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 purely quantitative form of partial recessive IFN-γR2 deficiency caused... Publications CDG: An Online Server for Detecting Biologically Closest Disease-Causing... Publications Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated... Publications BRIP1 coding variants are associated with a high risk of hepatocellular... Publications A novel genetic architecture of infectious diseases. Publications Gene transfer into hematopoietic stem cells reduces HLH manifestations... Publications An Optimized Lentiviral Vector Efficiently Corrects the Human Sickle Cell... Publications A Nontoxic Transduction Enhancer Enables Highly Efficient Lentiviral Transduction... Publications Loss of ARHGEF1 causes a human primary antibody deficiency. Publications Gene transfer into hematopoietic stem cells reduces HLH manifestations... Publications Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leuko... Publications A novel, highly potent and selective phosphodiesterase-9 inhibitor for... Publications Depdc5 knockdown causes mTOR-dependent motor hyperactivity in zebrafis... Publications TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome... Publications Gamma-aminobutyric acidergic transmission underlies interictal epileptogenicity... Pagination First page Previous Page … Page 19 Page 20 Page 21 Page 22 Current page 23 Page 24 Page 25 Page 26 Page 27 … 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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