---
_id: '14020'
abstract:
- lang: eng
  text: We report the observation of macroscopic field-free orientation, i.e., more
    than 73% of CO molecules pointing in the same direction. This is achieved through
    an all-optical scheme operating at high particle densities (>10(17)  cm(-3)) that
    combines one-color (ω) and two-color (ω+2ω) nonresonant femtosecond laser pulses.
    We show that the achieved orientation solely relies on the hyperpolarizability
    interaction as opposed to an ionization-depletion mechanism, thus, opening a wide
    range of applications. The achieved strong orientation enables us to reveal the
    molecular-frame anisotropies of the photorecombination amplitudes and phases caused
    by a shape resonance. The resonance appears as a local maximum in the even-harmonic
    emission around 28 eV. In contrast, the odd-harmonic emission is suppressed in
    this spectral region through the combined effects of an asymmetric photorecombination
    phase and a subcycle Stark effect, generic for polar molecules, that we experimentally
    identify.
article_number: '023001'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: P. M.
  full_name: Kraus, P. M.
  last_name: Kraus
- first_name: Denitsa Rangelova
  full_name: Baykusheva, Denitsa Rangelova
  id: 71b4d059-2a03-11ee-914d-dfa3beed6530
  last_name: Baykusheva
- first_name: H. J.
  full_name: Wörner, H. J.
  last_name: Wörner
citation:
  ama: Kraus PM, Baykusheva DR, Wörner HJ. Two-pulse field-free orientation reveals
    anisotropy of molecular shape resonance. <i>Physical Review Letters</i>. 2014;113(2).
    doi:<a href="https://doi.org/10.1103/physrevlett.113.023001">10.1103/physrevlett.113.023001</a>
  apa: Kraus, P. M., Baykusheva, D. R., &#38; Wörner, H. J. (2014). Two-pulse field-free
    orientation reveals anisotropy of molecular shape resonance. <i>Physical Review
    Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/physrevlett.113.023001">https://doi.org/10.1103/physrevlett.113.023001</a>
  chicago: Kraus, P. M., Denitsa Rangelova Baykusheva, and H. J. Wörner. “Two-Pulse
    Field-Free Orientation Reveals Anisotropy of Molecular Shape Resonance.” <i>Physical
    Review Letters</i>. American Physical Society, 2014. <a href="https://doi.org/10.1103/physrevlett.113.023001">https://doi.org/10.1103/physrevlett.113.023001</a>.
  ieee: P. M. Kraus, D. R. Baykusheva, and H. J. Wörner, “Two-pulse field-free orientation
    reveals anisotropy of molecular shape resonance,” <i>Physical Review Letters</i>,
    vol. 113, no. 2. American Physical Society, 2014.
  ista: Kraus PM, Baykusheva DR, Wörner HJ. 2014. Two-pulse field-free orientation
    reveals anisotropy of molecular shape resonance. Physical Review Letters. 113(2),
    023001.
  mla: Kraus, P. M., et al. “Two-Pulse Field-Free Orientation Reveals Anisotropy of
    Molecular Shape Resonance.” <i>Physical Review Letters</i>, vol. 113, no. 2, 023001,
    American Physical Society, 2014, doi:<a href="https://doi.org/10.1103/physrevlett.113.023001">10.1103/physrevlett.113.023001</a>.
  short: P.M. Kraus, D.R. Baykusheva, H.J. Wörner, Physical Review Letters 113 (2014).
date_created: 2023-08-10T06:38:38Z
date_published: 2014-07-11T00:00:00Z
date_updated: 2023-08-22T09:02:56Z
day: '11'
doi: 10.1103/physrevlett.113.023001
extern: '1'
external_id:
  arxiv:
  - '1311.3923'
  pmid:
  - '25062172'
intvolume: '       113'
issue: '2'
keyword:
- General Physics and Astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1311.3923
month: '07'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review Letters
publication_identifier:
  eissn:
  - 1079-7114
  issn:
  - 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Two-pulse field-free orientation reveals anisotropy of molecular shape resonance
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 113
year: '2014'
...
---
_id: '10384'
abstract:
- lang: eng
  text: 'Recent studies aimed at investigating artificial analogs of bacterial colonies
    have shown that low-density suspensions of self-propelled particles confined in
    two dimensions can assemble into finite aggregates that merge and split, but have
    a typical size that remains constant (living clusters). In this Letter, we address
    the problem of the formation of living clusters and crystals of active particles
    in three dimensions. We study two systems: self-propelled particles interacting
    via a generic attractive potential and colloids that can move toward each other
    as a result of active agents (e.g., by molecular motors). In both cases, fluidlike
    “living” clusters form. We explain this general feature in terms of the balance
    between active forces and regression to thermodynamic equilibrium. This balance
    can be quantified in terms of a dimensionless number that allows us to collapse
    the observed clustering behavior onto a universal curve. We also discuss how active
    motion affects the kinetics of crystal formation.'
acknowledgement: This work was supported by the ERC Advanced Grant 227758, the National
  Science Foundation under Career Grant No. DMR-0846426, the Wolfson Merit Award 2007/R3
  of the Royal Society of London and the EPSRC Programme Grant EP/I001352/1. BMM acknowledge
  T. Curk and A. Ballard for useful discussions. C. V. acknowledges financial support
  from a Juan de la Cierva Fellowship, from the Marie Curie Integration Grant PCIG-GA-2011-303941
  ANISOKINEQ, and from the National Project FIS2010- 16159. S. A-U acknowledges support
  from the Alexander von Humboldt Foundation.
article_number: '245702'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: B. M.
  full_name: Mognetti, B. M.
  last_name: Mognetti
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
- first_name: S.
  full_name: Angioletti-Uberti, S.
  last_name: Angioletti-Uberti
- first_name: A.
  full_name: Cacciuto, A.
  last_name: Cacciuto
- first_name: C.
  full_name: Valeriani, C.
  last_name: Valeriani
- first_name: D.
  full_name: Frenkel, D.
  last_name: Frenkel
citation:
  ama: Mognetti BM, Šarić A, Angioletti-Uberti S, Cacciuto A, Valeriani C, Frenkel
    D. Living clusters and crystals from low-density suspensions of active colloids.
    <i>Physical Review Letters</i>. 2013;111(24). doi:<a href="https://doi.org/10.1103/physrevlett.111.245702">10.1103/physrevlett.111.245702</a>
  apa: Mognetti, B. M., Šarić, A., Angioletti-Uberti, S., Cacciuto, A., Valeriani,
    C., &#38; Frenkel, D. (2013). Living clusters and crystals from low-density suspensions
    of active colloids. <i>Physical Review Letters</i>. American Physical Society.
    <a href="https://doi.org/10.1103/physrevlett.111.245702">https://doi.org/10.1103/physrevlett.111.245702</a>
  chicago: Mognetti, B. M., Anđela Šarić, S. Angioletti-Uberti, A. Cacciuto, C. Valeriani,
    and D. Frenkel. “Living Clusters and Crystals from Low-Density Suspensions of
    Active Colloids.” <i>Physical Review Letters</i>. American Physical Society, 2013.
    <a href="https://doi.org/10.1103/physrevlett.111.245702">https://doi.org/10.1103/physrevlett.111.245702</a>.
  ieee: B. M. Mognetti, A. Šarić, S. Angioletti-Uberti, A. Cacciuto, C. Valeriani,
    and D. Frenkel, “Living clusters and crystals from low-density suspensions of
    active colloids,” <i>Physical Review Letters</i>, vol. 111, no. 24. American Physical
    Society, 2013.
  ista: Mognetti BM, Šarić A, Angioletti-Uberti S, Cacciuto A, Valeriani C, Frenkel
    D. 2013. Living clusters and crystals from low-density suspensions of active colloids.
    Physical Review Letters. 111(24), 245702.
  mla: Mognetti, B. M., et al. “Living Clusters and Crystals from Low-Density Suspensions
    of Active Colloids.” <i>Physical Review Letters</i>, vol. 111, no. 24, 245702,
    American Physical Society, 2013, doi:<a href="https://doi.org/10.1103/physrevlett.111.245702">10.1103/physrevlett.111.245702</a>.
  short: B.M. Mognetti, A. Šarić, S. Angioletti-Uberti, A. Cacciuto, C. Valeriani,
    D. Frenkel, Physical Review Letters 111 (2013).
date_created: 2021-11-29T13:29:31Z
date_published: 2013-12-11T00:00:00Z
date_updated: 2021-11-29T14:05:19Z
day: '11'
doi: 10.1103/physrevlett.111.245702
extern: '1'
external_id:
  arxiv:
  - '1311.4681'
  pmid:
  - '24483677'
intvolume: '       111'
issue: '24'
keyword:
- general physics and astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1311.4681
month: '12'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review Letters
publication_identifier:
  eissn:
  - 1079-7114
  issn:
  - 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Living clusters and crystals from low-density suspensions of active colloids
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 111
year: '2013'
...
---
_id: '7776'
abstract:
- lang: eng
  text: We present an analysis of finite-size effects in jammed packings of N soft,
    frictionless spheres at zero temperature. There is a 1/N correction to the discrete
    jump in the contact number at the transition so that jammed packings exist only
    above isostaticity. As a result, the canonical power-law scalings of the contact
    number and elastic moduli break down at low pressure. These quantities exhibit
    scaling collapse with a nontrivial scaling function, demonstrating that the jamming
    transition can be considered a phase transition. Scaling is achieved as a function
    of N in both two and three dimensions, indicating an upper critical dimension
    of 2.
article_number: '095704'
article_processing_charge: No
article_type: original
author:
- first_name: Carl Peter
  full_name: Goodrich, Carl Peter
  id: EB352CD2-F68A-11E9-89C5-A432E6697425
  last_name: Goodrich
  orcid: 0000-0002-1307-5074
- first_name: Andrea J.
  full_name: Liu, Andrea J.
  last_name: Liu
- first_name: Sidney R.
  full_name: Nagel, Sidney R.
  last_name: Nagel
citation:
  ama: Goodrich CP, Liu AJ, Nagel SR. Finite-size scaling at the jamming transition.
    <i>Physical Review Letters</i>. 2012;109(9). doi:<a href="https://doi.org/10.1103/physrevlett.109.095704">10.1103/physrevlett.109.095704</a>
  apa: Goodrich, C. P., Liu, A. J., &#38; Nagel, S. R. (2012). Finite-size scaling
    at the jamming transition. <i>Physical Review Letters</i>. American Physical Society.
    <a href="https://doi.org/10.1103/physrevlett.109.095704">https://doi.org/10.1103/physrevlett.109.095704</a>
  chicago: Goodrich, Carl Peter, Andrea J. Liu, and Sidney R. Nagel. “Finite-Size
    Scaling at the Jamming Transition.” <i>Physical Review Letters</i>. American Physical
    Society, 2012. <a href="https://doi.org/10.1103/physrevlett.109.095704">https://doi.org/10.1103/physrevlett.109.095704</a>.
  ieee: C. P. Goodrich, A. J. Liu, and S. R. Nagel, “Finite-size scaling at the jamming
    transition,” <i>Physical Review Letters</i>, vol. 109, no. 9. American Physical
    Society, 2012.
  ista: Goodrich CP, Liu AJ, Nagel SR. 2012. Finite-size scaling at the jamming transition.
    Physical Review Letters. 109(9), 095704.
  mla: Goodrich, Carl Peter, et al. “Finite-Size Scaling at the Jamming Transition.”
    <i>Physical Review Letters</i>, vol. 109, no. 9, 095704, American Physical Society,
    2012, doi:<a href="https://doi.org/10.1103/physrevlett.109.095704">10.1103/physrevlett.109.095704</a>.
  short: C.P. Goodrich, A.J. Liu, S.R. Nagel, Physical Review Letters 109 (2012).
date_created: 2020-04-30T11:44:12Z
date_published: 2012-08-27T00:00:00Z
date_updated: 2021-01-12T08:15:27Z
day: '27'
doi: 10.1103/physrevlett.109.095704
extern: '1'
intvolume: '       109'
issue: '9'
language:
- iso: eng
month: '08'
oa_version: None
publication: Physical Review Letters
publication_identifier:
  issn:
  - 0031-9007
  - 1079-7114
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
status: public
title: Finite-size scaling at the jamming transition
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 109
year: '2012'
...
---
_id: '10387'
abstract:
- lang: eng
  text: We report numerical simulations of membrane tubulation driven by large colloidal
    particles. Using Monte Carlo simulations we study how the process depends on particle
    size and binding strength, and present accurate free energy calculations to sort
    out how tube formation compares with the competing budding process. We find that
    tube formation is a result of the collective behavior of the particles adhering
    on the surface, and it occurs for binding strengths that are smaller than those
    required for budding. We also find that long linear aggregates of particles forming
    on the membrane surface act as nucleation seeds for tubulation by lowering the
    free energy barrier associated to the process.
article_number: '188101'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
- first_name: Angelo
  full_name: Cacciuto, Angelo
  last_name: Cacciuto
citation:
  ama: Šarić A, Cacciuto A. Mechanism of membrane tube formation induced by adhesive
    nanocomponents. <i>Physical Review Letters</i>. 2012;109(18). doi:<a href="https://doi.org/10.1103/physrevlett.109.188101">10.1103/physrevlett.109.188101</a>
  apa: Šarić, A., &#38; Cacciuto, A. (2012). Mechanism of membrane tube formation
    induced by adhesive nanocomponents. <i>Physical Review Letters</i>. American Physical
    Society. <a href="https://doi.org/10.1103/physrevlett.109.188101">https://doi.org/10.1103/physrevlett.109.188101</a>
  chicago: Šarić, Anđela, and Angelo Cacciuto. “Mechanism of Membrane Tube Formation
    Induced by Adhesive Nanocomponents.” <i>Physical Review Letters</i>. American
    Physical Society, 2012. <a href="https://doi.org/10.1103/physrevlett.109.188101">https://doi.org/10.1103/physrevlett.109.188101</a>.
  ieee: A. Šarić and A. Cacciuto, “Mechanism of membrane tube formation induced by
    adhesive nanocomponents,” <i>Physical Review Letters</i>, vol. 109, no. 18. American
    Physical Society, 2012.
  ista: Šarić A, Cacciuto A. 2012. Mechanism of membrane tube formation induced by
    adhesive nanocomponents. Physical Review Letters. 109(18), 188101.
  mla: Šarić, Anđela, and Angelo Cacciuto. “Mechanism of Membrane Tube Formation Induced
    by Adhesive Nanocomponents.” <i>Physical Review Letters</i>, vol. 109, no. 18,
    188101, American Physical Society, 2012, doi:<a href="https://doi.org/10.1103/physrevlett.109.188101">10.1103/physrevlett.109.188101</a>.
  short: A. Šarić, A. Cacciuto, Physical Review Letters 109 (2012).
date_created: 2021-11-29T14:08:00Z
date_published: 2012-10-31T00:00:00Z
date_updated: 2021-11-29T14:29:25Z
day: '31'
doi: 10.1103/physrevlett.109.188101
extern: '1'
external_id:
  arxiv:
  - '1206.3528'
  pmid:
  - '23215334'
intvolume: '       109'
issue: '18'
keyword:
- general physics and astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1206.3528
month: '10'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review Letters
publication_identifier:
  eissn:
  - 1079-7114
  issn:
  - 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Mechanism of membrane tube formation induced by adhesive nanocomponents
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 109
year: '2012'
...
---
_id: '10388'
abstract:
- lang: eng
  text: Using computer simulations, we show that lipid membranes can mediate linear
    aggregation of spherical nanoparticles binding to it for a wide range of biologically
    relevant bending rigidities. This result is in net contrast with the isotropic
    aggregation of nanoparticles on fluid interfaces or the expected clustering of
    isotropic insertions in biological membranes. We present a phase diagram indicating
    where linear aggregation is expected and compute explicitly the free-energy barriers
    associated with linear and isotropic aggregation. Finally, we provide simple scaling
    arguments to explain this phenomenology.
acknowledgement: "This work was supported by the National Science Foundation under
  Career Grant No. DMR-0846426.\r\n"
article_number: '118101'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
- first_name: Angelo
  full_name: Cacciuto, Angelo
  last_name: Cacciuto
citation:
  ama: Šarić A, Cacciuto A. Fluid membranes can drive linear aggregation of adsorbed
    spherical nanoparticles. <i>Physical Review Letters</i>. 2012;108(11). doi:<a
    href="https://doi.org/10.1103/physrevlett.108.118101">10.1103/physrevlett.108.118101</a>
  apa: Šarić, A., &#38; Cacciuto, A. (2012). Fluid membranes can drive linear aggregation
    of adsorbed spherical nanoparticles. <i>Physical Review Letters</i>. American
    Physical Society. <a href="https://doi.org/10.1103/physrevlett.108.118101">https://doi.org/10.1103/physrevlett.108.118101</a>
  chicago: Šarić, Anđela, and Angelo Cacciuto. “Fluid Membranes Can Drive Linear Aggregation
    of Adsorbed Spherical Nanoparticles.” <i>Physical Review Letters</i>. American
    Physical Society, 2012. <a href="https://doi.org/10.1103/physrevlett.108.118101">https://doi.org/10.1103/physrevlett.108.118101</a>.
  ieee: A. Šarić and A. Cacciuto, “Fluid membranes can drive linear aggregation of
    adsorbed spherical nanoparticles,” <i>Physical Review Letters</i>, vol. 108, no.
    11. American Physical Society, 2012.
  ista: Šarić A, Cacciuto A. 2012. Fluid membranes can drive linear aggregation of
    adsorbed spherical nanoparticles. Physical Review Letters. 108(11), 118101.
  mla: Šarić, Anđela, and Angelo Cacciuto. “Fluid Membranes Can Drive Linear Aggregation
    of Adsorbed Spherical Nanoparticles.” <i>Physical Review Letters</i>, vol. 108,
    no. 11, 118101, American Physical Society, 2012, doi:<a href="https://doi.org/10.1103/physrevlett.108.118101">10.1103/physrevlett.108.118101</a>.
  short: A. Šarić, A. Cacciuto, Physical Review Letters 108 (2012).
date_created: 2021-11-29T14:30:05Z
date_published: 2012-03-14T00:00:00Z
date_updated: 2021-11-29T15:12:13Z
day: '14'
doi: 10.1103/physrevlett.108.118101
extern: '1'
external_id:
  arxiv:
  - '1201.0036'
  pmid:
  - '22540513'
intvolume: '       108'
issue: '11'
keyword:
- general physics and astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1201.0036
month: '03'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review Letters
publication_identifier:
  eissn:
  - 1079-7114
  issn:
  - 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Fluid membranes can drive linear aggregation of adsorbed spherical nanoparticles
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 108
year: '2012'
...
---
_id: '10391'
abstract:
- lang: eng
  text: We use numerical simulations to show how a fully flexible filament binding
    to a deformable cylindrical surface may acquire a macroscopic persistence length
    and a helical conformation. This is a result of the nontrivial elastic response
    to deformations of elastic sheets. We find that the filament’s helical pitch is
    completely determined by the mechanical properties of the surface, and can be
    easily tuned by varying the surface stretching rigidity. We propose simple scaling
    arguments to understand the physical mechanism behind this phenomenon and present
    a phase diagram indicating under what conditions one should expect a fully flexible
    chain to behave as a helical semiflexible filament. Finally, we discuss the implications
    of our results.
acknowledgement: This work was supported by the National Science Foundation under
  Career Grant No. DMR-0846426.
article_number: '226101'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Anđela
  full_name: Šarić, Anđela
  id: bf63d406-f056-11eb-b41d-f263a6566d8b
  last_name: Šarić
  orcid: 0000-0002-7854-2139
- first_name: Josep C.
  full_name: Pàmies, Josep C.
  last_name: Pàmies
- first_name: Angelo
  full_name: Cacciuto, Angelo
  last_name: Cacciuto
citation:
  ama: Šarić A, Pàmies JC, Cacciuto A. Effective elasticity of a flexible filament
    bound to a deformable cylindrical surface. <i>Physical Review Letters</i>. 2010;104(22).
    doi:<a href="https://doi.org/10.1103/physrevlett.104.226101">10.1103/physrevlett.104.226101</a>
  apa: Šarić, A., Pàmies, J. C., &#38; Cacciuto, A. (2010). Effective elasticity of
    a flexible filament bound to a deformable cylindrical surface. <i>Physical Review
    Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/physrevlett.104.226101">https://doi.org/10.1103/physrevlett.104.226101</a>
  chicago: Šarić, Anđela, Josep C. Pàmies, and Angelo Cacciuto. “Effective Elasticity
    of a Flexible Filament Bound to a Deformable Cylindrical Surface.” <i>Physical
    Review Letters</i>. American Physical Society, 2010. <a href="https://doi.org/10.1103/physrevlett.104.226101">https://doi.org/10.1103/physrevlett.104.226101</a>.
  ieee: A. Šarić, J. C. Pàmies, and A. Cacciuto, “Effective elasticity of a flexible
    filament bound to a deformable cylindrical surface,” <i>Physical Review Letters</i>,
    vol. 104, no. 22. American Physical Society, 2010.
  ista: Šarić A, Pàmies JC, Cacciuto A. 2010. Effective elasticity of a flexible filament
    bound to a deformable cylindrical surface. Physical Review Letters. 104(22), 226101.
  mla: Šarić, Anđela, et al. “Effective Elasticity of a Flexible Filament Bound to
    a Deformable Cylindrical Surface.” <i>Physical Review Letters</i>, vol. 104, no.
    22, 226101, American Physical Society, 2010, doi:<a href="https://doi.org/10.1103/physrevlett.104.226101">10.1103/physrevlett.104.226101</a>.
  short: A. Šarić, J.C. Pàmies, A. Cacciuto, Physical Review Letters 104 (2010).
date_created: 2021-11-29T15:14:33Z
date_published: 2010-06-03T00:00:00Z
date_updated: 2021-11-30T08:11:19Z
day: '03'
doi: 10.1103/physrevlett.104.226101
extern: '1'
external_id:
  arxiv:
  - '1005.2429'
  pmid:
  - '20867183'
intvolume: '       104'
issue: '22'
keyword:
- general physics and astronomy
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1005.2429
month: '06'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review Letters
publication_identifier:
  eissn:
  - 1079-7114
  issn:
  - 0031-9007
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Effective elasticity of a flexible filament bound to a deformable cylindrical
  surface
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 104
year: '2010'
...