MeCP2 Repression Goes Nonglobal
Author:
Affiliation:
1. The authors are at the Wellcome Trust Centre for Cell Biology, University of Edinburgh, The King's Buildings, Edinburgh EH9 3JR, UK.
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference12 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
2. Nonlinear partial differential equations and applications: Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain
3. Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2
4. DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation
5. RETRACTED: A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos
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