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STAT3 Signaling in Polycystic Kidney Disease
Mutations in the gene coding for the integral membrane protein polycystin-1 (PC1) are the cause of most cases of autosomal-dominant polycystic kidney disease (ADPKD), a very common disease that leads to kidney failure and currently lacks approved treatment. Recent work has revealed that PC1 can regu...
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| Publicado no: | Drug Discov Today Dis Mech |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4624194/ https://ncbi.nlm.nih.gov/pubmed/26523147 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ddmec.2013.03.001 |
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