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MeCP2 as an activator of gene expression
Rett Syndrome is a neurodevelopmental disorder that primarily affects females and is caused by mutations in the methyl-CpG-binding-protein 2 (MeCP2) gene. Initially, MeCP2 had been shown to be a repressor of gene transcription. In their 2008 paper, Chahrour and colleagues (DOI: 10.1126/science.11532...
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| Pubblicato in: | Trends Neurosci |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5909705/ https://ncbi.nlm.nih.gov/pubmed/29405930 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tins.2017.11.005 |
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