Vascular Dysfunction in a Mouse Model of Rett Syndrome and Effects of Curcumin Treatment

Mutations in the coding sequence of the X-linked gene MeCP2 (Methyl CpG–binding protein) are present in around 80% of patients with Rett Syndrome, a common cause of intellectual disability in female and to date without any effective pharmacological treatment. A relevant, and so far unexplored featur...

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Detalles Bibliográficos
Autores principales: Panighini, Anna, Duranti, Emiliano, Santini, Ferruccio, Maffei, Margherita, Pizzorusso, Tommaso, Funel, Niccola, Taddei, Stefano, Bernardini, Nunzia, Ippolito, Chiara, Virdis, Agostino, Costa, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660336/
https://www.ncbi.nlm.nih.gov/pubmed/23705018
http://dx.doi.org/10.1371/journal.pone.0064863

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3660336/
https://www.ncbi.nlm.nih.gov/pubmed/23705018
http://dx.doi.org/10.1371/journal.pone.0064863

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