Lataa...
Recent advances in MeCP2 structure and function
Mutations in methyl DNA binding protein 2 (MeCP2) cause the neurodevelopmental disorder Rett syndrome (RTT). The mechanism(s) by which the native MeCP2 protein operates in the cell are not well understood. Historically, MeCP2 has been characterized as a proximal gene silencer with 2 functional domai...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2009
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2874317/ https://ncbi.nlm.nih.gov/pubmed/19234536 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1139/o08-115 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|