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Genetic Modifiers of MeCP2 Function in Drosophila

The levels of methyl-CpG–binding protein 2 (MeCP2) are critical for normal post-natal development and function of the nervous system. Loss of function of MeCP2, a transcriptional regulator involved in chromatin remodeling, causes classic Rett syndrome (RTT) as well as other related conditions charac...

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Main Authors: Cukier, Holly N., Perez, Alma M., Collins, Ann L., Zhou, Zhaolan, Zoghbi, Huda Y., Botas, Juan
格式: Artigo
語言:Inglês
出版: Public Library of Science 2008
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2518867/
https://ncbi.nlm.nih.gov/pubmed/18773074
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1000179
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