6 results match your criteria: "UPMC Paris Universitas[Affiliation]"

Ceramides and sphingomyelinases in senile plaques.

Neurobiol Dis

May 2014

Laboratoire de Neuropathologie Escourolle, Hôpital de la Salpêtrière, AP-HP, Paris, France; Centre de recherche de l'ICM, UPMC, INSERM UMR S 975, CNRS UMR 7225, France; Equipe de Statistique Appliquée, ESPCI Paris Tech, Paris, France.

The senile plaque is a hallmark lesion of Alzheimer disease (AD). We compared, without a priori, the lipidome of the senile plaques and of the adjacent plaque-free neuropil. The analysis by liquid chromatography coupled with electrospray ionization mass spectrometry revealed that laser microdissected senile plaques were enriched in saturated ceramides Cer(d18:1/18:0) and Cer(d18:1/20:0) by 33 and 78% respectively with respect to the surrounding neuropil.

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Combining contemporary and ancient DNA in population genetic and phylogeographical studies.

Mol Ecol Resour

September 2010

INRA, UMR CBGP (INRA/IRD/Cirad/Montpellier SupAgro), Campus International de Baillarguet, CS 30016, F-34988 Montferrier-sur-Lez Cedex, France Laboratoire Ecologie et Evolution, CNRS UMR 7625, UPMC Paris Universitas, Ecole Normale Supérieure, Paris, France Centre for Ecology, Evolution and Conservation, School of Biological Sciences, University of East Anglia, Norwich NR4 7TJ, UK.

The analysis of ancient DNA in a population genetic or phylogeographical framework is an emerging field, as traditional analytical tools were largely developed for the purpose of analysing data sampled from a single time point. Markov chain Monte Carlo approaches have been successfully developed for the analysis of heterochronous sequence data from closed panmictic populations. However, attributing genetic differences between temporal samples to mutational events between time points requires the consideration of other factors that may also result in genetic differentiation.

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Single-layered chrysotile nanotubes: A quantum mechanical ab initio simulation.

J Chem Phys

November 2009

Institut des Sciences de la Terre de Paris (UMR 7193, UPMC-CNRS), UPMC-Paris Universitas, Paris 75005, France.

Chrysotile single-layered nanotubes, obtained by wrapping the Mg(3)Si(2)O(5)(OH)(4) lizardite monolayer along the (n,-n) hexagonal lattice vector, are simulated at the ab initio level by using an all electron 6-31G( *) basis set and the B3LYP functional for n varying from 14 to 24 (the nanotube radius R referred to the oxygen connecting the Mg and Si layers increases from 20 to 35 A). Because of the full exploitation of the helical symmetry, recently implemented in the CRYSTAL code, the computational cost for the full self-consistent field (SCF) and gradient calculation increases only by a factor of 2 and 1.2, respectively, when passing from the lizardite monolayer [18 atoms and 236 AOs (atomic orbitals) in the unit cell] to the (24, -24) tube (864 atoms and 11,328 AOs).

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Epidemiologic studies support the premise that Allium vegetables may lower the risk of cancers. The beneficial effects appear related to the organosulfur products generated upon processing of Allium. Leukemia cells from patients with acute myeloid leukemia (AML) display high proliferative capacity and have a reduced capacity of undergoing apoptosis and maturation.

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Nanotubes can be characterized by a very high point symmetry, comparable or even larger than the one of the most symmetric crystalline systems (cubic, 48 point symmetry operators). For example, N = 2n rototranslation symmetry operators connect the atoms of the (n,0) nanotubes. This symmetry is fully exploited in the CRYSTAL code.

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Using classical population genetics tools with heterochroneous data: time matters!

PLoS One

August 2009

Laboratoire d'Ecologie et Evolution, CNRS UMR 7625, UPMC Paris Universitas, Ecole Normale Supérieure, Paris, France.

Background: New polymorphism datasets from heterochroneous data have arisen thanks to recent advances in experimental and microbial molecular evolution, and the sequencing of ancient DNA (aDNA). However, classical tools for population genetics analyses do not take into account heterochrony between subsets, despite potential bias on neutrality and population structure tests. Here, we characterize the extent of such possible biases using serial coalescent simulations.

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