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Functional Profiling of Human MeCP2 by Automated Data Comparison Analysis and Computerized Expression Pathway Modeling
OBJECTIVES: Methyl-CpG binding protein 2 (MeCP2) is a ubiquitous epigenetic factor that represses gene expression by modifying chromatin. Mutations in the MeCP2 gene cause Rett syndrome, a progressive neurodevelopmental disorder. Recent studies also have shown that MeCP2 plays a role in carcinogenes...
Autores principales: | Kim, Injoo, Lee, Shin Hae, Jeong, Jinwoo, Park, Jun Hyung, Yoo, Mi Ae, Kim, Cheol Min |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Medical Informatics
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871842/ https://www.ncbi.nlm.nih.gov/pubmed/27200222 http://dx.doi.org/10.4258/hir.2016.22.2.120 |
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