Institution
Centre national de la recherche scientifique
Government•Paris, France•
About: Centre national de la recherche scientifique is a government organization based out in Paris, France. It is known for research contribution in the topics: Population & Catalysis. The organization has 239077 authors who have published 382421 publications receiving 13670943 citations.
Topics: Population, Catalysis, Magnetization, Thin film, Laser
Papers published on a yearly basis
Papers
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TL;DR: A new method for multiple sequence alignment that provides a dramatic improvement in accuracy with a modest sacrifice in speed as compared to the most commonly used alternatives but avoids the most serious pitfalls caused by the greedy nature of this algorithm.
6,727 citations
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TL;DR: MadGraph5 aMC@NLO as discussed by the authors is a computer program capable of handling all these computations, including parton-level fixed order, shower-matched, merged, in a unified framework whose defining features are flexibility, high level of parallelisation and human intervention limited to input physics quantities.
Abstract: We discuss the theoretical bases that underpin the automation of the computations of tree-level and next-to-leading order cross sections, of their matching to parton shower simulations, and of the merging of matched samples that differ by light-parton multiplicities. We present a computer program, MadGraph5 aMC@NLO, capable of handling all these computations — parton-level fixed order, shower-matched, merged — in a unified framework whose defining features are flexibility, high level of parallelisation, and human intervention limited to input physics quantities. We demonstrate the potential of the program by presenting selected phenomenological applications relevant to the LHC and to a 1-TeV e + e − collider. While next-to-leading order results are restricted to QCD corrections to SM processes in the first public version, we show that from the user viewpoint no changes have to be expected in the case of corrections due to any given renormalisable Lagrangian, and that the implementation of these are well under way.
6,509 citations
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Macquarie University1, University of Minnesota2, Stanford University3, Simón Bolívar University4, Wageningen University and Research Centre5, Smithsonian Environmental Research Center6, University of Alaska Fairbanks7, VU University Amsterdam8, University of Zurich9, Centre national de la recherche scientifique10, Curtin University11, Tohoku University12, University of Wisconsin–Eau Claire13, Landcare Research14, University of Concepción15, University of Cape Town16, University of Tartu17, Polish Academy of Sciences18, University of Tokyo19, Utrecht University20, University of Western Australia21, Charles Darwin University22, Ural State University23, University of Toronto24, Texas A&M University25, University of Córdoba (Spain)26
TL;DR: Reliable quantification of the leaf economics spectrum and its interaction with climate will prove valuable for modelling nutrient fluxes and vegetation boundaries under changing land-use and climate.
Abstract: Bringing together leaf trait data spanning 2,548 species and 175 sites we describe, for the first time at global scale, a universal spectrum of leaf economics consisting of key chemical, structural and physiological properties. The spectrum runs from quick to slow return on investments of nutrients and dry mass in leaves, and operates largely independently of growth form, plant functional type or biome. Categories along the spectrum would, in general, describe leaf economic variation at the global scale better than plant functional types, because functional types overlap substantially in their leaf traits. Overall, modulation of leaf traits and trait relationships by climate is surprisingly modest, although some striking and significant patterns can be seen. Reliable quantification of the leaf economics spectrum and its interaction with climate will prove valuable for modelling nutrient fluxes and vegetation boundaries under changing land-use and climate.
6,360 citations
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TL;DR: Together, these properties make PEI a promising vector for gene therapy and an outstanding core for the design of more sophisticated devices because its efficiency relies on extensive lysosome buffering that protects DNA from nuclease degradation, and consequent lysOSomal swelling and rupture that provide an escape mechanism for the PEI/DNA particles.
Abstract: Several polycations possessing substantial buffering capacity below physiological pH, such as lipopolyamines and polyamidoamine polymers, are efficient transfection agents per se--i.e., without the addition of cell targeting or membrane-disruption agents. This observation led us to test the cationic polymer polyethylenimine (PEI) for its gene-delivery potential. Indeed, every third atom of PEI is a protonable amino nitrogen atom, which makes the polymeric network an effective "proton sponge" at virtually any pH. Luciferase reporter gene transfer with this polycation into a variety of cell lines and primary cells gave results comparable to, or even better than, lipopolyamines. Cytotoxicity was low and seen only at concentrations well above those required for optimal transfection. Delivery of oligonucleotides into embryonic neurons was followed by using a fluorescent probe. Virtually all neurons showed nuclear labeling, with no toxic effects. The optimal PEI cation/anion balance for in vitro transfection is only slightly on the cationic side, which is advantageous for in vivo delivery. Indeed, intracerebral luciferase gene transfer into newborn mice gave results comparable (for a given amount of DNA) to the in vitro transfection of primary rat brain endothelial cells or chicken embryonic neurons. Together, these properties make PEI a promising vector for gene therapy and an outstanding core for the design of more sophisticated devices. Our hypothesis is that its efficiency relies on extensive lysosome buffering that protects DNA from nuclease degradation, and consequent lysosomal swelling and rupture that provide an escape mechanism for the PEI/DNA particles.
6,213 citations
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TL;DR: This review focuses on the characterization of EVs and on currently proposed mechanisms for their formation, targeting, and function.
Abstract: Cells release into the extracellular environment diverse types of membrane vesicles of endosomal and plasma membrane origin called exosomes and microvesicles, respectively. These extracellular vesicles (EVs) represent an important mode of intercellular communication by serving as vehicles for transfer between cells of membrane and cytosolic proteins, lipids, and RNA. Deficiencies in our knowledge of the molecular mechanisms for EV formation and lack of methods to interfere with the packaging of cargo or with vesicle release, however, still hamper identification of their physiological relevance in vivo. In this review, we focus on the characterization of EVs and on currently proposed mechanisms for their formation, targeting, and function.
6,141 citations
Authors
Showing all 239423 results
Name | H-index | Papers | Citations |
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Guido Kroemer | 236 | 1404 | 246571 |
Trevor W. Robbins | 231 | 1137 | 164437 |
Robert J. Lefkowitz | 214 | 860 | 147995 |
Pierre Chambon | 211 | 884 | 161565 |
Bruce M. Spiegelman | 179 | 434 | 158009 |
Tony Hunter | 175 | 593 | 124726 |
Kari Alitalo | 174 | 817 | 114231 |
Didier Raoult | 173 | 3267 | 153016 |
Marc G. Caron | 173 | 674 | 99802 |
Sophie Henrot-Versille | 171 | 957 | 157040 |
George F. Koob | 171 | 935 | 112521 |
Richard H. Friend | 169 | 1182 | 140032 |
Philippe Froguel | 166 | 820 | 118816 |
Marc A. Pfeffer | 166 | 765 | 133043 |
Anders Björklund | 165 | 769 | 84268 |