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Neurobiology of Disease|December 16, 2016
A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndromeValerie Matagne, Yann Ehinger, Lydia Saidi, et al.Brain Research|June 15, 2018
Correcting deregulated Fxyd1 expression rescues deficits in neuronal arborization and potassium homeostasis in MeCP2 deficient male miceValerie Matagne, Joyce Wondolowski, Matthew Frerking, et al.Nature Communications|December 17, 2015
Epigenetic regulation of puberty via Zinc finger protein-mediated transcriptional repressionAlejandro Lomniczi, Hollis Wright, Juan Manuel Castellano, et al.International Journal of Molecular Sciences|April 30, 2021
Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male Mouse Model of Rett SyndromeYann Ehinger, Valerie Matagne, Valérie Cunin, et al.Human Molecular Genetics|February 21, 2007
FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null miceVivianne Deng, Valerie Matagne, Fatima Banine, et al.Pharmaceutics|August 28, 2021
Ultrasound-Mediated Blood-Brain Barrier Opening Improves Whole Brain Gene Delivery in MiceMarie-Solenne Felix, Emilie Borloz, Khaled Metwally, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 22, 2006
Deletion of the Ttf1 gene in differentiated neurons disrupts female reproduction without impairing basal ganglia functionClaudio Mastronardi, Gregory G Smiley, Jacob Raber, et al.Pageof 2