---
_id: '8472'
abstract:
- lang: eng
  text: Characterization of protein dynamics by solid-state NMR spectroscopy requires
    robust and accurate measurement protocols, which are not yet fully developed.
    In this study, we investigate the backbone dynamics of microcrystalline ubiquitin
    using different approaches. A rotational-echo double-resonance type (REDOR-type)
    methodology allows one to accurately measure 1H−15N order parameters in highly
    deuterated samples. We show that the systematic errors in the REDOR experiment
    are as low as 1% or even less, giving access to accurate data for the amplitudes
    of backbone mobility. Combining such dipolar-coupling-derived order parameters
    with autocorrelated and cross-correlated 15N relaxation rates, we are able to
    quantitate amplitudes and correlation times of backbone dynamics on picosecond
    and nanosecond time scales in a residue-resolved manner. While the mobility on
    picosecond time scales appears to have rather uniform amplitude throughout the
    protein, we unambiguously identify and quantitate nanosecond mobility with order
    parameters S2 as low as 0.8 in some regions of the protein, where nanosecond dynamics
    has also been revealed in solution state. The methodology used here, a combination
    of accurate dipolar-coupling measurements and different relaxation parameters,
    yields details about dynamics on different time scales and can be applied to solid
    protein samples such as amyloid fibrils or membrane proteins.
article_processing_charge: No
article_type: original
author:
- first_name: Paul
  full_name: Schanda, Paul
  id: 7B541462-FAF6-11E9-A490-E8DFE5697425
  last_name: Schanda
  orcid: 0000-0002-9350-7606
- first_name: Beat H.
  full_name: Meier, Beat H.
  last_name: Meier
- first_name: Matthias
  full_name: Ernst, Matthias
  last_name: Ernst
citation:
  ama: Schanda P, Meier BH, Ernst M. Quantitative analysis of protein backbone dynamics
    in microcrystalline ubiquitin by solid-state NMR spectroscopy. <i>Journal of the
    American Chemical Society</i>. 2010;132(45):15957-15967. doi:<a href="https://doi.org/10.1021/ja100726a">10.1021/ja100726a</a>
  apa: Schanda, P., Meier, B. H., &#38; Ernst, M. (2010). Quantitative analysis of
    protein backbone dynamics in microcrystalline ubiquitin by solid-state NMR spectroscopy.
    <i>Journal of the American Chemical Society</i>. American Chemical Society. <a
    href="https://doi.org/10.1021/ja100726a">https://doi.org/10.1021/ja100726a</a>
  chicago: Schanda, Paul, Beat H. Meier, and Matthias Ernst. “Quantitative Analysis
    of Protein Backbone Dynamics in Microcrystalline Ubiquitin by Solid-State NMR
    Spectroscopy.” <i>Journal of the American Chemical Society</i>. American Chemical
    Society, 2010. <a href="https://doi.org/10.1021/ja100726a">https://doi.org/10.1021/ja100726a</a>.
  ieee: P. Schanda, B. H. Meier, and M. Ernst, “Quantitative analysis of protein backbone
    dynamics in microcrystalline ubiquitin by solid-state NMR spectroscopy,” <i>Journal
    of the American Chemical Society</i>, vol. 132, no. 45. American Chemical Society,
    pp. 15957–15967, 2010.
  ista: Schanda P, Meier BH, Ernst M. 2010. Quantitative analysis of protein backbone
    dynamics in microcrystalline ubiquitin by solid-state NMR spectroscopy. Journal
    of the American Chemical Society. 132(45), 15957–15967.
  mla: Schanda, Paul, et al. “Quantitative Analysis of Protein Backbone Dynamics in
    Microcrystalline Ubiquitin by Solid-State NMR Spectroscopy.” <i>Journal of the
    American Chemical Society</i>, vol. 132, no. 45, American Chemical Society, 2010,
    pp. 15957–67, doi:<a href="https://doi.org/10.1021/ja100726a">10.1021/ja100726a</a>.
  short: P. Schanda, B.H. Meier, M. Ernst, Journal of the American Chemical Society
    132 (2010) 15957–15967.
date_created: 2020-09-18T10:11:13Z
date_published: 2010-10-26T00:00:00Z
date_updated: 2021-01-12T08:19:30Z
day: '26'
doi: 10.1021/ja100726a
extern: '1'
intvolume: '       132'
issue: '45'
language:
- iso: eng
month: '10'
oa_version: None
page: 15957-15967
publication: Journal of the American Chemical Society
publication_identifier:
  issn:
  - 0002-7863
  - 1520-5126
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
status: public
title: Quantitative analysis of protein backbone dynamics in microcrystalline ubiquitin
  by solid-state NMR spectroscopy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 132
year: '2010'
...
---
_id: '8473'
abstract:
- lang: eng
  text: β2-microglobulin (β2m), the light chain of class I major histocompatibility
    complex, is responsible for the dialysis-related amyloidosis and, in patients
    undergoing long term dialysis, the full-length and chemically unmodified β2m converts
    into amyloid fibrils. The protein, belonging to the immunoglobulin superfamily,
    in common to other members of this family, experiences during its folding a long-lived
    intermediate associated to the trans-to-cis isomerization of Pro-32 that has been
    addressed as the precursor of the amyloid fibril formation. In this respect, previous
    studies on the W60G β2m mutant, showing that the lack of Trp-60 prevents fibril
    formation in mild aggregating condition, prompted us to reinvestigate the refolding
    kinetics of wild type and W60G β2m at atomic resolution by real-time NMR. The
    analysis, conducted at ambient temperature by the band selective flip angle short
    transient real-time two-dimensional NMR techniques and probing the β2m states
    every 15 s, revealed a more complex folding energy landscape than previously reported
    for wild type β2m, involving more than a single intermediate species, and shedding
    new light into the fibrillogenic pathway. Moreover, a significant difference in
    the kinetic scheme previously characterized by optical spectroscopic methods was
    discovered for the W60G β2m mutant.
article_processing_charge: No
article_type: original
author:
- first_name: Alessandra
  full_name: Corazza, Alessandra
  last_name: Corazza
- first_name: Enrico
  full_name: Rennella, Enrico
  last_name: Rennella
- first_name: Paul
  full_name: Schanda, Paul
  id: 7B541462-FAF6-11E9-A490-E8DFE5697425
  last_name: Schanda
  orcid: 0000-0002-9350-7606
- first_name: Maria Chiara
  full_name: Mimmi, Maria Chiara
  last_name: Mimmi
- first_name: Thomas
  full_name: Cutuil, Thomas
  last_name: Cutuil
- first_name: Sara
  full_name: Raimondi, Sara
  last_name: Raimondi
- first_name: Sofia
  full_name: Giorgetti, Sofia
  last_name: Giorgetti
- first_name: Federico
  full_name: Fogolari, Federico
  last_name: Fogolari
- first_name: Paolo
  full_name: Viglino, Paolo
  last_name: Viglino
- first_name: Lucio
  full_name: Frydman, Lucio
  last_name: Frydman
- first_name: Maayan
  full_name: Gal, Maayan
  last_name: Gal
- first_name: Vittorio
  full_name: Bellotti, Vittorio
  last_name: Bellotti
- first_name: Bernhard
  full_name: Brutscher, Bernhard
  last_name: Brutscher
- first_name: Gennaro
  full_name: Esposito, Gennaro
  last_name: Esposito
citation:
  ama: Corazza A, Rennella E, Schanda P, et al. Native-unlike long-lived intermediates
    along the folding pathway of the amyloidogenic protein β2-Microglobulin revealed
    by real-time two-dimensional NMR. <i>Journal of Biological Chemistry</i>. 2010;285(8):5827-5835.
    doi:<a href="https://doi.org/10.1074/jbc.m109.061168">10.1074/jbc.m109.061168</a>
  apa: Corazza, A., Rennella, E., Schanda, P., Mimmi, M. C., Cutuil, T., Raimondi,
    S., … Esposito, G. (2010). Native-unlike long-lived intermediates along the folding
    pathway of the amyloidogenic protein β2-Microglobulin revealed by real-time two-dimensional
    NMR. <i>Journal of Biological Chemistry</i>. American Society for Biochemistry
    &#38; Molecular Biology. <a href="https://doi.org/10.1074/jbc.m109.061168">https://doi.org/10.1074/jbc.m109.061168</a>
  chicago: Corazza, Alessandra, Enrico Rennella, Paul Schanda, Maria Chiara Mimmi,
    Thomas Cutuil, Sara Raimondi, Sofia Giorgetti, et al. “Native-Unlike Long-Lived
    Intermediates along the Folding Pathway of the Amyloidogenic Protein Β2-Microglobulin
    Revealed by Real-Time Two-Dimensional NMR.” <i>Journal of Biological Chemistry</i>.
    American Society for Biochemistry &#38; Molecular Biology, 2010. <a href="https://doi.org/10.1074/jbc.m109.061168">https://doi.org/10.1074/jbc.m109.061168</a>.
  ieee: A. Corazza <i>et al.</i>, “Native-unlike long-lived intermediates along the
    folding pathway of the amyloidogenic protein β2-Microglobulin revealed by real-time
    two-dimensional NMR,” <i>Journal of Biological Chemistry</i>, vol. 285, no. 8.
    American Society for Biochemistry &#38; Molecular Biology, pp. 5827–5835, 2010.
  ista: Corazza A, Rennella E, Schanda P, Mimmi MC, Cutuil T, Raimondi S, Giorgetti
    S, Fogolari F, Viglino P, Frydman L, Gal M, Bellotti V, Brutscher B, Esposito
    G. 2010. Native-unlike long-lived intermediates along the folding pathway of the
    amyloidogenic protein β2-Microglobulin revealed by real-time two-dimensional NMR.
    Journal of Biological Chemistry. 285(8), 5827–5835.
  mla: Corazza, Alessandra, et al. “Native-Unlike Long-Lived Intermediates along the
    Folding Pathway of the Amyloidogenic Protein Β2-Microglobulin Revealed by Real-Time
    Two-Dimensional NMR.” <i>Journal of Biological Chemistry</i>, vol. 285, no. 8,
    American Society for Biochemistry &#38; Molecular Biology, 2010, pp. 5827–35,
    doi:<a href="https://doi.org/10.1074/jbc.m109.061168">10.1074/jbc.m109.061168</a>.
  short: A. Corazza, E. Rennella, P. Schanda, M.C. Mimmi, T. Cutuil, S. Raimondi,
    S. Giorgetti, F. Fogolari, P. Viglino, L. Frydman, M. Gal, V. Bellotti, B. Brutscher,
    G. Esposito, Journal of Biological Chemistry 285 (2010) 5827–5835.
date_created: 2020-09-18T10:11:23Z
date_published: 2010-02-19T00:00:00Z
date_updated: 2021-01-12T08:19:31Z
day: '19'
doi: 10.1074/jbc.m109.061168
extern: '1'
intvolume: '       285'
issue: '8'
keyword:
- Cell Biology
- Biochemistry
- Molecular Biology
language:
- iso: eng
month: '02'
oa_version: None
page: 5827-5835
publication: Journal of Biological Chemistry
publication_identifier:
  issn:
  - 0021-9258
  - 1083-351X
publication_status: published
publisher: American Society for Biochemistry & Molecular Biology
quality_controlled: '1'
status: public
title: Native-unlike long-lived intermediates along the folding pathway of the amyloidogenic
  protein β2-Microglobulin revealed by real-time two-dimensional NMR
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 285
year: '2010'
...
---
_id: '8506'
article_processing_charge: No
author:
- first_name: Brian R.
  full_name: Hunt, Brian R.
  last_name: Hunt
- first_name: Vadim
  full_name: Kaloshin, Vadim
  id: FE553552-CDE8-11E9-B324-C0EBE5697425
  last_name: Kaloshin
  orcid: 0000-0002-6051-2628
citation:
  ama: 'Hunt BR, Kaloshin V. Prevalence. In: <i>Handbook of Dynamical Systems</i>.
    Vol 3. Elsevier; 2010:43-87. doi:<a href="https://doi.org/10.1016/s1874-575x(10)00310-3">10.1016/s1874-575x(10)00310-3</a>'
  apa: Hunt, B. R., &#38; Kaloshin, V. (2010). Prevalence. In <i>Handbook of Dynamical
    Systems</i> (Vol. 3, pp. 43–87). Elsevier. <a href="https://doi.org/10.1016/s1874-575x(10)00310-3">https://doi.org/10.1016/s1874-575x(10)00310-3</a>
  chicago: Hunt, Brian R., and Vadim Kaloshin. “Prevalence.” In <i>Handbook of Dynamical
    Systems</i>, 3:43–87. Elsevier, 2010. <a href="https://doi.org/10.1016/s1874-575x(10)00310-3">https://doi.org/10.1016/s1874-575x(10)00310-3</a>.
  ieee: B. R. Hunt and V. Kaloshin, “Prevalence,” in <i>Handbook of Dynamical Systems</i>,
    vol. 3, Elsevier, 2010, pp. 43–87.
  ista: 'Hunt BR, Kaloshin V. 2010.Prevalence. In: Handbook of Dynamical Systems.
    vol. 3, 43–87.'
  mla: Hunt, Brian R., and Vadim Kaloshin. “Prevalence.” <i>Handbook of Dynamical
    Systems</i>, vol. 3, Elsevier, 2010, pp. 43–87, doi:<a href="https://doi.org/10.1016/s1874-575x(10)00310-3">10.1016/s1874-575x(10)00310-3</a>.
  short: B.R. Hunt, V. Kaloshin, in:, Handbook of Dynamical Systems, Elsevier, 2010,
    pp. 43–87.
date_created: 2020-09-18T10:47:48Z
date_published: 2010-01-01T00:00:00Z
date_updated: 2021-01-12T08:19:45Z
day: '01'
doi: 10.1016/s1874-575x(10)00310-3
extern: '1'
intvolume: '         3'
language:
- iso: eng
month: '01'
oa_version: None
page: 43-87
publication: Handbook of Dynamical Systems
publication_identifier:
  isbn:
  - '9780444531414'
  issn:
  - 1874-575X
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: Prevalence
type: book_chapter
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 3
year: '2010'
...
---
_id: '8507'
abstract:
- lang: eng
  text: "We study a Cr nearly integrable Hamiltonian system  defined on \U0001D54B3
    × ℝ3. Let  and µΣ1 be the restriction of Lebesgue measure on \U0001D54B3 × ℝ3
    to ∑. We prove there is a perturbation ,  and an orbit (q(t), p(t)): ℝ → \U0001D54B3
    × ℝ3 of the Hamiltonian equation  such that ."
article_processing_charge: No
author:
- first_name: Vadim
  full_name: Kaloshin, Vadim
  id: FE553552-CDE8-11E9-B324-C0EBE5697425
  last_name: Kaloshin
  orcid: 0000-0002-6051-2628
- first_name: KE
  full_name: ZHANG, KE
  last_name: ZHANG
- first_name: YONG
  full_name: ZHENG, YONG
  last_name: ZHENG
citation:
  ama: 'Kaloshin V, ZHANG K, ZHENG Y. Almost dense orbit on energy surface. In: <i>XVIth
    International Congress on Mathematical Physics</i>. World Scientific; 2010:314-322.
    doi:<a href="https://doi.org/10.1142/9789814304634_0017">10.1142/9789814304634_0017</a>'
  apa: 'Kaloshin, V., ZHANG, K., &#38; ZHENG, Y. (2010). Almost dense orbit on energy
    surface. In <i>XVIth International Congress on Mathematical Physics</i> (pp. 314–322).
    Prague, Czech Republic: World Scientific. <a href="https://doi.org/10.1142/9789814304634_0017">https://doi.org/10.1142/9789814304634_0017</a>'
  chicago: Kaloshin, Vadim, KE ZHANG, and YONG ZHENG. “Almost Dense Orbit on Energy
    Surface.” In <i>XVIth International Congress on Mathematical Physics</i>, 314–22.
    World Scientific, 2010. <a href="https://doi.org/10.1142/9789814304634_0017">https://doi.org/10.1142/9789814304634_0017</a>.
  ieee: V. Kaloshin, K. ZHANG, and Y. ZHENG, “Almost dense orbit on energy surface,”
    in <i>XVIth International Congress on Mathematical Physics</i>, Prague, Czech
    Republic, 2010, pp. 314–322.
  ista: Kaloshin V, ZHANG K, ZHENG Y. 2010. Almost dense orbit on energy surface.
    XVIth International Congress on Mathematical Physics. International Congress on
    Mathematical Physics, 314–322.
  mla: Kaloshin, Vadim, et al. “Almost Dense Orbit on Energy Surface.” <i>XVIth International
    Congress on Mathematical Physics</i>, World Scientific, 2010, pp. 314–22, doi:<a
    href="https://doi.org/10.1142/9789814304634_0017">10.1142/9789814304634_0017</a>.
  short: V. Kaloshin, K. ZHANG, Y. ZHENG, in:, XVIth International Congress on Mathematical
    Physics, World Scientific, 2010, pp. 314–322.
conference:
  end_date: 2009-08-08
  location: Prague, Czech Republic
  name: International Congress on Mathematical Physics
  start_date: 2009-08-03
date_created: 2020-09-18T10:47:56Z
date_published: 2010-03-01T00:00:00Z
date_updated: 2021-01-12T08:19:46Z
day: '01'
doi: 10.1142/9789814304634_0017
extern: '1'
language:
- iso: eng
month: '03'
oa_version: None
page: 314-322
publication: XVIth International Congress on Mathematical Physics
publication_identifier:
  isbn:
  - '9789814304627'
  - '9789814304634'
publication_status: published
publisher: World Scientific
quality_controlled: '1'
status: public
title: Almost dense orbit on energy surface
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2010'
...
---
_id: '857'
abstract:
- lang: eng
  text: 'The need to maintain the structural and functional integrity of an evolving
    protein severely restricts the repertoire of acceptable amino-acid substitutions.
    However, it is not known whether these restrictions impose a global limit on how
    far homologous protein sequences can diverge from each other. Here we explore
    the limits of protein evolution using sequence divergence data. We formulate a
    computational approach to study the rate of divergence of distant protein sequences
    and measure this rate for ancient proteins, those that were present in the last
    universal common ancestor. We show that ancient proteins are still diverging from
    each other, indicating an ongoing expansion of the protein sequence universe.
    The slow rate of this divergence is imposed by the sparseness of functional protein
    sequences in sequence space and the ruggedness of the protein fitness landscape:
    98 per cent of sites cannot accept an amino-acid substitution at any given moment
    but a vast majority of all sites may eventually be permitted to evolve when other,
    compensatory, changes occur. Thus, 3.5 × 10 9 yr has not been enough to reach
    the limit of divergent evolution of proteins, and for most proteins the limit
    of sequence similarity imposed by common function may not exceed that of random
    sequences.'
acknowledgement: |
  We thank E. Koonin, Y. Wolf, A. Lobkovsky, D. Petrov, D. Ivankov, J. Sharpe, B. Lehner, Y. Jaeger, P. Vlasov, M. Ptitsyn and M. Roytberg for discussions and A. Kondrashov for extensive feedback on our manuscript. We thank D. Tawfik for inspiring us to start the investigation of the functional limits in sequence space.
author:
- first_name: Inna
  full_name: Povolotskaya, Inna
  last_name: Povolotskaya
- first_name: Fyodor
  full_name: Fyodor Kondrashov
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
citation:
  ama: Povolotskaya I, Kondrashov F. Sequence space and the ongoing expansion of the
    protein universe. <i>Nature</i>. 2010;465(7300):922-926. doi:<a href="https://doi.org/10.1038/nature09105">10.1038/nature09105</a>
  apa: Povolotskaya, I., &#38; Kondrashov, F. (2010). Sequence space and the ongoing
    expansion of the protein universe. <i>Nature</i>. Nature Publishing Group. <a
    href="https://doi.org/10.1038/nature09105">https://doi.org/10.1038/nature09105</a>
  chicago: Povolotskaya, Inna, and Fyodor Kondrashov. “Sequence Space and the Ongoing
    Expansion of the Protein Universe.” <i>Nature</i>. Nature Publishing Group, 2010.
    <a href="https://doi.org/10.1038/nature09105">https://doi.org/10.1038/nature09105</a>.
  ieee: I. Povolotskaya and F. Kondrashov, “Sequence space and the ongoing expansion
    of the protein universe,” <i>Nature</i>, vol. 465, no. 7300. Nature Publishing
    Group, pp. 922–926, 2010.
  ista: Povolotskaya I, Kondrashov F. 2010. Sequence space and the ongoing expansion
    of the protein universe. Nature. 465(7300), 922–926.
  mla: Povolotskaya, Inna, and Fyodor Kondrashov. “Sequence Space and the Ongoing
    Expansion of the Protein Universe.” <i>Nature</i>, vol. 465, no. 7300, Nature
    Publishing Group, 2010, pp. 922–26, doi:<a href="https://doi.org/10.1038/nature09105">10.1038/nature09105</a>.
  short: I. Povolotskaya, F. Kondrashov, Nature 465 (2010) 922–926.
date_created: 2018-12-11T11:48:52Z
date_published: 2010-06-17T00:00:00Z
date_updated: 2021-01-12T08:20:05Z
day: '17'
doi: 10.1038/nature09105
extern: 1
intvolume: '       465'
issue: '7300'
month: '06'
page: 922 - 926
publication: Nature
publication_status: published
publisher: Nature Publishing Group
publist_id: '6791'
quality_controlled: 0
status: public
title: Sequence space and the ongoing expansion of the protein universe
type: journal_article
volume: 465
year: '2010'
...
---
_id: '862'
abstract:
- lang: eng
  text: A long-standing controversy in evolutionary biology is whether or not evolving
    lineages can cross valleys on the fitness landscape that correspond to low-fitness
    genotypes, which can eventually enable them to reach isolated fitness peaks1-9.
    Here we study the fitness landscapes traversed by switches between different AU
    and GC Watson-Crick nucleotide pairs at complementary sites of mitochondrial transfer
    RNA stem regions in 83 mammalian species. We find that such Watson-Crick switches
    occur 30-40 times more slowly than pairs of neutral substitutions, and that alleles
    corresponding to GU and AC non-Watson-Crick intermediate states segregate within
    human populations at low frequencies, similar to those of non-synonymous alleles.
    Substitutions leading to a Watson-Crick switch are strongly correlated, especially
    in mitochondrial tRNAs encoded on the GT-nucleotide-rich strand of the mitochondrial
    genome. Using these data we estimate that a typical Watson-Crick switch involves
    crossing a fitness valley of a depth of about 10-3 or even about 10-2, with AC
    intermediates being slightly more deleterious than GU intermediates. This compensatory
    evolution must proceed through rare intermediate variants that never reach fixation.
    The ubiquitous nature of compensatory evolution in mammalian mitochondrial tRNAs
    and other molecules implies that simultaneous fixation of two alleles that are
    individually deleterious may be a common phenomenon at the molecular level.
acknowledgement: We thank H. Innan, M. Laessig, R. Guigo, I. Povolotskaya, D. Ivankov
  and M. Breen for thoughtful discussions and critical reading of the manuscript.
author:
- first_name: Margarita
  full_name: Meer, Margarita V
  last_name: Meer
- first_name: Alexey
  full_name: Kondrashov, Alexey S
  last_name: Kondrashov
- first_name: Yael
  full_name: Artzy-Randrup, Yael
  last_name: Artzy Randrup
- first_name: Fyodor
  full_name: Fyodor Kondrashov
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
citation:
  ama: Meer M, Kondrashov A, Artzy Randrup Y, Kondrashov F. Compensatory evolution
    in mitochondrial tRNAs navigates valleys of low fitness. <i>Nature</i>. 2010;464(7286):279-282.
    doi:<a href="https://doi.org/10.1038/nature08691">10.1038/nature08691</a>
  apa: Meer, M., Kondrashov, A., Artzy Randrup, Y., &#38; Kondrashov, F. (2010). Compensatory
    evolution in mitochondrial tRNAs navigates valleys of low fitness. <i>Nature</i>.
    Nature Publishing Group. <a href="https://doi.org/10.1038/nature08691">https://doi.org/10.1038/nature08691</a>
  chicago: Meer, Margarita, Alexey Kondrashov, Yael Artzy Randrup, and Fyodor Kondrashov.
    “Compensatory Evolution in Mitochondrial TRNAs Navigates Valleys of Low Fitness.”
    <i>Nature</i>. Nature Publishing Group, 2010. <a href="https://doi.org/10.1038/nature08691">https://doi.org/10.1038/nature08691</a>.
  ieee: M. Meer, A. Kondrashov, Y. Artzy Randrup, and F. Kondrashov, “Compensatory
    evolution in mitochondrial tRNAs navigates valleys of low fitness,” <i>Nature</i>,
    vol. 464, no. 7286. Nature Publishing Group, pp. 279–282, 2010.
  ista: Meer M, Kondrashov A, Artzy Randrup Y, Kondrashov F. 2010. Compensatory evolution
    in mitochondrial tRNAs navigates valleys of low fitness. Nature. 464(7286), 279–282.
  mla: Meer, Margarita, et al. “Compensatory Evolution in Mitochondrial TRNAs Navigates
    Valleys of Low Fitness.” <i>Nature</i>, vol. 464, no. 7286, Nature Publishing
    Group, 2010, pp. 279–82, doi:<a href="https://doi.org/10.1038/nature08691">10.1038/nature08691</a>.
  short: M. Meer, A. Kondrashov, Y. Artzy Randrup, F. Kondrashov, Nature 464 (2010)
    279–282.
date_created: 2018-12-11T11:48:54Z
date_published: 2010-03-11T00:00:00Z
date_updated: 2021-01-12T08:20:20Z
day: '11'
doi: 10.1038/nature08691
extern: 1
intvolume: '       464'
issue: '7286'
month: '03'
page: 279 - 282
publication: Nature
publication_status: published
publisher: Nature Publishing Group
publist_id: '6784'
quality_controlled: 0
status: public
title: Compensatory evolution in mitochondrial tRNAs navigates valleys of low fitness
type: journal_article
volume: 464
year: '2010'
...
---
_id: '872'
abstract:
- lang: eng
  text: The rate of spontaneous mutation in natural populations is a fundamental parameter
    for many evolutionary phenomena. Because the rate of mutation is generally low,
    most of what is currently known about mutation has been obtained through indirect,
    complex and imprecise methodological approaches. However, in the past few years
    genome-wide sequencing of closely related individuals has made it possible to
    estimate the rates of mutation directly at the level of the DNA, avoiding most
    of the problems associated with using indirect methods. Here, we review the methods
    used in the past with an emphasis on next generation sequencing, which may soon
    make the accurate measurement of spontaneous mutation rates a matter of routine.
author:
- first_name: Fyodor
  full_name: Fyodor Kondrashov
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
- first_name: Alexey
  full_name: Kondrashov, Alexey S
  last_name: Kondrashov
citation:
  ama: Kondrashov F, Kondrashov A. Measurements of spontaneous rates of mutations
    in the recent past and the near future. <i>Philosophical Transactions of the Royal
    Society of London Series B, Biological Sciences</i>. 2010;365(1544):1169-1176.
    doi:<a href="https://doi.org/10.1098/rstb.2009.0286">10.1098/rstb.2009.0286</a>
  apa: Kondrashov, F., &#38; Kondrashov, A. (2010). Measurements of spontaneous rates
    of mutations in the recent past and the near future. <i>Philosophical Transactions
    of the Royal Society of London. Series B, Biological Sciences</i>. Royal Society,
    The. <a href="https://doi.org/10.1098/rstb.2009.0286">https://doi.org/10.1098/rstb.2009.0286</a>
  chicago: Kondrashov, Fyodor, and Alexey Kondrashov. “Measurements of Spontaneous
    Rates of Mutations in the Recent Past and the near Future.” <i>Philosophical Transactions
    of the Royal Society of London. Series B, Biological Sciences</i>. Royal Society,
    The, 2010. <a href="https://doi.org/10.1098/rstb.2009.0286">https://doi.org/10.1098/rstb.2009.0286</a>.
  ieee: F. Kondrashov and A. Kondrashov, “Measurements of spontaneous rates of mutations
    in the recent past and the near future,” <i>Philosophical Transactions of the
    Royal Society of London. Series B, Biological Sciences</i>, vol. 365, no. 1544.
    Royal Society, The, pp. 1169–1176, 2010.
  ista: Kondrashov F, Kondrashov A. 2010. Measurements of spontaneous rates of mutations
    in the recent past and the near future. Philosophical Transactions of the Royal
    Society of London. Series B, Biological Sciences. 365(1544), 1169–1176.
  mla: Kondrashov, Fyodor, and Alexey Kondrashov. “Measurements of Spontaneous Rates
    of Mutations in the Recent Past and the near Future.” <i>Philosophical Transactions
    of the Royal Society of London. Series B, Biological Sciences</i>, vol. 365, no.
    1544, Royal Society, The, 2010, pp. 1169–76, doi:<a href="https://doi.org/10.1098/rstb.2009.0286">10.1098/rstb.2009.0286</a>.
  short: F. Kondrashov, A. Kondrashov, Philosophical Transactions of the Royal Society
    of London. Series B, Biological Sciences 365 (2010) 1169–1176.
date_created: 2018-12-11T11:48:57Z
date_published: 2010-04-27T00:00:00Z
date_updated: 2021-01-12T08:20:43Z
day: '27'
doi: 10.1098/rstb.2009.0286
extern: 1
intvolume: '       365'
issue: '1544'
month: '04'
page: 1169 - 1176
publication: Philosophical Transactions of the Royal Society of London. Series B,
  Biological Sciences
publication_status: published
publisher: Royal Society, The
publist_id: '6772'
quality_controlled: 0
status: public
title: Measurements of spontaneous rates of mutations in the recent past and the near
  future
type: journal_article
volume: 365
year: '2010'
...
---
_id: '884'
abstract:
- lang: eng
  text: 'Background: Divergence of two independently evolving sequences that originated
    from a common ancestor can be described by two parameters, the asymptotic level
    of divergence E and the rate r at which this level of divergence is approached.
    Constant negative selection impedes allele replacements and, therefore, is routinely
    assumed to decelerate sequence divergence. However, its impact on E and on r has
    not been formally investigated.Results: Strong selection that favors only one
    allele can make E arbitrarily small and r arbitrarily large. In contrast, in the
    case of 4 possible alleles and equal mutation rates, the lowest value of r, attained
    when two alleles confer equal fitnesses and the other two are strongly deleterious,
    is only two times lower than its value under selective neutrality.Conclusions:
    Constant selection can strongly constrain the level of sequence divergence, but
    cannot reduce substantially the rate at which this level is approached. In particular,
    under any constant selection the divergence of sequences that accumulated one
    substitution per neutral site since their origin from the common ancestor must
    already constitute at least one half of the asymptotic divergence at sites under
    such selection.Reviewers: This article was reviewed by Drs. Nicolas Galtier, Sergei
    Maslov, and Nick Grishin.'
author:
- first_name: Alexey
  full_name: Kondrashov, Alexey S
  last_name: Kondrashov
- first_name: Inna
  full_name: Povolotskaya, Inna
  last_name: Povolotskaya
- first_name: Dmitry
  full_name: Ivankov, Dmitry N
  last_name: Ivankov
- first_name: Fyodor
  full_name: Fyodor Kondrashov
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
citation:
  ama: Kondrashov A, Povolotskaya I, Ivankov D, Kondrashov F. Rate of sequence divergence
    under constant selection. <i>Biology Direct</i>. 2010;5. doi:<a href="https://doi.org/10.1186/1745-6150-5-5">10.1186/1745-6150-5-5</a>
  apa: Kondrashov, A., Povolotskaya, I., Ivankov, D., &#38; Kondrashov, F. (2010).
    Rate of sequence divergence under constant selection. <i>Biology Direct</i>. BioMed
    Central. <a href="https://doi.org/10.1186/1745-6150-5-5">https://doi.org/10.1186/1745-6150-5-5</a>
  chicago: Kondrashov, Alexey, Inna Povolotskaya, Dmitry Ivankov, and Fyodor Kondrashov.
    “Rate of Sequence Divergence under Constant Selection.” <i>Biology Direct</i>.
    BioMed Central, 2010. <a href="https://doi.org/10.1186/1745-6150-5-5">https://doi.org/10.1186/1745-6150-5-5</a>.
  ieee: A. Kondrashov, I. Povolotskaya, D. Ivankov, and F. Kondrashov, “Rate of sequence
    divergence under constant selection,” <i>Biology Direct</i>, vol. 5. BioMed Central,
    2010.
  ista: Kondrashov A, Povolotskaya I, Ivankov D, Kondrashov F. 2010. Rate of sequence
    divergence under constant selection. Biology Direct. 5.
  mla: Kondrashov, Alexey, et al. “Rate of Sequence Divergence under Constant Selection.”
    <i>Biology Direct</i>, vol. 5, BioMed Central, 2010, doi:<a href="https://doi.org/10.1186/1745-6150-5-5">10.1186/1745-6150-5-5</a>.
  short: A. Kondrashov, I. Povolotskaya, D. Ivankov, F. Kondrashov, Biology Direct
    5 (2010).
date_created: 2018-12-11T11:49:00Z
date_published: 2010-01-21T00:00:00Z
date_updated: 2021-01-12T08:21:15Z
day: '21'
doi: 10.1186/1745-6150-5-5
extern: 1
intvolume: '         5'
month: '01'
publication: Biology Direct
publication_status: published
publisher: BioMed Central
publist_id: '6762'
quality_controlled: 0
status: public
title: Rate of sequence divergence under constant selection
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
volume: 5
year: '2010'
...
---
_id: '89'
abstract:
- lang: eng
  text: We demonstrate the operation of a device that can produce chitosan nanoparticles
    in a tunable size range from 50-300 nm with small size dispersion. A piezoelectric
    oscillator operated at megahertz frequencies is used to aerosolize a solution
    containing dissolved chitosan. The solvent is then evaporated from the aerosolized
    droplets in a heat pipe, leaving monodisperse nanoparticles to be collected. The
    nanoparticle size is controlled both by the concentration of the dissolved polymer
    and by the size of the aerosol droplets that are created. Our device can be used
    with any polymer or polymer/therapeutic combination that can be prepared in a
    homogeneous solution and vaporized.
acknowledgement: This work was supported by the National Science Foundation under
  Grants PHY-0456898 and PHY-0757989, and acknowledgment is made to the Donors of
  the Petroleum Research Fund administered by the American Chemical Society for partial
  support of this research.
author:
- first_name: Ian
  full_name: Wright, Ian
  last_name: Wright
- first_name: Andrew P
  full_name: Higginbotham, Andrew P
  id: 4AD6785A-F248-11E8-B48F-1D18A9856A87
  last_name: Higginbotham
  orcid: 0000-0003-2607-2363
- first_name: Shenda
  full_name: Baker, Shenda
  last_name: Baker
- first_name: Tom
  full_name: Donnelly, Tom
  last_name: Donnelly
citation:
  ama: Wright I, Higginbotham AP, Baker S, Donnelly T. Generation of nanoparticles
    of controlled size using ultrasonic piezoelectric oscillators in solution. <i>ACS
    Applied Materials and Interfaces</i>. 2010;2(8):2360-2364. doi:<a href="https://doi.org/10.1021/am100375w">10.1021/am100375w</a>
  apa: Wright, I., Higginbotham, A. P., Baker, S., &#38; Donnelly, T. (2010). Generation
    of nanoparticles of controlled size using ultrasonic piezoelectric oscillators
    in solution. <i>ACS Applied Materials and Interfaces</i>. American Chemical Society.
    <a href="https://doi.org/10.1021/am100375w">https://doi.org/10.1021/am100375w</a>
  chicago: Wright, Ian, Andrew P Higginbotham, Shenda Baker, and Tom Donnelly. “Generation
    of Nanoparticles of Controlled Size Using Ultrasonic Piezoelectric Oscillators
    in Solution.” <i>ACS Applied Materials and Interfaces</i>. American Chemical Society,
    2010. <a href="https://doi.org/10.1021/am100375w">https://doi.org/10.1021/am100375w</a>.
  ieee: I. Wright, A. P. Higginbotham, S. Baker, and T. Donnelly, “Generation of nanoparticles
    of controlled size using ultrasonic piezoelectric oscillators in solution,” <i>ACS
    Applied Materials and Interfaces</i>, vol. 2, no. 8. American Chemical Society,
    pp. 2360–2364, 2010.
  ista: Wright I, Higginbotham AP, Baker S, Donnelly T. 2010. Generation of nanoparticles
    of controlled size using ultrasonic piezoelectric oscillators in solution. ACS
    Applied Materials and Interfaces. 2(8), 2360–2364.
  mla: Wright, Ian, et al. “Generation of Nanoparticles of Controlled Size Using Ultrasonic
    Piezoelectric Oscillators in Solution.” <i>ACS Applied Materials and Interfaces</i>,
    vol. 2, no. 8, American Chemical Society, 2010, pp. 2360–64, doi:<a href="https://doi.org/10.1021/am100375w">10.1021/am100375w</a>.
  short: I. Wright, A.P. Higginbotham, S. Baker, T. Donnelly, ACS Applied Materials
    and Interfaces 2 (2010) 2360–2364.
date_created: 2018-12-11T11:44:34Z
date_published: 2010-07-20T00:00:00Z
date_updated: 2021-01-12T08:21:17Z
day: '20'
doi: 10.1021/am100375w
extern: '1'
external_id:
  pmid:
  - '    20735108'
intvolume: '         2'
issue: '8'
language:
- iso: eng
month: '07'
oa_version: None
page: 2360 - 2364
pmid: 1
publication: ACS Applied Materials and Interfaces
publication_status: published
publisher: American Chemical Society
publist_id: '7965'
quality_controlled: '1'
status: public
title: Generation of nanoparticles of controlled size using ultrasonic piezoelectric
  oscillators in solution
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 2
year: '2010'
...
---
_id: '891'
abstract:
- lang: eng
  text: Gene duplications and their subsequent divergence play an important part in
    the evolution of novel gene functions. Several models for the emergence, maintenance
    and evolution of gene copies have been proposed. However, a clear consensus on
    how gene duplications are fixed and maintained in genomes is lacking. Here, we
    present a comprehensive classification of the models that are relevant to all
    stages of the evolution of gene duplications. Each model predicts a unique combination
    of evolutionary dynamics and functional properties. Setting out these predictions
    is an important step towards identifying the main mechanisms that are involved
    in the evolution of gene duplications.
acknowledgement: |
  We thank M. Lynch for insightful comments on the manuscript.
author:
- first_name: Hideki
  full_name: Innan, Hideki
  last_name: Innan
- first_name: Fyodor
  full_name: Fyodor Kondrashov
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
citation:
  ama: 'Innan H, Kondrashov F. The evolution of gene duplications: Classifying and
    distinguishing between models. <i>Nature Reviews Genetics</i>. 2010;11(2):97-108.
    doi:<a href="https://doi.org/10.1038/nrg2689">10.1038/nrg2689</a>'
  apa: 'Innan, H., &#38; Kondrashov, F. (2010). The evolution of gene duplications:
    Classifying and distinguishing between models. <i>Nature Reviews Genetics</i>.
    Nature Publishing Group. <a href="https://doi.org/10.1038/nrg2689">https://doi.org/10.1038/nrg2689</a>'
  chicago: 'Innan, Hideki, and Fyodor Kondrashov. “The Evolution of Gene Duplications:
    Classifying and Distinguishing between Models.” <i>Nature Reviews Genetics</i>.
    Nature Publishing Group, 2010. <a href="https://doi.org/10.1038/nrg2689">https://doi.org/10.1038/nrg2689</a>.'
  ieee: 'H. Innan and F. Kondrashov, “The evolution of gene duplications: Classifying
    and distinguishing between models,” <i>Nature Reviews Genetics</i>, vol. 11, no.
    2. Nature Publishing Group, pp. 97–108, 2010.'
  ista: 'Innan H, Kondrashov F. 2010. The evolution of gene duplications: Classifying
    and distinguishing between models. Nature Reviews Genetics. 11(2), 97–108.'
  mla: 'Innan, Hideki, and Fyodor Kondrashov. “The Evolution of Gene Duplications:
    Classifying and Distinguishing between Models.” <i>Nature Reviews Genetics</i>,
    vol. 11, no. 2, Nature Publishing Group, 2010, pp. 97–108, doi:<a href="https://doi.org/10.1038/nrg2689">10.1038/nrg2689</a>.'
  short: H. Innan, F. Kondrashov, Nature Reviews Genetics 11 (2010) 97–108.
date_created: 2018-12-11T11:49:03Z
date_published: 2010-02-01T00:00:00Z
date_updated: 2021-01-12T08:21:19Z
day: '01'
doi: 10.1038/nrg2689
extern: 1
intvolume: '        11'
issue: '2'
month: '02'
page: 97 - 108
publication: Nature Reviews Genetics
publication_status: published
publisher: Nature Publishing Group
publist_id: '6755'
quality_controlled: 0
status: public
title: 'The evolution of gene duplications: Classifying and distinguishing between
  models'
type: journal_article
volume: 11
year: '2010'
...
---
_id: '901'
abstract:
- lang: eng
  text: 'Background: Surveying deleterious variation in human populations is crucial
    for our understanding, diagnosis and potential treatment of human genetic pathologies.
    A number of recent genome-wide analyses focused on the prevalence of segregating
    deleterious alleles in the nuclear genome. However, such studies have not been
    conducted for the mitochondrial genome.Results: We present a systematic survey
    of polymorphisms in the human mitochondrial genome, including those predicted
    to be deleterious and those that correspond to known pathogenic mutations. Analyzing
    4458 completely sequenced mitochondrial genomes we characterize the genetic diversity
    of different types of single nucleotide polymorphisms (SNPs) in African (L haplotypes)
    and non-African (M and N haplotypes) populations. We find that the overall level
    of polymorphism is higher in the mitochondrial compared to the nuclear genome,
    although the mitochondrial genome appears to be under stronger selection as indicated
    by proportionally fewer nonsynonymous than synonymous substitutions. The African
    mitochondrial genomes show higher heterozygosity, a greater number of polymorphic
    sites and higher frequencies of polymorphisms for synonymous, benign and damaging
    polymorphism than non-African genomes. However, African genomes carry significantly
    fewer SNPs that have been previously characterized as pathogenic compared to non-African
    genomes.Conclusions: Finding SNPs classified as pathogenic to be the only category
    of polymorphisms that are more abundant in non-African genomes is best explained
    by a systematic ascertainment bias that favours the discovery of pathogenic polymorphisms
    segregating in non-African populations. This further suggests that, contrary to
    the common disease-common variant hypothesis, pathogenic mutations are largely
    population-specific and different SNPs may be associated with the same disease
    in different populations. Therefore, to obtain a comprehensive picture of the
    deleterious variability in the human population, as well as to improve the diagnostics
    of individuals carrying African mitochondrial haplotypes, it is necessary to survey
    different populations independently.Reviewers: This article was reviewed by Dr
    Mikhail Gelfand, Dr Vasily Ramensky (nominated by Dr Eugene Koonin) and Dr David
    Rand (nominated by Dr Laurence Hurst).'
acknowledgement: We thank Ivan Adzhubei and Shamil Sunyaev for extensive assistance
  with PolyPhen 2 and insightful discussion. We thank the Spanish Ministry of Science
  and Innovation, Plan Nacional Program grant BFU2009-09271 for funding.
author:
- first_name: Michael
  full_name: Breen, Michael S
  last_name: Breen
- first_name: Fyodor
  full_name: Fyodor Kondrashov
  id: 44FDEF62-F248-11E8-B48F-1D18A9856A87
  last_name: Kondrashov
  orcid: 0000-0001-8243-4694
citation:
  ama: Breen M, Kondrashov F. Mitochondrial pathogenic mutations are population-specific.
    <i>Biology Direct</i>. 2010;5. doi:<a href="https://doi.org/10.1186/1745-6150-5-68">10.1186/1745-6150-5-68</a>
  apa: Breen, M., &#38; Kondrashov, F. (2010). Mitochondrial pathogenic mutations
    are population-specific. <i>Biology Direct</i>. BioMed Central. <a href="https://doi.org/10.1186/1745-6150-5-68">https://doi.org/10.1186/1745-6150-5-68</a>
  chicago: Breen, Michael, and Fyodor Kondrashov. “Mitochondrial Pathogenic Mutations
    Are Population-Specific.” <i>Biology Direct</i>. BioMed Central, 2010. <a href="https://doi.org/10.1186/1745-6150-5-68">https://doi.org/10.1186/1745-6150-5-68</a>.
  ieee: M. Breen and F. Kondrashov, “Mitochondrial pathogenic mutations are population-specific,”
    <i>Biology Direct</i>, vol. 5. BioMed Central, 2010.
  ista: Breen M, Kondrashov F. 2010. Mitochondrial pathogenic mutations are population-specific.
    Biology Direct. 5.
  mla: Breen, Michael, and Fyodor Kondrashov. “Mitochondrial Pathogenic Mutations
    Are Population-Specific.” <i>Biology Direct</i>, vol. 5, BioMed Central, 2010,
    doi:<a href="https://doi.org/10.1186/1745-6150-5-68">10.1186/1745-6150-5-68</a>.
  short: M. Breen, F. Kondrashov, Biology Direct 5 (2010).
date_created: 2018-12-11T11:49:06Z
date_published: 2010-12-31T00:00:00Z
date_updated: 2021-01-12T08:21:46Z
day: '31'
doi: 10.1186/1745-6150-5-68
extern: 1
intvolume: '         5'
month: '12'
publication: Biology Direct
publication_status: published
publisher: BioMed Central
publist_id: '6749'
quality_controlled: 0
status: public
title: Mitochondrial pathogenic mutations are population-specific
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
volume: 5
year: '2010'
...
---
_id: '9012'
abstract:
- lang: eng
  text: In this Letter, we characterize experimentally the diffusiophoretic motion
    of colloids and λ-DNA toward higher concentration of solutes, using microfluidic
    technology to build spatially and temporally controlled concentration gradients.
    We then demonstrate that segregation and spatial patterning of the particles can
    be achieved from temporal variations of the solute concentration profile. This
    segregation takes the form of a strong trapping potential, stemming from an osmotically
    induced rectification mechanism of the solute time-dependent variations. Depending
    on the spatial and temporal symmetry of the solute signal, localization patterns
    with various shapes can be achieved. These results highlight the role of solute
    contrasts in out-of-equilibrium processes occurring in soft matter.
article_number: '138302'
article_processing_charge: No
article_type: letter_note
arxiv: 1
author:
- first_name: Jérémie A
  full_name: Palacci, Jérémie A
  id: 8fb92548-2b22-11eb-b7c1-a3f0d08d7c7d
  last_name: Palacci
  orcid: 0000-0002-7253-9465
- first_name: Benjamin
  full_name: Abécassis, Benjamin
  last_name: Abécassis
- first_name: Cécile
  full_name: Cottin-Bizonne, Cécile
  last_name: Cottin-Bizonne
- first_name: Christophe
  full_name: Ybert, Christophe
  last_name: Ybert
- first_name: Lydéric
  full_name: Bocquet, Lydéric
  last_name: Bocquet
citation:
  ama: Palacci JA, Abécassis B, Cottin-Bizonne C, Ybert C, Bocquet L. Colloidal motility
    and pattern formation under rectified diffusiophoresis. <i>Physical Review Letters</i>.
    2010;104(13). doi:<a href="https://doi.org/10.1103/physrevlett.104.138302">10.1103/physrevlett.104.138302</a>
  apa: Palacci, J. A., Abécassis, B., Cottin-Bizonne, C., Ybert, C., &#38; Bocquet,
    L. (2010). Colloidal motility and pattern formation under rectified diffusiophoresis.
    <i>Physical Review Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/physrevlett.104.138302">https://doi.org/10.1103/physrevlett.104.138302</a>
  chicago: Palacci, Jérémie A, Benjamin Abécassis, Cécile Cottin-Bizonne, Christophe
    Ybert, and Lydéric Bocquet. “Colloidal Motility and Pattern Formation under Rectified
    Diffusiophoresis.” <i>Physical Review Letters</i>. American Physical Society,
    2010. <a href="https://doi.org/10.1103/physrevlett.104.138302">https://doi.org/10.1103/physrevlett.104.138302</a>.
  ieee: J. A. Palacci, B. Abécassis, C. Cottin-Bizonne, C. Ybert, and L. Bocquet,
    “Colloidal motility and pattern formation under rectified diffusiophoresis,” <i>Physical
    Review Letters</i>, vol. 104, no. 13. American Physical Society, 2010.
  ista: Palacci JA, Abécassis B, Cottin-Bizonne C, Ybert C, Bocquet L. 2010. Colloidal
    motility and pattern formation under rectified diffusiophoresis. Physical Review
    Letters. 104(13), 138302.
  mla: Palacci, Jérémie A., et al. “Colloidal Motility and Pattern Formation under
    Rectified Diffusiophoresis.” <i>Physical Review Letters</i>, vol. 104, no. 13,
    138302, American Physical Society, 2010, doi:<a href="https://doi.org/10.1103/physrevlett.104.138302">10.1103/physrevlett.104.138302</a>.
  short: J.A. Palacci, B. Abécassis, C. Cottin-Bizonne, C. Ybert, L. Bocquet, Physical
    Review Letters 104 (2010).
date_created: 2021-01-19T10:25:04Z
date_published: 2010-04-02T00:00:00Z
date_updated: 2023-02-23T13:46:40Z
day: '02'
doi: 10.1103/physrevlett.104.138302
extern: '1'
external_id:
  arxiv:
  - '1004.1256 '
  pmid:
  - '20481918'
intvolume: '       104'
issue: '13'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1004.1256
month: '04'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review Letters
publication_identifier:
  eissn:
  - '10797114'
  issn:
  - '00319007'
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Colloidal motility and pattern formation under rectified diffusiophoresis
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 104
year: '2010'
...
---
_id: '9013'
abstract:
- lang: eng
  text: In this Letter, we investigate experimentally the nonequilibrium steady state
    of an active colloidal suspension under gravity field. The active particles are
    made of chemically powered colloids, showing self propulsion in the presence of
    an added fuel, here hydrogen peroxide. The active suspension is studied in a dedicated
    microfluidic device, made of permeable gel microstructures. Both the microdynamics
    of individual colloids and the global stationary state of the suspension under
    gravity are measured with optical microscopy. This yields a direct measurement
    of the effective temperature of the active system as a function of the particle
    activity, on the basis of the fluctuation-dissipation relationship. Our work is
    a first step in the experimental exploration of the out-of-equilibrium properties
    of active colloidal systems.
article_number: '088304'
article_processing_charge: No
article_type: letter_note
arxiv: 1
author:
- first_name: Jérémie A
  full_name: Palacci, Jérémie A
  id: 8fb92548-2b22-11eb-b7c1-a3f0d08d7c7d
  last_name: Palacci
  orcid: 0000-0002-7253-9465
- first_name: Cécile
  full_name: Cottin-Bizonne, Cécile
  last_name: Cottin-Bizonne
- first_name: Christophe
  full_name: Ybert, Christophe
  last_name: Ybert
- first_name: Lydéric
  full_name: Bocquet, Lydéric
  last_name: Bocquet
citation:
  ama: Palacci JA, Cottin-Bizonne C, Ybert C, Bocquet L. Sedimentation and effective
    temperature of active colloidal suspensions. <i>Physical Review Letters</i>. 2010;105(8).
    doi:<a href="https://doi.org/10.1103/physrevlett.105.088304">10.1103/physrevlett.105.088304</a>
  apa: Palacci, J. A., Cottin-Bizonne, C., Ybert, C., &#38; Bocquet, L. (2010). Sedimentation
    and effective temperature of active colloidal suspensions. <i>Physical Review
    Letters</i>. American Physical Society . <a href="https://doi.org/10.1103/physrevlett.105.088304">https://doi.org/10.1103/physrevlett.105.088304</a>
  chicago: Palacci, Jérémie A, Cécile Cottin-Bizonne, Christophe Ybert, and Lydéric
    Bocquet. “Sedimentation and Effective Temperature of Active Colloidal Suspensions.”
    <i>Physical Review Letters</i>. American Physical Society , 2010. <a href="https://doi.org/10.1103/physrevlett.105.088304">https://doi.org/10.1103/physrevlett.105.088304</a>.
  ieee: J. A. Palacci, C. Cottin-Bizonne, C. Ybert, and L. Bocquet, “Sedimentation
    and effective temperature of active colloidal suspensions,” <i>Physical Review
    Letters</i>, vol. 105, no. 8. American Physical Society , 2010.
  ista: Palacci JA, Cottin-Bizonne C, Ybert C, Bocquet L. 2010. Sedimentation and
    effective temperature of active colloidal suspensions. Physical Review Letters.
    105(8), 088304.
  mla: Palacci, Jérémie A., et al. “Sedimentation and Effective Temperature of Active
    Colloidal Suspensions.” <i>Physical Review Letters</i>, vol. 105, no. 8, 088304,
    American Physical Society , 2010, doi:<a href="https://doi.org/10.1103/physrevlett.105.088304">10.1103/physrevlett.105.088304</a>.
  short: J.A. Palacci, C. Cottin-Bizonne, C. Ybert, L. Bocquet, Physical Review Letters
    105 (2010).
date_created: 2021-01-19T10:26:33Z
date_published: 2010-08-20T00:00:00Z
date_updated: 2023-02-23T13:46:42Z
day: '20'
doi: 10.1103/physrevlett.105.088304
extern: '1'
external_id:
  arxiv:
  - '1004.4340'
  pmid:
  - '20868136'
intvolume: '       105'
issue: '8'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1004.4340
month: '08'
oa: 1
oa_version: Preprint
pmid: 1
publication: Physical Review Letters
publication_identifier:
  eissn:
  - '10797114'
  issn:
  - '00319007'
publication_status: published
publisher: 'American Physical Society '
quality_controlled: '1'
scopus_import: '1'
status: public
title: Sedimentation and effective temperature of active colloidal suspensions
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 105
year: '2010'
...
---
_id: '9145'
abstract:
- lang: eng
  text: "We have found a new way to express the solutions of the RSM (Reynolds Stress
    Model) equations that allows us to present the turbulent diffusivities for heat,
    salt and momentum in a way that is considerably simpler and thus easier to implement
    than in previous work. The RSM provides the dimensionless mixing efficiencies
    Γα (α stands for heat, salt and momentum). However, to compute the diffusivities,
    one needs additional information, specifically, the dissipation ε. Since a dynamic
    equation for the latter that includes the physical processes relevant to the ocean
    is still not available, one must resort to different sources of information outside
    the RSM to obtain a complete Mixing Scheme usable in OGCMs.\r\nAs for the RSM
    results, we show that the Γα’s are functions of both Ri and Rρ (Richardson number
    and density ratio representing double diffusion, DD); the Γα are different for
    heat, salt and momentum; in the case of heat, the traditional value Γh = 0.2 is
    valid only in the presence of strong shear (when DD is inoperative) while when
    shear subsides, NATRE data show that Γh can be three times as large, a result
    that we reproduce. The salt Γs is given in terms of Γh. The momentum Γm has thus
    far been guessed with different prescriptions while the RSM provides a well defined
    expression for Γm(Ri, Rρ). Having tested Γh, we then test the momentum Γm by showing
    that the turbulent Prandtl number Γm/Γh vs. Ri reproduces the available data quite
    well.\r\n\r\nAs for the dissipation ε, we use different representations, one for
    the mixed layer (ML), one for the thermocline and one for the ocean’s bottom.
    For the ML, we adopt a procedure analogous to the one successfully used in PB
    (planetary boundary layer) studies; for the thermocline, we employ an expression
    for the variable εN−2 from studies of the internal gravity waves spectra which
    includes a latitude dependence; for the ocean bottom, we adopt the enhanced bottom
    diffusivity expression used by previous authors but with a state of the art internal
    tidal energy formulation and replace the fixed Γα = 0.2 with the RSM result that
    brings into the problem the Ri, Rρ dependence of the Γα; the unresolved bottom
    drag, which has thus far been either ignored or modeled with heuristic relations,
    is modeled using a formalism we previously developed and tested in PBL studies.\r\nWe
    carried out several tests without an OGCM. Prandtl and flux Richardson numbers
    vs. Ri. The RSM model reproduces both types of data satisfactorily. DD and Mixing
    efficiency Γh(Ri, Rρ). The RSM model reproduces well the NATRE data. Bimodal ε-distribution.
    NATRE data show that ε(Ri < 1) ≈ 10ε(Ri > 1), which our model reproduces. Heat
    to salt flux ratio. In the Ri ≫ 1 regime, the RSM predictions reproduce the data
    satisfactorily. NATRE mass diffusivity. The z-profile of the mass diffusivity
    reproduces well the measurements at NATRE. The local form of the mixing scheme
    is algebraic with one cubic equation to solve."
article_processing_charge: No
article_type: original
author:
- first_name: V.M.
  full_name: Canuto, V.M.
  last_name: Canuto
- first_name: A.M.
  full_name: Howard, A.M.
  last_name: Howard
- first_name: Y.
  full_name: Cheng, Y.
  last_name: Cheng
- first_name: Caroline J
  full_name: Muller, Caroline J
  id: f978ccb0-3f7f-11eb-b193-b0e2bd13182b
  last_name: Muller
  orcid: 0000-0001-5836-5350
- first_name: A.
  full_name: Leboissetier, A.
  last_name: Leboissetier
- first_name: S.R.
  full_name: Jayne, S.R.
  last_name: Jayne
citation:
  ama: 'Canuto VM, Howard AM, Cheng Y, Muller CJ, Leboissetier A, Jayne SR. Ocean
    turbulence, III: New GISS vertical mixing scheme. <i>Ocean Modelling</i>. 2010;34(3-4):70-91.
    doi:<a href="https://doi.org/10.1016/j.ocemod.2010.04.006">10.1016/j.ocemod.2010.04.006</a>'
  apa: 'Canuto, V. M., Howard, A. M., Cheng, Y., Muller, C. J., Leboissetier, A.,
    &#38; Jayne, S. R. (2010). Ocean turbulence, III: New GISS vertical mixing scheme.
    <i>Ocean Modelling</i>. Elsevier. <a href="https://doi.org/10.1016/j.ocemod.2010.04.006">https://doi.org/10.1016/j.ocemod.2010.04.006</a>'
  chicago: 'Canuto, V.M., A.M. Howard, Y. Cheng, Caroline J Muller, A. Leboissetier,
    and S.R. Jayne. “Ocean Turbulence, III: New GISS Vertical Mixing Scheme.” <i>Ocean
    Modelling</i>. Elsevier, 2010. <a href="https://doi.org/10.1016/j.ocemod.2010.04.006">https://doi.org/10.1016/j.ocemod.2010.04.006</a>.'
  ieee: 'V. M. Canuto, A. M. Howard, Y. Cheng, C. J. Muller, A. Leboissetier, and
    S. R. Jayne, “Ocean turbulence, III: New GISS vertical mixing scheme,” <i>Ocean
    Modelling</i>, vol. 34, no. 3–4. Elsevier, pp. 70–91, 2010.'
  ista: 'Canuto VM, Howard AM, Cheng Y, Muller CJ, Leboissetier A, Jayne SR. 2010.
    Ocean turbulence, III: New GISS vertical mixing scheme. Ocean Modelling. 34(3–4),
    70–91.'
  mla: 'Canuto, V. M., et al. “Ocean Turbulence, III: New GISS Vertical Mixing Scheme.”
    <i>Ocean Modelling</i>, vol. 34, no. 3–4, Elsevier, 2010, pp. 70–91, doi:<a href="https://doi.org/10.1016/j.ocemod.2010.04.006">10.1016/j.ocemod.2010.04.006</a>.'
  short: V.M. Canuto, A.M. Howard, Y. Cheng, C.J. Muller, A. Leboissetier, S.R. Jayne,
    Ocean Modelling 34 (2010) 70–91.
date_created: 2021-02-15T14:40:19Z
date_published: 2010-05-12T00:00:00Z
date_updated: 2022-01-24T13:51:35Z
day: '12'
doi: 10.1016/j.ocemod.2010.04.006
extern: '1'
intvolume: '        34'
issue: 3-4
keyword:
- Computer Science (miscellaneous)
- Geotechnical Engineering and Engineering Geology
- Atmospheric Science
- Oceanography
language:
- iso: eng
month: '05'
oa_version: None
page: 70-91
publication: Ocean Modelling
publication_identifier:
  issn:
  - 1463-5003
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: 'Ocean turbulence, III: New GISS vertical mixing scheme'
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 34
year: '2010'
...
---
_id: '9146'
abstract:
- lang: eng
  text: "The factors governing the rate of change in the amount of atmospheric water
    vapor are analyzed in simulations of climate change. The global-mean amount of
    water vapor is estimated to increase at a differential rate of 7.3% K − 1 with
    respect to global-mean surface air temperature in the multi-model mean. Larger
    rates of change result if the fractional change is evaluated over a finite change
    in temperature (e.g., 8.2% K − 1 for a 3 K warming), and rates of change of zonal-mean
    column water vapor range from 6 to 12% K − 1 depending on latitude.\r\nClausius–Clapeyron
    scaling is directly evaluated using an invariant distribution of monthly-mean
    relative humidity, giving a rate of 7.4% K − 1 for global-mean water vapor. There
    are deviations from Clausius–Clapeyron scaling of zonal-mean column water vapor
    in the tropics and mid-latitudes, but they largely cancel in the global mean.
    A purely thermodynamic scaling based on a saturated troposphere gives a higher
    global rate of 7.9% K − 1.\r\nSurface specific humidity increases at a rate of
    5.7% K − 1, considerably lower than the rate for global-mean water vapor. Surface
    specific humidity closely follows Clausius–Clapeyron scaling over ocean. But there
    are widespread decreases in surface relative humidity over land (by more than
    1% K − 1 in many regions), and it is argued that decreases of this magnitude could
    result from the land/ocean contrast in surface warming."
article_number: '025207'
article_processing_charge: No
article_type: original
author:
- first_name: P A
  full_name: O’Gorman, P A
  last_name: O’Gorman
- first_name: Caroline J
  full_name: Muller, Caroline J
  id: f978ccb0-3f7f-11eb-b193-b0e2bd13182b
  last_name: Muller
  orcid: 0000-0001-5836-5350
citation:
  ama: O’Gorman PA, Muller CJ. How closely do changes in surface and column water
    vapor follow Clausius–Clapeyron scaling in climate change simulations? <i>Environmental
    Research Letters</i>. 2010;5(2). doi:<a href="https://doi.org/10.1088/1748-9326/5/2/025207">10.1088/1748-9326/5/2/025207</a>
  apa: O’Gorman, P. A., &#38; Muller, C. J. (2010). How closely do changes in surface
    and column water vapor follow Clausius–Clapeyron scaling in climate change simulations?
    <i>Environmental Research Letters</i>. IOP Publishing. <a href="https://doi.org/10.1088/1748-9326/5/2/025207">https://doi.org/10.1088/1748-9326/5/2/025207</a>
  chicago: O’Gorman, P A, and Caroline J Muller. “How Closely Do Changes in Surface
    and Column Water Vapor Follow Clausius–Clapeyron Scaling in Climate Change Simulations?”
    <i>Environmental Research Letters</i>. IOP Publishing, 2010. <a href="https://doi.org/10.1088/1748-9326/5/2/025207">https://doi.org/10.1088/1748-9326/5/2/025207</a>.
  ieee: P. A. O’Gorman and C. J. Muller, “How closely do changes in surface and column
    water vapor follow Clausius–Clapeyron scaling in climate change simulations?,”
    <i>Environmental Research Letters</i>, vol. 5, no. 2. IOP Publishing, 2010.
  ista: O’Gorman PA, Muller CJ. 2010. How closely do changes in surface and column
    water vapor follow Clausius–Clapeyron scaling in climate change simulations? Environmental
    Research Letters. 5(2), 025207.
  mla: O’Gorman, P. A., and Caroline J. Muller. “How Closely Do Changes in Surface
    and Column Water Vapor Follow Clausius–Clapeyron Scaling in Climate Change Simulations?”
    <i>Environmental Research Letters</i>, vol. 5, no. 2, 025207, IOP Publishing,
    2010, doi:<a href="https://doi.org/10.1088/1748-9326/5/2/025207">10.1088/1748-9326/5/2/025207</a>.
  short: P.A. O’Gorman, C.J. Muller, Environmental Research Letters 5 (2010).
date_created: 2021-02-15T14:40:46Z
date_published: 2010-04-09T00:00:00Z
date_updated: 2022-01-24T13:51:02Z
day: '09'
doi: 10.1088/1748-9326/5/2/025207
extern: '1'
intvolume: '         5'
issue: '2'
keyword:
- Renewable Energy
- Sustainability and the Environment
- Public Health
- Environmental and Occupational Health
- General Environmental Science
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1088/1748-9326/5/2/025207
month: '04'
oa: 1
oa_version: Published Version
publication: Environmental Research Letters
publication_identifier:
  issn:
  - 1748-9326
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
status: public
title: How closely do changes in surface and column water vapor follow Clausius–Clapeyron
  scaling in climate change simulations?
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 5
year: '2010'
...
---
_id: '920'
abstract:
- lang: eng
  text: Most eukaryotic cells sense and respond to the mechanical properties of their
    surroundings. This can strongly influence their collective behavior in embryonic
    development, tissue function, and wound healing. We use a deformable substrate
    to measure collective behavior in cell motion due to substrate mediated cell-cell
    interactions. We quantify spatial and temporal correlations in migration velocity
    and substrate deformation, and show that cooperative cell-driven patterns of substrate
    deformation mediate long-distance mechanical coupling between cells and control
    collective cell migration.
acknowledgement: "This work was supported by the NSF (DMR-0602684) and the Harvard
  MRSEC (DMR-0820484).\r\nWe would like to thank Dr. James Butler for helpful conversations."
article_processing_charge: No
author:
- first_name: Thomas
  full_name: Angelini, Thomas
  last_name: Angelini
- first_name: Edouard B
  full_name: Hannezo, Edouard B
  id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
  last_name: Hannezo
  orcid: 0000-0001-6005-1561
- first_name: Xavier
  full_name: Trepat, Xavier
  last_name: Trepat
- first_name: Jeffrey
  full_name: Fredberg, Jeffrey
  last_name: Fredberg
- first_name: David
  full_name: Weitz, David
  last_name: Weitz
citation:
  ama: Angelini T, Hannezo EB, Trepat X, Fredberg J, Weitz D. Cell migration driven
    by cooperative substrate deformation patterns. <i>Physical Review Letters</i>.
    2010;104(16). doi:<a href="https://doi.org/10.1103/PhysRevLett.104.168104">10.1103/PhysRevLett.104.168104</a>
  apa: Angelini, T., Hannezo, E. B., Trepat, X., Fredberg, J., &#38; Weitz, D. (2010).
    Cell migration driven by cooperative substrate deformation patterns. <i>Physical
    Review Letters</i>. American Physical Society. <a href="https://doi.org/10.1103/PhysRevLett.104.168104">https://doi.org/10.1103/PhysRevLett.104.168104</a>
  chicago: Angelini, Thomas, Edouard B Hannezo, Xavier Trepat, Jeffrey Fredberg, and
    David Weitz. “Cell Migration Driven by Cooperative Substrate Deformation Patterns.”
    <i>Physical Review Letters</i>. American Physical Society, 2010. <a href="https://doi.org/10.1103/PhysRevLett.104.168104">https://doi.org/10.1103/PhysRevLett.104.168104</a>.
  ieee: T. Angelini, E. B. Hannezo, X. Trepat, J. Fredberg, and D. Weitz, “Cell migration
    driven by cooperative substrate deformation patterns,” <i>Physical Review Letters</i>,
    vol. 104, no. 16. American Physical Society, 2010.
  ista: Angelini T, Hannezo EB, Trepat X, Fredberg J, Weitz D. 2010. Cell migration
    driven by cooperative substrate deformation patterns. Physical Review Letters.
    104(16).
  mla: Angelini, Thomas, et al. “Cell Migration Driven by Cooperative Substrate Deformation
    Patterns.” <i>Physical Review Letters</i>, vol. 104, no. 16, American Physical
    Society, 2010, doi:<a href="https://doi.org/10.1103/PhysRevLett.104.168104">10.1103/PhysRevLett.104.168104</a>.
  short: T. Angelini, E.B. Hannezo, X. Trepat, J. Fredberg, D. Weitz, Physical Review
    Letters 104 (2010).
date_created: 2018-12-11T11:49:12Z
date_published: 2010-04-23T00:00:00Z
date_updated: 2021-01-12T08:21:55Z
day: '23'
doi: 10.1103/PhysRevLett.104.168104
extern: '1'
intvolume: '       104'
issue: '16'
language:
- iso: eng
month: '04'
oa_version: None
publication: Physical Review Letters
publication_status: published
publisher: American Physical Society
publist_id: '6523'
status: public
title: Cell migration driven by cooperative substrate deformation patterns
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 104
year: '2010'
...
---
_id: '7078'
abstract:
- lang: eng
  text: We report resonant ultrasound spectroscopy (RUS), dilatometry/magnetostriction,
    magnetotransport, magnetization, specific-heat, and 119Sn Mössbauer spectroscopy
    measurements on SnTe and Sn0.995Cr0.005Te. Hall measurements at T=77 K indicate
    that our Bridgman-grown single crystals have a p-type carrier concentration of
    3.4×1019 cm−3 and that our Cr-doped crystals have an n-type concentration of 5.8×1022 cm−3.
    Although our SnTe crystals are diamagnetic over the temperature range 2≤T≤1100 K,
    the Cr-doped crystals are room-temperature ferromagnets with a Curie temperature
    of 294 K. For each sample type, three-terminal capacitive dilatometry measurements
    detect a subtle 0.5 μm distortion at Tc≈85 K. Whereas our RUS measurements on
    SnTe show elastic hardening near the structural transition, pointing to co-elastic
    behavior, similar measurements on Sn0.995Cr0.005Te show a pronounced softening,
    pointing to ferroelastic behavior. Effective Debye temperature, θD, values of
    SnTe obtained from 119Sn Mössbauer studies show a hardening of phonons in the
    range 60–115 K (θD=162 K) as compared with the 100–300 K range (θD=150 K). In
    addition, a precursor softening extending over approximately 100 K anticipates
    this collapse at the critical temperature and quantitative analysis over three
    decades of its reduced modulus finds ΔC44/C44=A|(T−T0)/T0|−κ with κ=0.50±0.02,
    a value indicating a three-dimensional softening of phonon branches at a temperature
    T0∼75 K, considerably below Tc. We suggest that the differences in these two types
    of elastic behaviors lie in the absence of elastic domain-wall motion in the one
    case and their nucleation in the other.
article_number: '184112'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: E. K. H.
  full_name: Salje, E. K. H.
  last_name: Salje
- first_name: D. J.
  full_name: Safarik, D. J.
  last_name: Safarik
- first_name: Kimberly A
  full_name: Modic, Kimberly A
  id: 13C26AC0-EB69-11E9-87C6-5F3BE6697425
  last_name: Modic
  orcid: 0000-0001-9760-3147
- first_name: J. E.
  full_name: Gubernatis, J. E.
  last_name: Gubernatis
- first_name: J. C.
  full_name: Cooley, J. C.
  last_name: Cooley
- first_name: R. D.
  full_name: Taylor, R. D.
  last_name: Taylor
- first_name: B.
  full_name: Mihaila, B.
  last_name: Mihaila
- first_name: A.
  full_name: Saxena, A.
  last_name: Saxena
- first_name: T.
  full_name: Lookman, T.
  last_name: Lookman
- first_name: J. L.
  full_name: Smith, J. L.
  last_name: Smith
- first_name: R. A.
  full_name: Fisher, R. A.
  last_name: Fisher
- first_name: M.
  full_name: Pasternak, M.
  last_name: Pasternak
- first_name: C. P.
  full_name: Opeil, C. P.
  last_name: Opeil
- first_name: T.
  full_name: Siegrist, T.
  last_name: Siegrist
- first_name: P. B.
  full_name: Littlewood, P. B.
  last_name: Littlewood
- first_name: J. C.
  full_name: Lashley, J. C.
  last_name: Lashley
citation:
  ama: 'Salje EKH, Safarik DJ, Modic KA, et al. Tin telluride: A weakly co-elastic
    metal. <i>Physical Review B</i>. 2010;82(18). doi:<a href="https://doi.org/10.1103/physrevb.82.184112">10.1103/physrevb.82.184112</a>'
  apa: 'Salje, E. K. H., Safarik, D. J., Modic, K. A., Gubernatis, J. E., Cooley,
    J. C., Taylor, R. D., … Lashley, J. C. (2010). Tin telluride: A weakly co-elastic
    metal. <i>Physical Review B</i>. APS. <a href="https://doi.org/10.1103/physrevb.82.184112">https://doi.org/10.1103/physrevb.82.184112</a>'
  chicago: 'Salje, E. K. H., D. J. Safarik, Kimberly A Modic, J. E. Gubernatis, J.
    C. Cooley, R. D. Taylor, B. Mihaila, et al. “Tin Telluride: A Weakly Co-Elastic
    Metal.” <i>Physical Review B</i>. APS, 2010. <a href="https://doi.org/10.1103/physrevb.82.184112">https://doi.org/10.1103/physrevb.82.184112</a>.'
  ieee: 'E. K. H. Salje <i>et al.</i>, “Tin telluride: A weakly co-elastic metal,”
    <i>Physical Review B</i>, vol. 82, no. 18. APS, 2010.'
  ista: 'Salje EKH, Safarik DJ, Modic KA, Gubernatis JE, Cooley JC, Taylor RD, Mihaila
    B, Saxena A, Lookman T, Smith JL, Fisher RA, Pasternak M, Opeil CP, Siegrist T,
    Littlewood PB, Lashley JC. 2010. Tin telluride: A weakly co-elastic metal. Physical
    Review B. 82(18), 184112.'
  mla: 'Salje, E. K. H., et al. “Tin Telluride: A Weakly Co-Elastic Metal.” <i>Physical
    Review B</i>, vol. 82, no. 18, 184112, APS, 2010, doi:<a href="https://doi.org/10.1103/physrevb.82.184112">10.1103/physrevb.82.184112</a>.'
  short: E.K.H. Salje, D.J. Safarik, K.A. Modic, J.E. Gubernatis, J.C. Cooley, R.D.
    Taylor, B. Mihaila, A. Saxena, T. Lookman, J.L. Smith, R.A. Fisher, M. Pasternak,
    C.P. Opeil, T. Siegrist, P.B. Littlewood, J.C. Lashley, Physical Review B 82 (2010).
date_created: 2019-11-19T13:46:28Z
date_published: 2010-11-18T00:00:00Z
date_updated: 2021-01-12T08:11:44Z
day: '18'
doi: 10.1103/physrevb.82.184112
extern: '1'
external_id:
  arxiv:
  - '1011.1445'
intvolume: '        82'
issue: '18'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1011.1445
month: '11'
oa: 1
oa_version: Preprint
publication: Physical Review B
publication_identifier:
  issn:
  - 1098-0121
  - 1550-235X
publication_status: published
publisher: APS
quality_controlled: '1'
status: public
title: 'Tin telluride: A weakly co-elastic metal'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 82
year: '2010'
...
---
_id: '7079'
abstract:
- lang: eng
  text: We have observed that reacting Pb:Te:Ag:Se in a 1:1:1.9:1 molar ratio gives
    rise to what appears to be a predominantly single-phase alloy, which crystallizes
    in the PbSe cF8 fcc structure. However, further investigation of the structure
    using energy dispersive x-ray analysis reveals the presence of two phases, PbSe
    and β-Ag2Te, with identical lattice parameters. The total thermal conductivity
    of the formed alloy is remarkably low for a crystalline material, κT<0.6W∕mK at
    675K, it is reproducible, and in addition, the compound has good mechanical properties.
article_number: '033519'
article_processing_charge: No
article_type: original
author:
- first_name: Fivos R.
  full_name: Drymiotis, Fivos R.
  last_name: Drymiotis
- first_name: Tyler B.
  full_name: Drye, Tyler B.
  last_name: Drye
- first_name: Yisha
  full_name: Wang, Yisha
  last_name: Wang
- first_name: Jian
  full_name: He, Jian
  last_name: He
- first_name: Daniel
  full_name: Rhodes, Daniel
  last_name: Rhodes
- first_name: Kimberly A
  full_name: Modic, Kimberly A
  id: 13C26AC0-EB69-11E9-87C6-5F3BE6697425
  last_name: Modic
  orcid: 0000-0001-9760-3147
- first_name: Samantha
  full_name: Cawthorne, Samantha
  last_name: Cawthorne
- first_name: Qiu Run
  full_name: Zhang, Qiu Run
  last_name: Zhang
citation:
  ama: Drymiotis FR, Drye TB, Wang Y, et al. Structure formation and very low thermal
    conductivity in Pb:Te:Ag:Se mixtures. <i>Journal of Applied Physics</i>. 2010;107(3).
    doi:<a href="https://doi.org/10.1063/1.3284946">10.1063/1.3284946</a>
  apa: Drymiotis, F. R., Drye, T. B., Wang, Y., He, J., Rhodes, D., Modic, K. A.,
    … Zhang, Q. R. (2010). Structure formation and very low thermal conductivity in
    Pb:Te:Ag:Se mixtures. <i>Journal of Applied Physics</i>. AIP. <a href="https://doi.org/10.1063/1.3284946">https://doi.org/10.1063/1.3284946</a>
  chicago: Drymiotis, Fivos R., Tyler B. Drye, Yisha Wang, Jian He, Daniel Rhodes,
    Kimberly A Modic, Samantha Cawthorne, and Qiu Run Zhang. “Structure Formation
    and Very Low Thermal Conductivity in Pb:Te:Ag:Se Mixtures.” <i>Journal of Applied
    Physics</i>. AIP, 2010. <a href="https://doi.org/10.1063/1.3284946">https://doi.org/10.1063/1.3284946</a>.
  ieee: F. R. Drymiotis <i>et al.</i>, “Structure formation and very low thermal conductivity
    in Pb:Te:Ag:Se mixtures,” <i>Journal of Applied Physics</i>, vol. 107, no. 3.
    AIP, 2010.
  ista: Drymiotis FR, Drye TB, Wang Y, He J, Rhodes D, Modic KA, Cawthorne S, Zhang
    QR. 2010. Structure formation and very low thermal conductivity in Pb:Te:Ag:Se
    mixtures. Journal of Applied Physics. 107(3), 033519.
  mla: Drymiotis, Fivos R., et al. “Structure Formation and Very Low Thermal Conductivity
    in Pb:Te:Ag:Se Mixtures.” <i>Journal of Applied Physics</i>, vol. 107, no. 3,
    033519, AIP, 2010, doi:<a href="https://doi.org/10.1063/1.3284946">10.1063/1.3284946</a>.
  short: F.R. Drymiotis, T.B. Drye, Y. Wang, J. He, D. Rhodes, K.A. Modic, S. Cawthorne,
    Q.R. Zhang, Journal of Applied Physics 107 (2010).
date_created: 2019-11-19T13:47:24Z
date_published: 2010-02-09T00:00:00Z
date_updated: 2021-01-12T08:11:44Z
day: '09'
doi: 10.1063/1.3284946
extern: '1'
intvolume: '       107'
issue: '3'
language:
- iso: eng
month: '02'
oa_version: None
publication: Journal of Applied Physics
publication_identifier:
  issn:
  - 0021-8979
  - 1089-7550
publication_status: published
publisher: AIP
quality_controlled: '1'
status: public
title: Structure formation and very low thermal conductivity in Pb:Te:Ag:Se mixtures
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 107
year: '2010'
...
---
_id: '7318'
abstract:
- lang: eng
  text: The decomposition reaction of H2O2 aqueous solutions (H2O2 - H2O + 1/2O2)
    catalyzed by transition metal oxide powders has been compared with the charging
    voltage of nonaqueous Li-O2 cells containing the same catalyst. An inverse linear
    relationship between Ln k (rate constant for the H2O2 decomposition) and the charging
    voltage has been found, despite differences in media and possible mechanistic
    differences. The results suggest that the decomposition may be a reliable, useful,
    and fast screening tool for materials that promote the charging process of the
    Li-O2 battery and may ultimately give insight into the charging mechanism.
article_number: A180
article_processing_charge: No
article_type: letter_note
author:
- first_name: V.
  full_name: Giordani, V.
  last_name: Giordani
- first_name: Stefan Alexander
  full_name: Freunberger, Stefan Alexander
  id: A8CA28E6-CE23-11E9-AD2D-EC27E6697425
  last_name: Freunberger
  orcid: 0000-0003-2902-5319
- first_name: P. G.
  full_name: Bruce, P. G.
  last_name: Bruce
- first_name: J.-M.
  full_name: Tarascon, J.-M.
  last_name: Tarascon
- first_name: D.
  full_name: Larcher, D.
  last_name: Larcher
citation:
  ama: Giordani V, Freunberger SA, Bruce PG, Tarascon J-M, Larcher D. H2O2 decomposition
    reaction as selecting tool for catalysts in Li–O2 cells. <i>Electrochemical and
    Solid-State Letters</i>. 2010;13(12). doi:<a href="https://doi.org/10.1149/1.3494045">10.1149/1.3494045</a>
  apa: Giordani, V., Freunberger, S. A., Bruce, P. G., Tarascon, J.-M., &#38; Larcher,
    D. (2010). H2O2 decomposition reaction as selecting tool for catalysts in Li–O2
    cells. <i>Electrochemical and Solid-State Letters</i>. The Electrochemical Society.
    <a href="https://doi.org/10.1149/1.3494045">https://doi.org/10.1149/1.3494045</a>
  chicago: Giordani, V., Stefan Alexander Freunberger, P. G. Bruce, J.-M. Tarascon,
    and D. Larcher. “H2O2 Decomposition Reaction as Selecting Tool for Catalysts in
    Li–O2 Cells.” <i>Electrochemical and Solid-State Letters</i>. The Electrochemical
    Society, 2010. <a href="https://doi.org/10.1149/1.3494045">https://doi.org/10.1149/1.3494045</a>.
  ieee: V. Giordani, S. A. Freunberger, P. G. Bruce, J.-M. Tarascon, and D. Larcher,
    “H2O2 decomposition reaction as selecting tool for catalysts in Li–O2 cells,”
    <i>Electrochemical and Solid-State Letters</i>, vol. 13, no. 12. The Electrochemical
    Society, 2010.
  ista: Giordani V, Freunberger SA, Bruce PG, Tarascon J-M, Larcher D. 2010. H2O2
    decomposition reaction as selecting tool for catalysts in Li–O2 cells. Electrochemical
    and Solid-State Letters. 13(12), A180.
  mla: Giordani, V., et al. “H2O2 Decomposition Reaction as Selecting Tool for Catalysts
    in Li–O2 Cells.” <i>Electrochemical and Solid-State Letters</i>, vol. 13, no.
    12, A180, The Electrochemical Society, 2010, doi:<a href="https://doi.org/10.1149/1.3494045">10.1149/1.3494045</a>.
  short: V. Giordani, S.A. Freunberger, P.G. Bruce, J.-M. Tarascon, D. Larcher, Electrochemical
    and Solid-State Letters 13 (2010).
date_created: 2020-01-15T12:21:06Z
date_published: 2010-10-04T00:00:00Z
date_updated: 2021-01-12T08:13:01Z
day: '04'
doi: 10.1149/1.3494045
extern: '1'
intvolume: '        13'
issue: '12'
language:
- iso: eng
month: '10'
oa_version: None
publication: Electrochemical and Solid-State Letters
publication_identifier:
  issn:
  - 1099-0062
publication_status: published
publisher: The Electrochemical Society
quality_controlled: '1'
status: public
title: H2O2 decomposition reaction as selecting tool for catalysts in Li–O2 cells
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 13
year: '2010'
...
---
_id: '754'
abstract:
- lang: eng
  text: 'Most people believe that renaming is easy: simply choose a name at random;
    if more than one process selects the same name, then try again. We highlight the
    issues that occur when trying to implement such a scheme and shed new light on
    the read-write complexity of randomized renaming in an asynchronous environment.
    At the heart of our new perspective stands an adaptive implementation of a randomized
    test-and-set object, that has poly-logarithmic step complexity per operation,
    with high probability. Interestingly, our implementation is anonymous, as it does
    not require process identifiers. Based on this implementation, we present two
    new randomized renaming algorithms. The first ensures a tight namespace of n names
    using O( n log4 n) total steps, with high probability. This significantly improves
    on the complexity of the best previously known namespace-optimal algorithms. The
    second algorithm achieves a namespace of size k (1 + ε) using O( k log4 k / log2
    (1 + ε) ) total steps, both with high probability, where k is the total contention
    in the execution. It is the first adaptive randomized renaming algorithm, and
    it improves on existing deterministic solutions by providing a smaller namespace,
    and by lowering step complexity.'
acknowledgement: The work of Dan Alistarh is supported by the Swiss NCCR MICS project.
  The work of Hagit Attiya is supported in part by the Israel Science Foundation (grant
  number 953/06).
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
- first_name: Hagit
  full_name: Attiya, Hagit
  last_name: Attiya
- first_name: Seth
  full_name: Gilbert, Seth
  last_name: Gilbert
- first_name: Andrei
  full_name: Giurgiu, Andrei
  last_name: Giurgiu
- first_name: Rachid
  full_name: Guerraoui, Rachid
  last_name: Guerraoui
citation:
  ama: 'Alistarh D-A, Attiya H, Gilbert S, Giurgiu A, Guerraoui R. Fast randomized
    test-and-set and renaming. In: Vol 6343 LNCS. Springer; 2010:94-108. doi:<a href="https://doi.org/10.1007/978-3-642-15763-9_9">10.1007/978-3-642-15763-9_9</a>'
  apa: 'Alistarh, D.-A., Attiya, H., Gilbert, S., Giurgiu, A., &#38; Guerraoui, R.
    (2010). Fast randomized test-and-set and renaming (Vol. 6343 LNCS, pp. 94–108).
    Presented at the DISC: Distributed Computing, Springer. <a href="https://doi.org/10.1007/978-3-642-15763-9_9">https://doi.org/10.1007/978-3-642-15763-9_9</a>'
  chicago: Alistarh, Dan-Adrian, Hagit Attiya, Seth Gilbert, Andrei Giurgiu, and Rachid
    Guerraoui. “Fast Randomized Test-and-Set and Renaming,” 6343 LNCS:94–108. Springer,
    2010. <a href="https://doi.org/10.1007/978-3-642-15763-9_9">https://doi.org/10.1007/978-3-642-15763-9_9</a>.
  ieee: 'D.-A. Alistarh, H. Attiya, S. Gilbert, A. Giurgiu, and R. Guerraoui, “Fast
    randomized test-and-set and renaming,” presented at the DISC: Distributed Computing,
    2010, vol. 6343 LNCS, pp. 94–108.'
  ista: 'Alistarh D-A, Attiya H, Gilbert S, Giurgiu A, Guerraoui R. 2010. Fast randomized
    test-and-set and renaming. DISC: Distributed Computing, LNCS, vol. 6343 LNCS,
    94–108.'
  mla: Alistarh, Dan-Adrian, et al. <i>Fast Randomized Test-and-Set and Renaming</i>.
    Vol. 6343 LNCS, Springer, 2010, pp. 94–108, doi:<a href="https://doi.org/10.1007/978-3-642-15763-9_9">10.1007/978-3-642-15763-9_9</a>.
  short: D.-A. Alistarh, H. Attiya, S. Gilbert, A. Giurgiu, R. Guerraoui, in:, Springer,
    2010, pp. 94–108.
conference:
  name: 'DISC: Distributed Computing'
date_created: 2018-12-11T11:48:19Z
date_published: 2010-01-01T00:00:00Z
date_updated: 2023-02-23T13:10:21Z
day: '01'
doi: 10.1007/978-3-642-15763-9_9
extern: '1'
language:
- iso: eng
month: '01'
oa_version: None
page: 94 - 108
publication_status: published
publisher: Springer
publist_id: '6900'
status: public
title: Fast randomized test-and-set and renaming
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 6343 LNCS
year: '2010'
...
