Résultat de recherche

Common homozygosity for predicted loss-of-function variants reveals both...

World Sickle Cell Day: Hope for treatment with a new gene therapy appr...

Editing a γ-globin repressor binding site restores fetal hemoglobin synthesis...

Give hope to sick children

Partnership research - Imagine launches a website dedicated to industr...

Discovery of a genetic defect at the origin of fulminant hepatitis A

Michel Polak

Discovery of the origin of a new rare eye disease and consequences for...

Sabrina Méchaussier, rewarded at the biggest European meeting of gene...

Shy? Outgoing? And if we had a brain signature for our level of sociab...

The origin of an inherited antibody immunodeficiency first described 56...

From Dysgammaglobulinemia to Autosomal-Dominant Activation-Induced Cytidine...

A Clinician Friendly Data Warehouse Oriented Toward Narrative Reports:...

Next Generation Phenotyping Using Narrative Reports in a Rare Disease Clinical...

1% of cases of tuberculosis in Europe would be because of a specific genetic...

Finding Patients Using Similarity Measures in a Rare Diseases-Oriented...

Taxation: The gift in kind

Maison Alaïa, a loyal supporter of Imagine

Type 1 Interferon Deficiency: A Blood based Signature for Detecting Patients...

Impaired type I interferon activity and inflammatory responses in severe...