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Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns

CHD7 is a member of the chromodomain helicase DNA binding domain family of ATP-dependent chromatin remodeling enzymes. De novo mutation of the CHD7 gene is a major cause of CHARGE syndrome, a genetic disease characterized by a complex constellation of birth defects (Coloboma of the eye, Heart defect...

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Detaylı Bibliyografya
Asıl Yazarlar: Schnetz, Michael P., Bartels, Cynthia F., Shastri, Kuntal, Balasubramanian, Dheepa, Zentner, Gabriel E., Balaji, Ravishankar, Zhang, Xiaodong, Song, Lingyun, Wang, Zhenghe, LaFramboise, Thomas, Crawford, Gregory E., Scacheri, Peter C.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Cold Spring Harbor Laboratory Press 2009
Konular:
Letter
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2665778/
https://ncbi.nlm.nih.gov/pubmed/19251738
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.086983.108
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