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 [Cilia and heart morphogenesis]. Publications Segmented filamentous bacterium uses secondary and tertiary lymphoid tissues... Publications The BLNK adaptor protein has a nonredundant role in human B-cell diffe... Publications Successful RAG1-SCID gene therapy depends on the level of RAG1 express... Publications Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical... Publications Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical... Publications Myhre syndrome. Publications RAS-associated lymphoproliferative disease evolves into severe juvenile... Publications Transgenic kallikrein 5 mice reproduce major cutaneous and systemic hallmarks... Publications CLP1 founder mutation links tRNA splicing and maturation to cerebellar... Publications Recombination-activating gene 1 (Rag1)-deficient mice with severe combined... Publications XYLT1 mutations in Desbuquois dysplasia type 2. Publications XYLT1 mutations in Desbuquois dysplasia type 2. Publications Mutations in endothelin 1 cause recessive auriculocondylar syndrome and... Publications Recurrent mutations in epigenetic regulators, RHOA and FYN kinase in peripheral... Pagination First page Previous Page … Page 42 Page 43 Page 44 Page 45 Current page 46 Page 47 Page 48 Page 49 Page 50 … Page Next Last page Newsletter Discoveries, advances, portaits... Find out the latest research news and medical innovations. Votre email Valider Data Privacy Policy
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