---
_id: '12104'
abstract:
- lang: eng
  text: We study ergodic decompositions of Dirichlet spaces under intertwining via
    unitary order isomorphisms. We show that the ergodic decomposition of a quasi-regular
    Dirichlet space is unique up to a unique isomorphism of the indexing space. Furthermore,
    every unitary order isomorphism intertwining two quasi-regular Dirichlet spaces
    is decomposable over their ergodic decompositions up to conjugation via an isomorphism
    of the corresponding indexing spaces.
acknowledgement: Research supported by the Austrian Science Fund (FWF) grant F65 at
  the Institute of Science and Technology Austria and by the European Research Council
  (ERC) (Grant agreement No. 716117 awarded to Prof. Dr. Jan Maas). L.D.S. gratefully
  acknowledges funding of his current position by the Austrian Science Fund (FWF)
  through the ESPRIT Programme (Grant No. 208). M.W. gratefully acknowledges funding
  of his current position by the Austrian Science Fund (FWF) through the ESPRIT Programme
  (Grant No. 156).
article_number: '9'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Lorenzo
  full_name: Dello Schiavo, Lorenzo
  id: ECEBF480-9E4F-11EA-B557-B0823DDC885E
  last_name: Dello Schiavo
  orcid: 0000-0002-9881-6870
- first_name: Melchior
  full_name: Wirth, Melchior
  id: 88644358-0A0E-11EA-8FA5-49A33DDC885E
  last_name: Wirth
  orcid: 0000-0002-0519-4241
citation:
  ama: Dello Schiavo L, Wirth M. Ergodic decompositions of Dirichlet forms under order
    isomorphisms. <i>Journal of Evolution Equations</i>. 2023;23(1). doi:<a href="https://doi.org/10.1007/s00028-022-00859-7">10.1007/s00028-022-00859-7</a>
  apa: Dello Schiavo, L., &#38; Wirth, M. (2023). Ergodic decompositions of Dirichlet
    forms under order isomorphisms. <i>Journal of Evolution Equations</i>. Springer
    Nature. <a href="https://doi.org/10.1007/s00028-022-00859-7">https://doi.org/10.1007/s00028-022-00859-7</a>
  chicago: Dello Schiavo, Lorenzo, and Melchior Wirth. “Ergodic Decompositions of
    Dirichlet Forms under Order Isomorphisms.” <i>Journal of Evolution Equations</i>.
    Springer Nature, 2023. <a href="https://doi.org/10.1007/s00028-022-00859-7">https://doi.org/10.1007/s00028-022-00859-7</a>.
  ieee: L. Dello Schiavo and M. Wirth, “Ergodic decompositions of Dirichlet forms
    under order isomorphisms,” <i>Journal of Evolution Equations</i>, vol. 23, no.
    1. Springer Nature, 2023.
  ista: Dello Schiavo L, Wirth M. 2023. Ergodic decompositions of Dirichlet forms
    under order isomorphisms. Journal of Evolution Equations. 23(1), 9.
  mla: Dello Schiavo, Lorenzo, and Melchior Wirth. “Ergodic Decompositions of Dirichlet
    Forms under Order Isomorphisms.” <i>Journal of Evolution Equations</i>, vol. 23,
    no. 1, 9, Springer Nature, 2023, doi:<a href="https://doi.org/10.1007/s00028-022-00859-7">10.1007/s00028-022-00859-7</a>.
  short: L. Dello Schiavo, M. Wirth, Journal of Evolution Equations 23 (2023).
date_created: 2023-01-08T23:00:53Z
date_published: 2023-01-01T00:00:00Z
date_updated: 2023-06-28T11:54:35Z
day: '01'
ddc:
- '510'
department:
- _id: JaMa
doi: 10.1007/s00028-022-00859-7
ec_funded: 1
external_id:
  isi:
  - '000906214600004'
file:
- access_level: open_access
  checksum: 1f34f3e2cb521033de6154f274ea3a4e
  content_type: application/pdf
  creator: dernst
  date_created: 2023-01-20T10:45:06Z
  date_updated: 2023-01-20T10:45:06Z
  file_id: '12325'
  file_name: 2023_JourEvolutionEquations_DelloSchiavo.pdf
  file_size: 422612
  relation: main_file
  success: 1
file_date_updated: 2023-01-20T10:45:06Z
has_accepted_license: '1'
intvolume: '        23'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: fc31cba2-9c52-11eb-aca3-ff467d239cd2
  grant_number: F6504
  name: Taming Complexity in Partial Differential Systems
- _id: 256E75B8-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '716117'
  name: Optimal Transport and Stochastic Dynamics
- _id: 34dbf174-11ca-11ed-8bc3-afe9d43d4b9c
  grant_number: E208
  name: Configuration Spaces over Non-Smooth Spaces
- _id: 34c6ea2d-11ca-11ed-8bc3-c04f3c502833
  grant_number: ESP156_N
  name: Gradient flow techniques for quantum Markov semigroups
publication: Journal of Evolution Equations
publication_identifier:
  eissn:
  - 1424-3202
  issn:
  - 1424-3199
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Ergodic decompositions of Dirichlet forms under order isomorphisms
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 23
year: '2023'
...
---
_id: '12105'
abstract:
- lang: eng
  text: Data-driven dimensionality reduction methods such as proper orthogonal decomposition
    and dynamic mode decomposition have proven to be useful for exploring complex
    phenomena within fluid dynamics and beyond. A well-known challenge for these techniques
    is posed by the continuous symmetries, e.g. translations and rotations, of the
    system under consideration, as drifts in the data dominate the modal expansions
    without providing an insight into the dynamics of the problem. In the present
    study, we address this issue for fluid flows in rectangular channels by formulating
    a continuous symmetry reduction method that eliminates the translations in the
    streamwise and spanwise directions simultaneously. We demonstrate our method by
    computing the symmetry-reduced dynamic mode decomposition (SRDMD) of sliding windows
    of data obtained from the transitional plane-Couette and turbulent plane-Poiseuille
    flow simulations. In the former setting, SRDMD captures the dynamics in the vicinity
    of the invariant solutions with translation symmetries, i.e. travelling waves
    and relative periodic orbits, whereas in the latter, our calculations reveal episodes
    of turbulent time evolution that can be approximated by a low-dimensional linear
    expansion.
acknowledgement: "E.M. acknowledges funding from the ISTplus fellowship programme.
  G.Y. and B.H. acknowledge\r\na grant from the Simons Foundation (662960, BH)."
article_number: A10
article_processing_charge: Yes (via OA deal)
article_type: original
arxiv: 1
author:
- first_name: Elena
  full_name: Marensi, Elena
  id: 0BE7553A-1004-11EA-B805-18983DDC885E
  last_name: Marensi
- first_name: Gökhan
  full_name: Yalniz, Gökhan
  id: 66E74FA2-D8BF-11E9-8249-8DE2E5697425
  last_name: Yalniz
  orcid: 0000-0002-8490-9312
- first_name: Björn
  full_name: Hof, Björn
  id: 3A374330-F248-11E8-B48F-1D18A9856A87
  last_name: Hof
  orcid: 0000-0003-2057-2754
- first_name: Nazmi B
  full_name: Budanur, Nazmi B
  id: 3EA1010E-F248-11E8-B48F-1D18A9856A87
  last_name: Budanur
  orcid: 0000-0003-0423-5010
citation:
  ama: Marensi E, Yalniz G, Hof B, Budanur NB. Symmetry-reduced dynamic mode decomposition
    of near-wall turbulence. <i>Journal of Fluid Mechanics</i>. 2023;954. doi:<a href="https://doi.org/10.1017/jfm.2022.1001">10.1017/jfm.2022.1001</a>
  apa: Marensi, E., Yalniz, G., Hof, B., &#38; Budanur, N. B. (2023). Symmetry-reduced
    dynamic mode decomposition of near-wall turbulence. <i>Journal of Fluid Mechanics</i>.
    Cambridge University Press. <a href="https://doi.org/10.1017/jfm.2022.1001">https://doi.org/10.1017/jfm.2022.1001</a>
  chicago: Marensi, Elena, Gökhan Yalniz, Björn Hof, and Nazmi B Budanur. “Symmetry-Reduced
    Dynamic Mode Decomposition of near-Wall Turbulence.” <i>Journal of Fluid Mechanics</i>.
    Cambridge University Press, 2023. <a href="https://doi.org/10.1017/jfm.2022.1001">https://doi.org/10.1017/jfm.2022.1001</a>.
  ieee: E. Marensi, G. Yalniz, B. Hof, and N. B. Budanur, “Symmetry-reduced dynamic
    mode decomposition of near-wall turbulence,” <i>Journal of Fluid Mechanics</i>,
    vol. 954. Cambridge University Press, 2023.
  ista: Marensi E, Yalniz G, Hof B, Budanur NB. 2023. Symmetry-reduced dynamic mode
    decomposition of near-wall turbulence. Journal of Fluid Mechanics. 954, A10.
  mla: Marensi, Elena, et al. “Symmetry-Reduced Dynamic Mode Decomposition of near-Wall
    Turbulence.” <i>Journal of Fluid Mechanics</i>, vol. 954, A10, Cambridge University
    Press, 2023, doi:<a href="https://doi.org/10.1017/jfm.2022.1001">10.1017/jfm.2022.1001</a>.
  short: E. Marensi, G. Yalniz, B. Hof, N.B. Budanur, Journal of Fluid Mechanics 954
    (2023).
date_created: 2023-01-08T23:00:53Z
date_published: 2023-01-10T00:00:00Z
date_updated: 2023-08-01T12:53:23Z
day: '10'
ddc:
- '530'
department:
- _id: BjHo
doi: 10.1017/jfm.2022.1001
external_id:
  arxiv:
  - '2101.07516'
  isi:
  - '000903336600001'
file:
- access_level: open_access
  checksum: 9224f987caefe5dd85a70814d3cce65c
  content_type: application/pdf
  creator: dernst
  date_created: 2023-02-02T12:34:54Z
  date_updated: 2023-02-02T12:34:54Z
  file_id: '12489'
  file_name: 2023_JourFluidMechanics_Marensi.pdf
  file_size: 1931647
  relation: main_file
  success: 1
file_date_updated: 2023-02-02T12:34:54Z
has_accepted_license: '1'
intvolume: '       954'
isi: 1
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
project:
- _id: 238598C6-32DE-11EA-91FC-C7463DDC885E
  grant_number: '662960'
  name: 'Revisiting the Turbulence Problem Using Statistical Mechanics: Experimental
    Studies on Transitional and Turbulent Flows'
publication: Journal of Fluid Mechanics
publication_identifier:
  eissn:
  - 1469-7645
  issn:
  - 0022-1120
publication_status: published
publisher: Cambridge University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: Symmetry-reduced dynamic mode decomposition of near-wall turbulence
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 954
year: '2023'
...
---
_id: '12106'
abstract:
- lang: eng
  text: Regulation of chromatin states involves the dynamic interplay between different
    histone modifications to control gene expression. Recent advances have enabled
    mapping of histone marks in single cells, but most methods are constrained to
    profile only one histone mark per cell. Here, we present an integrated experimental
    and computational framework, scChIX-seq (single-cell chromatin immunocleavage
    and unmixing sequencing), to map several histone marks in single cells. scChIX-seq
    multiplexes two histone marks together in single cells, then computationally deconvolves
    the signal using training data from respective histone mark profiles. This framework
    learns the cell-type-specific correlation structure between histone marks, and
    therefore does not require a priori assumptions of their genomic distributions.
    Using scChIX-seq, we demonstrate multimodal analysis of histone marks in single
    cells across a range of mark combinations. Modeling dynamics of in vitro macrophage
    differentiation enables integrated analysis of chromatin velocity. Overall, scChIX-seq
    unlocks systematic interrogation of the interplay between histone modifications
    in single cells.
acknowledgement: We thank M. van Loenhout for experimental advice on purifying cell
  types from the bone marrow, R. van der Linden for expertise with FACS and M. Blotenburg
  for help with cell typing the mouse organogenesis dataset. We thank M. Saraswat
  and O. Stegle for discussions on multinomial distributions. This work was supported
  by a European Research Council Advanced grant (ERC-AdG 742225-IntScOmics); Nederlandse
  Organisatie voor Wetenschappelijk Onderzoek (NWO) TOP grant (NWO CW 714.016.001)
  and NWO grant (OCENW.GROOT.2019.017); the Swiss National Science Foundation Early
  Postdoc Mobility (P2ELP3-184488 to P.Z. and P2BSP3-174991 to J.Y.); Marie Sklodowska-Curie
  Actions Postdoc (798573 to P.Z.) and the Human Frontier for Science Program Long-Term
  Fellowships (LT000209-2018-L to P.Z. and LT000097-2019-L to J.Y.). This work is
  part of the Oncode Institute which is financed partly by the Dutch Cancer Society.
article_processing_charge: No
article_type: original
author:
- first_name: Jake
  full_name: Yeung, Jake
  id: 123012b2-db30-11eb-b4d8-a35840c0551b
  last_name: Yeung
  orcid: 0000-0003-1732-1559
- first_name: Maria
  full_name: Florescu, Maria
  last_name: Florescu
- first_name: Peter
  full_name: Zeller, Peter
  last_name: Zeller
- first_name: Buys Anton
  full_name: De Barbanson, Buys Anton
  last_name: De Barbanson
- first_name: Max D.
  full_name: Wellenstein, Max D.
  last_name: Wellenstein
- first_name: Alexander
  full_name: Van Oudenaarden, Alexander
  last_name: Van Oudenaarden
citation:
  ama: Yeung J, Florescu M, Zeller P, De Barbanson BA, Wellenstein MD, Van Oudenaarden
    A. scChIX-seq infers dynamic relationships between histone modifications in single
    cells. <i>Nature Biotechnology</i>. 2023;41:813–823. doi:<a href="https://doi.org/10.1038/s41587-022-01560-3">10.1038/s41587-022-01560-3</a>
  apa: Yeung, J., Florescu, M., Zeller, P., De Barbanson, B. A., Wellenstein, M. D.,
    &#38; Van Oudenaarden, A. (2023). scChIX-seq infers dynamic relationships between
    histone modifications in single cells. <i>Nature Biotechnology</i>. Springer Nature.
    <a href="https://doi.org/10.1038/s41587-022-01560-3">https://doi.org/10.1038/s41587-022-01560-3</a>
  chicago: Yeung, Jake, Maria Florescu, Peter Zeller, Buys Anton De Barbanson, Max
    D. Wellenstein, and Alexander Van Oudenaarden. “ScChIX-Seq Infers Dynamic Relationships
    between Histone Modifications in Single Cells.” <i>Nature Biotechnology</i>. Springer
    Nature, 2023. <a href="https://doi.org/10.1038/s41587-022-01560-3">https://doi.org/10.1038/s41587-022-01560-3</a>.
  ieee: J. Yeung, M. Florescu, P. Zeller, B. A. De Barbanson, M. D. Wellenstein, and
    A. Van Oudenaarden, “scChIX-seq infers dynamic relationships between histone modifications
    in single cells,” <i>Nature Biotechnology</i>, vol. 41. Springer Nature, pp. 813–823,
    2023.
  ista: Yeung J, Florescu M, Zeller P, De Barbanson BA, Wellenstein MD, Van Oudenaarden
    A. 2023. scChIX-seq infers dynamic relationships between histone modifications
    in single cells. Nature Biotechnology. 41, 813–823.
  mla: Yeung, Jake, et al. “ScChIX-Seq Infers Dynamic Relationships between Histone
    Modifications in Single Cells.” <i>Nature Biotechnology</i>, vol. 41, Springer
    Nature, 2023, pp. 813–823, doi:<a href="https://doi.org/10.1038/s41587-022-01560-3">10.1038/s41587-022-01560-3</a>.
  short: J. Yeung, M. Florescu, P. Zeller, B.A. De Barbanson, M.D. Wellenstein, A.
    Van Oudenaarden, Nature Biotechnology 41 (2023) 813–823.
date_created: 2023-01-08T23:00:53Z
date_published: 2023-06-01T00:00:00Z
date_updated: 2023-08-16T11:32:33Z
day: '01'
ddc:
- '570'
department:
- _id: ScienComp
doi: 10.1038/s41587-022-01560-3
external_id:
  isi:
  - '000909067600003'
file:
- access_level: open_access
  checksum: 668447a1c8d360b68f8aaf9e08ed644f
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T11:30:45Z
  date_updated: 2023-08-16T11:30:45Z
  file_id: '14066'
  file_name: 2023_NatureBioTech_Yeung.pdf
  file_size: 12040976
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T11:30:45Z
has_accepted_license: '1'
intvolume: '        41'
isi: 1
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
page: 813–823
publication: Nature Biotechnology
publication_identifier:
  eissn:
  - 1546-1696
  issn:
  - 1087-0156
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: scChIX-seq infers dynamic relationships between histone modifications in single
  cells
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 41
year: '2023'
...
---
_id: '12113'
abstract:
- lang: eng
  text: The power factor of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate)
    (PEDOT:PSS) film can be significantly improved by optimizing the oxidation level
    of the film in oxidation and reduction processes. However, precise control over
    the oxidation and reduction effects in PEDOT:PSS remains a challenge, which greatly
    sacrifices both S and σ. Here, we propose a two-step post-treatment using a mixture
    of ethylene glycol (EG) and Arginine (Arg) and sulfuric acid (H2SO4) in sequence
    to engineer high-performance PEDOT:PSS thermoelectric films. The high-polarity
    EG dopant removes the excess non-ionized PSS and induces benzenoid-to-quinoid
    conformational change in the PEDOT:PSS films. In particular, basic amino acid
    Arg tunes the oxidation level of PEDOT:PSS and prevents the films from over-oxidation
    during H2SO4 post-treatment, leading to increased S. The following H2SO4 post-treatment
    further induces highly orientated lamellar stacking microstructures to increase
    σ, yielding a maximum power factor of 170.6 μW m−1 K−2 at 460 K. Moreover, a novel
    trigonal-shape thermoelectric device is designed and assembled by the as-prepared
    PEDOT:PSS films in order to harvest heat via a vertical temperature gradient.
    An output power density of 33 μW cm−2 is generated at a temperature difference
    of 40 K, showing the potential application for low-grade wearable electronic devices.
acknowledgement: Scientific Research Program Funded by Shaanxi Provincial Education
  Department (Program No.22JY012), Natural Science Basic Research Program of Shaanxi
  (Grant No.2022JZ-31), Young Talent fund of University Association for Science and
  Technology in Shaanxi, China (Grant No.20210411), China Postdoctoral Science Foundation
  (Grant No. 2021M692621), the Foundation of Shaanxi University of Science & Technology
  (Grant No. 2017GBJ-03), Open Foundation of Key Laboratory of Auxiliary Chemistry
  and Technology for Chemical Industry, Ministry of Education, Shaanxi University
  of Science and Technology (Grant No. KFKT2022-15), and Open Foundation of Shaanxi
  Collaborative Innovation Center of Industrial Auxiliary Chemistry and Technology,
  Shaanxi University of Science and Technology (Grant No. KFKT2022-15).
article_number: '156101'
article_processing_charge: No
article_type: original
author:
- first_name: Li
  full_name: Zhang, Li
  last_name: Zhang
- first_name: Xingyu
  full_name: Liu, Xingyu
  last_name: Liu
- first_name: Ting
  full_name: Wu, Ting
  last_name: Wu
- first_name: Shengduo
  full_name: Xu, Shengduo
  id: 12ab8624-4c8a-11ec-9e11-e1ac2438f22f
  last_name: Xu
- first_name: Guoquan
  full_name: Suo, Guoquan
  last_name: Suo
- first_name: Xiaohui
  full_name: Ye, Xiaohui
  last_name: Ye
- first_name: Xiaojiang
  full_name: Hou, Xiaojiang
  last_name: Hou
- first_name: Yanling
  full_name: Yang, Yanling
  last_name: Yang
- first_name: Qingfeng
  full_name: Liu, Qingfeng
  last_name: Liu
- first_name: Hongqiang
  full_name: Wang, Hongqiang
  last_name: Wang
citation:
  ama: Zhang L, Liu X, Wu T, et al. Two-step post-treatment to deliver high performance
    thermoelectric device with vertical temperature gradient. <i>Applied Surface Science</i>.
    2023;613. doi:<a href="https://doi.org/10.1016/j.apsusc.2022.156101">10.1016/j.apsusc.2022.156101</a>
  apa: Zhang, L., Liu, X., Wu, T., Xu, S., Suo, G., Ye, X., … Wang, H. (2023). Two-step
    post-treatment to deliver high performance thermoelectric device with vertical
    temperature gradient. <i>Applied Surface Science</i>. Elsevier. <a href="https://doi.org/10.1016/j.apsusc.2022.156101">https://doi.org/10.1016/j.apsusc.2022.156101</a>
  chicago: Zhang, Li, Xingyu Liu, Ting Wu, Shengduo Xu, Guoquan Suo, Xiaohui Ye, Xiaojiang
    Hou, Yanling Yang, Qingfeng Liu, and Hongqiang Wang. “Two-Step Post-Treatment
    to Deliver High Performance Thermoelectric Device with Vertical Temperature Gradient.”
    <i>Applied Surface Science</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.apsusc.2022.156101">https://doi.org/10.1016/j.apsusc.2022.156101</a>.
  ieee: L. Zhang <i>et al.</i>, “Two-step post-treatment to deliver high performance
    thermoelectric device with vertical temperature gradient,” <i>Applied Surface
    Science</i>, vol. 613. Elsevier, 2023.
  ista: Zhang L, Liu X, Wu T, Xu S, Suo G, Ye X, Hou X, Yang Y, Liu Q, Wang H. 2023.
    Two-step post-treatment to deliver high performance thermoelectric device with
    vertical temperature gradient. Applied Surface Science. 613, 156101.
  mla: Zhang, Li, et al. “Two-Step Post-Treatment to Deliver High Performance Thermoelectric
    Device with Vertical Temperature Gradient.” <i>Applied Surface Science</i>, vol.
    613, 156101, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.apsusc.2022.156101">10.1016/j.apsusc.2022.156101</a>.
  short: L. Zhang, X. Liu, T. Wu, S. Xu, G. Suo, X. Ye, X. Hou, Y. Yang, Q. Liu, H.
    Wang, Applied Surface Science 613 (2023).
date_created: 2023-01-12T11:55:02Z
date_published: 2023-03-15T00:00:00Z
date_updated: 2023-08-14T11:47:06Z
day: '15'
department:
- _id: MaIb
doi: 10.1016/j.apsusc.2022.156101
external_id:
  isi:
  - '000911497000001'
intvolume: '       613'
isi: 1
keyword:
- Surfaces
- Coatings and Films
- Condensed Matter Physics
- Surfaces and Interfaces
- General Physics and Astronomy
- General Chemistry
language:
- iso: eng
month: '03'
oa_version: None
publication: Applied Surface Science
publication_identifier:
  issn:
  - 0169-4332
publication_status: epub_ahead
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Two-step post-treatment to deliver high performance thermoelectric device with
  vertical temperature gradient
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 613
year: '2023'
...
---
_id: '12114'
abstract:
- lang: eng
  text: 'Probing the dynamics of aromatic side chains provides important insights
    into the behavior of a protein because flips of aromatic rings in a protein’s
    hydrophobic core report on breathing motion involving a large part of the protein.
    Inherently invisible to crystallography, aromatic motions have been primarily
    studied by solution NMR. The question how packing of proteins in crystals affects
    ring flips has, thus, remained largely unexplored. Here we apply magic-angle spinning
    NMR, advanced phenylalanine 1H-13C/2H isotope labeling and MD simulation to a
    protein in three different crystal packing environments to shed light onto possible
    impact of packing on ring flips. The flips of the two Phe residues in ubiquitin,
    both surface exposed, appear remarkably conserved in the different crystal forms,
    even though the intermolecular packing is quite different: Phe4 flips on a ca.
    10–20 ns time scale, and Phe45 are broadened in all crystals, presumably due to
    µs motion. Our findings suggest that intramolecular influences are more important
    for ring flips than intermolecular (packing) effects.'
acknowledgement: The NMR platform in Grenoble is part of the Grenoble Instruct-ERIC
  center (ISBG; UAR 3518 CNRS-CEA-UGA-EMBL) within the Grenoble Partnership for Structural
  Biology (PSB), supported by FRISBI (ANR-10-INBS-0005-02) and GRAL, financed within
  the University Grenoble Alpes graduate school (Ecoles Universitaires de Recherche)
  CBH-EUR-GS (ANR-17-EURE-0003). This work was supported by the European Research
  Council (StG-2012-311318-ProtDyn2Function to P.S.) and used the platforms of the
  Grenoble Instruct Center (ISBG; UMS 3518 CNRS-CEA-UJF-EMBL) with support from FRISBI
  (ANR-10-INSB-05–02) and GRAL (ANR-10-LABX-49–01) within the Grenoble Partnership
  for Structural Biology (PSB). We would like to thank Sergei Izmailov for developing
  and maintaining the pyxmolpp2 library. N.R.S. acknowledges support from St. Petersburg
  State University in a form of the grant 92425251 and the access to the MRR, MCT
  and CAMR resource centers. P.S. thanks Malcolm Levitt for pointing out the fact
  that “tensor asymmetry” is better called “tensor biaxiality”.
article_number: '100079'
article_processing_charge: No
article_type: original
author:
- first_name: Diego F.
  full_name: Gauto, Diego F.
  last_name: Gauto
- first_name: Olga O.
  full_name: Lebedenko, Olga O.
  last_name: Lebedenko
- first_name: Lea Marie
  full_name: Becker, Lea Marie
  id: 36336939-eb97-11eb-a6c2-c83f1214ca79
  last_name: Becker
  orcid: 0000-0002-6401-5151
- first_name: Isabel
  full_name: Ayala, Isabel
  last_name: Ayala
- first_name: Roman
  full_name: Lichtenecker, Roman
  last_name: Lichtenecker
- first_name: Nikolai R.
  full_name: Skrynnikov, Nikolai R.
  last_name: Skrynnikov
- first_name: Paul
  full_name: Schanda, Paul
  id: 7B541462-FAF6-11E9-A490-E8DFE5697425
  last_name: Schanda
  orcid: 0000-0002-9350-7606
citation:
  ama: 'Gauto DF, Lebedenko OO, Becker LM, et al. Aromatic ring flips in differently
    packed ubiquitin protein crystals from MAS NMR and MD. <i>Journal of Structural
    Biology: X</i>. 2023;7. doi:<a href="https://doi.org/10.1016/j.yjsbx.2022.100079">10.1016/j.yjsbx.2022.100079</a>'
  apa: 'Gauto, D. F., Lebedenko, O. O., Becker, L. M., Ayala, I., Lichtenecker, R.,
    Skrynnikov, N. R., &#38; Schanda, P. (2023). Aromatic ring flips in differently
    packed ubiquitin protein crystals from MAS NMR and MD. <i>Journal of Structural
    Biology: X</i>. Elsevier. <a href="https://doi.org/10.1016/j.yjsbx.2022.100079">https://doi.org/10.1016/j.yjsbx.2022.100079</a>'
  chicago: 'Gauto, Diego F., Olga O. Lebedenko, Lea Marie Becker, Isabel Ayala, Roman
    Lichtenecker, Nikolai R. Skrynnikov, and Paul Schanda. “Aromatic Ring Flips in
    Differently Packed Ubiquitin Protein Crystals from MAS NMR and MD.” <i>Journal
    of Structural Biology: X</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.yjsbx.2022.100079">https://doi.org/10.1016/j.yjsbx.2022.100079</a>.'
  ieee: 'D. F. Gauto <i>et al.</i>, “Aromatic ring flips in differently packed ubiquitin
    protein crystals from MAS NMR and MD,” <i>Journal of Structural Biology: X</i>,
    vol. 7. Elsevier, 2023.'
  ista: 'Gauto DF, Lebedenko OO, Becker LM, Ayala I, Lichtenecker R, Skrynnikov NR,
    Schanda P. 2023. Aromatic ring flips in differently packed ubiquitin protein crystals
    from MAS NMR and MD. Journal of Structural Biology: X. 7, 100079.'
  mla: 'Gauto, Diego F., et al. “Aromatic Ring Flips in Differently Packed Ubiquitin
    Protein Crystals from MAS NMR and MD.” <i>Journal of Structural Biology: X</i>,
    vol. 7, 100079, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.yjsbx.2022.100079">10.1016/j.yjsbx.2022.100079</a>.'
  short: 'D.F. Gauto, O.O. Lebedenko, L.M. Becker, I. Ayala, R. Lichtenecker, N.R.
    Skrynnikov, P. Schanda, Journal of Structural Biology: X 7 (2023).'
date_created: 2023-01-12T11:55:38Z
date_published: 2023-01-01T00:00:00Z
date_updated: 2023-08-16T09:37:25Z
day: '01'
ddc:
- '570'
department:
- _id: PaSc
doi: 10.1016/j.yjsbx.2022.100079
external_id:
  pmid:
  - '36578472'
file:
- access_level: open_access
  checksum: b4b1c10a31018aafe053b7d55a470e54
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T09:36:28Z
  date_updated: 2023-08-16T09:36:28Z
  file_id: '14064'
  file_name: 2023_JourStrucBiologyX_Gauto.pdf
  file_size: 5132322
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T09:36:28Z
has_accepted_license: '1'
intvolume: '         7'
keyword:
- Structural Biology
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
pmid: 1
publication: 'Journal of Structural Biology: X'
publication_identifier:
  issn:
  - 2590-1524
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Aromatic ring flips in differently packed ubiquitin protein crystals from MAS
  NMR and MD
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 7
year: '2023'
...
---
_id: '12115'
acknowledgement: This work was supported by European Commission’s Seventh Framework
  Programme under Grant Agreement No. 279113 (OCTIPS; www.octips.eu).
article_processing_charge: No
article_type: original
author:
- first_name: Jacek
  full_name: Glajzer, Jacek
  last_name: Glajzer
- first_name: Dan Cacsire
  full_name: Castillo-Tong, Dan Cacsire
  last_name: Castillo-Tong
- first_name: Rolf
  full_name: Richter, Rolf
  last_name: Richter
- first_name: Ignace
  full_name: Vergote, Ignace
  last_name: Vergote
- first_name: Hagen
  full_name: Kulbe, Hagen
  last_name: Kulbe
- first_name: Adriaan
  full_name: Vanderstichele, Adriaan
  last_name: Vanderstichele
- first_name: Ilary
  full_name: Ruscito, Ilary
  last_name: Ruscito
- first_name: Fabian
  full_name: Trillsch, Fabian
  last_name: Trillsch
- first_name: Alexander
  full_name: Mustea, Alexander
  last_name: Mustea
- first_name: Caroline
  full_name: Kreuzinger, Caroline
  id: 382077BA-F248-11E8-B48F-1D18A9856A87
  last_name: Kreuzinger
- first_name: Charlie
  full_name: Gourley, Charlie
  last_name: Gourley
- first_name: Hani
  full_name: Gabra, Hani
  last_name: Gabra
- first_name: Eliane T.
  full_name: Taube, Eliane T.
  last_name: Taube
- first_name: Oliver
  full_name: Dorigo, Oliver
  last_name: Dorigo
- first_name: David
  full_name: Horst, David
  last_name: Horst
- first_name: Carlotta
  full_name: Keunecke, Carlotta
  last_name: Keunecke
- first_name: Joanna
  full_name: Baum, Joanna
  last_name: Baum
- first_name: Timothy
  full_name: Angelotti, Timothy
  last_name: Angelotti
- first_name: Jalid
  full_name: Sehouli, Jalid
  last_name: Sehouli
- first_name: Elena Ioana
  full_name: Braicu, Elena Ioana
  last_name: Braicu
citation:
  ama: 'Glajzer J, Castillo-Tong DC, Richter R, et al. ASO Visual Abstract: Impact
    of BRCA mutation status on tumor dissemination pattern, surgical outcome, and
    patient survival in primary and recurrent high-grade serous ovarian cancer (HGSOC).
    A multicenter, retrospective study of the ovarian cancer therapy—innovative models
    prolong survival (OCTIPS) consortium. <i>Annals of Surgical Oncology</i>. 2023;30:46-47.
    doi:<a href="https://doi.org/10.1245/s10434-022-12681-z">10.1245/s10434-022-12681-z</a>'
  apa: 'Glajzer, J., Castillo-Tong, D. C., Richter, R., Vergote, I., Kulbe, H., Vanderstichele,
    A., … Braicu, E. I. (2023). ASO Visual Abstract: Impact of BRCA mutation status
    on tumor dissemination pattern, surgical outcome, and patient survival in primary
    and recurrent high-grade serous ovarian cancer (HGSOC). A multicenter, retrospective
    study of the ovarian cancer therapy—innovative models prolong survival (OCTIPS)
    consortium. <i>Annals of Surgical Oncology</i>. Springer Nature. <a href="https://doi.org/10.1245/s10434-022-12681-z">https://doi.org/10.1245/s10434-022-12681-z</a>'
  chicago: 'Glajzer, Jacek, Dan Cacsire Castillo-Tong, Rolf Richter, Ignace Vergote,
    Hagen Kulbe, Adriaan Vanderstichele, Ilary Ruscito, et al. “ASO Visual Abstract:
    Impact of BRCA Mutation Status on Tumor Dissemination Pattern, Surgical Outcome,
    and Patient Survival in Primary and Recurrent High-Grade Serous Ovarian Cancer
    (HGSOC). A Multicenter, Retrospective Study of the Ovarian Cancer Therapy—Innovative
    Models Prolong Survival (OCTIPS) Consortium.” <i>Annals of Surgical Oncology</i>.
    Springer Nature, 2023. <a href="https://doi.org/10.1245/s10434-022-12681-z">https://doi.org/10.1245/s10434-022-12681-z</a>.'
  ieee: 'J. Glajzer <i>et al.</i>, “ASO Visual Abstract: Impact of BRCA mutation status
    on tumor dissemination pattern, surgical outcome, and patient survival in primary
    and recurrent high-grade serous ovarian cancer (HGSOC). A multicenter, retrospective
    study of the ovarian cancer therapy—innovative models prolong survival (OCTIPS)
    consortium,” <i>Annals of Surgical Oncology</i>, vol. 30. Springer Nature, pp.
    46–47, 2023.'
  ista: 'Glajzer J, Castillo-Tong DC, Richter R, Vergote I, Kulbe H, Vanderstichele
    A, Ruscito I, Trillsch F, Mustea A, Kreuzinger C, Gourley C, Gabra H, Taube ET,
    Dorigo O, Horst D, Keunecke C, Baum J, Angelotti T, Sehouli J, Braicu EI. 2023.
    ASO Visual Abstract: Impact of BRCA mutation status on tumor dissemination pattern,
    surgical outcome, and patient survival in primary and recurrent high-grade serous
    ovarian cancer (HGSOC). A multicenter, retrospective study of the ovarian cancer
    therapy—innovative models prolong survival (OCTIPS) consortium. Annals of Surgical
    Oncology. 30, 46–47.'
  mla: 'Glajzer, Jacek, et al. “ASO Visual Abstract: Impact of BRCA Mutation Status
    on Tumor Dissemination Pattern, Surgical Outcome, and Patient Survival in Primary
    and Recurrent High-Grade Serous Ovarian Cancer (HGSOC). A Multicenter, Retrospective
    Study of the Ovarian Cancer Therapy—Innovative Models Prolong Survival (OCTIPS)
    Consortium.” <i>Annals of Surgical Oncology</i>, vol. 30, Springer Nature, 2023,
    pp. 46–47, doi:<a href="https://doi.org/10.1245/s10434-022-12681-z">10.1245/s10434-022-12681-z</a>.'
  short: J. Glajzer, D.C. Castillo-Tong, R. Richter, I. Vergote, H. Kulbe, A. Vanderstichele,
    I. Ruscito, F. Trillsch, A. Mustea, C. Kreuzinger, C. Gourley, H. Gabra, E.T.
    Taube, O. Dorigo, D. Horst, C. Keunecke, J. Baum, T. Angelotti, J. Sehouli, E.I.
    Braicu, Annals of Surgical Oncology 30 (2023) 46–47.
date_created: 2023-01-12T11:56:22Z
date_published: 2023-01-01T00:00:00Z
date_updated: 2023-09-05T15:18:36Z
day: '01'
department:
- _id: JoDa
doi: 10.1245/s10434-022-12681-z
external_id:
  isi:
  - '000879151800001'
intvolume: '        30'
isi: 1
keyword:
- Oncology
- Surgery
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1245/s10434-022-12681-z
month: '01'
oa: 1
oa_version: Published Version
page: 46-47
publication: Annals of Surgical Oncology
publication_identifier:
  eissn:
  - 1534-4681
  issn:
  - 1068-9265
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  record:
  - id: '12205'
    relation: other
    status: public
scopus_import: '1'
status: public
title: 'ASO Visual Abstract: Impact of BRCA mutation status on tumor dissemination
  pattern, surgical outcome, and patient survival in primary and recurrent high-grade
  serous ovarian cancer (HGSOC). A multicenter, retrospective study of the ovarian
  cancer therapy—innovative models prolong survival (OCTIPS) consortium'
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 30
year: '2023'
...
---
_id: '12158'
abstract:
- lang: eng
  text: 'Post-translational histone modifications modulate chromatin activity to affect
    gene expression. How chromatin states underlie lineage choice in single cells
    is relatively unexplored. We develop sort-assisted single-cell chromatin immunocleavage
    (sortChIC) and map active (H3K4me1 and H3K4me3) and repressive (H3K27me3 and H3K9me3)
    histone modifications in the mouse bone marrow. During differentiation, hematopoietic
    stem and progenitor cells (HSPCs) acquire active chromatin states mediated by
    cell-type-specifying transcription factors, which are unique for each lineage.
    By contrast, most alterations in repressive marks during differentiation occur
    independent of the final cell type. Chromatin trajectory analysis shows that lineage
    choice at the chromatin level occurs at the progenitor stage. Joint profiling
    of H3K4me1 and H3K9me3 demonstrates that cell types within the myeloid lineage
    have distinct active chromatin but share similar myeloid-specific heterochromatin
    states. This implies a hierarchical regulation of chromatin during hematopoiesis:
    heterochromatin dynamics distinguish differentiation trajectories and lineages,
    while euchromatin dynamics reflect cell types within lineages.'
acknowledgement: We thank A. Giladi for sharing mRNA abundance tables of cell types
  together with J. van den Berg for critical reading of the manuscript. We thank M.
  Bartosovic for sharing method comparison data. pK19pA-MN was a gift from Ulrich
  Laemmli (Addgene plasmid 86973, http://n2t.net/addgene:86973; RRID:Addgene_86973).
  Figure 8 is adopted from Hematopoiesis (human) diagram by A. Rad and M. Häggström
  under CC-BY-SA 3.0 license. This work was supported by European Research Council
  Advanced under grant ERC-AdG 742225-IntScOmics and Nederlandse Organisatie voor
  Wetenschappelijk Onderzoek (NWO) TOP award NWO-CW 714.016.001. The SNF (P2BSP3-174991),
  HFSP (LT000209/2018-L) and Marie Skłodowska-Curie Actions (798573) supported P.Z.
  The SNF (P2ELP3_184488) and HFSP (LT000097/2019-L) supported J.Y. and the EMBO LTF
  (ALTF 1197–2019) supported V.B. This work is part of the Oncode Institute, which
  is partly financed by the Dutch Cancer Society. The funders had no role in study
  design, data collection and analysis, decision to publish or preparation of the
  manuscript.
article_processing_charge: No
article_type: review
author:
- first_name: Peter
  full_name: Zeller, Peter
  last_name: Zeller
- first_name: Jake
  full_name: Yeung, Jake
  id: 123012b2-db30-11eb-b4d8-a35840c0551b
  last_name: Yeung
  orcid: 0000-0003-1732-1559
- first_name: Helena
  full_name: Viñas Gaza, Helena
  last_name: Viñas Gaza
- first_name: Buys Anton
  full_name: de Barbanson, Buys Anton
  last_name: de Barbanson
- first_name: Vivek
  full_name: Bhardwaj, Vivek
  last_name: Bhardwaj
- first_name: Maria
  full_name: Florescu, Maria
  last_name: Florescu
- first_name: Reinier
  full_name: van der Linden, Reinier
  last_name: van der Linden
- first_name: Alexander
  full_name: van Oudenaarden, Alexander
  last_name: van Oudenaarden
citation:
  ama: Zeller P, Yeung J, Viñas Gaza H, et al. Single-cell sortChIC identifies hierarchical
    chromatin dynamics during hematopoiesis. <i>Nature Genetics</i>. 2023;55:333-345.
    doi:<a href="https://doi.org/10.1038/s41588-022-01260-3">10.1038/s41588-022-01260-3</a>
  apa: Zeller, P., Yeung, J., Viñas Gaza, H., de Barbanson, B. A., Bhardwaj, V., Florescu,
    M., … van Oudenaarden, A. (2023). Single-cell sortChIC identifies hierarchical
    chromatin dynamics during hematopoiesis. <i>Nature Genetics</i>. Springer Nature.
    <a href="https://doi.org/10.1038/s41588-022-01260-3">https://doi.org/10.1038/s41588-022-01260-3</a>
  chicago: Zeller, Peter, Jake Yeung, Helena Viñas Gaza, Buys Anton de Barbanson,
    Vivek Bhardwaj, Maria Florescu, Reinier van der Linden, and Alexander van Oudenaarden.
    “Single-Cell SortChIC Identifies Hierarchical Chromatin Dynamics during Hematopoiesis.”
    <i>Nature Genetics</i>. Springer Nature, 2023. <a href="https://doi.org/10.1038/s41588-022-01260-3">https://doi.org/10.1038/s41588-022-01260-3</a>.
  ieee: P. Zeller <i>et al.</i>, “Single-cell sortChIC identifies hierarchical chromatin
    dynamics during hematopoiesis,” <i>Nature Genetics</i>, vol. 55. Springer Nature,
    pp. 333–345, 2023.
  ista: Zeller P, Yeung J, Viñas Gaza H, de Barbanson BA, Bhardwaj V, Florescu M,
    van der Linden R, van Oudenaarden A. 2023. Single-cell sortChIC identifies hierarchical
    chromatin dynamics during hematopoiesis. Nature Genetics. 55, 333–345.
  mla: Zeller, Peter, et al. “Single-Cell SortChIC Identifies Hierarchical Chromatin
    Dynamics during Hematopoiesis.” <i>Nature Genetics</i>, vol. 55, Springer Nature,
    2023, pp. 333–45, doi:<a href="https://doi.org/10.1038/s41588-022-01260-3">10.1038/s41588-022-01260-3</a>.
  short: P. Zeller, J. Yeung, H. Viñas Gaza, B.A. de Barbanson, V. Bhardwaj, M. Florescu,
    R. van der Linden, A. van Oudenaarden, Nature Genetics 55 (2023) 333–345.
date_created: 2023-01-12T12:09:09Z
date_published: 2023-02-01T00:00:00Z
date_updated: 2023-02-27T07:48:24Z
day: '01'
ddc:
- '570'
- '000'
department:
- _id: ScienComp
doi: 10.1038/s41588-022-01260-3
file:
- access_level: open_access
  checksum: 6fdb8e34fbeea63edd0f2c6c2cc5823e
  content_type: application/pdf
  creator: dernst
  date_created: 2023-02-27T07:46:45Z
  date_updated: 2023-02-27T07:46:45Z
  file_id: '12688'
  file_name: 2023_NatureGenetics_Zeller.pdf
  file_size: 21484855
  relation: main_file
  success: 1
file_date_updated: 2023-02-27T07:46:45Z
has_accepted_license: '1'
intvolume: '        55'
keyword:
- Genetics
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: 333-345
publication: Nature Genetics
publication_identifier:
  eissn:
  - 1546-1718
  issn:
  - 1061-4036
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Single-cell sortChIC identifies hierarchical chromatin dynamics during hematopoiesis
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 55
year: '2023'
...
---
_id: '12159'
abstract:
- lang: eng
  text: The term “haplotype block” is commonly used in the developing field of haplotype-based
    inference methods. We argue that the term should be defined based on the structure
    of the Ancestral Recombination Graph (ARG), which contains complete information
    on the ancestry of a sample. We use simulated examples to demonstrate key features
    of the relationship between haplotype blocks and ancestral structure, emphasizing
    the stochasticity of the processes that generate them. Even the simplest cases
    of neutrality or of a “hard” selective sweep produce a rich structure, often missed
    by commonly used statistics. We highlight a number of novel methods for inferring
    haplotype structure, based on the full ARG, or on a sequence of trees, and illustrate
    how they can be used to define haplotype blocks using an empirical data set. While
    the advent of new, computationally efficient methods makes it possible to apply
    these concepts broadly, they (and additional new methods) could benefit from adding
    features to explore haplotype blocks, as we define them. Understanding and applying
    the concept of the haplotype block will be essential to fully exploit long and
    linked-read sequencing technologies.
acknowledgement: 'We thank the Barton group for useful discussion and feedback during
  the writing of this article. Comments from Roger Butlin, Molly Schumer''s Group,
  the tskit development team, editors and three reviewers greatly improved the manuscript.
  Funding was provided by SCAS (Natural Sciences Programme, Knut and Alice Wallenberg
  Foundation), an FWF Wittgenstein grant (PT1001Z211), an FWF standalone grant (grant
  P 32166), and an ERC Advanced Grant. YFC was supported by the Max Planck Society
  and an ERC Proof of Concept Grant #101069216 (HAPLOTAGGING).'
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Daria
  full_name: Shipilina, Daria
  id: 428A94B0-F248-11E8-B48F-1D18A9856A87
  last_name: Shipilina
  orcid: 0000-0002-1145-9226
- first_name: Arka
  full_name: Pal, Arka
  id: 6AAB2240-CA9A-11E9-9C1A-D9D1E5697425
  last_name: Pal
  orcid: 0000-0002-4530-8469
- first_name: Sean
  full_name: Stankowski, Sean
  id: 43161670-5719-11EA-8025-FABC3DDC885E
  last_name: Stankowski
- first_name: Yingguang Frank
  full_name: Chan, Yingguang Frank
  last_name: Chan
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: Shipilina D, Pal A, Stankowski S, Chan YF, Barton NH. On the origin and structure
    of haplotype blocks. <i>Molecular Ecology</i>. 2023;32(6):1441-1457. doi:<a href="https://doi.org/10.1111/mec.16793">10.1111/mec.16793</a>
  apa: Shipilina, D., Pal, A., Stankowski, S., Chan, Y. F., &#38; Barton, N. H. (2023).
    On the origin and structure of haplotype blocks. <i>Molecular Ecology</i>. Wiley.
    <a href="https://doi.org/10.1111/mec.16793">https://doi.org/10.1111/mec.16793</a>
  chicago: Shipilina, Daria, Arka Pal, Sean Stankowski, Yingguang Frank Chan, and
    Nicholas H Barton. “On the Origin and Structure of Haplotype Blocks.” <i>Molecular
    Ecology</i>. Wiley, 2023. <a href="https://doi.org/10.1111/mec.16793">https://doi.org/10.1111/mec.16793</a>.
  ieee: D. Shipilina, A. Pal, S. Stankowski, Y. F. Chan, and N. H. Barton, “On the
    origin and structure of haplotype blocks,” <i>Molecular Ecology</i>, vol. 32,
    no. 6. Wiley, pp. 1441–1457, 2023.
  ista: Shipilina D, Pal A, Stankowski S, Chan YF, Barton NH. 2023. On the origin
    and structure of haplotype blocks. Molecular Ecology. 32(6), 1441–1457.
  mla: Shipilina, Daria, et al. “On the Origin and Structure of Haplotype Blocks.”
    <i>Molecular Ecology</i>, vol. 32, no. 6, Wiley, 2023, pp. 1441–57, doi:<a href="https://doi.org/10.1111/mec.16793">10.1111/mec.16793</a>.
  short: D. Shipilina, A. Pal, S. Stankowski, Y.F. Chan, N.H. Barton, Molecular Ecology
    32 (2023) 1441–1457.
date_created: 2023-01-12T12:09:17Z
date_published: 2023-03-01T00:00:00Z
date_updated: 2023-08-16T08:18:47Z
day: '01'
ddc:
- '570'
department:
- _id: NiBa
doi: 10.1111/mec.16793
external_id:
  isi:
  - '000900762000001'
  pmid:
  - '36433653'
file:
- access_level: open_access
  checksum: b10e0f8fa3dc4d72aaf77a557200978a
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T08:15:41Z
  date_updated: 2023-08-16T08:15:41Z
  file_id: '14062'
  file_name: 2023_MolecularEcology_Shipilina.pdf
  file_size: 7144607
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T08:15:41Z
has_accepted_license: '1'
intvolume: '        32'
isi: 1
issue: '6'
keyword:
- Genetics
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 1441-1457
pmid: 1
project:
- _id: 05959E1C-7A3F-11EA-A408-12923DDC885E
  grant_number: P32166
  name: The maintenance of alternative adaptive peaks in snapdragons
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: The Wittgenstein Prize
- _id: bd6958e0-d553-11ed-ba76-86eba6a76c00
  grant_number: '101055327'
  name: Understanding the evolution of continuous genomes
publication: Molecular Ecology
publication_identifier:
  eissn:
  - 1365-294X
  issn:
  - 0962-1083
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: On the origin and structure of haplotype blocks
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 32
year: '2023'
...
---
_id: '12162'
abstract:
- lang: eng
  text: Homeostatic balance in the intestinal epithelium relies on a fast cellular
    turnover, which is coordinated by an intricate interplay between biochemical signalling,
    mechanical forces and organ geometry. We review recent modelling approaches that
    have been developed to understand different facets of this remarkable homeostatic
    equilibrium. Existing models offer different, albeit complementary, perspectives
    on the problem. First, biomechanical models aim to explain the local and global
    mechanical stresses driving cell renewal as well as tissue shape maintenance.
    Second, compartmental models provide insights into the conditions necessary to
    keep a constant flow of cells with well-defined ratios of cell types, and how
    perturbations can lead to an unbalance of relative compartment sizes. A third
    family of models address, at the cellular level, the nature and regulation of
    stem fate choices that are necessary to fuel cellular turnover. We also review
    how these different approaches are starting to be integrated together across scales,
    to provide quantitative predictions and new conceptual frameworks to think about
    the dynamics of cell renewal in complex tissues.
acknowledgement: "This work received funding from the ERC under the European Union’s
  Horizon 2020 research and innovation programme (grant agreement No. 851288 to E.H.).\r\nB.
  C-M wants to acknowledge the support of the field of excellence Complexity of Life,
  in Basic Research and Innovation of the University of Graz."
article_processing_charge: Yes (via OA deal)
article_type: review
author:
- first_name: Bernat
  full_name: Corominas-Murtra, Bernat
  id: 43BE2298-F248-11E8-B48F-1D18A9856A87
  last_name: Corominas-Murtra
  orcid: 0000-0001-9806-5643
- first_name: Edouard B
  full_name: Hannezo, Edouard B
  id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
  last_name: Hannezo
  orcid: 0000-0001-6005-1561
citation:
  ama: Corominas-Murtra B, Hannezo EB. Modelling the dynamics of mammalian gut homeostasis.
    <i>Seminars in Cell &#38; Developmental Biology</i>. 2023;150-151:58-65. doi:<a
    href="https://doi.org/10.1016/j.semcdb.2022.11.005">10.1016/j.semcdb.2022.11.005</a>
  apa: Corominas-Murtra, B., &#38; Hannezo, E. B. (2023). Modelling the dynamics of
    mammalian gut homeostasis. <i>Seminars in Cell &#38; Developmental Biology</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.semcdb.2022.11.005">https://doi.org/10.1016/j.semcdb.2022.11.005</a>
  chicago: Corominas-Murtra, Bernat, and Edouard B Hannezo. “Modelling the Dynamics
    of Mammalian Gut Homeostasis.” <i>Seminars in Cell &#38; Developmental Biology</i>.
    Elsevier, 2023. <a href="https://doi.org/10.1016/j.semcdb.2022.11.005">https://doi.org/10.1016/j.semcdb.2022.11.005</a>.
  ieee: B. Corominas-Murtra and E. B. Hannezo, “Modelling the dynamics of mammalian
    gut homeostasis,” <i>Seminars in Cell &#38; Developmental Biology</i>, vol. 150–151.
    Elsevier, pp. 58–65, 2023.
  ista: Corominas-Murtra B, Hannezo EB. 2023. Modelling the dynamics of mammalian
    gut homeostasis. Seminars in Cell &#38; Developmental Biology. 150–151, 58–65.
  mla: Corominas-Murtra, Bernat, and Edouard B. Hannezo. “Modelling the Dynamics of
    Mammalian Gut Homeostasis.” <i>Seminars in Cell &#38; Developmental Biology</i>,
    vol. 150–151, Elsevier, 2023, pp. 58–65, doi:<a href="https://doi.org/10.1016/j.semcdb.2022.11.005">10.1016/j.semcdb.2022.11.005</a>.
  short: B. Corominas-Murtra, E.B. Hannezo, Seminars in Cell &#38; Developmental Biology
    150–151 (2023) 58–65.
date_created: 2023-01-12T12:09:47Z
date_published: 2023-12-02T00:00:00Z
date_updated: 2024-01-16T13:22:32Z
day: '02'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.1016/j.semcdb.2022.11.005
ec_funded: 1
external_id:
  isi:
  - '001053522200001'
  pmid:
  - '36470715'
file:
- access_level: open_access
  checksum: c619887cf130f4649bf3035417186004
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-08T10:16:04Z
  date_updated: 2024-01-08T10:16:04Z
  file_id: '14741'
  file_name: 2023_SeminarsCellDevBiology_CorominasMurtra.pdf
  file_size: 1343750
  relation: main_file
  success: 1
file_date_updated: 2024-01-08T10:16:04Z
has_accepted_license: '1'
isi: 1
keyword:
- Cell Biology
- Developmental Biology
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
page: 58-65
pmid: 1
project:
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '851288'
  name: Design Principles of Branching Morphogenesis
publication: Seminars in Cell & Developmental Biology
publication_identifier:
  issn:
  - 1084-9521
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Modelling the dynamics of mammalian gut homeostasis
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 150-151
year: '2023'
...
---
_id: '12163'
abstract:
- lang: eng
  text: Small GTPases play essential roles in the organization of eukaryotic cells.
    In recent years, it has become clear that their intracellular functions result
    from intricate biochemical networks of the GTPase and their regulators that dynamically
    bind to a membrane surface. Due to the inherent complexities of their interactions,
    however, revealing the underlying mechanisms of action is often difficult to achieve
    from in vivo studies. This review summarizes in vitro reconstitution approaches
    developed to obtain a better mechanistic understanding of how small GTPase activities
    are regulated in space and time.
acknowledgement: The authors acknowledge support from IST Austria and helpful comments
  from the anonymous reviewers that helped to improve this manuscript. We apologize
  to the authors of primary literature and outstanding research not cited here due
  to space restraints.
article_processing_charge: Yes (via OA deal)
article_type: review
author:
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
- first_name: Albert
  full_name: Auer, Albert
  id: 3018E8C2-F248-11E8-B48F-1D18A9856A87
  last_name: Auer
  orcid: 0000-0002-3580-2906
- first_name: Gabriel
  full_name: Brognara, Gabriel
  id: D96FFDA0-A884-11E9-9968-DC26E6697425
  last_name: Brognara
- first_name: Hanifatul R
  full_name: Budiman, Hanifatul R
  id: 55380f95-15b2-11ec-abd3-aff8e230696b
  last_name: Budiman
- first_name: Lukasz M
  full_name: Kowalski, Lukasz M
  id: e3a512e2-4bbe-11eb-a68a-e3857a7844c2
  last_name: Kowalski
- first_name: Ivana
  full_name: Matijevic, Ivana
  id: 83c17ce3-15b2-11ec-abd3-f486545870bd
  last_name: Matijevic
citation:
  ama: Loose M, Auer A, Brognara G, Budiman HR, Kowalski LM, Matijevic I. In vitro
    reconstitution of small GTPase regulation. <i>FEBS Letters</i>. 2023;597(6):762-777.
    doi:<a href="https://doi.org/10.1002/1873-3468.14540">10.1002/1873-3468.14540</a>
  apa: Loose, M., Auer, A., Brognara, G., Budiman, H. R., Kowalski, L. M., &#38; Matijevic,
    I. (2023). In vitro reconstitution of small GTPase regulation. <i>FEBS Letters</i>.
    Wiley. <a href="https://doi.org/10.1002/1873-3468.14540">https://doi.org/10.1002/1873-3468.14540</a>
  chicago: Loose, Martin, Albert Auer, Gabriel Brognara, Hanifatul R Budiman, Lukasz
    M Kowalski, and Ivana Matijevic. “In Vitro Reconstitution of Small GTPase Regulation.”
    <i>FEBS Letters</i>. Wiley, 2023. <a href="https://doi.org/10.1002/1873-3468.14540">https://doi.org/10.1002/1873-3468.14540</a>.
  ieee: M. Loose, A. Auer, G. Brognara, H. R. Budiman, L. M. Kowalski, and I. Matijevic,
    “In vitro reconstitution of small GTPase regulation,” <i>FEBS Letters</i>, vol.
    597, no. 6. Wiley, pp. 762–777, 2023.
  ista: Loose M, Auer A, Brognara G, Budiman HR, Kowalski LM, Matijevic I. 2023. In
    vitro reconstitution of small GTPase regulation. FEBS Letters. 597(6), 762–777.
  mla: Loose, Martin, et al. “In Vitro Reconstitution of Small GTPase Regulation.”
    <i>FEBS Letters</i>, vol. 597, no. 6, Wiley, 2023, pp. 762–77, doi:<a href="https://doi.org/10.1002/1873-3468.14540">10.1002/1873-3468.14540</a>.
  short: M. Loose, A. Auer, G. Brognara, H.R. Budiman, L.M. Kowalski, I. Matijevic,
    FEBS Letters 597 (2023) 762–777.
date_created: 2023-01-12T12:09:58Z
date_published: 2023-03-01T00:00:00Z
date_updated: 2023-08-16T08:32:29Z
day: '01'
ddc:
- '570'
department:
- _id: MaLo
doi: 10.1002/1873-3468.14540
external_id:
  isi:
  - '000891573000001'
  pmid:
  - '36448231'
file:
- access_level: open_access
  checksum: 7492244d3f9c5faa1347ef03f6e5bc84
  content_type: application/pdf
  creator: dernst
  date_created: 2023-08-16T08:31:04Z
  date_updated: 2023-08-16T08:31:04Z
  file_id: '14063'
  file_name: 2023_FEBSLetters_Loose.pdf
  file_size: 3148143
  relation: main_file
  success: 1
file_date_updated: 2023-08-16T08:31:04Z
has_accepted_license: '1'
intvolume: '       597'
isi: 1
issue: '6'
keyword:
- Cell Biology
- Genetics
- Molecular Biology
- Biochemistry
- Structural Biology
- Biophysics
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: 762-777
pmid: 1
publication: FEBS Letters
publication_identifier:
  eissn:
  - 1873-3468
  issn:
  - 0014-5793
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: In vitro reconstitution of small GTPase regulation
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 597
year: '2023'
...
---
_id: '12164'
abstract:
- lang: eng
  text: 'A shared-memory counter is a widely-used and well-studied concurrent object.
    It supports two operations: An Inc operation that increases its value by 1 and
    a Read operation that returns its current value. In Jayanti et al (SIAM J Comput,
    30(2), 2000), Jayanti, Tan and Toueg proved a linear lower bound on the worst-case
    step complexity of obstruction-free implementations, from read-write registers,
    of a large class of shared objects that includes counters. The lower bound leaves
    open the question of finding counter implementations with sub-linear amortized
    step complexity. In this work, we address this gap. We show that n-process, wait-free
    and linearizable counters can be implemented from read-write registers with O(log2n)
    amortized step complexity. This is the first counter algorithm from read-write
    registers that provides sub-linear amortized step complexity in executions of
    arbitrary length. Since a logarithmic lower bound on the amortized step complexity
    of obstruction-free counter implementations exists, our upper bound is within
    a logarithmic factor of the optimal. The worst-case step complexity of the construction
    remains linear, which is optimal. This is obtained thanks to a new max register
    construction with O(logn) amortized step complexity in executions of arbitrary
    length in which the value stored in the register does not grow too quickly. We
    then leverage an existing counter algorithm by Aspnes, Attiya and Censor-Hillel
    [1] in which we “plug” our max register implementation to show that it remains
    linearizable while achieving O(log2n) amortized step complexity.'
acknowledgement: A preliminary version of this work appeared in DISC’19. Mirza Ahad
  Baig, Alessia Milani and Corentin Travers are supported by ANR projects Descartes
  and FREDDA. Mirza Ahad Baig is supported by UMI Relax. Danny Hendler is supported
  by the Israel Science Foundation (Grants 380/18 and 1425/22).
article_processing_charge: No
article_type: original
author:
- first_name: Mirza Ahad
  full_name: Baig, Mirza Ahad
  id: 3EDE6DE4-AA5A-11E9-986D-341CE6697425
  last_name: Baig
- first_name: Danny
  full_name: Hendler, Danny
  last_name: Hendler
- first_name: Alessia
  full_name: Milani, Alessia
  last_name: Milani
- first_name: Corentin
  full_name: Travers, Corentin
  last_name: Travers
citation:
  ama: Baig MA, Hendler D, Milani A, Travers C. Long-lived counters with polylogarithmic
    amortized step complexity. <i>Distributed Computing</i>. 2023;36:29-43. doi:<a
    href="https://doi.org/10.1007/s00446-022-00439-5">10.1007/s00446-022-00439-5</a>
  apa: Baig, M. A., Hendler, D., Milani, A., &#38; Travers, C. (2023). Long-lived
    counters with polylogarithmic amortized step complexity. <i>Distributed Computing</i>.
    Springer Nature. <a href="https://doi.org/10.1007/s00446-022-00439-5">https://doi.org/10.1007/s00446-022-00439-5</a>
  chicago: Baig, Mirza Ahad, Danny Hendler, Alessia Milani, and Corentin Travers.
    “Long-Lived Counters with Polylogarithmic Amortized Step Complexity.” <i>Distributed
    Computing</i>. Springer Nature, 2023. <a href="https://doi.org/10.1007/s00446-022-00439-5">https://doi.org/10.1007/s00446-022-00439-5</a>.
  ieee: M. A. Baig, D. Hendler, A. Milani, and C. Travers, “Long-lived counters with
    polylogarithmic amortized step complexity,” <i>Distributed Computing</i>, vol.
    36. Springer Nature, pp. 29–43, 2023.
  ista: Baig MA, Hendler D, Milani A, Travers C. 2023. Long-lived counters with polylogarithmic
    amortized step complexity. Distributed Computing. 36, 29–43.
  mla: Baig, Mirza Ahad, et al. “Long-Lived Counters with Polylogarithmic Amortized
    Step Complexity.” <i>Distributed Computing</i>, vol. 36, Springer Nature, 2023,
    pp. 29–43, doi:<a href="https://doi.org/10.1007/s00446-022-00439-5">10.1007/s00446-022-00439-5</a>.
  short: M.A. Baig, D. Hendler, A. Milani, C. Travers, Distributed Computing 36 (2023)
    29–43.
date_created: 2023-01-12T12:10:08Z
date_published: 2023-03-01T00:00:00Z
date_updated: 2023-08-16T08:39:36Z
day: '01'
department:
- _id: KrPi
doi: 10.1007/s00446-022-00439-5
external_id:
  isi:
  - '000890138700001'
intvolume: '        36'
isi: 1
keyword:
- Computational Theory and Mathematics
- Computer Networks and Communications
- Hardware and Architecture
- Theoretical Computer Science
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://drops.dagstuhl.de/opus/volltexte/2019/11310/
month: '03'
oa: 1
oa_version: Preprint
page: 29-43
publication: Distributed Computing
publication_identifier:
  eissn:
  - 1432-0452
  issn:
  - 0178-2770
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Long-lived counters with polylogarithmic amortized step complexity
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 36
year: '2023'
...
---
_id: '12165'
abstract:
- lang: eng
  text: It may come as a surprise that a phenomenon as ubiquitous and prominent as
    the transition from laminar to turbulent flow has resisted combined efforts by
    physicists, engineers and mathematicians, and remained unresolved for almost one
    and a half centuries. In recent years, various studies have proposed analogies
    to directed percolation, a well-known universality class in statistical mechanics,
    which describes a non-equilibrium phase transition from a fluctuating active phase
    into an absorbing state. It is this unlikely relation between the multiscale,
    high-dimensional dynamics that signify the transition process in virtually all
    flows of practical relevance, and the arguably most basic non-equilibrium phase
    transition, that so far has mainly been the subject of model studies, which I
    review in this Perspective.
article_processing_charge: No
article_type: original
author:
- first_name: Björn
  full_name: Hof, Björn
  id: 3A374330-F248-11E8-B48F-1D18A9856A87
  last_name: Hof
  orcid: 0000-0003-2057-2754
citation:
  ama: Hof B. Directed percolation and the transition to turbulence. <i>Nature Reviews
    Physics</i>. 2023;5:62-72. doi:<a href="https://doi.org/10.1038/s42254-022-00539-y">10.1038/s42254-022-00539-y</a>
  apa: Hof, B. (2023). Directed percolation and the transition to turbulence. <i>Nature
    Reviews Physics</i>. Springer Nature. <a href="https://doi.org/10.1038/s42254-022-00539-y">https://doi.org/10.1038/s42254-022-00539-y</a>
  chicago: Hof, Björn. “Directed Percolation and the Transition to Turbulence.” <i>Nature
    Reviews Physics</i>. Springer Nature, 2023. <a href="https://doi.org/10.1038/s42254-022-00539-y">https://doi.org/10.1038/s42254-022-00539-y</a>.
  ieee: B. Hof, “Directed percolation and the transition to turbulence,” <i>Nature
    Reviews Physics</i>, vol. 5. Springer Nature, pp. 62–72, 2023.
  ista: Hof B. 2023. Directed percolation and the transition to turbulence. Nature
    Reviews Physics. 5, 62–72.
  mla: Hof, Björn. “Directed Percolation and the Transition to Turbulence.” <i>Nature
    Reviews Physics</i>, vol. 5, Springer Nature, 2023, pp. 62–72, doi:<a href="https://doi.org/10.1038/s42254-022-00539-y">10.1038/s42254-022-00539-y</a>.
  short: B. Hof, Nature Reviews Physics 5 (2023) 62–72.
date_created: 2023-01-12T12:10:18Z
date_published: 2023-01-01T00:00:00Z
date_updated: 2023-08-01T12:50:48Z
day: '01'
department:
- _id: BjHo
doi: 10.1038/s42254-022-00539-y
external_id:
  isi:
  - '000890148700002'
intvolume: '         5'
isi: 1
keyword:
- General Physics and Astronomy
language:
- iso: eng
month: '01'
oa_version: None
page: 62-72
publication: Nature Reviews Physics
publication_identifier:
  eissn:
  - 2522-5820
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Directed percolation and the transition to turbulence
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 5
year: '2023'
...
---
_id: '12172'
abstract:
- lang: eng
  text: In industrial reactors and equipment, non-ideality is quite a common phenomenon
    rather than an exception. These deviations from ideality impact the process's
    overall efficiency and the effectiveness of the equipment. To recognize the associated
    non-ideality, one needs to have enough understanding of the formulation of the
    equations and in-depth knowledge of the residence time distribution (RTD) data
    of real reactors. In the current work, step input and pulse input were used to
    create RTD data for Cascade continuous stirred tank reactors (CSTRs). For the
    aforementioned configuration, experiments were run at various flow rates to validate
    the developed characteristic equations. To produce RTD data, distilled water was
    utilized as the flowing fluid, and NaOH was the tracer substance. The ideal behavior
    of tracer concentration exits age distribution, and cumulative fraction for each
    setup and each input was plotted and experimental results were compared with perfect
    behavior. Deviation of concentration exit age distribution and cumulative fractional
    distribution from ideal behavior is more in pulse input as compared to a step
    input. For ideal cases, the exit age distribution curve and cumulative fraction
    curves are independent of the type of input. But a significant difference was
    observed for the two cases, which may be due to non-measurable fluctuations in
    volumetric flow rate, non-achievement of instant injection of tracer in case of
    pulse input, and slight variations in the sampling period. Further, with increasing
    flow rate, concentration, exit age, and cumulative fractional curves shifted upward,
    and this behavior matches with the actual case.
article_processing_charge: No
article_type: original
author:
- first_name: Bushra
  full_name: Khatoon, Bushra
  last_name: Khatoon
- first_name: Shoaib
  full_name: Kamil, Shoaib
  id: 185a19af-dc7d-11ea-9b2f-8eb2201959e9
  last_name: Kamil
- first_name: Hitesh
  full_name: Babu, Hitesh
  last_name: Babu
- first_name: M.
  full_name: Siraj Alam, M.
  last_name: Siraj Alam
citation:
  ama: 'Khatoon B, Kamil S, Babu H, Siraj Alam M. Experimental analysis of Cascade
    CSTRs with step and pulse inputs. <i>Materials Today: Proceedings</i>. 2023;78(Part
    1):40-47. doi:<a href="https://doi.org/10.1016/j.matpr.2022.11.037">10.1016/j.matpr.2022.11.037</a>'
  apa: 'Khatoon, B., Kamil, S., Babu, H., &#38; Siraj Alam, M. (2023). Experimental
    analysis of Cascade CSTRs with step and pulse inputs. <i>Materials Today: Proceedings</i>.
    Elsevier. <a href="https://doi.org/10.1016/j.matpr.2022.11.037">https://doi.org/10.1016/j.matpr.2022.11.037</a>'
  chicago: 'Khatoon, Bushra, Shoaib Kamil, Hitesh Babu, and M. Siraj Alam. “Experimental
    Analysis of Cascade CSTRs with Step and Pulse Inputs.” <i>Materials Today: Proceedings</i>.
    Elsevier, 2023. <a href="https://doi.org/10.1016/j.matpr.2022.11.037">https://doi.org/10.1016/j.matpr.2022.11.037</a>.'
  ieee: 'B. Khatoon, S. Kamil, H. Babu, and M. Siraj Alam, “Experimental analysis
    of Cascade CSTRs with step and pulse inputs,” <i>Materials Today: Proceedings</i>,
    vol. 78, no. Part 1. Elsevier, pp. 40–47, 2023.'
  ista: 'Khatoon B, Kamil S, Babu H, Siraj Alam M. 2023. Experimental analysis of
    Cascade CSTRs with step and pulse inputs. Materials Today: Proceedings. 78(Part
    1), 40–47.'
  mla: 'Khatoon, Bushra, et al. “Experimental Analysis of Cascade CSTRs with Step
    and Pulse Inputs.” <i>Materials Today: Proceedings</i>, vol. 78, no. Part 1, Elsevier,
    2023, pp. 40–47, doi:<a href="https://doi.org/10.1016/j.matpr.2022.11.037">10.1016/j.matpr.2022.11.037</a>.'
  short: 'B. Khatoon, S. Kamil, H. Babu, M. Siraj Alam, Materials Today: Proceedings
    78 (2023) 40–47.'
date_created: 2023-01-12T12:11:26Z
date_published: 2023-03-20T00:00:00Z
date_updated: 2023-08-16T09:08:11Z
day: '20'
department:
- _id: BjHo
doi: 10.1016/j.matpr.2022.11.037
intvolume: '        78'
issue: Part 1
keyword:
- General Medicine
language:
- iso: eng
month: '03'
oa_version: None
page: 40-47
publication: 'Materials Today: Proceedings'
publication_identifier:
  issn:
  - 2214-7853
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Experimental analysis of Cascade CSTRs with step and pulse inputs
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 78
year: '2023'
...
---
_id: '12183'
abstract:
- lang: eng
  text: We consider a gas of n bosonic particles confined in a box [−ℓ/2,ℓ/2]3 with
    Neumann boundary conditions. We prove Bose–Einstein condensation in the Gross–Pitaevskii
    regime, with an optimal bound on the condensate depletion. Moreover, our lower
    bound for the ground state energy in a small box [−ℓ/2,ℓ/2]3 implies (via Neumann
    bracketing) a lower bound for the ground state energy of N bosons in a large box
    [−L/2,L/2]3 with density ρ=N/L3 in the thermodynamic limit.
acknowledgement: Funding from the European Union’s Horizon 2020 research and innovation
  programme under the ERC grant agreement No 694227 is gratefully acknowledged.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Chiara
  full_name: Boccato, Chiara
  id: 342E7E22-F248-11E8-B48F-1D18A9856A87
  last_name: Boccato
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
citation:
  ama: Boccato C, Seiringer R. The Bose Gas in a box with Neumann boundary conditions.
    <i>Annales Henri Poincare</i>. 2023;24:1505-1560. doi:<a href="https://doi.org/10.1007/s00023-022-01252-3">10.1007/s00023-022-01252-3</a>
  apa: Boccato, C., &#38; Seiringer, R. (2023). The Bose Gas in a box with Neumann
    boundary conditions. <i>Annales Henri Poincare</i>. Springer Nature. <a href="https://doi.org/10.1007/s00023-022-01252-3">https://doi.org/10.1007/s00023-022-01252-3</a>
  chicago: Boccato, Chiara, and Robert Seiringer. “The Bose Gas in a Box with Neumann
    Boundary Conditions.” <i>Annales Henri Poincare</i>. Springer Nature, 2023. <a
    href="https://doi.org/10.1007/s00023-022-01252-3">https://doi.org/10.1007/s00023-022-01252-3</a>.
  ieee: C. Boccato and R. Seiringer, “The Bose Gas in a box with Neumann boundary
    conditions,” <i>Annales Henri Poincare</i>, vol. 24. Springer Nature, pp. 1505–1560,
    2023.
  ista: Boccato C, Seiringer R. 2023. The Bose Gas in a box with Neumann boundary
    conditions. Annales Henri Poincare. 24, 1505–1560.
  mla: Boccato, Chiara, and Robert Seiringer. “The Bose Gas in a Box with Neumann
    Boundary Conditions.” <i>Annales Henri Poincare</i>, vol. 24, Springer Nature,
    2023, pp. 1505–60, doi:<a href="https://doi.org/10.1007/s00023-022-01252-3">10.1007/s00023-022-01252-3</a>.
  short: C. Boccato, R. Seiringer, Annales Henri Poincare 24 (2023) 1505–1560.
date_created: 2023-01-15T23:00:52Z
date_published: 2023-05-01T00:00:00Z
date_updated: 2023-08-16T11:34:03Z
day: '01'
department:
- _id: RoSe
doi: 10.1007/s00023-022-01252-3
ec_funded: 1
external_id:
  arxiv:
  - '2205.15284'
  isi:
  - '000910751800002'
intvolume: '        24'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.2205.15284
month: '05'
oa: 1
oa_version: Preprint
page: 1505-1560
project:
- _id: 25C6DC12-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '694227'
  name: Analysis of quantum many-body systems
publication: Annales Henri Poincare
publication_identifier:
  issn:
  - 1424-0637
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: The Bose Gas in a box with Neumann boundary conditions
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2023'
...
---
_id: '12205'
abstract:
- lang: eng
  text: "Background: This study seeks to evaluate the impact of breast cancer (BRCA)
    gene status on tumor dissemination pattern, surgical outcome and survival in a
    multicenter cohort of paired primary ovarian cancer (pOC) and recurrent ovarian
    cancer (rOC).\r\n\r\nPatients and Methods: Medical records and follow-up data
    from 190 patients were gathered retrospectively. All patients had surgery at pOC
    and at least one further rOC surgery at four European high-volume centers. Patients
    were divided into one cohort with confirmed mutation for BRCA1 and/or BRCA2 (BRCAmut)
    and a second cohort with BRCA wild type or unknown (BRCAwt). Patterns of tumor
    presentation, surgical outcome and survival data were analyzed between the two
    groups.\r\n\r\nResults: Patients with BRCAmut disease were on average 4 years
    younger and had significantly more tumor involvement upon diagnosis. Patients
    with BRCAmut disease showed higher debulking rates at all stages. Multivariate
    analysis showed that only patient age had significant predictive value for complete
    tumor resection in pOC. At rOC, however, only BRCAmut status significantly correlated
    with optimal debulking. Patients with BRCAmut disease showed significantly prolonged
    overall survival (OS) by 24.3 months. Progression-free survival (PFS) was prolonged
    in the BRCAmut group at all stages as well, reaching statistical significance
    during recurrence.\r\n\r\nConclusions: Patients with BRCAmut disease showed a
    more aggressive course of disease with earlier onset and more extensive tumor
    dissemination at pOC. However, surgical outcome and OS were significantly better
    in patients with BRCAmut disease compared with patients with BRCAwt disease. We
    therefore propose to consider BRCAmut status in regard to patient selection for
    cytoreductive surgery, especially in rOC."
acknowledgement: "E.I.B. is a Feodor Lynen fellow of the Humboldt Foundation and a
  participant of the Charité Clinical Scientist Program funded by the Charité Universitätsmedizin
  Berlin and the Berlin Institute of Health. This work was supported by European Commission’s
  Seventh Framework Programme under grant agreement no. 279113 (OCTIPS; www.octips.eu).\r\nOpen
  Access funding enabled and organized by Projekt DEAL."
article_processing_charge: No
article_type: original
author:
- first_name: Jacek
  full_name: Glajzer, Jacek
  last_name: Glajzer
- first_name: Dan Cacsire
  full_name: Castillo-Tong, Dan Cacsire
  last_name: Castillo-Tong
- first_name: Rolf
  full_name: Richter, Rolf
  last_name: Richter
- first_name: Ignace
  full_name: Vergote, Ignace
  last_name: Vergote
- first_name: Hagen
  full_name: Kulbe, Hagen
  last_name: Kulbe
- first_name: Adriaan
  full_name: Vanderstichele, Adriaan
  last_name: Vanderstichele
- first_name: Ilary
  full_name: Ruscito, Ilary
  last_name: Ruscito
- first_name: Fabian
  full_name: Trillsch, Fabian
  last_name: Trillsch
- first_name: Alexander
  full_name: Mustea, Alexander
  last_name: Mustea
- first_name: Caroline
  full_name: Kreuzinger, Caroline
  id: 382077BA-F248-11E8-B48F-1D18A9856A87
  last_name: Kreuzinger
- first_name: Charlie
  full_name: Gourley, Charlie
  last_name: Gourley
- first_name: Hani
  full_name: Gabra, Hani
  last_name: Gabra
- first_name: Eliane T.
  full_name: Taube, Eliane T.
  last_name: Taube
- first_name: Oliver
  full_name: Dorigo, Oliver
  last_name: Dorigo
- first_name: David
  full_name: Horst, David
  last_name: Horst
- first_name: Carlotta
  full_name: Keunecke, Carlotta
  last_name: Keunecke
- first_name: Joanna
  full_name: Baum, Joanna
  last_name: Baum
- first_name: Timothy
  full_name: Angelotti, Timothy
  last_name: Angelotti
- first_name: Jalid
  full_name: Sehouli, Jalid
  last_name: Sehouli
- first_name: Elena Ioana
  full_name: Braicu, Elena Ioana
  last_name: Braicu
citation:
  ama: 'Glajzer J, Castillo-Tong DC, Richter R, et al. Impact of BRCA mutation status
    on tumor dissemination pattern, surgical outcome and patient survival in primary
    and recurrent high-grade serous ovarian cancer: A multicenter retrospective study
    by the Ovarian Cancer Therapy-Innovative Models Prolong Survival (OCTIPS) consortium.
    <i>Annals of Surgical Oncology</i>. 2023;30:35-45. doi:<a href="https://doi.org/10.1245/s10434-022-12459-3">10.1245/s10434-022-12459-3</a>'
  apa: 'Glajzer, J., Castillo-Tong, D. C., Richter, R., Vergote, I., Kulbe, H., Vanderstichele,
    A., … Braicu, E. I. (2023). Impact of BRCA mutation status on tumor dissemination
    pattern, surgical outcome and patient survival in primary and recurrent high-grade
    serous ovarian cancer: A multicenter retrospective study by the Ovarian Cancer
    Therapy-Innovative Models Prolong Survival (OCTIPS) consortium. <i>Annals of Surgical
    Oncology</i>. Springer Nature. <a href="https://doi.org/10.1245/s10434-022-12459-3">https://doi.org/10.1245/s10434-022-12459-3</a>'
  chicago: 'Glajzer, Jacek, Dan Cacsire Castillo-Tong, Rolf Richter, Ignace Vergote,
    Hagen Kulbe, Adriaan Vanderstichele, Ilary Ruscito, et al. “Impact of BRCA Mutation
    Status on Tumor Dissemination Pattern, Surgical Outcome and Patient Survival in
    Primary and Recurrent High-Grade Serous Ovarian Cancer: A Multicenter Retrospective
    Study by the Ovarian Cancer Therapy-Innovative Models Prolong Survival (OCTIPS) Consortium.”
    <i>Annals of Surgical Oncology</i>. Springer Nature, 2023. <a href="https://doi.org/10.1245/s10434-022-12459-3">https://doi.org/10.1245/s10434-022-12459-3</a>.'
  ieee: 'J. Glajzer <i>et al.</i>, “Impact of BRCA mutation status on tumor dissemination
    pattern, surgical outcome and patient survival in primary and recurrent high-grade
    serous ovarian cancer: A multicenter retrospective study by the Ovarian Cancer
    Therapy-Innovative Models Prolong Survival (OCTIPS) consortium,” <i>Annals of
    Surgical Oncology</i>, vol. 30. Springer Nature, pp. 35–45, 2023.'
  ista: 'Glajzer J, Castillo-Tong DC, Richter R, Vergote I, Kulbe H, Vanderstichele
    A, Ruscito I, Trillsch F, Mustea A, Kreuzinger C, Gourley C, Gabra H, Taube ET,
    Dorigo O, Horst D, Keunecke C, Baum J, Angelotti T, Sehouli J, Braicu EI. 2023.
    Impact of BRCA mutation status on tumor dissemination pattern, surgical outcome
    and patient survival in primary and recurrent high-grade serous ovarian cancer:
    A multicenter retrospective study by the Ovarian Cancer Therapy-Innovative Models
    Prolong Survival (OCTIPS) consortium. Annals of Surgical Oncology. 30, 35–45.'
  mla: 'Glajzer, Jacek, et al. “Impact of BRCA Mutation Status on Tumor Dissemination
    Pattern, Surgical Outcome and Patient Survival in Primary and Recurrent High-Grade
    Serous Ovarian Cancer: A Multicenter Retrospective Study by the Ovarian Cancer
    Therapy-Innovative Models Prolong Survival (OCTIPS) Consortium.” <i>Annals of
    Surgical Oncology</i>, vol. 30, Springer Nature, 2023, pp. 35–45, doi:<a href="https://doi.org/10.1245/s10434-022-12459-3">10.1245/s10434-022-12459-3</a>.'
  short: J. Glajzer, D.C. Castillo-Tong, R. Richter, I. Vergote, H. Kulbe, A. Vanderstichele,
    I. Ruscito, F. Trillsch, A. Mustea, C. Kreuzinger, C. Gourley, H. Gabra, E.T.
    Taube, O. Dorigo, D. Horst, C. Keunecke, J. Baum, T. Angelotti, J. Sehouli, E.I.
    Braicu, Annals of Surgical Oncology 30 (2023) 35–45.
date_created: 2023-01-16T09:44:36Z
date_published: 2023-01-01T00:00:00Z
date_updated: 2023-09-05T15:18:37Z
day: '01'
ddc:
- '610'
department:
- _id: JoDa
doi: 10.1245/s10434-022-12459-3
external_id:
  isi:
  - '000852125500006'
file:
- access_level: open_access
  checksum: 36a1200e1011f4b2155a8041d0308f34
  content_type: application/pdf
  creator: dernst
  date_created: 2023-02-02T13:01:20Z
  date_updated: 2023-02-02T13:01:20Z
  file_id: '12490'
  file_name: 2023_AnnalsSurgicalOncology_Glajzer.pdf
  file_size: 365865
  relation: main_file
  success: 1
file_date_updated: 2023-02-02T13:01:20Z
has_accepted_license: '1'
intvolume: '        30'
isi: 1
keyword:
- Oncology
- Surgery
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 35-45
publication: Annals of Surgical Oncology
publication_identifier:
  eissn:
  - 1534-4681
  issn:
  - 1068-9265
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  record:
  - id: '12115'
    relation: other
    status: public
scopus_import: '1'
status: public
title: 'Impact of BRCA mutation status on tumor dissemination pattern, surgical outcome
  and patient survival in primary and recurrent high-grade serous ovarian cancer:
  A multicenter retrospective study by the Ovarian Cancer Therapy-Innovative Models
  Prolong Survival (OCTIPS) consortium'
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: 30
year: '2023'
...
---
_id: '12287'
abstract:
- lang: eng
  text: We present criteria for establishing a triangulation of a manifold. Given
    a manifold M, a simplicial complex A, and a map H from the underlying space of
    A to M, our criteria are presented in local coordinate charts for M, and ensure
    that H is a homeomorphism. These criteria do not require a differentiable structure,
    or even an explicit metric on M. No Delaunay property of A is assumed. The result
    provides a triangulation guarantee for algorithms that construct a simplicial
    complex by working in local coordinate patches. Because the criteria are easily
    verified in such a setting, they are expected to be of general use.
acknowledgement: "This work has been funded by the European Research Council under
  the European Union’s ERC Grant Agreement number 339025 GUDHI (Algorithmic Foundations
  of Geometric Understanding in Higher Dimensions). Arijit Ghosh is supported by Ramanujan
  Fellowship (No. SB/S2/RJN-064/2015). Part of this work was done when Arijit Ghosh
  was a Researcher at Max-Planck-Institute for Informatics, Germany, supported by
  the IndoGerman Max Planck Center for Computer Science (IMPECS). Mathijs Wintraecken
  also received funding from the European Union’s Horizon 2020 research and innovation
  programme under the Marie Skłodowska-Curie grant agreement No. 754411 and the Austrian
  Science Fund (FWF): M-3073. A part of the results described in this paper were presented
  at SoCG 2018 and in [3]. \r\nOpen access funding provided by the Austrian Science
  Fund (FWF)."
article_processing_charge: No
article_type: original
author:
- first_name: Jean-Daniel
  full_name: Boissonnat, Jean-Daniel
  last_name: Boissonnat
- first_name: Ramsay
  full_name: Dyer, Ramsay
  last_name: Dyer
- first_name: Arijit
  full_name: Ghosh, Arijit
  last_name: Ghosh
- first_name: Mathijs
  full_name: Wintraecken, Mathijs
  id: 307CFBC8-F248-11E8-B48F-1D18A9856A87
  last_name: Wintraecken
  orcid: 0000-0002-7472-2220
citation:
  ama: Boissonnat J-D, Dyer R, Ghosh A, Wintraecken M. Local criteria for triangulating
    general manifolds. <i>Discrete &#38; Computational Geometry</i>. 2023;69:156-191.
    doi:<a href="https://doi.org/10.1007/s00454-022-00431-7">10.1007/s00454-022-00431-7</a>
  apa: Boissonnat, J.-D., Dyer, R., Ghosh, A., &#38; Wintraecken, M. (2023). Local
    criteria for triangulating general manifolds. <i>Discrete &#38; Computational
    Geometry</i>. Springer Nature. <a href="https://doi.org/10.1007/s00454-022-00431-7">https://doi.org/10.1007/s00454-022-00431-7</a>
  chicago: Boissonnat, Jean-Daniel, Ramsay Dyer, Arijit Ghosh, and Mathijs Wintraecken.
    “Local Criteria for Triangulating General Manifolds.” <i>Discrete &#38; Computational
    Geometry</i>. Springer Nature, 2023. <a href="https://doi.org/10.1007/s00454-022-00431-7">https://doi.org/10.1007/s00454-022-00431-7</a>.
  ieee: J.-D. Boissonnat, R. Dyer, A. Ghosh, and M. Wintraecken, “Local criteria for
    triangulating general manifolds,” <i>Discrete &#38; Computational Geometry</i>,
    vol. 69. Springer Nature, pp. 156–191, 2023.
  ista: Boissonnat J-D, Dyer R, Ghosh A, Wintraecken M. 2023. Local criteria for triangulating
    general manifolds. Discrete &#38; Computational Geometry. 69, 156–191.
  mla: Boissonnat, Jean-Daniel, et al. “Local Criteria for Triangulating General Manifolds.”
    <i>Discrete &#38; Computational Geometry</i>, vol. 69, Springer Nature, 2023,
    pp. 156–91, doi:<a href="https://doi.org/10.1007/s00454-022-00431-7">10.1007/s00454-022-00431-7</a>.
  short: J.-D. Boissonnat, R. Dyer, A. Ghosh, M. Wintraecken, Discrete &#38; Computational
    Geometry 69 (2023) 156–191.
date_created: 2023-01-16T10:04:06Z
date_published: 2023-01-01T00:00:00Z
date_updated: 2023-08-01T12:47:32Z
day: '01'
ddc:
- '510'
department:
- _id: HeEd
doi: 10.1007/s00454-022-00431-7
ec_funded: 1
external_id:
  isi:
  - '000862193600001'
file:
- access_level: open_access
  checksum: 46352e0ee71e460848f88685ca852681
  content_type: application/pdf
  creator: dernst
  date_created: 2023-02-02T11:01:10Z
  date_updated: 2023-02-02T11:01:10Z
  file_id: '12488'
  file_name: 2023_DiscreteCompGeometry_Boissonnat.pdf
  file_size: 582850
  relation: main_file
  success: 1
file_date_updated: 2023-02-02T11:01:10Z
has_accepted_license: '1'
intvolume: '        69'
isi: 1
keyword:
- Computational Theory and Mathematics
- Discrete Mathematics and Combinatorics
- Geometry and Topology
- Theoretical Computer Science
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: 156-191
project:
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
- _id: fc390959-9c52-11eb-aca3-afa58bd282b2
  grant_number: M03073
  name: Learning and triangulating manifolds via collapses
publication: Discrete & Computational Geometry
publication_identifier:
  eissn:
  - 1432-0444
  issn:
  - 0179-5376
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Local criteria for triangulating general manifolds
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 69
year: '2023'
...
---
_id: '12313'
abstract:
- lang: eng
  text: Let P be a nontorsion point on an elliptic curve defined over a number field
    K and consider the sequence {Bn}n∈N of the denominators of x(nP). We prove that
    every term of the sequence of the Bn has a primitive divisor for n greater than
    an effectively computable constant that we will explicitly compute. This constant
    will depend only on the model defining the curve.
acknowledgement: "This paper is part of the author’s PhD thesis at Università of Pisa.
  Moreover, this\r\nproject has received funding from the European Union’s Horizon
  2020 research\r\nand innovation programme under the Marie Skłodowska-Curie Grant
  Agreement\r\nNo. 101034413. I thank the referee for many helpful comments."
article_processing_charge: Yes (in subscription journal)
article_type: original
arxiv: 1
author:
- first_name: Matteo
  full_name: Verzobio, Matteo
  id: 7aa8f170-131e-11ed-88e1-a9efd01027cb
  last_name: Verzobio
  orcid: 0000-0002-0854-0306
citation:
  ama: Verzobio M. Some effectivity results for primitive divisors of elliptic divisibility 
    sequences. <i>Pacific Journal of Mathematics</i>. 2023;325(2):331-351. doi:<a
    href="https://doi.org/10.2140/pjm.2023.325.331">10.2140/pjm.2023.325.331</a>
  apa: Verzobio, M. (2023). Some effectivity results for primitive divisors of elliptic
    divisibility  sequences. <i>Pacific Journal of Mathematics</i>. Mathematical Sciences
    Publishers. <a href="https://doi.org/10.2140/pjm.2023.325.331">https://doi.org/10.2140/pjm.2023.325.331</a>
  chicago: Verzobio, Matteo. “Some Effectivity Results for Primitive Divisors of Elliptic
    Divisibility  Sequences.” <i>Pacific Journal of Mathematics</i>. Mathematical
    Sciences Publishers, 2023. <a href="https://doi.org/10.2140/pjm.2023.325.331">https://doi.org/10.2140/pjm.2023.325.331</a>.
  ieee: M. Verzobio, “Some effectivity results for primitive divisors of elliptic
    divisibility  sequences,” <i>Pacific Journal of Mathematics</i>, vol. 325, no.
    2. Mathematical Sciences Publishers, pp. 331–351, 2023.
  ista: Verzobio M. 2023. Some effectivity results for primitive divisors of elliptic
    divisibility  sequences. Pacific Journal of Mathematics. 325(2), 331–351.
  mla: Verzobio, Matteo. “Some Effectivity Results for Primitive Divisors of Elliptic
    Divisibility  Sequences.” <i>Pacific Journal of Mathematics</i>, vol. 325, no.
    2, Mathematical Sciences Publishers, 2023, pp. 331–51, doi:<a href="https://doi.org/10.2140/pjm.2023.325.331">10.2140/pjm.2023.325.331</a>.
  short: M. Verzobio, Pacific Journal of Mathematics 325 (2023) 331–351.
date_created: 2023-01-16T11:46:19Z
date_published: 2023-11-03T00:00:00Z
date_updated: 2023-12-13T11:18:14Z
day: '03'
ddc:
- '510'
department:
- _id: TiBr
doi: 10.2140/pjm.2023.325.331
ec_funded: 1
external_id:
  arxiv:
  - '2001.02987'
  isi:
  - '001104766900001'
file:
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month: '11'
oa: 1
oa_version: Published Version
page: 331-351
project:
- _id: fc2ed2f7-9c52-11eb-aca3-c01059dda49c
  call_identifier: H2020
  grant_number: '101034413'
  name: 'IST-BRIDGE: International postdoctoral program'
publication: Pacific Journal of Mathematics
publication_identifier:
  eissn:
  - 0030-8730
publication_status: published
publisher: Mathematical Sciences Publishers
quality_controlled: '1'
scopus_import: '1'
status: public
title: Some effectivity results for primitive divisors of elliptic divisibility  sequences
tmp:
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  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 325
year: '2023'
...
---
_id: '12329'
abstract:
- lang: eng
  text: In this article, we develop two independent and new approaches to model epidemic
    spread in a network. Contrary to the most studied models, those developed here
    allow for contacts with different probabilities of transmitting the disease (transmissibilities).
    We then examine each of these models using some mean field type approximations.
    The first model looks at the late-stage effects of an epidemic outbreak and allows
    for the computation of the probability that a given vertex was infected. This
    computation is based on a mean field approximation and only depends on the number
    of contacts and their transmissibilities. This approach shares many similarities
    with percolation models in networks. The second model we develop is a dynamic
    model which we analyze using a mean field approximation which highly reduces the
    dimensionality of the system. In particular, the original system which individually
    analyses each vertex of the network is reduced to one with as many equations as
    different transmissibilities. Perhaps the greatest contribution of this article
    is the observation that, in both these models, the existence and size of an epidemic
    outbreak are linked to the properties of a matrix which we call the R-matrix.
    This is a generalization of the basic reproduction number which more precisely
    characterizes the main routes of infection.
acknowledgement: Gonçalo Oliveira is supported by the NOMIS Foundation, Fundação Serrapilheira
  1812-27395, by CNPq grants 428959/2018-0 and 307475/2018-2, and by FAPERJ through
  the grant Jovem Cientista do Nosso Estado E-26/202.793/2019.
article_number: '468'
article_processing_charge: No
article_type: original
author:
- first_name: Arturo
  full_name: Gómez, Arturo
  last_name: Gómez
- first_name: Goncalo
  full_name: Oliveira, Goncalo
  id: 58abbde8-f455-11eb-a497-98c8fd71b905
  last_name: Oliveira
citation:
  ama: Gómez A, Oliveira G. New approaches to epidemic modeling on networks. <i>Scientific
    Reports</i>. 2023;13. doi:<a href="https://doi.org/10.1038/s41598-022-19827-9">10.1038/s41598-022-19827-9</a>
  apa: Gómez, A., &#38; Oliveira, G. (2023). New approaches to epidemic modeling on
    networks. <i>Scientific Reports</i>. Springer Nature. <a href="https://doi.org/10.1038/s41598-022-19827-9">https://doi.org/10.1038/s41598-022-19827-9</a>
  chicago: Gómez, Arturo, and Goncalo Oliveira. “New Approaches to Epidemic Modeling
    on Networks.” <i>Scientific Reports</i>. Springer Nature, 2023. <a href="https://doi.org/10.1038/s41598-022-19827-9">https://doi.org/10.1038/s41598-022-19827-9</a>.
  ieee: A. Gómez and G. Oliveira, “New approaches to epidemic modeling on networks,”
    <i>Scientific Reports</i>, vol. 13. Springer Nature, 2023.
  ista: Gómez A, Oliveira G. 2023. New approaches to epidemic modeling on networks.
    Scientific Reports. 13, 468.
  mla: Gómez, Arturo, and Goncalo Oliveira. “New Approaches to Epidemic Modeling on
    Networks.” <i>Scientific Reports</i>, vol. 13, 468, Springer Nature, 2023, doi:<a
    href="https://doi.org/10.1038/s41598-022-19827-9">10.1038/s41598-022-19827-9</a>.
  short: A. Gómez, G. Oliveira, Scientific Reports 13 (2023).
date_created: 2023-01-22T23:00:55Z
date_published: 2023-01-10T00:00:00Z
date_updated: 2023-08-01T12:31:40Z
day: '10'
ddc:
- '510'
department:
- _id: TaHa
doi: 10.1038/s41598-022-19827-9
external_id:
  isi:
  - '001003345000051'
file:
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file_date_updated: 2023-01-23T07:53:23Z
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isi: 1
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
publication: Scientific Reports
publication_identifier:
  eissn:
  - 2045-2322
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: New approaches to epidemic modeling on networks
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 13
year: '2023'
...
---
_id: '12330'
abstract:
- lang: eng
  text: 'The design and implementation of efficient concurrent data structures has
    seen significant attention. However, most of this work has focused on concurrent
    data structures providing good worst-case guarantees, although, in real workloads,
    objects are often accessed at different rates. Efficient distribution-adaptive
    data structures, such as splay-trees, are known in the sequential case; however,
    they often are hard to translate efficiently to the concurrent case. We investigate
    distribution-adaptive concurrent data structures, and propose a new design called
    the splay-list. At a high level, the splay-list is similar to a standard skip-list,
    with the key distinction that the height of each element adapts dynamically to
    its access rate: popular elements “move up,” whereas rarely-accessed elements
    decrease in height. We show that the splay-list provides order-optimal amortized
    complexity bounds for a subset of operations, while being amenable to efficient
    concurrent implementation. Experiments show that the splay-list can leverage distribution-adaptivity
    for performance, and can outperform the only previously-known distribution-adaptive
    concurrent design in certain workloads.'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Vitalii
  full_name: Aksenov, Vitalii
  id: 2980135A-F248-11E8-B48F-1D18A9856A87
  last_name: Aksenov
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
- first_name: Alexandra
  full_name: Drozdova, Alexandra
  last_name: Drozdova
- first_name: Amirkeivan
  full_name: Mohtashami, Amirkeivan
  last_name: Mohtashami
citation:
  ama: 'Aksenov V, Alistarh D-A, Drozdova A, Mohtashami A. The splay-list: A distribution-adaptive
    concurrent skip-list. <i>Distributed Computing</i>. 2023;36:395-418. doi:<a href="https://doi.org/10.1007/s00446-022-00441-x">10.1007/s00446-022-00441-x</a>'
  apa: 'Aksenov, V., Alistarh, D.-A., Drozdova, A., &#38; Mohtashami, A. (2023). The
    splay-list: A distribution-adaptive concurrent skip-list. <i>Distributed Computing</i>.
    Springer Nature. <a href="https://doi.org/10.1007/s00446-022-00441-x">https://doi.org/10.1007/s00446-022-00441-x</a>'
  chicago: 'Aksenov, Vitalii, Dan-Adrian Alistarh, Alexandra Drozdova, and Amirkeivan
    Mohtashami. “The Splay-List: A Distribution-Adaptive Concurrent Skip-List.” <i>Distributed
    Computing</i>. Springer Nature, 2023. <a href="https://doi.org/10.1007/s00446-022-00441-x">https://doi.org/10.1007/s00446-022-00441-x</a>.'
  ieee: 'V. Aksenov, D.-A. Alistarh, A. Drozdova, and A. Mohtashami, “The splay-list:
    A distribution-adaptive concurrent skip-list,” <i>Distributed Computing</i>, vol.
    36. Springer Nature, pp. 395–418, 2023.'
  ista: 'Aksenov V, Alistarh D-A, Drozdova A, Mohtashami A. 2023. The splay-list:
    A distribution-adaptive concurrent skip-list. Distributed Computing. 36, 395–418.'
  mla: 'Aksenov, Vitalii, et al. “The Splay-List: A Distribution-Adaptive Concurrent
    Skip-List.” <i>Distributed Computing</i>, vol. 36, Springer Nature, 2023, pp.
    395–418, doi:<a href="https://doi.org/10.1007/s00446-022-00441-x">10.1007/s00446-022-00441-x</a>.'
  short: V. Aksenov, D.-A. Alistarh, A. Drozdova, A. Mohtashami, Distributed Computing
    36 (2023) 395–418.
date_created: 2023-01-22T23:00:55Z
date_published: 2023-09-01T00:00:00Z
date_updated: 2025-07-22T14:06:00Z
day: '01'
department:
- _id: DaAl
doi: 10.1007/s00446-022-00441-x
external_id:
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  - '2008.01009'
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  - '000913424000001'
  oaworkID:
  - w4390499170
intvolume: '        36'
isi: 1
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.2008.01009
month: '09'
oa: 1
oa_version: Preprint
oaworkID: 1
page: 395-418
publication: Distributed Computing
publication_identifier:
  eissn:
  - 1432-0452
  issn:
  - 0178-2770
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'The splay-list: A distribution-adaptive concurrent skip-list'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 36
year: '2023'
...
---
_id: '12331'
abstract:
- lang: eng
  text: High carrier mobility is critical to improving thermoelectric performance
    over a broad temperature range. However, traditional doping inevitably deteriorates
    carrier mobility. Herein, we develop a strategy for fine tuning of defects to
    improve carrier mobility. To begin, n-type PbTe is created by compensating for
    the intrinsic Pb vacancy in bare PbTe. Excess Pb2+ reduces vacancy scattering,
    resulting in a high carrier mobility of ∼3400 cm2 V–1 s–1. Then, excess Ag is
    introduced to compensate for the remaining intrinsic Pb vacancies. We find that
    excess Ag exhibits a dynamic doping process with increasing temperatures, increasing
    both the carrier concentration and carrier mobility throughout a wide temperature
    range; specifically, an ultrahigh carrier mobility ∼7300 cm2 V–1 s–1 is obtained
    for Pb1.01Te + 0.002Ag at 300 K. Moreover, the dynamic doping-induced high carrier
    concentration suppresses the bipolar thermal conductivity at high temperatures.
    The final step is using iodine to optimize the carrier concentration to ∼1019
    cm–3. Ultimately, a maximum ZT value of ∼1.5 and a large average ZTave value of
    ∼1.0 at 300–773 K are obtained for Pb1.01Te0.998I0.002 + 0.002Ag. These findings
    demonstrate that fine tuning of defects with <0.5% impurities can remarkably enhance
    carrier mobility and improve thermoelectric performance.
acknowledgement: The National Key Research and Development Program of China (2018YFA0702100),
  the Basic Science Center Project of the National Natural Science Foundation of China
  (51788104), the National Natural Science Foundation of China (51571007 and 51772012),
  the Beijing Natural Science Foundation (JQ18004), the 111 Project (B17002), the
  National Science Fund for Distinguished Young Scholars (51925101), and the FWF “Lise
  Meitner Fellowship” (grant agreement M2889-N). Open Access is funded by the Austrian
  Science Fund (FWF).
article_processing_charge: No
article_type: original
author:
- first_name: Siqi
  full_name: Wang, Siqi
  last_name: Wang
- first_name: Cheng
  full_name: Chang, Cheng
  id: 9E331C2E-9F27-11E9-AE48-5033E6697425
  last_name: Chang
  orcid: 0000-0002-9515-4277
- first_name: Shulin
  full_name: Bai, Shulin
  last_name: Bai
- first_name: Bingchao
  full_name: Qin, Bingchao
  last_name: Qin
- first_name: Yingcai
  full_name: Zhu, Yingcai
  last_name: Zhu
- first_name: Shaoping
  full_name: Zhan, Shaoping
  last_name: Zhan
- first_name: Junqing
  full_name: Zheng, Junqing
  last_name: Zheng
- first_name: Shuwei
  full_name: Tang, Shuwei
  last_name: Tang
- first_name: Li Dong
  full_name: Zhao, Li Dong
  last_name: Zhao
citation:
  ama: Wang S, Chang C, Bai S, et al. Fine tuning of defects enables high carrier
    mobility and enhanced thermoelectric performance of n-type PbTe. <i>Chemistry
    of Materials</i>. 2023;35(2):755-763. doi:<a href="https://doi.org/10.1021/acs.chemmater.2c03542">10.1021/acs.chemmater.2c03542</a>
  apa: Wang, S., Chang, C., Bai, S., Qin, B., Zhu, Y., Zhan, S., … Zhao, L. D. (2023).
    Fine tuning of defects enables high carrier mobility and enhanced thermoelectric
    performance of n-type PbTe. <i>Chemistry of Materials</i>. American Chemical Society.
    <a href="https://doi.org/10.1021/acs.chemmater.2c03542">https://doi.org/10.1021/acs.chemmater.2c03542</a>
  chicago: Wang, Siqi, Cheng Chang, Shulin Bai, Bingchao Qin, Yingcai Zhu, Shaoping
    Zhan, Junqing Zheng, Shuwei Tang, and Li Dong Zhao. “Fine Tuning of Defects Enables
    High Carrier Mobility and Enhanced Thermoelectric Performance of N-Type PbTe.”
    <i>Chemistry of Materials</i>. American Chemical Society, 2023. <a href="https://doi.org/10.1021/acs.chemmater.2c03542">https://doi.org/10.1021/acs.chemmater.2c03542</a>.
  ieee: S. Wang <i>et al.</i>, “Fine tuning of defects enables high carrier mobility
    and enhanced thermoelectric performance of n-type PbTe,” <i>Chemistry of Materials</i>,
    vol. 35, no. 2. American Chemical Society, pp. 755–763, 2023.
  ista: Wang S, Chang C, Bai S, Qin B, Zhu Y, Zhan S, Zheng J, Tang S, Zhao LD. 2023.
    Fine tuning of defects enables high carrier mobility and enhanced thermoelectric
    performance of n-type PbTe. Chemistry of Materials. 35(2), 755–763.
  mla: Wang, Siqi, et al. “Fine Tuning of Defects Enables High Carrier Mobility and
    Enhanced Thermoelectric Performance of N-Type PbTe.” <i>Chemistry of Materials</i>,
    vol. 35, no. 2, American Chemical Society, 2023, pp. 755–63, doi:<a href="https://doi.org/10.1021/acs.chemmater.2c03542">10.1021/acs.chemmater.2c03542</a>.
  short: S. Wang, C. Chang, S. Bai, B. Qin, Y. Zhu, S. Zhan, J. Zheng, S. Tang, L.D.
    Zhao, Chemistry of Materials 35 (2023) 755–763.
date_created: 2023-01-22T23:00:55Z
date_published: 2023-01-24T00:00:00Z
date_updated: 2023-08-14T12:57:44Z
day: '24'
ddc:
- '540'
department:
- _id: MaIb
doi: 10.1021/acs.chemmater.2c03542
external_id:
  isi:
  - '000914749700001'
file:
- access_level: open_access
  checksum: b21dca2aa7a80c068bc256bdd1fea9df
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  date_created: 2023-08-14T12:57:25Z
  date_updated: 2023-08-14T12:57:25Z
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file_date_updated: 2023-08-14T12:57:25Z
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language:
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month: '01'
oa: 1
oa_version: Published Version
page: 755-763
project:
- _id: 9B8804FC-BA93-11EA-9121-9846C619BF3A
  grant_number: M02889
  name: Bottom-up Engineering for Thermoelectric Applications
publication: Chemistry of Materials
publication_identifier:
  eissn:
  - 1520-5002
  issn:
  - 0897-4756
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Fine tuning of defects enables high carrier mobility and enhanced thermoelectric
  performance of n-type PbTe
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 35
year: '2023'
...
