Résultat de recherche

Patrick Revy et Erika Brunet

Gene transfer into hematopoietic stem cells reduces HLH manifestations...

AK2 deficiency compromises the mitochondrial energy metabolism required...

Human T-lymphoid progenitors generated in a feeder-cell-free Delta-like-4...

IFI : Votre impôt au service des enfants atteints de maladies génét...

Les origines des troubles du spectre de l’autisme

Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leuko...

Biallelic mutations in neurofascin cause neurodevelopmental impairment...

De novo mutation screening in childhood-onset cerebellar atrophy identifies...

Utility of whole exome sequencing for the early diagnosis of pediatric-onset...

Cytomégalovirus et déficience en NOS2 ne font pas bon ménage

Innate immune cells, major actors of sickle cell disease pathophysiolo...

A novel, highly potent and selective phosphodiesterase-9 inhibitor for...

Enhanced Renewal of Erythroid Progenitors in Myelodysplastic Anemia by...

FAS and RAS related Apoptosis defects: From autoimmunity to leukemia.

Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a...

Autoimmune lymphoproliferative syndrome with somatic Fas mutations.

Mutations in Fas associated with human lymphoproliferative syndrome and...

Inactivation of the Fas gene by Alu insertion: retrotransposition in an...

Inherited and somatic CD3zeta mutations in a patient with T-cell defic...