A carregar...

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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Saxena, Alka, Tang, Dave, Carninci, Piero
Formato: Artigo
Idioma:Inglês
Publicado em: IOS Press 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3810717/
https://ncbi.nlm.nih.gov/pubmed/22976001
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/DMA-2012-0932
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!