載入...
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...
Na minha lista:
| 發表在: | Trends Neurosci |
|---|---|
| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2018
|
| 主題: | |
| 在線閱讀: | 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 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|