Neurogenomics and Neuronal Physiopathology
The focus on glutamatergic signaling and metabolism is supported by previous accumulated evidence from the team reporting various genetic alterations affecting the structure, the development and/or the function of excitatory glutamatergic neuronal connections in patients with neurodevelopmental disorders (ID and/or autism), as well as abnormal molecular signatures supporting perturbations in glutamate initiated signaling pathways and converging towards glutamate‐mediated excitotoxicity in ALS.
Members (Phd students excluded)
ANDRES | Christian | PUPH1 |
ARPIN | Stéphanie | PH |
AUGÉ-GOUILLOU | Corinne | PU1 |
BENZ DE BRETAGNE | Isabelle | PH |
BLASCO | Hélène | MCUPH |
CHERPI- ANTAR | Catherine | TCH |
CORCIA | Philippe | PUPH |
COUDERT | Edouard | ATER |
DE TOFFOL | Bertrand | PUPH1 |
GENTY | Murielle | ADT |
JAILLET | Jérôme | TCH |
LAUMONNIER | Frédéric | CR1 |
LEVER | David | CDI.C |
LIMOUSIN | Nadège | PH |
MAROUILLAT | Sylviane | IE |
MINIER | Frédéric | MCF |
MOIZARD | Marie-Pierre | IR |
RAYNAUD | Martine | PH |
RENAULT | Sylvaine | MCF |
RONCE | Nathalie | IR |
THEPAULT | Rose-Anne | TCH |
TOUTAIN | Annick | PUPH |
UNG | Devina | ATER |
VONWILL | Sandrine | IR |
VOURC'H | Patrick | PUPH |