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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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Genes Dev
Main Authors: Ma, Shenghong, Guan, Kun-Liang
Format: Artigo
Jezik:Inglês
Izdano: Cold Spring Harbor Laboratory Press 2018
Teme:
Online dostop: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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