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A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing
Mutations in MECP2 (methyl CpG binding protein 2) are linked to the severe postnatal neurodevelopmental disorder Rett Syndrome (RTT). MeCP2 was originally characterized as a transcriptional repressor that preferentially bound methylated DNA, however, recent data indicates MeCP2 is a multifunctional...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3148018/ https://ncbi.nlm.nih.gov/pubmed/21070191 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BSR20100124 |
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