---
_id: '8570'
abstract:
- lang: eng
  text: 'This report presents the results of a friendly competition for formal verification
    of continuous and hybrid systems with linear continuous dynamics. The friendly
    competition took place as part of the workshop Applied Verification for Continuous
    and Hybrid Systems (ARCH) in 2019. In its third edition, seven tools have been
    applied to solve six different benchmark problems in the category for linear continuous
    dynamics (in alphabetical order): CORA, CORA/SX, HyDRA, Hylaa, JuliaReach, SpaceEx,
    and XSpeed. This report is a snapshot of the current landscape of tools and the
    types of benchmarks they are particularly suited for. Due to the diversity of
    problems, we are not ranking tools, yet the presented results provide one of the
    most complete assessments of tools for the safety verification of continuous and
    hybrid systems with linear continuous dynamics up to this date.</jats:p>'
article_processing_charge: No
author:
- first_name: Matthias
  full_name: Althoff, Matthias
  last_name: Althoff
- first_name: Stanley
  full_name: Bak, Stanley
  last_name: Bak
- first_name: Marcelo
  full_name: Forets, Marcelo
  last_name: Forets
- first_name: Goran
  full_name: Frehse, Goran
  last_name: Frehse
- first_name: Niklas
  full_name: Kochdumper, Niklas
  last_name: Kochdumper
- first_name: Rajarshi
  full_name: Ray, Rajarshi
  last_name: Ray
- first_name: Christian
  full_name: Schilling, Christian
  id: 3A2F4DCE-F248-11E8-B48F-1D18A9856A87
  last_name: Schilling
  orcid: 0000-0003-3658-1065
- first_name: Stefan
  full_name: Schupp, Stefan
  last_name: Schupp
citation:
  ama: 'Althoff M, Bak S, Forets M, et al. ARCH-COMP19 Category Report: Continuous
    and hybrid systems with linear continuous dynamics. In: <i>EPiC Series in Computing</i>.
    Vol 61. EasyChair; 2019:14-40. doi:<a href="https://doi.org/10.29007/bj1w">10.29007/bj1w</a>'
  apa: 'Althoff, M., Bak, S., Forets, M., Frehse, G., Kochdumper, N., Ray, R., … Schupp,
    S. (2019). ARCH-COMP19 Category Report: Continuous and hybrid systems with linear
    continuous dynamics. In <i>EPiC Series in Computing</i> (Vol. 61, pp. 14–40).
    Montreal, Canada: EasyChair. <a href="https://doi.org/10.29007/bj1w">https://doi.org/10.29007/bj1w</a>'
  chicago: 'Althoff, Matthias, Stanley Bak, Marcelo Forets, Goran Frehse, Niklas Kochdumper,
    Rajarshi Ray, Christian Schilling, and Stefan Schupp. “ARCH-COMP19 Category Report:
    Continuous and Hybrid Systems with Linear Continuous Dynamics.” In <i>EPiC Series
    in Computing</i>, 61:14–40. EasyChair, 2019. <a href="https://doi.org/10.29007/bj1w">https://doi.org/10.29007/bj1w</a>.'
  ieee: 'M. Althoff <i>et al.</i>, “ARCH-COMP19 Category Report: Continuous and hybrid
    systems with linear continuous dynamics,” in <i>EPiC Series in Computing</i>,
    Montreal, Canada, 2019, vol. 61, pp. 14–40.'
  ista: 'Althoff M, Bak S, Forets M, Frehse G, Kochdumper N, Ray R, Schilling C, Schupp
    S. 2019. ARCH-COMP19 Category Report: Continuous and hybrid systems with linear
    continuous dynamics. EPiC Series in Computing. ARCH: International Workshop on
    Applied Verification on Continuous and Hybrid Systems vol. 61, 14–40.'
  mla: 'Althoff, Matthias, et al. “ARCH-COMP19 Category Report: Continuous and Hybrid
    Systems with Linear Continuous Dynamics.” <i>EPiC Series in Computing</i>, vol.
    61, EasyChair, 2019, pp. 14–40, doi:<a href="https://doi.org/10.29007/bj1w">10.29007/bj1w</a>.'
  short: M. Althoff, S. Bak, M. Forets, G. Frehse, N. Kochdumper, R. Ray, C. Schilling,
    S. Schupp, in:, EPiC Series in Computing, EasyChair, 2019, pp. 14–40.
conference:
  end_date: 2019-04-15
  location: Montreal, Canada
  name: 'ARCH: International Workshop on Applied Verification on Continuous and Hybrid
    Systems'
  start_date: 2019-04-15
corr_author: '1'
date_created: 2020-09-26T14:23:54Z
date_published: 2019-05-25T00:00:00Z
date_updated: 2026-06-18T19:33:41Z
day: '25'
ddc:
- '000'
department:
- _id: ToHe
doi: 10.29007/bj1w
intvolume: '        61'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://easychair.org/publications/open/1gbP
month: '05'
oa: 1
oa_version: Published Version
page: 14-40
publication: EPiC Series in Computing
publication_identifier:
  eissn:
  - 2398-7340
publication_status: published
publisher: EasyChair
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'ARCH-COMP19 Category Report: Continuous and hybrid systems with linear continuous
  dynamics'
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 61
year: '2019'
...
---
_id: '8693'
abstract:
- lang: eng
  text: We review V. I. Arnold’s 1963 celebrated paper [1] Proof of A. N. Kolmogorov’s
    Theorem on the Conservation of Conditionally Periodic Motions with a Small Variation
    in the Hamiltonian, and prove that, optimising Arnold’s scheme, one can get “sharp”
    asymptotic quantitative conditions (as ε → 0, ε being the strength of the perturbation).
    All constants involved are explicitly computed.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Luigi
  full_name: Chierchia, Luigi
  last_name: Chierchia
- first_name: Edmond
  full_name: Koudjinan, Edmond
  id: 52DF3E68-AEFA-11EA-95A4-124A3DDC885E
  last_name: Koudjinan
  orcid: 0000-0003-2640-4049
citation:
  ama: Chierchia L, Koudjinan E. V. I. Arnold’s “pointwise” KAM theorem. <i>Regular
    and Chaotic Dynamics</i>. 2019;24:583–606. doi:<a href="https://doi.org/10.1134/S1560354719060017">10.1134/S1560354719060017</a>
  apa: Chierchia, L., &#38; Koudjinan, E. (2019). V. I. Arnold’s “pointwise” KAM theorem.
    <i>Regular and Chaotic Dynamics</i>. Springer. <a href="https://doi.org/10.1134/S1560354719060017">https://doi.org/10.1134/S1560354719060017</a>
  chicago: Chierchia, Luigi, and Edmond Koudjinan. “V. I. Arnold’s ‘Pointwise’ KAM
    Theorem.” <i>Regular and Chaotic Dynamics</i>. Springer, 2019. <a href="https://doi.org/10.1134/S1560354719060017">https://doi.org/10.1134/S1560354719060017</a>.
  ieee: L. Chierchia and E. Koudjinan, “V. I. Arnold’s ‘pointwise’ KAM theorem,” <i>Regular
    and Chaotic Dynamics</i>, vol. 24. Springer, pp. 583–606, 2019.
  ista: Chierchia L, Koudjinan E. 2019. V. I. Arnold’s “pointwise” KAM theorem. Regular
    and Chaotic Dynamics. 24, 583–606.
  mla: Chierchia, Luigi, and Edmond Koudjinan. “V. I. Arnold’s ‘Pointwise’ KAM Theorem.”
    <i>Regular and Chaotic Dynamics</i>, vol. 24, Springer, 2019, pp. 583–606, doi:<a
    href="https://doi.org/10.1134/S1560354719060017">10.1134/S1560354719060017</a>.
  short: L. Chierchia, E. Koudjinan, Regular and Chaotic Dynamics 24 (2019) 583–606.
date_created: 2020-10-21T15:25:45Z
date_published: 2019-12-10T00:00:00Z
date_updated: 2021-01-12T08:20:34Z
day: '10'
doi: 10.1134/S1560354719060017
extern: '1'
external_id:
  arxiv:
  - '1908.02523'
intvolume: '        24'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1908.02523
month: '12'
oa: 1
oa_version: Preprint
page: 583–606
publication: Regular and Chaotic Dynamics
publication_status: published
publisher: Springer
quality_controlled: '1'
status: public
title: V. I. Arnold’s “pointwise” KAM theorem
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 24
year: '2019'
...
---
_id: '9016'
abstract:
- lang: eng
  text: Inhibiting the histone H3–ASF1 (anti‐silencing function 1) protein–protein
    interaction (PPI) represents a potential approach for treating numerous cancers.
    As an α‐helix‐mediated PPI, constraining the key histone H3 helix (residues 118–135)
    is a strategy through which chemical probes might be elaborated to test this hypothesis.
    In this work, variant H3118–135 peptides bearing pentenylglycine residues at the
    i and i+4 positions were constrained by olefin metathesis. Biophysical analyses
    revealed that promotion of a bioactive helical conformation depends on the position
    at which the constraint is introduced, but that the potency of binding towards
    ASF1 is unaffected by the constraint and instead that enthalpy–entropy compensation
    occurs.
article_processing_charge: No
article_type: original
author:
- first_name: May M
  full_name: Bakail, May M
  id: FB3C3F8E-522F-11EA-B186-22963DDC885E
  last_name: Bakail
  orcid: 0000-0002-9592-1587
- first_name: Silvia
  full_name: Rodriguez‐Marin, Silvia
  last_name: Rodriguez‐Marin
- first_name: Zsófia
  full_name: Hegedüs, Zsófia
  last_name: Hegedüs
- first_name: Marie E.
  full_name: Perrin, Marie E.
  last_name: Perrin
- first_name: Françoise
  full_name: Ochsenbein, Françoise
  last_name: Ochsenbein
- first_name: Andrew J.
  full_name: Wilson, Andrew J.
  last_name: Wilson
citation:
  ama: Bakail MM, Rodriguez‐Marin S, Hegedüs Z, Perrin ME, Ochsenbein F, Wilson AJ.
    Recognition of ASF1 by using hydrocarbon‐constrained peptides. <i>ChemBioChem</i>.
    2019;20(7):891-895. doi:<a href="https://doi.org/10.1002/cbic.201800633">10.1002/cbic.201800633</a>
  apa: Bakail, M. M., Rodriguez‐Marin, S., Hegedüs, Z., Perrin, M. E., Ochsenbein,
    F., &#38; Wilson, A. J. (2019). Recognition of ASF1 by using hydrocarbon‐constrained
    peptides. <i>ChemBioChem</i>. Wiley. <a href="https://doi.org/10.1002/cbic.201800633">https://doi.org/10.1002/cbic.201800633</a>
  chicago: Bakail, May M, Silvia Rodriguez‐Marin, Zsófia Hegedüs, Marie E. Perrin,
    Françoise Ochsenbein, and Andrew J. Wilson. “Recognition of ASF1 by Using Hydrocarbon‐constrained
    Peptides.” <i>ChemBioChem</i>. Wiley, 2019. <a href="https://doi.org/10.1002/cbic.201800633">https://doi.org/10.1002/cbic.201800633</a>.
  ieee: M. M. Bakail, S. Rodriguez‐Marin, Z. Hegedüs, M. E. Perrin, F. Ochsenbein,
    and A. J. Wilson, “Recognition of ASF1 by using hydrocarbon‐constrained peptides,”
    <i>ChemBioChem</i>, vol. 20, no. 7. Wiley, pp. 891–895, 2019.
  ista: Bakail MM, Rodriguez‐Marin S, Hegedüs Z, Perrin ME, Ochsenbein F, Wilson AJ.
    2019. Recognition of ASF1 by using hydrocarbon‐constrained peptides. ChemBioChem.
    20(7), 891–895.
  mla: Bakail, May M., et al. “Recognition of ASF1 by Using Hydrocarbon‐constrained
    Peptides.” <i>ChemBioChem</i>, vol. 20, no. 7, Wiley, 2019, pp. 891–95, doi:<a
    href="https://doi.org/10.1002/cbic.201800633">10.1002/cbic.201800633</a>.
  short: M.M. Bakail, S. Rodriguez‐Marin, Z. Hegedüs, M.E. Perrin, F. Ochsenbein,
    A.J. Wilson, ChemBioChem 20 (2019) 891–895.
date_created: 2021-01-19T10:59:14Z
date_published: 2019-04-01T00:00:00Z
date_updated: 2023-02-23T13:46:48Z
day: '01'
doi: 10.1002/cbic.201800633
extern: '1'
intvolume: '        20'
issue: '7'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: ' https://doi.org/10.1002/cbic.201800633'
month: '04'
oa: 1
oa_version: Published Version
page: 891-895
publication: ChemBioChem
publication_identifier:
  issn:
  - 1439-4227
  - 1439-7633
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Recognition of ASF1 by using hydrocarbon‐constrained peptides
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 20
year: '2019'
...
---
_id: '9018'
abstract:
- lang: eng
  text: Anti-silencing function 1 (ASF1) is a conserved H3-H4 histone chaperone involved
    in histone dynamics during replication, transcription, and DNA repair. Overexpressed
    in proliferating tissues including many tumors, ASF1 has emerged as a promising
    therapeutic target. Here, we combine structural, computational, and biochemical
    approaches to design peptides that inhibit the ASF1-histone interaction. Starting
    from the structure of the human ASF1-histone complex, we developed a rational
    design strategy combining epitope tethering and optimization of interface contacts
    to identify a potent peptide inhibitor with a dissociation constant of 3 nM. When
    introduced into cultured cells, the inhibitors impair cell proliferation, perturb
    cell-cycle progression, and reduce cell migration and invasion in a manner commensurate
    with their affinity for ASF1. Finally, we find that direct injection of the most
    potent ASF1 peptide inhibitor in mouse allografts reduces tumor growth. Our results
    open new avenues to use ASF1 inhibitors as promising leads for cancer therapy.
article_processing_charge: No
article_type: original
author:
- first_name: May M
  full_name: Bakail, May M
  id: FB3C3F8E-522F-11EA-B186-22963DDC885E
  last_name: Bakail
  orcid: 0000-0002-9592-1587
- first_name: Albane
  full_name: Gaubert, Albane
  last_name: Gaubert
- first_name: Jessica
  full_name: Andreani, Jessica
  last_name: Andreani
- first_name: Gwenaëlle
  full_name: Moal, Gwenaëlle
  last_name: Moal
- first_name: Guillaume
  full_name: Pinna, Guillaume
  last_name: Pinna
- first_name: Ekaterina
  full_name: Boyarchuk, Ekaterina
  last_name: Boyarchuk
- first_name: Marie-Cécile
  full_name: Gaillard, Marie-Cécile
  last_name: Gaillard
- first_name: Regis
  full_name: Courbeyrette, Regis
  last_name: Courbeyrette
- first_name: Carl
  full_name: Mann, Carl
  last_name: Mann
- first_name: Jean-Yves
  full_name: Thuret, Jean-Yves
  last_name: Thuret
- first_name: Bérengère
  full_name: Guichard, Bérengère
  last_name: Guichard
- first_name: Brice
  full_name: Murciano, Brice
  last_name: Murciano
- first_name: Nicolas
  full_name: Richet, Nicolas
  last_name: Richet
- first_name: Adeline
  full_name: Poitou, Adeline
  last_name: Poitou
- first_name: Claire
  full_name: Frederic, Claire
  last_name: Frederic
- first_name: Marie-Hélène
  full_name: Le Du, Marie-Hélène
  last_name: Le Du
- first_name: Morgane
  full_name: Agez, Morgane
  last_name: Agez
- first_name: Caroline
  full_name: Roelants, Caroline
  last_name: Roelants
- first_name: Zachary A.
  full_name: Gurard-Levin, Zachary A.
  last_name: Gurard-Levin
- first_name: Geneviève
  full_name: Almouzni, Geneviève
  last_name: Almouzni
- first_name: Nadia
  full_name: Cherradi, Nadia
  last_name: Cherradi
- first_name: Raphael
  full_name: Guerois, Raphael
  last_name: Guerois
- first_name: Françoise
  full_name: Ochsenbein, Françoise
  last_name: Ochsenbein
citation:
  ama: Bakail MM, Gaubert A, Andreani J, et al. Design on a rational basis of high-affinity
    peptides inhibiting the histone chaperone ASF1. <i>Cell Chemical Biology</i>.
    2019;26(11):1573-1585.e10. doi:<a href="https://doi.org/10.1016/j.chembiol.2019.09.002">10.1016/j.chembiol.2019.09.002</a>
  apa: Bakail, M. M., Gaubert, A., Andreani, J., Moal, G., Pinna, G., Boyarchuk, E.,
    … Ochsenbein, F. (2019). Design on a rational basis of high-affinity peptides
    inhibiting the histone chaperone ASF1. <i>Cell Chemical Biology</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.chembiol.2019.09.002">https://doi.org/10.1016/j.chembiol.2019.09.002</a>
  chicago: Bakail, May M, Albane Gaubert, Jessica Andreani, Gwenaëlle Moal, Guillaume
    Pinna, Ekaterina Boyarchuk, Marie-Cécile Gaillard, et al. “Design on a Rational
    Basis of High-Affinity Peptides Inhibiting the Histone Chaperone ASF1.” <i>Cell
    Chemical Biology</i>. Elsevier, 2019. <a href="https://doi.org/10.1016/j.chembiol.2019.09.002">https://doi.org/10.1016/j.chembiol.2019.09.002</a>.
  ieee: M. M. Bakail <i>et al.</i>, “Design on a rational basis of high-affinity peptides
    inhibiting the histone chaperone ASF1,” <i>Cell Chemical Biology</i>, vol. 26,
    no. 11. Elsevier, p. 1573–1585.e10, 2019.
  ista: Bakail MM, Gaubert A, Andreani J, Moal G, Pinna G, Boyarchuk E, Gaillard M-C,
    Courbeyrette R, Mann C, Thuret J-Y, Guichard B, Murciano B, Richet N, Poitou A,
    Frederic C, Le Du M-H, Agez M, Roelants C, Gurard-Levin ZA, Almouzni G, Cherradi
    N, Guerois R, Ochsenbein F. 2019. Design on a rational basis of high-affinity
    peptides inhibiting the histone chaperone ASF1. Cell Chemical Biology. 26(11),
    1573–1585.e10.
  mla: Bakail, May M., et al. “Design on a Rational Basis of High-Affinity Peptides
    Inhibiting the Histone Chaperone ASF1.” <i>Cell Chemical Biology</i>, vol. 26,
    no. 11, Elsevier, 2019, p. 1573–1585.e10, doi:<a href="https://doi.org/10.1016/j.chembiol.2019.09.002">10.1016/j.chembiol.2019.09.002</a>.
  short: M.M. Bakail, A. Gaubert, J. Andreani, G. Moal, G. Pinna, E. Boyarchuk, M.-C.
    Gaillard, R. Courbeyrette, C. Mann, J.-Y. Thuret, B. Guichard, B. Murciano, N.
    Richet, A. Poitou, C. Frederic, M.-H. Le Du, M. Agez, C. Roelants, Z.A. Gurard-Levin,
    G. Almouzni, N. Cherradi, R. Guerois, F. Ochsenbein, Cell Chemical Biology 26
    (2019) 1573–1585.e10.
date_created: 2021-01-19T11:04:50Z
date_published: 2019-11-21T00:00:00Z
date_updated: 2023-02-23T13:46:53Z
day: '21'
doi: 10.1016/j.chembiol.2019.09.002
extern: '1'
external_id:
  pmid:
  - '31543461'
intvolume: '        26'
issue: '11'
keyword:
- Clinical Biochemistry
- Molecular Medicine
- Biochemistry
- Molecular Biology
- Pharmacology
- Drug Discovery
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.chembiol.2019.09.002
month: '11'
oa: 1
oa_version: Published Version
page: 1573-1585.e10
pmid: 1
publication: Cell Chemical Biology
publication_identifier:
  issn:
  - 2451-9456
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: Design on a rational basis of high-affinity peptides inhibiting the histone
  chaperone ASF1
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 26
year: '2019'
...
---
_id: '9060'
abstract:
- lang: eng
  text: Molecular motors are essential to the living, generating fluctuations that
    boost transport and assist assembly. Active colloids, that consume energy to move,
    hold similar potential for man-made materials controlled by forces generated from
    within. Yet, their use as a powerhouse in materials science lacks. Here we show
    a massive acceleration of the annealing of a monolayer of passive beads by moderate
    addition of self-propelled microparticles. We rationalize our observations with
    a model of collisions that drive active fluctuations and activate the annealing.
    The experiment is quantitatively compared with Brownian dynamic simulations that
    further unveil a dynamical transition in the mechanism of annealing. Active dopants
    travel uniformly in the system or co-localize at the grain boundaries as a result
    of the persistence of their motion. Our findings uncover the potential of internal
    activity to control materials and lay the groundwork for the rise of materials
    science beyond equilibrium.
article_number: '3380'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Sophie
  full_name: Ramananarivo, Sophie
  last_name: Ramananarivo
- first_name: Etienne
  full_name: Ducrot, Etienne
  last_name: Ducrot
- first_name: Jérémie A
  full_name: Palacci, Jérémie A
  id: 8fb92548-2b22-11eb-b7c1-a3f0d08d7c7d
  last_name: Palacci
  orcid: 0000-0002-7253-9465
citation:
  ama: Ramananarivo S, Ducrot E, Palacci JA. Activity-controlled annealing of colloidal
    monolayers. <i>Nature Communications</i>. 2019;10(1). doi:<a href="https://doi.org/10.1038/s41467-019-11362-y">10.1038/s41467-019-11362-y</a>
  apa: Ramananarivo, S., Ducrot, E., &#38; Palacci, J. A. (2019). Activity-controlled
    annealing of colloidal monolayers. <i>Nature Communications</i>. Springer Nature.
    <a href="https://doi.org/10.1038/s41467-019-11362-y">https://doi.org/10.1038/s41467-019-11362-y</a>
  chicago: Ramananarivo, Sophie, Etienne Ducrot, and Jérémie A Palacci. “Activity-Controlled
    Annealing of Colloidal Monolayers.” <i>Nature Communications</i>. Springer Nature,
    2019. <a href="https://doi.org/10.1038/s41467-019-11362-y">https://doi.org/10.1038/s41467-019-11362-y</a>.
  ieee: S. Ramananarivo, E. Ducrot, and J. A. Palacci, “Activity-controlled annealing
    of colloidal monolayers,” <i>Nature Communications</i>, vol. 10, no. 1. Springer
    Nature, 2019.
  ista: Ramananarivo S, Ducrot E, Palacci JA. 2019. Activity-controlled annealing
    of colloidal monolayers. Nature Communications. 10(1), 3380.
  mla: Ramananarivo, Sophie, et al. “Activity-Controlled Annealing of Colloidal Monolayers.”
    <i>Nature Communications</i>, vol. 10, no. 1, 3380, Springer Nature, 2019, doi:<a
    href="https://doi.org/10.1038/s41467-019-11362-y">10.1038/s41467-019-11362-y</a>.
  short: S. Ramananarivo, E. Ducrot, J.A. Palacci, Nature Communications 10 (2019).
date_created: 2021-02-02T13:43:36Z
date_published: 2019-07-29T00:00:00Z
date_updated: 2023-02-23T13:47:59Z
day: '29'
ddc:
- '530'
doi: 10.1038/s41467-019-11362-y
extern: '1'
external_id:
  arxiv:
  - '1909.07382'
  pmid:
  - '31358762'
file:
- access_level: open_access
  checksum: 70c6e5d6fbea0932b0669505ab6633ec
  content_type: application/pdf
  creator: cziletti
  date_created: 2021-02-02T13:47:21Z
  date_updated: 2021-02-02T13:47:21Z
  file_id: '9061'
  file_name: 2019_NatureComm_Ramananarivo.pdf
  file_size: 2820337
  relation: main_file
  success: 1
file_date_updated: 2021-02-02T13:47:21Z
has_accepted_license: '1'
intvolume: '        10'
issue: '1'
keyword:
- General Biochemistry
- Genetics and Molecular Biology
- General Physics and Astronomy
- General Chemistry
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
  issn:
  - 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Activity-controlled annealing of colloidal monolayers
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 10
year: '2019'
...
---
_id: '9261'
abstract:
- lang: eng
  text: 'Bending-active structures are able to efficiently produce complex curved
    shapes starting from flat panels. The desired deformation of the panels derives
    from the proper selection of their elastic properties. Optimized panels, called
    FlexMaps, are designed such that, once they are bent and assembled, the resulting
    static equilibrium configuration matches a desired input 3D shape. The FlexMaps
    elastic properties are controlled by locally varying spiraling geometric mesostructures,
    which are optimized in size and shape to match the global curvature (i.e., bending
    requests) of the target shape. The design pipeline starts from a quad mesh representing
    the input 3D shape, which defines the edge size and the total amount of spirals:
    every quad will embed one spiral. Then, an optimization algorithm tunes the geometry
    of the spirals by using a simplified pre-computed rod model. This rod model is
    derived from a non-linear regression algorithm which approximates the non-linear
    behavior of solid FEM spiral models subject to hundreds of load combinations.
    This innovative pipeline has been applied to the project of a lightweight plywood
    pavilion named FlexMaps Pavilion, which is a single-layer piecewise twisted arc
    that fits a bounding box of 3.90x3.96x3.25 meters.'
article_processing_charge: No
author:
- first_name: Francesco
  full_name: Laccone, Francesco
  last_name: Laccone
- first_name: Luigi
  full_name: Malomo, Luigi
  last_name: Malomo
- first_name: Jesus
  full_name: Perez Rodriguez, Jesus
  id: 2DC83906-F248-11E8-B48F-1D18A9856A87
  last_name: Perez Rodriguez
- first_name: Nico
  full_name: Pietroni, Nico
  last_name: Pietroni
- first_name: Federico
  full_name: Ponchio, Federico
  last_name: Ponchio
- first_name: Bernd
  full_name: Bickel, Bernd
  id: 49876194-F248-11E8-B48F-1D18A9856A87
  last_name: Bickel
  orcid: 0000-0001-6511-9385
- first_name: Paolo
  full_name: Cignoni, Paolo
  last_name: Cignoni
citation:
  ama: 'Laccone F, Malomo L, Perez Rodriguez J, et al. FlexMaps Pavilion: A twisted
    arc made of mesostructured flat flexible panels. In: <i>IASS Symposium 2019 -
    60th Anniversary Symposium of the International Association for Shell and Spatial
    Structures; Structural Membranes 2019 - 9th International Conference on Textile
    Composites and Inflatable Structures, FORM and FORCE</i>. International Center
    for Numerical Methods in Engineering; 2019:509-515.'
  apa: 'Laccone, F., Malomo, L., Perez Rodriguez, J., Pietroni, N., Ponchio, F., Bickel,
    B., &#38; Cignoni, P. (2019). FlexMaps Pavilion: A twisted arc made of mesostructured
    flat flexible panels. In <i>IASS Symposium 2019 - 60th Anniversary Symposium of
    the International Association for Shell and Spatial Structures; Structural Membranes
    2019 - 9th International Conference on Textile Composites and Inflatable Structures,
    FORM and FORCE</i> (pp. 509–515). Barcelona, Spain: International Center for Numerical
    Methods in Engineering.'
  chicago: 'Laccone, Francesco, Luigi Malomo, Jesus Perez Rodriguez, Nico Pietroni,
    Federico Ponchio, Bernd Bickel, and Paolo Cignoni. “FlexMaps Pavilion: A Twisted
    Arc Made of Mesostructured Flat Flexible Panels.” In <i>IASS Symposium 2019 -
    60th Anniversary Symposium of the International Association for Shell and Spatial
    Structures; Structural Membranes 2019 - 9th International Conference on Textile
    Composites and Inflatable Structures, FORM and FORCE</i>, 509–15. International
    Center for Numerical Methods in Engineering, 2019.'
  ieee: 'F. Laccone <i>et al.</i>, “FlexMaps Pavilion: A twisted arc made of mesostructured
    flat flexible panels,” in <i>IASS Symposium 2019 - 60th Anniversary Symposium
    of the International Association for Shell and Spatial Structures; Structural
    Membranes 2019 - 9th International Conference on Textile Composites and Inflatable
    Structures, FORM and FORCE</i>, Barcelona, Spain, 2019, pp. 509–515.'
  ista: 'Laccone F, Malomo L, Perez Rodriguez J, Pietroni N, Ponchio F, Bickel B,
    Cignoni P. 2019. FlexMaps Pavilion: A twisted arc made of mesostructured flat
    flexible panels. IASS Symposium 2019 - 60th Anniversary Symposium of the International
    Association for Shell and Spatial Structures; Structural Membranes 2019 - 9th
    International Conference on Textile Composites and Inflatable Structures, FORM
    and FORCE. IASS: International Association for Shell and Spatial Structures, 509–515.'
  mla: 'Laccone, Francesco, et al. “FlexMaps Pavilion: A Twisted Arc Made of Mesostructured
    Flat Flexible Panels.” <i>IASS Symposium 2019 - 60th Anniversary Symposium of
    the International Association for Shell and Spatial Structures; Structural Membranes
    2019 - 9th International Conference on Textile Composites and Inflatable Structures,
    FORM and FORCE</i>, International Center for Numerical Methods in Engineering,
    2019, pp. 509–15.'
  short: F. Laccone, L. Malomo, J. Perez Rodriguez, N. Pietroni, F. Ponchio, B. Bickel,
    P. Cignoni, in:, IASS Symposium 2019 - 60th Anniversary Symposium of the International
    Association for Shell and Spatial Structures; Structural Membranes 2019 - 9th
    International Conference on Textile Composites and Inflatable Structures, FORM
    and FORCE, International Center for Numerical Methods in Engineering, 2019, pp.
    509–515.
conference:
  end_date: 2019-10-10
  location: Barcelona, Spain
  name: 'IASS: International Association for Shell and Spatial Structures'
  start_date: 2019-10-07
date_created: 2021-03-21T23:01:21Z
date_published: 2019-10-10T00:00:00Z
date_updated: 2023-09-08T11:21:54Z
day: '10'
department:
- _id: BeBi
external_id:
  isi:
  - '000563497600059'
isi: 1
language:
- iso: eng
month: '10'
oa_version: None
page: 509-515
publication: IASS Symposium 2019 - 60th Anniversary Symposium of the International
  Association for Shell and Spatial Structures; Structural Membranes 2019 - 9th International
  Conference on Textile Composites and Inflatable Structures, FORM and FORCE
publication_identifier:
  isbn:
  - '9788412110104'
  issn:
  - 2518-6582
publication_status: published
publisher: International Center for Numerical Methods in Engineering
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'FlexMaps Pavilion: A twisted arc made of mesostructured flat flexible panels'
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
year: '2019'
...
---
_id: '9460'
abstract:
- lang: eng
  text: Epigenetic reprogramming is required for proper regulation of gene expression
    in eukaryotic organisms. In Arabidopsis, active DNA demethylation is crucial for
    seed viability, pollen function, and successful reproduction. The DEMETER (DME)
    DNA glycosylase initiates localized DNA demethylation in vegetative and central
    cells, so-called companion cells that are adjacent to sperm and egg gametes, respectively.
    In rice, the central cell genome displays local DNA hypomethylation, suggesting
    that active DNA demethylation also occurs in rice; however, the enzyme responsible
    for this process is unknown. One candidate is the rice REPRESSOR OF SILENCING
    1a (ROS1a) gene, which is related to DME and is essential for rice seed viability
    and pollen function. Here, we report genome-wide analyses of DNA methylation in
    wild-type and ros1a mutant sperm and vegetative cells. We find that the rice vegetative
    cell genome is locally hypomethylated compared with sperm by a process that requires
    ROS1a activity. We show that many ROS1a target sequences in the vegetative cell
    are hypomethylated in the rice central cell, suggesting that ROS1a also demethylates
    the central cell genome. Similar to Arabidopsis, we show that sperm non-CG methylation
    is indirectly promoted by DNA demethylation in the vegetative cell. These results
    reveal that DNA glycosylase-mediated DNA demethylation processes are conserved
    in Arabidopsis and rice, plant species that diverged 150 million years ago. Finally,
    although global non-CG methylation levels of sperm and egg differ, the maternal
    and paternal embryo genomes show similar non-CG methylation levels, suggesting
    that rice gamete genomes undergo dynamic DNA methylation reprogramming after cell
    fusion.
article_processing_charge: No
article_type: original
author:
- first_name: M. Yvonne
  full_name: Kim, M. Yvonne
  last_name: Kim
- first_name: Akemi
  full_name: Ono, Akemi
  last_name: Ono
- first_name: Stefan
  full_name: Scholten, Stefan
  last_name: Scholten
- first_name: Tetsu
  full_name: Kinoshita, Tetsu
  last_name: Kinoshita
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Takashi
  full_name: Okamoto, Takashi
  last_name: Okamoto
- first_name: Robert L.
  full_name: Fischer, Robert L.
  last_name: Fischer
citation:
  ama: Kim MY, Ono A, Scholten S, et al. DNA demethylation by ROS1a in rice vegetative
    cells promotes methylation in sperm. <i>Proceedings of the National Academy of
    Sciences</i>. 2019;116(19):9652-9657. doi:<a href="https://doi.org/10.1073/pnas.1821435116">10.1073/pnas.1821435116</a>
  apa: Kim, M. Y., Ono, A., Scholten, S., Kinoshita, T., Zilberman, D., Okamoto, T.,
    &#38; Fischer, R. L. (2019). DNA demethylation by ROS1a in rice vegetative cells
    promotes methylation in sperm. <i>Proceedings of the National Academy of Sciences</i>.
    National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1821435116">https://doi.org/10.1073/pnas.1821435116</a>
  chicago: Kim, M. Yvonne, Akemi Ono, Stefan Scholten, Tetsu Kinoshita, Daniel Zilberman,
    Takashi Okamoto, and Robert L. Fischer. “DNA Demethylation by ROS1a in Rice Vegetative
    Cells Promotes Methylation in Sperm.” <i>Proceedings of the National Academy of
    Sciences</i>. National Academy of Sciences, 2019. <a href="https://doi.org/10.1073/pnas.1821435116">https://doi.org/10.1073/pnas.1821435116</a>.
  ieee: M. Y. Kim <i>et al.</i>, “DNA demethylation by ROS1a in rice vegetative cells
    promotes methylation in sperm,” <i>Proceedings of the National Academy of Sciences</i>,
    vol. 116, no. 19. National Academy of Sciences, pp. 9652–9657, 2019.
  ista: Kim MY, Ono A, Scholten S, Kinoshita T, Zilberman D, Okamoto T, Fischer RL.
    2019. DNA demethylation by ROS1a in rice vegetative cells promotes methylation
    in sperm. Proceedings of the National Academy of Sciences. 116(19), 9652–9657.
  mla: Kim, M. Yvonne, et al. “DNA Demethylation by ROS1a in Rice Vegetative Cells
    Promotes Methylation in Sperm.” <i>Proceedings of the National Academy of Sciences</i>,
    vol. 116, no. 19, National Academy of Sciences, 2019, pp. 9652–57, doi:<a href="https://doi.org/10.1073/pnas.1821435116">10.1073/pnas.1821435116</a>.
  short: M.Y. Kim, A. Ono, S. Scholten, T. Kinoshita, D. Zilberman, T. Okamoto, R.L.
    Fischer, Proceedings of the National Academy of Sciences 116 (2019) 9652–9657.
date_created: 2021-06-04T12:38:20Z
date_published: 2019-05-07T00:00:00Z
date_updated: 2021-12-14T07:52:30Z
day: '07'
ddc:
- '580'
department:
- _id: DaZi
doi: 10.1073/pnas.1821435116
extern: '1'
external_id:
  pmid:
  - '31000601'
file:
- access_level: open_access
  checksum: 5b0ae3779b8b21b5223bd2d3cceede3a
  content_type: application/pdf
  creator: asandaue
  date_created: 2021-06-04T12:50:47Z
  date_updated: 2021-06-04T12:50:47Z
  file_id: '9461'
  file_name: 2019_PNAS_Kim.pdf
  file_size: 1142540
  relation: main_file
  success: 1
file_date_updated: 2021-06-04T12:50:47Z
has_accepted_license: '1'
intvolume: '       116'
issue: '19'
keyword:
- Multidisciplinary
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '05'
oa: 1
oa_version: Published Version
page: 9652-9657
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: DNA demethylation by ROS1a in rice vegetative cells promotes methylation in
  sperm
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 116
year: '2019'
...
---
_id: '9530'
abstract:
- lang: eng
  text: "Background\r\nDNA methylation of active genes, also known as gene body methylation,
    is found in many animal and plant genomes. Despite this, the transcriptional and
    developmental role of such methylation remains poorly understood. Here, we explore
    the dynamic range of DNA methylation in honey bee, a model organism for gene body
    methylation.\r\n\r\nResults\r\nOur data show that CG methylation in gene bodies
    globally fluctuates during honey bee development. However, these changes cause
    no gene expression alterations. Intriguingly, despite the global alterations,
    tissue-specific CG methylation patterns of complete genes or exons are rare, implying
    robust maintenance of genic methylation during development. Additionally, we show
    that CG methylation maintenance fluctuates in somatic cells, while reaching maximum
    fidelity in sperm cells. Finally, unlike universally present CG methylation, we
    discovered non-CG methylation specifically in bee heads that resembles such methylation
    in mammalian brain tissue.\r\n\r\nConclusions\r\nBased on these results, we propose
    that gene body CG methylation can oscillate during development if it is kept to
    a level adequate to preserve function. Additionally, our data suggest that heightened
    non-CG methylation is a conserved regulator of animal nervous systems."
article_number: '62'
article_processing_charge: No
article_type: original
author:
- first_name: Keith D.
  full_name: Harris, Keith D.
  last_name: Harris
- first_name: James P. B.
  full_name: Lloyd, James P. B.
  last_name: Lloyd
- first_name: Katherine
  full_name: Domb, Katherine
  last_name: Domb
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Assaf
  full_name: Zemach, Assaf
  last_name: Zemach
citation:
  ama: Harris KD, Lloyd JPB, Domb K, Zilberman D, Zemach A. DNA methylation is maintained
    with high fidelity in the honey bee germline and exhibits global non-functional
    fluctuations during somatic development. <i>Epigenetics and Chromatin</i>. 2019;12.
    doi:<a href="https://doi.org/10.1186/s13072-019-0307-4">10.1186/s13072-019-0307-4</a>
  apa: Harris, K. D., Lloyd, J. P. B., Domb, K., Zilberman, D., &#38; Zemach, A. (2019).
    DNA methylation is maintained with high fidelity in the honey bee germline and
    exhibits global non-functional fluctuations during somatic development. <i>Epigenetics
    and Chromatin</i>. Springer Nature. <a href="https://doi.org/10.1186/s13072-019-0307-4">https://doi.org/10.1186/s13072-019-0307-4</a>
  chicago: Harris, Keith D., James P. B. Lloyd, Katherine Domb, Daniel Zilberman,
    and Assaf Zemach. “DNA Methylation Is Maintained with High Fidelity in the Honey
    Bee Germline and Exhibits Global Non-Functional Fluctuations during Somatic Development.”
    <i>Epigenetics and Chromatin</i>. Springer Nature, 2019. <a href="https://doi.org/10.1186/s13072-019-0307-4">https://doi.org/10.1186/s13072-019-0307-4</a>.
  ieee: K. D. Harris, J. P. B. Lloyd, K. Domb, D. Zilberman, and A. Zemach, “DNA methylation
    is maintained with high fidelity in the honey bee germline and exhibits global
    non-functional fluctuations during somatic development,” <i>Epigenetics and Chromatin</i>,
    vol. 12. Springer Nature, 2019.
  ista: Harris KD, Lloyd JPB, Domb K, Zilberman D, Zemach A. 2019. DNA methylation
    is maintained with high fidelity in the honey bee germline and exhibits global
    non-functional fluctuations during somatic development. Epigenetics and Chromatin.
    12, 62.
  mla: Harris, Keith D., et al. “DNA Methylation Is Maintained with High Fidelity
    in the Honey Bee Germline and Exhibits Global Non-Functional Fluctuations during
    Somatic Development.” <i>Epigenetics and Chromatin</i>, vol. 12, 62, Springer
    Nature, 2019, doi:<a href="https://doi.org/10.1186/s13072-019-0307-4">10.1186/s13072-019-0307-4</a>.
  short: K.D. Harris, J.P.B. Lloyd, K. Domb, D. Zilberman, A. Zemach, Epigenetics
    and Chromatin 12 (2019).
date_created: 2021-06-08T09:21:51Z
date_published: 2019-10-10T00:00:00Z
date_updated: 2021-12-14T07:53:00Z
day: '10'
ddc:
- '570'
department:
- _id: DaZi
doi: 10.1186/s13072-019-0307-4
extern: '1'
external_id:
  pmid:
  - '31601251'
file:
- access_level: open_access
  checksum: 86ff50a7517891511af2733c76c81b67
  content_type: application/pdf
  creator: asandaue
  date_created: 2021-06-08T09:29:19Z
  date_updated: 2021-06-08T09:29:19Z
  file_id: '9531'
  file_name: 2019_EpigeneticsAndChromatin_Harris.pdf
  file_size: 3221067
  relation: main_file
  success: 1
file_date_updated: 2021-06-08T09:29:19Z
has_accepted_license: '1'
intvolume: '        12'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
pmid: 1
publication: Epigenetics and Chromatin
publication_identifier:
  eissn:
  - 1756-8935
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: DNA methylation is maintained with high fidelity in the honey bee germline
  and exhibits global non-functional fluctuations during somatic development
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: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 12
year: '2019'
...
---
_id: '9580'
abstract:
- lang: eng
  text: An r-cut of a k-uniform hypergraph H is a partition of the vertex set of H
    into r parts and the size of the cut is the number of edges which have a vertex
    in each part. A classical result of Edwards says that every m-edge graph has a
    2-cut of size m/2+Ω)(m−−√) and this is best possible. That is, there exist cuts
    which exceed the expected size of a random cut by some multiple of the standard
    deviation. We study analogues of this and related results in hypergraphs. First,
    we observe that similarly to graphs, every m-edge k-uniform hypergraph has an
    r-cut whose size is Ω(m−−√) larger than the expected size of a random r-cut. Moreover,
    in the case where k = 3 and r = 2 this bound is best possible and is attained
    by Steiner triple systems. Surprisingly, for all other cases (that is, if k ≥
    4 or r ≥ 3), we show that every m-edge k-uniform hypergraph has an r-cut whose
    size is Ω(m5/9) larger than the expected size of a random r-cut. This is a significant
    difference in behaviour, since the amount by which the size of the largest cut
    exceeds the expected size of a random cut is now considerably larger than the
    standard deviation.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: David
  full_name: Conlon, David
  last_name: Conlon
- first_name: Jacob
  full_name: Fox, Jacob
  last_name: Fox
- first_name: Matthew Alan
  full_name: Kwan, Matthew Alan
  id: 5fca0887-a1db-11eb-95d1-ca9d5e0453b3
  last_name: Kwan
  orcid: 0000-0002-4003-7567
- first_name: Benny
  full_name: Sudakov, Benny
  last_name: Sudakov
citation:
  ama: Conlon D, Fox J, Kwan MA, Sudakov B. Hypergraph cuts above the average. <i>Israel
    Journal of Mathematics</i>. 2019;233(1):67-111. doi:<a href="https://doi.org/10.1007/s11856-019-1897-z">10.1007/s11856-019-1897-z</a>
  apa: Conlon, D., Fox, J., Kwan, M. A., &#38; Sudakov, B. (2019). Hypergraph cuts
    above the average. <i>Israel Journal of Mathematics</i>. Springer. <a href="https://doi.org/10.1007/s11856-019-1897-z">https://doi.org/10.1007/s11856-019-1897-z</a>
  chicago: Conlon, David, Jacob Fox, Matthew Alan Kwan, and Benny Sudakov. “Hypergraph
    Cuts above the Average.” <i>Israel Journal of Mathematics</i>. Springer, 2019.
    <a href="https://doi.org/10.1007/s11856-019-1897-z">https://doi.org/10.1007/s11856-019-1897-z</a>.
  ieee: D. Conlon, J. Fox, M. A. Kwan, and B. Sudakov, “Hypergraph cuts above the
    average,” <i>Israel Journal of Mathematics</i>, vol. 233, no. 1. Springer, pp.
    67–111, 2019.
  ista: Conlon D, Fox J, Kwan MA, Sudakov B. 2019. Hypergraph cuts above the average.
    Israel Journal of Mathematics. 233(1), 67–111.
  mla: Conlon, David, et al. “Hypergraph Cuts above the Average.” <i>Israel Journal
    of Mathematics</i>, vol. 233, no. 1, Springer, 2019, pp. 67–111, doi:<a href="https://doi.org/10.1007/s11856-019-1897-z">10.1007/s11856-019-1897-z</a>.
  short: D. Conlon, J. Fox, M.A. Kwan, B. Sudakov, Israel Journal of Mathematics 233
    (2019) 67–111.
date_created: 2021-06-21T13:36:02Z
date_published: 2019-08-01T00:00:00Z
date_updated: 2023-02-23T14:01:41Z
day: '01'
doi: 10.1007/s11856-019-1897-z
extern: '1'
external_id:
  arxiv:
  - '1803.08462'
intvolume: '       233'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1803.08462
month: '08'
oa: 1
oa_version: Preprint
page: 67-111
publication: Israel Journal of Mathematics
publication_identifier:
  eissn:
  - 1565-8511
  issn:
  - 0021-2172
publication_status: published
publisher: Springer
quality_controlled: '1'
scopus_import: '1'
status: public
title: Hypergraph cuts above the average
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 233
year: '2019'
...
---
_id: '9585'
abstract:
- lang: eng
  text: An n-vertex graph is called C-Ramsey if it has no clique or independent set
    of size C log n. All known constructions of Ramsey graphs involve randomness in
    an essential way, and there is an ongoing line of research towards showing that
    in fact all Ramsey graphs must obey certain “richness” properties characteristic
    of random graphs. More than 25 years ago, Erdős, Faudree and Sós conjectured that
    in any C-Ramsey graph there are Ω(n^5/2) induced subgraphs, no pair of which have
    the same numbers of vertices and edges. Improving on earlier results of Alon,
    Balogh, Kostochka and Samotij, in this paper we prove this conjecture.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Matthew Alan
  full_name: Kwan, Matthew Alan
  id: 5fca0887-a1db-11eb-95d1-ca9d5e0453b3
  last_name: Kwan
  orcid: 0000-0002-4003-7567
- first_name: Benny
  full_name: Sudakov, Benny
  last_name: Sudakov
citation:
  ama: Kwan MA, Sudakov B. Proof of a conjecture on induced subgraphs of Ramsey graphs.
    <i>Transactions of the American Mathematical Society</i>. 2019;372(8):5571-5594.
    doi:<a href="https://doi.org/10.1090/tran/7729">10.1090/tran/7729</a>
  apa: Kwan, M. A., &#38; Sudakov, B. (2019). Proof of a conjecture on induced subgraphs
    of Ramsey graphs. <i>Transactions of the American Mathematical Society</i>. American
    Mathematical Society. <a href="https://doi.org/10.1090/tran/7729">https://doi.org/10.1090/tran/7729</a>
  chicago: Kwan, Matthew Alan, and Benny Sudakov. “Proof of a Conjecture on Induced
    Subgraphs of Ramsey Graphs.” <i>Transactions of the American Mathematical Society</i>.
    American Mathematical Society, 2019. <a href="https://doi.org/10.1090/tran/7729">https://doi.org/10.1090/tran/7729</a>.
  ieee: M. A. Kwan and B. Sudakov, “Proof of a conjecture on induced subgraphs of
    Ramsey graphs,” <i>Transactions of the American Mathematical Society</i>, vol.
    372, no. 8. American Mathematical Society, pp. 5571–5594, 2019.
  ista: Kwan MA, Sudakov B. 2019. Proof of a conjecture on induced subgraphs of Ramsey
    graphs. Transactions of the American Mathematical Society. 372(8), 5571–5594.
  mla: Kwan, Matthew Alan, and Benny Sudakov. “Proof of a Conjecture on Induced Subgraphs
    of Ramsey Graphs.” <i>Transactions of the American Mathematical Society</i>, vol.
    372, no. 8, American Mathematical Society, 2019, pp. 5571–94, doi:<a href="https://doi.org/10.1090/tran/7729">10.1090/tran/7729</a>.
  short: M.A. Kwan, B. Sudakov, Transactions of the American Mathematical Society
    372 (2019) 5571–5594.
date_created: 2021-06-22T09:31:45Z
date_published: 2019-10-15T00:00:00Z
date_updated: 2023-02-23T14:01:50Z
day: '15'
doi: 10.1090/tran/7729
extern: '1'
external_id:
  arxiv:
  - '1712.05656'
intvolume: '       372'
issue: '8'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1090/tran/7729
month: '10'
oa: 1
oa_version: Submitted Version
page: 5571-5594
publication: Transactions of the American Mathematical Society
publication_identifier:
  eissn:
  - 1088-6850
  issn:
  - 0002-9947
publication_status: published
publisher: American Mathematical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Proof of a conjecture on induced subgraphs of Ramsey graphs
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 372
year: '2019'
...
---
_id: '9586'
abstract:
- lang: eng
  text: "Consider integers  \U0001D458,ℓ  such that  0⩽ℓ⩽(\U0001D4582) . Given a large
    graph  \U0001D43A , what is the fraction of  \U0001D458 -vertex subsets of  \U0001D43A
    \ which span exactly  ℓ  edges? When  \U0001D43A  is empty or complete, and  ℓ
    \ is zero or  (\U0001D4582) , this fraction can be exactly 1. On the other hand,
    if  ℓ  is far from these extreme values, one might expect that this fraction is
    substantially smaller than 1. This was recently proved by Alon, Hefetz, Krivelevich,
    and Tyomkyn who initiated the systematic study of this question and proposed several
    natural conjectures.\r\nLet  ℓ∗=min{ℓ,(\U0001D4582)−ℓ} . Our main result is that
    for any  \U0001D458  and  ℓ , the fraction of  \U0001D458 -vertex subsets that
    span  ℓ  edges is at most  log\U0001D442(1)(ℓ∗/\U0001D458)√ \U0001D458/ℓ∗, which
    is best-possible up to the logarithmic factor. This improves on multiple results
    of Alon, Hefetz, Krivelevich, and Tyomkyn, and resolves one of their conjectures.
    In addition, we also make some first steps towards some analogous questions for
    hypergraphs.\r\nOur proofs involve some Ramsey-type arguments, and a number of
    different probabilistic tools, such as polynomial anticoncentration inequalities,
    hypercontractivity, and a coupling trick for random variables defined on a ‘slice’
    of the Boolean hypercube."
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Matthew Alan
  full_name: Kwan, Matthew Alan
  id: 5fca0887-a1db-11eb-95d1-ca9d5e0453b3
  last_name: Kwan
  orcid: 0000-0002-4003-7567
- first_name: Benny
  full_name: Sudakov, Benny
  last_name: Sudakov
- first_name: Tuan
  full_name: Tran, Tuan
  last_name: Tran
citation:
  ama: Kwan MA, Sudakov B, Tran T. Anticoncentration for subgraph statistics. <i>Journal
    of the London Mathematical Society</i>. 2019;99(3):757-777. doi:<a href="https://doi.org/10.1112/jlms.12192">10.1112/jlms.12192</a>
  apa: Kwan, M. A., Sudakov, B., &#38; Tran, T. (2019). Anticoncentration for subgraph
    statistics. <i>Journal of the London Mathematical Society</i>. Wiley. <a href="https://doi.org/10.1112/jlms.12192">https://doi.org/10.1112/jlms.12192</a>
  chicago: Kwan, Matthew Alan, Benny Sudakov, and Tuan Tran. “Anticoncentration for
    Subgraph Statistics.” <i>Journal of the London Mathematical Society</i>. Wiley,
    2019. <a href="https://doi.org/10.1112/jlms.12192">https://doi.org/10.1112/jlms.12192</a>.
  ieee: M. A. Kwan, B. Sudakov, and T. Tran, “Anticoncentration for subgraph statistics,”
    <i>Journal of the London Mathematical Society</i>, vol. 99, no. 3. Wiley, pp.
    757–777, 2019.
  ista: Kwan MA, Sudakov B, Tran T. 2019. Anticoncentration for subgraph statistics.
    Journal of the London Mathematical Society. 99(3), 757–777.
  mla: Kwan, Matthew Alan, et al. “Anticoncentration for Subgraph Statistics.” <i>Journal
    of the London Mathematical Society</i>, vol. 99, no. 3, Wiley, 2019, pp. 757–77,
    doi:<a href="https://doi.org/10.1112/jlms.12192">10.1112/jlms.12192</a>.
  short: M.A. Kwan, B. Sudakov, T. Tran, Journal of the London Mathematical Society
    99 (2019) 757–777.
date_created: 2021-06-22T09:46:03Z
date_published: 2019-05-03T00:00:00Z
date_updated: 2023-02-23T14:01:53Z
day: '03'
doi: 10.1112/jlms.12192
extern: '1'
external_id:
  arxiv:
  - '1807.05202'
intvolume: '        99'
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1807.05202
month: '05'
oa: 1
oa_version: Preprint
page: 757-777
publication: Journal of the London Mathematical Society
publication_identifier:
  eissn:
  - 1469-7750
  issn:
  - 0024-6107
publication_status: published
publisher: Wiley
quality_controlled: '1'
scopus_import: '1'
status: public
title: Anticoncentration for subgraph statistics
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 99
year: '2019'
...
---
_id: '9677'
abstract:
- lang: eng
  text: Progress in the atomic-scale modeling of matter over the past decade has been
    tremendous. This progress has been brought about by improvements in methods for
    evaluating interatomic forces that work by either solving the electronic structure
    problem explicitly, or by computing accurate approximations of the solution and
    by the development of techniques that use the Born–Oppenheimer (BO) forces to
    move the atoms on the BO potential energy surface. As a consequence of these developments
    it is now possible to identify stable or metastable states, to sample configurations
    consistent with the appropriate thermodynamic ensemble, and to estimate the kinetics
    of reactions and phase transitions. All too often, however, progress is slowed
    down by the bottleneck associated with implementing new optimization algorithms
    and/or sampling techniques into the many existing electronic-structure and empirical-potential
    codes. To address this problem, we are thus releasing a new version of the i-PI
    software. This piece of software is an easily extensible framework for implementing
    advanced atomistic simulation techniques using interatomic potentials and forces
    calculated by an external driver code. While the original version of the code
    (Ceriotti et al., 2014) was developed with a focus on path integral molecular
    dynamics techniques, this second release of i-PI not only includes several new
    advanced path integral methods, but also offers other classes of algorithms. In
    other words, i-PI is moving towards becoming a universal force engine that is
    both modular and tightly coupled to the driver codes that evaluate the potential
    energy surface and its derivatives.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Venkat
  full_name: Kapil, Venkat
  last_name: Kapil
- first_name: Mariana
  full_name: Rossi, Mariana
  last_name: Rossi
- first_name: Ondrej
  full_name: Marsalek, Ondrej
  last_name: Marsalek
- first_name: Riccardo
  full_name: Petraglia, Riccardo
  last_name: Petraglia
- first_name: Yair
  full_name: Litman, Yair
  last_name: Litman
- first_name: Thomas
  full_name: Spura, Thomas
  last_name: Spura
- first_name: Bingqing
  full_name: Cheng, Bingqing
  id: cbe3cda4-d82c-11eb-8dc7-8ff94289fcc9
  last_name: Cheng
  orcid: 0000-0002-3584-9632
- first_name: Alice
  full_name: Cuzzocrea, Alice
  last_name: Cuzzocrea
- first_name: Robert H.
  full_name: Meißner, Robert H.
  last_name: Meißner
- first_name: David M.
  full_name: Wilkins, David M.
  last_name: Wilkins
- first_name: Benjamin A.
  full_name: Helfrecht, Benjamin A.
  last_name: Helfrecht
- first_name: Przemysław
  full_name: Juda, Przemysław
  last_name: Juda
- first_name: Sébastien P.
  full_name: Bienvenue, Sébastien P.
  last_name: Bienvenue
- first_name: Wei
  full_name: Fang, Wei
  last_name: Fang
- first_name: Jan
  full_name: Kessler, Jan
  last_name: Kessler
- first_name: Igor
  full_name: Poltavsky, Igor
  last_name: Poltavsky
- first_name: Steven
  full_name: Vandenbrande, Steven
  last_name: Vandenbrande
- first_name: Jelle
  full_name: Wieme, Jelle
  last_name: Wieme
- first_name: Clemence
  full_name: Corminboeuf, Clemence
  last_name: Corminboeuf
- first_name: Thomas D.
  full_name: Kühne, Thomas D.
  last_name: Kühne
- first_name: David E.
  full_name: Manolopoulos, David E.
  last_name: Manolopoulos
- first_name: Thomas E.
  full_name: Markland, Thomas E.
  last_name: Markland
- first_name: Jeremy O.
  full_name: Richardson, Jeremy O.
  last_name: Richardson
- first_name: Alexandre
  full_name: Tkatchenko, Alexandre
  last_name: Tkatchenko
- first_name: Gareth A.
  full_name: Tribello, Gareth A.
  last_name: Tribello
- first_name: Veronique
  full_name: Van Speybroeck, Veronique
  last_name: Van Speybroeck
- first_name: Michele
  full_name: Ceriotti, Michele
  last_name: Ceriotti
citation:
  ama: 'Kapil V, Rossi M, Marsalek O, et al. i-PI 2.0: A universal force engine for
    advanced molecular simulations. <i>Computer Physics Communications</i>. 2019;236:214-223.
    doi:<a href="https://doi.org/10.1016/j.cpc.2018.09.020">10.1016/j.cpc.2018.09.020</a>'
  apa: 'Kapil, V., Rossi, M., Marsalek, O., Petraglia, R., Litman, Y., Spura, T.,
    … Ceriotti, M. (2019). i-PI 2.0: A universal force engine for advanced molecular
    simulations. <i>Computer Physics Communications</i>. Elsevier. <a href="https://doi.org/10.1016/j.cpc.2018.09.020">https://doi.org/10.1016/j.cpc.2018.09.020</a>'
  chicago: 'Kapil, Venkat, Mariana Rossi, Ondrej Marsalek, Riccardo Petraglia, Yair
    Litman, Thomas Spura, Bingqing Cheng, et al. “I-PI 2.0: A Universal Force Engine
    for Advanced Molecular Simulations.” <i>Computer Physics Communications</i>. Elsevier,
    2019. <a href="https://doi.org/10.1016/j.cpc.2018.09.020">https://doi.org/10.1016/j.cpc.2018.09.020</a>.'
  ieee: 'V. Kapil <i>et al.</i>, “i-PI 2.0: A universal force engine for advanced
    molecular simulations,” <i>Computer Physics Communications</i>, vol. 236. Elsevier,
    pp. 214–223, 2019.'
  ista: 'Kapil V, Rossi M, Marsalek O, Petraglia R, Litman Y, Spura T, Cheng B, Cuzzocrea
    A, Meißner RH, Wilkins DM, Helfrecht BA, Juda P, Bienvenue SP, Fang W, Kessler
    J, Poltavsky I, Vandenbrande S, Wieme J, Corminboeuf C, Kühne TD, Manolopoulos
    DE, Markland TE, Richardson JO, Tkatchenko A, Tribello GA, Van Speybroeck V, Ceriotti
    M. 2019. i-PI 2.0: A universal force engine for advanced molecular simulations.
    Computer Physics Communications. 236, 214–223.'
  mla: 'Kapil, Venkat, et al. “I-PI 2.0: A Universal Force Engine for Advanced Molecular
    Simulations.” <i>Computer Physics Communications</i>, vol. 236, Elsevier, 2019,
    pp. 214–23, doi:<a href="https://doi.org/10.1016/j.cpc.2018.09.020">10.1016/j.cpc.2018.09.020</a>.'
  short: V. Kapil, M. Rossi, O. Marsalek, R. Petraglia, Y. Litman, T. Spura, B. Cheng,
    A. Cuzzocrea, R.H. Meißner, D.M. Wilkins, B.A. Helfrecht, P. Juda, S.P. Bienvenue,
    W. Fang, J. Kessler, I. Poltavsky, S. Vandenbrande, J. Wieme, C. Corminboeuf,
    T.D. Kühne, D.E. Manolopoulos, T.E. Markland, J.O. Richardson, A. Tkatchenko,
    G.A. Tribello, V. Van Speybroeck, M. Ceriotti, Computer Physics Communications
    236 (2019) 214–223.
date_created: 2021-07-16T08:53:01Z
date_published: 2019-03-01T00:00:00Z
date_updated: 2021-08-09T12:37:16Z
day: '01'
doi: 10.1016/j.cpc.2018.09.020
extern: '1'
external_id:
  arxiv:
  - '1808.03824'
intvolume: '       236'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1808.03824
month: '03'
oa: 1
oa_version: Preprint
page: 214-223
publication: Computer Physics Communications
publication_identifier:
  issn:
  - 0010-4655
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'i-PI 2.0: A universal force engine for advanced molecular simulations'
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 236
year: '2019'
...
---
_id: '9680'
abstract:
- lang: eng
  text: Atomistic modeling of phase transitions, chemical reactions, or other rare
    events that involve overcoming high free energy barriers usually entails prohibitively
    long simulation times. Introducing a bias potential as a function of an appropriately
    chosen set of collective variables can significantly accelerate the exploration
    of phase space, albeit at the price of distorting the distribution of microstates.
    Efficient reweighting to recover the unbiased distribution can be nontrivial when
    employing adaptive sampling techniques such as metadynamics, variationally enhanced
    sampling, or parallel bias metadynamics, in which the system evolves in a quasi-equilibrium
    manner under a time-dependent bias. We introduce an iterative unbiasing scheme
    that makes efficient use of all the trajectory data and that does not require
    the distribution to be evaluated on a grid. The method can thus be used even when
    the bias has a high dimensionality. We benchmark this approach against some of
    the existing schemes on model systems with different complexity and dimensionality.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: F.
  full_name: Giberti, F.
  last_name: Giberti
- first_name: Bingqing
  full_name: Cheng, Bingqing
  id: cbe3cda4-d82c-11eb-8dc7-8ff94289fcc9
  last_name: Cheng
  orcid: 0000-0002-3584-9632
- first_name: G. A.
  full_name: Tribello, G. A.
  last_name: Tribello
- first_name: M.
  full_name: Ceriotti, M.
  last_name: Ceriotti
citation:
  ama: Giberti F, Cheng B, Tribello GA, Ceriotti M. Iterative unbiasing of quasi-equilibrium
    sampling. <i>Journal of Chemical Theory and Computation</i>. 2019;16(1):100-107.
    doi:<a href="https://doi.org/10.1021/acs.jctc.9b00907">10.1021/acs.jctc.9b00907</a>
  apa: Giberti, F., Cheng, B., Tribello, G. A., &#38; Ceriotti, M. (2019). Iterative
    unbiasing of quasi-equilibrium sampling. <i>Journal of Chemical Theory and Computation</i>.
    American Chemical Society. <a href="https://doi.org/10.1021/acs.jctc.9b00907">https://doi.org/10.1021/acs.jctc.9b00907</a>
  chicago: Giberti, F., Bingqing Cheng, G. A. Tribello, and M. Ceriotti. “Iterative
    Unbiasing of Quasi-Equilibrium Sampling.” <i>Journal of Chemical Theory and Computation</i>.
    American Chemical Society, 2019. <a href="https://doi.org/10.1021/acs.jctc.9b00907">https://doi.org/10.1021/acs.jctc.9b00907</a>.
  ieee: F. Giberti, B. Cheng, G. A. Tribello, and M. Ceriotti, “Iterative unbiasing
    of quasi-equilibrium sampling,” <i>Journal of Chemical Theory and Computation</i>,
    vol. 16, no. 1. American Chemical Society, pp. 100–107, 2019.
  ista: Giberti F, Cheng B, Tribello GA, Ceriotti M. 2019. Iterative unbiasing of
    quasi-equilibrium sampling. Journal of Chemical Theory and Computation. 16(1),
    100–107.
  mla: Giberti, F., et al. “Iterative Unbiasing of Quasi-Equilibrium Sampling.” <i>Journal
    of Chemical Theory and Computation</i>, vol. 16, no. 1, American Chemical Society,
    2019, pp. 100–07, doi:<a href="https://doi.org/10.1021/acs.jctc.9b00907">10.1021/acs.jctc.9b00907</a>.
  short: F. Giberti, B. Cheng, G.A. Tribello, M. Ceriotti, Journal of Chemical Theory
    and Computation 16 (2019) 100–107.
date_created: 2021-07-19T06:56:45Z
date_published: 2019-01-14T00:00:00Z
date_updated: 2021-08-09T12:37:37Z
day: '14'
doi: 10.1021/acs.jctc.9b00907
extern: '1'
external_id:
  arxiv:
  - '1911.01140'
  pmid:
  - '31743021'
intvolume: '        16'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1911.01140
month: '01'
oa: 1
oa_version: Preprint
page: 100-107
pmid: 1
publication: Journal of Chemical Theory and Computation
publication_identifier:
  eissn:
  - 1549-9626
  issn:
  - 1549-9618
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Iterative unbiasing of quasi-equilibrium sampling
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 16
year: '2019'
...
---
_id: '9689'
abstract:
- lang: eng
  text: A central goal of computational physics and chemistry is to predict material
    properties by using first-principles methods based on the fundamental laws of
    quantum mechanics. However, the high computational costs of these methods typically
    prevent rigorous predictions of macroscopic quantities at finite temperatures,
    such as heat capacity, density, and chemical potential. Here, we enable such predictions
    by marrying advanced free-energy methods with data-driven machine-learning interatomic
    potentials. We show that, for the ubiquitous and technologically essential system
    of water, a first-principles thermodynamic description not only leads to excellent
    agreement with experiments, but also reveals the crucial role of nuclear quantum
    fluctuations in modulating the thermodynamic stabilities of different phases of
    water.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Bingqing
  full_name: Cheng, Bingqing
  id: cbe3cda4-d82c-11eb-8dc7-8ff94289fcc9
  last_name: Cheng
  orcid: 0000-0002-3584-9632
- first_name: Edgar A.
  full_name: Engel, Edgar A.
  last_name: Engel
- first_name: Jörg
  full_name: Behler, Jörg
  last_name: Behler
- first_name: Christoph
  full_name: Dellago, Christoph
  last_name: Dellago
- first_name: Michele
  full_name: Ceriotti, Michele
  last_name: Ceriotti
citation:
  ama: Cheng B, Engel EA, Behler J, Dellago C, Ceriotti M. Ab initio thermodynamics
    of liquid and solid water. <i>Proceedings of the National Academy of Sciences</i>.
    2019;116(4):1110-1115. doi:<a href="https://doi.org/10.1073/pnas.1815117116">10.1073/pnas.1815117116</a>
  apa: Cheng, B., Engel, E. A., Behler, J., Dellago, C., &#38; Ceriotti, M. (2019).
    Ab initio thermodynamics of liquid and solid water. <i>Proceedings of the National
    Academy of Sciences</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.1815117116">https://doi.org/10.1073/pnas.1815117116</a>
  chicago: Cheng, Bingqing, Edgar A. Engel, Jörg Behler, Christoph Dellago, and Michele
    Ceriotti. “Ab Initio Thermodynamics of Liquid and Solid Water.” <i>Proceedings
    of the National Academy of Sciences</i>. National Academy of Sciences, 2019. <a
    href="https://doi.org/10.1073/pnas.1815117116">https://doi.org/10.1073/pnas.1815117116</a>.
  ieee: B. Cheng, E. A. Engel, J. Behler, C. Dellago, and M. Ceriotti, “Ab initio
    thermodynamics of liquid and solid water,” <i>Proceedings of the National Academy
    of Sciences</i>, vol. 116, no. 4. National Academy of Sciences, pp. 1110–1115,
    2019.
  ista: Cheng B, Engel EA, Behler J, Dellago C, Ceriotti M. 2019. Ab initio thermodynamics
    of liquid and solid water. Proceedings of the National Academy of Sciences. 116(4),
    1110–1115.
  mla: Cheng, Bingqing, et al. “Ab Initio Thermodynamics of Liquid and Solid Water.”
    <i>Proceedings of the National Academy of Sciences</i>, vol. 116, no. 4, National
    Academy of Sciences, 2019, pp. 1110–15, doi:<a href="https://doi.org/10.1073/pnas.1815117116">10.1073/pnas.1815117116</a>.
  short: B. Cheng, E.A. Engel, J. Behler, C. Dellago, M. Ceriotti, Proceedings of
    the National Academy of Sciences 116 (2019) 1110–1115.
date_created: 2021-07-19T10:17:09Z
date_published: 2019-01-22T00:00:00Z
date_updated: 2023-02-23T14:05:08Z
day: '22'
doi: 10.1073/pnas.1815117116
extern: '1'
external_id:
  arxiv:
  - '1811.08630'
  pmid:
  - '30610171'
intvolume: '       116'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1073/pnas.1815117116
month: '01'
oa: 1
oa_version: Published Version
page: 1110-1115
pmid: 1
publication: Proceedings of the National Academy of Sciences
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: Ab initio thermodynamics of liquid and solid water
type: journal_article
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
volume: 116
year: '2019'
...
---
_id: '9726'
abstract:
- lang: eng
  text: A detailed description of the two stochastic models, table of parameters,
    supplementary data for Figures 4 and 5, parameter dependence of the results, and
    an analysis on motors with different force–velocity functions (PDF)
article_processing_charge: No
author:
- first_name: Mehmet C
  full_name: Ucar, Mehmet C
  id: 50B2A802-6007-11E9-A42B-EB23E6697425
  last_name: Ucar
  orcid: 0000-0003-0506-4217
- first_name: Reinhard
  full_name: Lipowsky, Reinhard
  last_name: Lipowsky
citation:
  ama: Ucar MC, Lipowsky R. Supplementary information - Collective force generation
    by molecular motors is determined by strain-induced unbinding. 2019. doi:<a href="https://doi.org/10.1021/acs.nanolett.9b04445.s001">10.1021/acs.nanolett.9b04445.s001</a>
  apa: Ucar, M. C., &#38; Lipowsky, R. (2019). Supplementary information - Collective
    force generation by molecular motors is determined by strain-induced unbinding.
    American Chemical Society . <a href="https://doi.org/10.1021/acs.nanolett.9b04445.s001">https://doi.org/10.1021/acs.nanolett.9b04445.s001</a>
  chicago: Ucar, Mehmet C, and Reinhard Lipowsky. “Supplementary Information - Collective
    Force Generation by Molecular Motors Is Determined by Strain-Induced Unbinding.”
    American Chemical Society , 2019. <a href="https://doi.org/10.1021/acs.nanolett.9b04445.s001">https://doi.org/10.1021/acs.nanolett.9b04445.s001</a>.
  ieee: M. C. Ucar and R. Lipowsky, “Supplementary information - Collective force
    generation by molecular motors is determined by strain-induced unbinding.” American
    Chemical Society , 2019.
  ista: Ucar MC, Lipowsky R. 2019. Supplementary information - Collective force generation
    by molecular motors is determined by strain-induced unbinding, American Chemical
    Society , <a href="https://doi.org/10.1021/acs.nanolett.9b04445.s001">10.1021/acs.nanolett.9b04445.s001</a>.
  mla: Ucar, Mehmet C., and Reinhard Lipowsky. <i>Supplementary Information - Collective
    Force Generation by Molecular Motors Is Determined by Strain-Induced Unbinding</i>.
    American Chemical Society , 2019, doi:<a href="https://doi.org/10.1021/acs.nanolett.9b04445.s001">10.1021/acs.nanolett.9b04445.s001</a>.
  short: M.C. Ucar, R. Lipowsky, (2019).
date_created: 2021-07-27T09:51:46Z
date_published: 2019-12-19T00:00:00Z
date_updated: 2026-06-18T19:17:32Z
day: '19'
department:
- _id: EdHa
doi: 10.1021/acs.nanolett.9b04445.s001
month: '12'
oa_version: Published Version
publisher: 'American Chemical Society '
related_material:
  record:
  - id: '7166'
    relation: used_in_publication
    status: public
status: public
title: Supplementary information - Collective force generation by molecular motors
  is determined by strain-induced unbinding
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2019'
...
---
_id: '9731'
abstract:
- lang: eng
  text: OGs with putative pseudogenes by the number of affected genomes in different
    chlamydial species. Frameshift and nonsense mutations located less than 60 bp
    upstreamof the gene end or present in a single genome from the corresponding OG
    were excluded. (CSV 31 kb)
article_processing_charge: No
author:
- first_name: Olga
  full_name: Sigalova, Olga
  last_name: Sigalova
- first_name: Andrei
  full_name: Chaplin, Andrei
  last_name: Chaplin
- first_name: Olga
  full_name: Bochkareva, Olga
  id: C4558D3C-6102-11E9-A62E-F418E6697425
  last_name: Bochkareva
  orcid: 0000-0003-1006-6639
- first_name: Pavel
  full_name: Shelyakin, Pavel
  last_name: Shelyakin
- first_name: Vsevolod
  full_name: Filaretov, Vsevolod
  last_name: Filaretov
- first_name: Evgeny
  full_name: Akkuratov, Evgeny
  last_name: Akkuratov
- first_name: Valentina
  full_name: Burskaia, Valentina
  last_name: Burskaia
- first_name: Mikhail S.
  full_name: Gelfand, Mikhail S.
  last_name: Gelfand
citation:
  ama: Sigalova O, Chaplin A, Bochkareva O, et al. Additional file 11 of Chlamydia
    pan-genomic analysis reveals balance between host adaptation and selective pressure
    to genome reduction. 2019. doi:<a href="https://doi.org/10.6084/m9.figshare.9808772.v1">10.6084/m9.figshare.9808772.v1</a>
  apa: Sigalova, O., Chaplin, A., Bochkareva, O., Shelyakin, P., Filaretov, V., Akkuratov,
    E., … Gelfand, M. S. (2019). Additional file 11 of Chlamydia pan-genomic analysis
    reveals balance between host adaptation and selective pressure to genome reduction.
    Springer Nature. <a href="https://doi.org/10.6084/m9.figshare.9808772.v1">https://doi.org/10.6084/m9.figshare.9808772.v1</a>
  chicago: Sigalova, Olga, Andrei Chaplin, Olga Bochkareva, Pavel Shelyakin, Vsevolod
    Filaretov, Evgeny Akkuratov, Valentina Burskaia, and Mikhail S. Gelfand. “Additional
    File 11 of Chlamydia Pan-Genomic Analysis Reveals Balance between Host Adaptation
    and Selective Pressure to Genome Reduction.” Springer Nature, 2019. <a href="https://doi.org/10.6084/m9.figshare.9808772.v1">https://doi.org/10.6084/m9.figshare.9808772.v1</a>.
  ieee: O. Sigalova <i>et al.</i>, “Additional file 11 of Chlamydia pan-genomic analysis
    reveals balance between host adaptation and selective pressure to genome reduction.”
    Springer Nature, 2019.
  ista: Sigalova O, Chaplin A, Bochkareva O, Shelyakin P, Filaretov V, Akkuratov E,
    Burskaia V, Gelfand MS. 2019. Additional file 11 of Chlamydia pan-genomic analysis
    reveals balance between host adaptation and selective pressure to genome reduction,
    Springer Nature, <a href="https://doi.org/10.6084/m9.figshare.9808772.v1">10.6084/m9.figshare.9808772.v1</a>.
  mla: Sigalova, Olga, et al. <i>Additional File 11 of Chlamydia Pan-Genomic Analysis
    Reveals Balance between Host Adaptation and Selective Pressure to Genome Reduction</i>.
    Springer Nature, 2019, doi:<a href="https://doi.org/10.6084/m9.figshare.9808772.v1">10.6084/m9.figshare.9808772.v1</a>.
  short: O. Sigalova, A. Chaplin, O. Bochkareva, P. Shelyakin, V. Filaretov, E. Akkuratov,
    V. Burskaia, M.S. Gelfand, (2019).
date_created: 2021-07-27T14:09:11Z
date_published: 2019-09-12T00:00:00Z
date_updated: 2026-04-03T09:39:40Z
day: '12'
department:
- _id: FyKo
doi: 10.6084/m9.figshare.9808772.v1
main_file_link:
- open_access: '1'
  url: https://doi.org/10.6084/m9.figshare.9808772.v1
month: '09'
oa: 1
oa_version: Published Version
publisher: Springer Nature
related_material:
  record:
  - id: '6898'
    relation: used_in_publication
    status: public
status: public
title: Additional file 11 of Chlamydia pan-genomic analysis reveals balance between
  host adaptation and selective pressure to genome reduction
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2019'
...
---
_id: '9783'
abstract:
- lang: eng
  text: Predicted frameshift and nonsense mutations in Chlamydial pan-genome. For
    the analysis of putative pseudogenes, events located less than 60 bp. away from
    gene end or present in a single genome from the corresponding OG were excluded.
    (CSV 600 kb)
article_processing_charge: No
author:
- first_name: Olga M.
  full_name: Sigalova, Olga M.
  last_name: Sigalova
- first_name: Andrei V.
  full_name: Chaplin, Andrei V.
  last_name: Chaplin
- first_name: Olga
  full_name: Bochkareva, Olga
  id: C4558D3C-6102-11E9-A62E-F418E6697425
  last_name: Bochkareva
  orcid: 0000-0003-1006-6639
- first_name: Pavel V.
  full_name: Shelyakin, Pavel V.
  last_name: Shelyakin
- first_name: Vsevolod A.
  full_name: Filaretov, Vsevolod A.
  last_name: Filaretov
- first_name: Evgeny E.
  full_name: Akkuratov, Evgeny E.
  last_name: Akkuratov
- first_name: Valentina
  full_name: Burskaia, Valentina
  last_name: Burskaia
- first_name: Mikhail S.
  full_name: Gelfand, Mikhail S.
  last_name: Gelfand
citation:
  ama: Sigalova OM, Chaplin AV, Bochkareva O, et al. Additional file 10 of Chlamydia
    pan-genomic analysis reveals balance between host adaptation and selective pressure
    to genome reduction. 2019. doi:<a href="https://doi.org/10.6084/m9.figshare.9808760.v1">10.6084/m9.figshare.9808760.v1</a>
  apa: Sigalova, O. M., Chaplin, A. V., Bochkareva, O., Shelyakin, P. V., Filaretov,
    V. A., Akkuratov, E. E., … Gelfand, M. S. (2019). Additional file 10 of Chlamydia
    pan-genomic analysis reveals balance between host adaptation and selective pressure
    to genome reduction. Springer Nature. <a href="https://doi.org/10.6084/m9.figshare.9808760.v1">https://doi.org/10.6084/m9.figshare.9808760.v1</a>
  chicago: Sigalova, Olga M., Andrei V. Chaplin, Olga Bochkareva, Pavel V. Shelyakin,
    Vsevolod A. Filaretov, Evgeny E. Akkuratov, Valentina Burskaia, and Mikhail S.
    Gelfand. “Additional File 10 of Chlamydia Pan-Genomic Analysis Reveals Balance
    between Host Adaptation and Selective Pressure to Genome Reduction.” Springer
    Nature, 2019. <a href="https://doi.org/10.6084/m9.figshare.9808760.v1">https://doi.org/10.6084/m9.figshare.9808760.v1</a>.
  ieee: O. M. Sigalova <i>et al.</i>, “Additional file 10 of Chlamydia pan-genomic
    analysis reveals balance between host adaptation and selective pressure to genome
    reduction.” Springer Nature, 2019.
  ista: Sigalova OM, Chaplin AV, Bochkareva O, Shelyakin PV, Filaretov VA, Akkuratov
    EE, Burskaia V, Gelfand MS. 2019. Additional file 10 of Chlamydia pan-genomic
    analysis reveals balance between host adaptation and selective pressure to genome
    reduction, Springer Nature, <a href="https://doi.org/10.6084/m9.figshare.9808760.v1">10.6084/m9.figshare.9808760.v1</a>.
  mla: Sigalova, Olga M., et al. <i>Additional File 10 of Chlamydia Pan-Genomic Analysis
    Reveals Balance between Host Adaptation and Selective Pressure to Genome Reduction</i>.
    Springer Nature, 2019, doi:<a href="https://doi.org/10.6084/m9.figshare.9808760.v1">10.6084/m9.figshare.9808760.v1</a>.
  short: O.M. Sigalova, A.V. Chaplin, O. Bochkareva, P.V. Shelyakin, V.A. Filaretov,
    E.E. Akkuratov, V. Burskaia, M.S. Gelfand, (2019).
date_created: 2021-08-06T07:59:56Z
date_published: 2019-09-12T00:00:00Z
date_updated: 2026-04-03T09:39:40Z
day: '12'
department:
- _id: FyKo
doi: 10.6084/m9.figshare.9808760.v1
main_file_link:
- open_access: '1'
  url: https://doi.org/10.6084/m9.figshare.9808760.v1
month: '09'
oa: 1
oa_version: Published Version
publisher: Springer Nature
related_material:
  record:
  - id: '6898'
    relation: used_in_publication
    status: public
status: public
title: Additional file 10 of Chlamydia pan-genomic analysis reveals balance between
  host adaptation and selective pressure to genome reduction
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2019'
...
---
_id: '9784'
abstract:
- lang: eng
  text: 'Additional file 1: Table S1. Kinetics of MDA-MB-231 cell growth in either
    the presence or absence of 100Â mg/L glyphosate. Cell counts are given at day-1
    of seeding flasks and following 6-days of continuous culture. Note: no differences
    in cell numbers were observed between negative control and glyphosate treated
    cultures.'
article_processing_charge: No
author:
- first_name: Michael N.
  full_name: Antoniou, Michael N.
  last_name: Antoniou
- first_name: Armel
  full_name: Nicolas, Armel
  id: 2A103192-F248-11E8-B48F-1D18A9856A87
  last_name: Nicolas
- first_name: Robin
  full_name: Mesnage, Robin
  last_name: Mesnage
- first_name: Martina
  full_name: Biserni, Martina
  last_name: Biserni
- first_name: Francesco V.
  full_name: Rao, Francesco V.
  last_name: Rao
- first_name: Cristina Vazquez
  full_name: Martin, Cristina Vazquez
  last_name: Martin
citation:
  ama: Antoniou MN, Nicolas A, Mesnage R, Biserni M, Rao FV, Martin CV. MOESM1 of
    Glyphosate does not substitute for glycine in proteins of actively dividing mammalian
    cells. 2019. doi:<a href="https://doi.org/10.6084/m9.figshare.9411761.v1">10.6084/m9.figshare.9411761.v1</a>
  apa: Antoniou, M. N., Nicolas, A., Mesnage, R., Biserni, M., Rao, F. V., &#38; Martin,
    C. V. (2019). MOESM1 of Glyphosate does not substitute for glycine in proteins
    of actively dividing mammalian cells. Springer Nature. <a href="https://doi.org/10.6084/m9.figshare.9411761.v1">https://doi.org/10.6084/m9.figshare.9411761.v1</a>
  chicago: Antoniou, Michael N., Armel Nicolas, Robin Mesnage, Martina Biserni, Francesco
    V. Rao, and Cristina Vazquez Martin. “MOESM1 of Glyphosate Does Not Substitute
    for Glycine in Proteins of Actively Dividing Mammalian Cells.” Springer Nature,
    2019. <a href="https://doi.org/10.6084/m9.figshare.9411761.v1">https://doi.org/10.6084/m9.figshare.9411761.v1</a>.
  ieee: M. N. Antoniou, A. Nicolas, R. Mesnage, M. Biserni, F. V. Rao, and C. V. Martin,
    “MOESM1 of Glyphosate does not substitute for glycine in proteins of actively
    dividing mammalian cells.” Springer Nature, 2019.
  ista: Antoniou MN, Nicolas A, Mesnage R, Biserni M, Rao FV, Martin CV. 2019. MOESM1
    of Glyphosate does not substitute for glycine in proteins of actively dividing
    mammalian cells, Springer Nature, <a href="https://doi.org/10.6084/m9.figshare.9411761.v1">10.6084/m9.figshare.9411761.v1</a>.
  mla: Antoniou, Michael N., et al. <i>MOESM1 of Glyphosate Does Not Substitute for
    Glycine in Proteins of Actively Dividing Mammalian Cells</i>. Springer Nature,
    2019, doi:<a href="https://doi.org/10.6084/m9.figshare.9411761.v1">10.6084/m9.figshare.9411761.v1</a>.
  short: M.N. Antoniou, A. Nicolas, R. Mesnage, M. Biserni, F.V. Rao, C.V. Martin,
    (2019).
date_created: 2021-08-06T08:14:05Z
date_published: 2019-08-09T00:00:00Z
date_updated: 2023-02-23T12:52:29Z
day: '09'
department:
- _id: LifeSc
doi: 10.6084/m9.figshare.9411761.v1
main_file_link:
- open_access: '1'
  url: https://doi.org/10.6084/m9.figshare.9411761.v1
month: '08'
oa: 1
oa_version: Published Version
publisher: Springer Nature
related_material:
  record:
  - id: '6819'
    relation: used_in_publication
    status: public
status: public
title: MOESM1 of Glyphosate does not substitute for glycine in proteins of actively
  dividing mammalian cells
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2019'
...
---
_id: '9786'
article_processing_charge: No
author:
- first_name: Jakob
  full_name: Ruess, Jakob
  id: 4A245D00-F248-11E8-B48F-1D18A9856A87
  last_name: Ruess
  orcid: 0000-0003-1615-3282
- first_name: Maros
  full_name: Pleska, Maros
  id: 4569785E-F248-11E8-B48F-1D18A9856A87
  last_name: Pleska
  orcid: 0000-0001-7460-7479
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
- first_name: Gašper
  full_name: Tkačik, Gašper
  id: 3D494DCA-F248-11E8-B48F-1D18A9856A87
  last_name: Tkačik
  orcid: 0000-0002-6699-1455
citation:
  ama: Ruess J, Pleska M, Guet CC, Tkačik G. Supporting text and results. 2019. doi:<a
    href="https://doi.org/10.1371/journal.pcbi.1007168.s001">10.1371/journal.pcbi.1007168.s001</a>
  apa: Ruess, J., Pleska, M., Guet, C. C., &#38; Tkačik, G. (2019). Supporting text
    and results. Public Library of Science. <a href="https://doi.org/10.1371/journal.pcbi.1007168.s001">https://doi.org/10.1371/journal.pcbi.1007168.s001</a>
  chicago: Ruess, Jakob, Maros Pleska, Calin C Guet, and Gašper Tkačik. “Supporting
    Text and Results.” Public Library of Science, 2019. <a href="https://doi.org/10.1371/journal.pcbi.1007168.s001">https://doi.org/10.1371/journal.pcbi.1007168.s001</a>.
  ieee: J. Ruess, M. Pleska, C. C. Guet, and G. Tkačik, “Supporting text and results.”
    Public Library of Science, 2019.
  ista: Ruess J, Pleska M, Guet CC, Tkačik G. 2019. Supporting text and results, Public
    Library of Science, <a href="https://doi.org/10.1371/journal.pcbi.1007168.s001">10.1371/journal.pcbi.1007168.s001</a>.
  mla: Ruess, Jakob, et al. <i>Supporting Text and Results</i>. Public Library of
    Science, 2019, doi:<a href="https://doi.org/10.1371/journal.pcbi.1007168.s001">10.1371/journal.pcbi.1007168.s001</a>.
  short: J. Ruess, M. Pleska, C.C. Guet, G. Tkačik, (2019).
date_created: 2021-08-06T08:23:43Z
date_published: 2019-07-02T00:00:00Z
date_updated: 2025-04-15T07:33:55Z
day: '02'
department:
- _id: CaGu
- _id: GaTk
doi: 10.1371/journal.pcbi.1007168.s001
month: '07'
oa_version: Published Version
publisher: Public Library of Science
related_material:
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    relation: used_in_publication
    status: public
status: public
title: Supporting text and results
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2019'
...
---
_id: '9789'
article_processing_charge: No
author:
- first_name: Victoria
  full_name: Pokusaeva, Victoria
  id: 3184041C-F248-11E8-B48F-1D18A9856A87
  last_name: Pokusaeva
  orcid: 0000-0001-7660-444X
- first_name: Dinara R.
  full_name: Usmanova, Dinara R.
  last_name: Usmanova
- first_name: Ekaterina V.
  full_name: Putintseva, Ekaterina V.
  last_name: Putintseva
- first_name: Lorena
  full_name: Espinar, Lorena
  last_name: Espinar
- first_name: Karen
  full_name: Sarkisyan, Karen
  id: 39A7BF80-F248-11E8-B48F-1D18A9856A87
  last_name: Sarkisyan
  orcid: 0000-0002-5375-6341
- first_name: Alexander S.
  full_name: Mishin, Alexander S.
  last_name: Mishin
- first_name: Natalya S.
  full_name: Bogatyreva, Natalya S.
  last_name: Bogatyreva
- first_name: Dmitry
  full_name: Ivankov, Dmitry
  id: 49FF1036-F248-11E8-B48F-1D18A9856A87
  last_name: Ivankov
  orcid: 0000-0002-8224-4118
- first_name: Arseniy
  full_name: Akopyan, Arseniy
  id: 430D2C90-F248-11E8-B48F-1D18A9856A87
  last_name: Akopyan
  orcid: 0000-0002-2548-617X
- first_name: Sergey
  full_name: Avvakumov, Sergey
  id: 3827DAC8-F248-11E8-B48F-1D18A9856A87
  last_name: Avvakumov
  orcid: 0000-0002-7840-5062
- first_name: Inna S.
  full_name: Povolotskaya, Inna S.
  last_name: Povolotskaya
- first_name: Guillaume J.
  full_name: Filion, Guillaume J.
  last_name: Filion
- first_name: Lucas B.
  full_name: Carey, Lucas B.
  last_name: Carey
- first_name: Fyodor
  full_name: Kondrashov, Fyodor
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
citation:
  ama: Pokusaeva V, Usmanova DR, Putintseva EV, et al. Multiple alignment of His3
    orthologues. 2019. doi:<a href="https://doi.org/10.1371/journal.pgen.1008079.s010">10.1371/journal.pgen.1008079.s010</a>
  apa: Pokusaeva, V., Usmanova, D. R., Putintseva, E. V., Espinar, L., Sarkisyan,
    K., Mishin, A. S., … Kondrashov, F. (2019). Multiple alignment of His3 orthologues.
    Public Library of Science. <a href="https://doi.org/10.1371/journal.pgen.1008079.s010">https://doi.org/10.1371/journal.pgen.1008079.s010</a>
  chicago: Pokusaeva, Victoria, Dinara R. Usmanova, Ekaterina V. Putintseva, Lorena
    Espinar, Karen Sarkisyan, Alexander S. Mishin, Natalya S. Bogatyreva, et al. “Multiple
    Alignment of His3 Orthologues.” Public Library of Science, 2019. <a href="https://doi.org/10.1371/journal.pgen.1008079.s010">https://doi.org/10.1371/journal.pgen.1008079.s010</a>.
  ieee: V. Pokusaeva <i>et al.</i>, “Multiple alignment of His3 orthologues.” Public
    Library of Science, 2019.
  ista: Pokusaeva V, Usmanova DR, Putintseva EV, Espinar L, Sarkisyan K, Mishin AS,
    Bogatyreva NS, Ivankov D, Akopyan A, Avvakumov S, Povolotskaya IS, Filion GJ,
    Carey LB, Kondrashov F. 2019. Multiple alignment of His3 orthologues, Public Library
    of Science, <a href="https://doi.org/10.1371/journal.pgen.1008079.s010">10.1371/journal.pgen.1008079.s010</a>.
  mla: Pokusaeva, Victoria, et al. <i>Multiple Alignment of His3 Orthologues</i>.
    Public Library of Science, 2019, doi:<a href="https://doi.org/10.1371/journal.pgen.1008079.s010">10.1371/journal.pgen.1008079.s010</a>.
  short: V. Pokusaeva, D.R. Usmanova, E.V. Putintseva, L. Espinar, K. Sarkisyan, A.S.
    Mishin, N.S. Bogatyreva, D. Ivankov, A. Akopyan, S. Avvakumov, I.S. Povolotskaya,
    G.J. Filion, L.B. Carey, F. Kondrashov, (2019).
date_created: 2021-08-06T08:38:50Z
date_published: 2019-04-10T00:00:00Z
date_updated: 2026-04-03T09:45:18Z
day: '10'
department:
- _id: FyKo
doi: 10.1371/journal.pgen.1008079.s010
month: '04'
oa_version: Published Version
publisher: Public Library of Science
related_material:
  record:
  - id: '6419'
    relation: used_in_publication
    status: public
status: public
title: Multiple alignment of His3 orthologues
type: research_data_reference
user_id: 6785fbc1-c503-11eb-8a32-93094b40e1cf
year: '2019'
...
