Résultat de recherche

Long-term outcomes of lentiviral gene therapy for the β-hemoglobinopathies:...

Base-editing-mediated dissection of a γ-globin cis-regulatory element...

Novel lentiviral vectors for gene therapy of sickle cell disease combining...

Autoantibodies against type I interferon : detected and active in chil...

Identification of a new genetic disease responsible for pulmonary alveolar...

CENTOGENE and the Laboratory of Human Genetics of Infectious Diseases at...

A new mutation implicated in autoimmune lymphoproliferative syndrome

A wave of deep intronic mutations in X-linked Alport syndrome.

VNtyper enables accurate alignment-free genotyping of MUC1 coding VNTR...

Overcoming the challenges associated with identification of deep intronic...

The genetic landscape and clinical spectrum of nephronophthisis and related...

Fluid shear stress triggers cholesterol biosynthesis and uptake in inner...

Meta-analysis of single-cell and single-nucleus transcriptomics reveals...

Repurposing small molecules for nephronophthisis and related renal cil...

Agonists of prostaglandin E2 receptors as potential first in class treatment...

The renal inflammatory network of nephronophthisis.

Targeted next-generation sequencing in a large series of fetuses with severe...

Anne-Marie Laurencine, Hygiene, Safety and Environment Coordinator

Discovery of a frequent genetic cause of autoimmunity From rare to frequent...

Identification of a new key player in the immune control of Epstein-Barr...