MeCP2 in Rett syndrome: transcriptional repressor or chromatin architectural protein?
Author:
Funder
National Institutes of Health
National Institute of Environmental Health Sciences
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics
Reference38 articles.
1. DNA methylation and human disease;Robertson;Nat Rev Genet,2005
2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
3. Methyl CpG-binding proteins and transcriptional repression;Wade;Bioessays,2001
4. Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex;Nan;Nature,1998
5. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription;Jones;Nat Genet,1998
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