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Polycystic kidney disease: a Hippo connection
Mutations in PKD1 and PKD2 are the leading cause of autosomal dominant polycystic kidney disease (ADPKD). In this issue of Genes & Development, a report by Cai and colleagues (pp. 781–793) reveals new insight into the molecular basis by which PKD1 deficiency leads to cystic kidney pathogenesis....
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| Vydáno v: | Genes Dev |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Cold Spring Harbor Laboratory Press
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6049516/ https://ncbi.nlm.nih.gov/pubmed/29921661 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gad.316570.118 |
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