Epigenome: what we learned from Rett syndrome, a neurological disease caused by mutation of a methyl-CpG binding protein
Author:
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Reference10 articles.
1. 1) Obi T, Nishioka K, Ross OA, et al. Clinicopathologic study of a SNCA gene duplication patient with Parkinson disease and dementia. Neurology 2008;70:238-241.
2. 2) Kubota T, Das S, Christian SL, et al. Methylation-specific PCR simplifies imprinting analysis. Nat Genet 1997;16:16-17.
3. 3) Weaver IC, Cervoni N, Champagne FA, et al. Epigenetic programming by maternal behavior. Nat Neurosci 2004;7:847-854.
4. 4) Amir RE, Van den Veyver IB, Wan M, et al. Rett syndrome is caused by mutations in X-linked MECP2; encoding methyl-CpG-binding protein 2. Nat Genet 1999;23:185-188.
5. 5) Miyake K, Hirasawa T, Soutome M, et al. The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndrome. BMC Neurosci 2011;12:81.
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