee, S. E., Darrous, L., Patxot, M., Läll, K., Fischer, K., Mägi, R., …
    Robinson, M. R. (2023). Genetic insights into the age-specific biological mechanisms
    governing human ovarian aging. <i>American Journal of Human Genetics</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.ajhg.2023.07.006">https://doi.org/10.1016/j.ajhg.2023.07.006</a>
  chicago: Ojavee, Sven E., Liza Darrous, Marion Patxot, Kristi Läll, Krista Fischer,
    Reedik Mägi, Zoltan Kutalik, and Matthew Richard Robinson. “Genetic Insights into
    the Age-Specific Biological Mechanisms Governing Human Ovarian Aging.” <i>American
    Journal of Human Genetics</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.ajhg.2023.07.006">https://doi.org/10.1016/j.ajhg.2023.07.006</a>.
  ieee: S. E. Ojavee <i>et al.</i>, “Genetic insights into the age-specific biological
    mechanisms governing human ovarian aging,” <i>American Journal of Human Genetics</i>,
    vol. 110, no. 9. Elsevier, pp. 1549–1563, 2023.
  ista: Ojavee SE, Darrous L, Patxot M, Läll K, Fischer K, Mägi R, Kutalik Z, Robinson
    MR. 2023. Genetic insights into the age-specific biological mechanisms governing
    human ovarian aging. American Journal of Human Genetics. 110(9), 1549–1563.
  mla: Ojavee, Sven E., et al. “Genetic Insights into the Age-Specific Biological
    Mechanisms Governing Human Ovarian Aging.” <i>American Journal of Human Genetics</i>,
    vol. 110, no. 9, Elsevier, 2023, pp. 1549–63, doi:<a href="https://doi.org/10.1016/j.ajhg.2023.07.006">10.1016/j.ajhg.2023.07.006</a>.
  short: S.E. Ojavee, L. Darrous, M. Patxot, K. Läll, K. Fischer, R. Mägi, Z. Kutalik,
    M.R. Robinson, American Journal of Human Genetics 110 (2023) 1549–1563.
date_created: 2023-09-03T22:01:15Z
date_published: 2023-09-07T00:00:00Z
date_updated: 2024-01-30T13:21:05Z
day: '07'
ddc:
- '570'
department:
- _id: MaRo
doi: 10.1016/j.ajhg.2023.07.006
external_id:
  pmid:
  - '37543033'
file:
- access_level: open_access
  checksum: 4108b031dc726ae6b4a5ae7e021ba188
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-30T13:20:35Z
  date_updated: 2024-01-30T13:20:35Z
  file_id: '14912'
  file_name: 2023_AJHG_Ojavee.pdf
  file_size: 2551276
  relation: main_file
  success: 1
file_date_updated: 2024-01-30T13:20:35Z
has_accepted_license: '1'
intvolume: '       110'
issue: '9'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 1549-1563
pmid: 1
publication: American Journal of Human Genetics
publication_identifier:
  eissn:
  - 1537-6605
  issn:
  - 0002-9297
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Genetic insights into the age-specific biological mechanisms governing human
  ovarian aging
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: 110
year: '2023'
...
---
_id: '14259'
abstract:
- lang: eng
  text: "We provide a learning-based technique for guessing a winning strategy in
    a parity game originating from an LTL synthesis problem. A cheaply obtained guess
    can be useful in several applications. Not only can the guessed strategy be applied
    as best-effort in cases where the game’s huge size prohibits rigorous approaches,
    but it can also increase the scalability of rigorous LTL synthesis in several
    ways. Firstly, checking whether a guessed strategy is winning is easier than constructing
    one. Secondly, even if the guess is wrong in some places, it can be fixed by strategy
    iteration faster than constructing one from scratch. Thirdly, the guess can be
    used in on-the-fly approaches to prioritize exploration in the most fruitful directions.\r\nIn
    contrast to previous works, we (i) reflect the highly structured logical information
    in game’s states, the so-called semantic labelling, coming from the recent LTL-to-automata
    translations, and (ii) learn to reflect it properly by learning from previously
    solved games, bringing the solving process closer to human-like reasoning."
acknowledgement: This research was funded in part by the German Research Foundation
  (DFG) project 427755713 Group-By Objectives in Probabilistic Verification (GOPro).
alternative_title:
- LNCS
article_processing_charge: Yes (in subscription journal)
author:
- first_name: Jan
  full_name: Kretinsky, Jan
  id: 44CEF464-F248-11E8-B48F-1D18A9856A87
  last_name: Kretinsky
  orcid: 0000-0002-8122-2881
- first_name: Tobias
  full_name: Meggendorfer, Tobias
  id: b21b0c15-30a2-11eb-80dc-f13ca25802e1
  last_name: Meggendorfer
  orcid: 0000-0002-1712-2165
- first_name: Maximilian
  full_name: Prokop, Maximilian
  last_name: Prokop
- first_name: Sabine
  full_name: Rieder, Sabine
  last_name: Rieder
citation:
  ama: 'Kretinsky J, Meggendorfer T, Prokop M, Rieder S. Guessing winning policies
    in LTL synthesis by semantic learning. In: <i>35th International Conference on
    Computer Aided Verification </i>. Vol 13964. Springer Nature; 2023:390-414. doi:<a
    href="https://doi.org/10.1007/978-3-031-37706-8_20">10.1007/978-3-031-37706-8_20</a>'
  apa: 'Kretinsky, J., Meggendorfer, T., Prokop, M., &#38; Rieder, S. (2023). Guessing
    winning policies in LTL synthesis by semantic learning. In <i>35th International
    Conference on Computer Aided Verification </i> (Vol. 13964, pp. 390–414). Paris,
    France: Springer Nature. <a href="https://doi.org/10.1007/978-3-031-37706-8_20">https://doi.org/10.1007/978-3-031-37706-8_20</a>'
  chicago: Kretinsky, Jan, Tobias Meggendorfer, Maximilian Prokop, and Sabine Rieder.
    “Guessing Winning Policies in LTL Synthesis by Semantic Learning.” In <i>35th
    International Conference on Computer Aided Verification </i>, 13964:390–414. Springer
    Nature, 2023. <a href="https://doi.org/10.1007/978-3-031-37706-8_20">https://doi.org/10.1007/978-3-031-37706-8_20</a>.
  ieee: J. Kretinsky, T. Meggendorfer, M. Prokop, and S. Rieder, “Guessing winning
    policies in LTL synthesis by semantic learning,” in <i>35th International Conference
    on Computer Aided Verification </i>, Paris, France, 2023, vol. 13964, pp. 390–414.
  ista: 'Kretinsky J, Meggendorfer T, Prokop M, Rieder S. 2023. Guessing winning policies
    in LTL synthesis by semantic learning. 35th International Conference on Computer
    Aided Verification . CAV: Computer Aided Verification, LNCS, vol. 13964, 390–414.'
  mla: Kretinsky, Jan, et al. “Guessing Winning Policies in LTL Synthesis by Semantic
    Learning.” <i>35th International Conference on Computer Aided Verification </i>,
    vol. 13964, Springer Nature, 2023, pp. 390–414, doi:<a href="https://doi.org/10.1007/978-3-031-37706-8_20">10.1007/978-3-031-37706-8_20</a>.
  short: J. Kretinsky, T. Meggendorfer, M. Prokop, S. Rieder, in:, 35th International
    Conference on Computer Aided Verification , Springer Nature, 2023, pp. 390–414.
conference:
  end_date: 2023-07-22
  location: Paris, France
  name: 'CAV: Computer Aided Verification'
  start_date: 2023-07-17
date_created: 2023-09-03T22:01:16Z
date_published: 2023-07-17T00:00:00Z
date_updated: 2023-09-06T08:27:33Z
day: '17'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1007/978-3-031-37706-8_20
file:
- access_level: open_access
  checksum: ed66278b61bb869e1baba3d9b9081271
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T08:25:50Z
  date_updated: 2023-09-06T08:25:50Z
  file_id: '14276'
  file_name: 2023_LNCS_CAV_Kretinsky.pdf
  file_size: 428354
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T08:25:50Z
has_accepted_license: '1'
intvolume: '     13964'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 390-414
publication: '35th International Conference on Computer Aided Verification '
publication_identifier:
  eissn:
  - 1611-3349
  isbn:
  - '9783031377051'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Guessing winning policies in LTL synthesis by semantic learning
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: 13964
year: '2023'
...
---
_id: '14260'
abstract:
- lang: eng
  text: "This paper presents Lincheck, a new practical and user-friendly framework
    for testing concurrent algorithms on the Java Virtual Machine (JVM). Lincheck
    provides a simple and declarative way to write concurrent tests: instead of describing
    how to perform the test, users specify what to test by declaring all the operations
    to examine; the framework automatically handles the rest. As a result, tests written
    with Lincheck are concise and easy to understand. The framework automatically
    generates a set of concurrent scenarios, examines them using stress-testing or
    bounded model checking, and verifies that the results of each invocation are correct.
    Notably, if an error is detected via model checking, Lincheck provides an easy-to-follow
    trace to reproduce it, significantly simplifying the bug investigation.\r\n\r\nTo
    the best of our knowledge, Lincheck is the first production-ready tool on the
    JVM that offers such a simple way of writing concurrent tests, without requiring
    special skills or expertise. We successfully integrated Lincheck in the development
    process of several large projects, such as Kotlin Coroutines, and identified new
    bugs in popular concurrency libraries, such as a race in Java’s standard ConcurrentLinkedDeque
    and a liveliness bug in Java’s AbstractQueuedSynchronizer framework, which is
    used in most of the synchronization primitives. We believe that Lincheck can significantly
    improve the quality and productivity of concurrent algorithms research and development
    and become the state-of-the-art tool for checking their correctness."
alternative_title:
- LNCS
article_processing_charge: Yes (in subscription journal)
author:
- first_name: Nikita
  full_name: Koval, Nikita
  id: 2F4DB10C-F248-11E8-B48F-1D18A9856A87
  last_name: Koval
- first_name: Alexander
  full_name: Fedorov, Alexander
  id: 2e711909-896a-11ed-bdf8-eb0f5a2984c6
  last_name: Fedorov
- first_name: Maria
  full_name: Sokolova, Maria
  last_name: Sokolova
- first_name: Dmitry
  full_name: Tsitelov, Dmitry
  last_name: Tsitelov
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
citation:
  ama: 'Koval N, Fedorov A, Sokolova M, Tsitelov D, Alistarh D-A. Lincheck: A practical
    framework for testing concurrent data structures on JVM. In: <i>35th International
    Conference on Computer Aided Verification </i>. Vol 13964. Springer Nature; 2023:156-169.
    doi:<a href="https://doi.org/10.1007/978-3-031-37706-8_8">10.1007/978-3-031-37706-8_8</a>'
  apa: 'Koval, N., Fedorov, A., Sokolova, M., Tsitelov, D., &#38; Alistarh, D.-A.
    (2023). Lincheck: A practical framework for testing concurrent data structures
    on JVM. In <i>35th International Conference on Computer Aided Verification </i>
    (Vol. 13964, pp. 156–169). Paris, France: Springer Nature. <a href="https://doi.org/10.1007/978-3-031-37706-8_8">https://doi.org/10.1007/978-3-031-37706-8_8</a>'
  chicago: 'Koval, Nikita, Alexander Fedorov, Maria Sokolova, Dmitry Tsitelov, and
    Dan-Adrian Alistarh. “Lincheck: A Practical Framework for Testing Concurrent Data
    Structures on JVM.” In <i>35th International Conference on Computer Aided Verification
    </i>, 13964:156–69. Springer Nature, 2023. <a href="https://doi.org/10.1007/978-3-031-37706-8_8">https://doi.org/10.1007/978-3-031-37706-8_8</a>.'
  ieee: 'N. Koval, A. Fedorov, M. Sokolova, D. Tsitelov, and D.-A. Alistarh, “Lincheck:
    A practical framework for testing concurrent data structures on JVM,” in <i>35th
    International Conference on Computer Aided Verification </i>, Paris, France, 2023,
    vol. 13964, pp. 156–169.'
  ista: 'Koval N, Fedorov A, Sokolova M, Tsitelov D, Alistarh D-A. 2023. Lincheck:
    A practical framework for testing concurrent data structures on JVM. 35th International
    Conference on Computer Aided Verification . CAV: Computer Aided Verification,
    LNCS, vol. 13964, 156–169.'
  mla: 'Koval, Nikita, et al. “Lincheck: A Practical Framework for Testing Concurrent
    Data Structures on JVM.” <i>35th International Conference on Computer Aided Verification
    </i>, vol. 13964, Springer Nature, 2023, pp. 156–69, doi:<a href="https://doi.org/10.1007/978-3-031-37706-8_8">10.1007/978-3-031-37706-8_8</a>.'
  short: N. Koval, A. Fedorov, M. Sokolova, D. Tsitelov, D.-A. Alistarh, in:, 35th
    International Conference on Computer Aided Verification , Springer Nature, 2023,
    pp. 156–169.
conference:
  end_date: 2023-07-22
  location: Paris, France
  name: 'CAV: Computer Aided Verification'
  start_date: 2023-07-17
date_created: 2023-09-03T22:01:16Z
date_published: 2023-07-17T00:00:00Z
date_updated: 2024-02-27T07:46:52Z
day: '17'
ddc:
- '000'
department:
- _id: DaAl
- _id: GradSch
doi: 10.1007/978-3-031-37706-8_8
file:
- access_level: open_access
  checksum: c346016393123a0a2338ad4d976f61bc
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T08:16:25Z
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  file_name: 2023_LNCS_Koval.pdf
  file_size: 421408
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has_accepted_license: '1'
intvolume: '     13964'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 156-169
publication: '35th International Conference on Computer Aided Verification '
publication_identifier:
  eissn:
  - 1611-3349
  isbn:
  - '9783031377051'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
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scopus_import: '1'
status: public
title: 'Lincheck: A practical framework for testing concurrent data structures on JVM'
tmp:
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  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: 13964
year: '2023'
...
---
_id: '14261'
abstract:
- lang: eng
  text: In this work, a generalized, adapted Numerov implementation capable of determining
    band structures of periodic quantum systems is outlined. Based on the input potential,
    the presented approach numerically solves the Schrödinger equation in position
    space at each momentum space point. Thus, in addition to the band structure, the
    method inherently provides information about the state functions and probability
    densities in position space at each momentum space point considered. The generalized,
    adapted Numerov framework provided reliable estimates for a variety of increasingly
    complex test suites in one, two, and three dimensions. The accuracy of the proposed
    methodology was benchmarked against results obtained for the analytically solvable
    Kronig-Penney model. Furthermore, the presented numerical solver was applied to
    a model potential representing a 2D optical lattice being a challenging application
    relevant, for example, in the field of quantum computing.
acknowledgement: Financial supports for this work via a PhD scholarship for J. Gamper
  issued by the Leopold-Franzens-University of Innsbruck (Vicerector Prof. Dr Ulrike
  Tanzer) are gratefully acknowledged. The computational results presented have been
  achieved (in part) using the HPC infrastructure of the University of Innsbruck.
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Jakob
  full_name: Gamper, Jakob
  last_name: Gamper
- first_name: Florian
  full_name: Kluibenschedl, Florian
  id: 7499e70e-eb2c-11ec-b98b-f925648bc9d9
  last_name: Kluibenschedl
- first_name: Alexander K.H.
  full_name: Weiss, Alexander K.H.
  last_name: Weiss
- first_name: Thomas S.
  full_name: Hofer, Thomas S.
  last_name: Hofer
citation:
  ama: Gamper J, Kluibenschedl F, Weiss AKH, Hofer TS. Accessing position space wave
    functions in band structure calculations of periodic systems - a generalized,
    adapted numerov implementation for one-, two-, and three-dimensional quantum problems.
    <i>Journal of Physical Chemistry Letters</i>. 2023;14(33):7395-7403. doi:<a href="https://doi.org/10.1021/acs.jpclett.3c01707">10.1021/acs.jpclett.3c01707</a>
  apa: Gamper, J., Kluibenschedl, F., Weiss, A. K. H., &#38; Hofer, T. S. (2023).
    Accessing position space wave functions in band structure calculations of periodic
    systems - a generalized, adapted numerov implementation for one-, two-, and three-dimensional
    quantum problems. <i>Journal of Physical Chemistry Letters</i>. American Chemical
    Society. <a href="https://doi.org/10.1021/acs.jpclett.3c01707">https://doi.org/10.1021/acs.jpclett.3c01707</a>
  chicago: Gamper, Jakob, Florian Kluibenschedl, Alexander K.H. Weiss, and Thomas
    S. Hofer. “Accessing Position Space Wave Functions in Band Structure Calculations
    of Periodic Systems - a Generalized, Adapted Numerov Implementation for One-,
    Two-, and Three-Dimensional Quantum Problems.” <i>Journal of Physical Chemistry
    Letters</i>. American Chemical Society, 2023. <a href="https://doi.org/10.1021/acs.jpclett.3c01707">https://doi.org/10.1021/acs.jpclett.3c01707</a>.
  ieee: J. Gamper, F. Kluibenschedl, A. K. H. Weiss, and T. S. Hofer, “Accessing position
    space wave functions in band structure calculations of periodic systems - a generalized,
    adapted numerov implementation for one-, two-, and three-dimensional quantum problems,”
    <i>Journal of Physical Chemistry Letters</i>, vol. 14, no. 33. American Chemical
    Society, pp. 7395–7403, 2023.
  ista: Gamper J, Kluibenschedl F, Weiss AKH, Hofer TS. 2023. Accessing position space
    wave functions in band structure calculations of periodic systems - a generalized,
    adapted numerov implementation for one-, two-, and three-dimensional quantum problems.
    Journal of Physical Chemistry Letters. 14(33), 7395–7403.
  mla: Gamper, Jakob, et al. “Accessing Position Space Wave Functions in Band Structure
    Calculations of Periodic Systems - a Generalized, Adapted Numerov Implementation
    for One-, Two-, and Three-Dimensional Quantum Problems.” <i>Journal of Physical
    Chemistry Letters</i>, vol. 14, no. 33, American Chemical Society, 2023, pp. 7395–403,
    doi:<a href="https://doi.org/10.1021/acs.jpclett.3c01707">10.1021/acs.jpclett.3c01707</a>.
  short: J. Gamper, F. Kluibenschedl, A.K.H. Weiss, T.S. Hofer, Journal of Physical
    Chemistry Letters 14 (2023) 7395–7403.
date_created: 2023-09-03T22:01:16Z
date_published: 2023-08-11T00:00:00Z
date_updated: 2023-09-06T11:04:31Z
day: '11'
ddc:
- '530'
- '540'
department:
- _id: GradSch
doi: 10.1021/acs.jpclett.3c01707
external_id:
  isi:
  - '001048165800001'
  pmid:
  - '37566743'
file:
- access_level: open_access
  checksum: 637454e2b3a357498d8d622d241c4bf6
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T07:32:39Z
  date_updated: 2023-09-06T07:32:39Z
  file_id: '14272'
  file_name: 2023_JourPhysChemistry_Gamper.pdf
  file_size: 4986859
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T07:32:39Z
has_accepted_license: '1'
intvolume: '        14'
isi: 1
issue: '33'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: 7395-7403
pmid: 1
publication: Journal of Physical Chemistry Letters
publication_identifier:
  eissn:
  - 1948-7185
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Accessing position space wave functions in band structure calculations of periodic
  systems - a generalized, adapted numerov implementation for one-, two-, and three-dimensional
  quantum problems
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 14
year: '2023'
...
---
_id: '14274'
abstract:
- lang: eng
  text: Immune responses rely on the rapid and coordinated migration of leukocytes.
    Whereas it is well established that single-cell migration is often guided by gradients
    of chemokines and other chemoattractants, it remains poorly understood how these
    gradients are generated, maintained, and modulated. By combining experimental
    data with theory on leukocyte chemotaxis guided by the G protein–coupled receptor
    (GPCR) CCR7, we demonstrate that in addition to its role as the sensory receptor
    that steers migration, CCR7 also acts as a generator and a modulator of chemotactic
    gradients. Upon exposure to the CCR7 ligand CCL19, dendritic cells (DCs) effectively
    internalize the receptor and ligand as part of the canonical GPCR desensitization
    response. We show that CCR7 internalization also acts as an effective sink for
    the chemoattractant, dynamically shaping the spatiotemporal distribution of the
    chemokine. This mechanism drives complex collective migration patterns, enabling
    DCs to create or sharpen chemotactic gradients. We further show that these self-generated
    gradients can sustain the long-range guidance of DCs, adapt collective migration
    patterns to the size and geometry of the environment, and provide a guidance cue
    for other comigrating cells. Such a dual role of CCR7 as a GPCR that both senses
    and consumes its ligand can thus provide a novel mode of cellular self-organization.
acknowledgement: "We thank I. de Vries and the Scientific Service Units (Life Sciences,
  Bioimaging, Nanofabrication, Preclinical and Miba Machine Shop) of the Institute
  of Science and Technology Austria for excellent support, as well as all the rotation
  students assisting in the laboratory work (B. Zens, H. Schön, and D. Babic).\r\nThis
  work was supported by grants from the European Research Council under the European
  Union’s Horizon 2020 research to M.S. (grant agreement no. 724373) and to E.H. (grant
  agreement no. 851288), and a grant by the Austrian Science Fund (DK Nanocell W1250-B20)
  to M.S. J.A. was supported by the Jenny and Antti Wihuri Foundation and Research
  Council of Finland's Flagship Programme InFLAMES (decision number: 357910). M.C.U.
  was supported by the European Union’s Horizon 2020 research and innovation programme
  under the Marie Skłodowska-Curie grant agreement no. 754411."
article_number: adc9584
article_processing_charge: No
article_type: original
author:
- first_name: Jonna H
  full_name: Alanko, Jonna H
  id: 2CC12E8C-F248-11E8-B48F-1D18A9856A87
  last_name: Alanko
  orcid: 0000-0002-7698-3061
- 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: Nikola
  full_name: Canigova, Nikola
  id: 3795523E-F248-11E8-B48F-1D18A9856A87
  last_name: Canigova
  orcid: 0000-0002-8518-5926
- first_name: Julian A
  full_name: Stopp, Julian A
  id: 489E3F00-F248-11E8-B48F-1D18A9856A87
  last_name: Stopp
- first_name: Jan
  full_name: Schwarz, Jan
  id: 346C1EC6-F248-11E8-B48F-1D18A9856A87
  last_name: Schwarz
- first_name: Jack
  full_name: Merrin, Jack
  id: 4515C308-F248-11E8-B48F-1D18A9856A87
  last_name: Merrin
  orcid: 0000-0001-5145-4609
- 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: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
citation:
  ama: Alanko JH, Ucar MC, Canigova N, et al. CCR7 acts as both a sensor and a sink
    for CCL19 to coordinate collective leukocyte migration. <i>Science Immunology</i>.
    2023;8(87). doi:<a href="https://doi.org/10.1126/sciimmunol.adc9584">10.1126/sciimmunol.adc9584</a>
  apa: Alanko, J. H., Ucar, M. C., Canigova, N., Stopp, J. A., Schwarz, J., Merrin,
    J., … Sixt, M. K. (2023). CCR7 acts as both a sensor and a sink for CCL19 to coordinate
    collective leukocyte migration. <i>Science Immunology</i>. American Association
    for the Advancement of Science. <a href="https://doi.org/10.1126/sciimmunol.adc9584">https://doi.org/10.1126/sciimmunol.adc9584</a>
  chicago: Alanko, Jonna H, Mehmet C Ucar, Nikola Canigova, Julian A Stopp, Jan Schwarz,
    Jack Merrin, Edouard B Hannezo, and Michael K Sixt. “CCR7 Acts as Both a Sensor
    and a Sink for CCL19 to Coordinate Collective Leukocyte Migration.” <i>Science
    Immunology</i>. American Association for the Advancement of Science, 2023. <a
    href="https://doi.org/10.1126/sciimmunol.adc9584">https://doi.org/10.1126/sciimmunol.adc9584</a>.
  ieee: J. H. Alanko <i>et al.</i>, “CCR7 acts as both a sensor and a sink for CCL19
    to coordinate collective leukocyte migration,” <i>Science Immunology</i>, vol.
    8, no. 87. American Association for the Advancement of Science, 2023.
  ista: Alanko JH, Ucar MC, Canigova N, Stopp JA, Schwarz J, Merrin J, Hannezo EB,
    Sixt MK. 2023. CCR7 acts as both a sensor and a sink for CCL19 to coordinate collective
    leukocyte migration. Science Immunology. 8(87), adc9584.
  mla: Alanko, Jonna H., et al. “CCR7 Acts as Both a Sensor and a Sink for CCL19 to
    Coordinate Collective Leukocyte Migration.” <i>Science Immunology</i>, vol. 8,
    no. 87, adc9584, American Association for the Advancement of Science, 2023, doi:<a
    href="https://doi.org/10.1126/sciimmunol.adc9584">10.1126/sciimmunol.adc9584</a>.
  short: J.H. Alanko, M.C. Ucar, N. Canigova, J.A. Stopp, J. Schwarz, J. Merrin, E.B.
    Hannezo, M.K. Sixt, Science Immunology 8 (2023).
date_created: 2023-09-06T08:07:51Z
date_published: 2023-09-01T00:00:00Z
date_updated: 2023-12-21T14:30:01Z
day: '01'
department:
- _id: MiSi
- _id: EdHa
- _id: NanoFab
doi: 10.1126/sciimmunol.adc9584
ec_funded: 1
external_id:
  isi:
  - '001062110600003'
  pmid:
  - '37656776'
intvolume: '         8'
isi: 1
issue: '87'
keyword:
- General Medicine
- Immunology
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1126/sciimmunol.adc9584
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 25FE9508-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '724373'
  name: Cellular navigation along spatial gradients
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '851288'
  name: Design Principles of Branching Morphogenesis
- _id: 265E2996-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W01250-B20
  name: Nano-Analytics of Cellular Systems
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Science Immunology
publication_identifier:
  issn:
  - 2470-9468
publication_status: published
publisher: American Association for the Advancement of Science
quality_controlled: '1'
related_material:
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    relation: research_data
    status: public
  - id: '14697'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: CCR7 acts as both a sensor and a sink for CCL19 to coordinate collective leukocyte
  migration
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2023'
...
---
_id: '14277'
abstract:
- lang: eng
  text: Living tissues are characterized by an intrinsically mechanochemical interplay
    of active physical forces and complex biochemical signaling pathways. Either feature
    alone can give rise to complex emergent phenomena, for example, mechanically driven
    glassy dynamics and rigidity transitions, or chemically driven reaction-diffusion
    instabilities. An important question is how to quantitatively assess the contribution
    of these different cues to the large-scale dynamics of biological materials. We
    address this in Madin-Darby canine kidney (MDCK) monolayers, considering both
    mechanochemical feedback between extracellular signal-regulated kinase (ERK) signaling
    activity and cellular density as well as a mechanically active tissue rheology
    via a self-propelled vertex model. We show that the relative strength of active
    migration forces to mechanochemical couplings controls a transition from a uniform
    active glass to periodic spatiotemporal waves. We parametrize the model from published
    experimental data sets on MDCK monolayers and use it to make new predictions on
    the correlation functions of cellular dynamics and the dynamics of topological
    defects associated with the oscillatory phase of cells. Interestingly, MDCK monolayers
    are best described by an intermediary parameter region in which both mechanochemical
    couplings and noisy active propulsion have a strong influence on the dynamics.
    Finally, we study how tissue rheology and ERK waves produce feedback on one another
    and uncover a mechanism via which tissue fluidity can be controlled by mechanochemical
    waves at both the local and global levels.
acknowledgement: We thank all members of the Hannezo group for discussions and suggestions,
  as well as Sound Wai Phow for technical assistance. This work received funding from
  the European Research Council under the EU Horizon 2020 research and innovation
  program Grant Agreement No. 851288 (E.H.), JSPS KAKENHI Grant No. 21H05290, and
  the Ministry of Education under the Research Centres of Excellence program through
  the MBI at NUS.
article_number: '013001'
article_processing_charge: Yes
article_type: original
author:
- first_name: Daniel R
  full_name: Boocock, Daniel R
  id: 453AF628-F248-11E8-B48F-1D18A9856A87
  last_name: Boocock
  orcid: 0000-0002-1585-2631
- first_name: Tsuyoshi
  full_name: Hirashima, Tsuyoshi
  last_name: Hirashima
- first_name: Edouard B
  full_name: Hannezo, Edouard B
  id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
  last_name: Hannezo
  orcid: 0000-0001-6005-1561
citation:
  ama: Boocock DR, Hirashima T, Hannezo EB. Interplay between mechanochemical patterning
    and glassy dynamics in cellular monolayers. <i>PRX Life</i>. 2023;1(1). doi:<a
    href="https://doi.org/10.1103/prxlife.1.013001">10.1103/prxlife.1.013001</a>
  apa: Boocock, D. R., Hirashima, T., &#38; Hannezo, E. B. (2023). Interplay between
    mechanochemical patterning and glassy dynamics in cellular monolayers. <i>PRX
    Life</i>. American Physical Society. <a href="https://doi.org/10.1103/prxlife.1.013001">https://doi.org/10.1103/prxlife.1.013001</a>
  chicago: Boocock, Daniel R, Tsuyoshi Hirashima, and Edouard B Hannezo. “Interplay
    between Mechanochemical Patterning and Glassy Dynamics in Cellular Monolayers.”
    <i>PRX Life</i>. American Physical Society, 2023. <a href="https://doi.org/10.1103/prxlife.1.013001">https://doi.org/10.1103/prxlife.1.013001</a>.
  ieee: D. R. Boocock, T. Hirashima, and E. B. Hannezo, “Interplay between mechanochemical
    patterning and glassy dynamics in cellular monolayers,” <i>PRX Life</i>, vol.
    1, no. 1. American Physical Society, 2023.
  ista: Boocock DR, Hirashima T, Hannezo EB. 2023. Interplay between mechanochemical
    patterning and glassy dynamics in cellular monolayers. PRX Life. 1(1), 013001.
  mla: Boocock, Daniel R., et al. “Interplay between Mechanochemical Patterning and
    Glassy Dynamics in Cellular Monolayers.” <i>PRX Life</i>, vol. 1, no. 1, 013001,
    American Physical Society, 2023, doi:<a href="https://doi.org/10.1103/prxlife.1.013001">10.1103/prxlife.1.013001</a>.
  short: D.R. Boocock, T. Hirashima, E.B. Hannezo, PRX Life 1 (2023).
date_created: 2023-09-06T08:30:59Z
date_published: 2023-07-20T00:00:00Z
date_updated: 2023-09-15T06:39:17Z
day: '20'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.1103/prxlife.1.013001
ec_funded: 1
file:
- access_level: open_access
  checksum: f881d98c89eb9f1aa136d7b781511553
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-15T06:30:50Z
  date_updated: 2023-09-15T06:30:50Z
  file_id: '14335'
  file_name: 2023_PRXLife_Boocock.pdf
  file_size: 2559520
  relation: main_file
  success: 1
file_date_updated: 2023-09-15T06:30:50Z
has_accepted_license: '1'
intvolume: '         1'
issue: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '851288'
  name: Design Principles of Branching Morphogenesis
publication: PRX Life
publication_identifier:
  issn:
  - 2835-8279
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
status: public
title: Interplay between mechanochemical patterning and glassy dynamics in cellular
  monolayers
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: 1
year: '2023'
...
---
_id: '14279'
abstract:
- lang: eng
  text: "The zip file includes source data used in the manuscript \"CCR7 acts as both
    a sensor and a sink for CCL19 to coordinate collective leukocyte migration\",
    as well as a representative Jupyter notebook to reproduce the main figures. Please
    see the preprint on bioRxiv and the DOI link there to access the final published
    version. Note the title change between the preprint and the published manuscript.\r\nA
    sample script for particle-based simulations of collective chemotaxis by self-generated
    gradients is also included (see Self-generated_chemotaxis_sample_script.ipynb)
    to generate exemplary cell trajectories. A detailed description of the simulation
    setup is provided in the supplementary information of the manuscipt."
article_processing_charge: No
author:
- first_name: Mehmet C
  full_name: Ucar, Mehmet C
  id: 50B2A802-6007-11E9-A42B-EB23E6697425
  last_name: Ucar
  orcid: 0000-0003-0506-4217
citation:
  ama: Ucar MC. Source data for the manuscript “CCR7 acts as both a sensor and a sink
    for CCL19 to coordinate collective leukocyte migration.” 2023. doi:<a href="https://doi.org/10.5281/ZENODO.8133960">10.5281/ZENODO.8133960</a>
  apa: Ucar, M. C. (2023). Source data for the manuscript “CCR7 acts as both a sensor
    and a sink for CCL19 to coordinate collective leukocyte migration.” Zenodo. <a
    href="https://doi.org/10.5281/ZENODO.8133960">https://doi.org/10.5281/ZENODO.8133960</a>
  chicago: Ucar, Mehmet C. “Source Data for the Manuscript ‘CCR7 Acts as Both a Sensor
    and a Sink for CCL19 to Coordinate Collective Leukocyte Migration.’” Zenodo, 2023.
    <a href="https://doi.org/10.5281/ZENODO.8133960">https://doi.org/10.5281/ZENODO.8133960</a>.
  ieee: M. C. Ucar, “Source data for the manuscript ‘CCR7 acts as both a sensor and
    a sink for CCL19 to coordinate collective leukocyte migration.’” Zenodo, 2023.
  ista: Ucar MC. 2023. Source data for the manuscript ‘CCR7 acts as both a sensor
    and a sink for CCL19 to coordinate collective leukocyte migration’, Zenodo, <a
    href="https://doi.org/10.5281/ZENODO.8133960">10.5281/ZENODO.8133960</a>.
  mla: Ucar, Mehmet C. <i>Source Data for the Manuscript “CCR7 Acts as Both a Sensor
    and a Sink for CCL19 to Coordinate Collective Leukocyte Migration.”</i> Zenodo,
    2023, doi:<a href="https://doi.org/10.5281/ZENODO.8133960">10.5281/ZENODO.8133960</a>.
  short: M.C. Ucar, (2023).
date_created: 2023-09-06T08:39:25Z
date_published: 2023-07-11T00:00:00Z
date_updated: 2023-10-03T11:42:58Z
day: '11'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.5281/ZENODO.8133960
has_accepted_license: '1'
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5281/zenodo.8133960
month: '07'
oa: 1
oa_version: Published Version
publisher: Zenodo
related_material:
  record:
  - id: '14274'
    relation: used_in_publication
    status: public
status: public
title: Source data for the manuscript "CCR7 acts as both a sensor and a sink for CCL19
  to coordinate collective leukocyte migration"
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: research_data_reference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '14280'
abstract:
- lang: eng
  text: "Cell division in Escherichia coli is performed by the divisome, a multi-protein
    complex composed of more than 30 proteins. The divisome spans from the cytoplasm
    through the inner membrane to the cell wall and the outer membrane. Divisome assembly
    is initiated by a cytoskeletal structure, the so-called Z-ring, which localizes
    at the center of the E. coli cell and determines the position of the future cell
    septum. The Z-ring is composed of the highly conserved bacterial tubulin homologue
    FtsZ, which forms treadmilling filaments. These filaments are recruited to the
    inner membrane by FtsA, a highly conserved bacterial actin homologue. FtsA interacts
    with other proteins in the periplasm and thus connects the cytoplasmic and periplasmic
    components of the divisome. \r\nA previous model postulated that FtsA regulates
    maturation of the divisome by switching from an oligomeric, inactive state to
    a monomeric and active state. This model was based mostly on in vivo studies,
    as a biochemical characterization of FtsA has been hampered by difficulties in
    purifying the protein. Here, we studied FtsA using an in vitro reconstitution
    approach and aimed to answer two questions: (i) How are dynamics from cytoplasmic,
    treadmilling FtsZ filaments coupled to proteins acting in the periplasmic space
    and (ii) How does FtsA regulate the maturation of the divisome?\r\nWe found that
    the cytoplasmic peptides of the transmembrane proteins FtsN and FtsQ interact
    directly with FtsA and can follow the spatiotemporal signal of FtsA/Z filaments.
    When we investigated the underlying mechanism by imaging single molecules of FtsNcyto,
    we found the peptide to interact transiently with FtsA. An in depth analysis of
    the single molecule trajectories helped to postulate a model where PG synthases
    follow the dynamics of FtsZ by a diffusion and capture mechanism. \r\nFollowing
    up on these findings we were interested in how the self-interaction of FtsA changes
    when it encounters FtsNcyto and if we can confirm the proposed oligomer-monomer
    switch. For this, we compared the behavior of the previously identified, hyperactive
    mutant FtsA R286W with wildtype FtsA. The mutant outperforms WT in mirroring and
    transmitting the spatiotemporal signal of treadmilling FtsZ filaments. Surprisingly
    however, we found that this was not due to a difference in the self-interaction
    strength of the two variants, but a difference in their membrane residence time.
    Furthermore, in contrast to our expectations, upon binding of FtsNcyto the measured
    self-interaction of FtsA actually increased. \r\nWe propose that FtsNcyto induces
    a rearrangement of the oligomeric architecture of FtsA. In further consequence
    this change leads to more persistent FtsZ filaments which results in a defined
    signalling zone, allowing formation of the mature divisome. The observed difference
    between FtsA WT and R286W is due to the vastly different membrane turnover of
    the proteins. R286W cycles 5-10x faster compared to WT which allows to sample
    FtsZ filaments at faster frequencies. These findings can explain the observed
    differences in toxicity for overexpression of FtsA WT and R286W and help to understand
    how FtsA regulates divisome maturation."
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Philipp
  full_name: Radler, Philipp
  id: 40136C2A-F248-11E8-B48F-1D18A9856A87
  last_name: Radler
  orcid: '0000-0001-9198-2182 '
citation:
  ama: Radler P. Spatiotemporal signaling during assembly of the bacterial divisome.
    2023. doi:<a href="https://doi.org/10.15479/at:ista:14280">10.15479/at:ista:14280</a>
  apa: Radler, P. (2023). <i>Spatiotemporal signaling during assembly of the bacterial
    divisome</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:14280">https://doi.org/10.15479/at:ista:14280</a>
  chicago: Radler, Philipp. “Spatiotemporal Signaling during Assembly of the Bacterial
    Divisome.” Institute of Science and Technology Austria, 2023. <a href="https://doi.org/10.15479/at:ista:14280">https://doi.org/10.15479/at:ista:14280</a>.
  ieee: P. Radler, “Spatiotemporal signaling during assembly of the bacterial divisome,”
    Institute of Science and Technology Austria, 2023.
  ista: Radler P. 2023. Spatiotemporal signaling during assembly of the bacterial
    divisome. Institute of Science and Technology Austria.
  mla: Radler, Philipp. <i>Spatiotemporal Signaling during Assembly of the Bacterial
    Divisome</i>. Institute of Science and Technology Austria, 2023, doi:<a href="https://doi.org/10.15479/at:ista:14280">10.15479/at:ista:14280</a>.
  short: P. Radler, Spatiotemporal Signaling during Assembly of the Bacterial Divisome,
    Institute of Science and Technology Austria, 2023.
date_created: 2023-09-06T10:58:25Z
date_published: 2023-09-25T00:00:00Z
date_updated: 2024-02-21T12:35:18Z
day: '25'
ddc:
- '572'
degree_awarded: PhD
department:
- _id: GradSch
- _id: MaLo
doi: 10.15479/at:ista:14280
ec_funded: 1
file:
- access_level: closed
  checksum: 87eef11fbc5c7df0826f12a3a629b444
  content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
  creator: pradler
  date_created: 2023-10-04T10:11:53Z
  date_updated: 2023-10-04T10:28:35Z
  file_id: '14390'
  file_name: PhD Thesis_Philipp Radler_20231004.docx
  file_size: 114932847
  relation: source_file
- access_level: closed
  checksum: 3253e099b7126469d941fd9419d68b4f
  content_type: application/pdf
  creator: pradler
  date_created: 2023-10-04T10:11:21Z
  date_updated: 2023-10-04T10:28:35Z
  embargo: 2024-10-04
  embargo_to: open_access
  file_id: '14391'
  file_name: PhD Thesis_Philipp Radler_20231004.pdf
  file_size: 37838778
  relation: main_file
file_date_updated: 2023-10-04T10:28:35Z
has_accepted_license: '1'
keyword:
- Cell Division
- Reconstitution
- FtsZ
- FtsA
- Divisome
- E.coli
language:
- iso: eng
month: '09'
oa_version: Published Version
page: '156'
project:
- _id: 2595697A-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '679239'
  name: Self-Organization of the Bacterial Cell
- _id: fc38323b-9c52-11eb-aca3-ff8afb4a011d
  grant_number: P34607
  name: "Understanding bacterial cell division by in vitro\r\nreconstitution"
- _id: 2596EAB6-B435-11E9-9278-68D0E5697425
  grant_number: ALTF 2015-1163
  name: Synthesis of bacterial cell wall
- _id: 259B655A-B435-11E9-9278-68D0E5697425
  grant_number: LT000824/2016
  name: Reconstitution of bacterial cell wall sythesis
publication_identifier:
  isbn:
  - 978-3-99078-033-6
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '11373'
    relation: part_of_dissertation
    status: public
  - id: '7387'
    relation: part_of_dissertation
    status: public
  - id: '10934'
    relation: research_data
    status: public
status: public
supervisor:
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
title: Spatiotemporal signaling during assembly of the bacterial divisome
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: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2023'
...
---
_id: '14281'
abstract:
- lang: eng
  text: In nature, proteins that switch between two conformations in response to environmental
    stimuli structurally transduce biochemical information in a manner analogous to
    how transistors control information flow in computing devices. Designing proteins
    with two distinct but fully structured conformations is a challenge for protein
    design as it requires sculpting an energy landscape with two distinct minima.
    Here we describe the design of “hinge” proteins that populate one designed state
    in the absence of ligand and a second designed state in the presence of ligand.
    X-ray crystallography, electron microscopy, double electron-electron resonance
    spectroscopy, and binding measurements demonstrate that despite the significant
    structural differences the two states are designed with atomic level accuracy
    and that the conformational and binding equilibria are closely coupled.
article_processing_charge: No
article_type: original
author:
- first_name: Florian M
  full_name: Praetorius, Florian M
  id: dfec9381-4341-11ee-8fd8-faa02bba7d62
  last_name: Praetorius
- first_name: Philip J. Y.
  full_name: Leung, Philip J. Y.
  last_name: Leung
- first_name: Maxx H.
  full_name: Tessmer, Maxx H.
  last_name: Tessmer
- first_name: Adam
  full_name: Broerman, Adam
  last_name: Broerman
- first_name: Cullen
  full_name: Demakis, Cullen
  last_name: Demakis
- first_name: Acacia F.
  full_name: Dishman, Acacia F.
  last_name: Dishman
- first_name: Arvind
  full_name: Pillai, Arvind
  last_name: Pillai
- first_name: Abbas
  full_name: Idris, Abbas
  last_name: Idris
- first_name: David
  full_name: Juergens, David
  last_name: Juergens
- first_name: Justas
  full_name: Dauparas, Justas
  last_name: Dauparas
- first_name: Xinting
  full_name: Li, Xinting
  last_name: Li
- first_name: Paul M.
  full_name: Levine, Paul M.
  last_name: Levine
- first_name: Mila
  full_name: Lamb, Mila
  last_name: Lamb
- first_name: Ryanne K.
  full_name: Ballard, Ryanne K.
  last_name: Ballard
- first_name: Stacey R.
  full_name: Gerben, Stacey R.
  last_name: Gerben
- first_name: Hannah
  full_name: Nguyen, Hannah
  last_name: Nguyen
- first_name: Alex
  full_name: Kang, Alex
  last_name: Kang
- first_name: Banumathi
  full_name: Sankaran, Banumathi
  last_name: Sankaran
- first_name: Asim K.
  full_name: Bera, Asim K.
  last_name: Bera
- first_name: Brian F.
  full_name: Volkman, Brian F.
  last_name: Volkman
- first_name: Jeff
  full_name: Nivala, Jeff
  last_name: Nivala
- first_name: Stefan
  full_name: Stoll, Stefan
  last_name: Stoll
- first_name: David
  full_name: Baker, David
  last_name: Baker
citation:
  ama: Praetorius FM, Leung PJY, Tessmer MH, et al. Design of stimulus-responsive
    two-state hinge proteins. <i>Science</i>. 2023;381(6659):754-760. doi:<a href="https://doi.org/10.1126/science.adg7731">10.1126/science.adg7731</a>
  apa: Praetorius, F. M., Leung, P. J. Y., Tessmer, M. H., Broerman, A., Demakis,
    C., Dishman, A. F., … Baker, D. (2023). Design of stimulus-responsive two-state
    hinge proteins. <i>Science</i>. American Association for the Advancement of Science.
    <a href="https://doi.org/10.1126/science.adg7731">https://doi.org/10.1126/science.adg7731</a>
  chicago: Praetorius, Florian M, Philip J. Y. Leung, Maxx H. Tessmer, Adam Broerman,
    Cullen Demakis, Acacia F. Dishman, Arvind Pillai, et al. “Design of Stimulus-Responsive
    Two-State Hinge Proteins.” <i>Science</i>. American Association for the Advancement
    of Science, 2023. <a href="https://doi.org/10.1126/science.adg7731">https://doi.org/10.1126/science.adg7731</a>.
  ieee: F. M. Praetorius <i>et al.</i>, “Design of stimulus-responsive two-state hinge
    proteins,” <i>Science</i>, vol. 381, no. 6659. American Association for the Advancement
    of Science, pp. 754–760, 2023.
  ista: Praetorius FM, Leung PJY, Tessmer MH, Broerman A, Demakis C, Dishman AF, Pillai
    A, Idris A, Juergens D, Dauparas J, Li X, Levine PM, Lamb M, Ballard RK, Gerben
    SR, Nguyen H, Kang A, Sankaran B, Bera AK, Volkman BF, Nivala J, Stoll S, Baker
    D. 2023. Design of stimulus-responsive two-state hinge proteins. Science. 381(6659),
    754–760.
  mla: Praetorius, Florian M., et al. “Design of Stimulus-Responsive Two-State Hinge
    Proteins.” <i>Science</i>, vol. 381, no. 6659, American Association for the Advancement
    of Science, 2023, pp. 754–60, doi:<a href="https://doi.org/10.1126/science.adg7731">10.1126/science.adg7731</a>.
  short: F.M. Praetorius, P.J.Y. Leung, M.H. Tessmer, A. Broerman, C. Demakis, A.F.
    Dishman, A. Pillai, A. Idris, D. Juergens, J. Dauparas, X. Li, P.M. Levine, M.
    Lamb, R.K. Ballard, S.R. Gerben, H. Nguyen, A. Kang, B. Sankaran, A.K. Bera, B.F.
    Volkman, J. Nivala, S. Stoll, D. Baker, Science 381 (2023) 754–760.
date_created: 2023-09-06T12:04:23Z
date_published: 2023-08-17T00:00:00Z
date_updated: 2023-11-07T12:42:09Z
day: '17'
doi: 10.1126/science.adg7731
extern: '1'
external_id:
  pmid:
  - '37590357'
intvolume: '       381'
issue: '6659'
language:
- iso: eng
month: '08'
oa_version: None
page: 754-760
pmid: 1
publication: Science
publication_identifier:
  eissn:
  - 1095-9203
  issn:
  - 0036-8075
publication_status: published
publisher: American Association for the Advancement of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: Design of stimulus-responsive two-state hinge proteins
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 381
year: '2023'
...
---
_id: '14294'
abstract:
- lang: eng
  text: Growth factors and cytokines signal by binding to the extracellular domains
    of their receptors and drive association and transphosphorylation of the receptor
    intracellular tyrosine kinase domains, initiating downstream signaling cascades.
    To enable systematic exploration of how receptor valency and geometry affects
    signaling outcomes, we designed cyclic homo-oligomers with up to 8 subunits using
    repeat protein building blocks that can be modularly extended. By incorporating
    a de novo designed fibroblast growth-factor receptor (FGFR) binding module into
    these scaffolds, we generated a series of synthetic signaling ligands that exhibit
    potent valency- and geometry-dependent Ca2+ release and MAPK pathway activation.
    The high specificity of the designed agonists reveal distinct roles for two FGFR
    splice variants in driving endothelial and mesenchymal cell fates during early
    vascular development. The ability to incorporate receptor binding domains and
    repeat extensions in a modular fashion makes our designed scaffolds broadly useful
    for probing and manipulating cellular signaling pathways.
article_processing_charge: No
author:
- first_name: Natasha I
  full_name: Edman, Natasha I
  last_name: Edman
- first_name: Rachel L
  full_name: Redler, Rachel L
  last_name: Redler
- first_name: Ashish
  full_name: Phal, Ashish
  last_name: Phal
- first_name: Thomas
  full_name: Schlichthaerle, Thomas
  last_name: Schlichthaerle
- first_name: Sanjay R
  full_name: Srivatsan, Sanjay R
  last_name: Srivatsan
- first_name: Ali
  full_name: Etemadi, Ali
  last_name: Etemadi
- first_name: Seong
  full_name: An, Seong
  last_name: An
- first_name: Andrew
  full_name: Favor, Andrew
  last_name: Favor
- first_name: Devon
  full_name: Ehnes, Devon
  last_name: Ehnes
- first_name: Zhe
  full_name: Li, Zhe
  last_name: Li
- first_name: Florian M
  full_name: Praetorius, Florian M
  id: dfec9381-4341-11ee-8fd8-faa02bba7d62
  last_name: Praetorius
- first_name: Max
  full_name: Gordon, Max
  last_name: Gordon
- first_name: Wei
  full_name: Yang, Wei
  last_name: Yang
- first_name: Brian
  full_name: Coventry, Brian
  last_name: Coventry
- first_name: Derrick R
  full_name: Hicks, Derrick R
  last_name: Hicks
- first_name: Longxing
  full_name: Cao, Longxing
  last_name: Cao
- first_name: Neville
  full_name: Bethel, Neville
  last_name: Bethel
- first_name: Piper
  full_name: Heine, Piper
  last_name: Heine
- first_name: Analisa N
  full_name: Murray, Analisa N
  last_name: Murray
- first_name: Stacey
  full_name: Gerben, Stacey
  last_name: Gerben
- first_name: Lauren
  full_name: Carter, Lauren
  last_name: Carter
- first_name: Marcos
  full_name: Miranda, Marcos
  last_name: Miranda
- first_name: Babak
  full_name: Negahdari, Babak
  last_name: Negahdari
- first_name: Sangwon
  full_name: Lee, Sangwon
  last_name: Lee
- first_name: Cole
  full_name: Trapnell, Cole
  last_name: Trapnell
- first_name: Lance
  full_name: Stewart, Lance
  last_name: Stewart
- first_name: Damian C
  full_name: Ekiert, Damian C
  last_name: Ekiert
- first_name: Joseph
  full_name: Schlessinger, Joseph
  last_name: Schlessinger
- first_name: Jay
  full_name: Shendure, Jay
  last_name: Shendure
- first_name: Gira
  full_name: Bhabha, Gira
  last_name: Bhabha
- first_name: Hannele
  full_name: Ruohola-Baker, Hannele
  last_name: Ruohola-Baker
- first_name: David
  full_name: Baker, David
  last_name: Baker
citation:
  ama: Edman NI, Redler RL, Phal A, et al. Modulation of FGF pathway signaling and
    vascular differentiation using designed oligomeric assemblies. <i>bioRxiv</i>.
    doi:<a href="https://doi.org/10.1101/2023.03.14.532666">10.1101/2023.03.14.532666</a>
  apa: Edman, N. I., Redler, R. L., Phal, A., Schlichthaerle, T., Srivatsan, S. R.,
    Etemadi, A., … Baker, D. (n.d.). Modulation of FGF pathway signaling and vascular
    differentiation using designed oligomeric assemblies. <i>bioRxiv</i>. <a href="https://doi.org/10.1101/2023.03.14.532666">https://doi.org/10.1101/2023.03.14.532666</a>
  chicago: Edman, Natasha I, Rachel L Redler, Ashish Phal, Thomas Schlichthaerle,
    Sanjay R Srivatsan, Ali Etemadi, Seong An, et al. “Modulation of FGF Pathway Signaling
    and Vascular Differentiation Using Designed Oligomeric Assemblies.” <i>BioRxiv</i>,
    n.d. <a href="https://doi.org/10.1101/2023.03.14.532666">https://doi.org/10.1101/2023.03.14.532666</a>.
  ieee: N. I. Edman <i>et al.</i>, “Modulation of FGF pathway signaling and vascular
    differentiation using designed oligomeric assemblies,” <i>bioRxiv</i>. .
  ista: Edman NI, Redler RL, Phal A, Schlichthaerle T, Srivatsan SR, Etemadi A, An
    S, Favor A, Ehnes D, Li Z, Praetorius FM, Gordon M, Yang W, Coventry B, Hicks
    DR, Cao L, Bethel N, Heine P, Murray AN, Gerben S, Carter L, Miranda M, Negahdari
    B, Lee S, Trapnell C, Stewart L, Ekiert DC, Schlessinger J, Shendure J, Bhabha
    G, Ruohola-Baker H, Baker D. Modulation of FGF pathway signaling and vascular
    differentiation using designed oligomeric assemblies. bioRxiv, <a href="https://doi.org/10.1101/2023.03.14.532666">10.1101/2023.03.14.532666</a>.
  mla: Edman, Natasha I., et al. “Modulation of FGF Pathway Signaling and Vascular
    Differentiation Using Designed Oligomeric Assemblies.” <i>BioRxiv</i>, doi:<a
    href="https://doi.org/10.1101/2023.03.14.532666">10.1101/2023.03.14.532666</a>.
  short: N.I. Edman, R.L. Redler, A. Phal, T. Schlichthaerle, S.R. Srivatsan, A. Etemadi,
    S. An, A. Favor, D. Ehnes, Z. Li, F.M. Praetorius, M. Gordon, W. Yang, B. Coventry,
    D.R. Hicks, L. Cao, N. Bethel, P. Heine, A.N. Murray, S. Gerben, L. Carter, M.
    Miranda, B. Negahdari, S. Lee, C. Trapnell, L. Stewart, D.C. Ekiert, J. Schlessinger,
    J. Shendure, G. Bhabha, H. Ruohola-Baker, D. Baker, BioRxiv (n.d.).
date_created: 2023-09-06T12:31:49Z
date_published: 2023-03-15T00:00:00Z
date_updated: 2023-11-07T12:21:58Z
day: '15'
doi: 10.1101/2023.03.14.532666
extern: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/2023.03.14.532666
month: '03'
oa: 1
oa_version: Preprint
publication: bioRxiv
publication_status: submitted
status: public
title: Modulation of FGF pathway signaling and vascular differentiation using designed
  oligomeric assemblies
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '14313'
abstract:
- lang: eng
  text: To respond to auxin, the chief orchestrator of their multicellularity, plants
    evolved multiple receptor systems and signal transduction cascades. Despite decades
    of research, however, we are still lacking a satisfactory synthesis of various
    auxin signaling mechanisms. The chief discrepancy and historical controversy of
    the field is that of rapid and slow auxin effects on plant physiology and development.
    How is it possible that ions begin to trickle across the plasma membrane as soon
    as auxin enters the cell, even though the best-characterized transcriptional auxin
    pathway can take effect only after tens of minutes? Recently, unexpected progress
    has been made in understanding this and other unknowns of auxin signaling. We
    provide a perspective on these exciting developments and concepts whose general
    applicability might have ramifications beyond auxin signaling.
acknowledgement: The opening quote is not intended to reflect any political views
  of the authors. The authors by no means endorse the rhetoric of Donald Rumsfeld
  or the 2003 invasion of Iraq by the United States. Nevertheless, Rumsfeld's quote
  led to both public and academic debates on the concept of known and unknown unknowns,
  which can be applied to the recent unexpected developments in the auxin signaling
  field. We thank Linlin Qi and Huihuang Chen for their suggestions on figure presentation
  and inspiring discussions of TIR1/AFB signaling. Finally, we thank Aroosa Hussain
  for discussion of Greek mythology.
article_number: '102443'
article_processing_charge: No
article_type: review
author:
- first_name: Lukas
  full_name: Fiedler, Lukas
  id: 7c417475-8972-11ed-ae7b-8b674ca26986
  last_name: Fiedler
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: 'Fiedler L, Friml J. Rapid auxin signaling: Unknowns old and new. <i>Current
    Opinion in Plant Biology</i>. 2023;75(10). doi:<a href="https://doi.org/10.1016/j.pbi.2023.102443">10.1016/j.pbi.2023.102443</a>'
  apa: 'Fiedler, L., &#38; Friml, J. (2023). Rapid auxin signaling: Unknowns old and
    new. <i>Current Opinion in Plant Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.pbi.2023.102443">https://doi.org/10.1016/j.pbi.2023.102443</a>'
  chicago: 'Fiedler, Lukas, and Jiří Friml. “Rapid Auxin Signaling: Unknowns Old and
    New.” <i>Current Opinion in Plant Biology</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.pbi.2023.102443">https://doi.org/10.1016/j.pbi.2023.102443</a>.'
  ieee: 'L. Fiedler and J. Friml, “Rapid auxin signaling: Unknowns old and new,” <i>Current
    Opinion in Plant Biology</i>, vol. 75, no. 10. Elsevier, 2023.'
  ista: 'Fiedler L, Friml J. 2023. Rapid auxin signaling: Unknowns old and new. Current
    Opinion in Plant Biology. 75(10), 102443.'
  mla: 'Fiedler, Lukas, and Jiří Friml. “Rapid Auxin Signaling: Unknowns Old and New.”
    <i>Current Opinion in Plant Biology</i>, vol. 75, no. 10, 102443, Elsevier, 2023,
    doi:<a href="https://doi.org/10.1016/j.pbi.2023.102443">10.1016/j.pbi.2023.102443</a>.'
  short: L. Fiedler, J. Friml, Current Opinion in Plant Biology 75 (2023).
date_created: 2023-09-10T22:01:11Z
date_published: 2023-10-01T00:00:00Z
date_updated: 2023-11-07T08:17:13Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1016/j.pbi.2023.102443
external_id:
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  - '37666097'
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publication_identifier:
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publication_status: published
publisher: Elsevier
quality_controlled: '1'
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status: public
title: 'Rapid auxin signaling: Unknowns old and new'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 75
year: '2023'
...
---
_id: '14314'
abstract:
- lang: eng
  text: The execution of cognitive functions requires coordinated circuit activity
    across different brain areas that involves the associated firing of neuronal assemblies.
    Here, we tested the circuit mechanism behind assembly interactions between the
    hippocampus and the medial prefrontal cortex (mPFC) of adult rats by recording
    neuronal populations during a rule-switching task. We identified functionally
    coupled CA1-mPFC cells that synchronized their activity beyond that expected from
    common spatial coding or oscillatory firing. When such cell pairs fired together,
    the mPFC cell strongly phase locked to CA1 theta oscillations and maintained consistent
    theta firing phases, independent of the theta timing of their CA1 counterpart.
    These functionally connected CA1-mPFC cells formed interconnected assemblies.
    While firing together with their CA1 assembly partners, mPFC cells fired along
    specific theta sequences. Our results suggest that upregulated theta oscillatory
    firing of mPFC cells can signal transient interactions with specific CA1 assemblies,
    thus enabling distributed computations.
acknowledgement: We thank A. Cumpelik, H. Chiossi, and L. Bollman for comments on
  an earlier version of this manuscript. This work was funded by EU-FP7 MC-ITN IN-SENS
  (grant 607616).
article_number: '113015'
article_processing_charge: Yes
article_type: original
author:
- first_name: Michele
  full_name: Nardin, Michele
  id: 30BD0376-F248-11E8-B48F-1D18A9856A87
  last_name: Nardin
  orcid: 0000-0001-8849-6570
- first_name: Karola
  full_name: Käfer, Karola
  id: 2DAA49AA-F248-11E8-B48F-1D18A9856A87
  last_name: Käfer
- first_name: Federico
  full_name: Stella, Federico
  id: 39AF1E74-F248-11E8-B48F-1D18A9856A87
  last_name: Stella
  orcid: 0000-0001-9439-3148
- first_name: Jozsef L
  full_name: Csicsvari, Jozsef L
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
citation:
  ama: Nardin M, Käfer K, Stella F, Csicsvari JL. Theta oscillations as a substrate
    for medial prefrontal-hippocampal assembly interactions. <i>Cell Reports</i>.
    2023;42(9). doi:<a href="https://doi.org/10.1016/j.celrep.2023.113015">10.1016/j.celrep.2023.113015</a>
  apa: Nardin, M., Käfer, K., Stella, F., &#38; Csicsvari, J. L. (2023). Theta oscillations
    as a substrate for medial prefrontal-hippocampal assembly interactions. <i>Cell
    Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2023.113015">https://doi.org/10.1016/j.celrep.2023.113015</a>
  chicago: Nardin, Michele, Karola Käfer, Federico Stella, and Jozsef L Csicsvari.
    “Theta Oscillations as a Substrate for Medial Prefrontal-Hippocampal Assembly
    Interactions.” <i>Cell Reports</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.celrep.2023.113015">https://doi.org/10.1016/j.celrep.2023.113015</a>.
  ieee: M. Nardin, K. Käfer, F. Stella, and J. L. Csicsvari, “Theta oscillations as
    a substrate for medial prefrontal-hippocampal assembly interactions,” <i>Cell
    Reports</i>, vol. 42, no. 9. Elsevier, 2023.
  ista: Nardin M, Käfer K, Stella F, Csicsvari JL. 2023. Theta oscillations as a substrate
    for medial prefrontal-hippocampal assembly interactions. Cell Reports. 42(9),
    113015.
  mla: Nardin, Michele, et al. “Theta Oscillations as a Substrate for Medial Prefrontal-Hippocampal
    Assembly Interactions.” <i>Cell Reports</i>, vol. 42, no. 9, 113015, Elsevier,
    2023, doi:<a href="https://doi.org/10.1016/j.celrep.2023.113015">10.1016/j.celrep.2023.113015</a>.
  short: M. Nardin, K. Käfer, F. Stella, J.L. Csicsvari, Cell Reports 42 (2023).
date_created: 2023-09-10T22:01:11Z
date_published: 2023-09-26T00:00:00Z
date_updated: 2023-09-15T07:14:12Z
day: '26'
ddc:
- '570'
department:
- _id: JoCs
doi: 10.1016/j.celrep.2023.113015
ec_funded: 1
external_id:
  pmid:
  - '37632747'
file:
- access_level: open_access
  checksum: ca77a304fb813c292550b8604b0fb41d
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-15T07:12:46Z
  date_updated: 2023-09-15T07:12:46Z
  file_id: '14337'
  file_name: 2023_CellPress_Nardin.pdf
  file_size: 4879455
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file_date_updated: 2023-09-15T07:12:46Z
has_accepted_license: '1'
intvolume: '        42'
issue: '9'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 257BBB4C-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '607616'
  name: Inter-and intracellular signalling in schizophrenia
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Theta oscillations as a substrate for medial prefrontal-hippocampal assembly
  interactions
tmp:
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  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
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...
