piRNAs Warrant Investigation in Rett Syndrome: An Omics Perspective

Mutations in the MECP2 gene are found in a large proportion of girls with Rett Syndrome. Despite extensive research, the principal role of MeCP2 protein remains elusive. Is MeCP2 a regulator of genes, acting in concert with co-activators and co-repressors, predominantly as an activator of target gen...

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Detalles Bibliográficos
Autores principales: Saxena, Alka, Tang, Dave, Carninci, Piero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2012
Materias:
Other
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810717/
https://www.ncbi.nlm.nih.gov/pubmed/22976001
http://dx.doi.org/10.3233/DMA-2012-0932

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810717/
https://www.ncbi.nlm.nih.gov/pubmed/22976001
http://dx.doi.org/10.3233/DMA-2012-0932

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