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Recent advances in MeCP2 structure and function

Mutations in methyl DNA binding protein 2 (MeCP2) cause the neurodevelopmental disorder Rett syndrome (RTT). The mechanism(s) by which the native MeCP2 protein operates in the cell are not well understood. Historically, MeCP2 has been characterized as a proximal gene silencer with 2 functional domai...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Hite, Kristopher C., Adams, Valerie H., Hansen, Jeffrey C.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2009
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2874317/
https://ncbi.nlm.nih.gov/pubmed/19234536
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1139/o08-115
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