Filter Filter By date Start date End date By Team Michel Polak Alessandra Pierani Patrick Revy & Erika Brunet Sigolène Meilhac Laurent Abel Jeanne Amiel et Laurence Legeai‑Mallet Antonio Rausell Isabelle André Vincent Cantagrel Jean-Laurent Casanova Nadine Cerf-Bensussan Yanick Crow Olivier Hermine & Thiago Trovati Maciel Alain Hovnanian Edor Kabashi Sylvain Latour Valérie Cormier-Daire Mickaël Ménager Gaël Ménasché et Fernando Sepulveda Annarita Miccio Frédéric Rieux-Laucat Agnès Rötig Jean-Michel Rozet Sophie Saunier et Corinne Antignac Matias Simons Nathalie Boddaert Sabine Sarnacki et Isabelle Bloch Yves Ville Anne DUMAINE Patrick Nitschké Corinne Cordier Meriem Garfa-Traoré Sylvie Fabrega Marie-Alexandra Alyanakian Sophie Berissi Chiara Guerrera Pierre David Nathalie Lefort Claude Besmond Marcelo Simon Sola LEAT Nathalie Boddaert Travail en collaboration : Unité de Recherche clinique-Centre d’investigation clinique (URC-CIC) Travail en collaboration : Département de Biothérapie, Centre d'Investigation Clinique pour les Thérapies Innovantes Salma Kotti Nicolas Garcelon Mickaël Ménager Michela Deleidi Annarita Miccio Annarita Miccio Jean Michel Rozet Sara Bizzotto Elodie Bal Bana Jabri Hossein Khonsari Karim Wahbi Lucile Couronné Denis Jabaudon, Thomas Blauwblomme et Rima Nabbout Bana Jabri Céline GRECO Filter Reset 0 results match your search. Publications A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated... Publications Graded defects in cytotoxicity determine severity of hemophagocytic lymphohistiocytosis... Publications Diagnosis of autoimmune lymphoproliferative syndrome caused by FAS deficiency... Publications WDR34 mutations that cause short-rib polydactyly syndrome type III/severe... Publications Elevated expression of the V-ATPase C subunit triggers JNK-dependent cell... Publications Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome... Publications Extracting 3D cell parameters from dense tissue environments: application... Publications AMPD2 regulates GTP synthesis and is mutated in a potentially treatable... Publications Deletion of the LTR enhancer/promoter has no impact on the integration... Publications OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking... Publications OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking... Publications Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS... Publications EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia. Publications Nup153 and Nup98 bind the HIV-1 core and contribute to the early steps... Publications Resolving cell lineage contributions to the ventricular conduction system... Pagination First page Previous Page … Page 43 Page 44 Page 45 Page 46 Current page 47 Page 48 Page 49 Page 50 Page 51 … Page Next Last page Newsletter Discoveries, advances, portaits... Find out the latest research news and medical innovations. Votre email Valider Data Privacy Policy
