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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Detalles Bibliográficos
Autores principales: Cukier, Holly N., Perez, Alma M., Collins, Ann L., Zhou, Zhaolan, Zoghbi, Huda Y., Botas, Juan
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518867/
https://www.ncbi.nlm.nih.gov/pubmed/18773074
http://dx.doi.org/10.1371/journal.pgen.1000179

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518867/
https://www.ncbi.nlm.nih.gov/pubmed/18773074
http://dx.doi.org/10.1371/journal.pgen.1000179

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