---
_id: '12334'
abstract:
- lang: eng
  text: Regulation of the Arp2/3 complex is required for productive nucleation of
    branched actin networks. An emerging aspect of regulation is the incorporation
    of subunit isoforms into the Arp2/3 complex. Specifically, both ArpC5 subunit
    isoforms, ArpC5 and ArpC5L, have been reported to fine-tune nucleation activity
    and branch junction stability. We have combined reverse genetics and cellular
    structural biology to describe how ArpC5 and ArpC5L differentially affect cell
    migration. Both define the structural stability of ArpC1 in branch junctions and,
    in turn, by determining protrusion characteristics, affect protein dynamics and
    actin network ultrastructure. ArpC5 isoforms also affect the positioning of members
    of the Ena/Vasodilator-stimulated phosphoprotein (VASP) family of actin filament
    elongators, which mediate ArpC5 isoform–specific effects on the actin assembly
    level. Our results suggest that ArpC5 and Ena/VASP proteins are part of a signaling
    pathway enhancing cell migration.</jats:p>
acknowledged_ssus:
- _id: ScienComp
- _id: LifeSc
- _id: Bio
- _id: EM-Fac
acknowledgement: "We would like to thank K. von Peinen and B. Denker (Helmholtz Centre
  for Infection Research, Braunschweig, Germany) for experimental and technical assistance,
  respectively.\r\nThis research was supported by the Scientific Service Units (SSUs)
  of ISTA through resources provided by Scientific Computing (SciComp), the Life Science
  Facility (LSF), the Imaging and Optics facility (IOF), and the Electron Microscopy
  Facility (EMF). We acknowledge support from ISTA and from the Austrian Science Fund
  (FWF) (P33367) to F.K.M.S., from the Research Training Group GRK2223 and the Helmholtz
  Society to K.R,. and from the Deutsche Forschungsgemeinschaft (DFG) to J.F. and
  K.R."
article_number: add6495
article_processing_charge: No
article_type: original
author:
- first_name: Florian
  full_name: Fäßler, Florian
  id: 404F5528-F248-11E8-B48F-1D18A9856A87
  last_name: Fäßler
  orcid: 0000-0001-7149-769X
- first_name: Manjunath
  full_name: Javoor, Manjunath
  id: 305ab18b-dc7d-11ea-9b2f-b58195228ea2
  last_name: Javoor
- first_name: Julia
  full_name: Datler, Julia
  id: 3B12E2E6-F248-11E8-B48F-1D18A9856A87
  last_name: Datler
  orcid: 0000-0002-3616-8580
- first_name: Hermann
  full_name: Döring, Hermann
  last_name: Döring
- first_name: Florian
  full_name: Hofer, Florian
  id: b9d234ba-9e33-11ed-95b6-cd561df280e6
  last_name: Hofer
- first_name: Georgi A
  full_name: Dimchev, Georgi A
  id: 38C393BE-F248-11E8-B48F-1D18A9856A87
  last_name: Dimchev
  orcid: 0000-0001-8370-6161
- first_name: Victor-Valentin
  full_name: Hodirnau, Victor-Valentin
  id: 3661B498-F248-11E8-B48F-1D18A9856A87
  last_name: Hodirnau
- first_name: Jan
  full_name: Faix, Jan
  last_name: Faix
- first_name: Klemens
  full_name: Rottner, Klemens
  last_name: Rottner
- first_name: Florian KM
  full_name: Schur, Florian KM
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
citation:
  ama: Fäßler F, Javoor M, Datler J, et al. ArpC5 isoforms regulate Arp2/3 complex–dependent
    protrusion through differential Ena/VASP positioning. <i>Science Advances</i>.
    2023;9(3). doi:<a href="https://doi.org/10.1126/sciadv.add6495">10.1126/sciadv.add6495</a>
  apa: Fäßler, F., Javoor, M., Datler, J., Döring, H., Hofer, F., Dimchev, G. A.,
    … Schur, F. K. (2023). ArpC5 isoforms regulate Arp2/3 complex–dependent protrusion
    through differential Ena/VASP positioning. <i>Science Advances</i>. American Association
    for the Advancement of Science. <a href="https://doi.org/10.1126/sciadv.add6495">https://doi.org/10.1126/sciadv.add6495</a>
  chicago: Fäßler, Florian, Manjunath Javoor, Julia Datler, Hermann Döring, Florian
    Hofer, Georgi A Dimchev, Victor-Valentin Hodirnau, Jan Faix, Klemens Rottner,
    and Florian KM Schur. “ArpC5 Isoforms Regulate Arp2/3 Complex–Dependent Protrusion
    through Differential Ena/VASP Positioning.” <i>Science Advances</i>. American
    Association for the Advancement of Science, 2023. <a href="https://doi.org/10.1126/sciadv.add6495">https://doi.org/10.1126/sciadv.add6495</a>.
  ieee: F. Fäßler <i>et al.</i>, “ArpC5 isoforms regulate Arp2/3 complex–dependent
    protrusion through differential Ena/VASP positioning,” <i>Science Advances</i>,
    vol. 9, no. 3. American Association for the Advancement of Science, 2023.
  ista: Fäßler F, Javoor M, Datler J, Döring H, Hofer F, Dimchev GA, Hodirnau V-V,
    Faix J, Rottner K, Schur FK. 2023. ArpC5 isoforms regulate Arp2/3 complex–dependent
    protrusion through differential Ena/VASP positioning. Science Advances. 9(3),
    add6495.
  mla: Fäßler, Florian, et al. “ArpC5 Isoforms Regulate Arp2/3 Complex–Dependent Protrusion
    through Differential Ena/VASP Positioning.” <i>Science Advances</i>, vol. 9, no.
    3, add6495, American Association for the Advancement of Science, 2023, doi:<a
    href="https://doi.org/10.1126/sciadv.add6495">10.1126/sciadv.add6495</a>.
  short: F. Fäßler, M. Javoor, J. Datler, H. Döring, F. Hofer, G.A. Dimchev, V.-V.
    Hodirnau, J. Faix, K. Rottner, F.K. Schur, Science Advances 9 (2023).
date_created: 2023-01-23T07:26:42Z
date_published: 2023-01-20T00:00:00Z
date_updated: 2023-11-21T08:05:35Z
day: '20'
ddc:
- '570'
department:
- _id: FlSc
- _id: EM-Fac
doi: 10.1126/sciadv.add6495
external_id:
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  grant_number: P33367
  name: Structure and isoform diversity of the Arp2/3 complex
publication: Science Advances
publication_identifier:
  issn:
  - 2375-2548
publication_status: published
publisher: American Association for the Advancement of Science
quality_controlled: '1'
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title: ArpC5 isoforms regulate Arp2/3 complex–dependent protrusion through differential
  Ena/VASP positioning
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: 9
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...
---
_id: '12349'
abstract:
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  text: Statistics of natural scenes are not uniform - their structure varies dramatically
    from ground to sky. It remains unknown whether these non-uniformities are reflected
    in the large-scale organization of the early visual system and what benefits such
    adaptations would confer. Here, by relying on the efficient coding hypothesis,
    we predict that changes in the structure of receptive fields across visual space
    increase the efficiency of sensory coding. We show experimentally that, in agreement
    with our predictions, receptive fields of retinal ganglion cells change their
    shape along the dorsoventral retinal axis, with a marked surround asymmetry at
    the visual horizon. Our work demonstrates that, according to principles of efficient
    coding, the panoramic structure of natural scenes is exploited by the retina across
    space and cell-types.
acknowledged_ssus:
- _id: ScienComp
- _id: PreCl
- _id: LifeSc
- _id: Bio
acknowledgement: We thank Hiroki Asari for sharing the dataset of naturalistic images,
  Anton Sumser for sharing visual stimulus code, Yoav Ben Simon for initial explorative
  work with the generation of AAVs, and Tomas Vega-Zuñiga for help with immunostainings.
  We also thank Gasper Tkacik and members of the Neuroethology group for their comments
  on the manuscript. This research was supported by the Scientific Service Units of
  IST Austria through resources provided by Scientific Computing, the Preclinical
  Facility, the Lab Support Facility, and the Imaging and Optics Facility. This work
  was supported by European Union Horizon 2020 Marie Skłodowska-Curie grant 665385
  (DG), Austrian Science Fund (FWF) stand-alone grant P 34015 (WM), Human Frontiers
  Science Program LT000256/2018-L (AS), EMBO ALTF 1098-2017 (AS) and the European
  Research Council Starting Grant 756502 (MJ).
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Divyansh
  full_name: Gupta, Divyansh
  id: 2A485EBE-F248-11E8-B48F-1D18A9856A87
  last_name: Gupta
  orcid: 0000-0001-7400-6665
- first_name: Wiktor F
  full_name: Mlynarski, Wiktor F
  id: 358A453A-F248-11E8-B48F-1D18A9856A87
  last_name: Mlynarski
- first_name: Anton L
  full_name: Sumser, Anton L
  id: 3320A096-F248-11E8-B48F-1D18A9856A87
  last_name: Sumser
  orcid: 0000-0002-4792-1881
- first_name: Olga
  full_name: Symonova, Olga
  id: 3C0C7BC6-F248-11E8-B48F-1D18A9856A87
  last_name: Symonova
  orcid: 0000-0003-2012-9947
- first_name: Jan
  full_name: Svaton, Jan
  id: f7f724c3-9d6f-11ed-9f44-e5c5f3a5bee2
  last_name: Svaton
  orcid: 0000-0002-6198-2939
- first_name: Maximilian A
  full_name: Jösch, Maximilian A
  id: 2BD278E6-F248-11E8-B48F-1D18A9856A87
  last_name: Jösch
  orcid: 0000-0002-3937-1330
citation:
  ama: Gupta D, Mlynarski WF, Sumser AL, Symonova O, Svaton J, Jösch MA. Panoramic
    visual statistics shape retina-wide organization of receptive fields. <i>Nature
    Neuroscience</i>. 2023;26:606-614. doi:<a href="https://doi.org/10.1038/s41593-023-01280-0">10.1038/s41593-023-01280-0</a>
  apa: Gupta, D., Mlynarski, W. F., Sumser, A. L., Symonova, O., Svaton, J., &#38;
    Jösch, M. A. (2023). Panoramic visual statistics shape retina-wide organization
    of receptive fields. <i>Nature Neuroscience</i>. Springer Nature. <a href="https://doi.org/10.1038/s41593-023-01280-0">https://doi.org/10.1038/s41593-023-01280-0</a>
  chicago: Gupta, Divyansh, Wiktor F Mlynarski, Anton L Sumser, Olga Symonova, Jan
    Svaton, and Maximilian A Jösch. “Panoramic Visual Statistics Shape Retina-Wide
    Organization of Receptive Fields.” <i>Nature Neuroscience</i>. Springer Nature,
    2023. <a href="https://doi.org/10.1038/s41593-023-01280-0">https://doi.org/10.1038/s41593-023-01280-0</a>.
  ieee: D. Gupta, W. F. Mlynarski, A. L. Sumser, O. Symonova, J. Svaton, and M. A.
    Jösch, “Panoramic visual statistics shape retina-wide organization of receptive
    fields,” <i>Nature Neuroscience</i>, vol. 26. Springer Nature, pp. 606–614, 2023.
  ista: Gupta D, Mlynarski WF, Sumser AL, Symonova O, Svaton J, Jösch MA. 2023. Panoramic
    visual statistics shape retina-wide organization of receptive fields. Nature Neuroscience.
    26, 606–614.
  mla: Gupta, Divyansh, et al. “Panoramic Visual Statistics Shape Retina-Wide Organization
    of Receptive Fields.” <i>Nature Neuroscience</i>, vol. 26, Springer Nature, 2023,
    pp. 606–14, doi:<a href="https://doi.org/10.1038/s41593-023-01280-0">10.1038/s41593-023-01280-0</a>.
  short: D. Gupta, W.F. Mlynarski, A.L. Sumser, O. Symonova, J. Svaton, M.A. Jösch,
    Nature Neuroscience 26 (2023) 606–614.
date_created: 2023-01-23T14:14:19Z
date_published: 2023-04-01T00:00:00Z
date_updated: 2023-10-04T11:41:05Z
day: '01'
ddc:
- '570'
department:
- _id: GradSch
- _id: MaJö
doi: 10.1038/s41593-023-01280-0
ec_funded: 1
external_id:
  isi:
  - '000955258300002'
  pmid:
  - '36959418'
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tmp:
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abstract:
- lang: eng
  text: 'Statistics of natural scenes are not uniform - their structure varies dramatically
    from ground to sky. It remains unknown whether these non-uniformities are reflected
    in the large-scale organization of the early visual system and what benefits such
    adaptations would confer. Here, by relying on the efficient coding hypothesis,
    we predict that changes in the structure of receptive fields across visual space
    increase the efficiency of sensory coding. We show experimentally that, in agreement
    with our predictions, receptive fields of retinal ganglion cells change their
    shape along the dorsoventral retinal axis, with a marked surround asymmetry at
    the visual horizon. Our work demonstrates that, according to principles of efficient
    coding, the panoramic structure of natural scenes is exploited by the retina across
    space and cell-types. '
acknowledged_ssus:
- _id: ScienComp
- _id: M-Shop
- _id: Bio
- _id: PreCl
- _id: LifeSc
article_processing_charge: No
author:
- first_name: Divyansh
  full_name: Gupta, Divyansh
  id: 2A485EBE-F248-11E8-B48F-1D18A9856A87
  last_name: Gupta
  orcid: 0000-0001-7400-6665
- first_name: Anton L
  full_name: Sumser, Anton L
  id: 3320A096-F248-11E8-B48F-1D18A9856A87
  last_name: Sumser
  orcid: 0000-0002-4792-1881
- first_name: Maximilian A
  full_name: Jösch, Maximilian A
  id: 2BD278E6-F248-11E8-B48F-1D18A9856A87
  last_name: Jösch
  orcid: 0000-0002-3937-1330
citation:
  ama: 'Gupta D, Sumser AL, Jösch MA. Research Data for: Panoramic visual statistics
    shape retina-wide organization of receptive fields. 2023. doi:<a href="https://doi.org/10.15479/AT:ISTA:12370">10.15479/AT:ISTA:12370</a>'
  apa: 'Gupta, D., Sumser, A. L., &#38; Jösch, M. A. (2023). Research Data for: Panoramic
    visual statistics shape retina-wide organization of receptive fields. Institute
    of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:12370">https://doi.org/10.15479/AT:ISTA:12370</a>'
  chicago: 'Gupta, Divyansh, Anton L Sumser, and Maximilian A Jösch. “Research Data
    for: Panoramic Visual Statistics Shape Retina-Wide Organization of Receptive Fields.”
    Institute of Science and Technology Austria, 2023. <a href="https://doi.org/10.15479/AT:ISTA:12370">https://doi.org/10.15479/AT:ISTA:12370</a>.'
  ieee: 'D. Gupta, A. L. Sumser, and M. A. Jösch, “Research Data for: Panoramic visual
    statistics shape retina-wide organization of receptive fields.” Institute of Science
    and Technology Austria, 2023.'
  ista: 'Gupta D, Sumser AL, Jösch MA. 2023. Research Data for: Panoramic visual statistics
    shape retina-wide organization of receptive fields, Institute of Science and Technology
    Austria, <a href="https://doi.org/10.15479/AT:ISTA:12370">10.15479/AT:ISTA:12370</a>.'
  mla: 'Gupta, Divyansh, et al. <i>Research Data for: Panoramic Visual Statistics
    Shape Retina-Wide Organization of Receptive Fields</i>. Institute of Science and
    Technology Austria, 2023, doi:<a href="https://doi.org/10.15479/AT:ISTA:12370">10.15479/AT:ISTA:12370</a>.'
  short: D. Gupta, A.L. Sumser, M.A. Jösch, (2023).
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  id: 3C0C7BC6-F248-11E8-B48F-1D18A9856A87
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- contributor_type: researcher
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date_created: 2023-01-25T12:45:18Z
date_published: 2023-01-26T00:00:00Z
date_updated: 2023-10-04T11:41:04Z
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doi: 10.15479/AT:ISTA:12370
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file_date_updated: 2023-01-26T10:51:34Z
has_accepted_license: '1'
license: https://creativecommons.org/licenses/by-nc-sa/4.0/
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 626c45b5-2b32-11ec-9570-e509828c1ba6
  grant_number: P34015
  name: Efficient coding with biophysical realism
- _id: 2634E9D2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '756502'
  name: Circuits of Visual Attention
- _id: 266D407A-B435-11E9-9278-68D0E5697425
  grant_number: LT000256
  name: Neuronal networks of salience and spatial detection in the murine superior
    colliculus
- _id: 264FEA02-B435-11E9-9278-68D0E5697425
  grant_number: ALTF 1098-2017
  name: Connecting sensory with motor processing in the superior colliculus
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '12349'
    relation: used_in_publication
    status: public
status: public
title: 'Research Data for: Panoramic visual statistics shape retina-wide organization
  of receptive fields'
tmp:
  image: /images/cc_by_nc_sa.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC
    BY-NC-SA 4.0)
  short: CC BY-NC-SA (4.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '12406'
abstract:
- lang: eng
  text: Let X be a sufficiently large positive integer. We prove that one may choose
    a subset S of primes with cardinality O(logX) such that a positive proportion
    of integers less than X can be represented by x2+py2 for at least one p∈S.
acknowledgement: "This article is a version the author’s master thesis at the University
  of Bonn. The author would like to thank his advisor Valentin Blomer for introducing
  the problem, and giving generous feedback and encouragement along the way, especially
  during the global pandemic.\r\nThe author thanks Edgar Assing for his lectures on
  analytic number theory. Finally, the author is grateful to the anonymous referees
  for their valuable time and comments.\r\n"
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Yijie
  full_name: Diao, Yijie
  id: 7b7eb4ca-eb2c-11ec-b98b-accec0b20c3b
  last_name: Diao
  orcid: 0000-0002-4989-5330
citation:
  ama: Diao Y. Density of the union of positive diagonal binary quadratic forms. <i>Acta
    Arithmetica</i>. 2023;207:1-17. doi:<a href="https://doi.org/10.4064/aa210830-24-11">10.4064/aa210830-24-11</a>
  apa: Diao, Y. (2023). Density of the union of positive diagonal binary quadratic
    forms. <i>Acta Arithmetica</i>. Instytut Matematyczny. <a href="https://doi.org/10.4064/aa210830-24-11">https://doi.org/10.4064/aa210830-24-11</a>
  chicago: Diao, Yijie. “Density of the Union of Positive Diagonal Binary Quadratic
    Forms.” <i>Acta Arithmetica</i>. Instytut Matematyczny, 2023. <a href="https://doi.org/10.4064/aa210830-24-11">https://doi.org/10.4064/aa210830-24-11</a>.
  ieee: Y. Diao, “Density of the union of positive diagonal binary quadratic forms,”
    <i>Acta Arithmetica</i>, vol. 207. Instytut Matematyczny, pp. 1–17, 2023.
  ista: Diao Y. 2023. Density of the union of positive diagonal binary quadratic forms.
    Acta Arithmetica. 207, 1–17.
  mla: Diao, Yijie. “Density of the Union of Positive Diagonal Binary Quadratic Forms.”
    <i>Acta Arithmetica</i>, vol. 207, Instytut Matematyczny, 2023, pp. 1–17, doi:<a
    href="https://doi.org/10.4064/aa210830-24-11">10.4064/aa210830-24-11</a>.
  short: Y. Diao, Acta Arithmetica 207 (2023) 1–17.
date_created: 2023-01-26T21:17:04Z
date_published: 2023-01-09T00:00:00Z
date_updated: 2023-10-17T09:15:17Z
day: '09'
department:
- _id: GradSch
doi: 10.4064/aa210830-24-11
external_id:
  arxiv:
  - '2103.08268'
  isi:
  - '000912903000001'
intvolume: '       207'
isi: 1
keyword:
- Algebra
- Number Theory
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.2103.08268
month: '01'
oa: 1
oa_version: Preprint
page: 1-17
publication: Acta Arithmetica
publication_identifier:
  eissn:
  - 1730-6264
  issn:
  - 0065-1036
publication_status: published
publisher: Instytut Matematyczny
quality_controlled: '1'
status: public
title: Density of the union of positive diagonal binary quadratic forms
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 207
year: '2023'
...
---
_id: '12407'
abstract:
- lang: eng
  text: "As the complexity and criticality of software increase every year, so does
    the importance of run-time monitoring. Third-party monitoring, with limited knowledge
    of the monitored software, and best-effort monitoring, which keeps pace with the
    monitored software, are especially valuable, yet underexplored areas of run-time
    monitoring. Most existing monitoring frameworks do not support their combination
    because they either require access to the monitored code for instrumentation purposes
    or the processing of all observed events, or both.\r\n\r\nWe present a middleware
    framework, VAMOS, for the run-time monitoring of software which is explicitly
    designed to support third-party and best-effort scenarios. The design goals of
    VAMOS are (i) efficiency (keeping pace at low overhead), (ii) flexibility (the
    ability to monitor black-box code through a variety of different event channels,
    and the connectability to monitors written in different specification languages),
    and (iii) ease-of-use. To achieve its goals, VAMOS combines aspects of event broker
    and event recognition systems with aspects of stream processing systems.\r\n\r\nWe
    implemented a prototype toolchain for VAMOS and conducted experiments including
    a case study of monitoring for data races. The results indicate that VAMOS enables
    writing useful yet efficient monitors, is compatible with a variety of event sources
    and monitor specifications, and simplifies key aspects of setting up a monitoring
    system from scratch."
acknowledgement: "This work was supported in part by the ERC-2020-AdG 101020093. \r\nThe
  authors would like to thank the anonymous FASE reviewers for their valuable feedback
  and suggestions."
alternative_title:
- IST Austria Technical Report
article_processing_charge: No
author:
- first_name: Marek
  full_name: Chalupa, Marek
  id: 87e34708-d6c6-11ec-9f5b-9391e7be2463
  last_name: Chalupa
- first_name: Fabian
  full_name: Mühlböck, Fabian
  id: 6395C5F6-89DF-11E9-9C97-6BDFE5697425
  last_name: Mühlböck
  orcid: 0000-0003-1548-0177
- first_name: Stefanie
  full_name: Muroya Lei, Stefanie
  id: a376de31-8972-11ed-ae7b-d0251c13c8ff
  last_name: Muroya Lei
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000-0002-2985-7724
citation:
  ama: 'Chalupa M, Mühlböck F, Muroya Lei S, Henzinger TA. <i>VAMOS: Middleware for
    Best-Effort Third-Party Monitoring</i>. Institute of Science and Technology Austria;
    2023. doi:<a href="https://doi.org/10.15479/AT:ISTA:12407">10.15479/AT:ISTA:12407</a>'
  apa: 'Chalupa, M., Mühlböck, F., Muroya Lei, S., &#38; Henzinger, T. A. (2023).
    <i>VAMOS: Middleware for Best-Effort Third-Party Monitoring</i>. Institute of
    Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:12407">https://doi.org/10.15479/AT:ISTA:12407</a>'
  chicago: 'Chalupa, Marek, Fabian Mühlböck, Stefanie Muroya Lei, and Thomas A Henzinger.
    <i>VAMOS: Middleware for Best-Effort Third-Party Monitoring</i>. Institute of
    Science and Technology Austria, 2023. <a href="https://doi.org/10.15479/AT:ISTA:12407">https://doi.org/10.15479/AT:ISTA:12407</a>.'
  ieee: 'M. Chalupa, F. Mühlböck, S. Muroya Lei, and T. A. Henzinger, <i>VAMOS: Middleware
    for Best-Effort Third-Party Monitoring</i>. Institute of Science and Technology
    Austria, 2023.'
  ista: 'Chalupa M, Mühlböck F, Muroya Lei S, Henzinger TA. 2023. VAMOS: Middleware
    for Best-Effort Third-Party Monitoring, Institute of Science and Technology Austria,
    38p.'
  mla: 'Chalupa, Marek, et al. <i>VAMOS: Middleware for Best-Effort Third-Party Monitoring</i>.
    Institute of Science and Technology Austria, 2023, doi:<a href="https://doi.org/10.15479/AT:ISTA:12407">10.15479/AT:ISTA:12407</a>.'
  short: 'M. Chalupa, F. Mühlböck, S. Muroya Lei, T.A. Henzinger, VAMOS: Middleware
    for Best-Effort Third-Party Monitoring, Institute of Science and Technology Austria,
    2023.'
date_created: 2023-01-27T03:18:08Z
date_published: 2023-01-27T00:00:00Z
date_updated: 2023-04-25T07:19:06Z
day: '27'
ddc:
- '005'
department:
- _id: ToHe
doi: 10.15479/AT:ISTA:12407
ec_funded: 1
file:
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  creator: fmuehlbo
  date_created: 2023-01-27T03:18:34Z
  date_updated: 2023-01-27T03:18:34Z
  file_id: '12408'
  file_name: main.pdf
  file_size: 662409
  relation: main_file
  success: 1
file_date_updated: 2023-01-27T03:18:34Z
has_accepted_license: '1'
keyword:
- runtime monitoring
- best effort
- third party
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: '38'
project:
- _id: 62781420-2b32-11ec-9570-8d9b63373d4d
  call_identifier: H2020
  grant_number: '101020093'
  name: Vigilant Algorithmic Monitoring of Software
publication_identifier:
  eissn:
  - 2664-1690
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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  - id: '12856'
    relation: later_version
    status: public
status: public
title: 'VAMOS: Middleware for Best-Effort Third-Party Monitoring'
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: technical_report
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '12421'
abstract:
- lang: eng
  text: The actin cytoskeleton plays a key role in cell migration and cellular morphodynamics
    in most eukaryotes. The ability of the actin cytoskeleton to assemble and disassemble
    in a spatiotemporally controlled manner allows it to form higher-order structures,
    which can generate forces required for a cell to explore and navigate through
    its environment. It is regulated not only via a complex synergistic and competitive
    interplay between actin-binding proteins (ABP), but also by filament biochemistry
    and filament geometry. The lack of structural insights into how geometry and ABPs
    regulate the actin cytoskeleton limits our understanding of the molecular mechanisms
    that define actin cytoskeleton remodeling and, in turn, impact emerging cell migration
    characteristics. With the advent of cryo-electron microscopy (cryo-EM) and advanced
    computational methods, it is now possible to define these molecular mechanisms
    involving actin and its interactors at both atomic and ultra-structural levels
    in vitro and in cellulo. In this review, we will provide an overview of the available
    cryo-EM methods, applicable to further our understanding of the actin cytoskeleton,
    specifically in the context of cell migration. We will discuss how these methods
    have been employed to elucidate ABP- and geometry-defined regulatory mechanisms
    in initiating, maintaining, and disassembling cellular actin networks in migratory
    protrusions.
acknowledgement: 'We apologize for not being able to mention and cite additional excellent
  work that would have fit the scope of this review, due to space restraints. We thank
  Jesse Hansen for comments on the manuscript. We acknowledge support from the Austrian
  Science Fund (FWF): P33367 and the Institute of Science and Technology Austria.'
article_processing_charge: No
article_type: original
author:
- first_name: Florian
  full_name: Fäßler, Florian
  id: 404F5528-F248-11E8-B48F-1D18A9856A87
  last_name: Fäßler
  orcid: 0000-0001-7149-769X
- first_name: Manjunath
  full_name: Javoor, Manjunath
  id: 305ab18b-dc7d-11ea-9b2f-b58195228ea2
  last_name: Javoor
- first_name: Florian KM
  full_name: Schur, Florian KM
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
citation:
  ama: Fäßler F, Javoor M, Schur FK. Deciphering the molecular mechanisms of actin
    cytoskeleton regulation in cell migration using cryo-EM. <i>Biochemical Society
    Transactions</i>. 2023;51(1):87-99. doi:<a href="https://doi.org/10.1042/bst20220221">10.1042/bst20220221</a>
  apa: Fäßler, F., Javoor, M., &#38; Schur, F. K. (2023). Deciphering the molecular
    mechanisms of actin cytoskeleton regulation in cell migration using cryo-EM. <i>Biochemical
    Society Transactions</i>. Portland Press. <a href="https://doi.org/10.1042/bst20220221">https://doi.org/10.1042/bst20220221</a>
  chicago: Fäßler, Florian, Manjunath Javoor, and Florian KM Schur. “Deciphering the
    Molecular Mechanisms of Actin Cytoskeleton Regulation in Cell Migration Using
    Cryo-EM.” <i>Biochemical Society Transactions</i>. Portland Press, 2023. <a href="https://doi.org/10.1042/bst20220221">https://doi.org/10.1042/bst20220221</a>.
  ieee: F. Fäßler, M. Javoor, and F. K. Schur, “Deciphering the molecular mechanisms
    of actin cytoskeleton regulation in cell migration using cryo-EM,” <i>Biochemical
    Society Transactions</i>, vol. 51, no. 1. Portland Press, pp. 87–99, 2023.
  ista: Fäßler F, Javoor M, Schur FK. 2023. Deciphering the molecular mechanisms of
    actin cytoskeleton regulation in cell migration using cryo-EM. Biochemical Society
    Transactions. 51(1), 87–99.
  mla: Fäßler, Florian, et al. “Deciphering the Molecular Mechanisms of Actin Cytoskeleton
    Regulation in Cell Migration Using Cryo-EM.” <i>Biochemical Society Transactions</i>,
    vol. 51, no. 1, Portland Press, 2023, pp. 87–99, doi:<a href="https://doi.org/10.1042/bst20220221">10.1042/bst20220221</a>.
  short: F. Fäßler, M. Javoor, F.K. Schur, Biochemical Society Transactions 51 (2023)
    87–99.
date_created: 2023-01-27T10:08:19Z
date_published: 2023-02-01T00:00:00Z
date_updated: 2023-08-01T12:55:32Z
day: '01'
ddc:
- '570'
department:
- _id: FlSc
doi: 10.1042/bst20220221
external_id:
  isi:
  - '000926043100001'
file:
- access_level: open_access
  checksum: 4e7069845e3dad22bb44fb71ec624c60
  content_type: application/pdf
  creator: dernst
  date_created: 2023-03-16T07:58:16Z
  date_updated: 2023-03-16T07:58:16Z
  file_id: '12728'
  file_name: 2023_BioChemicalSocietyTransactions_Faessler.pdf
  file_size: 10045006
  relation: main_file
  success: 1
file_date_updated: 2023-03-16T07:58:16Z
has_accepted_license: '1'
intvolume: '        51'
isi: 1
issue: '1'
keyword:
- Biochemistry
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 87-99
project:
- _id: 9B954C5C-BA93-11EA-9121-9846C619BF3A
  grant_number: P33367
  name: Structure and isoform diversity of the Arp2/3 complex
publication: Biochemical Society Transactions
publication_identifier:
  eissn:
  - 1470-8752
  issn:
  - 0300-5127
publication_status: published
publisher: Portland Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Deciphering the molecular mechanisms of actin cytoskeleton regulation in cell
  migration using cryo-EM
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 51
year: '2023'
...
---
_id: '12427'
abstract:
- lang: eng
  text: 'Let k be a number field and X a smooth, geometrically integral quasi-projective
    variety over k. For any linear algebraic group G over k and any G-torsor g : Z
    → X, we observe that if the étale-Brauer obstruction is the only one for strong
    approximation off a finite set of places S for all twists of Z by elements in
    H^1(k, G), then the étale-Brauer obstruction is the only one for strong approximation
    off a finite set of places S for X. As an application, we show that any homogeneous
    space of the form G/H with G a connected linear algebraic group over k satisfies
    strong approximation off the infinite places with étale-Brauer obstruction, under
    some compactness assumptions when k is totally real. We also prove more refined
    strong approximation results for homogeneous spaces of the form G/H with G semisimple
    simply connected and H finite, using the theory of torsors and descent.'
article_processing_charge: No
article_type: original
author:
- first_name: Francesca
  full_name: Balestrieri, Francesca
  id: 3ACCD756-F248-11E8-B48F-1D18A9856A87
  last_name: Balestrieri
citation:
  ama: Balestrieri F. Some remarks on strong approximation and applications to homogeneous
    spaces of linear algebraic groups. <i>Proceedings of the American Mathematical
    Society</i>. 2023;151(3):907-914. doi:<a href="https://doi.org/10.1090/proc/15239">10.1090/proc/15239</a>
  apa: Balestrieri, F. (2023). Some remarks on strong approximation and applications
    to homogeneous spaces of linear algebraic groups. <i>Proceedings of the American
    Mathematical Society</i>. American Mathematical Society. <a href="https://doi.org/10.1090/proc/15239">https://doi.org/10.1090/proc/15239</a>
  chicago: Balestrieri, Francesca. “Some Remarks on Strong Approximation and Applications
    to Homogeneous Spaces of Linear Algebraic Groups.” <i>Proceedings of the American
    Mathematical Society</i>. American Mathematical Society, 2023. <a href="https://doi.org/10.1090/proc/15239">https://doi.org/10.1090/proc/15239</a>.
  ieee: F. Balestrieri, “Some remarks on strong approximation and applications to
    homogeneous spaces of linear algebraic groups,” <i>Proceedings of the American
    Mathematical Society</i>, vol. 151, no. 3. American Mathematical Society, pp.
    907–914, 2023.
  ista: Balestrieri F. 2023. Some remarks on strong approximation and applications
    to homogeneous spaces of linear algebraic groups. Proceedings of the American
    Mathematical Society. 151(3), 907–914.
  mla: Balestrieri, Francesca. “Some Remarks on Strong Approximation and Applications
    to Homogeneous Spaces of Linear Algebraic Groups.” <i>Proceedings of the American
    Mathematical Society</i>, vol. 151, no. 3, American Mathematical Society, 2023,
    pp. 907–14, doi:<a href="https://doi.org/10.1090/proc/15239">10.1090/proc/15239</a>.
  short: F. Balestrieri, Proceedings of the American Mathematical Society 151 (2023)
    907–914.
date_created: 2023-01-29T23:00:58Z
date_published: 2023-01-01T00:00:00Z
date_updated: 2023-08-01T13:03:32Z
day: '01'
department:
- _id: TiBr
doi: 10.1090/proc/15239
external_id:
  isi:
  - '000898440000001'
intvolume: '       151'
isi: 1
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://hal.science/hal-03013498/
month: '01'
oa: 1
oa_version: Preprint
page: 907-914
publication: Proceedings of the American Mathematical Society
publication_identifier:
  eissn:
  - 1088-6826
  issn:
  - 0002-9939
publication_status: published
publisher: American Mathematical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Some remarks on strong approximation and applications to homogeneous spaces
  of linear algebraic groups
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 151
year: '2023'
...
---
_id: '12428'
abstract:
- lang: eng
  text: The mammary gland consists of a bilayered epithelial structure with an extensively
    branched morphology. The majority of this epithelial tree is laid down during
    puberty, during which actively proliferating terminal end buds repeatedly elongate
    and bifurcate to form the basic structure of the ductal tree. Mammary ducts consist
    of a basal and luminal cell layer with a multitude of identified sub-lineages
    within both layers. The understanding of how these different cell lineages are
    cooperatively driving branching morphogenesis is a problem of crossing multiple
    scales, as this requires information on the macroscopic branched structure of
    the gland, as well as data on single-cell dynamics driving the morphogenic program.
    Here we describe a method to combine genetic lineage tracing with whole-gland
    branching analysis. Quantitative data on the global organ structure can be used
    to derive a model for mammary gland branching morphogenesis and provide a backbone
    on which the dynamics of individual cell lineages can be simulated and compared
    to lineage-tracing approaches. Eventually, these quantitative models and experiments
    allow to understand the couplings between the macroscopic shape of the mammary
    gland and the underlying single-cell dynamics driving branching morphogenesis.
alternative_title:
- Methods in Molecular Biology
article_processing_charge: No
author:
- 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: Colinda L.G.J.
  full_name: Scheele, Colinda L.G.J.
  last_name: Scheele
citation:
  ama: 'Hannezo EB, Scheele CLGJ. A Guide Toward Multi-scale and Quantitative Branching
    Analysis in the Mammary Gland. In: Margadant C, ed. <i>Cell Migration in Three
    Dimensions</i>. Vol 2608. MIMB. Springer Nature; 2023:183-205. doi:<a href="https://doi.org/10.1007/978-1-0716-2887-4_12">10.1007/978-1-0716-2887-4_12</a>'
  apa: Hannezo, E. B., &#38; Scheele, C. L. G. J. (2023). A Guide Toward Multi-scale
    and Quantitative Branching Analysis in the Mammary Gland. In C. Margadant (Ed.),
    <i>Cell Migration in Three Dimensions</i> (Vol. 2608, pp. 183–205). Springer Nature.
    <a href="https://doi.org/10.1007/978-1-0716-2887-4_12">https://doi.org/10.1007/978-1-0716-2887-4_12</a>
  chicago: Hannezo, Edouard B, and Colinda L.G.J. Scheele. “A Guide Toward Multi-Scale
    and Quantitative Branching Analysis in the Mammary Gland.” In <i>Cell Migration
    in Three Dimensions</i>, edited by Coert Margadant, 2608:183–205. MIMB. Springer
    Nature, 2023. <a href="https://doi.org/10.1007/978-1-0716-2887-4_12">https://doi.org/10.1007/978-1-0716-2887-4_12</a>.
  ieee: E. B. Hannezo and C. L. G. J. Scheele, “A Guide Toward Multi-scale and Quantitative
    Branching Analysis in the Mammary Gland,” in <i>Cell Migration in Three Dimensions</i>,
    vol. 2608, C. Margadant, Ed. Springer Nature, 2023, pp. 183–205.
  ista: 'Hannezo EB, Scheele CLGJ. 2023.A Guide Toward Multi-scale and Quantitative
    Branching Analysis in the Mammary Gland. In: Cell Migration in Three Dimensions.
    Methods in Molecular Biology, vol. 2608, 183–205.'
  mla: Hannezo, Edouard B., and Colinda L. G. J. Scheele. “A Guide Toward Multi-Scale
    and Quantitative Branching Analysis in the Mammary Gland.” <i>Cell Migration in
    Three Dimensions</i>, edited by Coert Margadant, vol. 2608, Springer Nature, 2023,
    pp. 183–205, doi:<a href="https://doi.org/10.1007/978-1-0716-2887-4_12">10.1007/978-1-0716-2887-4_12</a>.
  short: E.B. Hannezo, C.L.G.J. Scheele, in:, C. Margadant (Ed.), Cell Migration in
    Three Dimensions, Springer Nature, 2023, pp. 183–205.
date_created: 2023-01-29T23:00:58Z
date_published: 2023-01-19T00:00:00Z
date_updated: 2023-02-03T10:58:56Z
day: '19'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.1007/978-1-0716-2887-4_12
editor:
- first_name: Coert
  full_name: Margadant, Coert
  last_name: Margadant
external_id:
  pmid:
  - '36653709'
file:
- access_level: open_access
  checksum: aec1b8d3ba938ddf9d8fcb777f3c38ee
  content_type: application/pdf
  creator: dernst
  date_created: 2023-02-03T10:56:39Z
  date_updated: 2023-02-03T10:56:39Z
  file_id: '12500'
  file_name: 2023_MIMB_Hannezo.pdf
  file_size: 826598
  relation: main_file
  success: 1
file_date_updated: 2023-02-03T10:56:39Z
has_accepted_license: '1'
intvolume: '      2608'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 183-205
pmid: 1
publication: Cell Migration in Three Dimensions
publication_identifier:
  eisbn:
  - '9781071628874'
  eissn:
  - 1940-6029
  isbn:
  - '9781071628867'
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
series_title: MIMB
status: public
title: A Guide Toward Multi-scale and Quantitative Branching Analysis in the Mammary
  Gland
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: book_chapter
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 2608
year: '2023'
...
---
_id: '12429'
abstract:
- lang: eng
  text: In this paper, we consider traces at initial times for functions with mixed
    time-space smoothness. Such results are often needed in the theory of evolution
    equations. Our result extends and unifies many previous results. Our main improvement
    is that we can allow general interpolation couples. The abstract results are applied
    to regularity problems for fractional evolution equations and stochastic evolution
    equations, where uniform trace estimates on the half-line are shown.
acknowledgement: The first author has been partially supported by the Nachwuchsring—Network
  for the promotion of young scientists—at TU Kaiserslautern. The second and third
  authors were supported by the Vidi subsidy 639.032.427 of the Netherlands Organisation
  for Scientific Research (NWO).
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Antonio
  full_name: Agresti, Antonio
  id: 673cd0cc-9b9a-11eb-b144-88f30e1fbb72
  last_name: Agresti
  orcid: 0000-0002-9573-2962
- first_name: Nick
  full_name: Lindemulder, Nick
  last_name: Lindemulder
- first_name: Mark
  full_name: Veraar, Mark
  last_name: Veraar
citation:
  ama: Agresti A, Lindemulder N, Veraar M. On the trace embedding and its applications
    to evolution equations. <i>Mathematische Nachrichten</i>. 2023;296(4):1319-1350.
    doi:<a href="https://doi.org/10.1002/mana.202100192">10.1002/mana.202100192</a>
  apa: Agresti, A., Lindemulder, N., &#38; Veraar, M. (2023). On the trace embedding
    and its applications to evolution equations. <i>Mathematische Nachrichten</i>.
    Wiley. <a href="https://doi.org/10.1002/mana.202100192">https://doi.org/10.1002/mana.202100192</a>
  chicago: Agresti, Antonio, Nick Lindemulder, and Mark Veraar. “On the Trace Embedding
    and Its Applications to Evolution Equations.” <i>Mathematische Nachrichten</i>.
    Wiley, 2023. <a href="https://doi.org/10.1002/mana.202100192">https://doi.org/10.1002/mana.202100192</a>.
  ieee: A. Agresti, N. Lindemulder, and M. Veraar, “On the trace embedding and its
    applications to evolution equations,” <i>Mathematische Nachrichten</i>, vol. 296,
    no. 4. Wiley, pp. 1319–1350, 2023.
  ista: Agresti A, Lindemulder N, Veraar M. 2023. On the trace embedding and its applications
    to evolution equations. Mathematische Nachrichten. 296(4), 1319–1350.
  mla: Agresti, Antonio, et al. “On the Trace Embedding and Its Applications to Evolution
    Equations.” <i>Mathematische Nachrichten</i>, vol. 296, no. 4, Wiley, 2023, pp.
    1319–50, doi:<a href="https://doi.org/10.1002/mana.202100192">10.1002/mana.202100192</a>.
  short: A. Agresti, N. Lindemulder, M. Veraar, Mathematische Nachrichten 296 (2023)
    1319–1350.
date_created: 2023-01-29T23:00:59Z
date_published: 2023-04-01T00:00:00Z
date_updated: 2023-08-16T11:41:42Z
day: '01'
ddc:
- '510'
department:
- _id: JuFi
doi: 10.1002/mana.202100192
external_id:
  arxiv:
  - '2104.05063'
  isi:
  - '000914134900001'
file:
- access_level: open_access
  checksum: 6f099f1d064173784d1a27716a2cc795
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T11:40:02Z
  date_updated: 2023-08-16T11:40:02Z
  file_id: '14067'
  file_name: 2023_MathNachrichten_Agresti.pdf
  file_size: 449280
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T11:40:02Z
has_accepted_license: '1'
intvolume: '       296'
isi: 1
issue: '4'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc/4.0/
month: '04'
oa: 1
oa_version: Published Version
page: 1319-1350
publication: Mathematische Nachrichten
publication_identifier:
  eissn:
  - 1522-2616
  issn:
  - 0025-584X
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: On the trace embedding and its applications to evolution equations
tmp:
  image: /images/cc_by_nc.png
  legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
  short: CC BY-NC (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 296
year: '2023'
...
---
_id: '12430'
abstract:
- lang: eng
  text: We study the time evolution of the Nelson model in a mean-field limit in which
    N nonrelativistic bosons weakly couple (with respect to the particle number) to
    a positive or zero mass quantized scalar field. Our main result is the derivation
    of the Bogoliubov dynamics and higher-order corrections. More precisely, we prove
    the convergence of the approximate wave function to the many-body wave function
    in norm, with a convergence rate proportional to the number of corrections taken
    into account in the approximation. We prove an analogous result for the unitary
    propagator. As an application, we derive a simple system of partial differential
    equations describing the time evolution of the first- and second-order approximations
    to the one-particle reduced density matrices of the particles and the quantum
    field, respectively.
article_number: '2350006'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Marco
  full_name: Falconi, Marco
  last_name: Falconi
- first_name: Nikolai K
  full_name: Leopold, Nikolai K
  id: 4BC40BEC-F248-11E8-B48F-1D18A9856A87
  last_name: Leopold
  orcid: 0000-0002-0495-6822
- first_name: David Johannes
  full_name: Mitrouskas, David Johannes
  id: cbddacee-2b11-11eb-a02e-a2e14d04e52d
  last_name: Mitrouskas
- first_name: Sören P
  full_name: Petrat, Sören P
  id: 40AC02DC-F248-11E8-B48F-1D18A9856A87
  last_name: Petrat
  orcid: 0000-0002-9166-5889
citation:
  ama: Falconi M, Leopold NK, Mitrouskas DJ, Petrat SP. Bogoliubov dynamics and higher-order
    corrections for the regularized Nelson model. <i>Reviews in Mathematical Physics</i>.
    2023;35(4). doi:<a href="https://doi.org/10.1142/S0129055X2350006X">10.1142/S0129055X2350006X</a>
  apa: Falconi, M., Leopold, N. K., Mitrouskas, D. J., &#38; Petrat, S. P. (2023).
    Bogoliubov dynamics and higher-order corrections for the regularized Nelson model.
    <i>Reviews in Mathematical Physics</i>. World Scientific Publishing. <a href="https://doi.org/10.1142/S0129055X2350006X">https://doi.org/10.1142/S0129055X2350006X</a>
  chicago: Falconi, Marco, Nikolai K Leopold, David Johannes Mitrouskas, and Sören
    P Petrat. “Bogoliubov Dynamics and Higher-Order Corrections for the Regularized
    Nelson Model.” <i>Reviews in Mathematical Physics</i>. World Scientific Publishing,
    2023. <a href="https://doi.org/10.1142/S0129055X2350006X">https://doi.org/10.1142/S0129055X2350006X</a>.
  ieee: M. Falconi, N. K. Leopold, D. J. Mitrouskas, and S. P. Petrat, “Bogoliubov
    dynamics and higher-order corrections for the regularized Nelson model,” <i>Reviews
    in Mathematical Physics</i>, vol. 35, no. 4. World Scientific Publishing, 2023.
  ista: Falconi M, Leopold NK, Mitrouskas DJ, Petrat SP. 2023. Bogoliubov dynamics
    and higher-order corrections for the regularized Nelson model. Reviews in Mathematical
    Physics. 35(4), 2350006.
  mla: Falconi, Marco, et al. “Bogoliubov Dynamics and Higher-Order Corrections for
    the Regularized Nelson Model.” <i>Reviews in Mathematical Physics</i>, vol. 35,
    no. 4, 2350006, World Scientific Publishing, 2023, doi:<a href="https://doi.org/10.1142/S0129055X2350006X">10.1142/S0129055X2350006X</a>.
  short: M. Falconi, N.K. Leopold, D.J. Mitrouskas, S.P. Petrat, Reviews in Mathematical
    Physics 35 (2023).
date_created: 2023-01-29T23:00:59Z
date_published: 2023-01-09T00:00:00Z
date_updated: 2023-08-16T11:47:27Z
day: '09'
department:
- _id: RoSe
doi: 10.1142/S0129055X2350006X
external_id:
  arxiv:
  - '2110.00458'
  isi:
  - '000909760300001'
intvolume: '        35'
isi: 1
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: ' https://doi.org/10.48550/arXiv.2110.00458'
month: '01'
oa: 1
oa_version: Preprint
publication: Reviews in Mathematical Physics
publication_identifier:
  issn:
  - 0129-055X
publication_status: published
publisher: World Scientific Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Bogoliubov dynamics and higher-order corrections for the regularized Nelson
  model
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 35
year: '2023'
...
---
_id: '12467'
abstract:
- lang: eng
  text: Safety and liveness are elementary concepts of computation, and the foundation
    of many verification paradigms. The safety-liveness classification of boolean
    properties characterizes whether a given property can be falsified by observing
    a finite prefix of an infinite computation trace (always for safety, never for
    liveness). In quantitative specification and verification, properties assign not
    truth values, but quantitative values to infinite traces (e.g., a cost, or the
    distance to a boolean property). We introduce quantitative safety and liveness,
    and we prove that our definitions induce conservative quantitative generalizations
    of both (1)~the safety-progress hierarchy of boolean properties and (2)~the safety-liveness
    decomposition of boolean properties. In particular, we show that every quantitative
    property can be written as the pointwise minimum of a quantitative safety property
    and a quantitative liveness property. Consequently, like boolean properties, also
    quantitative properties can be min-decomposed into safety and liveness parts,
    or alternatively, max-decomposed into co-safety and co-liveness parts. Moreover,
    quantitative properties can be approximated naturally. We prove that every quantitative
    property that has both safe and co-safe approximations can be monitored arbitrarily
    precisely by a monitor that uses only a finite number of states.
acknowledgement: We thank the anonymous reviewers for their helpful comments. This
  work was supported in part by the ERC-2020-AdG 101020093.
alternative_title:
- LNCS
article_processing_charge: No
arxiv: 1
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000-0002-2985-7724
- first_name: Nicolas Adrien
  full_name: Mazzocchi, Nicolas Adrien
  id: b26baa86-3308-11ec-87b0-8990f34baa85
  last_name: Mazzocchi
- first_name: Naci E
  full_name: Sarac, Naci E
  id: 8C6B42F8-C8E6-11E9-A03A-F2DCE5697425
  last_name: Sarac
citation:
  ama: 'Henzinger TA, Mazzocchi NA, Sarac NE. Quantitative safety and liveness. In:
    <i>26th International Conference Foundations of Software Science and Computation
    Structures</i>. Vol 13992. Springer Nature; 2023:349-370. doi:<a href="https://doi.org/10.1007/978-3-031-30829-1_17">10.1007/978-3-031-30829-1_17</a>'
  apa: 'Henzinger, T. A., Mazzocchi, N. A., &#38; Sarac, N. E. (2023). Quantitative
    safety and liveness. In <i>26th International Conference Foundations of Software
    Science and Computation Structures</i> (Vol. 13992, pp. 349–370). Paris, France:
    Springer Nature. <a href="https://doi.org/10.1007/978-3-031-30829-1_17">https://doi.org/10.1007/978-3-031-30829-1_17</a>'
  chicago: Henzinger, Thomas A, Nicolas Adrien Mazzocchi, and Naci E Sarac. “Quantitative
    Safety and Liveness.” In <i>26th International Conference Foundations of Software
    Science and Computation Structures</i>, 13992:349–70. Springer Nature, 2023. <a
    href="https://doi.org/10.1007/978-3-031-30829-1_17">https://doi.org/10.1007/978-3-031-30829-1_17</a>.
  ieee: T. A. Henzinger, N. A. Mazzocchi, and N. E. Sarac, “Quantitative safety and
    liveness,” in <i>26th International Conference Foundations of Software Science
    and Computation Structures</i>, Paris, France, 2023, vol. 13992, pp. 349–370.
  ista: 'Henzinger TA, Mazzocchi NA, Sarac NE. 2023. Quantitative safety and liveness.
    26th International Conference Foundations of Software Science and Computation
    Structures. FOSSACS: Foundations of Software Science and Computation Structures,
    LNCS, vol. 13992, 349–370.'
  mla: Henzinger, Thomas A., et al. “Quantitative Safety and Liveness.” <i>26th International
    Conference Foundations of Software Science and Computation Structures</i>, vol.
    13992, Springer Nature, 2023, pp. 349–70, doi:<a href="https://doi.org/10.1007/978-3-031-30829-1_17">10.1007/978-3-031-30829-1_17</a>.
  short: T.A. Henzinger, N.A. Mazzocchi, N.E. Sarac, in:, 26th International Conference
    Foundations of Software Science and Computation Structures, Springer Nature, 2023,
    pp. 349–370.
conference:
  end_date: 2023-04-27
  location: Paris, France
  name: 'FOSSACS: Foundations of Software Science and Computation Structures'
  start_date: 2023-04-22
date_created: 2023-01-31T07:23:56Z
date_published: 2023-04-21T00:00:00Z
date_updated: 2023-07-14T11:20:27Z
day: '21'
ddc:
- '000'
department:
- _id: GradSch
- _id: ToHe
doi: 10.1007/978-3-031-30829-1_17
ec_funded: 1
external_id:
  arxiv:
  - '2301.11175'
file:
- access_level: open_access
  checksum: 981025aed580b6b27c426cb8856cf63e
  content_type: application/pdf
  creator: esarac
  date_created: 2023-01-31T07:22:21Z
  date_updated: 2023-01-31T07:22:21Z
  file_id: '12468'
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  creator: dernst
  date_created: 2023-06-19T10:28:09Z
  date_updated: 2023-06-19T10:28:09Z
  file_id: '13153'
  file_name: 2023_LNCS_HenzingerT.pdf
  file_size: 1048171
  relation: main_file
  success: 1
file_date_updated: 2023-06-19T10:28:09Z
has_accepted_license: '1'
intvolume: '     13992'
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
page: 349-370
project:
- _id: 62781420-2b32-11ec-9570-8d9b63373d4d
  call_identifier: H2020
  grant_number: '101020093'
  name: Vigilant Algorithmic Monitoring of Software
publication: 26th International Conference Foundations of Software Science and Computation
  Structures
publication_identifier:
  eissn:
  - 1611-3349
  isbn:
  - '9783031308284'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Quantitative safety and liveness
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: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 13992
year: '2023'
...
---
_id: '12469'
abstract:
- lang: eng
  text: 'Hosts can carry many viruses in their bodies, but not all of them cause disease.
    We studied ants as a social host to determine both their overall viral repertoire
    and the subset of actively infecting viruses across natural populations of three
    subfamilies: the Argentine ant (Linepithema humile, Dolichoderinae), the invasive
    garden ant (Lasius neglectus, Formicinae) and the red ant (Myrmica rubra, Myrmicinae).
    We used a dual sequencing strategy to reconstruct complete virus genomes by RNA-seq
    and to simultaneously determine the small interfering RNAs (siRNAs) by small RNA
    sequencing (sRNA-seq), which constitute the host antiviral RNAi immune response.
    This approach led to the discovery of 41 novel viruses in ants and revealed a
    host ant-specific RNAi response (21 vs. 22 nt siRNAs) in the different ant species.
    The efficiency of the RNAi response (sRNA/RNA read count ratio) depended on the
    virus and the respective ant species, but not its population. Overall, we found
    the highest virus abundance and diversity per population in Li. humile, followed
    by La. neglectus and M. rubra. Argentine ants also shared a high proportion of
    viruses between populations, whilst overlap was nearly absent in M. rubra. Only
    one of the 59 viruses was found to infect two of the ant species as hosts, revealing
    high host-specificity in active infections. In contrast, six viruses actively
    infected one ant species, but were found as contaminants only in the others. Disentangling
    spillover of disease-causing infection from non-infecting contamination across
    species is providing relevant information for disease ecology and ecosystem management.'
acknowledgement: "We thank D.J. Obbard for sharing the details of the dual RNA-seq/sRNA-seq
  approach, S.\r\nMetzler and R. Ferrigato for the photographs (Figure 1), M. Konrad,
  B. Casillas-Perez, C.D.\r\nPull and X. Espadaler for help with ant collection, and
  the Social Immunity Team at IST\r\nAustria, in particular J. Robb, A. Franschitz,
  E. Naderlinger, E. Dawson and B. Casillas-Perez\r\nfor support and comments on the
  manuscript. The study was funded by the Austrian Science\r\nFund (FWF; M02076-B25
  to MAF) and the Academy of Finland (343022 to LV). "
article_number: '1119002'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Lumi
  full_name: Viljakainen, Lumi
  last_name: Viljakainen
- first_name: Matthias
  full_name: Fürst, Matthias
  id: 393B1196-F248-11E8-B48F-1D18A9856A87
  last_name: Fürst
  orcid: 0000-0002-3712-925X
- first_name: Anna V
  full_name: Grasse, Anna V
  id: 406F989C-F248-11E8-B48F-1D18A9856A87
  last_name: Grasse
- first_name: Jaana
  full_name: Jurvansuu, Jaana
  last_name: Jurvansuu
- first_name: Jinook
  full_name: Oh, Jinook
  id: 403169A4-080F-11EA-9993-BF3F3DDC885E
  last_name: Oh
  orcid: 0000-0001-7425-2372
- first_name: Lassi
  full_name: Tolonen, Lassi
  last_name: Tolonen
- first_name: Thomas
  full_name: Eder, Thomas
  last_name: Eder
- first_name: Thomas
  full_name: Rattei, Thomas
  last_name: Rattei
- first_name: Sylvia
  full_name: Cremer, Sylvia
  id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
  last_name: Cremer
  orcid: 0000-0002-2193-3868
citation:
  ama: Viljakainen L, Fürst M, Grasse AV, et al. Antiviral immune response reveals
    host-specific virus infections in natural ant populations. <i>Frontiers in Microbiology</i>.
    2023;14. doi:<a href="https://doi.org/10.3389/fmicb.2023.1119002">10.3389/fmicb.2023.1119002</a>
  apa: Viljakainen, L., Fürst, M., Grasse, A. V., Jurvansuu, J., Oh, J., Tolonen,
    L., … Cremer, S. (2023). Antiviral immune response reveals host-specific virus
    infections in natural ant populations. <i>Frontiers in Microbiology</i>. Frontiers.
    <a href="https://doi.org/10.3389/fmicb.2023.1119002">https://doi.org/10.3389/fmicb.2023.1119002</a>
  chicago: Viljakainen, Lumi, Matthias Fürst, Anna V Grasse, Jaana Jurvansuu, Jinook
    Oh, Lassi Tolonen, Thomas Eder, Thomas Rattei, and Sylvia Cremer. “Antiviral Immune
    Response Reveals Host-Specific Virus Infections in Natural Ant Populations.” <i>Frontiers
    in Microbiology</i>. Frontiers, 2023. <a href="https://doi.org/10.3389/fmicb.2023.1119002">https://doi.org/10.3389/fmicb.2023.1119002</a>.
  ieee: L. Viljakainen <i>et al.</i>, “Antiviral immune response reveals host-specific
    virus infections in natural ant populations,” <i>Frontiers in Microbiology</i>,
    vol. 14. Frontiers, 2023.
  ista: Viljakainen L, Fürst M, Grasse AV, Jurvansuu J, Oh J, Tolonen L, Eder T, Rattei
    T, Cremer S. 2023. Antiviral immune response reveals host-specific virus infections
    in natural ant populations. Frontiers in Microbiology. 14, 1119002.
  mla: Viljakainen, Lumi, et al. “Antiviral Immune Response Reveals Host-Specific
    Virus Infections in Natural Ant Populations.” <i>Frontiers in Microbiology</i>,
    vol. 14, 1119002, Frontiers, 2023, doi:<a href="https://doi.org/10.3389/fmicb.2023.1119002">10.3389/fmicb.2023.1119002</a>.
  short: L. Viljakainen, M. Fürst, A.V. Grasse, J. Jurvansuu, J. Oh, L. Tolonen, T.
    Eder, T. Rattei, S. Cremer, Frontiers in Microbiology 14 (2023).
date_created: 2023-01-31T08:13:40Z
date_published: 2023-03-16T00:00:00Z
date_updated: 2023-08-01T12:39:58Z
day: '16'
ddc:
- '570'
department:
- _id: SyCr
doi: 10.3389/fmicb.2023.1119002
external_id:
  isi:
  - '000961542100001'
  pmid:
  - 'PPR559293 '
file:
- access_level: open_access
  checksum: cd52292963acce1111634d9fac08c699
  content_type: application/pdf
  creator: dernst
  date_created: 2023-04-17T07:49:09Z
  date_updated: 2023-04-17T07:49:09Z
  file_id: '12843'
  file_name: 2023_FrontMicrobiology_Viljakainen.pdf
  file_size: 4866332
  relation: main_file
  success: 1
file_date_updated: 2023-04-17T07:49:09Z
has_accepted_license: '1'
intvolume: '        14'
isi: 1
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 25DF61D8-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: M02076
  name: Viral pathogens and social immunity in ants
publication: Frontiers in Microbiology
publication_identifier:
  eissn:
  - 1664-302X
publication_status: published
publisher: Frontiers
quality_controlled: '1'
scopus_import: '1'
status: public
title: Antiviral immune response reveals host-specific virus infections in natural
  ant populations
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 14
year: '2023'
...
---
_id: '12470'
abstract:
- lang: eng
  text: "The brain is an exceptionally sophisticated organ consisting of billions
    of cells and trillions of \r\nconnections that orchestrate our cognition and behavior.
    To decode its complex connectivity, it is \r\npivotal to disentangle its intricate
    architecture spanning from cm-sized circuits down to tens of \r\nnm-small synapses.\r\nTo
    achieve this goal, I developed CATS – Comprehensive Analysis of nervous Tissue
    across \r\nScales, a versatile toolbox for obtaining a holistic view of nervous
    tissue context with (super\x02resolution) fluorescence microscopy. CATS combines
    comprehensive labeling of the extracellular\r\nspace, that is compatible with
    chemical fixation, with information on molecular markers, super\x02resolved data
    acquisition and machine-learning based data analysis for segmentation and synapse
    \r\nidentification.\r\nI used CATS to analyze key features of nervous tissue connectivity,
    ranging from whole tissue \r\narchitecture, neuronal in- and output-fields, down
    to synapse morphology.\r\nFocusing on the hippocampal circuitry, I quantified
    synaptic transmission properties of mossy \r\nfiber boutons and analyzed the connectivity
    pattern of dentate gyrus granule cells with CA3 \r\npyramidal neurons. This shows
    that CATS is a viable tool to study hallmarks of neuronal \r\nconnectivity with
    light microscopy."
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: PreCl
- _id: EM-Fac
- _id: M-Shop
- _id: ScienComp
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Julia M
  full_name: Michalska, Julia M
  id: 443DB6DE-F248-11E8-B48F-1D18A9856A87
  last_name: Michalska
  orcid: 0000-0003-3862-1235
citation:
  ama: Michalska JM. A versatile toolbox for the comprehensive analysis of nervous
    tissue organization with light microscopy. 2023. doi:<a href="https://doi.org/10.15479/at:ista:12470">10.15479/at:ista:12470</a>
  apa: Michalska, J. M. (2023). <i>A versatile toolbox for the comprehensive analysis
    of nervous tissue organization with light microscopy</i>. Institute of Science
    and Technology Austria. <a href="https://doi.org/10.15479/at:ista:12470">https://doi.org/10.15479/at:ista:12470</a>
  chicago: Michalska, Julia M. “A Versatile Toolbox for the Comprehensive Analysis
    of Nervous Tissue Organization with Light Microscopy.” Institute of Science and
    Technology Austria, 2023. <a href="https://doi.org/10.15479/at:ista:12470">https://doi.org/10.15479/at:ista:12470</a>.
  ieee: J. M. Michalska, “A versatile toolbox for the comprehensive analysis of nervous
    tissue organization with light microscopy,” Institute of Science and Technology
    Austria, 2023.
  ista: Michalska JM. 2023. A versatile toolbox for the comprehensive analysis of
    nervous tissue organization with light microscopy. Institute of Science and Technology
    Austria.
  mla: Michalska, Julia M. <i>A Versatile Toolbox for the Comprehensive Analysis of
    Nervous Tissue Organization with Light Microscopy</i>. Institute of Science and
    Technology Austria, 2023, doi:<a href="https://doi.org/10.15479/at:ista:12470">10.15479/at:ista:12470</a>.
  short: J.M. Michalska, A Versatile Toolbox for the Comprehensive Analysis of Nervous
    Tissue Organization with Light Microscopy, Institute of Science and Technology
    Austria, 2023.
date_created: 2023-01-31T15:10:53Z
date_published: 2023-01-09T00:00:00Z
date_updated: 2023-08-31T12:26:58Z
day: '09'
ddc:
- '610'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JoDa
doi: 10.15479/at:ista:12470
ec_funded: 1
file:
- access_level: open_access
  checksum: 1a2306e5f59f52df598e7ecfadf921ac
  content_type: application/pdf
  creator: cchlebak
  date_created: 2023-01-31T15:11:42Z
  date_updated: 2023-07-27T22:30:54Z
  embargo: 2023-07-09
  file_id: '12471'
  file_name: 20230109_PhD_thesis_JM_final.pdf
  file_size: 41771714
  relation: main_file
- access_level: closed
  checksum: 0bebbdee0773443959e1f6ab8caf281f
  content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
  creator: cchlebak
  date_created: 2023-01-31T15:11:51Z
  date_updated: 2023-07-10T22:30:04Z
  embargo_to: open_access
  file_id: '12472'
  file_name: 20230109_PhD_thesis_JM_final.docx
  file_size: 66983464
  relation: source_file
file_date_updated: 2023-07-27T22:30:54Z
has_accepted_license: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: '201'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 26AA4EF2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W1232-B24
  name: Molecular Drug Targets
publication_identifier:
  isbn:
  - ' 978-3-99078-026-8'
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '11943'
    relation: part_of_dissertation
    status: public
  - id: '11950'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Johann G
  full_name: Danzl, Johann G
  id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87
  last_name: Danzl
  orcid: 0000-0001-8559-3973
title: A versatile toolbox for the comprehensive analysis of nervous tissue organization
  with light microscopy
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: '12478'
abstract:
- lang: eng
  text: In Gram negative bacteria, the multiple antibiotic resistance or mar operon,
    is known to control the expression of multi-drug efflux genes that protect bacteria
    from a wide range of drugs. As many different chemical compounds can induce this
    operon, identifying the parameters that govern the dynamics of its induction is
    crucial to better characterize the processes of tolerance and resistance. Most
    experiments have assumed that the properties of the mar transcriptional network
    can be inferred from population measurements. However, measurements from an asynchronous
    population of cells can mask underlying phenotypic variations of single cells.
    We monitored the activity of the mar promoter in single Escherichia coli cells
    in linear micro-colonies and established that the response to a steady level of
    inducer was most heterogeneous within individual colonies for an intermediate
    value of inducer. Specifically, sub-lineages defined by contiguous daughter-cells
    exhibited similar promoter activity, whereas activity was greatly variable between
    different sub-lineages. Specific sub-trees of uniform promoter activity persisted
    over several generations. Statistical analyses of the lineages suggest that the
    presence of these sub-trees is the signature of an inducible memory of the promoter
    state that is transmitted from mother to daughter cells. This single-cell study
    reveals that the degree of epigenetic inheritance changes as a function of inducer
    concentration, suggesting that phenotypic inheritance may be an inducible phenotype.
acknowledgement: This work was supported by NIH P50 award P50GM081892-02 to the University
  of Chicago, a catalyst grant from the Chicago Biomedical Consortium with support
  from The Searle Funds at The Chicago Community Trust to PC, and a Yen Fellowship
  to CCG. MA was partially supported by PAPIIT-UNAM grant IN-11322.
article_number: '1049255'
article_processing_charge: Yes
article_type: original
author:
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
- first_name: L
  full_name: Bruneaux, L
  last_name: Bruneaux
- first_name: P
  full_name: Oikonomou, P
  last_name: Oikonomou
- first_name: M
  full_name: Aldana, M
  last_name: Aldana
- first_name: P
  full_name: Cluzel, P
  last_name: Cluzel
citation:
  ama: Guet CC, Bruneaux L, Oikonomou P, Aldana M, Cluzel P. Monitoring lineages of
    growing and dividing bacteria reveals an inducible memory of <i>mar</i> operon
    expression. <i>Frontiers in Microbiology</i>. 2023;14. doi:<a href="https://doi.org/10.3389/fmicb.2023.1049255">10.3389/fmicb.2023.1049255</a>
  apa: Guet, C. C., Bruneaux, L., Oikonomou, P., Aldana, M., &#38; Cluzel, P. (2023).
    Monitoring lineages of growing and dividing bacteria reveals an inducible memory
    of <i>mar</i> operon expression. <i>Frontiers in Microbiology</i>. Frontiers.
    <a href="https://doi.org/10.3389/fmicb.2023.1049255">https://doi.org/10.3389/fmicb.2023.1049255</a>
  chicago: Guet, Calin C, L Bruneaux, P Oikonomou, M Aldana, and P Cluzel. “Monitoring
    Lineages of Growing and Dividing Bacteria Reveals an Inducible Memory of <i>Mar</i>
    Operon Expression.” <i>Frontiers in Microbiology</i>. Frontiers, 2023. <a href="https://doi.org/10.3389/fmicb.2023.1049255">https://doi.org/10.3389/fmicb.2023.1049255</a>.
  ieee: C. C. Guet, L. Bruneaux, P. Oikonomou, M. Aldana, and P. Cluzel, “Monitoring
    lineages of growing and dividing bacteria reveals an inducible memory of <i>mar</i>
    operon expression,” <i>Frontiers in Microbiology</i>, vol. 14. Frontiers, 2023.
  ista: Guet CC, Bruneaux L, Oikonomou P, Aldana M, Cluzel P. 2023. Monitoring lineages
    of growing and dividing bacteria reveals an inducible memory of <i>mar</i> operon
    expression. Frontiers in Microbiology. 14, 1049255.
  mla: Guet, Calin C., et al. “Monitoring Lineages of Growing and Dividing Bacteria
    Reveals an Inducible Memory of <i>Mar</i> Operon Expression.” <i>Frontiers in
    Microbiology</i>, vol. 14, 1049255, Frontiers, 2023, doi:<a href="https://doi.org/10.3389/fmicb.2023.1049255">10.3389/fmicb.2023.1049255</a>.
  short: C.C. Guet, L. Bruneaux, P. Oikonomou, M. Aldana, P. Cluzel, Frontiers in
    Microbiology 14 (2023).
date_created: 2023-02-02T08:13:28Z
date_published: 2023-06-20T00:00:00Z
date_updated: 2023-08-02T06:25:04Z
day: '20'
ddc:
- '570'
department:
- _id: CaGu
doi: 10.3389/fmicb.2023.1049255
external_id:
  isi:
  - '001030002600001'
  pmid:
  - '37485524'
file:
- access_level: open_access
  checksum: 7dd322347512afaa5daf72a0154f2f07
  content_type: application/pdf
  creator: dernst
  date_created: 2023-07-31T07:16:34Z
  date_updated: 2023-07-31T07:16:34Z
  file_id: '13322'
  file_name: 2023_FrontiersMicrobiology_Guet.pdf
  file_size: 6452841
  relation: main_file
  success: 1
file_date_updated: 2023-07-31T07:16:34Z
has_accepted_license: '1'
intvolume: '        14'
isi: 1
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
publication: Frontiers in Microbiology
publication_identifier:
  eissn:
  - 1664-302X
publication_status: published
publisher: Frontiers
quality_controlled: '1'
scopus_import: '1'
status: public
title: Monitoring lineages of growing and dividing bacteria reveals an inducible memory
  of <i>mar</i> operon expression
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: '12486'
abstract:
- lang: eng
  text: This paper is concerned with the problem of regularization by noise of systems
    of reaction–diffusion equations with mass control. It is known that strong solutions
    to such systems of PDEs may blow-up in finite time. Moreover, for many systems
    of practical interest, establishing whether the blow-up occurs or not is an open
    question. Here we prove that a suitable multiplicative noise of transport type
    has a regularizing effect. More precisely, for both a sufficiently noise intensity
    and a high spectrum, the blow-up of strong solutions is delayed up to an arbitrary
    large time. Global existence is shown for the case of exponentially decreasing
    mass. The proofs combine and extend recent developments in regularization by noise
    and in the Lp(Lq)-approach to stochastic PDEs, highlighting new connections between
    the two areas.
acknowledgement: "The author has received funding from the European Research Council
  (ERC) under the European Union’s Horizon 2020 research and innovation programme
  (Grant Agreement No. 948819).\r\nThe author thanks Lorenzo Dello Schiavo, Lucio
  Galeati and Mark Veraar for helpful comments. The author acknowledges Caterina Balzotti
  for her support in creating the picture. The author\r\nthanks the anonymous referee
  for helpful comments. "
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Antonio
  full_name: Agresti, Antonio
  id: 673cd0cc-9b9a-11eb-b144-88f30e1fbb72
  last_name: Agresti
  orcid: 0000-0002-9573-2962
citation:
  ama: 'Agresti A. Delayed blow-up and enhanced diffusion by transport noise for systems
    of reaction-diffusion equations. <i>Stochastics and Partial Differential Equations:
    Analysis and Computations</i>. 2023. doi:<a href="https://doi.org/10.1007/s40072-023-00319-4">10.1007/s40072-023-00319-4</a>'
  apa: 'Agresti, A. (2023). Delayed blow-up and enhanced diffusion by transport noise
    for systems of reaction-diffusion equations. <i>Stochastics and Partial Differential
    Equations: Analysis and Computations</i>. Springer Nature. <a href="https://doi.org/10.1007/s40072-023-00319-4">https://doi.org/10.1007/s40072-023-00319-4</a>'
  chicago: 'Agresti, Antonio. “Delayed Blow-up and Enhanced Diffusion by Transport
    Noise for Systems of Reaction-Diffusion Equations.” <i>Stochastics and Partial
    Differential Equations: Analysis and Computations</i>. Springer Nature, 2023.
    <a href="https://doi.org/10.1007/s40072-023-00319-4">https://doi.org/10.1007/s40072-023-00319-4</a>.'
  ieee: 'A. Agresti, “Delayed blow-up and enhanced diffusion by transport noise for
    systems of reaction-diffusion equations,” <i>Stochastics and Partial Differential
    Equations: Analysis and Computations</i>. Springer Nature, 2023.'
  ista: 'Agresti A. 2023. Delayed blow-up and enhanced diffusion by transport noise
    for systems of reaction-diffusion equations. Stochastics and Partial Differential
    Equations: Analysis and Computations.'
  mla: 'Agresti, Antonio. “Delayed Blow-up and Enhanced Diffusion by Transport Noise
    for Systems of Reaction-Diffusion Equations.” <i>Stochastics and Partial Differential
    Equations: Analysis and Computations</i>, Springer Nature, 2023, doi:<a href="https://doi.org/10.1007/s40072-023-00319-4">10.1007/s40072-023-00319-4</a>.'
  short: 'A. Agresti, Stochastics and Partial Differential Equations: Analysis and
    Computations (2023).'
date_created: 2023-02-02T10:45:47Z
date_published: 2023-11-28T00:00:00Z
date_updated: 2023-12-18T07:53:45Z
day: '28'
ddc:
- '510'
department:
- _id: JuFi
doi: 10.1007/s40072-023-00319-4
ec_funded: 1
external_id:
  arxiv:
  - '2207.08293'
has_accepted_license: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1007/s40072-023-00319-4
month: '11'
oa: 1
oa_version: Submitted Version
project:
- _id: 0aa76401-070f-11eb-9043-b5bb049fa26d
  call_identifier: H2020
  grant_number: '948819'
  name: Bridging Scales in Random Materials
publication: 'Stochastics and Partial Differential Equations: Analysis and Computations'
publication_identifier:
  eissn:
  - 2194-041X
  issn:
  - 2194-0401
publication_status: epub_ahead
publisher: Springer Nature
scopus_import: '1'
status: public
title: Delayed blow-up and enhanced diffusion by transport noise for systems of reaction-diffusion
  equations
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
year: '2023'
...
---
_id: '12487'
abstract:
- lang: eng
  text: Sleep plays a key role in preserving brain function, keeping the brain network
    in a state that ensures optimal computational capabilities. Empirical evidence
    indicates that such a state is consistent with criticality, where scale-free neuronal
    avalanches emerge. However, the relationship between sleep, emergent avalanches,
    and criticality remains poorly understood. Here we fully characterize the critical
    behavior of avalanches during sleep, and study their relationship with the sleep
    macro- and micro-architecture, in particular the cyclic alternating pattern (CAP).
    We show that avalanche size and duration distributions exhibit robust power laws
    with exponents approximately equal to −3/2 e −2, respectively. Importantly, we
    find that sizes scale as a power law of the durations, and that all critical exponents
    for neuronal avalanches obey robust scaling relations, which are consistent with
    the mean-field directed percolation universality class. Our analysis demonstrates
    that avalanche dynamics depends on the position within the NREM-REM cycles, with
    the avalanche density increasing in the descending phases and decreasing in the
    ascending phases of sleep cycles. Moreover, we show that, within NREM sleep, avalanche
    occurrence correlates with CAP activation phases, particularly A1, which are the
    expression of slow wave sleep propensity and have been proposed to be beneficial
    for cognitive processes. The results suggest that neuronal avalanches, and thus
    tuning to criticality, actively contribute to sleep development and play a role
    in preserving network function. Such findings, alongside characterization of the
    universality class for avalanches, open new avenues to the investigation of functional
    role of criticality during sleep with potential clinical application.</jats:p><jats:sec><jats:title>Significance
    statement</jats:title><jats:p>We fully characterize the critical behavior of neuronal
    avalanches during sleep, and show that avalanches follow precise scaling laws
    that are consistent with the mean-field directed percolation universality class.
    The analysis provides first evidence of a functional relationship between avalanche
    occurrence, slow-wave sleep dynamics, sleep stage transitions and occurrence of
    CAP phase A during NREM sleep. Because CAP is considered one of the major guardians
    of NREM sleep that allows the brain to dynamically react to external perturbation
    and contributes to the cognitive consolidation processes occurring in sleep, our
    observations suggest that neuronal avalanches at criticality are associated with
    flexible response to external inputs and to cognitive processes, a key assumption
    of the critical brain hypothesis.
acknowledgement: FL acknowledges support from the European Union’s Horizon 2020 research
  and innovation program under the Marie Sklodowska-Curie Grant Agreement No. 754411,
  and from the Austrian Science Fund (FWF) under the Lise Meitner fellowship No. PT1013M03318.
  IA acknowledges financial support from the MIUR PRIN 2017WZFTZP.
article_processing_charge: Yes
article_type: original
author:
- first_name: Silvia
  full_name: Scarpetta, Silvia
  last_name: Scarpetta
- first_name: Niccolò
  full_name: Morrisi, Niccolò
  last_name: Morrisi
- first_name: Carlotta
  full_name: Mutti, Carlotta
  last_name: Mutti
- first_name: Nicoletta
  full_name: Azzi, Nicoletta
  last_name: Azzi
- first_name: Irene
  full_name: Trippi, Irene
  last_name: Trippi
- first_name: Rosario
  full_name: Ciliento, Rosario
  last_name: Ciliento
- first_name: Ilenia
  full_name: Apicella, Ilenia
  last_name: Apicella
- first_name: Giovanni
  full_name: Messuti, Giovanni
  last_name: Messuti
- first_name: Marianna
  full_name: Angiolelli, Marianna
  last_name: Angiolelli
- first_name: Fabrizio
  full_name: Lombardi, Fabrizio
  id: A057D288-3E88-11E9-986D-0CF4E5697425
  last_name: Lombardi
  orcid: 0000-0003-2623-5249
- first_name: Liborio
  full_name: Parrino, Liborio
  last_name: Parrino
- first_name: Anna Elisabetta
  full_name: Vaudano, Anna Elisabetta
  last_name: Vaudano
citation:
  ama: Scarpetta S, Morrisi N, Mutti C, et al. Criticality of neuronal avalanches
    in human sleep and their relationship with sleep macro- and micro-architecture.
    <i>iScience</i>. 2023;26(10):107840. doi:<a href="https://doi.org/10.1016/j.isci.2023.107840">10.1016/j.isci.2023.107840</a>
  apa: Scarpetta, S., Morrisi, N., Mutti, C., Azzi, N., Trippi, I., Ciliento, R.,
    … Vaudano, A. E. (2023). Criticality of neuronal avalanches in human sleep and
    their relationship with sleep macro- and micro-architecture. <i>IScience</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.isci.2023.107840">https://doi.org/10.1016/j.isci.2023.107840</a>
  chicago: Scarpetta, Silvia, Niccolò Morrisi, Carlotta Mutti, Nicoletta Azzi, Irene
    Trippi, Rosario Ciliento, Ilenia Apicella, et al. “Criticality of Neuronal Avalanches
    in Human Sleep and Their Relationship with Sleep Macro- and Micro-Architecture.”
    <i>IScience</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.isci.2023.107840">https://doi.org/10.1016/j.isci.2023.107840</a>.
  ieee: S. Scarpetta <i>et al.</i>, “Criticality of neuronal avalanches in human sleep
    and their relationship with sleep macro- and micro-architecture,” <i>iScience</i>,
    vol. 26, no. 10. Elsevier, p. 107840, 2023.
  ista: Scarpetta S, Morrisi N, Mutti C, Azzi N, Trippi I, Ciliento R, Apicella I,
    Messuti G, Angiolelli M, Lombardi F, Parrino L, Vaudano AE. 2023. Criticality
    of neuronal avalanches in human sleep and their relationship with sleep macro-
    and micro-architecture. iScience. 26(10), 107840.
  mla: Scarpetta, Silvia, et al. “Criticality of Neuronal Avalanches in Human Sleep
    and Their Relationship with Sleep Macro- and Micro-Architecture.” <i>IScience</i>,
    vol. 26, no. 10, Elsevier, 2023, p. 107840, doi:<a href="https://doi.org/10.1016/j.isci.2023.107840">10.1016/j.isci.2023.107840</a>.
  short: S. Scarpetta, N. Morrisi, C. Mutti, N. Azzi, I. Trippi, R. Ciliento, I. Apicella,
    G. Messuti, M. Angiolelli, F. Lombardi, L. Parrino, A.E. Vaudano, IScience 26
    (2023) 107840.
date_created: 2023-02-02T10:50:17Z
date_published: 2023-10-20T00:00:00Z
date_updated: 2023-12-13T11:11:24Z
day: '20'
ddc:
- '570'
department:
- _id: GaTk
doi: 10.1016/j.isci.2023.107840
ec_funded: 1
external_id:
  isi:
  - '001082331200001'
  pmid:
  - '37766992'
file:
- access_level: open_access
  checksum: f499836af172ecc9865de4bb41fa99d1
  content_type: application/pdf
  creator: dernst
  date_created: 2023-10-09T07:23:46Z
  date_updated: 2023-10-09T07:23:46Z
  file_id: '14412'
  file_name: 2023_iScience_Scarpetta.pdf
  file_size: 4872708
  relation: main_file
  success: 1
file_date_updated: 2023-10-09T07:23:46Z
has_accepted_license: '1'
intvolume: '        26'
isi: 1
issue: '10'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
page: '107840'
pmid: 1
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
- _id: eb943429-77a9-11ec-83b8-9f471cdf5c67
  grant_number: M03318
  name: Functional Advantages of Critical Brain Dynamics
publication: iScience
publication_identifier:
  eissn:
  - 2589-0042
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Criticality of neuronal avalanches in human sleep and their relationship with
  sleep macro- and micro-architecture
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 26
year: '2023'
...
---
_id: '12491'
abstract:
- lang: eng
  text: "The extracellular matrix (ECM) is a hydrated and complex three-dimensional
    network consisting of proteins, polysaccharides, and water. It provides structural
    scaffolding for the cells embedded within it and is essential in regulating numerous
    physiological processes, including cell migration and proliferation, wound healing,
    and stem cell fate. \r\nDespite extensive study, detailed structural knowledge
    of ECM components in physiologically relevant conditions is still rudimentary.
    This is due to methodological limitations in specimen preparation protocols which
    are incompatible with keeping large samples, such as the ECM, in their native
    state for subsequent imaging. Conventional electron microscopy (EM) techniques
    rely on fixation, dehydration, contrasting, and sectioning. This results in the
    alteration of a highly hydrated environment and the potential introduction of
    artifacts. Other structural biology techniques, such as nuclear magnetic resonance
    (NMR) spectroscopy and X-ray crystallography, allow high-resolution analysis of
    protein structures but only work on homogenous and purified samples, hence lacking
    contextual information. Currently, no approach exists for the ultrastructural
    and structural study of extracellular components under native conditions in a
    physiological, 3D environment. \r\nIn this thesis, I have developed a workflow
    that allows for the ultrastructural analysis of the ECM in near-native conditions
    at molecular resolution. The developments I introduced include implementing a
    novel specimen preparation workflow for cell-derived matrices (CDMs) to render
    them compatible with ion-beam milling and subsequent high-resolution cryo-electron
    tomography (ET). \r\nTo this end, I have established protocols to generate CDMs
    grown over several weeks on EM grids that are compatible with downstream cryo-EM
    sample preparation and imaging techniques. Characterization of these ECMs confirmed
    that they contain essential ECM components such as collagen I, collagen VI, and
    fibronectin I in high abundance and hence represent a bona fide biologically-relevant
    sample. I successfully optimized vitrification of these specimens by testing various
    vitrification techniques and cryoprotectants. \r\nIn order to obtain high-resolution
    molecular insights into the ultrastructure and organization of CDMs, I established
    cryo-focused ion beam scanning electron microscopy (FIBSEM) on these challenging
    and complex specimens. I explored different approaches for the creation of thin
    cryo-lamellae by FIB milling and succeeded in optimizing the cryo-lift-out technique,
    resulting in high-quality lamellae of approximately 200 nm thickness. \r\nHigh-resolution
    Cryo-ET of these lamellae revealed for the first time the architecture of native
    CDM in the context of matrix-secreting cells. This allowed for the in situ visualization
    of fibrillar matrix proteins such as collagen, laying the foundation for future
    structural and ultrastructural characterization of these proteins in their near-native
    environment. \r\nIn summary, in this thesis, I present a novel workflow that combines
    state-of-the-art cryo-EM specimen preparation and imaging technologies to permit
    characterization of the ECM, an important tissue component in higher organisms.
    This innovative and highly versatile workflow will enable addressing far-reaching
    questions on ECM architecture, composition, and reciprocal ECM-cell interactions."
acknowledged_ssus:
- _id: EM-Fac
- _id: LifeSc
- _id: Bio
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Bettina
  full_name: Zens, Bettina
  id: 45FD126C-F248-11E8-B48F-1D18A9856A87
  last_name: Zens
citation:
  ama: Zens B. Ultrastructural characterization of natively preserved extracellular
    matrix by cryo-electron tomography. 2023. doi:<a href="https://doi.org/10.15479/at:ista:12491">10.15479/at:ista:12491</a>
  apa: Zens, B. (2023). <i>Ultrastructural characterization of natively preserved
    extracellular matrix by cryo-electron tomography</i>. Institute of Science and
    Technology Austria. <a href="https://doi.org/10.15479/at:ista:12491">https://doi.org/10.15479/at:ista:12491</a>
  chicago: Zens, Bettina. “Ultrastructural Characterization of Natively Preserved
    Extracellular Matrix by Cryo-Electron Tomography.” Institute of Science and Technology
    Austria, 2023. <a href="https://doi.org/10.15479/at:ista:12491">https://doi.org/10.15479/at:ista:12491</a>.
  ieee: B. Zens, “Ultrastructural characterization of natively preserved extracellular
    matrix by cryo-electron tomography,” Institute of Science and Technology Austria,
    2023.
  ista: Zens B. 2023. Ultrastructural characterization of natively preserved extracellular
    matrix by cryo-electron tomography. Institute of Science and Technology Austria.
  mla: Zens, Bettina. <i>Ultrastructural Characterization of Natively Preserved Extracellular
    Matrix by Cryo-Electron Tomography</i>. Institute of Science and Technology Austria,
    2023, doi:<a href="https://doi.org/10.15479/at:ista:12491">10.15479/at:ista:12491</a>.
  short: B. Zens, Ultrastructural Characterization of Natively Preserved Extracellular
    Matrix by Cryo-Electron Tomography, Institute of Science and Technology Austria,
    2023.
date_created: 2023-02-02T14:50:20Z
date_published: 2023-02-02T00:00:00Z
date_updated: 2024-02-08T23:30:05Z
day: '02'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: FlSc
doi: 10.15479/at:ista:12491
file:
- access_level: open_access
  checksum: 069d87f025e0799bf9e3c375664264f2
  content_type: application/pdf
  creator: bzens
  date_created: 2023-02-07T13:07:38Z
  date_updated: 2024-02-08T23:30:04Z
  embargo: 2024-02-07
  file_id: '12527'
  file_name: PhDThesis_BettinaZens_2023_final.pdf
  file_size: 23082464
  relation: main_file
- access_level: closed
  checksum: 8c66ed203495d6e078ed1002a866520c
  content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
  creator: bzens
  date_created: 2023-02-07T13:09:05Z
  date_updated: 2024-02-08T23:30:04Z
  embargo_to: open_access
  file_id: '12528'
  file_name: PhDThesis_BettinaZens_2023_final.docx
  file_size: 106169509
  relation: source_file
file_date_updated: 2024-02-08T23:30:04Z
has_accepted_license: '1'
keyword:
- cryo-EM
- cryo-ET
- FIB milling
- method development
- FIBSEM
- extracellular matrix
- ECM
- cell-derived matrices
- CDMs
- cell culture
- high pressure freezing
- HPF
- structural biology
- tomography
- collagen
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: '187'
project:
- _id: eba3b5f6-77a9-11ec-83b8-cf0905748aa3
  name: Integrated visual proteomics of reciprocal cell-extracellular matrix interactions
- _id: 059B463C-7A3F-11EA-A408-12923DDC885E
  name: NÖ-Fonds Preis für die Jungforscherin des Jahres am IST Austria
publication_identifier:
  isbn:
  - 978-3-99078-027-5
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '8586'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Florian KM
  full_name: Schur, Florian KM
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
title: Ultrastructural characterization of natively preserved extracellular matrix
  by cryo-electron tomography
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2023'
...
---
_id: '12497'
abstract:
- lang: eng
  text: Aromatic side chains are important reporters of the plasticity of proteins,
    and often form important contacts in protein–protein interactions. We studied
    aromatic residues in the two structurally homologous cross-β amyloid fibrils HET-s,
    and  HELLF by employing a specific isotope-labeling approach and magic-angle-spinning
    NMR. The dynamic behavior of the aromatic residues Phe and Tyr indicates that
    the hydrophobic amyloid core is rigid, without any sign of "breathing motions"
    over hundreds of milliseconds at least. Aromatic residues exposed at the fibril
    surface have a rigid ring axis but undergo ring flips on a variety of time scales
    from nanoseconds to microseconds. Our approach provides direct insight into hydrophobic-core
    motions, enabling a better evaluation of the conformational heterogeneity generated
    from an NMR structural ensemble of such amyloid cross-β architecture.
article_processing_charge: No
author:
- first_name: Lea Marie
  full_name: Becker, Lea Marie
  id: 36336939-eb97-11eb-a6c2-c83f1214ca79
  last_name: Becker
  orcid: 0000-0002-6401-5151
- first_name: Paul
  full_name: Schanda, Paul
  id: 7B541462-FAF6-11E9-A490-E8DFE5697425
  last_name: Schanda
  orcid: 0000-0002-9350-7606
citation:
  ama: 'Becker LM, Schanda P. Research data to: The rigid core and flexible surface
    of amyloid fibrils probed by magic-angle-spinning NMR spectroscopy of aromatic
    residues. 2023. doi:<a href="https://doi.org/10.15479/AT:ISTA:12497">10.15479/AT:ISTA:12497</a>'
  apa: 'Becker, L. M., &#38; Schanda, P. (2023). Research data to: The rigid core
    and flexible surface of amyloid fibrils probed by magic-angle-spinning NMR spectroscopy
    of aromatic residues. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:12497">https://doi.org/10.15479/AT:ISTA:12497</a>'
  chicago: 'Becker, Lea Marie, and Paul Schanda. “Research Data to: The Rigid Core
    and Flexible Surface of Amyloid Fibrils Probed by Magic-Angle-Spinning NMR Spectroscopy
    of Aromatic Residues.” Institute of Science and Technology Austria, 2023. <a href="https://doi.org/10.15479/AT:ISTA:12497">https://doi.org/10.15479/AT:ISTA:12497</a>.'
  ieee: 'L. M. Becker and P. Schanda, “Research data to: The rigid core and flexible
    surface of amyloid fibrils probed by magic-angle-spinning NMR spectroscopy of
    aromatic residues.” Institute of Science and Technology Austria, 2023.'
  ista: 'Becker LM, Schanda P. 2023. Research data to: The rigid core and flexible
    surface of amyloid fibrils probed by magic-angle-spinning NMR spectroscopy of
    aromatic residues, Institute of Science and Technology Austria, <a href="https://doi.org/10.15479/AT:ISTA:12497">10.15479/AT:ISTA:12497</a>.'
  mla: 'Becker, Lea Marie, and Paul Schanda. <i>Research Data to: The Rigid Core and
    Flexible Surface of Amyloid Fibrils Probed by Magic-Angle-Spinning NMR Spectroscopy
    of Aromatic Residues</i>. Institute of Science and Technology Austria, 2023, doi:<a
    href="https://doi.org/10.15479/AT:ISTA:12497">10.15479/AT:ISTA:12497</a>.'
  short: L.M. Becker, P. Schanda, (2023).
contributor:
- contributor_type: researcher
  first_name: Mélanie
  last_name: Berbon
- contributor_type: researcher
  first_name: Alicia
  last_name: Vallet
- contributor_type: researcher
  first_name: Axelle
  last_name: Grelard
- contributor_type: researcher
  first_name: Estelle
  last_name: Morvan
- contributor_type: researcher
  first_name: Benjamin
  last_name: Bardiaux
- contributor_type: researcher
  first_name: Roman
  last_name: Lichtenecker
- contributor_type: researcher
  first_name: Matthias
  last_name: Ernst
- contributor_type: researcher
  first_name: Antoine
  last_name: Loquet
- contributor_type: contact_person
  first_name: Paul
  id: 7B541462-FAF6-11E9-A490-E8DFE5697425
  last_name: Schanda
  orcid: 0000-0002-9350-7606
- contributor_type: researcher
  first_name: Lea Marie
  id: 36336939-eb97-11eb-a6c2-c83f1214ca79
  last_name: Becker
  orcid: 0000-0002-6401-5151
date_created: 2023-02-03T08:08:02Z
date_published: 2023-03-23T00:00:00Z
date_updated: 2024-02-21T12:14:06Z
day: '23'
ddc:
- '572'
department:
- _id: GradSch
- _id: PaSc
doi: 10.15479/AT:ISTA:12497
file:
- access_level: open_access
  checksum: fd9a28620a81a82991fb70f4fd6591d9
  content_type: application/zip
  creator: lbecker
  date_created: 2023-03-23T10:03:16Z
  date_updated: 2023-03-24T09:34:20Z
  file_id: '12743'
  file_name: Research_Data.zip
  file_size: 87018103
  relation: main_file
- access_level: open_access
  checksum: 30ebdfb600af118fcf8518b6efe0b7e9
  content_type: text/plain
  creator: dernst
  date_created: 2023-03-24T07:13:55Z
  date_updated: 2023-03-24T09:42:03Z
  file_id: '12755'
  file_name: README.txt
  file_size: 747
  relation: main_file
file_date_updated: 2023-03-24T09:42:03Z
has_accepted_license: '1'
keyword:
- aromatic side chains
- isotopic labeling
- protein dynamics
- ring flips
- spin relaxation
month: '03'
oa: 1
oa_version: Published Version
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '12675'
    relation: used_in_publication
    status: public
status: public
title: 'Research data to: The rigid core and flexible surface of amyloid fibrils probed
  by magic-angle-spinning NMR spectroscopy of aromatic residues'
tmp:
  image: /images/cc_by_nc.png
  legal_code_url: https://creativecommons.org/licenses/by-nc/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
  short: CC BY-NC (4.0)
type: research_data
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '12514'
abstract:
- lang: eng
  text: The concept of a “speciation continuum” has gained popularity in recent decades.
    It emphasizes speciation as a continuous process that may be studied by comparing
    contemporary population pairs that show differing levels of divergence. In their
    recent perspective article in Evolution, Stankowski and Ravinet provided a valuable
    service by formally defining the speciation continuum as a continuum of reproductive
    isolation, based on opinions gathered from a survey of speciation researchers.
    While we agree that the speciation continuum has been a useful concept to advance
    the understanding of the speciation process, some intrinsic limitations exist.
    Here, we advocate for a multivariate extension, the speciation hypercube, first
    proposed by Dieckmann et al. in 2004, but rarely used since. We extend the idea
    of the speciation cube and suggest it has strong conceptual and practical advantages
    over a one-dimensional model. We illustrate how the speciation hypercube can be
    used to visualize and compare different speciation trajectories, providing new
    insights into the processes and mechanisms of speciation. A key strength of the
    speciation hypercube is that it provides a unifying framework for speciation research,
    as it allows questions from apparently disparate subfields to be addressed in
    a single conceptual model.
acknowledgement: "The authors of this article were supported by LMU Munich (J.B.W.W.),
  a James S. McDonnell Foundation postdoctoral fellowship (A.K.H.). P.N. received
  funding from the European Research Council (ERC) under the European Union’s Horizon
  2020 research and innovation program (Grant agreement No. 770826 EE-Dynamics).\r\nWe
  thank participants in the 2019 Gordon Conference on Speciation for the extensive
  conversation on this topic. Thanks to Dan Funk for providing permission to use data
  from Funk et al. 2006, and for comments on the manuscript."
article_processing_charge: No
article_type: original
author:
- first_name: Daniel I.
  full_name: Bolnick, Daniel I.
  last_name: Bolnick
- first_name: Amanda K.
  full_name: Hund, Amanda K.
  last_name: Hund
- first_name: Patrik
  full_name: Nosil, Patrik
  last_name: Nosil
- first_name: Foen
  full_name: Peng, Foen
  last_name: Peng
- first_name: Mark
  full_name: Ravinet, Mark
  last_name: Ravinet
- first_name: Sean
  full_name: Stankowski, Sean
  id: 43161670-5719-11EA-8025-FABC3DDC885E
  last_name: Stankowski
- first_name: Swapna
  full_name: Subramanian, Swapna
  last_name: Subramanian
- first_name: Jochen B.W.
  full_name: Wolf, Jochen B.W.
  last_name: Wolf
- first_name: Roman
  full_name: Yukilevich, Roman
  last_name: Yukilevich
citation:
  ama: 'Bolnick DI, Hund AK, Nosil P, et al. A multivariate view of the speciation
    continuum. <i>Evolution: International journal of organic evolution</i>. 2023;77(1):318-328.
    doi:<a href="https://doi.org/10.1093/evolut/qpac004">10.1093/evolut/qpac004</a>'
  apa: 'Bolnick, D. I., Hund, A. K., Nosil, P., Peng, F., Ravinet, M., Stankowski,
    S., … Yukilevich, R. (2023). A multivariate view of the speciation continuum.
    <i>Evolution: International Journal of Organic Evolution</i>. Oxford University
    Press. <a href="https://doi.org/10.1093/evolut/qpac004">https://doi.org/10.1093/evolut/qpac004</a>'
  chicago: 'Bolnick, Daniel I., Amanda K. Hund, Patrik Nosil, Foen Peng, Mark Ravinet,
    Sean Stankowski, Swapna Subramanian, Jochen B.W. Wolf, and Roman Yukilevich. “A
    Multivariate View of the Speciation Continuum.” <i>Evolution: International Journal
    of Organic Evolution</i>. Oxford University Press, 2023. <a href="https://doi.org/10.1093/evolut/qpac004">https://doi.org/10.1093/evolut/qpac004</a>.'
  ieee: 'D. I. Bolnick <i>et al.</i>, “A multivariate view of the speciation continuum,”
    <i>Evolution: International journal of organic evolution</i>, vol. 77, no. 1.
    Oxford University Press, pp. 318–328, 2023.'
  ista: 'Bolnick DI, Hund AK, Nosil P, Peng F, Ravinet M, Stankowski S, Subramanian
    S, Wolf JBW, Yukilevich R. 2023. A multivariate view of the speciation continuum.
    Evolution: International journal of organic evolution. 77(1), 318–328.'
  mla: 'Bolnick, Daniel I., et al. “A Multivariate View of the Speciation Continuum.”
    <i>Evolution: International Journal of Organic Evolution</i>, vol. 77, no. 1,
    Oxford University Press, 2023, pp. 318–28, doi:<a href="https://doi.org/10.1093/evolut/qpac004">10.1093/evolut/qpac004</a>.'
  short: 'D.I. Bolnick, A.K. Hund, P. Nosil, F. Peng, M. Ravinet, S. Stankowski, S.
    Subramanian, J.B.W. Wolf, R. Yukilevich, Evolution: International Journal of Organic
    Evolution 77 (2023) 318–328.'
date_created: 2023-02-05T23:00:59Z
date_published: 2023-01-01T00:00:00Z
date_updated: 2023-08-01T12:58:30Z
day: '01'
department:
- _id: NiBa
doi: 10.1093/evolut/qpac004
external_id:
  isi:
  - '001021686300024'
  pmid:
  - '36622661'
intvolume: '        77'
isi: 1
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1093/evolut/qpac004
month: '01'
oa: 1
oa_version: Published Version
page: 318-328
pmid: 1
publication: 'Evolution: International journal of organic evolution'
publication_identifier:
  eissn:
  - 1558-5646
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: A multivariate view of the speciation continuum
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 77
year: '2023'
...
---
_id: '12515'
abstract:
- lang: eng
  text: "Introduction: The olfactory system in most mammals is divided into several
    subsystems based on the anatomical locations of the neuroreceptor cells involved
    and the receptor families that are expressed. In addition to the main olfactory
    system and the vomeronasal system, a range of olfactory subsystems converge onto
    the transition zone located between the main olfactory bulb (MOB) and the accessory
    olfactory bulb (AOB), which has been termed the olfactory limbus (OL). The OL
    contains specialized glomeruli that receive noncanonical sensory afferences and
    which interact with the MOB and AOB. Little is known regarding the olfactory subsystems
    of mammals other than laboratory rodents.\r\nMethods: We have focused on characterizing
    the OL in the red fox by performing general and specific histological stainings
    on serial sections, using both single and double immunohistochemical and lectin-histochemical
    labeling techniques.\r\nResults: As a result, we have been able to determine that
    the OL of the red fox (Vulpes vulpes) displays an uncommonly high degree of development
    and complexity.\r\nDiscussion: This makes this species a novel mammalian model,
    the study of which could improve our understanding of the noncanonical pathways
    involved in the processing of chemosensory cues."
acknowledgement: This work was partially supported by a grant from “Consello Social
  Universidade de Santiago de Compostela” 2022-PU004.We would like to show special
  gratitude to Prof. Ludwig Wagner (Medical University, Vienna) for kindly providing
  us with the secretagogin antibody. We thank the Wildlife Recovery Centres of Galicia,
  Dirección Xeral de Patrimonio Natural (Xunta de Galicia, Spain), and Federación
  Galega de Caza for providing the red foxes used in this study.
article_number: '1097467'
article_processing_charge: No
article_type: original
author:
- first_name: Irene
  full_name: Ortiz-Leal, Irene
  last_name: Ortiz-Leal
- first_name: Mateo V.
  full_name: Torres, Mateo V.
  last_name: Torres
- first_name: Victor M
  full_name: Vargas Barroso, Victor M
  id: 2F55A9DE-F248-11E8-B48F-1D18A9856A87
  last_name: Vargas Barroso
- first_name: Luis Eusebio
  full_name: Fidalgo, Luis Eusebio
  last_name: Fidalgo
- first_name: Ana María
  full_name: López-Beceiro, Ana María
  last_name: López-Beceiro
- first_name: Jorge A.
  full_name: Larriva-Sahd, Jorge A.
  last_name: Larriva-Sahd
- first_name: Pablo
  full_name: Sánchez-Quinteiro, Pablo
  last_name: Sánchez-Quinteiro
citation:
  ama: Ortiz-Leal I, Torres MV, Vargas Barroso VM, et al. The olfactory limbus of
    the red fox (Vulpes vulpes). New insights regarding a noncanonical olfactory bulb
    pathway. <i>Frontiers in Neuroanatomy</i>. 2023;16. doi:<a href="https://doi.org/10.3389/fnana.2022.1097467">10.3389/fnana.2022.1097467</a>
  apa: Ortiz-Leal, I., Torres, M. V., Vargas Barroso, V. M., Fidalgo, L. E., López-Beceiro,
    A. M., Larriva-Sahd, J. A., &#38; Sánchez-Quinteiro, P. (2023). The olfactory
    limbus of the red fox (Vulpes vulpes). New insights regarding a noncanonical olfactory
    bulb pathway. <i>Frontiers in Neuroanatomy</i>. Frontiers. <a href="https://doi.org/10.3389/fnana.2022.1097467">https://doi.org/10.3389/fnana.2022.1097467</a>
  chicago: Ortiz-Leal, Irene, Mateo V. Torres, Victor M Vargas Barroso, Luis Eusebio
    Fidalgo, Ana María López-Beceiro, Jorge A. Larriva-Sahd, and Pablo Sánchez-Quinteiro.
    “The Olfactory Limbus of the Red Fox (Vulpes Vulpes). New Insights Regarding a
    Noncanonical Olfactory Bulb Pathway.” <i>Frontiers in Neuroanatomy</i>. Frontiers,
    2023. <a href="https://doi.org/10.3389/fnana.2022.1097467">https://doi.org/10.3389/fnana.2022.1097467</a>.
  ieee: I. Ortiz-Leal <i>et al.</i>, “The olfactory limbus of the red fox (Vulpes
    vulpes). New insights regarding a noncanonical olfactory bulb pathway,” <i>Frontiers
    in Neuroanatomy</i>, vol. 16. Frontiers, 2023.
  ista: Ortiz-Leal I, Torres MV, Vargas Barroso VM, Fidalgo LE, López-Beceiro AM,
    Larriva-Sahd JA, Sánchez-Quinteiro P. 2023. The olfactory limbus of the red fox
    (Vulpes vulpes). New insights regarding a noncanonical olfactory bulb pathway.
    Frontiers in Neuroanatomy. 16, 1097467.
  mla: Ortiz-Leal, Irene, et al. “The Olfactory Limbus of the Red Fox (Vulpes Vulpes).
    New Insights Regarding a Noncanonical Olfactory Bulb Pathway.” <i>Frontiers in
    Neuroanatomy</i>, vol. 16, 1097467, Frontiers, 2023, doi:<a href="https://doi.org/10.3389/fnana.2022.1097467">10.3389/fnana.2022.1097467</a>.
  short: I. Ortiz-Leal, M.V. Torres, V.M. Vargas Barroso, L.E. Fidalgo, A.M. López-Beceiro,
    J.A. Larriva-Sahd, P. Sánchez-Quinteiro, Frontiers in Neuroanatomy 16 (2023).
date_created: 2023-02-05T23:01:00Z
date_published: 2023-01-10T00:00:00Z
date_updated: 2023-08-16T11:37:52Z
day: '10'
ddc:
- '570'
department:
- _id: PeJo
doi: 10.3389/fnana.2022.1097467
external_id:
  isi:
  - '000919786900001'
  pmid:
  - '36704406'
file:
- access_level: open_access
  checksum: 49cd40f3bda6f267079427042e7d15e3
  content_type: application/pdf
  creator: dernst
  date_created: 2023-02-06T07:56:14Z
  date_updated: 2023-02-06T07:56:14Z
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  file_name: 2022_FrontiersNeuroanatomy_OrtizLeal.pdf
  file_size: 21943473
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file_date_updated: 2023-02-06T07:56:14Z
has_accepted_license: '1'
intvolume: '        16'
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language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
pmid: 1
publication: Frontiers in Neuroanatomy
publication_identifier:
  eissn:
  - 1662-5129
publication_status: published
publisher: Frontiers
quality_controlled: '1'
scopus_import: '1'
status: public
title: The olfactory limbus of the red fox (Vulpes vulpes). New insights regarding
  a noncanonical olfactory bulb pathway
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: 16
year: '2023'
...
