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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
Assuntos:
Articles
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados