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Role of PKR in the Inhibition of Proliferation and Translation by Polycystin-1
Autosomal dominant polycystic kidney disease (ADPKD) is mainly caused by mutations in the PKD1 (~85%) or PKD2 (~15%) gene which, respectively, encode polycystin-1 (PC1) and polycystin-2 (PC2). How PC1 regulates cell proliferation and apoptosis has been studied for decades but the underlying mechanis...
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| Publicado no: | Biomed Res Int |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6612395/ https://ncbi.nlm.nih.gov/pubmed/31341901 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/5320747 |
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