Résultat de recherche

A Missense LRRK2 Variant Is a Risk Factor for Excessive Inflammatory Responses...

Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered...

Impact of IL28B, APOH and ITPA Polymorphisms on Efficacy and Safety of...

Imagine annual report 2018

« C’est la première fois depuis que je fais des dons à des associations...

Le mécénat d’entreprise

An eQTL variant of ZXDC is associated with IFN-γ production following...

Genetics of human susceptibility to active and latent tuberculosis: present...

Human genetics of infectious diseases: Unique insights into immunological...

IRF4 haploinsufficiency in a family with Whipple's disease.

A novel genetic architecture of infectious diseases.

MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial...

Mariner is defective in myosin VIIA: a zebrafish model for human hereditary...

Un institut au cœur de Necker-Enfants malades

A genomic region encompassing a newly identified exon provides enhancing...

Travail en collaboration : Unité de Recherche clinique-Centre d’investigation...

Travail en collaboration : Département de Biothérapie, Centre d'Investigation...

Vivre avec l'ataxie de Friedreich : le témoignage d’Antony Feraud

1ère cérémonie de naming à Imagine

Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome...