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Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2)

Rett syndrome (RTT) is one of the most prevalent female mental disorders. De novo mutations in methyl CpG-binding protein 2 (MeCP2) are a major cause of RTT. MeCP2 regulates gene expression as a transcription regulator as well as through long-range chromatin interaction. Because MeCP2 is present on...

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Detalhes bibliográficos
Main Authors: Tanaka, Yoshiaki, Kim, Kun-Yong, Zhong, Mei, Pan, Xinghua, Weissman, Sherman Morton, Park, In-Hyun
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3900111/
https://ncbi.nlm.nih.gov/pubmed/24129406
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt500
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