Long-lasting beneficial effects of central serotonin receptor 7 stimulation in female mice modeling Rett syndrome

Rett syndrome (RTT) is a rare neurodevelopmental disorder, characterized by severe behavioral and physiological symptoms. Mutations in the methyl CpG binding protein 2 gene (MECP2) cause more than 95% of classic cases, and currently there is no cure for this devastating disorder. Recently we have de...

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Detalles Bibliográficos
Autores principales: De Filippis, Bianca, Chiodi, Valentina, Adriani, Walter, Lacivita, Enza, Mallozzi, Cinzia, Leopoldo, Marcello, Domenici, Maria Rosaria, Fuso, Andrea, Laviola, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396444/
https://www.ncbi.nlm.nih.gov/pubmed/25926782
http://dx.doi.org/10.3389/fnbeh.2015.00086

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396444/
https://www.ncbi.nlm.nih.gov/pubmed/25926782
http://dx.doi.org/10.3389/fnbeh.2015.00086

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