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The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis

Rett syndrome is a severe neurodevelopmental disorder mainly caused by mutations in the transcriptional regulator MeCP2. Although there is no effective therapy for Rett syndrome, the recently discovered disease reversibility in mice suggests that there are therapeutic possibilities. Identification o...

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Autores principales: Forlani, Greta, Giarda, Elisa, Ala, Ugo, Di Cunto, Ferdinando, Salani, Monica, Tupler, Rossella, Kilstrup-Nielsen, Charlotte, Landsberger, Nicoletta
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2010
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2908467/
https://ncbi.nlm.nih.gov/pubmed/20504995
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq214
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