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 Drosophila ATP6AP2/VhaPRR functions both as a novel planar cell polarity... Publications Distinct severity of HLH in both human and murine mutants with complete... Publications Human T-lymphoid progenitors generated in a feeder-cell-free Delta-like-4... Publications ALDH1A3 mutations cause recessive anophthalmia and microphthalmia. Publications Quantitative analysis of polarity in 3D reveals local cell coordination... Publications Early transcriptional changes linked to naturally occurring Huntington's... Publications Asymmetric fate of the posterior part of the second heart field results... Publications Lineage tree for the venous pole of the heart: clonal analysis clarifies... Publications Spastic paraplegia gene 7 in patients with spasticity and/or optic neu... Publications Gene therapy rescues cilia defects and restores olfactory function in a... Publications Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe... Publications Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe... Publications TCTN3 mutations cause Mohr-Majewski syndrome. Publications The GATA1-HS2 enhancer allows persistent and position-independent expression... Publications Terminal transport of lytic granules to the immune synapse is mediated... Pagination First page Previous Page … Page 44 Page 45 Page 46 Page 47 Current page 48 Page 49 Page 50 Page 51 Page 52 … 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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