Actualités

Clarifying the role of IKKα kinase in the function of the NF-κB inflammation pathway

Pedagogical interventions to help schoolchildren with learning difficulties

Enhanced bone repair with FGFR antagonists in a model of hypochondroplasia

A genetic cause of an inherited bone marrow failure identified

Jean-Laurent Casanova’s pioneering genetic discoveries earn him the 2025 Novo Nordisk Prize

Deciphering the genetic origin of language development disorders in children without intellectual disabilities, autism or apraxia of speech

PROFESSOR BANA JABRI TAKES OVER AS DIRECTOR OF INSTITUT IMAGINE

Evaluation of an innovative support programme for young patients with rare genetic epilepsies

Calls for Junior Group Leader at Institut Imagine

Amyotrophic lateral sclerosis: a defect in autophagy responsible for the disease

Incontinentia Pigmenti, a rare skin disease that also predisposes to viral infections

The fifth HEROES auction for the benefit of Institut Imagine reaches €10 million

The first inherited TNF deficiency in human underlies susceptibility to tuberculosis

Innov4-ePiK: Innovative diagnostic and therapeutic approaches in potassium channel developmental and epileptic encephalopathies (K-DEEs) using 4P for medicine.

The role of dendritic cells in papillomavirus infections: from the FLT3LG gene to therapeutic perspectives