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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 & Dopamine. The organization has 6541 authors who have published 11983 publications receiving 648742 citations. The organization is also known as: College de France.


Papers
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Journal ArticleDOI
TL;DR: It is demonstrated that inflammation-induced astroglial hemichannel activation plays a critical role in neuronal death and suggest a neuroprotective role of connexin43 hemichannels blockade.

149 citations

Journal ArticleDOI
TL;DR: A two-photon Fock state is prepared in a cavity sustaining a "source mode" and a "target mode," with a single circular Rydberg atom in a third-order Raman process.
Abstract: A two-photon Fock state is prepared in a cavity sustaining a "source mode" and a "target mode," with a single circular Rydberg atom. In a third-order Raman process, the atom emits a photon in the target while scattering one photon from the source into the target. The final two-photon state is probed by measuring by Ramsey interferometry the cavity light shifts induced by the target field on the same atom. Extensions to other multiphoton processes and to a new type of micromaser are briefly discussed.

149 citations

Journal ArticleDOI
TL;DR: The exact laws deduced from energetic considerations are found to be in excellent agreement with the data and it is shown how such tubes can be used to prevent bubbles from being trapped.

148 citations

Journal ArticleDOI
TL;DR: The mineral-mineral and mineral-biomolecule interfaces in bone tissue must be driven by metastable hydrated amorphous environments rich in HPO42− ions rather than by stable crystalline environments of hydroxyapatite structure.
Abstract: Some compositional and structural features of mature bone mineral particles remain unclear. They have been described as calcium-deficient and hydroxyl-deficient carbonated hydroxyapatite particles in which a fraction of the PO43− lattice sites are occupied by HPO42− ions. The time has come to revise this description since it has now been proven that the surface of mature bone mineral particles is not in the form of hydroxyapatite but rather in the form of hydrated amorphous calcium phosphate. Using a combination of dedicated solid-state nuclear magnetic resonance techniques, the hydrogen-bearing species present in bone mineral and especially the HPO42− ions were closely scrutinized. We show that these HPO42− ions are concentrated at the surface of bone mineral particles in the so-called amorphous surface layer whose thickness was estimated here to be about 0.8 nm for a 4-nm thick particle. We also show that their molar proportion is much higher than previously estimated since they stand for about half of the overall amount of inorganic phosphate ions that compose bone mineral. As such, the mineral-mineral and mineral-biomolecule interfaces in bone tissue must be driven by metastable hydrated amorphous environments rich in HPO42− ions rather than by stable crystalline environments of hydroxyapatite structure.

148 citations

Journal ArticleDOI
TL;DR: It is demonstrated in human and mouse that endothelial cells and myogenic progenitor cells interacted together to couple myogenesis and angiogenesis in vitro and in vivo during skeletal muscle regeneration.
Abstract: In skeletal muscle, new functions for vessels have recently emerged beyond oxygen and nutrient supply, through the interactions that vascular cells establish with muscle stem cells. Here, we demonstrate in human and mouse that endothelial cells (ECs) and myogenic progenitor cells (MPCs) interacted together to couple myogenesis and angiogenesis in vitro and in vivo during skeletal muscle regeneration. Kinetics of gene expression of ECs and MPCs sorted at different time points of regeneration identified three effectors secreted by both ECs and MPCs. Apelin, Oncostatin M, and Periostin were shown to control myogenesis/angiogenesis coupling in vitro and to be required for myogenesis and vessel formation during muscle regeneration in vivo. Furthermore, restorative macrophages, which have been previously shown to support myogenesis in vivo, were shown in a 3D triculture model to stimulate myogenesis/angiogenesis coupling, notably through Oncostatin M production. Our data demonstrate that restorative macrophages orchestrate muscle regeneration by controlling myogenesis/angiogenesis coupling.

148 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
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20238
202293
2021418
2020429
2019385
2018391