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IHU Imagine - Institut des maladies génétiques

2017-2018 (vague D)

Type de rapport
Rapport d’évaluation d’une entité de recherche
Campagne d'évaluation
2017-2018 (vague D)
Date de publication
2018-07-02
Etablissement(s)
Institut national de la santé et de la recherche médicale - INSERM, Université Paris Descartes
Domaine scientifique
Biologie, médecine et santé
Discipline
SVE Sciences du vivant et environnement
SVE3 Microbiologie, Immunité
SVE2 Biologie Cellulaire, Imagerie, Biologie Moléculaire, Biochimie, Génomique, Biologie Systémique, Développement, Biologie Structurale
Panel ERC
LS6 Immunity and infection: immunobiology, aetiology of immune disorders, microbiology, virology, parasitology, global and other infectious diseases, population dynamics of infectious diseases, veterinary medicine
Nom des équipes de l'unité
Human genetics of infectious diseases: Complex predisposition
Human genetics of infectious diseases : Monogenic predisposition
Genetics of mitochondrial disorders
Genetics in Ophthalmology
Origins and functions of skeletal stem cells in bone regeneration
CTGDM: unstable CTG repeat and myotonic dystrophy
Genetic and pathophysiological bases of auto-inflammatory diseases
Normal and pathological homeostasis of the immune system
Genome dynamics in the immune system (DGSI)
Lymphocyte activation and susceptibility to EBV
Immunogenetics of pediatric autoimmune diseases
Laboratory of cellular and molecular mechanisms of hematologic disorders and therapeutic implications
Hereditary kidney diseases : Pathophysiology of cystinosis and hereditary glomerular diseases
Laboratory of neurogenetics and neuroinflammation
Chromatin and gene regulation during development
Heart morphogenesis
The Clinical Bioinformatics laboratory
Epithelial biology and disease - Liliane Bettencourt Chair of Developmental Biology
Inflammatory Resp
Hereditary Kidney diseases : nephronophthisis and renal hypodysplasia
Human Lympho-hematopoiesis Lab
Laboratory of Intestinal Immunity
Molecular and pathophysiological bases of developmental brain disorders
Molecular and Physiopathological bases of osteochondrodysplasia
Genetic skin diseases : from disease mechanism to therapies
Embryology and genetics of human malformations
Mots-clés
Langue de rédaction du rapport
Anglais

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