Loading...
MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription
Mutations in the gene encoding the transcriptional repressor methyl-CpG binding protein 2 (MeCP2) cause the neurodevelopmental disorder Rett syndrome. Loss of function as well as increased dosage of MECP2 gene cause a host of neuropsychiatric disorders. To explore the molecular mechanism(s) underlyi...
Na minha lista:
| Main Authors: | , , , , , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2008
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2443785/ https://ncbi.nlm.nih.gov/pubmed/18511691 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/science.1153252 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|