New Golgipathy identified in NeuroDev team

New Golgipathy identified in NeuroDev team

The NeuroDev team publishes an article in Life Science Alliance [1] identifying the first human pathogenic variant of GORASP1, the gene encoding the Golgi stacking protein GRASP65, and demonstrating its consequences on glycosylation and mitotic progression. [1] S....
Sleep2Develop research program

Sleep2Develop research program

The Sleep2Develop program investigates the role of sleep as a promotor of neurodevelopment and identifies the sleep determinants of childhood development. This is rephrased as Sleep(to)Develop? or Sleep(to)Develop! Our sleep research combines clinical and...
Research program on CCHS

Research program on CCHS

Congenital central hypoventilation syndrome (CCHS), also known as Ondine’s curse, is a genetic disorder characterised by reduced or absent breathing during sleep. The SleepCmd team at NeuroDiderot (Inserm–Université Paris Cité) combines experimental research and...