scispace - formally typeset
Search or ask a question
Institution

Collège de France

EducationParis, France
About: Collège de France is a education organization based out in Paris, France. It is known for research contribution in the topics: Population & Receptor. The organization has 6541 authors who have published 11983 publications receiving 648742 citations. The organization is also known as: College de France.


Papers
More filters
Journal ArticleDOI
TL;DR: The molecular mechanism unraveled here points to a role for FMRP in modulation of actin dynamics, which is a key process in morphogenesis of dendritic spines, synaptic structures abnormally developed in Fragile X syndrome patient's brain.
Abstract: Fragile X syndrome, the most common form of inherited mental retardation, is caused by absence of FMRP, an RNA-binding protein implicated in regulation of mRNA translation and/or transport. We have previously shown that dFMR1, the Drosophila ortholog of FMRP, is genetically linked to the dRac1 GTPase, a key player in actin cytoskeleton remodeling. Here, we demonstrate that FMRP and the Rac1 pathway are connected in a model of murine fibroblasts. We show that Rac1 activation induces relocalization of four FMRP partners to actin ring areas. Moreover, Rac1-induced actin remodeling is altered in fibroblasts lacking FMRP or carrying a point-mutation in the KH1 or in the KH2 RNA-binding domain. In absence of wild-type FMRP, we found that phospho-ADF/Cofilin (P-Cofilin) level, a major mediator of Rac1 signaling, is lowered, whereas the level of protein phosphatase 2A catalytic subunit (PP2Ac), a P-Cofilin phosphatase, is increased. We show that FMRP binds with high affinity to the 5'-UTR of pp2acbeta mRNA and is thus a likely negative regulator of its translation. The molecular mechanism unraveled here points to a role for FMRP in modulation of actin dynamics, which is a key process in morphogenesis of dendritic spines, synaptic structures abnormally developed in Fragile X syndrome patient's brain.

160 citations

Journal ArticleDOI
TL;DR: In this article, a new alkali-deficient P2•Na2/3Mn7/9Zn2/9O2 phase using a more electronegative element (Zn) than Mg is reported.
Abstract: The revival of the Na‐ion battery concept has prompted intense research activities toward new sustainable Na‐based insertion compounds and their implementation in full Na‐ion cells. Efforts are parted between Na‐based polyanionic and layered compounds. For the latter, there has been a specific focus on Na‐deficient layered phases that show cationic and anionic redox activity similar to a Na0.67Mn0.72Mg0.28O2 phase. Herein, a new alkali‐deficient P2‐Na2/3Mn7/9Zn2/9O2 phase using a more electronegative element (Zn) than Mg is reported. Like its Mg counterpart, this phase shows anionic redox activity and no O2 release despite evidence of cationic migration. Density functional theory (DFT) calculations show that it is the presence of an oxygen nonbonding state that triggers the anionic redox activity in this material. The phase delivers a reversible capacity of 200 mAh g−1 in Na‐half cells with such a value be reduced to 140 mAh g−1 in full Na‐ion cells which additionally shows capacity decay upon cycling. These findings establish Na‐deficient layered oxides as a promising platform to further explore the underlying science behind O2 release in insertion compounds based on anionic redox activity.

160 citations

Journal ArticleDOI
TL;DR: In this article, the behavior of a liquid being pulled out along a vertical plate is discussed, assuming that, in equilibrium, the liquid has a finite contact angle θ e. Since the velocity of pull-outU is below a certain thresholdUm(θe), this may provide a general scheme of interpretation for reactive deposition.
Abstract: The behavior of a liquid being pulled out along a vertical plate is discussed, assuming that, in equilibrium, the liquid has a finite contact angleθe. Using a simplified form of the Huh-Scriven analysis for viscous friction, we show that a steady state solution (with a dynamic contact angleθ<θe) exists provided that the velocity of pull-outU is below a certain thresholdUm(θe). These considerations can be transposed (with a modification in numerical coefficients) to the case where the liquid is covered with a surfactant monolayer, to be transferred towards the solid in theY mode. SinceUm is predicted in terms of interfacial tensions, this may provide a general scheme of interpretation for “reactive” deposition.

160 citations

Journal ArticleDOI
TL;DR: In this paper, mesoporous MIL-100(Al, Cr or Fe) metal-organic frameworks were synthesized by a microwave-assisted solvothermal route with green solvents.
Abstract: Nanoparticles of mesoporous MIL-100(Al, Cr or Fe) metal–organic frameworks were synthesized by a microwave-assisted solvothermal route with green solvents. The optimization of yield, crystallinity, and particle size was achieved through the control of synthetic parameters such as temperature, heating rate, and dwelling time. The particle size strongly depends on the metallic cation and the metal and linker precursors; nanoparticles smaller than 100 nm were obtained for iron and chromium based MIL-100. Finally, stable colloidal solutions of iron and chromium MIL-100 nanoparticles were used for thin layer dip-coating deposition, which resulted in high optical quality thin films, the porosity of which was investigated by environmental ellipsometric porosimetry.

160 citations

Journal ArticleDOI
01 Feb 2019-Nature
TL;DR: Waveguide quantum electrodynamics is used to couple a single collective excitation of an atomic array to a nanoscale waveguide; the excitation is stored and later read out, generating guided single photons on demand.
Abstract: Considerable efforts have been recently devoted to combining ultracold atoms and nanophotonic devices1-4 to obtain not only better scalability and figures of merit than in free-space implementations, but also new paradigms for atom-photon interactions5. Dielectric waveguides offer a promising platform for such integration because they enable tight transverse confinement of the propagating light, strong photon-atom coupling in single-pass configurations and potentially long-range atom-atom interactions mediated by the guided photons. However, the preparation of non-classical quantum states in such atom-waveguide interfaces has not yet been realized. Here, by using arrays of individual caesium atoms trapped along an optical nanofibre6,7, we observe a single collective atomic excitation8,9 coupled to a nanoscale waveguide. The stored collective entangled state can be efficiently read out with an external laser pulse, leading to on-demand emission of a single photon into the guided mode. We characterize the emitted single photon via the suppression of the two-photon component and confirm the single character of the atomic excitation, which can be retrieved with an efficiency of about 25%. Our results demonstrate a capability that is essential for the emerging field of waveguide quantum electrodynamics, with applications to quantum networking, quantum nonlinear optics and quantum many-body physics10,11.

160 citations


Authors

Showing all 6597 results

NameH-indexPapersCitations
Pierre Chambon211884161565
Irving L. Weissman2011141172504
David R. Williams1782034138789
Kari Alitalo174817114231
Pierre Bourdieu153592194586
Stanislas Dehaene14945686539
Howard L. Weiner144104791424
Alain Fischer14377081680
Yves Agid14166974441
Michel Foucault140499191296
Jean-Pierre Changeux13867276462
Jean-Marie Tarascon136853137673
K. Ganga13227299004
Jacques Delabrouille13135494923
G. Patanchon12824187233
Network Information
Related Institutions (5)
Centre national de la recherche scientifique
382.4K papers, 13.6M citations

92% related

University of Paris
174.1K papers, 5M citations

92% related

Max Planck Society
406.2K papers, 19.5M citations

90% related

French Institute of Health and Medical Research
174.2K papers, 8.3M citations

90% related

École Normale Supérieure
99.4K papers, 3M citations

90% related

Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20238
202293
2021418
2020429
2019385
2018391