Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Claude Ferrec"'
Autor:
Jeanne Amiel, Sophie Julia, Catherine Vincent-Delorme, Christel Thauvin-Robinet, Paul Kuentz, Salima El Chehadeh, Stanislas Lyonnet, Bruno Leheup, Elodie Gautier, Odile Boute-Benejean, Nathalie Le Meur, Sandrine Marlin, Irène François, Delphine Héron, Marianne Till, Patrick Edery, Houda Karmous Benailly, Serge Romana, Nicole Philip, Patrick Callier, Valérie Cormier-Daire, Bénédicte Héron, Adeline Vigouroux-Castera, Mathilde Lefebvre, Chantal Missirian, Sylvie Odent, Fanny Morice-Picard, Roseline Caumes, Dominique Martin, Cédric Le Caignec, Nicolas Chassaing, Claire Benneteau, Anne-Laure Mosca-Boidron, Claude Ferrec, Anne-Marie Guerrot, Sylvie Manouvrier-Hanu, Eva Piparas, Damien Sanlaville, Florence Petit, Stéphanie Arpin, Sébastien Moutton, Marie-Pierre Alex-Cordier, Elodie Cretin, Laurence Faivre, Sabine Sigaudy, Tiffany Busa, Brigitte Gilbert-Dussardier, Sandra Chantot-Bastaraud, Julien Thevenon, Alexandra Afenjar, Annick Toutain, Boris Keren, Anne Philippe, Valérie Malan, Laetitia Lambert, Sandra Mercier, Elise Schaefer, James Lespinasse, Nathalie Marle, Sylvia Redon, Fabienne Giuliano, Isabelle Mortemousque, Philippe Khau Van Kien, Pierre Bitoun, Alice Goldenberg, Sophie Blesson, Michèle Marti-Dramard
Publikováno v:
Clinical Genetics. 89:630-635
Microarray-based comparative genomic hybridization (aCGH) is commonly used in diagnosing patients with intellectual disability (ID) with or without congenital malformation. Because aCGH interrogates with the whole genome, there is a risk of being con
Autor:
Claude Ferrec, Leena Peltonen, M. Gonul Ogur, Gilbert Vassart, Concepción de la Rúa, Bernard Mercier, Marianne Schwartz, Gunhild Beckman, Michel Samson, Victor Spitsyn, Marina Aksenova, Bjorn Grinde, László Tı́már, Pascale Cochaux, Guillermo Glover, Maurizio Ferrari, Marc Parmentier, Mireille Claustres, Antonio Cao, Frédérick Libert, Lars Beckman, Vaidutis Kučinskas, Sefik Güran, Andrew E. Czeizel, Joao Lavinha, C. Rosatelli
Publikováno v:
Human Molecular Genetics. 7:399-406
The chemokine receptor CCR5 is encoded by the CMKBR5 gene located on the p21.3 region of human chromosome 3, and constitutes the major co-receptor for the macrophage-tropic strains of HIV-1. A mutant allele of the CCR5 gene, Delta ccr5 , was shown to
Publikováno v:
Steroids. 73(11)
7alpha-Hydroxy-DHEA, 7beta-hydroxy-DHEA and 7beta-hydroxy-EpiA are native metabolites of dehydroepiandrosterone (DHEA) and epiandrosterone (EpiA). Since numerous steroids are reported to interfere with inflammatory and immune processes, our objective
Autor:
Françoise Denoyelle, Hélène Catros, Marie-Françoise Obstoy, Dominique Weil, Lucien Moati, Natalie Loundon, Rémy Couderc, Claude Ferrec, Valérie Drouin-Garraud, Alain Joannard, Bruno Delobel, Sébastien Schmerber, Hubert Journel, Sandrine Marlin, Delphine Feldmann, Christine Petit, Erea-Noel Garabedian, Jacques Leman
Publikováno v:
European journal of human genetics : EJHG. 12(4)
Mutations in GJB2 are the most common cause of congenital nonsyndromic hearing loss. The controversial allele variant M34T has been hypothesized to cause autosomal dominant or recessive nonsyndromic hearing impairment and some in vitro data has been
Autor:
A. Andriulli, Ph Deprez, Louis Le Bodic, Claude Ferrec, Philippe Lévy, Michel Robaskiewsicz, P. Ruszniewski, Jm Chen, Pascal Hammel
Publikováno v:
Gastroenterology. 120:A645-A645