---
_id: '159'
abstract:
- lang: eng
  text: L-type Ca2+ channels (LTCCs) play a crucial role in excitation-contraction
    coupling and release of hormones from secretory cells. They are targets of antihypertensive
    and antiarrhythmic drugs such as diltiazem. Here, we present a photoswitchable
    diltiazem, FHU-779, which can be used to reversibly block endogenous LTCCs by
    light. FHU-779 is as potent as diltiazem and can be used to place pancreatic β-cell
    function and cardiac activity under optical control.
article_processing_charge: No
article_type: original
author:
- first_name: Timm
  full_name: Fehrentz, Timm
  last_name: Fehrentz
- first_name: Florian
  full_name: Huber, Florian
  last_name: Huber
- first_name: Nina
  full_name: Hartrampf, Nina
  last_name: Hartrampf
- first_name: Tobias
  full_name: Bruegmann, Tobias
  last_name: Bruegmann
- first_name: James
  full_name: Frank, James
  last_name: Frank
- first_name: Nicholas
  full_name: Fine, Nicholas
  last_name: Fine
- first_name: Daniela
  full_name: Malan, Daniela
  last_name: Malan
- first_name: Johann G
  full_name: Danzl, Johann G
  id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87
  last_name: Danzl
  orcid: 0000-0001-8559-3973
- first_name: Denis
  full_name: Tikhonov, Denis
  last_name: Tikhonov
- first_name: Maritn
  full_name: Sumser, Maritn
  last_name: Sumser
- first_name: Philipp
  full_name: Sasse, Philipp
  last_name: Sasse
- first_name: David
  full_name: Hodson, David
  last_name: Hodson
- first_name: Boris
  full_name: Zhorov, Boris
  last_name: Zhorov
- first_name: Nikolaj
  full_name: Klocker, Nikolaj
  last_name: Klocker
- first_name: Dirk
  full_name: Trauner, Dirk
  last_name: Trauner
citation:
  ama: Fehrentz T, Huber F, Hartrampf N, et al. Optical control of L-type Ca2+ channels
    using a diltiazem photoswitch. <i>Nature Chemical Biology</i>. 2018;14(8):764-767.
    doi:<a href="https://doi.org/10.1038/s41589-018-0090-8">10.1038/s41589-018-0090-8</a>
  apa: Fehrentz, T., Huber, F., Hartrampf, N., Bruegmann, T., Frank, J., Fine, N.,
    … Trauner, D. (2018). Optical control of L-type Ca2+ channels using a diltiazem
    photoswitch. <i>Nature Chemical Biology</i>. Nature Publishing Group. <a href="https://doi.org/10.1038/s41589-018-0090-8">https://doi.org/10.1038/s41589-018-0090-8</a>
  chicago: Fehrentz, Timm, Florian Huber, Nina Hartrampf, Tobias Bruegmann, James
    Frank, Nicholas Fine, Daniela Malan, et al. “Optical Control of L-Type Ca2+ Channels
    Using a Diltiazem Photoswitch.” <i>Nature Chemical Biology</i>. Nature Publishing
    Group, 2018. <a href="https://doi.org/10.1038/s41589-018-0090-8">https://doi.org/10.1038/s41589-018-0090-8</a>.
  ieee: T. Fehrentz <i>et al.</i>, “Optical control of L-type Ca2+ channels using
    a diltiazem photoswitch,” <i>Nature Chemical Biology</i>, vol. 14, no. 8. Nature
    Publishing Group, pp. 764–767, 2018.
  ista: Fehrentz T, Huber F, Hartrampf N, Bruegmann T, Frank J, Fine N, Malan D, Danzl
    JG, Tikhonov D, Sumser M, Sasse P, Hodson D, Zhorov B, Klocker N, Trauner D. 2018.
    Optical control of L-type Ca2+ channels using a diltiazem photoswitch. Nature
    Chemical Biology. 14(8), 764–767.
  mla: Fehrentz, Timm, et al. “Optical Control of L-Type Ca2+ Channels Using a Diltiazem
    Photoswitch.” <i>Nature Chemical Biology</i>, vol. 14, no. 8, Nature Publishing
    Group, 2018, pp. 764–67, doi:<a href="https://doi.org/10.1038/s41589-018-0090-8">10.1038/s41589-018-0090-8</a>.
  short: T. Fehrentz, F. Huber, N. Hartrampf, T. Bruegmann, J. Frank, N. Fine, D.
    Malan, J.G. Danzl, D. Tikhonov, M. Sumser, P. Sasse, D. Hodson, B. Zhorov, N.
    Klocker, D. Trauner, Nature Chemical Biology 14 (2018) 764–767.
date_created: 2018-12-11T11:44:56Z
date_published: 2018-07-16T00:00:00Z
date_updated: 2023-09-13T09:36:35Z
day: '16'
ddc:
- '570'
department:
- _id: JoDa
doi: 10.1038/s41589-018-0090-8
external_id:
  isi:
  - '000438970200010'
file:
- access_level: open_access
  checksum: d42935094ec845f54a0688bf12986d62
  content_type: application/pdf
  creator: dernst
  date_created: 2020-05-14T12:14:09Z
  date_updated: 2020-07-14T12:45:03Z
  file_id: '7832'
  file_name: 2018_NatureChemicalBiology_Fehrentz.pdf
  file_size: 6321000
  relation: main_file
file_date_updated: 2020-07-14T12:45:03Z
has_accepted_license: '1'
intvolume: '        14'
isi: 1
issue: '8'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Submitted Version
page: 764 - 767
publication: Nature Chemical Biology
publication_status: published
publisher: Nature Publishing Group
publist_id: '7762'
quality_controlled: '1'
related_material:
  link:
  - relation: erratum
    url: https://doi.org/10.1038/s41589-021-00744-3
scopus_import: '1'
status: public
title: Optical control of L-type Ca2+ channels using a diltiazem photoswitch
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 14
year: '2018'
...
---
_id: '16'
abstract:
- lang: eng
  text: We report quantitative evidence of mixing-layer elastic instability in a viscoelastic
    fluid flow between two widely spaced obstacles hindering a channel flow at Re
    1 and Wi 1. Two mixing layers with nonuniform shear velocity profiles are formed
    in the region between the obstacles. The mixing-layer instability arises in the
    vicinity of an inflection point on the shear velocity profile with a steep variation
    in the elastic stress. The instability results in an intermittent appearance of
    small vortices in the mixing layers and an amplification of spatiotemporal averaged
    vorticity in the elastic turbulence regime. The latter is characterized through
    scaling of friction factor with Wi and both pressure and velocity spectra. Furthermore,
    the observations reported provide improved understanding of the stability of the
    mixing layer in a viscoelastic fluid at large elasticity, i.e., Wi 1 and Re 1
    and oppose the current view of suppression of vorticity solely by polymer additives.
acknowledgement: This work was partially supported by the Israel Science Foundation
  (ISF; Grant No. 882/15) and the Binational USA-Israel Foundation (BSF; Grant No.
  2016145).
article_number: '103303'
article_processing_charge: No
article_type: original
author:
- first_name: Atul
  full_name: Varshney, Atul
  id: 2A2006B2-F248-11E8-B48F-1D18A9856A87
  last_name: Varshney
  orcid: 0000-0002-3072-5999
- first_name: Victor
  full_name: Steinberg, Victor
  last_name: Steinberg
citation:
  ama: Varshney A, Steinberg V. Mixing layer instability and vorticity amplification
    in a creeping viscoelastic flow. <i>Physical Review Fluids</i>. 2018;3(10). doi:<a
    href="https://doi.org/10.1103/PhysRevFluids.3.103303">10.1103/PhysRevFluids.3.103303</a>
  apa: Varshney, A., &#38; Steinberg, V. (2018). Mixing layer instability and vorticity
    amplification in a creeping viscoelastic flow. <i>Physical Review Fluids</i>.
    American Physical Society. <a href="https://doi.org/10.1103/PhysRevFluids.3.103303">https://doi.org/10.1103/PhysRevFluids.3.103303</a>
  chicago: Varshney, Atul, and Victor Steinberg. “Mixing Layer Instability and Vorticity
    Amplification in a Creeping Viscoelastic Flow.” <i>Physical Review Fluids</i>.
    American Physical Society, 2018. <a href="https://doi.org/10.1103/PhysRevFluids.3.103303">https://doi.org/10.1103/PhysRevFluids.3.103303</a>.
  ieee: A. Varshney and V. Steinberg, “Mixing layer instability and vorticity amplification
    in a creeping viscoelastic flow,” <i>Physical Review Fluids</i>, vol. 3, no. 10.
    American Physical Society, 2018.
  ista: Varshney A, Steinberg V. 2018. Mixing layer instability and vorticity amplification
    in a creeping viscoelastic flow. Physical Review Fluids. 3(10), 103303.
  mla: Varshney, Atul, and Victor Steinberg. “Mixing Layer Instability and Vorticity
    Amplification in a Creeping Viscoelastic Flow.” <i>Physical Review Fluids</i>,
    vol. 3, no. 10, 103303, American Physical Society, 2018, doi:<a href="https://doi.org/10.1103/PhysRevFluids.3.103303">10.1103/PhysRevFluids.3.103303</a>.
  short: A. Varshney, V. Steinberg, Physical Review Fluids 3 (2018).
date_created: 2018-12-11T11:44:10Z
date_published: 2018-10-16T00:00:00Z
date_updated: 2025-04-14T07:44:02Z
day: '16'
ddc:
- '532'
department:
- _id: BjHo
doi: 10.1103/PhysRevFluids.3.103303
ec_funded: 1
external_id:
  isi:
  - '000447469200001'
file:
- access_level: open_access
  checksum: 7fc0a2322214d1c04debef36d5bf2e8a
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:13:56Z
  date_updated: 2020-07-14T12:45:04Z
  file_id: '5043'
  file_name: IST-2018-1062-v1+1_PhysRevFluids.3.103303.pdf
  file_size: 1838431
  relation: main_file
file_date_updated: 2020-07-14T12:45:04Z
has_accepted_license: '1'
intvolume: '         3'
isi: 1
issue: '10'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Submitted Version
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Physical Review Fluids
publication_status: published
publisher: American Physical Society
publist_id: '8039'
pubrep_id: '1062'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mixing layer instability and vorticity amplification in a creeping viscoelastic
  flow
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 3
year: '2018'
...
---
_id: '161'
abstract:
- lang: eng
  text: 'Which properties of metabolic networks can be derived solely from stoichiometry?
    Predictive results have been obtained by flux balance analysis (FBA), by postulating
    that cells set metabolic fluxes to maximize growth rate. Here we consider a generalization
    of FBA to single-cell level using maximum entropy modeling, which we extend and
    test experimentally. Specifically, we define for Escherichia coli metabolism a
    flux distribution that yields the experimental growth rate: the model, containing
    FBA as a limit, provides a better match to measured fluxes and it makes a wide
    range of predictions: on flux variability, regulation, and correlations; on the
    relative importance of stoichiometry vs. optimization; on scaling relations for
    growth rate distributions. We validate the latter here with single-cell data at
    different sub-inhibitory antibiotic concentrations. The model quantifies growth
    optimization as emerging from the interplay of competitive dynamics in the population
    and regulation of metabolism at the level of single cells.'
article_number: '2988'
article_processing_charge: No
author:
- first_name: Daniele
  full_name: De Martino, Daniele
  id: 3FF5848A-F248-11E8-B48F-1D18A9856A87
  last_name: De Martino
  orcid: 0000-0002-5214-4706
- first_name: Andersson Anna
  full_name: Mc, Andersson Anna
  last_name: Mc
- first_name: Tobias
  full_name: Bergmiller, Tobias
  id: 2C471CFA-F248-11E8-B48F-1D18A9856A87
  last_name: Bergmiller
  orcid: 0000-0001-5396-4346
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
- first_name: Gasper
  full_name: Tkacik, Gasper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkacik
  orcid: 0000-0002-6699-1455
citation:
  ama: De Martino D, Mc AA, Bergmiller T, Guet CC, Tkačik G. Statistical mechanics
    for metabolic networks during steady state growth. <i>Nature Communications</i>.
    2018;9(1). doi:<a href="https://doi.org/10.1038/s41467-018-05417-9">10.1038/s41467-018-05417-9</a>
  apa: De Martino, D., Mc, A. A., Bergmiller, T., Guet, C. C., &#38; Tkačik, G. (2018).
    Statistical mechanics for metabolic networks during steady state growth. <i>Nature
    Communications</i>. Springer Nature. <a href="https://doi.org/10.1038/s41467-018-05417-9">https://doi.org/10.1038/s41467-018-05417-9</a>
  chicago: De Martino, Daniele, Andersson Anna Mc, Tobias Bergmiller, Calin C Guet,
    and Gašper Tkačik. “Statistical Mechanics for Metabolic Networks during Steady
    State Growth.” <i>Nature Communications</i>. Springer Nature, 2018. <a href="https://doi.org/10.1038/s41467-018-05417-9">https://doi.org/10.1038/s41467-018-05417-9</a>.
  ieee: D. De Martino, A. A. Mc, T. Bergmiller, C. C. Guet, and G. Tkačik, “Statistical
    mechanics for metabolic networks during steady state growth,” <i>Nature Communications</i>,
    vol. 9, no. 1. Springer Nature, 2018.
  ista: De Martino D, Mc AA, Bergmiller T, Guet CC, Tkačik G. 2018. Statistical mechanics
    for metabolic networks during steady state growth. Nature Communications. 9(1),
    2988.
  mla: De Martino, Daniele, et al. “Statistical Mechanics for Metabolic Networks during
    Steady State Growth.” <i>Nature Communications</i>, vol. 9, no. 1, 2988, Springer
    Nature, 2018, doi:<a href="https://doi.org/10.1038/s41467-018-05417-9">10.1038/s41467-018-05417-9</a>.
  short: D. De Martino, A.A. Mc, T. Bergmiller, C.C. Guet, G. Tkačik, Nature Communications
    9 (2018).
date_created: 2018-12-11T11:44:57Z
date_published: 2018-07-30T00:00:00Z
date_updated: 2025-04-15T06:50:08Z
day: '30'
ddc:
- '570'
department:
- _id: GaTk
- _id: CaGu
doi: 10.1038/s41467-018-05417-9
ec_funded: 1
external_id:
  isi:
  - '000440149300021'
file:
- access_level: open_access
  checksum: 3ba7ab27b27723c7dcf633e8fc1f8f18
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T16:44:28Z
  date_updated: 2020-07-14T12:45:06Z
  file_id: '5728'
  file_name: 2018_NatureComm_DeMartino.pdf
  file_size: 1043205
  relation: main_file
file_date_updated: 2020-07-14T12:45:06Z
has_accepted_license: '1'
intvolume: '         9'
isi: 1
issue: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 254E9036-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P28844-B27
  name: Biophysics of information processing in gene regulation
- _id: 25681D80-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '291734'
  name: International IST Postdoc Fellowship Programme
publication: Nature Communications
publication_status: published
publisher: Springer Nature
publist_id: '7760'
quality_controlled: '1'
related_material:
  record:
  - id: '5587'
    relation: popular_science
    status: public
scopus_import: '1'
status: public
title: Statistical mechanics for metabolic networks during steady state growth
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 9
year: '2018'
...
---
_id: '162'
abstract:
- lang: eng
  text: 'Facial shape is the basis for facial recognition and categorization. Facial
    features reflect the underlying geometry of the skeletal structures. Here, we
    reveal that cartilaginous nasal capsule (corresponding to upper jaw and face)
    is shaped by signals generated by neural structures: brain and olfactory epithelium.
    Brain-derived Sonic Hedgehog (SHH) enables the induction of nasal septum and posterior
    nasal capsule, whereas the formation of a capsule roof is controlled by signals
    from the olfactory epithelium. Unexpectedly, the cartilage of the nasal capsule
    turned out to be important for shaping membranous facial bones during development.
    This suggests that conserved neurosensory structures could benefit from protection
    and have evolved signals inducing cranial cartilages encasing them. Experiments
    with mutant mice revealed that the genomic regulatory regions controlling production
    of SHH in the nervous system contribute to facial cartilage morphogenesis, which
    might be a mechanism responsible for the adaptive evolution of animal faces and
    snouts.'
article_number: e34465
article_processing_charge: No
author:
- first_name: Marketa
  full_name: Kaucka, Marketa
  last_name: Kaucka
- first_name: Julian
  full_name: Petersen, Julian
  last_name: Petersen
- first_name: Marketa
  full_name: Tesarova, Marketa
  last_name: Tesarova
- first_name: Bara
  full_name: Szarowska, Bara
  last_name: Szarowska
- first_name: Maria
  full_name: Kastriti, Maria
  last_name: Kastriti
- first_name: Meng
  full_name: Xie, Meng
  last_name: Xie
- first_name: Anna
  full_name: Kicheva, Anna
  id: 3959A2A0-F248-11E8-B48F-1D18A9856A87
  last_name: Kicheva
  orcid: 0000-0003-4509-4998
- first_name: Karl
  full_name: Annusver, Karl
  last_name: Annusver
- first_name: Maria
  full_name: Kasper, Maria
  last_name: Kasper
- first_name: Orsolya
  full_name: Symmons, Orsolya
  last_name: Symmons
- first_name: Leslie
  full_name: Pan, Leslie
  last_name: Pan
- first_name: Francois
  full_name: Spitz, Francois
  last_name: Spitz
- first_name: Jozef
  full_name: Kaiser, Jozef
  last_name: Kaiser
- first_name: Maria
  full_name: Hovorakova, Maria
  last_name: Hovorakova
- first_name: Tomas
  full_name: Zikmund, Tomas
  last_name: Zikmund
- first_name: Kazunori
  full_name: Sunadome, Kazunori
  last_name: Sunadome
- first_name: Michael P
  full_name: Matise, Michael P
  last_name: Matise
- first_name: Hui
  full_name: Wang, Hui
  last_name: Wang
- first_name: Ulrika
  full_name: Marklund, Ulrika
  last_name: Marklund
- first_name: Hind
  full_name: Abdo, Hind
  last_name: Abdo
- first_name: Patrik
  full_name: Ernfors, Patrik
  last_name: Ernfors
- first_name: Pascal
  full_name: Maire, Pascal
  last_name: Maire
- first_name: Maud
  full_name: Wurmser, Maud
  last_name: Wurmser
- first_name: Andrei S
  full_name: Chagin, Andrei S
  last_name: Chagin
- first_name: Kaj
  full_name: Fried, Kaj
  last_name: Fried
- first_name: Igor
  full_name: Adameyko, Igor
  last_name: Adameyko
citation:
  ama: Kaucka M, Petersen J, Tesarova M, et al. Signals from the brain and olfactory
    epithelium control shaping of the mammalian nasal capsule cartilage. <i>eLife</i>.
    2018;7. doi:<a href="https://doi.org/10.7554/eLife.34465">10.7554/eLife.34465</a>
  apa: Kaucka, M., Petersen, J., Tesarova, M., Szarowska, B., Kastriti, M., Xie, M.,
    … Adameyko, I. (2018). Signals from the brain and olfactory epithelium control
    shaping of the mammalian nasal capsule cartilage. <i>ELife</i>. eLife Sciences
    Publications. <a href="https://doi.org/10.7554/eLife.34465">https://doi.org/10.7554/eLife.34465</a>
  chicago: Kaucka, Marketa, Julian Petersen, Marketa Tesarova, Bara Szarowska, Maria
    Kastriti, Meng Xie, Anna Kicheva, et al. “Signals from the Brain and Olfactory
    Epithelium Control Shaping of the Mammalian Nasal Capsule Cartilage.” <i>ELife</i>.
    eLife Sciences Publications, 2018. <a href="https://doi.org/10.7554/eLife.34465">https://doi.org/10.7554/eLife.34465</a>.
  ieee: M. Kaucka <i>et al.</i>, “Signals from the brain and olfactory epithelium
    control shaping of the mammalian nasal capsule cartilage,” <i>eLife</i>, vol.
    7. eLife Sciences Publications, 2018.
  ista: Kaucka M, Petersen J, Tesarova M, Szarowska B, Kastriti M, Xie M, Kicheva
    A, Annusver K, Kasper M, Symmons O, Pan L, Spitz F, Kaiser J, Hovorakova M, Zikmund
    T, Sunadome K, Matise MP, Wang H, Marklund U, Abdo H, Ernfors P, Maire P, Wurmser
    M, Chagin AS, Fried K, Adameyko I. 2018. Signals from the brain and olfactory
    epithelium control shaping of the mammalian nasal capsule cartilage. eLife. 7,
    e34465.
  mla: Kaucka, Marketa, et al. “Signals from the Brain and Olfactory Epithelium Control
    Shaping of the Mammalian Nasal Capsule Cartilage.” <i>ELife</i>, vol. 7, e34465,
    eLife Sciences Publications, 2018, doi:<a href="https://doi.org/10.7554/eLife.34465">10.7554/eLife.34465</a>.
  short: M. Kaucka, J. Petersen, M. Tesarova, B. Szarowska, M. Kastriti, M. Xie, A.
    Kicheva, K. Annusver, M. Kasper, O. Symmons, L. Pan, F. Spitz, J. Kaiser, M. Hovorakova,
    T. Zikmund, K. Sunadome, M.P. Matise, H. Wang, U. Marklund, H. Abdo, P. Ernfors,
    P. Maire, M. Wurmser, A.S. Chagin, K. Fried, I. Adameyko, ELife 7 (2018).
date_created: 2018-12-11T11:44:57Z
date_published: 2018-06-13T00:00:00Z
date_updated: 2025-04-14T07:27:30Z
day: '13'
ddc:
- '571'
department:
- _id: AnKi
doi: 10.7554/eLife.34465
ec_funded: 1
external_id:
  isi:
  - '000436227500001'
file:
- access_level: open_access
  checksum: da2378cdcf6b5461dcde194e4d608343
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T16:41:58Z
  date_updated: 2020-07-14T12:45:07Z
  file_id: '5727'
  file_name: 2018_eLife_Kaucka.pdf
  file_size: 9816484
  relation: main_file
file_date_updated: 2020-07-14T12:45:07Z
has_accepted_license: '1'
intvolume: '         7'
isi: 1
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
project:
- _id: B6FC0238-B512-11E9-945C-1524E6697425
  call_identifier: H2020
  grant_number: '680037'
  name: Coordination of Patterning And Growth In the Spinal Cord
publication: eLife
publication_status: published
publisher: eLife Sciences Publications
publist_id: '7759'
quality_controlled: '1'
related_material:
  record:
  - id: '9838'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Signals from the brain and olfactory epithelium control shaping of the mammalian
  nasal capsule cartilage
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 7
year: '2018'
...
---
_id: '163'
abstract:
- lang: eng
  text: For ultrafast fixation of biological samples to avoid artifacts, high-pressure
    freezing (HPF) followed by freeze substitution (FS) is preferred over chemical
    fixation at room temperature. After HPF, samples are maintained at low temperature
    during dehydration and fixation, while avoiding damaging recrystallization. This
    is a notoriously slow process. McDonald and Webb demonstrated, in 2011, that sample
    agitation during FS dramatically reduces the necessary time. Then, in 2015, we
    (H.G. and S.R.) introduced an agitation module into the cryochamber of an automated
    FS unit and demonstrated that the preparation of algae could be shortened from
    days to a couple of hours. We argued that variability in the processing, reproducibility,
    and safety issues are better addressed using automated FS units. For dissemination,
    we started low-cost manufacturing of agitation modules for two of the most widely
    used FS units, the Automatic Freeze Substitution Systems, AFS(1) and AFS2, from
    Leica Microsystems, using three dimensional (3D)-printing of the major components.
    To test them, several labs independently used the modules on a wide variety of
    specimens that had previously been processed by manual agitation, or without agitation.
    We demonstrate that automated processing with sample agitation saves time, increases
    flexibility with respect to sample requirements and protocols, and produces data
    of at least as good quality as other approaches.
article_processing_charge: No
article_type: original
author:
- first_name: Siegfried
  full_name: Reipert, Siegfried
  last_name: Reipert
- first_name: Helmuth
  full_name: Goldammer, Helmuth
  last_name: Goldammer
- first_name: Christine
  full_name: Richardson, Christine
  last_name: Richardson
- first_name: Martin
  full_name: Goldberg, Martin
  last_name: Goldberg
- first_name: Timothy
  full_name: Hawkins, Timothy
  last_name: Hawkins
- first_name: Elena
  full_name: Hollergschwandtner, Elena
  id: 3C054040-F248-11E8-B48F-1D18A9856A87
  last_name: Hollergschwandtner
- first_name: Walter
  full_name: Kaufmann, Walter
  id: 3F99E422-F248-11E8-B48F-1D18A9856A87
  last_name: Kaufmann
  orcid: 0000-0001-9735-5315
- first_name: Sebastian
  full_name: Antreich, Sebastian
  last_name: Antreich
- first_name: York
  full_name: Stierhof, York
  last_name: Stierhof
citation:
  ama: 'Reipert S, Goldammer H, Richardson C, et al. Agitation modules: Flexible means
    to accelerate automated freeze substitution. <i>Journal of Histochemistry and
    Cytochemistry</i>. 2018;66(12):903-921. doi:<a href="https://doi.org/10.1369/0022155418786698">10.1369/0022155418786698</a>'
  apa: 'Reipert, S., Goldammer, H., Richardson, C., Goldberg, M., Hawkins, T., Saeckl,
    E., … Stierhof, Y. (2018). Agitation modules: Flexible means to accelerate automated
    freeze substitution. <i>Journal of Histochemistry and Cytochemistry</i>. SAGE
    Publications. <a href="https://doi.org/10.1369/0022155418786698">https://doi.org/10.1369/0022155418786698</a>'
  chicago: 'Reipert, Siegfried, Helmuth Goldammer, Christine Richardson, Martin Goldberg,
    Timothy Hawkins, Elena Saeckl, Walter Kaufmann, Sebastian Antreich, and York Stierhof.
    “Agitation Modules: Flexible Means to Accelerate Automated Freeze Substitution.”
    <i>Journal of Histochemistry and Cytochemistry</i>. SAGE Publications, 2018. <a
    href="https://doi.org/10.1369/0022155418786698">https://doi.org/10.1369/0022155418786698</a>.'
  ieee: 'S. Reipert <i>et al.</i>, “Agitation modules: Flexible means to accelerate
    automated freeze substitution,” <i>Journal of Histochemistry and Cytochemistry</i>,
    vol. 66, no. 12. SAGE Publications, pp. 903–921, 2018.'
  ista: 'Reipert S, Goldammer H, Richardson C, Goldberg M, Hawkins T, Saeckl E, Kaufmann
    W, Antreich S, Stierhof Y. 2018. Agitation modules: Flexible means to accelerate
    automated freeze substitution. Journal of Histochemistry and Cytochemistry. 66(12),
    903–921.'
  mla: 'Reipert, Siegfried, et al. “Agitation Modules: Flexible Means to Accelerate
    Automated Freeze Substitution.” <i>Journal of Histochemistry and Cytochemistry</i>,
    vol. 66, no. 12, SAGE Publications, 2018, pp. 903–21, doi:<a href="https://doi.org/10.1369/0022155418786698">10.1369/0022155418786698</a>.'
  short: S. Reipert, H. Goldammer, C. Richardson, M. Goldberg, T. Hawkins, E. Saeckl,
    W. Kaufmann, S. Antreich, Y. Stierhof, Journal of Histochemistry and Cytochemistry
    66 (2018) 903–921.
date_created: 2018-12-11T11:44:57Z
date_published: 2018-12-01T00:00:00Z
date_updated: 2023-10-17T08:42:24Z
day: '01'
department:
- _id: RySh
- _id: EM-Fac
doi: 10.1369/0022155418786698
external_id:
  isi:
  - '000452277700005'
  pmid:
  - '29969056'
intvolume: '        66'
isi: 1
issue: '12'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1369/0022155418786698
month: '12'
oa: 1
oa_version: Published Version
page: 903-921
pmid: 1
publication: Journal of Histochemistry and Cytochemistry
publication_identifier:
  issn:
  - 0022-1554
publication_status: published
publisher: SAGE Publications
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Agitation modules: Flexible means to accelerate automated freeze substitution'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 66
year: '2018'
...
---
_id: '17'
abstract:
- lang: eng
  text: Creeping flow of polymeric fluid without inertia exhibits elastic instabilities
    and elastic turbulence accompanied by drag enhancement due to elastic stress produced
    by flow-stretched polymers. However, in inertia-dominated flow at high Re and
    low fluid elasticity El, a reduction in turbulent frictional drag is caused by
    an intricate competition between inertial and elastic stresses. Here we explore
    the effect of inertia on the stability of viscoelastic flow in a broad range of
    control parameters El and (Re,Wi). We present the stability diagram of observed
    flow regimes in Wi-Re coordinates and find that the instabilities' onsets show
    an unexpectedly nonmonotonic dependence on El. Further, three distinct regions
    in the diagram are identified based on El. Strikingly, for high-elasticity fluids
    we discover a complete relaminarization of flow at Reynolds number in the range
    of 1 to 10, different from a well-known turbulent drag reduction. These counterintuitive
    effects may be explained by a finite polymer extensibility and a suppression of
    vorticity at high Wi. Our results call for further theoretical and numerical development
    to uncover the role of inertial effect on elastic turbulence in a viscoelastic
    flow.
article_number: '103302 '
article_processing_charge: No
author:
- first_name: Atul
  full_name: Varshney, Atul
  id: 2A2006B2-F248-11E8-B48F-1D18A9856A87
  last_name: Varshney
  orcid: 0000-0002-3072-5999
- first_name: Victor
  full_name: Steinberg, Victor
  last_name: Steinberg
citation:
  ama: Varshney A, Steinberg V. Drag enhancement and drag reduction in viscoelastic
    flow. <i>Physical Review Fluids</i>. 2018;3(10). doi:<a href="https://doi.org/10.1103/PhysRevFluids.3.103302">10.1103/PhysRevFluids.3.103302</a>
  apa: Varshney, A., &#38; Steinberg, V. (2018). Drag enhancement and drag reduction
    in viscoelastic flow. <i>Physical Review Fluids</i>. American Physical Society.
    <a href="https://doi.org/10.1103/PhysRevFluids.3.103302">https://doi.org/10.1103/PhysRevFluids.3.103302</a>
  chicago: Varshney, Atul, and Victor Steinberg. “Drag Enhancement and Drag Reduction
    in Viscoelastic Flow.” <i>Physical Review Fluids</i>. American Physical Society,
    2018. <a href="https://doi.org/10.1103/PhysRevFluids.3.103302">https://doi.org/10.1103/PhysRevFluids.3.103302</a>.
  ieee: A. Varshney and V. Steinberg, “Drag enhancement and drag reduction in viscoelastic
    flow,” <i>Physical Review Fluids</i>, vol. 3, no. 10. American Physical Society,
    2018.
  ista: Varshney A, Steinberg V. 2018. Drag enhancement and drag reduction in viscoelastic
    flow. Physical Review Fluids. 3(10), 103302.
  mla: Varshney, Atul, and Victor Steinberg. “Drag Enhancement and Drag Reduction
    in Viscoelastic Flow.” <i>Physical Review Fluids</i>, vol. 3, no. 10, 103302,
    American Physical Society, 2018, doi:<a href="https://doi.org/10.1103/PhysRevFluids.3.103302">10.1103/PhysRevFluids.3.103302</a>.
  short: A. Varshney, V. Steinberg, Physical Review Fluids 3 (2018).
date_created: 2018-12-11T11:44:11Z
date_published: 2018-10-15T00:00:00Z
date_updated: 2025-04-14T07:43:59Z
day: '15'
ddc:
- '532'
department:
- _id: BjHo
doi: 10.1103/PhysRevFluids.3.103302
ec_funded: 1
external_id:
  isi:
  - '000447311500001'
file:
- access_level: open_access
  checksum: e1445be33e8165114e96246275600750
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:10:14Z
  date_updated: 2020-07-14T12:45:12Z
  file_id: '4800'
  file_name: IST-2018-1061-v1+1_PhysRevFluids.3.103302.pdf
  file_size: 1409040
  relation: main_file
file_date_updated: 2020-07-14T12:45:12Z
has_accepted_license: '1'
intvolume: '         3'
isi: 1
issue: '10'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Physical Review Fluids
publication_status: published
publisher: American Physical Society
publist_id: '8038'
pubrep_id: '1061'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Drag enhancement and drag reduction in viscoelastic flow
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 3
year: '2018'
...
---
_id: '78'
abstract:
- lang: eng
  text: We provide a procedure for detecting the sub-segments of an incrementally
    observed Boolean signal ω that match a given temporal pattern ϕ. As a pattern
    specification language, we use timed regular expressions, a formalism well-suited
    for expressing properties of concurrent asynchronous behaviors embedded in metric
    time. We construct a timed automaton accepting the timed language denoted by ϕ
    and modify it slightly for the purpose of matching. We then apply zone-based reachability
    computation to this automaton while it reads ω, and retrieve all the matching
    segments from the results. Since the procedure is automaton based, it can be applied
    to patterns specified by other formalisms such as timed temporal logics reducible
    to timed automata or directly encoded as timed automata. The procedure has been
    implemented and its performance on synthetic examples is demonstrated.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Alexey
  full_name: Bakhirkin, Alexey
  last_name: Bakhirkin
- first_name: Thomas
  full_name: Ferrere, Thomas
  id: 40960E6E-F248-11E8-B48F-1D18A9856A87
  last_name: Ferrere
  orcid: 0000-0001-5199-3143
- first_name: Dejan
  full_name: Nickovic, Dejan
  last_name: Nickovic
- first_name: Oded
  full_name: Maler, Oded
  last_name: Maler
- first_name: Eugene
  full_name: Asarin, Eugene
  last_name: Asarin
citation:
  ama: 'Bakhirkin A, Ferrere T, Nickovic D, Maler O, Asarin E. Online timed pattern
    matching using automata. In: Vol 11022. Springer; 2018:215-232. doi:<a href="https://doi.org/10.1007/978-3-030-00151-3_13">10.1007/978-3-030-00151-3_13</a>'
  apa: 'Bakhirkin, A., Ferrere, T., Nickovic, D., Maler, O., &#38; Asarin, E. (2018).
    Online timed pattern matching using automata (Vol. 11022, pp. 215–232). Presented
    at the FORMATS: Formal Modeling and Analysis of Timed Systems, Bejing, China:
    Springer. <a href="https://doi.org/10.1007/978-3-030-00151-3_13">https://doi.org/10.1007/978-3-030-00151-3_13</a>'
  chicago: Bakhirkin, Alexey, Thomas Ferrere, Dejan Nickovic, Oded Maler, and Eugene
    Asarin. “Online Timed Pattern Matching Using Automata,” 11022:215–32. Springer,
    2018. <a href="https://doi.org/10.1007/978-3-030-00151-3_13">https://doi.org/10.1007/978-3-030-00151-3_13</a>.
  ieee: 'A. Bakhirkin, T. Ferrere, D. Nickovic, O. Maler, and E. Asarin, “Online timed
    pattern matching using automata,” presented at the FORMATS: Formal Modeling and
    Analysis of Timed Systems, Bejing, China, 2018, vol. 11022, pp. 215–232.'
  ista: 'Bakhirkin A, Ferrere T, Nickovic D, Maler O, Asarin E. 2018. Online timed
    pattern matching using automata. FORMATS: Formal Modeling and Analysis of Timed
    Systems, LNCS, vol. 11022, 215–232.'
  mla: Bakhirkin, Alexey, et al. <i>Online Timed Pattern Matching Using Automata</i>.
    Vol. 11022, Springer, 2018, pp. 215–32, doi:<a href="https://doi.org/10.1007/978-3-030-00151-3_13">10.1007/978-3-030-00151-3_13</a>.
  short: A. Bakhirkin, T. Ferrere, D. Nickovic, O. Maler, E. Asarin, in:, Springer,
    2018, pp. 215–232.
conference:
  end_date: 2018-09-06
  location: Bejing, China
  name: 'FORMATS: Formal Modeling and Analysis of Timed Systems'
  start_date: 2018-09-04
date_created: 2018-12-11T11:44:31Z
date_published: 2018-08-26T00:00:00Z
date_updated: 2025-04-15T06:26:03Z
day: '26'
ddc:
- '000'
department:
- _id: ToHe
doi: 10.1007/978-3-030-00151-3_13
external_id:
  isi:
  - '000884993200013'
file:
- access_level: open_access
  checksum: 436b7574934324cfa7d1d3986fddc65b
  content_type: application/pdf
  creator: dernst
  date_created: 2020-05-14T11:34:34Z
  date_updated: 2020-07-14T12:48:03Z
  file_id: '7831'
  file_name: 2018_LNCS_Bakhirkin.pdf
  file_size: 374851
  relation: main_file
file_date_updated: 2020-07-14T12:48:03Z
has_accepted_license: '1'
intvolume: '     11022'
isi: 1
language:
- iso: eng
month: '08'
oa: 1
oa_version: Submitted Version
page: 215 - 232
project:
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
publication_identifier:
  isbn:
  - 978-3-030-00150-6
publication_status: published
publisher: Springer
publist_id: '7976'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Online timed pattern matching using automata
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 11022
year: '2018'
...
---
_id: '7812'
abstract:
- lang: eng
  text: Deep neural networks (DNNs) continue to make significant advances, solving
    tasks from image classification to translation or reinforcement learning. One
    aspect of the field receiving considerable attention is efficiently executing
    deep models in resource-constrained environments, such as mobile or embedded devices.
    This paper focuses on this problem, and proposes two new compression methods,
    which jointly leverage weight quantization and distillation of larger teacher
    networks into smaller student networks. The first method we propose is called
    quantized distillation and leverages distillation during the training process,
    by incorporating distillation loss, expressed with respect to the teacher, into
    the training of a student network whose weights are quantized to a limited set
    of levels. The second method,  differentiable quantization, optimizes the location
    of quantization points through stochastic gradient descent, to better fit the
    behavior of the teacher model.  We validate both methods through experiments on
    convolutional and recurrent architectures. We show that quantized shallow students
    can reach similar accuracy levels to full-precision teacher models, while providing
    order of magnitude compression, and inference speedup that is linear in the depth
    reduction. In sum, our results enable DNNs for resource-constrained environments
    to leverage architecture and accuracy advances developed on more powerful devices.
acknowledgement: "We would like to thank Ce Zhang (ETH Zurich), Hantian Zhang (ETH
  Zurich) and Martin Jaggi ´\r\n(EPFL) for their support with experiments and valuable
  feedback.\r\n"
article_processing_charge: No
arxiv: 1
author:
- first_name: Antonio
  full_name: Polino, Antonio
  last_name: Polino
- first_name: Razvan
  full_name: Pascanu, Razvan
  last_name: Pascanu
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
citation:
  ama: 'Polino A, Pascanu R, Alistarh D-A. Model compression via distillation and
    quantization. In: <i>6th International Conference on Learning Representations</i>.
    ; 2018.'
  apa: Polino, A., Pascanu, R., &#38; Alistarh, D.-A. (2018). Model compression via
    distillation and quantization. In <i>6th International Conference on Learning
    Representations</i>. Vancouver, Canada.
  chicago: Polino, Antonio, Razvan Pascanu, and Dan-Adrian Alistarh. “Model Compression
    via Distillation and Quantization.” In <i>6th International Conference on Learning
    Representations</i>, 2018.
  ieee: A. Polino, R. Pascanu, and D.-A. Alistarh, “Model compression via distillation
    and quantization,” in <i>6th International Conference on Learning Representations</i>,
    Vancouver, Canada, 2018.
  ista: 'Polino A, Pascanu R, Alistarh D-A. 2018. Model compression via distillation
    and quantization. 6th International Conference on Learning Representations. ICLR:
    International Conference on Learning Representations.'
  mla: Polino, Antonio, et al. “Model Compression via Distillation and Quantization.”
    <i>6th International Conference on Learning Representations</i>, 2018.
  short: A. Polino, R. Pascanu, D.-A. Alistarh, in:, 6th International Conference
    on Learning Representations, 2018.
conference:
  end_date: 2018-05-03
  location: Vancouver, Canada
  name: 'ICLR: International Conference on Learning Representations'
  start_date: 2018-04-30
date_created: 2020-05-10T22:00:51Z
date_published: 2018-05-01T00:00:00Z
date_updated: 2025-06-30T10:04:44Z
day: '01'
ddc:
- '000'
department:
- _id: DaAl
external_id:
  arxiv:
  - '1802.05668'
file:
- access_level: open_access
  checksum: a4336c167978e81891970e4e4517a8c3
  content_type: application/pdf
  creator: dernst
  date_created: 2020-05-26T13:02:00Z
  date_updated: 2020-07-14T12:48:03Z
  file_id: '7894'
  file_name: 2018_ICLR_Polino.pdf
  file_size: 308339
  relation: main_file
file_date_updated: 2020-07-14T12:48:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
publication: 6th International Conference on Learning Representations
publication_status: published
quality_controlled: '1'
scopus_import: '1'
status: public
title: Model compression via distillation and quantization
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '79'
abstract:
- lang: eng
  text: 'Markov Decision Processes (MDPs) are a popular class of models suitable for
    solving control decision problems in probabilistic reactive systems. We consider
    parametric MDPs (pMDPs) that include parameters in some of the transition probabilities
    to account for stochastic uncertainties of the environment such as noise or input
    disturbances. We study pMDPs with reachability objectives where the parameter
    values are unknown and impossible to measure directly during execution, but there
    is a probability distribution known over the parameter values. We study for the
    first time computing parameter-independent strategies that are expectation optimal,
    i.e., optimize the expected reachability probability under the probability distribution
    over the parameters. We present an encoding of our problem to partially observable
    MDPs (POMDPs), i.e., a reduction of our problem to computing optimal strategies
    in POMDPs. We evaluate our method experimentally on several benchmarks: a motivating
    (repeated) learner model; a series of benchmarks of varying configurations of
    a robot moving on a grid; and a consensus protocol.'
alternative_title:
- LNCS
article_processing_charge: No
arxiv: 1
author:
- first_name: Sebastian
  full_name: Arming, Sebastian
  last_name: Arming
- first_name: Ezio
  full_name: Bartocci, Ezio
  last_name: Bartocci
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Joost P
  full_name: Katoen, Joost P
  id: 4524F760-F248-11E8-B48F-1D18A9856A87
  last_name: Katoen
- first_name: Ana
  full_name: Sokolova, Ana
  last_name: Sokolova
citation:
  ama: 'Arming S, Bartocci E, Chatterjee K, Katoen JP, Sokolova A. Parameter-independent
    strategies for pMDPs via POMDPs. In: Vol 11024. Springer; 2018:53-70. doi:<a href="https://doi.org/10.1007/978-3-319-99154-2_4">10.1007/978-3-319-99154-2_4</a>'
  apa: 'Arming, S., Bartocci, E., Chatterjee, K., Katoen, J. P., &#38; Sokolova, A.
    (2018). Parameter-independent strategies for pMDPs via POMDPs (Vol. 11024, pp.
    53–70). Presented at the QEST: Quantitative Evaluation of Systems, Beijing, China:
    Springer. <a href="https://doi.org/10.1007/978-3-319-99154-2_4">https://doi.org/10.1007/978-3-319-99154-2_4</a>'
  chicago: Arming, Sebastian, Ezio Bartocci, Krishnendu Chatterjee, Joost P Katoen,
    and Ana Sokolova. “Parameter-Independent Strategies for PMDPs via POMDPs,” 11024:53–70.
    Springer, 2018. <a href="https://doi.org/10.1007/978-3-319-99154-2_4">https://doi.org/10.1007/978-3-319-99154-2_4</a>.
  ieee: 'S. Arming, E. Bartocci, K. Chatterjee, J. P. Katoen, and A. Sokolova, “Parameter-independent
    strategies for pMDPs via POMDPs,” presented at the QEST: Quantitative Evaluation
    of Systems, Beijing, China, 2018, vol. 11024, pp. 53–70.'
  ista: 'Arming S, Bartocci E, Chatterjee K, Katoen JP, Sokolova A. 2018. Parameter-independent
    strategies for pMDPs via POMDPs. QEST: Quantitative Evaluation of Systems, LNCS,
    vol. 11024, 53–70.'
  mla: Arming, Sebastian, et al. <i>Parameter-Independent Strategies for PMDPs via
    POMDPs</i>. Vol. 11024, Springer, 2018, pp. 53–70, doi:<a href="https://doi.org/10.1007/978-3-319-99154-2_4">10.1007/978-3-319-99154-2_4</a>.
  short: S. Arming, E. Bartocci, K. Chatterjee, J.P. Katoen, A. Sokolova, in:, Springer,
    2018, pp. 53–70.
conference:
  end_date: 2018-09-07
  location: Beijing, China
  name: 'QEST: Quantitative Evaluation of Systems'
  start_date: 2018-09-04
date_created: 2018-12-11T11:44:31Z
date_published: 2018-08-15T00:00:00Z
date_updated: 2023-09-13T09:38:28Z
day: '15'
department:
- _id: KrCh
- _id: ToHe
doi: 10.1007/978-3-319-99154-2_4
external_id:
  arxiv:
  - '1806.05126'
  isi:
  - '000548912200004'
intvolume: '     11024'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1806.05126
month: '08'
oa: 1
oa_version: Preprint
page: 53-70
publication_status: published
publisher: Springer
publist_id: '7975'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Parameter-independent strategies for pMDPs via POMDPs
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 11024
year: '2018'
...
---
_id: '81'
abstract:
- lang: eng
  text: We solve the offline monitoring problem for timed propositional temporal logic
    (TPTL), interpreted over dense-time Boolean signals. The variant of TPTL we consider
    extends linear temporal logic (LTL) with clock variables and reset quantifiers,
    providing a mechanism to specify real-time constraints. We first describe a general
    monitoring algorithm based on an exhaustive computation of the set of satisfying
    clock assignments as a finite union of zones. We then propose a specialized monitoring
    algorithm for the one-variable case using a partition of the time domain based
    on the notion of region equivalence, whose complexity is linear in the length
    of the signal, thereby generalizing a known result regarding the monitoring of
    metric temporal logic (MTL). The region and zone representations of time constraints
    are known from timed automata verification and can also be used in the discrete-time
    case. Our prototype implementation appears to outperform previous discrete-time
    implementations of TPTL monitoring,
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Adrian
  full_name: Elgyütt, Adrian
  id: 4A2E9DBA-F248-11E8-B48F-1D18A9856A87
  last_name: Elgyütt
- first_name: Thomas
  full_name: Ferrere, Thomas
  id: 40960E6E-F248-11E8-B48F-1D18A9856A87
  last_name: Ferrere
  orcid: 0000-0001-5199-3143
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
citation:
  ama: 'Elgyütt A, Ferrere T, Henzinger TA. Monitoring temporal logic with clock variables.
    In: Vol 11022. Springer; 2018:53-70. doi:<a href="https://doi.org/10.1007/978-3-030-00151-3_4">10.1007/978-3-030-00151-3_4</a>'
  apa: 'Elgyütt, A., Ferrere, T., &#38; Henzinger, T. A. (2018). Monitoring temporal
    logic with clock variables (Vol. 11022, pp. 53–70). Presented at the FORMATS:
    Formal Modeling and Analysis of Timed Systems, Beijing, China: Springer. <a href="https://doi.org/10.1007/978-3-030-00151-3_4">https://doi.org/10.1007/978-3-030-00151-3_4</a>'
  chicago: Elgyütt, Adrian, Thomas Ferrere, and Thomas A Henzinger. “Monitoring Temporal
    Logic with Clock Variables,” 11022:53–70. Springer, 2018. <a href="https://doi.org/10.1007/978-3-030-00151-3_4">https://doi.org/10.1007/978-3-030-00151-3_4</a>.
  ieee: 'A. Elgyütt, T. Ferrere, and T. A. Henzinger, “Monitoring temporal logic with
    clock variables,” presented at the FORMATS: Formal Modeling and Analysis of Timed
    Systems, Beijing, China, 2018, vol. 11022, pp. 53–70.'
  ista: 'Elgyütt A, Ferrere T, Henzinger TA. 2018. Monitoring temporal logic with
    clock variables. FORMATS: Formal Modeling and Analysis of Timed Systems, LNCS,
    vol. 11022, 53–70.'
  mla: Elgyütt, Adrian, et al. <i>Monitoring Temporal Logic with Clock Variables</i>.
    Vol. 11022, Springer, 2018, pp. 53–70, doi:<a href="https://doi.org/10.1007/978-3-030-00151-3_4">10.1007/978-3-030-00151-3_4</a>.
  short: A. Elgyütt, T. Ferrere, T.A. Henzinger, in:, Springer, 2018, pp. 53–70.
conference:
  end_date: 2018-09-06
  location: Beijing, China
  name: 'FORMATS: Formal Modeling and Analysis of Timed Systems'
  start_date: 2018-09-04
date_created: 2018-12-11T11:44:31Z
date_published: 2018-08-26T00:00:00Z
date_updated: 2025-04-15T06:26:03Z
day: '26'
ddc:
- '000'
department:
- _id: ToHe
doi: 10.1007/978-3-030-00151-3_4
external_id:
  isi:
  - '000884993200004'
file:
- access_level: open_access
  checksum: e5d81c9b50a6bd9d8a2c16953aad7e23
  content_type: application/pdf
  creator: dernst
  date_created: 2020-10-09T06:24:21Z
  date_updated: 2020-10-09T06:24:21Z
  file_id: '8638'
  file_name: 2018_LNCS_Elgyuett.pdf
  file_size: 537219
  relation: main_file
  success: 1
file_date_updated: 2020-10-09T06:24:21Z
has_accepted_license: '1'
intvolume: '     11022'
isi: 1
language:
- iso: eng
month: '08'
oa: 1
oa_version: Submitted Version
page: 53 - 70
project:
- _id: 25F5A88A-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11402-N23
  name: Moderne Concurrency Paradigms
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
publication_status: published
publisher: Springer
publist_id: '7973'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Monitoring temporal logic with clock variables
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 11022
year: '2018'
...
---
_id: '82'
abstract:
- lang: eng
  text: In experimental cultures, when bacteria are mixed with lytic (virulent) bacteriophage,
    bacterial cells resistant to the phage commonly emerge and become the dominant
    population of bacteria. Following the ascent of resistant mutants, the densities
    of bacteria in these simple communities become limited by resources rather than
    the phage. Despite the evolution of resistant hosts, upon which the phage cannot
    replicate, the lytic phage population is most commonly maintained in an apparently
    stable state with the resistant bacteria. Several mechanisms have been put forward
    to account for this result. Here we report the results of population dynamic/evolution
    experiments with a virulent mutant of phage Lambda, λVIR, and Escherichia coli
    in serial transfer cultures. We show that, following the ascent of λVIR-resistant
    bacteria, λVIRis maintained in the majority of cases in maltose-limited minimal
    media and in all cases in nutrient-rich broth. Using mathematical models and experiments,
    we show that the dominant mechanism responsible for maintenance of λVIRin these
    resource-limited populations dominated by resistant E. coli is a high rate of
    either phenotypic or genetic transition from resistance to susceptibility—a hitherto
    undemonstrated mechanism we term &quot;leaky resistance.&quot; We discuss the
    implications of leaky resistance to our understanding of the conditions for the
    maintenance of phage in populations of bacteria—their “existence conditions.”.
article_number: '2005971'
article_processing_charge: Yes
author:
- first_name: Waqas
  full_name: Chaudhry, Waqas
  last_name: Chaudhry
- first_name: Maros
  full_name: Pleska, Maros
  id: 4569785E-F248-11E8-B48F-1D18A9856A87
  last_name: Pleska
  orcid: 0000-0001-7460-7479
- first_name: Nilang
  full_name: Shah, Nilang
  last_name: Shah
- first_name: Howard
  full_name: Weiss, Howard
  last_name: Weiss
- first_name: Ingrid
  full_name: Mccall, Ingrid
  last_name: Mccall
- first_name: Justin
  full_name: Meyer, Justin
  last_name: Meyer
- first_name: Animesh
  full_name: Gupta, Animesh
  last_name: Gupta
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
- first_name: Bruce
  full_name: Levin, Bruce
  last_name: Levin
citation:
  ama: Chaudhry W, Pleska M, Shah N, et al. Leaky resistance and the conditions for
    the existence of lytic bacteriophage. <i>PLoS Biology</i>. 2018;16(8). doi:<a
    href="https://doi.org/10.1371/journal.pbio.2005971">10.1371/journal.pbio.2005971</a>
  apa: Chaudhry, W., Pleska, M., Shah, N., Weiss, H., Mccall, I., Meyer, J., … Levin,
    B. (2018). Leaky resistance and the conditions for the existence of lytic bacteriophage.
    <i>PLoS Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.2005971">https://doi.org/10.1371/journal.pbio.2005971</a>
  chicago: Chaudhry, Waqas, Maros Pleska, Nilang Shah, Howard Weiss, Ingrid Mccall,
    Justin Meyer, Animesh Gupta, Calin C Guet, and Bruce Levin. “Leaky Resistance
    and the Conditions for the Existence of Lytic Bacteriophage.” <i>PLoS Biology</i>.
    Public Library of Science, 2018. <a href="https://doi.org/10.1371/journal.pbio.2005971">https://doi.org/10.1371/journal.pbio.2005971</a>.
  ieee: W. Chaudhry <i>et al.</i>, “Leaky resistance and the conditions for the existence
    of lytic bacteriophage,” <i>PLoS Biology</i>, vol. 16, no. 8. Public Library of
    Science, 2018.
  ista: Chaudhry W, Pleska M, Shah N, Weiss H, Mccall I, Meyer J, Gupta A, Guet CC,
    Levin B. 2018. Leaky resistance and the conditions for the existence of lytic
    bacteriophage. PLoS Biology. 16(8), 2005971.
  mla: Chaudhry, Waqas, et al. “Leaky Resistance and the Conditions for the Existence
    of Lytic Bacteriophage.” <i>PLoS Biology</i>, vol. 16, no. 8, 2005971, Public
    Library of Science, 2018, doi:<a href="https://doi.org/10.1371/journal.pbio.2005971">10.1371/journal.pbio.2005971</a>.
  short: W. Chaudhry, M. Pleska, N. Shah, H. Weiss, I. Mccall, J. Meyer, A. Gupta,
    C.C. Guet, B. Levin, PLoS Biology 16 (2018).
date_created: 2018-12-11T11:44:32Z
date_published: 2018-08-16T00:00:00Z
date_updated: 2023-09-13T08:45:41Z
day: '16'
ddc:
- '570'
department:
- _id: CaGu
doi: 10.1371/journal.pbio.2005971
external_id:
  isi:
  - '000443383300024'
file:
- access_level: open_access
  checksum: 527076f78265cd4ea192cd1569851587
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T12:55:31Z
  date_updated: 2020-07-14T12:48:10Z
  file_id: '5706'
  file_name: 2018_Plos_Chaudhry.pdf
  file_size: 4007095
  relation: main_file
file_date_updated: 2020-07-14T12:48:10Z
has_accepted_license: '1'
intvolume: '        16'
isi: 1
issue: '8'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
publication: PLoS Biology
publication_status: published
publisher: Public Library of Science
publist_id: '7972'
quality_controlled: '1'
related_material:
  record:
  - id: '9810'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Leaky resistance and the conditions for the existence of lytic bacteriophage
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 16
year: '2018'
...
---
_id: '8547'
abstract:
- lang: eng
  text: The cerebral cortex contains multiple hierarchically organized areas with
    distinctive cytoarchitectonical patterns, but the cellular mechanisms underlying
    the emergence of this diversity remain unclear. Here, we have quantitatively investigated
    the neuronal output of individual progenitor cells in the ventricular zone of
    the developing mouse neocortex using a combination of methods that together circumvent
    the biases and limitations of individual approaches. We found that individual
    cortical progenitor cells show a high degree of stochasticity and generate pyramidal
    cell lineages that adopt a wide range of laminar configurations. Mathematical
    modelling these lineage data suggests that a small number of progenitor cell populations,
    each generating pyramidal cells following different stochastic developmental programs,
    suffice to generate the heterogenous complement of pyramidal cell lineages that
    collectively build the complex cytoarchitecture of the neocortex.
acknowledgement: We thank I. Andrew and S.E. Bae for excellent technical assistance,
  F. Gage for plasmids, and K. Nave (Nex-Cre) for mouse colonies. We thank members
  of the Marín and Rico laboratories for stimulating discussions and ideas. Our research
  on this topic is supported by grants from the European Research Council (ERC-2017-AdG
  787355 to O.M and ERC2016-CoG 725780 to S.H.) and Wellcome Trust (103714MA) to O.M.
  L.L. was the recipient of an EMBO long-term postdoctoral fellowship, R.B. received
  support from FWF Lise-Meitner program (M 2416) and F.K.W. was supported by an EMBO
  postdoctoral fellowship and is currently a Marie Skłodowska-Curie Fellow from the
  European Commission under the H2020 Programme.
article_processing_charge: No
author:
- first_name: Alfredo
  full_name: Llorca, Alfredo
  last_name: Llorca
- first_name: Gabriele
  full_name: Ciceri, Gabriele
  last_name: Ciceri
- first_name: Robert J
  full_name: Beattie, Robert J
  id: 2E26DF60-F248-11E8-B48F-1D18A9856A87
  last_name: Beattie
  orcid: 0000-0002-8483-8753
- first_name: Fong K.
  full_name: Wong, Fong K.
  last_name: Wong
- first_name: Giovanni
  full_name: Diana, Giovanni
  last_name: Diana
- first_name: Eleni
  full_name: Serafeimidou, Eleni
  last_name: Serafeimidou
- first_name: Marian
  full_name: Fernández-Otero, Marian
  last_name: Fernández-Otero
- first_name: Carmen
  full_name: Streicher, Carmen
  id: 36BCB99C-F248-11E8-B48F-1D18A9856A87
  last_name: Streicher
- first_name: Sebastian J.
  full_name: Arnold, Sebastian J.
  last_name: Arnold
- first_name: Martin
  full_name: Meyer, Martin
  last_name: Meyer
- first_name: Simon
  full_name: Hippenmeyer, Simon
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
- first_name: Miguel
  full_name: Maravall, Miguel
  last_name: Maravall
- first_name: Oscar
  full_name: Marín, Oscar
  last_name: Marín
citation:
  ama: Llorca A, Ciceri G, Beattie RJ, et al. Heterogeneous progenitor cell behaviors
    underlie the assembly of neocortical cytoarchitecture. <i>bioRxiv</i>. doi:<a
    href="https://doi.org/10.1101/494088">10.1101/494088</a>
  apa: Llorca, A., Ciceri, G., Beattie, R. J., Wong, F. K., Diana, G., Serafeimidou,
    E., … Marín, O. (n.d.). Heterogeneous progenitor cell behaviors underlie the assembly
    of neocortical cytoarchitecture. <i>bioRxiv</i>. Cold Spring Harbor Laboratory.
    <a href="https://doi.org/10.1101/494088">https://doi.org/10.1101/494088</a>
  chicago: Llorca, Alfredo, Gabriele Ciceri, Robert J Beattie, Fong K. Wong, Giovanni
    Diana, Eleni Serafeimidou, Marian Fernández-Otero, et al. “Heterogeneous Progenitor
    Cell Behaviors Underlie the Assembly of Neocortical Cytoarchitecture.” <i>BioRxiv</i>.
    Cold Spring Harbor Laboratory, n.d. <a href="https://doi.org/10.1101/494088">https://doi.org/10.1101/494088</a>.
  ieee: A. Llorca <i>et al.</i>, “Heterogeneous progenitor cell behaviors underlie
    the assembly of neocortical cytoarchitecture,” <i>bioRxiv</i>. Cold Spring Harbor
    Laboratory.
  ista: Llorca A, Ciceri G, Beattie RJ, Wong FK, Diana G, Serafeimidou E, Fernández-Otero
    M, Streicher C, Arnold SJ, Meyer M, Hippenmeyer S, Maravall M, Marín O. Heterogeneous
    progenitor cell behaviors underlie the assembly of neocortical cytoarchitecture.
    bioRxiv, <a href="https://doi.org/10.1101/494088">10.1101/494088</a>.
  mla: Llorca, Alfredo, et al. “Heterogeneous Progenitor Cell Behaviors Underlie the
    Assembly of Neocortical Cytoarchitecture.” <i>BioRxiv</i>, Cold Spring Harbor
    Laboratory, doi:<a href="https://doi.org/10.1101/494088">10.1101/494088</a>.
  short: A. Llorca, G. Ciceri, R.J. Beattie, F.K. Wong, G. Diana, E. Serafeimidou,
    M. Fernández-Otero, C. Streicher, S.J. Arnold, M. Meyer, S. Hippenmeyer, M. Maravall,
    O. Marín, BioRxiv (n.d.).
date_created: 2020-09-21T12:01:50Z
date_published: 2018-12-13T00:00:00Z
date_updated: 2024-10-22T10:46:39Z
day: '13'
department:
- _id: SiHi
doi: 10.1101/494088
ec_funded: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/494088
month: '12'
oa: 1
oa_version: Preprint
project:
- _id: 260018B0-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '725780'
  name: Principles of Neural Stem Cell Lineage Progression in Cerebral Cortex Development
- _id: 264E56E2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: M02416
  name: Molecular Mechanisms Regulating Gliogenesis in the Neocortex
publication: bioRxiv
publication_status: submitted
publisher: Cold Spring Harbor Laboratory
status: public
title: Heterogeneous progenitor cell behaviors underlie the assembly of neocortical
  cytoarchitecture
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '86'
abstract:
- lang: eng
  text: Responsiveness—the requirement that every request to a system be eventually
    handled—is one of the fundamental liveness properties of a reactive system. Average
    response time is a quantitative measure for the responsiveness requirement used
    commonly in performance evaluation. We show how average response time can be computed
    on state-transition graphs, on Markov chains, and on game graphs. In all three
    cases, we give polynomial-time algorithms.
acknowledgement: 'This research was supported in part by the Austrian Science Fund
  (FWF) under grants S11402-N23, S11407-N23 (RiSE/SHiNE) and Z211-N23 (Wittgenstein
  Award), ERC Start grant (279307: Graph Games), Vienna Science and Technology Fund
  (WWTF) through project ICT15-003 and by the National Science Centre (NCN), Poland
  under grant 2014/15/D/ST6/04543.'
alternative_title:
- LNCS
author:
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Jan
  full_name: Otop, Jan
  id: 2FC5DA74-F248-11E8-B48F-1D18A9856A87
  last_name: Otop
citation:
  ama: 'Chatterjee K, Henzinger TA, Otop J. Computing average response time. In: Lohstroh
    M, Derler P, Sirjani M, eds. <i>Principles of Modeling</i>. Vol 10760. Springer;
    2018:143-161. doi:<a href="https://doi.org/10.1007/978-3-319-95246-8_9">10.1007/978-3-319-95246-8_9</a>'
  apa: Chatterjee, K., Henzinger, T. A., &#38; Otop, J. (2018). Computing average
    response time. In M. Lohstroh, P. Derler, &#38; M. Sirjani (Eds.), <i>Principles
    of Modeling</i> (Vol. 10760, pp. 143–161). Springer. <a href="https://doi.org/10.1007/978-3-319-95246-8_9">https://doi.org/10.1007/978-3-319-95246-8_9</a>
  chicago: Chatterjee, Krishnendu, Thomas A Henzinger, and Jan Otop. “Computing Average
    Response Time.” In <i>Principles of Modeling</i>, edited by Marten Lohstroh, Patricia
    Derler, and Marjan Sirjani, 10760:143–61. Springer, 2018. <a href="https://doi.org/10.1007/978-3-319-95246-8_9">https://doi.org/10.1007/978-3-319-95246-8_9</a>.
  ieee: K. Chatterjee, T. A. Henzinger, and J. Otop, “Computing average response time,”
    in <i>Principles of Modeling</i>, vol. 10760, M. Lohstroh, P. Derler, and M. Sirjani,
    Eds. Springer, 2018, pp. 143–161.
  ista: 'Chatterjee K, Henzinger TA, Otop J. 2018.Computing average response time.
    In: Principles of Modeling. LNCS, vol. 10760, 143–161.'
  mla: Chatterjee, Krishnendu, et al. “Computing Average Response Time.” <i>Principles
    of Modeling</i>, edited by Marten Lohstroh et al., vol. 10760, Springer, 2018,
    pp. 143–61, doi:<a href="https://doi.org/10.1007/978-3-319-95246-8_9">10.1007/978-3-319-95246-8_9</a>.
  short: K. Chatterjee, T.A. Henzinger, J. Otop, in:, M. Lohstroh, P. Derler, M. Sirjani
    (Eds.), Principles of Modeling, Springer, 2018, pp. 143–161.
date_created: 2018-12-11T11:44:33Z
date_published: 2018-07-20T00:00:00Z
date_updated: 2025-04-15T06:26:15Z
day: '20'
ddc:
- '000'
department:
- _id: KrCh
- _id: ToHe
doi: 10.1007/978-3-319-95246-8_9
ec_funded: 1
editor:
- first_name: Marten
  full_name: Lohstroh, Marten
  last_name: Lohstroh
- first_name: Patricia
  full_name: Derler, Patricia
  last_name: Derler
- first_name: Marjan
  full_name: Sirjani, Marjan
  last_name: Sirjani
file:
- access_level: open_access
  checksum: 9995c6ce6957333baf616fc4f20be597
  content_type: application/pdf
  creator: dernst
  date_created: 2019-11-19T08:22:18Z
  date_updated: 2020-07-14T12:48:14Z
  file_id: '7053'
  file_name: 2018_PrinciplesModeling_Chatterjee.pdf
  file_size: 516307
  relation: main_file
file_date_updated: 2020-07-14T12:48:14Z
has_accepted_license: '1'
intvolume: '     10760'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Submitted Version
page: 143 - 161
project:
- _id: 25832EC2-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S 11407_N23
  name: Rigorous Systems Engineering
- _id: 25863FF4-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11407
  name: Game Theory
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
- _id: 2581B60A-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '279307'
  name: 'Quantitative Graph Games: Theory and Applications'
- _id: 25892FC0-B435-11E9-9278-68D0E5697425
  grant_number: ICT15-003
  name: Efficient Algorithms for Computer Aided Verification
publication: Principles of Modeling
publication_status: published
publisher: Springer
publist_id: '7968'
quality_controlled: '1'
scopus_import: 1
status: public
title: Computing average response time
type: book_chapter
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 10760
year: '2018'
...
---
_id: '8618'
abstract:
- lang: eng
  text: The reversibly switchable fluorescent proteins (RSFPs) commonly used for RESOLFT
    nanoscopy have been developed from fluorescent proteins of the GFP superfamily.
    These proteins are bright, but exhibit several drawbacks such as relatively large
    size, oxygen-dependence, sensitivity to low pH, and limited switching speed. Therefore,
    RSFPs from other origins with improved properties need to be explored. Here, we
    report the development of two RSFPs based on the LOV domain of the photoreceptor
    protein YtvA from Bacillus subtilis. LOV domains obtain their fluorescence by
    association with the abundant cellular cofactor flavin mononucleotide (FMN). Under
    illumination with blue and ultraviolet light, they undergo a photocycle, making
    these proteins inherently photoswitchable. Our first improved variant, rsLOV1,
    can be used for RESOLFT imaging, whereas rsLOV2 proved useful for STED nanoscopy
    of living cells with a resolution of down to 50 nm. In addition to their smaller
    size compared to GFP-related proteins (17 kDa instead of 27 kDa) and their usability
    at low pH, rsLOV1 and rsLOV2 exhibit faster switching kinetics, switching on and
    off 3 times faster than rsEGFP2, the fastest-switching RSFP reported to date.
    Therefore, LOV-domain-based RSFPs have potential for applications where the switching
    speed of GFP-based proteins is limiting.
article_number: '2724'
article_processing_charge: No
article_type: original
author:
- first_name: Carola
  full_name: Gregor, Carola
  last_name: Gregor
- first_name: Sven C.
  full_name: Sidenstein, Sven C.
  last_name: Sidenstein
- first_name: Martin
  full_name: Andresen, Martin
  last_name: Andresen
- first_name: Steffen J.
  full_name: Sahl, Steffen J.
  last_name: Sahl
- first_name: Johann G
  full_name: Danzl, Johann G
  id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87
  last_name: Danzl
  orcid: 0000-0001-8559-3973
- first_name: Stefan W.
  full_name: Hell, Stefan W.
  last_name: Hell
citation:
  ama: Gregor C, Sidenstein SC, Andresen M, Sahl SJ, Danzl JG, Hell SW. Novel reversibly
    switchable fluorescent proteins for RESOLFT and STED nanoscopy engineered from
    the bacterial photoreceptor YtvA. <i>Scientific Reports</i>. 2018;8. doi:<a href="https://doi.org/10.1038/s41598-018-19947-1">10.1038/s41598-018-19947-1</a>
  apa: Gregor, C., Sidenstein, S. C., Andresen, M., Sahl, S. J., Danzl, J. G., &#38;
    Hell, S. W. (2018). Novel reversibly switchable fluorescent proteins for RESOLFT
    and STED nanoscopy engineered from the bacterial photoreceptor YtvA. <i>Scientific
    Reports</i>. Springer Nature. <a href="https://doi.org/10.1038/s41598-018-19947-1">https://doi.org/10.1038/s41598-018-19947-1</a>
  chicago: Gregor, Carola, Sven C. Sidenstein, Martin Andresen, Steffen J. Sahl, Johann
    G Danzl, and Stefan W. Hell. “Novel Reversibly Switchable Fluorescent Proteins
    for RESOLFT and STED Nanoscopy Engineered from the Bacterial Photoreceptor YtvA.”
    <i>Scientific Reports</i>. Springer Nature, 2018. <a href="https://doi.org/10.1038/s41598-018-19947-1">https://doi.org/10.1038/s41598-018-19947-1</a>.
  ieee: C. Gregor, S. C. Sidenstein, M. Andresen, S. J. Sahl, J. G. Danzl, and S.
    W. Hell, “Novel reversibly switchable fluorescent proteins for RESOLFT and STED
    nanoscopy engineered from the bacterial photoreceptor YtvA,” <i>Scientific Reports</i>,
    vol. 8. Springer Nature, 2018.
  ista: Gregor C, Sidenstein SC, Andresen M, Sahl SJ, Danzl JG, Hell SW. 2018. Novel
    reversibly switchable fluorescent proteins for RESOLFT and STED nanoscopy engineered
    from the bacterial photoreceptor YtvA. Scientific Reports. 8, 2724.
  mla: Gregor, Carola, et al. “Novel Reversibly Switchable Fluorescent Proteins for
    RESOLFT and STED Nanoscopy Engineered from the Bacterial Photoreceptor YtvA.”
    <i>Scientific Reports</i>, vol. 8, 2724, Springer Nature, 2018, doi:<a href="https://doi.org/10.1038/s41598-018-19947-1">10.1038/s41598-018-19947-1</a>.
  short: C. Gregor, S.C. Sidenstein, M. Andresen, S.J. Sahl, J.G. Danzl, S.W. Hell,
    Scientific Reports 8 (2018).
date_created: 2020-10-06T16:33:37Z
date_published: 2018-02-09T00:00:00Z
date_updated: 2024-10-21T06:02:43Z
day: '09'
ddc:
- '570'
department:
- _id: JoDa
doi: 10.1038/s41598-018-19947-1
external_id:
  isi:
  - '000424630400037'
  pmid:
  - '29426833'
file:
- access_level: open_access
  checksum: e642080fcbde9584c63544f587c74f03
  content_type: application/pdf
  creator: dernst
  date_created: 2020-10-06T16:35:16Z
  date_updated: 2020-10-06T16:35:16Z
  file_id: '8619'
  file_name: 2018_ScientificReports_Gregor.pdf
  file_size: 2818077
  relation: main_file
  success: 1
file_date_updated: 2020-10-06T16:35:16Z
has_accepted_license: '1'
intvolume: '         8'
isi: 1
keyword:
- Multidisciplinary
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
publication: Scientific Reports
publication_identifier:
  issn:
  - 2045-2322
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Novel reversibly switchable fluorescent proteins for RESOLFT and STED nanoscopy
  engineered from the bacterial photoreceptor YtvA
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 8
year: '2018'
...
---
_id: '913'
abstract:
- lang: eng
  text: Coordinated cell polarization in developing tissues is a recurrent theme in
    multicellular organisms. In plants, a directional distribution of the plant hormone
    auxin is at the core of many developmental programs. A feedback regulation of
    auxin on the polarized localization of PIN auxin transporters in individual cells
    has been proposed as a self-organizing mechanism for coordinated tissue polarization,
    but the molecular mechanisms linking auxin signalling to PIN-dependent auxin transport
    remain unknown. We performed a microarray-based approach to find regulators of
    the auxin-induced PIN relocation in the Arabidopsis thaliana root. We identified
    a subset of a family of phosphatidylinositol transfer proteins (PITP), the PATELLINs
    (PATL). Here, we show that PATLs are expressed in partially overlapping cells
    types in different tissues going through mitosis or initiating differentiation
    programs. PATLs are plasma membrane-associated proteins accumulated in Arabidopsis
    embryos, primary roots, lateral root primordia, and developing stomata. Higher
    order patl mutants display reduced PIN1 repolarization in response to auxin, shorter
    root apical meristem, and drastic defects in embryo and seedling development.
    This suggests PATLs redundantly play a crucial role in polarity and patterning
    in Arabidopsis.
article_number: jcs.204198
article_processing_charge: No
author:
- first_name: Ricardo
  full_name: Tejos, Ricardo
  last_name: Tejos
- first_name: Cecilia
  full_name: Rodríguez Furlán, Cecilia
  last_name: Rodríguez Furlán
- first_name: Maciek
  full_name: Adamowski, Maciek
  id: 45F536D2-F248-11E8-B48F-1D18A9856A87
  last_name: Adamowski
  orcid: 0000-0001-6463-5257
- first_name: Michael
  full_name: Sauer, Michael
  last_name: Sauer
- first_name: Lorena
  full_name: Norambuena, Lorena
  last_name: Norambuena
- first_name: Jirí
  full_name: Friml, Jirí
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: Tejos R, Rodríguez Furlán C, Adamowski M, Sauer M, Norambuena L, Friml J. PATELLINS
    are regulators of auxin mediated PIN1 relocation and plant development in Arabidopsis
    thaliana. <i>Journal of Cell Science</i>. 2018;131(2). doi:<a href="https://doi.org/10.1242/jcs.204198">10.1242/jcs.204198</a>
  apa: Tejos, R., Rodríguez Furlán, C., Adamowski, M., Sauer, M., Norambuena, L.,
    &#38; Friml, J. (2018). PATELLINS are regulators of auxin mediated PIN1 relocation
    and plant development in Arabidopsis thaliana. <i>Journal of Cell Science</i>.
    Company of Biologists. <a href="https://doi.org/10.1242/jcs.204198">https://doi.org/10.1242/jcs.204198</a>
  chicago: Tejos, Ricardo, Cecilia Rodríguez Furlán, Maciek Adamowski, Michael Sauer,
    Lorena Norambuena, and Jiří Friml. “PATELLINS Are Regulators of Auxin Mediated
    PIN1 Relocation and Plant Development in Arabidopsis Thaliana.” <i>Journal of
    Cell Science</i>. Company of Biologists, 2018. <a href="https://doi.org/10.1242/jcs.204198">https://doi.org/10.1242/jcs.204198</a>.
  ieee: R. Tejos, C. Rodríguez Furlán, M. Adamowski, M. Sauer, L. Norambuena, and
    J. Friml, “PATELLINS are regulators of auxin mediated PIN1 relocation and plant
    development in Arabidopsis thaliana,” <i>Journal of Cell Science</i>, vol. 131,
    no. 2. Company of Biologists, 2018.
  ista: Tejos R, Rodríguez Furlán C, Adamowski M, Sauer M, Norambuena L, Friml J.
    2018. PATELLINS are regulators of auxin mediated PIN1 relocation and plant development
    in Arabidopsis thaliana. Journal of Cell Science. 131(2), jcs. 204198.
  mla: Tejos, Ricardo, et al. “PATELLINS Are Regulators of Auxin Mediated PIN1 Relocation
    and Plant Development in Arabidopsis Thaliana.” <i>Journal of Cell Science</i>,
    vol. 131, no. 2, jcs. 204198, Company of Biologists, 2018, doi:<a href="https://doi.org/10.1242/jcs.204198">10.1242/jcs.204198</a>.
  short: R. Tejos, C. Rodríguez Furlán, M. Adamowski, M. Sauer, L. Norambuena, J.
    Friml, Journal of Cell Science 131 (2018).
corr_author: '1'
date_created: 2018-12-11T11:49:10Z
date_published: 2018-01-29T00:00:00Z
date_updated: 2025-07-10T12:01:38Z
day: '29'
ddc:
- '581'
department:
- _id: JiFr
doi: 10.1242/jcs.204198
ec_funded: 1
external_id:
  isi:
  - '000424842400019'
file:
- access_level: open_access
  checksum: bf156c20a4f117b4b932370d54cbac8c
  content_type: application/pdf
  creator: dernst
  date_created: 2019-04-12T08:46:32Z
  date_updated: 2020-07-14T12:48:15Z
  file_id: '6299'
  file_name: 2017_adamowski_PATELLINS_are.pdf
  file_size: 14925985
  relation: main_file
file_date_updated: 2020-07-14T12:48:15Z
has_accepted_license: '1'
intvolume: '       131'
isi: 1
issue: '2'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: 25716A02-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '282300'
  name: Polarity and subcellular dynamics in plants
publication: Journal of Cell Science
publication_identifier:
  issn:
  - 0021-9533
publication_status: published
publisher: Company of Biologists
publist_id: '6530'
pubrep_id: '988'
quality_controlled: '1'
scopus_import: '1'
status: public
title: PATELLINS are regulators of auxin mediated PIN1 relocation and plant development
  in Arabidopsis thaliana
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 131
year: '2018'
...
---
_id: '9229'
alternative_title:
- Molecular and cellular neuroscience
article_processing_charge: No
article_type: letter_note
author:
- first_name: Johann G
  full_name: Danzl, Johann G
  id: 42EFD3B6-F248-11E8-B48F-1D18A9856A87
  last_name: Danzl
  orcid: 0000-0001-8559-3973
citation:
  ama: Danzl JG. Diffraction-unlimited optical imaging for synaptic physiology. <i>Opera
    Medica et Physiologica</i>. 2018;4(S1):11. doi:<a href="https://doi.org/10.20388/omp2018.00s1.001">10.20388/omp2018.00s1.001</a>
  apa: Danzl, J. G. (2018). Diffraction-unlimited optical imaging for synaptic physiology.
    <i>Opera Medica et Physiologica</i>. Lobachevsky State University of Nizhny Novgorod.
    <a href="https://doi.org/10.20388/omp2018.00s1.001">https://doi.org/10.20388/omp2018.00s1.001</a>
  chicago: Danzl, Johann G. “Diffraction-Unlimited Optical Imaging for Synaptic Physiology.”
    <i>Opera Medica et Physiologica</i>. Lobachevsky State University of Nizhny Novgorod,
    2018. <a href="https://doi.org/10.20388/omp2018.00s1.001">https://doi.org/10.20388/omp2018.00s1.001</a>.
  ieee: J. G. Danzl, “Diffraction-unlimited optical imaging for synaptic physiology,”
    <i>Opera Medica et Physiologica</i>, vol. 4, no. S1. Lobachevsky State University
    of Nizhny Novgorod, p. 11, 2018.
  ista: Danzl JG. 2018. Diffraction-unlimited optical imaging for synaptic physiology.
    Opera Medica et Physiologica. 4(S1), 11.
  mla: Danzl, Johann G. “Diffraction-Unlimited Optical Imaging for Synaptic Physiology.”
    <i>Opera Medica et Physiologica</i>, vol. 4, no. S1, Lobachevsky State University
    of Nizhny Novgorod, 2018, p. 11, doi:<a href="https://doi.org/10.20388/omp2018.00s1.001">10.20388/omp2018.00s1.001</a>.
  short: J.G. Danzl, Opera Medica et Physiologica 4 (2018) 11.
date_created: 2021-03-07T23:01:25Z
date_published: 2018-06-30T00:00:00Z
date_updated: 2021-12-03T07:31:05Z
day: '30'
department:
- _id: JoDa
doi: 10.20388/omp2018.00s1.001
intvolume: '         4'
issue: S1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://operamedphys.org/content/molecular-and-cellular-neuroscience
month: '06'
oa: 1
oa_version: Published Version
page: '11'
publication: Opera Medica et Physiologica
publication_identifier:
  eissn:
  - 2500-2295
  issn:
  - 2500-2287
publication_status: published
publisher: Lobachevsky State University of Nizhny Novgorod
quality_controlled: '1'
scopus_import: '1'
status: public
title: Diffraction-unlimited optical imaging for synaptic physiology
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 4
year: '2018'
...
---
_id: '9471'
abstract:
- lang: eng
  text: The DEMETER (DME) DNA glycosylase catalyzes genome-wide DNA demethylation
    and is required for endosperm genomic imprinting and embryo viability. Targets
    of DME-mediated DNA demethylation reside in small, euchromatic, AT-rich transposons
    and at the boundaries of large transposons, but how DME interacts with these diverse
    chromatin states is unknown. The STRUCTURE SPECIFIC RECOGNITION PROTEIN 1 (SSRP1)
    subunit of the chromatin remodeler FACT (facilitates chromatin transactions),
    was previously shown to be involved in the DME-dependent regulation of genomic
    imprinting in Arabidopsis endosperm. Therefore, to investigate the interaction
    between DME and chromatin, we focused on the activity of the two FACT subunits,
    SSRP1 and SUPPRESSOR of TY16 (SPT16), during reproduction in Arabidopsis. We found
    that FACT colocalizes with nuclear DME in vivo, and that DME has two classes of
    target sites, the first being euchromatic and accessible to DME, but the second,
    representing over half of DME targets, requiring the action of FACT for DME-mediated
    DNA demethylation genome-wide. Our results show that the FACT-dependent DME targets
    are GC-rich heterochromatin domains with high nucleosome occupancy enriched with
    H3K9me2 and H3K27me1. Further, we demonstrate that heterochromatin-associated
    linker histone H1 specifically mediates the requirement for FACT at a subset of
    DME-target loci. Overall, our results demonstrate that FACT is required for DME
    targeting by facilitating its access to heterochromatin.
article_processing_charge: No
article_type: original
author:
- first_name: Jennifer M.
  full_name: Frost, Jennifer M.
  last_name: Frost
- first_name: M. Yvonne
  full_name: Kim, M. Yvonne
  last_name: Kim
- first_name: Guen Tae
  full_name: Park, Guen Tae
  last_name: Park
- first_name: Ping-Hung
  full_name: Hsieh, Ping-Hung
  last_name: Hsieh
- first_name: Miyuki
  full_name: Nakamura, Miyuki
  last_name: Nakamura
- first_name: Samuel J. H.
  full_name: Lin, Samuel J. H.
  last_name: Lin
- first_name: Hyunjin
  full_name: Yoo, Hyunjin
  last_name: Yoo
- first_name: Jaemyung
  full_name: Choi, Jaemyung
  last_name: Choi
- first_name: Yoko
  full_name: Ikeda, Yoko
  last_name: Ikeda
- first_name: Tetsu
  full_name: Kinoshita, Tetsu
  last_name: Kinoshita
- first_name: Yeonhee
  full_name: Choi, Yeonhee
  last_name: Choi
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Robert L.
  full_name: Fischer, Robert L.
  last_name: Fischer
citation:
  ama: Frost JM, Kim MY, Park GT, et al. FACT complex is required for DNA demethylation
    at heterochromatin during reproduction in Arabidopsis. <i>Proceedings of the National
    Academy of Sciences</i>. 2018;115(20):E4720-E4729. doi:<a href="https://doi.org/10.1073/pnas.1713333115">10.1073/pnas.1713333115</a>
  apa: Frost, J. M., Kim, M. Y., Park, G. T., Hsieh, P.-H., Nakamura, M., Lin, S.
    J. H., … Fischer, R. L. (2018). FACT complex is required for DNA demethylation
    at heterochromatin during reproduction in Arabidopsis. <i>Proceedings of the National
    Academy of Sciences</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1713333115">https://doi.org/10.1073/pnas.1713333115</a>
  chicago: Frost, Jennifer M., M. Yvonne Kim, Guen Tae Park, Ping-Hung Hsieh, Miyuki
    Nakamura, Samuel J. H. Lin, Hyunjin Yoo, et al. “FACT Complex Is Required for
    DNA Demethylation at Heterochromatin during Reproduction in Arabidopsis.” <i>Proceedings
    of the National Academy of Sciences</i>. National Academy of Sciences, 2018. <a
    href="https://doi.org/10.1073/pnas.1713333115">https://doi.org/10.1073/pnas.1713333115</a>.
  ieee: J. M. Frost <i>et al.</i>, “FACT complex is required for DNA demethylation
    at heterochromatin during reproduction in Arabidopsis,” <i>Proceedings of the
    National Academy of Sciences</i>, vol. 115, no. 20. National Academy of Sciences,
    pp. E4720–E4729, 2018.
  ista: Frost JM, Kim MY, Park GT, Hsieh P-H, Nakamura M, Lin SJH, Yoo H, Choi J,
    Ikeda Y, Kinoshita T, Choi Y, Zilberman D, Fischer RL. 2018. FACT complex is required
    for DNA demethylation at heterochromatin during reproduction in Arabidopsis. Proceedings
    of the National Academy of Sciences. 115(20), E4720–E4729.
  mla: Frost, Jennifer M., et al. “FACT Complex Is Required for DNA Demethylation
    at Heterochromatin during Reproduction in Arabidopsis.” <i>Proceedings of the
    National Academy of Sciences</i>, vol. 115, no. 20, National Academy of Sciences,
    2018, pp. E4720–29, doi:<a href="https://doi.org/10.1073/pnas.1713333115">10.1073/pnas.1713333115</a>.
  short: J.M. Frost, M.Y. Kim, G.T. Park, P.-H. Hsieh, M. Nakamura, S.J.H. Lin, H.
    Yoo, J. Choi, Y. Ikeda, T. Kinoshita, Y. Choi, D. Zilberman, R.L. Fischer, Proceedings
    of the National Academy of Sciences 115 (2018) E4720–E4729.
date_created: 2021-06-07T06:11:28Z
date_published: 2018-05-15T00:00:00Z
date_updated: 2021-12-14T07:53:40Z
day: '15'
ddc:
- '580'
department:
- _id: DaZi
doi: 10.1073/pnas.1713333115
extern: '1'
external_id:
  pmid:
  - '29712855'
file:
- access_level: open_access
  checksum: 810260dc0e3cc3033e15c19ad0dc123e
  content_type: application/pdf
  creator: asandaue
  date_created: 2021-06-07T06:16:38Z
  date_updated: 2021-06-07T06:16:38Z
  file_id: '9472'
  file_name: 2018_PNAS_Frost.pdf
  file_size: 3045260
  relation: main_file
  success: 1
file_date_updated: 2021-06-07T06:16:38Z
has_accepted_license: '1'
intvolume: '       115'
issue: '20'
keyword:
- Multidisciplinary
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '05'
oa: 1
oa_version: Published Version
page: E4720-E4729
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
related_material:
  link:
  - relation: earlier_version
    url: 'https://doi.org/10.1101/187674 '
scopus_import: '1'
status: public
title: FACT complex is required for DNA demethylation at heterochromatin during reproduction
  in Arabidopsis
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: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 115
year: '2018'
...
---
_id: '9807'
abstract:
- lang: eng
  text: Table S1. Genes with highest betweenness. Table S2. Local and Master regulators
    up-regulated. Table S3. Local and Master regulators down-regulated (XLSX 23 kb).
article_processing_charge: No
author:
- first_name: Juan
  full_name: Higareda Almaraz, Juan
  last_name: Higareda Almaraz
- first_name: Michael
  full_name: Karbiener, Michael
  last_name: Karbiener
- first_name: Maude
  full_name: Giroud, Maude
  last_name: Giroud
- first_name: Florian
  full_name: Pauler, Florian
  id: 48EA0138-F248-11E8-B48F-1D18A9856A87
  last_name: Pauler
  orcid: 0000-0002-7462-0048
- first_name: Teresa
  full_name: Gerhalter, Teresa
  last_name: Gerhalter
- first_name: Stephan
  full_name: Herzig, Stephan
  last_name: Herzig
- first_name: Marcel
  full_name: Scheideler, Marcel
  last_name: Scheideler
citation:
  ama: 'Higareda Almaraz J, Karbiener M, Giroud M, et al. Additional file 1: Of Norepinephrine
    triggers an immediate-early regulatory network response in primary human white
    adipocytes. 2018. doi:<a href="https://doi.org/10.6084/m9.figshare.7295339.v1">10.6084/m9.figshare.7295339.v1</a>'
  apa: 'Higareda Almaraz, J., Karbiener, M., Giroud, M., Pauler, F., Gerhalter, T.,
    Herzig, S., &#38; Scheideler, M. (2018). Additional file 1: Of Norepinephrine
    triggers an immediate-early regulatory network response in primary human white
    adipocytes. Springer Nature. <a href="https://doi.org/10.6084/m9.figshare.7295339.v1">https://doi.org/10.6084/m9.figshare.7295339.v1</a>'
  chicago: 'Higareda Almaraz, Juan, Michael Karbiener, Maude Giroud, Florian Pauler,
    Teresa Gerhalter, Stephan Herzig, and Marcel Scheideler. “Additional File 1: Of
    Norepinephrine Triggers an Immediate-Early Regulatory Network Response in Primary
    Human White Adipocytes.” Springer Nature, 2018. <a href="https://doi.org/10.6084/m9.figshare.7295339.v1">https://doi.org/10.6084/m9.figshare.7295339.v1</a>.'
  ieee: 'J. Higareda Almaraz <i>et al.</i>, “Additional file 1: Of Norepinephrine
    triggers an immediate-early regulatory network response in primary human white
    adipocytes.” Springer Nature, 2018.'
  ista: 'Higareda Almaraz J, Karbiener M, Giroud M, Pauler F, Gerhalter T, Herzig
    S, Scheideler M. 2018. Additional file 1: Of Norepinephrine triggers an immediate-early
    regulatory network response in primary human white adipocytes, Springer Nature,
    <a href="https://doi.org/10.6084/m9.figshare.7295339.v1">10.6084/m9.figshare.7295339.v1</a>.'
  mla: 'Higareda Almaraz, Juan, et al. <i>Additional File 1: Of Norepinephrine Triggers
    an Immediate-Early Regulatory Network Response in Primary Human White Adipocytes</i>.
    Springer Nature, 2018, doi:<a href="https://doi.org/10.6084/m9.figshare.7295339.v1">10.6084/m9.figshare.7295339.v1</a>.'
  short: J. Higareda Almaraz, M. Karbiener, M. Giroud, F. Pauler, T. Gerhalter, S.
    Herzig, M. Scheideler, (2018).
date_created: 2021-08-06T12:26:53Z
date_published: 2018-11-03T00:00:00Z
date_updated: 2023-09-13T09:10:47Z
day: '03'
department:
- _id: SiHi
doi: 10.6084/m9.figshare.7295339.v1
main_file_link:
- open_access: '1'
  url: https://doi.org/10.6084/m9.figshare.7295339.v1
month: '11'
oa: 1
oa_version: Published Version
publisher: Springer Nature
related_material:
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title: 'Additional file 1: Of Norepinephrine triggers an immediate-early regulatory
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type: research_data_reference
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...
---
_id: '9808'
abstract:
- lang: eng
  text: Table S4. Counts per Gene per Million Reads Mapped. (XLSX 2751 kb).
article_processing_charge: No
author:
- first_name: Juan
  full_name: Higareda Almaraz, Juan
  last_name: Higareda Almaraz
- first_name: Michael
  full_name: Karbiener, Michael
  last_name: Karbiener
- first_name: Maude
  full_name: Giroud, Maude
  last_name: Giroud
- first_name: Florian
  full_name: Pauler, Florian
  id: 48EA0138-F248-11E8-B48F-1D18A9856A87
  last_name: Pauler
  orcid: 0000-0002-7462-0048
- first_name: Teresa
  full_name: Gerhalter, Teresa
  last_name: Gerhalter
- first_name: Stephan
  full_name: Herzig, Stephan
  last_name: Herzig
- first_name: Marcel
  full_name: Scheideler, Marcel
  last_name: Scheideler
citation:
  ama: 'Higareda Almaraz J, Karbiener M, Giroud M, et al. Additional file 3: Of Norepinephrine
    triggers an immediate-early regulatory network response in primary human white
    adipocytes. 2018. doi:<a href="https://doi.org/10.6084/m9.figshare.7295369.v1">10.6084/m9.figshare.7295369.v1</a>'
  apa: 'Higareda Almaraz, J., Karbiener, M., Giroud, M., Pauler, F., Gerhalter, T.,
    Herzig, S., &#38; Scheideler, M. (2018). Additional file 3: Of Norepinephrine
    triggers an immediate-early regulatory network response in primary human white
    adipocytes. Springer Nature. <a href="https://doi.org/10.6084/m9.figshare.7295369.v1">https://doi.org/10.6084/m9.figshare.7295369.v1</a>'
  chicago: 'Higareda Almaraz, Juan, Michael Karbiener, Maude Giroud, Florian Pauler,
    Teresa Gerhalter, Stephan Herzig, and Marcel Scheideler. “Additional File 3: Of
    Norepinephrine Triggers an Immediate-Early Regulatory Network Response in Primary
    Human White Adipocytes.” Springer Nature, 2018. <a href="https://doi.org/10.6084/m9.figshare.7295369.v1">https://doi.org/10.6084/m9.figshare.7295369.v1</a>.'
  ieee: 'J. Higareda Almaraz <i>et al.</i>, “Additional file 3: Of Norepinephrine
    triggers an immediate-early regulatory network response in primary human white
    adipocytes.” Springer Nature, 2018.'
  ista: 'Higareda Almaraz J, Karbiener M, Giroud M, Pauler F, Gerhalter T, Herzig
    S, Scheideler M. 2018. Additional file 3: Of Norepinephrine triggers an immediate-early
    regulatory network response in primary human white adipocytes, Springer Nature,
    <a href="https://doi.org/10.6084/m9.figshare.7295369.v1">10.6084/m9.figshare.7295369.v1</a>.'
  mla: 'Higareda Almaraz, Juan, et al. <i>Additional File 3: Of Norepinephrine Triggers
    an Immediate-Early Regulatory Network Response in Primary Human White Adipocytes</i>.
    Springer Nature, 2018, doi:<a href="https://doi.org/10.6084/m9.figshare.7295369.v1">10.6084/m9.figshare.7295369.v1</a>.'
  short: J. Higareda Almaraz, M. Karbiener, M. Giroud, F. Pauler, T. Gerhalter, S.
    Herzig, M. Scheideler, (2018).
date_created: 2021-08-06T12:31:57Z
date_published: 2018-11-03T00:00:00Z
date_updated: 2023-09-13T09:10:47Z
day: '03'
department:
- _id: SiHi
doi: 10.6084/m9.figshare.7295369.v1
main_file_link:
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  url: https://doi.org/10.6084/m9.figshare.7295369.v1
month: '11'
oa: 1
oa_version: Published Version
publisher: Springer Nature
related_material:
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title: 'Additional file 3: Of Norepinephrine triggers an immediate-early regulatory
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type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
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...
---
_id: '9810'
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author:
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  full_name: Chaudhry, Waqas
  last_name: Chaudhry
- first_name: Maros
  full_name: Pleska, Maros
  id: 4569785E-F248-11E8-B48F-1D18A9856A87
  last_name: Pleska
  orcid: 0000-0001-7460-7479
- first_name: Nilang
  full_name: Shah, Nilang
  last_name: Shah
- first_name: Howard
  full_name: Weiss, Howard
  last_name: Weiss
- first_name: Ingrid
  full_name: Mccall, Ingrid
  last_name: Mccall
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  full_name: Meyer, Justin
  last_name: Meyer
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  full_name: Gupta, Animesh
  last_name: Gupta
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
- first_name: Bruce
  full_name: Levin, Bruce
  last_name: Levin
citation:
  ama: Chaudhry W, Pleska M, Shah N, et al. Numerical data used in figures. 2018.
    doi:<a href="https://doi.org/10.1371/journal.pbio.2005971.s008">10.1371/journal.pbio.2005971.s008</a>
  apa: Chaudhry, W., Pleska, M., Shah, N., Weiss, H., Mccall, I., Meyer, J., … Levin,
    B. (2018). Numerical data used in figures. Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.2005971.s008">https://doi.org/10.1371/journal.pbio.2005971.s008</a>
  chicago: Chaudhry, Waqas, Maros Pleska, Nilang Shah, Howard Weiss, Ingrid Mccall,
    Justin Meyer, Animesh Gupta, Calin C Guet, and Bruce Levin. “Numerical Data Used
    in Figures.” Public Library of Science, 2018. <a href="https://doi.org/10.1371/journal.pbio.2005971.s008">https://doi.org/10.1371/journal.pbio.2005971.s008</a>.
  ieee: W. Chaudhry <i>et al.</i>, “Numerical data used in figures.” Public Library
    of Science, 2018.
  ista: Chaudhry W, Pleska M, Shah N, Weiss H, Mccall I, Meyer J, Gupta A, Guet CC,
    Levin B. 2018. Numerical data used in figures, Public Library of Science, <a href="https://doi.org/10.1371/journal.pbio.2005971.s008">10.1371/journal.pbio.2005971.s008</a>.
  mla: Chaudhry, Waqas, et al. <i>Numerical Data Used in Figures</i>. Public Library
    of Science, 2018, doi:<a href="https://doi.org/10.1371/journal.pbio.2005971.s008">10.1371/journal.pbio.2005971.s008</a>.
  short: W. Chaudhry, M. Pleska, N. Shah, H. Weiss, I. Mccall, J. Meyer, A. Gupta,
    C.C. Guet, B. Levin, (2018).
date_created: 2021-08-06T12:43:44Z
date_published: 2018-08-16T00:00:00Z
date_updated: 2023-09-13T08:45:41Z
day: '16'
department:
- _id: CaGu
doi: 10.1371/journal.pbio.2005971.s008
month: '08'
oa_version: Published Version
publisher: Public Library of Science
related_material:
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title: Numerical data used in figures
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year: '2018'
...
