Author
Centre National de la Recherche ScientifiqueORCID 0000-0003-3964-2548Unclaimed ORCID profile · follow to get notified of new preprints
3 papers
Recent·Most cited
Ana Guardia, Almudena Fernández, Davide Seruggia…·Lluı́s Montoliu
The paper generates a mouse model of FHONDA syndrome with mutations in SLC38A8, showing normal pigmentation but visual deficits similar to albinism.
Giulia Albertini, Ivana D’Andrea, Mélanie Druart…·Anne Roumier
This study shows that serotonin signaling through microglial 5-HT2B receptors during early development is critical for normal neuronal circuit maturation and social behavior.
Takuma Kumamoto, Franck Maurinot, Raphaëlle Barry‐Martinet…·Jean Livet
This paper introduces a genetic switch called iOn that enables the identification of genomic integration events by triggering gene expression upon insertion, improving transgenesis in stem cells and model organisms.