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 Lentiviral vector integration in the human genome induces alternative splicing... Publications AON-mediated Exon Skipping Restores Ciliation in Fibroblasts Harboring... Publications AON-mediated Exon Skipping Restores Ciliation in Fibroblasts Harboring... Publications An activating Fgfr3 mutation affects trabecular bone formation via a paracrine... Publications Tangentially migrating transient glutamatergic neurons control neurogenesis... Publications Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations. Publications Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations. Publications Recurrent genomic instability of chromosome 1q in neural derivatives of... Publications Evolutionarily assembled cis-regulatory module at a human ciliopathy l... Publications A survey of 90 patients with autoimmune lymphoproliferative syndrome related... Publications TET2 and DNMT3A mutations in human T-cell lymphoma. Publications Cell lineages, growth and repair of the mouse heart. Publications Cell lineages, growth and repair of the mouse heart. Publications Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre... Publications Germline deletion of the miR-17∼92 cluster causes skeletal and growth... Pagination First page Previous Page … Page 45 Page 46 Page 47 Page 48 Current page 49 Page 50 Page 51 Page 52 Page 53 … 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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