---
_id: '14274'
abstract:
- lang: eng
  text: Immune responses rely on the rapid and coordinated migration of leukocytes.
    Whereas it is well established that single-cell migration is often guided by gradients
    of chemokines and other chemoattractants, it remains poorly understood how these
    gradients are generated, maintained, and modulated. By combining experimental
    data with theory on leukocyte chemotaxis guided by the G protein–coupled receptor
    (GPCR) CCR7, we demonstrate that in addition to its role as the sensory receptor
    that steers migration, CCR7 also acts as a generator and a modulator of chemotactic
    gradients. Upon exposure to the CCR7 ligand CCL19, dendritic cells (DCs) effectively
    internalize the receptor and ligand as part of the canonical GPCR desensitization
    response. We show that CCR7 internalization also acts as an effective sink for
    the chemoattractant, dynamically shaping the spatiotemporal distribution of the
    chemokine. This mechanism drives complex collective migration patterns, enabling
    DCs to create or sharpen chemotactic gradients. We further show that these self-generated
    gradients can sustain the long-range guidance of DCs, adapt collective migration
    patterns to the size and geometry of the environment, and provide a guidance cue
    for other comigrating cells. Such a dual role of CCR7 as a GPCR that both senses
    and consumes its ligand can thus provide a novel mode of cellular self-organization.
acknowledgement: "We thank I. de Vries and the Scientific Service Units (Life Sciences,
  Bioimaging, Nanofabrication, Preclinical and Miba Machine Shop) of the Institute
  of Science and Technology Austria for excellent support, as well as all the rotation
  students assisting in the laboratory work (B. Zens, H. Schön, and D. Babic).\r\nThis
  work was supported by grants from the European Research Council under the European
  Union’s Horizon 2020 research to M.S. (grant agreement no. 724373) and to E.H. (grant
  agreement no. 851288), and a grant by the Austrian Science Fund (DK Nanocell W1250-B20)
  to M.S. J.A. was supported by the Jenny and Antti Wihuri Foundation and Research
  Council of Finland's Flagship Programme InFLAMES (decision number: 357910). M.C.U.
  was supported by the European Union’s Horizon 2020 research and innovation programme
  under the Marie Skłodowska-Curie grant agreement no. 754411."
article_number: adc9584
article_processing_charge: No
article_type: original
author:
- first_name: Jonna H
  full_name: Alanko, Jonna H
  id: 2CC12E8C-F248-11E8-B48F-1D18A9856A87
  last_name: Alanko
  orcid: 0000-0002-7698-3061
- first_name: Mehmet C
  full_name: Ucar, Mehmet C
  id: 50B2A802-6007-11E9-A42B-EB23E6697425
  last_name: Ucar
  orcid: 0000-0003-0506-4217
- first_name: Nikola
  full_name: Canigova, Nikola
  id: 3795523E-F248-11E8-B48F-1D18A9856A87
  last_name: Canigova
  orcid: 0000-0002-8518-5926
- first_name: Julian A
  full_name: Stopp, Julian A
  id: 489E3F00-F248-11E8-B48F-1D18A9856A87
  last_name: Stopp
- first_name: Jan
  full_name: Schwarz, Jan
  id: 346C1EC6-F248-11E8-B48F-1D18A9856A87
  last_name: Schwarz
- first_name: Jack
  full_name: Merrin, Jack
  id: 4515C308-F248-11E8-B48F-1D18A9856A87
  last_name: Merrin
  orcid: 0000-0001-5145-4609
- first_name: Edouard B
  full_name: Hannezo, Edouard B
  id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
  last_name: Hannezo
  orcid: 0000-0001-6005-1561
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
citation:
  ama: Alanko JH, Ucar MC, Canigova N, et al. CCR7 acts as both a sensor and a sink
    for CCL19 to coordinate collective leukocyte migration. <i>Science Immunology</i>.
    2023;8(87). doi:<a href="https://doi.org/10.1126/sciimmunol.adc9584">10.1126/sciimmunol.adc9584</a>
  apa: Alanko, J. H., Ucar, M. C., Canigova, N., Stopp, J. A., Schwarz, J., Merrin,
    J., … Sixt, M. K. (2023). CCR7 acts as both a sensor and a sink for CCL19 to coordinate
    collective leukocyte migration. <i>Science Immunology</i>. American Association
    for the Advancement of Science. <a href="https://doi.org/10.1126/sciimmunol.adc9584">https://doi.org/10.1126/sciimmunol.adc9584</a>
  chicago: Alanko, Jonna H, Mehmet C Ucar, Nikola Canigova, Julian A Stopp, Jan Schwarz,
    Jack Merrin, Edouard B Hannezo, and Michael K Sixt. “CCR7 Acts as Both a Sensor
    and a Sink for CCL19 to Coordinate Collective Leukocyte Migration.” <i>Science
    Immunology</i>. American Association for the Advancement of Science, 2023. <a
    href="https://doi.org/10.1126/sciimmunol.adc9584">https://doi.org/10.1126/sciimmunol.adc9584</a>.
  ieee: J. H. Alanko <i>et al.</i>, “CCR7 acts as both a sensor and a sink for CCL19
    to coordinate collective leukocyte migration,” <i>Science Immunology</i>, vol.
    8, no. 87. American Association for the Advancement of Science, 2023.
  ista: Alanko JH, Ucar MC, Canigova N, Stopp JA, Schwarz J, Merrin J, Hannezo EB,
    Sixt MK. 2023. CCR7 acts as both a sensor and a sink for CCL19 to coordinate collective
    leukocyte migration. Science Immunology. 8(87), adc9584.
  mla: Alanko, Jonna H., et al. “CCR7 Acts as Both a Sensor and a Sink for CCL19 to
    Coordinate Collective Leukocyte Migration.” <i>Science Immunology</i>, vol. 8,
    no. 87, adc9584, American Association for the Advancement of Science, 2023, doi:<a
    href="https://doi.org/10.1126/sciimmunol.adc9584">10.1126/sciimmunol.adc9584</a>.
  short: J.H. Alanko, M.C. Ucar, N. Canigova, J.A. Stopp, J. Schwarz, J. Merrin, E.B.
    Hannezo, M.K. Sixt, Science Immunology 8 (2023).
corr_author: '1'
date_created: 2023-09-06T08:07:51Z
date_published: 2023-09-01T00:00:00Z
date_updated: 2026-09-30T22:30:39Z
day: '01'
ddc:
- '570'
department:
- _id: MiSi
- _id: EdHa
- _id: NanoFab
doi: 10.1126/sciimmunol.adc9584
ec_funded: 1
external_id:
  isi:
  - '001062110600003'
  pmid:
  - '37656776'
fulldoi: https://doi.org/10.1126/sciimmunol.adc9584
intvolume: '         8'
isi: 1
issue: '87'
keyword:
- General Medicine
- Immunology
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1126/sciimmunol.adc9584
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 25FE9508-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '724373'
  name: Cellular Navigation Along Spatial Gradients
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '851288'
  name: Design Principles of Branching Morphogenesis
- _id: 265E2996-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W01250-B20
  name: Nano-Analytics of Cellular Systems
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Science Immunology
publication_identifier:
  issn:
  - 2470-9468
publication_status: published
publisher: American Association for the Advancement of Science
quality_controlled: '1'
related_material:
  record:
  - id: '14279'
    relation: research_data
    status: public
  - id: '14697'
    relation: dissertation_contains
    status: public
  - id: '19745'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: CCR7 acts as both a sensor and a sink for CCL19 to coordinate collective leukocyte
  migration
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 8
year: '2023'
...
---
OA_place: publisher
_id: '14226'
abstract:
- lang: eng
  text: "We introduce the notion of a Faustian interchange in a 1-parameter family
    of smooth\r\nfunctions to generalize the medial axis to critical points of index
    larger than 0.\r\nWe construct and implement a general purpose algorithm for approximating
    such\r\ngeneralized medial axes."
alternative_title:
- ISTA Master's Thesis
article_processing_charge: No
author:
- first_name: Elizabeth R
  full_name: Stephenson, Elizabeth R
  id: 2D04F932-F248-11E8-B48F-1D18A9856A87
  last_name: Stephenson
  orcid: 0000-0002-6862-208X
citation:
  ama: Stephenson ER. Generalizing medial axes with homology switches. 2023. doi:<a
    href="https://doi.org/10.15479/at:ista:14226">10.15479/at:ista:14226</a>
  apa: Stephenson, E. R. (2023). <i>Generalizing medial axes with homology switches</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:14226">https://doi.org/10.15479/at:ista:14226</a>
  chicago: Stephenson, Elizabeth R. “Generalizing Medial Axes with Homology Switches.”
    Institute of Science and Technology Austria, 2023. <a href="https://doi.org/10.15479/at:ista:14226">https://doi.org/10.15479/at:ista:14226</a>.
  ieee: E. R. Stephenson, “Generalizing medial axes with homology switches,” Institute
    of Science and Technology Austria, 2023.
  ista: Stephenson ER. 2023. Generalizing medial axes with homology switches. Institute
    of Science and Technology Austria.
  mla: Stephenson, Elizabeth R. <i>Generalizing Medial Axes with Homology Switches</i>.
    Institute of Science and Technology Austria, 2023, doi:<a href="https://doi.org/10.15479/at:ista:14226">10.15479/at:ista:14226</a>.
  short: E.R. Stephenson, Generalizing Medial Axes with Homology Switches, Institute
    of Science and Technology Austria, 2023.
corr_author: '1'
date_created: 2023-08-24T13:01:18Z
date_published: 2023-08-24T00:00:00Z
date_updated: 2026-04-07T14:02:30Z
day: '24'
ddc:
- '500'
degree_awarded: MS
department:
- _id: GradSch
- _id: HeEd
doi: 10.15479/at:ista:14226
file:
- access_level: closed
  checksum: 453caf851d75c3478c10ed09bd242a91
  content_type: application/x-zip-compressed
  creator: cchlebak
  date_created: 2023-08-24T13:02:49Z
  date_updated: 2024-02-26T23:30:03Z
  embargo_to: open_access
  file_id: '14227'
  file_name: documents-export-2023-08-24.zip
  file_size: 15501411
  relation: source_file
- access_level: open_access
  checksum: 7349d29963d6695e555e171748648d9a
  content_type: application/pdf
  creator: cchlebak
  date_created: 2023-08-24T13:03:42Z
  date_updated: 2024-02-26T23:30:03Z
  embargo: 2024-02-25
  file_id: '14228'
  file_name: thesis_pdf_a.pdf
  file_size: 6854783
  relation: main_file
file_date_updated: 2024-02-26T23:30:03Z
fulldoi: https://doi.org/10.15479/at:ista:14226
has_accepted_license: '1'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: '43'
publication_identifier:
  issn:
  - 2791-4585
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
title: Generalizing medial axes with homology switches
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2023'
...
---
_id: '12159'
abstract:
- lang: eng
  text: The term “haplotype block” is commonly used in the developing field of haplotype-based
    inference methods. We argue that the term should be defined based on the structure
    of the Ancestral Recombination Graph (ARG), which contains complete information
    on the ancestry of a sample. We use simulated examples to demonstrate key features
    of the relationship between haplotype blocks and ancestral structure, emphasizing
    the stochasticity of the processes that generate them. Even the simplest cases
    of neutrality or of a “hard” selective sweep produce a rich structure, often missed
    by commonly used statistics. We highlight a number of novel methods for inferring
    haplotype structure, based on the full ARG, or on a sequence of trees, and illustrate
    how they can be used to define haplotype blocks using an empirical data set. While
    the advent of new, computationally efficient methods makes it possible to apply
    these concepts broadly, they (and additional new methods) could benefit from adding
    features to explore haplotype blocks, as we define them. Understanding and applying
    the concept of the haplotype block will be essential to fully exploit long and
    linked-read sequencing technologies.
acknowledgement: 'We thank the Barton group for useful discussion and feedback during
  the writing of this article. Comments from Roger Butlin, Molly Schumer''s Group,
  the tskit development team, editors and three reviewers greatly improved the manuscript.
  Funding was provided by SCAS (Natural Sciences Programme, Knut and Alice Wallenberg
  Foundation), an FWF Wittgenstein grant (PT1001Z211), an FWF standalone grant (grant
  P 32166), and an ERC Advanced Grant. YFC was supported by the Max Planck Society
  and an ERC Proof of Concept Grant #101069216 (HAPLOTAGGING).'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Daria
  full_name: Shipilina, Daria
  id: 428A94B0-F248-11E8-B48F-1D18A9856A87
  last_name: Shipilina
  orcid: 0000-0002-1145-9226
- first_name: Arka
  full_name: Pal, Arka
  id: 6AAB2240-CA9A-11E9-9C1A-D9D1E5697425
  last_name: Pal
  orcid: 0000-0002-4530-8469
- first_name: Sean
  full_name: Stankowski, Sean
  id: 43161670-5719-11EA-8025-FABC3DDC885E
  last_name: Stankowski
- first_name: Yingguang Frank
  full_name: Chan, Yingguang Frank
  last_name: Chan
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: Shipilina D, Pal A, Stankowski S, Chan YF, Barton NH. On the origin and structure
    of haplotype blocks. <i>Molecular Ecology</i>. 2023;32(6):1441-1457. doi:<a href="https://doi.org/10.1111/mec.16793">10.1111/mec.16793</a>
  apa: Shipilina, D., Pal, A., Stankowski, S., Chan, Y. F., &#38; Barton, N. H. (2023).
    On the origin and structure of haplotype blocks. <i>Molecular Ecology</i>. Wiley.
    <a href="https://doi.org/10.1111/mec.16793">https://doi.org/10.1111/mec.16793</a>
  chicago: Shipilina, Daria, Arka Pal, Sean Stankowski, Yingguang Frank Chan, and
    Nicholas H Barton. “On the Origin and Structure of Haplotype Blocks.” <i>Molecular
    Ecology</i>. Wiley, 2023. <a href="https://doi.org/10.1111/mec.16793">https://doi.org/10.1111/mec.16793</a>.
  ieee: D. Shipilina, A. Pal, S. Stankowski, Y. F. Chan, and N. H. Barton, “On the
    origin and structure of haplotype blocks,” <i>Molecular Ecology</i>, vol. 32,
    no. 6. Wiley, pp. 1441–1457, 2023.
  ista: Shipilina D, Pal A, Stankowski S, Chan YF, Barton NH. 2023. On the origin
    and structure of haplotype blocks. Molecular Ecology. 32(6), 1441–1457.
  mla: Shipilina, Daria, et al. “On the Origin and Structure of Haplotype Blocks.”
    <i>Molecular Ecology</i>, vol. 32, no. 6, Wiley, 2023, pp. 1441–57, doi:<a href="https://doi.org/10.1111/mec.16793">10.1111/mec.16793</a>.
  short: D. Shipilina, A. Pal, S. Stankowski, Y.F. Chan, N.H. Barton, Molecular Ecology
    32 (2023) 1441–1457.
corr_author: '1'
date_created: 2023-01-12T12:09:17Z
date_published: 2023-03-01T00:00:00Z
date_updated: 2026-09-30T22:30:43Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1111/mec.16793
external_id:
  isi:
  - '000900762000001'
  pmid:
  - '36433653'
file:
- access_level: open_access
  checksum: b10e0f8fa3dc4d72aaf77a557200978a
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T08:15:41Z
  date_updated: 2023-08-16T08:15:41Z
  file_id: '14062'
  file_name: 2023_MolecularEcology_Shipilina.pdf
  file_size: 7144607
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T08:15:41Z
fulldoi: https://doi.org/10.1111/mec.16793
has_accepted_license: '1'
intvolume: '        32'
isi: 1
issue: '6'
keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '03'
oa: 1
oa_version: Published Version
page: 1441-1457
pmid: 1
project:
- _id: 05959E1C-7A3F-11EA-A408-12923DDC885E
  grant_number: P32166
  name: Snapdragon Speciation
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
- _id: bd6958e0-d553-11ed-ba76-86eba6a76c00
  grant_number: '101055327'
  name: Understanding the evolution of continuous genomes
publication: Molecular Ecology
publication_identifier:
  eissn:
  - 1365-294X
  issn:
  - 0962-1083
publication_status: published
publisher: Wiley
quality_controlled: '1'
related_material:
  record:
  - id: '20694'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: On the origin and structure of haplotype blocks
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: 32
year: '2023'
...
---
OA_place: publisher
_id: '14510'
abstract:
- lang: eng
  text: "Clathrin-mediated endocytosis (CME) is vital for the regulation of plant
    growth and\r\ndevelopment by controlling plasma membrane protein composition and
    cargo uptake. CME\r\nrelies on the precise recruitment control of protein regulators
    for vesicle maturation and\r\nrelease. During the early stages of endocytosis,
    an area of flat membrane is remodelled by\r\nproteins to create a spherical vesicle
    against intracellular forces. After the Clathrin-coated\r\nvesicle (CCV) is fully
    formed, scission machinery releases it from the plasma membrane,\r\nand cargo
    proceeds for recycling or degradation through early endosomes / Trans Golgi\r\nnetwork.
    Protein machineries that mediate membrane bending and vesicle release in plants\r\nare
    unknown. However, studies show, that plant endocytosis is actin independent, thus\r\nindicating
    that plants utilize a unique mechanism to mediate membrane bending against highturgor
    pressure compared to other model systems. First, by using biochemical and advanced\r\nlive
    microscopy approaches we investigate the TPLATE complex, a plant-specific\r\nendocytosis
    protein complex. We found that TPLATE is peripherally associated with\r\nclathrin-coated
    vesicles and localises at the rim of endocytosis events. Next, our study of\r\nplant
    Dynamin-related protein 1C (DRP1C), which was hypothesised previously to play
    a\r\nrole in vesicle release, shows the recruitment of the protein already at
    the early stages of\r\nendocytosis. Moreover, DRP1C assembles into organised ring-like
    structures and is able to\r\ninduce membrane deformation and tubulation, suggesting
    its role also in membrane bending\r\nduring early CME. Based on the data from
    mammalian and yeast systems, plant DynaminRelated Proteins 2 and SH3P2 protein
    are strong candidates to be part of the plant vesicle\r\nscission machinery; however,
    their precise role in plant CME has not been yet elucidated.\r\nHere, we characterised
    DRP2s and SH3P2 roles in CME by combining high-resolution\r\nimaging of endocytic
    events in vivo and protein characterisation. Although DRP2s and\r\nSH3P2 arrive
    together during late CME and physically interact, genetic analysis using\r\n∆sh3p1,2,3
    mutant and complementation with non-DRP2-interacting SH3P2 variants suggest\r\nthat
    SH3P2 does not directly recruit DRP2s to the site of endocytosis. Summarising
    our\r\nresearch, these observations provide new important insights into the mechanism
    of plant\r\nCME and show that, despite plants posses many homologues of mammalian
    and yeast CME\r\ncomponents, they do not necessarily act in the same manner. "
acknowledged_ssus:
- _id: EM-Fac
- _id: Bio
- _id: LifeSc
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Nataliia
  full_name: Gnyliukh, Nataliia
  id: 390C1120-F248-11E8-B48F-1D18A9856A87
  last_name: Gnyliukh
  orcid: 0000-0002-2198-0509
citation:
  ama: Gnyliukh N. Mechanism of clathrin-coated vesicle  formation during endocytosis
    in plants. 2023. doi:<a href="https://doi.org/10.15479/at:ista:14510">10.15479/at:ista:14510</a>
  apa: Gnyliukh, N. (2023). <i>Mechanism of clathrin-coated vesicle  formation during
    endocytosis in plants</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:14510">https://doi.org/10.15479/at:ista:14510</a>
  chicago: Gnyliukh, Nataliia. “Mechanism of Clathrin-Coated Vesicle  Formation during
    Endocytosis in Plants.” Institute of Science and Technology Austria, 2023. <a
    href="https://doi.org/10.15479/at:ista:14510">https://doi.org/10.15479/at:ista:14510</a>.
  ieee: N. Gnyliukh, “Mechanism of clathrin-coated vesicle  formation during endocytosis
    in plants,” Institute of Science and Technology Austria, 2023.
  ista: Gnyliukh N. 2023. Mechanism of clathrin-coated vesicle  formation during endocytosis
    in plants. Institute of Science and Technology Austria.
  mla: Gnyliukh, Nataliia. <i>Mechanism of Clathrin-Coated Vesicle  Formation during
    Endocytosis in Plants</i>. Institute of Science and Technology Austria, 2023,
    doi:<a href="https://doi.org/10.15479/at:ista:14510">10.15479/at:ista:14510</a>.
  short: N. Gnyliukh, Mechanism of Clathrin-Coated Vesicle  Formation during Endocytosis
    in Plants, Institute of Science and Technology Austria, 2023.
corr_author: '1'
date_created: 2023-11-10T09:10:06Z
date_published: 2023-11-10T00:00:00Z
date_updated: 2026-09-30T22:30:56Z
day: '10'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JiFr
- _id: MaLo
doi: 10.15479/at:ista:14510
ec_funded: 1
file:
- access_level: closed
  checksum: 3d5e680bfc61f98e308c434f45cc9bd6
  content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
  creator: ngnyliuk
  date_created: 2023-11-20T09:18:51Z
  date_updated: 2024-11-23T23:30:38Z
  embargo_to: open_access
  file_id: '14567'
  file_name: Thesis_Gnyliukh_final_08_11_23.docx
  file_size: 20824903
  relation: source_file
- access_level: open_access
  checksum: bfc96d47fc4e7e857dd71656097214a4
  content_type: application/pdf
  creator: ngnyliuk
  date_created: 2023-11-20T09:23:11Z
  date_updated: 2024-11-23T23:30:38Z
  embargo: 2024-11-23
  file_id: '14568'
  file_name: Thesis_Gnyliukh_final_20_11_23.pdf
  file_size: 24871844
  relation: main_file
file_date_updated: 2024-11-23T23:30:38Z
fulldoi: https://doi.org/10.15479/at:ista:14510
has_accepted_license: '1'
keyword:
- Clathrin-Mediated Endocytosis
- vesicle scission
- Dynamin-Related Protein 2
- SH3P2
- TPLATE complex
- Total internal reflection fluorescence microscopy
- Arabidopsis thaliana
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: '180'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  isbn:
  - 978-3-99078-037-4
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '14591'
    relation: part_of_dissertation
    status: public
  - id: '9887'
    relation: part_of_dissertation
    status: public
  - id: '8139'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
title: Mechanism of clathrin-coated vesicle  formation during endocytosis in plants
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: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2023'
...
---
OA_place: repository
_id: '14591'
abstract:
- lang: eng
  text: Clathrin-mediated endocytosis (CME) is vital for the regulation of plant growth
    and development by controlling plasma membrane protein composition and cargo uptake.
    CME relies on the precise recruitment of regulators for vesicle maturation and
    release. Homologues of components of mammalian vesicle scission are strong candidates
    to be part of the scissin machinery in plants, but the precise roles of these
    proteins in this process is not fully understood. Here, we characterised the roles
    of Plant Dynamin-Related Proteins 2 (DRP2s) and SH3-domain containing protein
    2 (SH3P2), the plant homologue to Dynamins’ recruiters, like Endophilin and Amphiphysin,
    in the CME by combining high-resolution imaging of endocytic events in vivo and
    characterisation of the purified proteins in vitro. Although DRP2s and SH3P2 arrive
    similarly late during CME and physically interact, genetic analysis of the Dsh3p1,2,3
    triple-mutant and complementation assays with non-SH3P2-interacting DRP2 variants
    suggests that SH3P2 does not directly recruit DRP2s to the site of endocytosis.
    These observations imply that despite the presence of many well-conserved endocytic
    components, plants have acquired a distinct mechanism for CME. One Sentence Summary
    In contrast to predictions based on mammalian systems, plant Dynamin-related proteins
    2 are recruited to the site of Clathrin-mediated endocytosis independently of
    BAR-SH3 proteins.
acknowledged_ssus:
- _id: EM-Fac
- _id: LifeSc
- _id: Bio
article_processing_charge: No
author:
- first_name: Nataliia
  full_name: Gnyliukh, Nataliia
  id: 390C1120-F248-11E8-B48F-1D18A9856A87
  last_name: Gnyliukh
  orcid: 0000-0002-2198-0509
- first_name: Alexander J
  full_name: Johnson, Alexander J
  id: 46A62C3A-F248-11E8-B48F-1D18A9856A87
  last_name: Johnson
  orcid: 0000-0002-2739-8843
- first_name: Marie-Kristin
  full_name: Nagel, Marie-Kristin
  last_name: Nagel
- first_name: Aline
  full_name: Monzer, Aline
  id: 2DB5D88C-D7B3-11E9-B8FD-7907E6697425
  last_name: Monzer
- first_name: Annamaria
  full_name: Hlavata, Annamaria
  id: 36062FEC-F248-11E8-B48F-1D18A9856A87
  last_name: Hlavata
- first_name: Erika
  full_name: Isono, Erika
  last_name: Isono
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Gnyliukh N, Johnson AJ, Nagel M-K, et al. Role of dynamin-related proteins
    2 and SH3P2 in clathrin-mediated endocytosis in plants. <i>bioRxiv</i>. doi:<a
    href="https://doi.org/10.1101/2023.10.09.561523">10.1101/2023.10.09.561523</a>
  apa: Gnyliukh, N., Johnson, A. J., Nagel, M.-K., Monzer, A., Hlavata, A., Isono,
    E., … Friml, J. (n.d.). Role of dynamin-related proteins 2 and SH3P2 in clathrin-mediated
    endocytosis in plants. <i>bioRxiv</i>. <a href="https://doi.org/10.1101/2023.10.09.561523">https://doi.org/10.1101/2023.10.09.561523</a>
  chicago: Gnyliukh, Nataliia, Alexander J Johnson, Marie-Kristin Nagel, Aline Monzer,
    Annamaria Hlavata, Erika Isono, Martin Loose, and Jiří Friml. “Role of Dynamin-Related
    Proteins 2 and SH3P2 in Clathrin-Mediated Endocytosis in Plants.” <i>BioRxiv</i>,
    n.d. <a href="https://doi.org/10.1101/2023.10.09.561523">https://doi.org/10.1101/2023.10.09.561523</a>.
  ieee: N. Gnyliukh <i>et al.</i>, “Role of dynamin-related proteins 2 and SH3P2 in
    clathrin-mediated endocytosis in plants,” <i>bioRxiv</i>. .
  ista: Gnyliukh N, Johnson AJ, Nagel M-K, Monzer A, Hlavata A, Isono E, Loose M,
    Friml J. Role of dynamin-related proteins 2 and SH3P2 in clathrin-mediated endocytosis
    in plants. bioRxiv, <a href="https://doi.org/10.1101/2023.10.09.561523">10.1101/2023.10.09.561523</a>.
  mla: Gnyliukh, Nataliia, et al. “Role of Dynamin-Related Proteins 2 and SH3P2 in
    Clathrin-Mediated Endocytosis in Plants.” <i>BioRxiv</i>, doi:<a href="https://doi.org/10.1101/2023.10.09.561523">10.1101/2023.10.09.561523</a>.
  short: N. Gnyliukh, A.J. Johnson, M.-K. Nagel, A. Monzer, A. Hlavata, E. Isono,
    M. Loose, J. Friml, BioRxiv (n.d.).
corr_author: '1'
date_created: 2023-11-22T10:17:49Z
date_published: 2023-10-10T00:00:00Z
date_updated: 2026-09-30T22:30:56Z
day: '10'
department:
- _id: JiFr
- _id: MaLo
- _id: CaBe
doi: 10.1101/2023.10.09.561523
ec_funded: 1
fulldoi: https://doi.org/10.1101/2023.10.09.561523
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/2023.10.09.561523
month: '10'
oa: 1
oa_version: Preprint
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication: bioRxiv
publication_status: draft
related_material:
  record:
  - id: '15330'
    relation: later_version
    status: public
  - id: '14510'
    relation: dissertation_contains
    status: public
status: public
title: Role of dynamin-related proteins 2 and SH3P2 in clathrin-mediated endocytosis
  in plants
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
OA_place: publisher
_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.
corr_author: '1'
date_created: 2023-01-31T15:10:53Z
date_published: 2023-01-09T00:00:00Z
date_updated: 2026-07-06T12:50:45Z
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
fulldoi: https://doi.org/10.15479/at:ista:12470
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: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2023'
...
---
_id: '13117'
abstract:
- lang: eng
  text: The ability to control the direction of scattered light is crucial to provide
    flexibility and scalability for a wide range of on-chip applications, such as
    integrated photonics, quantum information processing, and nonlinear optics. Tunable
    directionality can be achieved by applying external magnetic fields that modify
    optical selection rules, by using nonlinear effects, or interactions with vibrations.
    However, these approaches are less suitable to control microwave photon propagation
    inside integrated superconducting quantum devices. Here, we demonstrate on-demand
    tunable directional scattering based on two periodically modulated transmon qubits
    coupled to a transmission line at a fixed distance. By changing the relative phase
    between the modulation tones, we realize unidirectional forward or backward photon
    scattering. Such an in-situ switchable mirror represents a versatile tool for
    intra- and inter-chip microwave photonic processors. In the future, a lattice
    of qubits can be used to realize topological circuits that exhibit strong nonreciprocity
    or chirality.
acknowledged_ssus:
- _id: M-Shop
- _id: NanoFab
acknowledgement: The authors thank W.D. Oliver for discussions, L. Drmic and P. Zielinski
  for software development, and the MIBA workshop and the IST nanofabrication facility
  for technical support. This work was supported by the Austrian Science Fund (FWF)
  through BeyondC (F7105) and IST Austria. E.R. is the recipient of a DOC fellowship
  of the Austrian Academy of Sciences at IST Austria. J.M.F. and M.Z. acknowledge
  support from the European Research Council under grant agreement No 758053 (ERC
  StG QUNNECT) and a NOMIS foundation research grant. The work of A.N.P. and A.V.P.
  has been supported by the Russian Science Foundation under the grant No 20-12-00194.
article_number: '2998'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Elena
  full_name: Redchenko, Elena
  id: 2C21D6E8-F248-11E8-B48F-1D18A9856A87
  last_name: Redchenko
- first_name: Alexander V.
  full_name: Poshakinskiy, Alexander V.
  last_name: Poshakinskiy
- first_name: Riya
  full_name: Sett, Riya
  id: 2E6D040E-F248-11E8-B48F-1D18A9856A87
  last_name: Sett
  orcid: 0000-0001-7641-8348
- first_name: Martin
  full_name: Zemlicka, Martin
  id: 2DCF8DE6-F248-11E8-B48F-1D18A9856A87
  last_name: Zemlicka
  orcid: 0009-0005-0878-3032
- first_name: Alexander N.
  full_name: Poddubny, Alexander N.
  last_name: Poddubny
- first_name: Johannes M
  full_name: Fink, Johannes M
  id: 4B591CBA-F248-11E8-B48F-1D18A9856A87
  last_name: Fink
  orcid: 0000-0001-8112-028X
citation:
  ama: Redchenko E, Poshakinskiy AV, Sett R, Zemlicka M, Poddubny AN, Fink JM. Tunable
    directional photon scattering from a pair of superconducting qubits. <i>Nature
    Communications</i>. 2023;14. doi:<a href="https://doi.org/10.1038/s41467-023-38761-6">10.1038/s41467-023-38761-6</a>
  apa: Redchenko, E., Poshakinskiy, A. V., Sett, R., Zemlicka, M., Poddubny, A. N.,
    &#38; Fink, J. M. (2023). Tunable directional photon scattering from a pair of
    superconducting qubits. <i>Nature Communications</i>. Springer Nature. <a href="https://doi.org/10.1038/s41467-023-38761-6">https://doi.org/10.1038/s41467-023-38761-6</a>
  chicago: Redchenko, Elena, Alexander V. Poshakinskiy, Riya Sett, Martin Zemlicka,
    Alexander N. Poddubny, and Johannes M Fink. “Tunable Directional Photon Scattering
    from a Pair of Superconducting Qubits.” <i>Nature Communications</i>. Springer
    Nature, 2023. <a href="https://doi.org/10.1038/s41467-023-38761-6">https://doi.org/10.1038/s41467-023-38761-6</a>.
  ieee: E. Redchenko, A. V. Poshakinskiy, R. Sett, M. Zemlicka, A. N. Poddubny, and
    J. M. Fink, “Tunable directional photon scattering from a pair of superconducting
    qubits,” <i>Nature Communications</i>, vol. 14. Springer Nature, 2023.
  ista: Redchenko E, Poshakinskiy AV, Sett R, Zemlicka M, Poddubny AN, Fink JM. 2023.
    Tunable directional photon scattering from a pair of superconducting qubits. Nature
    Communications. 14, 2998.
  mla: Redchenko, Elena, et al. “Tunable Directional Photon Scattering from a Pair
    of Superconducting Qubits.” <i>Nature Communications</i>, vol. 14, 2998, Springer
    Nature, 2023, doi:<a href="https://doi.org/10.1038/s41467-023-38761-6">10.1038/s41467-023-38761-6</a>.
  short: E. Redchenko, A.V. Poshakinskiy, R. Sett, M. Zemlicka, A.N. Poddubny, J.M.
    Fink, Nature Communications 14 (2023).
corr_author: '1'
date_created: 2023-06-04T22:01:02Z
date_published: 2023-05-24T00:00:00Z
date_updated: 2026-09-30T22:31:12Z
day: '24'
ddc:
- '530'
department:
- _id: JoFi
doi: 10.1038/s41467-023-38761-6
ec_funded: 1
external_id:
  arxiv:
  - '2205.03293'
  isi:
  - '001001099700002'
  pmid:
  - '37225689'
file:
- access_level: open_access
  checksum: a857df40f0882859c48a1ff1e2001ec2
  content_type: application/pdf
  creator: dernst
  date_created: 2023-06-06T07:31:20Z
  date_updated: 2023-06-06T07:31:20Z
  file_id: '13123'
  file_name: 2023_NaturePhysics_Redchenko.pdf
  file_size: 1654389
  relation: main_file
  success: 1
file_date_updated: 2023-06-06T07:31:20Z
fulldoi: https://doi.org/10.1038/s41467-023-38761-6
has_accepted_license: '1'
intvolume: '        14'
isi: 1
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 26336814-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '758053'
  name: A Fiber Optic Transceiver for Superconducting Qubits
- _id: 26B354CA-B435-11E9-9278-68D0E5697425
  name: Controllable Collective States of Superconducting Qubit Ensembles
- _id: eb9b30ac-77a9-11ec-83b8-871f581d53d2
  name: Protected states of quantum matter
- _id: bdb108fd-d553-11ed-ba76-83dc74a9864f
  grant_number: F07105
  name: QUANTUM INFORMATION SYSTEMS BEYOND CLASSICAL CAPABILITIES / P5- Integration
    of Superconducting Quantum Circuits
publication: Nature Communications
publication_identifier:
  eissn:
  - 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  record:
  - id: '13124'
    relation: research_data
    status: public
  - id: '19533'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Tunable directional photon scattering from a pair of superconducting qubits
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'
...
---
OA_place: publisher
_id: '14622'
abstract:
- lang: eng
  text: "This Ph.D. thesis presents a detailed investigation into Variational Quantum
    Algorithms\r\n(VQAs), a promising class of quantum algorithms that are well suited
    for near-term quantum\r\ncomputation due to their moderate hardware requirements
    and resilience to noise. Our\r\nprimary focus lies on two particular types of
    VQAs: the Quantum Approximate Optimization\r\nAlgorithm (QAOA), used for solving
    binary optimization problems, and the Variational Quantum\r\nEigensolver (VQE),
    utilized for finding ground states of quantum many-body systems.\r\nIn the first
    part of the thesis, we examine the issue of effective parameter initialization
    for\r\nthe QAOA. The work demonstrates that random initialization of the QAOA
    often leads to\r\nconvergence in local minima with sub-optimal performance. To
    mitigate this issue, we propose\r\nan initialization of QAOA parameters based
    on the Trotterized Quantum Annealing (TQA).\r\nWe show that TQA initialization
    leads to the same performance as the best of an exponentially\r\nscaling number
    of random initializations.\r\nThe second study introduces Transition States (TS),
    stationary points with a single direction\r\nof descent, as a tool for systematically
    exploring the QAOA optimization landscape. This\r\nleads us to propose a novel
    greedy parameter initialization strategy that guarantees for the\r\nenergy to
    decrease with increasing number of circuit layers.\r\nIn the third section, we
    extend the QAOA to qudit systems, which are higher-dimensional\r\ngeneralizations
    of qubits. This chapter provides theoretical insights and practical strategies
    for\r\nleveraging the increased computational power of qudits in the context of
    quantum optimization\r\nalgorithms and suggests a quantum circuit for implementing
    the algorithm on an ion trap\r\nquantum computer.\r\nFinally, we propose an algorithm
    to avoid “barren plateaus”, regions in parameter space with\r\nvanishing gradients
    that obstruct efficient parameter optimization. This novel approach relies\r\non
    defining a notion of weak barren plateaus based on the entropies of local reduced
    density\r\nmatrices and showcases how these can be efficiently quantified using
    shadow tomography.\r\nTo illustrate the approach we employ the strategy in the
    VQE and show that it allows to\r\nsuccessfully avoid barren plateaus in the initialization
    and throughout the optimization.\r\nTaken together, this thesis greatly enhances
    our understanding of parameter initialization and\r\noptimization in VQAs, expands
    the scope of QAOA to higher-dimensional quantum systems,\r\nand presents a method
    to address the challenge of barren plateaus using the VQE. These\r\ninsights are
    instrumental in advancing the field of near-term quantum computation."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Stefan
  full_name: Sack, Stefan
  id: dd622248-f6e0-11ea-865d-ce382a1c81a5
  last_name: Sack
  orcid: 0000-0001-5400-8508
citation:
  ama: 'Sack S. Improving variational quantum algorithms: Innovative initialization
    techniques and extensions to qudit systems. 2023. doi:<a href="https://doi.org/10.15479/at:ista:14622">10.15479/at:ista:14622</a>'
  apa: 'Sack, S. (2023). <i>Improving variational quantum algorithms: Innovative initialization
    techniques and extensions to qudit systems</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/at:ista:14622">https://doi.org/10.15479/at:ista:14622</a>'
  chicago: 'Sack, Stefan. “Improving Variational Quantum Algorithms: Innovative Initialization
    Techniques and Extensions to Qudit Systems.” Institute of Science and Technology
    Austria, 2023. <a href="https://doi.org/10.15479/at:ista:14622">https://doi.org/10.15479/at:ista:14622</a>.'
  ieee: 'S. Sack, “Improving variational quantum algorithms: Innovative initialization
    techniques and extensions to qudit systems,” Institute of Science and Technology
    Austria, 2023.'
  ista: 'Sack S. 2023. Improving variational quantum algorithms: Innovative initialization
    techniques and extensions to qudit systems. Institute of Science and Technology
    Austria.'
  mla: 'Sack, Stefan. <i>Improving Variational Quantum Algorithms: Innovative Initialization
    Techniques and Extensions to Qudit Systems</i>. Institute of Science and Technology
    Austria, 2023, doi:<a href="https://doi.org/10.15479/at:ista:14622">10.15479/at:ista:14622</a>.'
  short: 'S. Sack, Improving Variational Quantum Algorithms: Innovative Initialization
    Techniques and Extensions to Qudit Systems, Institute of Science and Technology
    Austria, 2023.'
corr_author: '1'
date_created: 2023-11-28T10:58:13Z
date_published: 2023-11-30T00:00:00Z
date_updated: 2026-09-14T08:36:32Z
day: '30'
ddc:
- '530'
degree_awarded: PhD
department:
- _id: GradSch
- _id: MaSe
doi: 10.15479/at:ista:14622
doi_confirm: '1'
ec_funded: 1
file:
- access_level: open_access
  checksum: 068fd3570506ec42b2faa390de784bc4
  content_type: application/pdf
  creator: ssack
  date_created: 2023-11-30T15:53:10Z
  date_updated: 2024-11-30T23:30:03Z
  embargo: 2024-11-30
  file_id: '14635'
  file_name: PhD_Thesis.pdf
  file_size: 11947523
  relation: main_file
- access_level: closed
  checksum: 0fa3bc0d108aed0ac59d2c6beef2220a
  content_type: application/zip
  creator: ssack
  date_created: 2023-11-30T15:54:11Z
  date_updated: 2024-11-30T23:30:03Z
  embargo_to: open_access
  file_id: '14636'
  file_name: PhD Thesis (1).zip
  file_size: 18422964
  relation: source_file
file_date_updated: 2024-11-30T23:30:03Z
fulldoi: https://doi.org/10.15479/at:ista:14622
has_accepted_license: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-sa/4.0/
month: '11'
oa: 1
oa_version: Published Version
page: '142'
project:
- _id: bd660c93-d553-11ed-ba76-fb0fb6f49c0d
  name: IBM PhD Nomination Fellowship - Stefan Sack
- _id: 23841C26-32DE-11EA-91FC-C7463DDC885E
  call_identifier: H2020
  grant_number: '850899'
  name: 'Non-Ergodic Quantum Matter: Universality, Dynamics and Control'
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '13125'
    relation: part_of_dissertation
    status: public
  - id: '11471'
    relation: part_of_dissertation
    status: public
  - id: '9760'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Maksym
  full_name: Serbyn, Maksym
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
title: 'Improving variational quantum algorithms: Innovative initialization techniques
  and extensions to qudit systems'
tmp:
  image: /images/cc_by_nc_sa.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC
    BY-NC-SA 4.0)
  short: CC BY-NC-SA (4.0)
type: dissertation
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '2023'
...
---
_id: '13125'
abstract:
- lang: eng
  text: 'The quantum approximate optimization algorithm (QAOA) is a variational quantum
    algorithm, where a quantum computer implements a variational ansatz consisting
    of p layers of alternating unitary operators and a classical computer is used
    to optimize the variational parameters. For a random initialization, the optimization
    typically leads to local minima with poor performance, motivating the search for
    initialization strategies of QAOA variational parameters. Although numerous heuristic
    initializations exist, an analytical understanding and performance guarantees
    for large p remain evasive.We introduce a greedy initialization of QAOA which
    guarantees improving performance with an increasing number of layers. Our main
    result is an analytic construction of 2p + 1 transition states—saddle points with
    a unique negative curvature direction—for QAOA with p + 1 layers that use the
    local minimum of QAOA with p layers. Transition states connect to new local minima,
    which are guaranteed to lower the energy compared to the minimum found for p layers.
    We use the GREEDY procedure to navigate the exponentially increasing with p number
    of local minima resulting from the recursive application of our analytic construction.
    The performance of the GREEDY procedure matches available initialization strategies
    while providing a guarantee for the minimal energy to decrease with an increasing
    number of layers p. '
acknowledgement: 'We thank V. Verteletskyi for a joint collaboration on numerical
  studies of the QAOA during his internship at ISTA that inspired analytic results
  on TS reported in this work. We acknowledge A. A. Mele and M. Brooks for discussions
  and D. Egger, P. Love, and D. Wierichs for valuable feedback on the manuscript.
  S.H.S., R.A.M., and M.S. acknowledge support by the European Research Council (ERC)
  under the European Union’s Horizon 2020 research and innovation program (Grant Agreement
  No. 850899). R.K. is supported by the SFB BeyondC (Grant No. F7107-N38) and the
  project QuantumReady (FFG 896217). '
article_number: '062404'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Stefan
  full_name: Sack, Stefan
  id: dd622248-f6e0-11ea-865d-ce382a1c81a5
  last_name: Sack
  orcid: 0000-0001-5400-8508
- first_name: Raimel A
  full_name: Medina Ramos, Raimel A
  id: CE680B90-D85A-11E9-B684-C920E6697425
  last_name: Medina Ramos
  orcid: 0000-0002-5383-2869
- first_name: Richard
  full_name: Kueng, Richard
  last_name: Kueng
- first_name: Maksym
  full_name: Serbyn, Maksym
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
citation:
  ama: Sack S, Medina Ramos RA, Kueng R, Serbyn M. Recursive greedy initialization
    of the quantum approximate optimization algorithm with guaranteed improvement.
    <i>Physical Review A</i>. 2023;107(6). doi:<a href="https://doi.org/10.1103/physreva.107.062404">10.1103/physreva.107.062404</a>
  apa: Sack, S., Medina Ramos, R. A., Kueng, R., &#38; Serbyn, M. (2023). Recursive
    greedy initialization of the quantum approximate optimization algorithm with guaranteed
    improvement. <i>Physical Review A</i>. American Physical Society. <a href="https://doi.org/10.1103/physreva.107.062404">https://doi.org/10.1103/physreva.107.062404</a>
  chicago: Sack, Stefan, Raimel A Medina Ramos, Richard Kueng, and Maksym Serbyn.
    “Recursive Greedy Initialization of the Quantum Approximate Optimization Algorithm
    with Guaranteed Improvement.” <i>Physical Review A</i>. American Physical Society,
    2023. <a href="https://doi.org/10.1103/physreva.107.062404">https://doi.org/10.1103/physreva.107.062404</a>.
  ieee: S. Sack, R. A. Medina Ramos, R. Kueng, and M. Serbyn, “Recursive greedy initialization
    of the quantum approximate optimization algorithm with guaranteed improvement,”
    <i>Physical Review A</i>, vol. 107, no. 6. American Physical Society, 2023.
  ista: Sack S, Medina Ramos RA, Kueng R, Serbyn M. 2023. Recursive greedy initialization
    of the quantum approximate optimization algorithm with guaranteed improvement.
    Physical Review A. 107(6), 062404.
  mla: Sack, Stefan, et al. “Recursive Greedy Initialization of the Quantum Approximate
    Optimization Algorithm with Guaranteed Improvement.” <i>Physical Review A</i>,
    vol. 107, no. 6, 062404, American Physical Society, 2023, doi:<a href="https://doi.org/10.1103/physreva.107.062404">10.1103/physreva.107.062404</a>.
  short: S. Sack, R.A. Medina Ramos, R. Kueng, M. Serbyn, Physical Review A 107 (2023).
corr_author: '1'
date_created: 2023-06-07T06:57:32Z
date_published: 2023-06-02T00:00:00Z
date_updated: 2026-09-30T22:31:16Z
day: '02'
ddc:
- '530'
department:
- _id: MaSe
doi: 10.1103/physreva.107.062404
ec_funded: 1
external_id:
  arxiv:
  - '2209.01159'
  isi:
  - '001016927100012'
file:
- access_level: open_access
  checksum: 0d71423888eeccaa60d8f41197f26306
  content_type: application/pdf
  creator: dernst
  date_created: 2023-06-13T07:28:36Z
  date_updated: 2023-06-13T07:28:36Z
  file_id: '13131'
  file_name: 2023_PhysRevA_Sack.pdf
  file_size: 2524611
  relation: main_file
  success: 1
file_date_updated: 2023-06-13T07:28:36Z
fulldoi: https://doi.org/10.1103/physreva.107.062404
has_accepted_license: '1'
intvolume: '       107'
isi: 1
issue: '6'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
project:
- _id: 23841C26-32DE-11EA-91FC-C7463DDC885E
  call_identifier: H2020
  grant_number: '850899'
  name: 'Non-Ergodic Quantum Matter: Universality, Dynamics and Control'
publication: Physical Review A
publication_identifier:
  eissn:
  - 2469-9934
  issn:
  - 2469-9926
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
related_material:
  record:
  - id: '17208'
    relation: dissertation_contains
    status: public
  - id: '14622'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Recursive greedy initialization of the quantum approximate optimization algorithm
  with guaranteed improvement
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: 107
year: '2023'
...
---
_id: '14032'
abstract:
- lang: eng
  text: Arrays of Josephson junctions are governed by a competition between superconductivity
    and repulsive Coulomb interactions, and are expected to exhibit diverging low-temperature
    resistance when interactions exceed a critical level. Here we report a study of
    the transport and microwave response of Josephson arrays with interactions exceeding
    this level. Contrary to expectations, we observe that the array resistance drops
    dramatically as the temperature is decreased—reminiscent of superconducting behaviour—and
    then saturates at low temperature. Applying a magnetic field, we eventually observe
    a transition to a highly resistive regime. These observations can be understood
    within a theoretical picture that accounts for the effect of thermal fluctuations
    on the insulating phase. On the basis of the agreement between experiment and
    theory, we suggest that apparent superconductivity in our Josephson arrays arises
    from melting the zero-temperature insulator.
acknowledged_ssus:
- _id: M-Shop
- _id: NanoFab
acknowledgement: We thank D. Haviland, J. Pekola, C. Ciuti, A. Bubis and A. Shnirman
  for helpful feedback on the paper. This research was supported by the Scientific
  Service Units of IST Austria through resources provided by the MIBA Machine Shop
  and the Nanofabrication Facility. Work supported by the Austrian FWF grant P33692-N
  (S.M., J.S. and A.P.H.), the European Union’s Horizon 2020 Research and Innovation
  programme under the Marie Skłodowska-Curie Grant Agreement No. 754411 (J.S.) and
  a NOMIS foundation research grant (J.M.F. and A.P.H.).
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Soham
  full_name: Mukhopadhyay, Soham
  id: FDE60288-A89D-11E9-947F-1AF6E5697425
  last_name: Mukhopadhyay
  orcid: 0000-0001-5263-5559
- first_name: Jorden L
  full_name: Senior, Jorden L
  id: 5479D234-2D30-11EA-89CC-40953DDC885E
  last_name: Senior
  orcid: 0000-0002-0672-9295
- first_name: Jaime
  full_name: Saez Mollejo, Jaime
  id: e0390f72-f6e0-11ea-865d-862393336714
  last_name: Saez Mollejo
- first_name: Denise
  full_name: Puglia, Denise
  id: 4D495994-AE37-11E9-AC72-31CAE5697425
  last_name: Puglia
  orcid: 0000-0003-1144-2763
- first_name: Martin
  full_name: Zemlicka, Martin
  id: 2DCF8DE6-F248-11E8-B48F-1D18A9856A87
  last_name: Zemlicka
  orcid: 0009-0005-0878-3032
- first_name: Johannes M
  full_name: Fink, Johannes M
  id: 4B591CBA-F248-11E8-B48F-1D18A9856A87
  last_name: Fink
  orcid: 0000-0001-8112-028X
- first_name: Andrew P
  full_name: Higginbotham, Andrew P
  id: 4AD6785A-F248-11E8-B48F-1D18A9856A87
  last_name: Higginbotham
  orcid: 0000-0003-2607-2363
citation:
  ama: Mukhopadhyay S, Senior JL, Saez Mollejo J, et al. Superconductivity from a
    melted insulator in Josephson junction arrays. <i>Nature Physics</i>. 2023;19:1630-1635.
    doi:<a href="https://doi.org/10.1038/s41567-023-02161-w">10.1038/s41567-023-02161-w</a>
  apa: Mukhopadhyay, S., Senior, J. L., Saez Mollejo, J., Puglia, D., Zemlicka, M.,
    Fink, J. M., &#38; Higginbotham, A. P. (2023). Superconductivity from a melted
    insulator in Josephson junction arrays. <i>Nature Physics</i>. Springer Nature.
    <a href="https://doi.org/10.1038/s41567-023-02161-w">https://doi.org/10.1038/s41567-023-02161-w</a>
  chicago: Mukhopadhyay, Soham, Jorden L Senior, Jaime Saez Mollejo, Denise Puglia,
    Martin Zemlicka, Johannes M Fink, and Andrew P Higginbotham. “Superconductivity
    from a Melted Insulator in Josephson Junction Arrays.” <i>Nature Physics</i>.
    Springer Nature, 2023. <a href="https://doi.org/10.1038/s41567-023-02161-w">https://doi.org/10.1038/s41567-023-02161-w</a>.
  ieee: S. Mukhopadhyay <i>et al.</i>, “Superconductivity from a melted insulator
    in Josephson junction arrays,” <i>Nature Physics</i>, vol. 19. Springer Nature,
    pp. 1630–1635, 2023.
  ista: Mukhopadhyay S, Senior JL, Saez Mollejo J, Puglia D, Zemlicka M, Fink JM,
    Higginbotham AP. 2023. Superconductivity from a melted insulator in Josephson
    junction arrays. Nature Physics. 19, 1630–1635.
  mla: Mukhopadhyay, Soham, et al. “Superconductivity from a Melted Insulator in Josephson
    Junction Arrays.” <i>Nature Physics</i>, vol. 19, Springer Nature, 2023, pp. 1630–35,
    doi:<a href="https://doi.org/10.1038/s41567-023-02161-w">10.1038/s41567-023-02161-w</a>.
  short: S. Mukhopadhyay, J.L. Senior, J. Saez Mollejo, D. Puglia, M. Zemlicka, J.M.
    Fink, A.P. Higginbotham, Nature Physics 19 (2023) 1630–1635.
corr_author: '1'
date_created: 2023-08-11T07:41:17Z
date_published: 2023-11-01T00:00:00Z
date_updated: 2026-09-30T22:31:19Z
day: '01'
ddc:
- '530'
department:
- _id: GradSch
- _id: AnHi
- _id: JoFi
doi: 10.1038/s41567-023-02161-w
ec_funded: 1
external_id:
  isi:
  - '001054563800006'
file:
- access_level: open_access
  checksum: 1fc86d71bfbf836e221c1e925343adc5
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-29T11:25:38Z
  date_updated: 2024-01-29T11:25:38Z
  file_id: '14899'
  file_name: 2023_NaturePhysics_Mukhopadhyay.pdf
  file_size: 1977706
  relation: main_file
  success: 1
file_date_updated: 2024-01-29T11:25:38Z
fulldoi: https://doi.org/10.1038/s41567-023-02161-w
has_accepted_license: '1'
intvolume: '        19'
isi: 1
keyword:
- General Physics and Astronomy
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: 1630-1635
project:
- _id: 0aa3608a-070f-11eb-9043-e9cd8a2bd931
  grant_number: P33692
  name: Cavity electromechanics across a quantum phase transition
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
- _id: eb9b30ac-77a9-11ec-83b8-871f581d53d2
  name: Protected states of quantum matter
publication: Nature Physics
publication_identifier:
  eissn:
  - 1745-2481
  issn:
  - 1745-2473
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  record:
  - id: '17881'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Superconductivity from a melted insulator in Josephson junction arrays
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 19
year: '2023'
...
---
_id: '13136'
abstract:
- lang: eng
  text: Despite its fundamental importance for development, the question of how organs
    achieve their correct size and shape is poorly understood. This complex process
    requires coordination between the generation of cell mass and the morphogenetic
    mechanisms that sculpt tissues. These processes are regulated by morphogen signalling
    pathways and mechanical forces. Yet, in many systems, it is unclear how biochemical
    and mechanical signalling are quantitatively interpreted to determine the behaviours
    of individual cells and how they contribute to growth and morphogenesis at the
    tissue scale. In this review, we discuss the development of the vertebrate neural
    tube and somites as an example of the state of knowledge, as well as the challenges
    in understanding the mechanisms of tissue size control in vertebrate organogenesis.
    We highlight how the recent advances in stem cell differentiation and organoid
    approaches can be harnessed to provide new insights into this question.
acknowledgement: 'We thank J. Briscoe for comments on the manuscript. Work in the
  AK lab is supported by ISTA, the European Research Council under Horizon Europe:
  grant 101044579, and Austrian Science Fund (FWF): F78 (Stem Cell Modulation). SR
  is supported by Gesellschaft für Forschungsförderung Niederösterreich m.b.H. fellowship
  SC19-011.'
article_number: '100459'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Thomas
  full_name: Minchington, Thomas
  id: 7d1648cb-19e9-11eb-8e7a-f8c037fb3e3f
  last_name: Minchington
- first_name: Stefanie
  full_name: Rus, Stefanie
  id: 4D9EC9B6-F248-11E8-B48F-1D18A9856A87
  last_name: Rus
  orcid: 0000-0001-8703-1093
- first_name: Anna
  full_name: Kicheva, Anna
  id: 3959A2A0-F248-11E8-B48F-1D18A9856A87
  last_name: Kicheva
  orcid: 0000-0003-4509-4998
citation:
  ama: Minchington T, Rus S, Kicheva A. Control of tissue dimensions in the developing
    neural tube and somites. <i>Current Opinion in Systems Biology</i>. 2023;35. doi:<a
    href="https://doi.org/10.1016/j.coisb.2023.100459">10.1016/j.coisb.2023.100459</a>
  apa: Minchington, T., Rus, S., &#38; Kicheva, A. (2023). Control of tissue dimensions
    in the developing neural tube and somites. <i>Current Opinion in Systems Biology</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.coisb.2023.100459">https://doi.org/10.1016/j.coisb.2023.100459</a>
  chicago: Minchington, Thomas, Stefanie Rus, and Anna Kicheva. “Control of Tissue
    Dimensions in the Developing Neural Tube and Somites.” <i>Current Opinion in Systems
    Biology</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.coisb.2023.100459">https://doi.org/10.1016/j.coisb.2023.100459</a>.
  ieee: T. Minchington, S. Rus, and A. Kicheva, “Control of tissue dimensions in the
    developing neural tube and somites,” <i>Current Opinion in Systems Biology</i>,
    vol. 35. Elsevier, 2023.
  ista: Minchington T, Rus S, Kicheva A. 2023. Control of tissue dimensions in the
    developing neural tube and somites. Current Opinion in Systems Biology. 35, 100459.
  mla: Minchington, Thomas, et al. “Control of Tissue Dimensions in the Developing
    Neural Tube and Somites.” <i>Current Opinion in Systems Biology</i>, vol. 35,
    100459, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.coisb.2023.100459">10.1016/j.coisb.2023.100459</a>.
  short: T. Minchington, S. Rus, A. Kicheva, Current Opinion in Systems Biology 35
    (2023).
corr_author: '1'
date_created: 2023-06-18T22:00:46Z
date_published: 2023-09-01T00:00:00Z
date_updated: 2026-09-30T22:31:18Z
day: '01'
ddc:
- '570'
department:
- _id: AnKi
doi: 10.1016/j.coisb.2023.100459
file:
- access_level: open_access
  checksum: 8a75c4e29fd9b62e3c50663c2265b173
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-29T11:06:45Z
  date_updated: 2024-01-29T11:06:45Z
  file_id: '14896'
  file_name: 2023_CurrOpSystBioloy_Minchington.pdf
  file_size: 598842
  relation: main_file
  success: 1
file_date_updated: 2024-01-29T11:06:45Z
fulldoi: https://doi.org/10.1016/j.coisb.2023.100459
has_accepted_license: '1'
intvolume: '        35'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '09'
oa: 1
oa_version: Published Version
project:
- _id: bd7e737f-d553-11ed-ba76-d69ffb5ee3aa
  grant_number: '101044579'
  name: Mechanisms of tissue size regulation in spinal cord development
- _id: 059DF620-7A3F-11EA-A408-12923DDC885E
  grant_number: F7802
  name: Stem Cell Modulation in Neural Development and Regeneration/ P02-Morphogen
    control of growth and pattern in the spinal cord
- _id: 9B9B39FA-BA93-11EA-9121-9846C619BF3A
  grant_number: SC19-011
  name: The regulatory logic of pattern formation in the vertebrate dorsal neural
    tube
publication: Current Opinion in Systems Biology
publication_identifier:
  eissn:
  - 2452-3100
publication_status: published
publisher: Elsevier
quality_controlled: '1'
related_material:
  record:
  - id: '19763'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Control of tissue dimensions in the developing neural tube and somites
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 35
year: '2023'
...
---
_id: '14613'
abstract:
- lang: eng
  text: 'Many insects carry an ancient X chromosome - the Drosophila Muller element
    F - that likely predates their origin. Interestingly, the X has undergone turnover
    in multiple fly species (Diptera) after being conserved for more than 450 MY.
    The long evolutionary distance between Diptera and other sequenced insect clades
    makes it difficult to infer what could have contributed to this sudden increase
    in rate of turnover. Here, we produce the first genome and transcriptome of a
    long overlooked sister-order to Diptera: Mecoptera. We compare the scorpionfly
    Panorpa cognata X-chromosome gene content, expression, and structure, to that
    of several dipteran species as well as more distantly-related insect orders (Orthoptera
    and Blattodea). We find high conservation of gene content between the mecopteran
    X and the dipteran Muller F element, as well as several shared biological features,
    such as the presence of dosage compensation and a low amount of genetic diversity,
    consistent with a low recombination rate. However, the two homologous X chromosomes
    differ strikingly in their size and number of genes they carry. Our results therefore
    support a common ancestry of the mecopteran and ancestral dipteran X chromosomes,
    and suggest that Muller element F shrank in size and gene content after the split
    of Diptera and Mecoptera, which may have contributed to its turnover in dipteran
    insects.'
acknowledged_ssus:
- _id: ScienComp
acknowledgement: "We thank the Vicoso lab for their assistance with specimen collection,
  and Tim Connallon for valuable comments and suggestions on earlier versions of the
  manuscript. Computational resources and support were provided by the Scientific
  Computing unit at the ISTA. This research was supported by grants from the Austrian
  Science Foundation to C.L.\r\n(FWF ESP 39), and to B.V. (FWF SFB F88-10)."
article_number: msad245
article_processing_charge: Yes
article_type: original
author:
- first_name: Clementine
  full_name: Lasne, Clementine
  id: 02225f57-50d2-11eb-9ed8-8c92b9a34237
  last_name: Lasne
  orcid: 0000-0002-1197-8616
- first_name: Marwan N
  full_name: Elkrewi, Marwan N
  id: 0B46FACA-A8E1-11E9-9BD3-79D1E5697425
  last_name: Elkrewi
  orcid: 0000-0002-5328-7231
- first_name: Melissa A
  full_name: Toups, Melissa A
  id: 4E099E4E-F248-11E8-B48F-1D18A9856A87
  last_name: Toups
  orcid: 0000-0002-9752-7380
- first_name: Lorena Alexandra
  full_name: Layana Franco, Lorena Alexandra
  id: 02814589-eb8f-11eb-b029-a70074f3f18f
  last_name: Layana Franco
  orcid: 0000-0002-1253-6297
- first_name: Ariana
  full_name: Macon, Ariana
  id: 2A0848E2-F248-11E8-B48F-1D18A9856A87
  last_name: Macon
- first_name: Beatriz
  full_name: Vicoso, Beatriz
  id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
  last_name: Vicoso
  orcid: 0000-0002-4579-8306
citation:
  ama: Lasne C, Elkrewi MN, Toups MA, Layana Franco LA, Macon A, Vicoso B. The scorpionfly
    (Panorpa cognata) genome highlights conserved and derived features of the peculiar
    dipteran X chromosome. <i>Molecular Biology and Evolution</i>. 2023;40(12). doi:<a
    href="https://doi.org/10.1093/molbev/msad245">10.1093/molbev/msad245</a>
  apa: Lasne, C., Elkrewi, M. N., Toups, M. A., Layana Franco, L. A., Macon, A., &#38;
    Vicoso, B. (2023). The scorpionfly (Panorpa cognata) genome highlights conserved
    and derived features of the peculiar dipteran X chromosome. <i>Molecular Biology
    and Evolution</i>. Oxford University Press. <a href="https://doi.org/10.1093/molbev/msad245">https://doi.org/10.1093/molbev/msad245</a>
  chicago: Lasne, Clementine, Marwan N Elkrewi, Melissa A Toups, Lorena Alexandra
    Layana Franco, Ariana Macon, and Beatriz Vicoso. “The Scorpionfly (Panorpa Cognata)
    Genome Highlights Conserved and Derived Features of the Peculiar Dipteran X Chromosome.”
    <i>Molecular Biology and Evolution</i>. Oxford University Press, 2023. <a href="https://doi.org/10.1093/molbev/msad245">https://doi.org/10.1093/molbev/msad245</a>.
  ieee: C. Lasne, M. N. Elkrewi, M. A. Toups, L. A. Layana Franco, A. Macon, and B.
    Vicoso, “The scorpionfly (Panorpa cognata) genome highlights conserved and derived
    features of the peculiar dipteran X chromosome,” <i>Molecular Biology and Evolution</i>,
    vol. 40, no. 12. Oxford University Press, 2023.
  ista: Lasne C, Elkrewi MN, Toups MA, Layana Franco LA, Macon A, Vicoso B. 2023.
    The scorpionfly (Panorpa cognata) genome highlights conserved and derived features
    of the peculiar dipteran X chromosome. Molecular Biology and Evolution. 40(12),
    msad245.
  mla: Lasne, Clementine, et al. “The Scorpionfly (Panorpa Cognata) Genome Highlights
    Conserved and Derived Features of the Peculiar Dipteran X Chromosome.” <i>Molecular
    Biology and Evolution</i>, vol. 40, no. 12, msad245, Oxford University Press,
    2023, doi:<a href="https://doi.org/10.1093/molbev/msad245">10.1093/molbev/msad245</a>.
  short: C. Lasne, M.N. Elkrewi, M.A. Toups, L.A. Layana Franco, A. Macon, B. Vicoso,
    Molecular Biology and Evolution 40 (2023).
corr_author: '1'
date_created: 2023-11-27T16:14:37Z
date_published: 2023-12-01T00:00:00Z
date_updated: 2026-09-30T22:31:19Z
day: '01'
ddc:
- '570'
department:
- _id: BeVi
doi: 10.1093/molbev/msad245
external_id:
  isi:
  - '001122489000003'
  pmid:
  - '37988296'
file:
- access_level: open_access
  checksum: 47c1c72fb499f26ea52d216b242208c8
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-02T11:39:38Z
  date_updated: 2024-01-02T11:39:38Z
  file_id: '14727'
  file_name: 2023_MolecularBioEvo_Lasne.pdf
  file_size: 8623505
  relation: main_file
  success: 1
file_date_updated: 2024-01-02T11:39:38Z
fulldoi: https://doi.org/10.1093/molbev/msad245
has_accepted_license: '1'
intvolume: '        40'
isi: 1
issue: '12'
keyword:
- Genetics
- Molecular Biology
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 34ae1506-11ca-11ed-8bc3-c14f4c474396
  grant_number: F8810
  name: The highjacking of meiosis for asexual reproduction
- _id: ebb230e0-77a9-11ec-83b8-87a37e0241d3
  grant_number: ESP39 49461
  name: Mechanisms and Evolution of Reproductive Plasticity
publication: Molecular Biology and Evolution
publication_identifier:
  eissn:
  - 1537-1719
  issn:
  - 0737-4038
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
related_material:
  link:
  - description: News on ISTA webpage
    relation: press_release
    url: https://ista.ac.at/en/news/on-the-hunt/
  record:
  - id: '14614'
    relation: research_data
    status: public
  - id: '19386'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: The scorpionfly (Panorpa cognata) genome highlights conserved and derived features
  of the peculiar dipteran X chromosome
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: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 40
year: '2023'
...
---
_id: '12521'
abstract:
- lang: eng
  text: Differentiated X chromosomes are expected to have higher rates of adaptive
    divergence than autosomes, if new beneficial mutations are recessive (the “faster-X
    effect”), largely because these mutations are immediately exposed to selection
    in males. The evolution of X chromosomes after they stop recombining in males,
    but before they become hemizygous, has not been well explored theoretically. We
    use the diffusion approximation to infer substitution rates of beneficial and
    deleterious mutations under such a scenario. Our results show that selection is
    less efficient on diploid X loci than on autosomal and hemizygous X loci under
    a wide range of parameters. This “slower-X” effect is stronger for genes affecting
    primarily (or only) male fitness, and for sexually antagonistic genes. These unusual
    dynamics suggest that some of the peculiar features of X chromosomes, such as
    the differential accumulation of genes with sex-specific functions, may start
    arising earlier than previously appreciated.
acknowledgement: We thank the Vicoso and Barton groups and ISTA Scientific Computing
  Unit. We also thank two anonymous reviewers for their valuable comments. This work
  was supported by the European Research Council under the European Union’s Horizon
  2020 research and innovation program (grant agreements no. 715257 and no. 716117).
article_number: qrac004
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Andrea
  full_name: Mrnjavac, Andrea
  id: 353FAC84-AE61-11E9-8BFC-00D3E5697425
  last_name: Mrnjavac
- first_name: Kseniia
  full_name: Khudiakova, Kseniia
  id: 4E6DC800-AE37-11E9-AC72-31CAE5697425
  last_name: Khudiakova
  orcid: 0000-0002-6246-1465
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
- first_name: Beatriz
  full_name: Vicoso, Beatriz
  id: 49E1C5C6-F248-11E8-B48F-1D18A9856A87
  last_name: Vicoso
  orcid: 0000-0002-4579-8306
citation:
  ama: 'Mrnjavac A, Khudiakova K, Barton NH, Vicoso B. Slower-X: Reduced efficiency
    of selection in the early stages of X chromosome evolution. <i>Evolution Letters</i>.
    2023;7(1). doi:<a href="https://doi.org/10.1093/evlett/qrac004">10.1093/evlett/qrac004</a>'
  apa: 'Mrnjavac, A., Khudiakova, K., Barton, N. H., &#38; Vicoso, B. (2023). Slower-X:
    Reduced efficiency of selection in the early stages of X chromosome evolution.
    <i>Evolution Letters</i>. Oxford University Press. <a href="https://doi.org/10.1093/evlett/qrac004">https://doi.org/10.1093/evlett/qrac004</a>'
  chicago: 'Mrnjavac, Andrea, Kseniia Khudiakova, Nicholas H Barton, and Beatriz Vicoso.
    “Slower-X: Reduced Efficiency of Selection in the Early Stages of X Chromosome
    Evolution.” <i>Evolution Letters</i>. Oxford University Press, 2023. <a href="https://doi.org/10.1093/evlett/qrac004">https://doi.org/10.1093/evlett/qrac004</a>.'
  ieee: 'A. Mrnjavac, K. Khudiakova, N. H. Barton, and B. Vicoso, “Slower-X: Reduced
    efficiency of selection in the early stages of X chromosome evolution,” <i>Evolution
    Letters</i>, vol. 7, no. 1. Oxford University Press, 2023.'
  ista: 'Mrnjavac A, Khudiakova K, Barton NH, Vicoso B. 2023. Slower-X: Reduced efficiency
    of selection in the early stages of X chromosome evolution. Evolution Letters.
    7(1), qrac004.'
  mla: 'Mrnjavac, Andrea, et al. “Slower-X: Reduced Efficiency of Selection in the
    Early Stages of X Chromosome Evolution.” <i>Evolution Letters</i>, vol. 7, no.
    1, qrac004, Oxford University Press, 2023, doi:<a href="https://doi.org/10.1093/evlett/qrac004">10.1093/evlett/qrac004</a>.'
  short: A. Mrnjavac, K. Khudiakova, N.H. Barton, B. Vicoso, Evolution Letters 7 (2023).
corr_author: '1'
date_created: 2023-02-06T13:59:12Z
date_published: 2023-02-01T00:00:00Z
date_updated: 2026-09-30T22:31:21Z
day: '01'
ddc:
- '570'
department:
- _id: GradSch
- _id: BeVi
doi: 10.1093/evlett/qrac004
ec_funded: 1
external_id:
  isi:
  - '001021692200001'
  pmid:
  - '37065438'
file:
- access_level: open_access
  checksum: a240a041cb9b9b7c8ba93a4706674a3f
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T11:43:33Z
  date_updated: 2023-08-16T11:43:33Z
  file_id: '14068'
  file_name: 2023_EvLetters_Mrnjavac.pdf
  file_size: 2592189
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T11:43:33Z
fulldoi: https://doi.org/10.1093/evlett/qrac004
has_accepted_license: '1'
intvolume: '         7'
isi: 1
issue: '1'
keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 256E75B8-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '716117'
  name: Optimal Transport and Stochastic Dynamics
- _id: 250BDE62-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715257'
  name: Prevalence and Influence of Sexual Antagonism on Genome Evolution
publication: Evolution Letters
publication_identifier:
  issn:
  - 2056-3744
publication_status: published
publisher: Oxford University Press
quality_controlled: '1'
related_material:
  record:
  - id: '18531'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: 'Slower-X: Reduced efficiency of selection in the early stages of X chromosome
  evolution'
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: 7
year: '2023'
...
---
OA_place: repository
OA_type: green
_id: '23012'
abstract:
- lang: eng
  text: The onset of turbulence in pipe flow has defied detailed understanding ever
    since Reynolds' first observations revealed the spatially-heterogeneous nature
    of the transition. While recent theoretical studies and experiments in simpler,
    shear-driven flows suggest that the onset of turbulence is a directed percolation
    non-equilibrium phase transition, whether these findings are generic and apply
    also to open or pressure-driven flows is unknown. In pipe flow, the extremely
    long time scales near the transition make direct observations of critical behavior
    virtually impossible. Here, we circumvent these limitations by experimentally
    characterizing all pairwise interactions between localized patches of turbulence
    ("puffs"), and using these interactions as input to renormalization group and
    computer simulations of minimal models that extrapolate to long length and time
    scales. We show that the universality class of the transition is directed percolation,
    from which emerges a jammed phase of puffs above the critical point. The stronger
    interactions in the jamming regime enable us to explicitly measure the turbulent
    fraction and confirm model predictions. Our work shows that directed percolation
    scaling applies beyond simple closed shear flows, and underscores how statistical
    mechanics can lead to profound, quantitative and predictive insights on turbulent
    flows and their phases.
article_processing_charge: No
author:
- first_name: Grégoire
  full_name: Lemoult, Grégoire
  last_name: Lemoult
citation:
  ama: Lemoult G. Directed percolation and puff jamming near the transition to pipe
    turbulence. 2023. doi:<a href="https://doi.org/10.5281/zenodo.10308791">10.5281/zenodo.10308791</a>
  apa: Lemoult, G. (2023). Directed percolation and puff jamming near the transition
    to pipe turbulence. Zenodo. <a href="https://doi.org/10.5281/zenodo.10308791">https://doi.org/10.5281/zenodo.10308791</a>
  chicago: Lemoult, Grégoire. “Directed Percolation and Puff Jamming near the Transition
    to Pipe Turbulence.” Zenodo, 2023. <a href="https://doi.org/10.5281/zenodo.10308791">https://doi.org/10.5281/zenodo.10308791</a>.
  ieee: G. Lemoult, “Directed percolation and puff jamming near the transition to
    pipe turbulence.” Zenodo, 2023.
  ista: Lemoult G. 2023. Directed percolation and puff jamming near the transition
    to pipe turbulence, Zenodo, <a href="https://doi.org/10.5281/zenodo.10308791">10.5281/zenodo.10308791</a>.
  mla: Lemoult, Grégoire. <i>Directed Percolation and Puff Jamming near the Transition
    to Pipe Turbulence</i>. Zenodo, 2023, doi:<a href="https://doi.org/10.5281/zenodo.10308791">10.5281/zenodo.10308791</a>.
  short: G. Lemoult, (2023).
date_created: 2026-10-01T07:47:57Z
date_published: 2023-12-08T00:00:00Z
date_updated: 2026-10-01T07:50:31Z
day: '08'
department:
- _id: BjHo
doi: 10.5281/zenodo.10308791
fulldoi: https://doi.org/10.5281/zenodo.10308791
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5281/zenodo.10308791
month: '12'
oa: 1
oa_version: None
publisher: Zenodo
related_material:
  record:
  - id: '17128'
    relation: used_in_publication
    status: public
status: public
title: Directed percolation and puff jamming near the transition to pipe turbulence
type: research_data_reference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
year: '2023'
...
---
_id: '10818'
abstract:
- lang: eng
  text: Microglia cells are active players in regulating synaptic development and
    plasticity in the brain. However, how they influence the normal functioning of
    synapses is largely unknown. In this study, we characterized the effects of pharmacological
    microglia depletion, achieved by administration of PLX5622, on hippocampal CA3-CA1
    synapses of adult wild type mice. Following microglial depletion, we observed
    a reduction of spontaneous and evoked glutamatergic activity associated with a
    decrease of dendritic spine density. We also observed the appearance of immature
    synaptic features and higher levels of plasticity. Microglia depleted mice showed
    a deficit in the acquisition of the Novel Object Recognition task. These events
    were accompanied by hippocampal astrogliosis, although in the absence ofneuroinflammatory
    condition. PLX-induced synaptic changes were absent in Cx3cr1−/− mice, highlighting
    the role of CX3CL1/CX3CR1 axis in microglia control of synaptic functioning. Remarkably,
    microglia repopulation after PLX5622 withdrawal was associated with the recovery
    of hippocampal synapses and learning functions. Altogether, these data demonstrate
    that microglia contribute to normal synaptic functioning in the adult brain and
    that their removal induces reversible changes in organization and activity of
    glutamatergic synapses.
acknowledgement: The work was supported by a grant from MIUR (PRIN 2017HPTFFC_003)
  to Davide Ragozzino and in part by funds to Silvia Di Angelantonio (CrestOptics-IIT
  JointLab for Advanced Microscopy) and Daniele Caprioli (Istituto Pasteur-Fondazione
  Cenci Bolognetti). Bernadette Basilico, and Laura Ferrucci were supported by the
  PhD program in Clinical-Experimental Neuroscience and Psychiatry, Sapienza University,
  Rome; Caterina Sanchini was supported by the PhD program in Life Science, Sapienza
  University, Rome and by the Italian Institute of Technology, Rome. The authors thank
  Alessandro Felici, Claudia Valeri, Arsenio Armagno, and Senthilkumar Deivasigamani
  for help with animal husbandry and transgenic colonies management. They also wish
  to thank Piotr Bregestovski and Michal Schwartz for helpful discussions and criticism.
  PLX5622 was provided under Materials Transfer Agreement by Plexxikon Inc. (Berkeley,
  CA). Open Access Funding provided by Universita degli Studi di Roma La Sapienza
  within the CRUI-CARE Agreement.
article_processing_charge: No
article_type: original
author:
- first_name: Bernadette
  full_name: Basilico, Bernadette
  id: 36035796-5ACA-11E9-A75E-7AF2E5697425
  last_name: Basilico
  orcid: 0000-0003-1843-3173
- first_name: Laura
  full_name: Ferrucci, Laura
  last_name: Ferrucci
- first_name: Patrizia
  full_name: Ratano, Patrizia
  last_name: Ratano
- first_name: Maria T.
  full_name: Golia, Maria T.
  last_name: Golia
- first_name: Alfonso
  full_name: Grimaldi, Alfonso
  last_name: Grimaldi
- first_name: Maria
  full_name: Rosito, Maria
  last_name: Rosito
- first_name: Valentina
  full_name: Ferretti, Valentina
  last_name: Ferretti
- first_name: Ingrid
  full_name: Reverte, Ingrid
  last_name: Reverte
- first_name: Caterina
  full_name: Sanchini, Caterina
  last_name: Sanchini
- first_name: Maria C.
  full_name: Marrone, Maria C.
  last_name: Marrone
- first_name: Maria
  full_name: Giubettini, Maria
  last_name: Giubettini
- first_name: Valeria
  full_name: De Turris, Valeria
  last_name: De Turris
- first_name: Debora
  full_name: Salerno, Debora
  last_name: Salerno
- first_name: Stefano
  full_name: Garofalo, Stefano
  last_name: Garofalo
- first_name: Marie‐Kim
  full_name: St‐Pierre, Marie‐Kim
  last_name: St‐Pierre
- first_name: Micael
  full_name: Carrier, Micael
  last_name: Carrier
- first_name: Massimiliano
  full_name: Renzi, Massimiliano
  last_name: Renzi
- first_name: Francesca
  full_name: Pagani, Francesca
  last_name: Pagani
- first_name: Brijesh
  full_name: Modi, Brijesh
  last_name: Modi
- first_name: Marcello
  full_name: Raspa, Marcello
  last_name: Raspa
- first_name: Ferdinando
  full_name: Scavizzi, Ferdinando
  last_name: Scavizzi
- first_name: Cornelius T.
  full_name: Gross, Cornelius T.
  last_name: Gross
- first_name: Silvia
  full_name: Marinelli, Silvia
  last_name: Marinelli
- first_name: Marie‐Ève
  full_name: Tremblay, Marie‐Ève
  last_name: Tremblay
- first_name: Daniele
  full_name: Caprioli, Daniele
  last_name: Caprioli
- first_name: Laura
  full_name: Maggi, Laura
  last_name: Maggi
- first_name: Cristina
  full_name: Limatola, Cristina
  last_name: Limatola
- first_name: Silvia
  full_name: Di Angelantonio, Silvia
  last_name: Di Angelantonio
- first_name: Davide
  full_name: Ragozzino, Davide
  last_name: Ragozzino
citation:
  ama: Basilico B, Ferrucci L, Ratano P, et al. Microglia control glutamatergic synapses
    in the adult mouse hippocampus. <i>Glia</i>. 2022;70(1):173-195. doi:<a href="https://doi.org/10.1002/glia.24101">10.1002/glia.24101</a>
  apa: Basilico, B., Ferrucci, L., Ratano, P., Golia, M. T., Grimaldi, A., Rosito,
    M., … Ragozzino, D. (2022). Microglia control glutamatergic synapses in the adult
    mouse hippocampus. <i>Glia</i>. Wiley. <a href="https://doi.org/10.1002/glia.24101">https://doi.org/10.1002/glia.24101</a>
  chicago: Basilico, Bernadette, Laura Ferrucci, Patrizia Ratano, Maria T. Golia,
    Alfonso Grimaldi, Maria Rosito, Valentina Ferretti, et al. “Microglia Control
    Glutamatergic Synapses in the Adult Mouse Hippocampus.” <i>Glia</i>. Wiley, 2022.
    <a href="https://doi.org/10.1002/glia.24101">https://doi.org/10.1002/glia.24101</a>.
  ieee: B. Basilico <i>et al.</i>, “Microglia control glutamatergic synapses in the
    adult mouse hippocampus,” <i>Glia</i>, vol. 70, no. 1. Wiley, pp. 173–195, 2022.
  ista: Basilico B, Ferrucci L, Ratano P, Golia MT, Grimaldi A, Rosito M, Ferretti
    V, Reverte I, Sanchini C, Marrone MC, Giubettini M, De Turris V, Salerno D, Garofalo
    S, St‐Pierre M, Carrier M, Renzi M, Pagani F, Modi B, Raspa M, Scavizzi F, Gross
    CT, Marinelli S, Tremblay M, Caprioli D, Maggi L, Limatola C, Di Angelantonio
    S, Ragozzino D. 2022. Microglia control glutamatergic synapses in the adult mouse
    hippocampus. Glia. 70(1), 173–195.
  mla: Basilico, Bernadette, et al. “Microglia Control Glutamatergic Synapses in the
    Adult Mouse Hippocampus.” <i>Glia</i>, vol. 70, no. 1, Wiley, 2022, pp. 173–95,
    doi:<a href="https://doi.org/10.1002/glia.24101">10.1002/glia.24101</a>.
  short: B. Basilico, L. Ferrucci, P. Ratano, M.T. Golia, A. Grimaldi, M. Rosito,
    V. Ferretti, I. Reverte, C. Sanchini, M.C. Marrone, M. Giubettini, V. De Turris,
    D. Salerno, S. Garofalo, M. St‐Pierre, M. Carrier, M. Renzi, F. Pagani, B. Modi,
    M. Raspa, F. Scavizzi, C.T. Gross, S. Marinelli, M. Tremblay, D. Caprioli, L.
    Maggi, C. Limatola, S. Di Angelantonio, D. Ragozzino, Glia 70 (2022) 173–195.
corr_author: '1'
date_created: 2022-03-04T08:53:37Z
date_published: 2022-01-01T00:00:00Z
date_updated: 2024-10-09T21:04:02Z
day: '01'
ddc:
- '570'
department:
- _id: GaNo
doi: 10.1002/glia.24101
external_id:
  isi:
  - '000708025800001'
  pmid:
  - '34661306'
file:
- access_level: open_access
  checksum: f10a897290e66c0a062e04ba91db6c17
  content_type: application/pdf
  creator: dernst
  date_created: 2022-03-04T08:55:27Z
  date_updated: 2022-03-04T08:55:27Z
  file_id: '10819'
  file_name: 2021_Glia_Basilico.pdf
  file_size: 5340294
  relation: main_file
  success: 1
file_date_updated: 2022-03-04T08:55:27Z
fulldoi: https://doi.org/10.1002/glia.24101
has_accepted_license: '1'
intvolume: '        70'
isi: 1
issue: '1'
keyword:
- Cellular and Molecular Neuroscience
- Neurology
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc/4.0/
month: '01'
oa: 1
oa_version: Published Version
page: 173-195
pmid: 1
publication: Glia
publication_identifier:
  eissn:
  - 1098-1136
  issn:
  - 0894-1491
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Microglia control glutamatergic synapses in the adult mouse hippocampus
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: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 70
year: '2022'
...
---
OA_type: closed access
_id: '10820'
abstract:
- lang: eng
  text: Streaky structures in the boundary layers are often generated by surface roughness
    elements and/or free-stream turbulence, and are known to have significant effects
    on boundary-layer instability. In this paper, we investigate the impact of two
    forms of streaks on the instability of supersonic boundary layers. The first concerns
    the streaks generated by an array of spanwise periodic and streamwise elongated
    surface roughness elements, and our interest is how these streaks influence the
    lower-branch viscous first modes, whose characteristic wavelength and frequency
    are on the classical triple-deck scales. By adapting the triple-deck theory in
    the incompressible regime to the supersonic one, we first derived a simplified
    system which allows for efficient calculation of the streaks. The asymptotic analysis
    simplifies a bi-global eigenvalue problem to a one-dimensional problem in the
    spanwise direction, showing that the instability is controlled at leading order
    solely by the spanwise-dependent wall shear. In the fundamental configuration,
    the streaks stabilize first modes at low frequencies but destabilize the high-frequency
    ones. In the subharmonic configuration, the streaks generally destabilize the
    first mode across the entire frequency band. Importantly, the spanwise even modes
    are of radiating nature, i.e. they emit acoustic waves spontaneously to the far
    field. Streaks of the second form are generated by low-frequency vortical disturbances
    representing free-stream turbulence. They alter the flow in the entire layer and
    their effects on instability are investigated by solving the inviscid bi-global
    eigenvalue problem. Different from the incompressible case, a multitude of compressible
    instability modes exists, of which the dominant mode is an inviscid instability
    associated with the spanwise shear. In addition, there exists a separate branch
    of instability modes that have smaller growth rates but are spontaneously radiating.
acknowledgement: The work is supported by the National Key Research and Development
  Program of China (No. 2016YFA0401200), the National Natural Science Foundation of
  China (Grant Nos. 91952202 and 11402167).
alternative_title:
- IUTAM
article_processing_charge: No
author:
- first_name: Jianxin
  full_name: Liu, Jianxin
  last_name: Liu
- first_name: Elena
  full_name: Marensi, Elena
  id: 0BE7553A-1004-11EA-B805-18983DDC885E
  last_name: Marensi
  orcid: 0000-0001-7173-4923
- first_name: Xuesong
  full_name: Wu, Xuesong
  last_name: Wu
citation:
  ama: 'Liu J, Marensi E, Wu X. Effects of streaky structures on the instability of
    supersonic boundary layers. In: <i>IUTAM Laminar-Turbulent Transition</i>. Vol
    38. Springer Nature; 2022:587-598. doi:<a href="https://doi.org/10.1007/978-3-030-67902-6_51">10.1007/978-3-030-67902-6_51</a>'
  apa: 'Liu, J., Marensi, E., &#38; Wu, X. (2022). Effects of streaky structures on
    the instability of supersonic boundary layers. In <i>IUTAM Laminar-Turbulent Transition</i>
    (Vol. 38, pp. 587–598). London, United Kingdom: Springer Nature. <a href="https://doi.org/10.1007/978-3-030-67902-6_51">https://doi.org/10.1007/978-3-030-67902-6_51</a>'
  chicago: Liu, Jianxin, Elena Marensi, and Xuesong Wu. “Effects of Streaky Structures
    on the Instability of Supersonic Boundary Layers.” In <i>IUTAM Laminar-Turbulent
    Transition</i>, 38:587–98. Springer Nature, 2022. <a href="https://doi.org/10.1007/978-3-030-67902-6_51">https://doi.org/10.1007/978-3-030-67902-6_51</a>.
  ieee: J. Liu, E. Marensi, and X. Wu, “Effects of streaky structures on the instability
    of supersonic boundary layers,” in <i>IUTAM Laminar-Turbulent Transition</i>,
    London, United Kingdom, 2022, vol. 38, pp. 587–598.
  ista: Liu J, Marensi E, Wu X. 2022. Effects of streaky structures on the instability
    of supersonic boundary layers. IUTAM Laminar-Turbulent Transition. IUTAM Symposium,
    IUTAM, vol. 38, 587–598.
  mla: Liu, Jianxin, et al. “Effects of Streaky Structures on the Instability of Supersonic
    Boundary Layers.” <i>IUTAM Laminar-Turbulent Transition</i>, vol. 38, Springer
    Nature, 2022, pp. 587–98, doi:<a href="https://doi.org/10.1007/978-3-030-67902-6_51">10.1007/978-3-030-67902-6_51</a>.
  short: J. Liu, E. Marensi, X. Wu, in:, IUTAM Laminar-Turbulent Transition, Springer
    Nature, 2022, pp. 587–598.
conference:
  end_date: 2019-09-06
  location: London, United Kingdom
  name: IUTAM Symposium
  start_date: 2019-09-02
date_created: 2022-03-04T09:14:34Z
date_published: 2022-01-01T00:00:00Z
date_updated: 2025-05-20T06:08:26Z
day: '01'
department:
- _id: BjHo
doi: 10.1007/978-3-030-67902-6_51
external_id:
  isi:
  - '000709087600051'
fulldoi: https://doi.org/10.1007/978-3-030-67902-6_51
intvolume: '        38'
isi: 1
language:
- iso: eng
month: '01'
oa_version: None
page: 587-598
publication: IUTAM Laminar-Turbulent Transition
publication_identifier:
  eisbn:
  - '9783030679026'
  eissn:
  - 1875-3493
  isbn:
  - '9783030679019'
  issn:
  - 1875-3507
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Effects of streaky structures on the instability of supersonic boundary layers
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 38
year: '2022'
...
---
_id: '10825'
abstract:
- lang: eng
  text: In development, lineage segregation is coordinated in time and space. An important
    example is the mammalian inner cell mass, in which the primitive endoderm (PrE,
    founder of the yolk sac) physically segregates from the epiblast (EPI, founder
    of the fetus). While the molecular requirements have been well studied, the physical
    mechanisms determining spatial segregation between EPI and PrE remain elusive.
    Here, we investigate the mechanical basis of EPI and PrE sorting. We find that
    rather than the differences in static cell surface mechanical parameters as in
    classical sorting models, it is the differences in surface fluctuations that robustly
    ensure physical lineage sorting. These differential surface fluctuations systematically
    correlate with differential cellular fluidity, which we propose together constitute
    a non-equilibrium sorting mechanism for EPI and PrE lineages. By combining experiments
    and modeling, we identify cell surface dynamics as a key factor orchestrating
    the correct spatial segregation of the founder embryonic lineages.
acknowledgement: We are grateful to H. Niwa for Dox regulatable PB vector; G. Charras
  for EzrinT567D cDNA; K. Jones for tdTomato ESCs, R26-Confetti ESCs, and laboratory
  assistance; M. Kinoshita for pPB-CAG-H2B-BFP plasmid; P. Humphreys and D. Clements
  for imaging support; G. Chu, P. Attlesey, and staff for animal husbandry; S. Pallett
  for laboratory assistance; C. Mulas for critical feedback on the project; T. Boroviak
  for single-cell RNA-seq; the EMBL Genomics Core Facility for sequencing; and M.
  Merkel for developing and sharing the original version of the 3D Voronoi code. This
  work was financially supported by BBSRC ( BB/Moo4023/1 and BB/T007044/1 to K.J.C.
  and J.N., Alert16 grant BB/R000042 to E.K.P.), Leverhulme Trust ( RPG-2014-080 to
  K.J.C. and J.N.), European Research Council ( 772798 -CellFateTech to K.J.C., 311637
  -MorphoCorDiv and 820188 -NanoMechShape to E.K.P., Starting Grant 851288 to E.H.,
  and 772426 -MeChemGui to K.F.), the Isaac Newton Trust (to E.K.P.), Medical Research
  Council UK (MRC program award MC_UU_00012/5 to E.K.P.), the European Union’s Horizon
  2020 research and innovation program under the Marie Sklodowska-Curie grant agreement
  no. 641639 ( ITN Biopol , H.D.B. and E.K.P.), the Alexander von Humboldt Foundation
  (Alexander von Humboldt Professorship to K.F.), EMBO ALTF 522-2021 (to P.S.), Centre
  for Trophoblast Research (Next Generation fellowship to S.A.), and JSPS Overseas
  Research Fellowships (to A.Y.). The Wellcome-MRC Cambridge Stem Cell Institute receives
  core funding from Wellcome Trust ( 203151/Z/16/Z ) and MRC ( MC_PC_17230 ). For
  the purpose of open access, the author has applied a CC BY public copyright licence
  to any Author Accepted Manuscript version arising from this submission.
article_processing_charge: No
article_type: original
author:
- first_name: Ayaka
  full_name: Yanagida, Ayaka
  last_name: Yanagida
- first_name: Elena
  full_name: Corujo-Simon, Elena
  last_name: Corujo-Simon
- first_name: Christopher K.
  full_name: Revell, Christopher K.
  last_name: Revell
- first_name: Preeti
  full_name: Sahu, Preeti
  id: 55BA52EE-A185-11EA-88FD-18AD3DDC885E
  last_name: Sahu
- first_name: Giuliano G.
  full_name: Stirparo, Giuliano G.
  last_name: Stirparo
- first_name: Irene M.
  full_name: Aspalter, Irene M.
  last_name: Aspalter
- first_name: Alex K.
  full_name: Winkel, Alex K.
  last_name: Winkel
- first_name: Ruby
  full_name: Peters, Ruby
  last_name: Peters
- first_name: Henry
  full_name: De Belly, Henry
  last_name: De Belly
- first_name: Davide A.D.
  full_name: Cassani, Davide A.D.
  last_name: Cassani
- first_name: Sarra
  full_name: Achouri, Sarra
  last_name: Achouri
- first_name: Raphael
  full_name: Blumenfeld, Raphael
  last_name: Blumenfeld
- first_name: Kristian
  full_name: Franze, Kristian
  last_name: Franze
- 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: Ewa K.
  full_name: Paluch, Ewa K.
  last_name: Paluch
- first_name: Jennifer
  full_name: Nichols, Jennifer
  last_name: Nichols
- first_name: Kevin J.
  full_name: Chalut, Kevin J.
  last_name: Chalut
citation:
  ama: Yanagida A, Corujo-Simon E, Revell CK, et al. Cell surface fluctuations regulate
    early embryonic lineage sorting. <i>Cell</i>. 2022;185(5):777-793.e20. doi:<a
    href="https://doi.org/10.1016/j.cell.2022.01.022">10.1016/j.cell.2022.01.022</a>
  apa: Yanagida, A., Corujo-Simon, E., Revell, C. K., Sahu, P., Stirparo, G. G., Aspalter,
    I. M., … Chalut, K. J. (2022). Cell surface fluctuations regulate early embryonic
    lineage sorting. <i>Cell</i>. Cell Press. <a href="https://doi.org/10.1016/j.cell.2022.01.022">https://doi.org/10.1016/j.cell.2022.01.022</a>
  chicago: Yanagida, Ayaka, Elena Corujo-Simon, Christopher K. Revell, Preeti Sahu,
    Giuliano G. Stirparo, Irene M. Aspalter, Alex K. Winkel, et al. “Cell Surface
    Fluctuations Regulate Early Embryonic Lineage Sorting.” <i>Cell</i>. Cell Press,
    2022. <a href="https://doi.org/10.1016/j.cell.2022.01.022">https://doi.org/10.1016/j.cell.2022.01.022</a>.
  ieee: A. Yanagida <i>et al.</i>, “Cell surface fluctuations regulate early embryonic
    lineage sorting,” <i>Cell</i>, vol. 185, no. 5. Cell Press, p. 777–793.e20, 2022.
  ista: Yanagida A, Corujo-Simon E, Revell CK, Sahu P, Stirparo GG, Aspalter IM, Winkel
    AK, Peters R, De Belly H, Cassani DAD, Achouri S, Blumenfeld R, Franze K, Hannezo
    EB, Paluch EK, Nichols J, Chalut KJ. 2022. Cell surface fluctuations regulate
    early embryonic lineage sorting. Cell. 185(5), 777–793.e20.
  mla: Yanagida, Ayaka, et al. “Cell Surface Fluctuations Regulate Early Embryonic
    Lineage Sorting.” <i>Cell</i>, vol. 185, no. 5, Cell Press, 2022, p. 777–793.e20,
    doi:<a href="https://doi.org/10.1016/j.cell.2022.01.022">10.1016/j.cell.2022.01.022</a>.
  short: A. Yanagida, E. Corujo-Simon, C.K. Revell, P. Sahu, G.G. Stirparo, I.M. Aspalter,
    A.K. Winkel, R. Peters, H. De Belly, D.A.D. Cassani, S. Achouri, R. Blumenfeld,
    K. Franze, E.B. Hannezo, E.K. Paluch, J. Nichols, K.J. Chalut, Cell 185 (2022)
    777–793.e20.
date_created: 2022-03-06T23:01:52Z
date_published: 2022-02-22T00:00:00Z
date_updated: 2025-07-10T11:50:00Z
day: '22'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.1016/j.cell.2022.01.022
ec_funded: 1
external_id:
  isi:
  - '000796293700007'
  pmid:
  - '35196500'
file:
- access_level: open_access
  checksum: ae305060e8031297771b89dae9e36a29
  content_type: application/pdf
  creator: dernst
  date_created: 2022-03-07T07:55:23Z
  date_updated: 2022-03-07T07:55:23Z
  file_id: '10831'
  file_name: 2022_Cell_Yanagida.pdf
  file_size: 8478995
  relation: main_file
  success: 1
file_date_updated: 2022-03-07T07:55:23Z
fulldoi: https://doi.org/10.1016/j.cell.2022.01.022
has_accepted_license: '1'
intvolume: '       185'
isi: 1
issue: '5'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 777-793.e20
pmid: 1
project:
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '851288'
  name: Design Principles of Branching Morphogenesis
publication: Cell
publication_identifier:
  eissn:
  - 1097-4172
  issn:
  - 0092-8674
publication_status: published
publisher: Cell Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Cell surface fluctuations regulate early embryonic lineage sorting
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: 185
year: '2022'
...
---
_id: '10826'
abstract:
- lang: eng
  text: Animals that lose one sensory modality often show augmented responses to other
    sensory inputs. The mechanisms underpinning this cross-modal plasticity are poorly
    understood. We probe such mechanisms by performing a forward genetic screen for
    mutants with enhanced O2 perception in Caenorhabditis elegans. Multiple mutants
    exhibiting increased O2 responsiveness concomitantly show defects in other sensory
    responses. One mutant, qui-1, defective in a conserved NACHT/WD40 protein, abolishes
    pheromone-evoked Ca2+ responses in the ADL pheromone-sensing neurons. At the same
    time, ADL responsiveness to pre-synaptic input from O2-sensing neurons is heightened
    in qui-1, and other sensory defective mutants, resulting in enhanced neurosecretion
    although not increased Ca2+ responses. Expressing qui-1 selectively in ADL rescues
    both the qui-1 ADL neurosecretory phenotype and enhanced escape from 21% O2. Profiling
    ADL neurons in qui-1 mutants highlights extensive changes in gene expression,
    notably of many neuropeptide receptors. We show that elevated ADL expression of
    the conserved neuropeptide receptor NPR-22 is necessary for enhanced ADL neurosecretion
    in qui-1 mutants, and is sufficient to confer increased ADL neurosecretion in
    control animals. Sensory loss can thus confer cross-modal plasticity by changing
    the peptidergic connectome.
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: ScienComp
acknowledgement: "We would like to thank Gemma Chandratillake and Merav Cohen for
  identifying mutants and José David Moñino Sánchez for his help on neurosecretion
  assays. We are grateful to Kaveh Ashrafi (UCSF), Piali Sengupta (Brandeis), and
  the Caenorhabditis Genetic Center (funded by National Institutes of Health Infrastructure
  Program P40 OD010440) for strains and reagents ... and Rebecca Butcher (Univ. Florida)
  for C9 pheromone. We thank Tim Stevens, Paula Freire-Pritchett, Alastair Crisp,
  GurpreetGhattaoraya, and Fabian Amman for help with bioinformatic analysis, Ekaterina
  Lashmanova for help with injections, Iris Hardege for strains, and Isabel Beets
  (KU Leuven) and members of the de Bono Lab for comments on the manuscript. We thank
  the CRUK Cambridge Research Institute Genomics Core for next generation sequencing
  and the Flow Cytometry Facility at LMB for FACS. This research was supported by
  the Scientific Service Units (SSU) of IST Austria through resources provided by
  the Bioimaging Facility (BIF), the Life Science Facility (LSF) and Scientific Computing
  (SciCo-p– Bioinformatics).\r\nThis work was supported by the Medical Research Council
  UK (Studentship to GV), an\r\nAdvanced ERC grant (269,058 ACMO to MdB), and a Wellcome
  Investigator Award (209504/Z/17/Z to MdB)."
article_number: e68040
article_processing_charge: No
article_type: original
author:
- first_name: Giulio
  full_name: Valperga, Giulio
  id: 67F289DE-0D8F-11EA-9BDD-54AE3DDC885E
  last_name: Valperga
  orcid: 0000-0001-6726-3890
- first_name: Mario
  full_name: De Bono, Mario
  id: 4E3FF80E-F248-11E8-B48F-1D18A9856A87
  last_name: De Bono
  orcid: 0000-0001-8347-0443
citation:
  ama: Valperga G, de Bono M. Impairing one sensory modality enhances another by reconfiguring
    peptidergic signalling in Caenorhabditis elegans. <i>eLife</i>. 2022;11. doi:<a
    href="https://doi.org/10.7554/eLife.68040">10.7554/eLife.68040</a>
  apa: Valperga, G., &#38; de Bono, M. (2022). Impairing one sensory modality enhances
    another by reconfiguring peptidergic signalling in Caenorhabditis elegans. <i>ELife</i>.
    eLife Sciences Publications. <a href="https://doi.org/10.7554/eLife.68040">https://doi.org/10.7554/eLife.68040</a>
  chicago: Valperga, Giulio, and Mario de Bono. “Impairing One Sensory Modality Enhances
    Another by Reconfiguring Peptidergic Signalling in Caenorhabditis Elegans.” <i>ELife</i>.
    eLife Sciences Publications, 2022. <a href="https://doi.org/10.7554/eLife.68040">https://doi.org/10.7554/eLife.68040</a>.
  ieee: G. Valperga and M. de Bono, “Impairing one sensory modality enhances another
    by reconfiguring peptidergic signalling in Caenorhabditis elegans,” <i>eLife</i>,
    vol. 11. eLife Sciences Publications, 2022.
  ista: Valperga G, de Bono M. 2022. Impairing one sensory modality enhances another
    by reconfiguring peptidergic signalling in Caenorhabditis elegans. eLife. 11,
    e68040.
  mla: Valperga, Giulio, and Mario de Bono. “Impairing One Sensory Modality Enhances
    Another by Reconfiguring Peptidergic Signalling in Caenorhabditis Elegans.” <i>ELife</i>,
    vol. 11, e68040, eLife Sciences Publications, 2022, doi:<a href="https://doi.org/10.7554/eLife.68040">10.7554/eLife.68040</a>.
  short: G. Valperga, M. de Bono, ELife 11 (2022).
corr_author: '1'
date_created: 2022-03-06T23:01:52Z
date_published: 2022-02-24T00:00:00Z
date_updated: 2026-04-02T12:45:39Z
day: '24'
ddc:
- '570'
department:
- _id: MaDe
doi: 10.7554/eLife.68040
external_id:
  isi:
  - '000763432300001'
  pmid:
  - '35201977'
file:
- access_level: open_access
  checksum: cc1b9bf866d0f61f965556e0dd03d3ac
  content_type: application/pdf
  creator: dernst
  date_created: 2022-03-07T07:39:25Z
  date_updated: 2022-03-07T07:39:25Z
  file_id: '10830'
  file_name: 2022_eLife_Valperga.pdf
  file_size: 4095591
  relation: main_file
  success: 1
file_date_updated: 2022-03-07T07:39:25Z
fulldoi: https://doi.org/10.7554/eLife.68040
has_accepted_license: '1'
intvolume: '        11'
isi: 1
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 23870BE8-32DE-11EA-91FC-C7463DDC885E
  grant_number: 209504/A/17/Z
  name: Molecular mechanisms of neural circuit function
publication: eLife
publication_identifier:
  eissn:
  - 2050-084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
scopus_import: '1'
status: public
title: Impairing one sensory modality enhances another by reconfiguring peptidergic
  signalling in Caenorhabditis elegans
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 11
year: '2022'
...
---
_id: '10828'
abstract:
- lang: eng
  text: Digital images enable quantitative analysis of material properties at micro
    and macro length scales, but choosing an appropriate resolution when acquiring
    the image is challenging. A high resolution means longer image acquisition and
    larger data requirements for a given sample, but if the resolution is too low,
    significant information may be lost. This paper studies the impact of changes
    in resolution on persistent homology, a tool from topological data analysis that
    provides a signature of structure in an image across all length scales. Given
    prior information about a function, the geometry of an object, or its density
    distribution at a given resolution, we provide methods to select the coarsest
    resolution yielding results within an acceptable tolerance. We present numerical
    case studies for an illustrative synthetic example and samples from porous materials
    where the theoretical bounds are unknown.
article_processing_charge: No
arxiv: 1
author:
- first_name: Teresa
  full_name: Heiss, Teresa
  id: 4879BB4E-F248-11E8-B48F-1D18A9856A87
  last_name: Heiss
  orcid: 0000-0002-1780-2689
- first_name: Sarah
  full_name: Tymochko, Sarah
  last_name: Tymochko
- first_name: Brittany
  full_name: Story, Brittany
  last_name: Story
- first_name: Adélie
  full_name: Garin, Adélie
  last_name: Garin
- first_name: Hoa
  full_name: Bui, Hoa
  last_name: Bui
- first_name: Bea
  full_name: Bleile, Bea
  last_name: Bleile
- first_name: Vanessa
  full_name: Robins, Vanessa
  last_name: Robins
citation:
  ama: 'Heiss T, Tymochko S, Story B, et al. The impact of changes in resolution on
    the persistent homology of images. In: <i>2021 IEEE International Conference on
    Big Data</i>. IEEE; 2022:3824-3834. doi:<a href="https://doi.org/10.1109/BigData52589.2021.9671483">10.1109/BigData52589.2021.9671483</a>'
  apa: 'Heiss, T., Tymochko, S., Story, B., Garin, A., Bui, H., Bleile, B., &#38;
    Robins, V. (2022). The impact of changes in resolution on the persistent homology
    of images. In <i>2021 IEEE International Conference on Big Data</i> (pp. 3824–3834).
    Orlando, FL, United States; Virtuell: IEEE. <a href="https://doi.org/10.1109/BigData52589.2021.9671483">https://doi.org/10.1109/BigData52589.2021.9671483</a>'
  chicago: Heiss, Teresa, Sarah Tymochko, Brittany Story, Adélie Garin, Hoa Bui, Bea
    Bleile, and Vanessa Robins. “The Impact of Changes in Resolution on the Persistent
    Homology of Images.” In <i>2021 IEEE International Conference on Big Data</i>,
    3824–34. IEEE, 2022. <a href="https://doi.org/10.1109/BigData52589.2021.9671483">https://doi.org/10.1109/BigData52589.2021.9671483</a>.
  ieee: T. Heiss <i>et al.</i>, “The impact of changes in resolution on the persistent
    homology of images,” in <i>2021 IEEE International Conference on Big Data</i>,
    Orlando, FL, United States; Virtuell, 2022, pp. 3824–3834.
  ista: 'Heiss T, Tymochko S, Story B, Garin A, Bui H, Bleile B, Robins V. 2022. The
    impact of changes in resolution on the persistent homology of images. 2021 IEEE
    International Conference on Big Data. Big Data: International Conference on Big
    Data, 3824–3834.'
  mla: Heiss, Teresa, et al. “The Impact of Changes in Resolution on the Persistent
    Homology of Images.” <i>2021 IEEE International Conference on Big Data</i>, IEEE,
    2022, pp. 3824–34, doi:<a href="https://doi.org/10.1109/BigData52589.2021.9671483">10.1109/BigData52589.2021.9671483</a>.
  short: T. Heiss, S. Tymochko, B. Story, A. Garin, H. Bui, B. Bleile, V. Robins,
    in:, 2021 IEEE International Conference on Big Data, IEEE, 2022, pp. 3824–3834.
conference:
  end_date: 2021-12-18
  location: Orlando, FL, United States; Virtuell
  name: 'Big Data: International Conference on Big Data'
  start_date: 2021-12-15
date_created: 2022-03-06T23:01:53Z
date_published: 2022-01-13T00:00:00Z
date_updated: 2026-04-07T12:54:09Z
day: '13'
department:
- _id: HeEd
doi: 10.1109/BigData52589.2021.9671483
external_id:
  arxiv:
  - '2111.05663'
  isi:
  - '000800559503126'
fulldoi: https://doi.org/10.1109/BigData52589.2021.9671483
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/2111.05663
month: '01'
oa: 1
oa_version: Preprint
page: 3824-3834
publication: 2021 IEEE International Conference on Big Data
publication_identifier:
  isbn:
  - '9781665439022'
publication_status: published
publisher: IEEE
quality_controlled: '1'
related_material:
  record:
  - id: '18667'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: The impact of changes in resolution on the persistent homology of images
type: conference
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
year: '2022'
...
---
_id: '10829'
abstract:
- lang: eng
  text: A novel multivariable system, combining a transistor with fiber optic-based
    surface plasmon resonance spectroscopy with the gate electrode simultaneously
    acting as the fiber optic sensor surface, is reported. The dual-mode sensor allows
    for discrimination of mass and charge contributions for binding assays on the
    same sensor surface. Furthermore, we optimize the sensor geometry by investigating
    the influence of the fiber area to transistor channel area ratio and distance.
    We show that larger fiber optic tip diameters are favorable for electronic and
    optical signals and demonstrate the reversibility of plasmon resonance wavelength
    shifts after electric field application. As a proof of principle, a layer-by-layer
    assembly of polyelectrolytes is performed to benchmark the system against multivariable
    sensing platforms with planar surface plasmon resonance configurations. Furthermore,
    the biosensing performance is assessed using a thrombin binding assay with surface-immobilized
    aptamers as receptors, allowing for the detection of medically relevant thrombin
    concentrations.
acknowledgement: "This project has received funding from the European Union’s Horizon
  2020 Research and Innovation Programme under the Marie Skłodowska-Curie grant agreement
  No. 813863-\r\nBORGES. Additionally, we gratefully acknowledge the financial support
  from the Austrian Research Promotion Agency (FFG; 870025 and 873541) for this research.
  The data that support the findings of this study are openly available in Zenodo
  (DOI: 10.5281/zenodo.5500360)"
article_processing_charge: No
article_type: original
author:
- first_name: Roger
  full_name: Hasler, Roger
  last_name: Hasler
- first_name: Ciril
  full_name: Reiner-Rozman, Ciril
  last_name: Reiner-Rozman
- first_name: Stefan
  full_name: Fossati, Stefan
  last_name: Fossati
- first_name: Patrik
  full_name: Aspermair, Patrik
  last_name: Aspermair
- first_name: Jakub
  full_name: Dostalek, Jakub
  last_name: Dostalek
- first_name: Seungho
  full_name: Lee, Seungho
  id: BB243B88-D767-11E9-B658-BC13E6697425
  last_name: Lee
  orcid: 0000-0002-6962-8598
- first_name: Maria
  full_name: Ibáñez, Maria
  id: 43C61214-F248-11E8-B48F-1D18A9856A87
  last_name: Ibáñez
  orcid: 0000-0001-5013-2843
- first_name: Johannes
  full_name: Bintinger, Johannes
  last_name: Bintinger
- first_name: Wolfgang
  full_name: Knoll, Wolfgang
  last_name: Knoll
citation:
  ama: Hasler R, Reiner-Rozman C, Fossati S, et al. Field-effect transistor with a
    plasmonic fiber optic gate electrode as a multivariable biosensor device. <i>ACS
    Sensors</i>. 2022;7(2):504-512. doi:<a href="https://doi.org/10.1021/acssensors.1c02313">10.1021/acssensors.1c02313</a>
  apa: Hasler, R., Reiner-Rozman, C., Fossati, S., Aspermair, P., Dostalek, J., Lee,
    S., … Knoll, W. (2022). Field-effect transistor with a plasmonic fiber optic gate
    electrode as a multivariable biosensor device. <i>ACS Sensors</i>. American Chemical
    Society. <a href="https://doi.org/10.1021/acssensors.1c02313">https://doi.org/10.1021/acssensors.1c02313</a>
  chicago: Hasler, Roger, Ciril Reiner-Rozman, Stefan Fossati, Patrik Aspermair, Jakub
    Dostalek, Seungho Lee, Maria Ibáñez, Johannes Bintinger, and Wolfgang Knoll. “Field-Effect
    Transistor with a Plasmonic Fiber Optic Gate Electrode as a Multivariable Biosensor
    Device.” <i>ACS Sensors</i>. American Chemical Society, 2022. <a href="https://doi.org/10.1021/acssensors.1c02313">https://doi.org/10.1021/acssensors.1c02313</a>.
  ieee: R. Hasler <i>et al.</i>, “Field-effect transistor with a plasmonic fiber optic
    gate electrode as a multivariable biosensor device,” <i>ACS Sensors</i>, vol.
    7, no. 2. American Chemical Society, pp. 504–512, 2022.
  ista: Hasler R, Reiner-Rozman C, Fossati S, Aspermair P, Dostalek J, Lee S, Ibáñez
    M, Bintinger J, Knoll W. 2022. Field-effect transistor with a plasmonic fiber
    optic gate electrode as a multivariable biosensor device. ACS Sensors. 7(2), 504–512.
  mla: Hasler, Roger, et al. “Field-Effect Transistor with a Plasmonic Fiber Optic
    Gate Electrode as a Multivariable Biosensor Device.” <i>ACS Sensors</i>, vol.
    7, no. 2, American Chemical Society, 2022, pp. 504–12, doi:<a href="https://doi.org/10.1021/acssensors.1c02313">10.1021/acssensors.1c02313</a>.
  short: R. Hasler, C. Reiner-Rozman, S. Fossati, P. Aspermair, J. Dostalek, S. Lee,
    M. Ibáñez, J. Bintinger, W. Knoll, ACS Sensors 7 (2022) 504–512.
date_created: 2022-03-06T23:01:54Z
date_published: 2022-02-08T00:00:00Z
date_updated: 2026-04-02T12:33:46Z
day: '08'
ddc:
- '540'
department:
- _id: MaIb
doi: 10.1021/acssensors.1c02313
external_id:
  isi:
  - '000765113000016'
  pmid:
  - '35134289'
file:
- access_level: open_access
  checksum: d704af7262cd484da9bb84b7d84e2b09
  content_type: application/pdf
  creator: dernst
  date_created: 2022-03-07T08:15:01Z
  date_updated: 2022-03-07T08:15:01Z
  file_id: '10832'
  file_name: 2022_ACSSensors_Hasler.pdf
  file_size: 2969415
  relation: main_file
  success: 1
file_date_updated: 2022-03-07T08:15:01Z
fulldoi: https://doi.org/10.1021/acssensors.1c02313
has_accepted_license: '1'
intvolume: '         7'
isi: 1
issue: '2'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 504-512
pmid: 1
publication: ACS Sensors
publication_identifier:
  eissn:
  - 2379-3694
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
related_material:
  record:
  - id: '10833'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Field-effect transistor with a plasmonic fiber optic gate electrode as a multivariable
  biosensor device
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
volume: 7
year: '2022'
...
