Loss of WSTF results in spontaneous fluctuations of heterochromatin formation and resolution, combined with substantial changes to gene expression.

Culver-Cochran, Ashley E; Chadwick, Brian P

Culver-Cochran, Ashley E; Chadwick, Brian P.

Affiliation

Chadwick BP; Department of Biological Science, Florida State University, Tallahassee, FL, USA. chadwick@bio.fsu.edu.

BMC Genomics ; 14: 740, 2013 Oct 29.

Article in En | MEDLINE | ID: mdl-24168170

Subject(s)

Heterochromatin/metabolism; Williams Syndrome/genetics; Base Sequence; Cell Line; Chromatin Assembly and Disassembly; Chromosomes, Human, X; Gene Knockout Techniques; Haploinsufficiency/genetics; Histones/genetics; Histones/metabolism; Humans; Promoter Regions, Genetic; Transcription Factors/deficiency; Transcription Factors/genetics; Transcription Factors/metabolism

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Heterochromatin / Williams Syndrome Type of study: Prognostic_studies Limits: Humans Language: En Journal: BMC Genomics Journal subject: GENETICA Year: 2013 Document type: Article Country of publication: United kingdom

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