6 results match your criteria: "Centre de Recherche des Cordeliers 15[Affiliation]"

Assessment of the breadth of binding promiscuity of heme towards human proteins.

Biol Chem

November 2022

Centre de Recherche des Cordeliers, INSERM, CNRS, Sorbonne Université, Université de Paris, Centre de Recherche des Cordeliers 15, rue de l'Ecole de Médecine, F-75006 Paris, France.

Heme regulates important biological processes by transient interactions with many human proteins. The goal of the present study was to assess extends of protein binding promiscuity of heme. To this end we evaluated interaction of heme with >9000 human proteins.

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[Not Available].

Bull Cancer

November 2016

Service d'immunologie biologique, hôpital européen Georges-Pompidou, 20, rue Leblanc, 75015 Paris; Inserm U970, Paris Cardiovascular Research Center - PARCC, 56, rue Leblanc, 75015 Paris, France ; UMR-S970, université Paris-Descartes, Sorbonne-Paris-Cité, Paris, France ; équipe labellisée ligue contre le cancer, 56, rue Leblanc, 75015 Paris, France.

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We developed a mathematical model of calcium (Ca(2+)) transport along the rat nephron to investigate the factors that promote hypercalciuria. The model is an extension of the flat medullary model of Hervy and Thomas (Am J Physiol Renal Physiol 284: F65-F81, 2003). It explicitly represents all the nephron segments beyond the proximal tubules and distinguishes between superficial and deep nephrons.

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Objective: Cystatin C, a protein coded by CST3 gene, is implicated in adipose tissue biology. Our hypothesis is that common variants in CST3 gene could play a role in the development of corpulence during lifetime.

Methods: Two tag SNPs were selected to capture all SNPs in the CST3 region.

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Purpose: This study investigates the effects of triamcinolone acetonide (TA) on retinal endothelial cells in vitro and explores the potential vascular toxic effect of TA injected into the vitreous cavity of rats in vivo.

Methods: Subconfluent endothelial cells were treated with either 0.1 mg/ml or 1 mg/ml TA in 1% ethanol.

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Cloned 20 years ago, GLUT2 is a facilitative glucose transporter in the liver, pancreas, intestine, kidney, and brain. It ensures large bidirectional fluxes of glucose in and out the cell due to its low affinity and high capacity. It also transports other dietary sugars, such as fructose and galactose, within the range of physiological concentrations.

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