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 Single-cell analysis reveals the continuum of human lympho-myeloid progenitor... Publications Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children... Publications Disease Evolution and Response to Rapamycin in Activated Phosphoinositide... Publications Constitutively-active FGFR3 disrupts primary cilium length and IFT20 trafficking... Publications Disease Evolution and Response to Rapamycin in Activated Phosphoinositide... Publications Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children... Publications The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity... Publications Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic... Publications Mutations in TUBB4B Cause a Distinctive Sensorineural Disease. Publications Mutations in TUBB4B Cause a Distinctive Sensorineural Disease. Publications Mutations in TUBB4B Cause a Distinctive Sensorineural Disease. Publications A predictive model of asymmetric morphogenesis from 3D reconstructions... Publications Targeted Inactivation of Bax Reveals a Subtype-Specific Mechanism of Cajal-Retzius... Publications Single-cell analysis identifies cellular markers of the HIV permissive... Publications DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis. Pagination First page Previous Page … Page 32 Page 33 Page 34 Page 35 Current page 36 Page 37 Page 38 Page 39 Page 40 … Page Next Last page Newsletter Discoveries, advances, portaits... Find out the latest research news and medical innovations. Votre email Valider Data Privacy Policy
