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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832002/
https://www.ncbi.nlm.nih.gov/pubmed/31441214
http://dx.doi.org/10.15252/embr.201948336

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832002/
https://www.ncbi.nlm.nih.gov/pubmed/31441214
http://dx.doi.org/10.15252/embr.201948336

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