The ion channel function of polycystin‐1 in the polycystin‐1/polycystin‐2 complex

Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in PKD1 or PKD2 gene, encoding the polycystic kidney disease protein polycystin‐1 and the transient receptor potential channel polycystin‐2 (also known as TRPP2), respectively. Polycystin‐1 and polycystin‐2 form a receptor–i...

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Bibliografiske detaljer
Udgivet i:EMBO Rep
Main Authors: Wang, Zhifei, Ng, Courtney, Liu, Xiong, Wang, Yan, Li, Bin, Kashyap, Parul, Chaudhry, Haroon A, Castro, Alexis, Kalontar, Enessa M, Ilyayev, Leah, Walker, Rebecca, Alexander, R Todd, Qian, Feng, Chen, Xing‐Zhen, Yu, Yong
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2019
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Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6832002/
https://ncbi.nlm.nih.gov/pubmed/31441214
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/embr.201948336
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