Yüklüyor......
Gemin proteins are required for efficient assembly of Sm-class ribonucleoproteins
Spinal muscular atrophy (SMA) is a neurodegenerative disease characterized by loss of spinal motor neurons. The gene encoding the survival of motor neurons (SMN) protein is mutated in >95% of SMA cases. SMN is the central component of a large oligomeric complex, including Gemins2–7, that is neces...
Kaydedildi:
| Asıl Yazarlar: | , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
National Academy of Sciences
2005
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1297697/ https://ncbi.nlm.nih.gov/pubmed/16301532 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0508947102 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|