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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Detaylı Bibliyografya
Yayımlandı:EMBO Rep
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2019
Konular:
Articles
Online Erişim: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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