CHD7 Targets Active Gene Enhancer Elements to Modulate ES Cell-Specific Gene Expression

CHD7 is one of nine members of the chromodomain helicase DNA–binding domain family of ATP–dependent chromatin remodeling enzymes found in mammalian cells. De novo mutation of CHD7 is a major cause of CHARGE syndrome, a genetic condition characterized by multiple congenital anomalies. To gain insight...

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Detalles Bibliográficos
Autores principales: Schnetz, Michael P., Handoko, Lusy, Akhtar-Zaidi, Batool, Bartels, Cynthia F., Pereira, C. Filipe, Fisher, Amanda G., Adams, David J., Flicek, Paul, Crawford, Gregory E., LaFramboise, Thomas, Tesar, Paul, Wei, Chia-Lin, Scacheri, Peter C.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2904778/
https://www.ncbi.nlm.nih.gov/pubmed/20657823
http://dx.doi.org/10.1371/journal.pgen.1001023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2904778/
https://www.ncbi.nlm.nih.gov/pubmed/20657823
http://dx.doi.org/10.1371/journal.pgen.1001023

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