Résultat de recherche

Clonal tracking in gene therapy patients reveals a diversity of human hematopoietic differentiation programs

Emmanuelle SIX, Adeline DENIS, Marianne DELVILLE, Steicy SOBRINO, Isabelle André, Marina Cavazzana

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A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiency.

Chantal LAGRESLE-PEYROU, Hanem SADEK, Cindy DA SILVA, Alexandrine GARRIGUE, Isabelle André, Marina Cavazzana

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Neural basis of interindividual variability in social perception in typically developing children and adolescents using diffusion tensor imaging.

Ana Saitovitch, Nathalie Boddaert, Monica Zilbovicius , Alice Vinçon-Leite, Hervé Lemaître, Elza Rechtman, Ludovic Fillon, David Grévent

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Developmental cell death regulates lineage-related interneuron-oligodendroglia functional clusters and oligodendrocyte homeostasis.

Alessandra Pierani

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Reallocation of Olfactory Cajal-Retzius Cells Shapes Neocortex Architecture.

Alessandra Pierani

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Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restriction.

Nadia Bahi-Buisson, Camille Maillard

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Mutations in TBR1 gene leads to cortical malformations and intellectual disability.

Nadia Bahi-Buisson, Camille Maillard

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Further refinement of COL4A1 and COL4A2 related cortical malformations.

Nadia Bahi-Buisson

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