Somatic Mutations in Renal Cyst Epithelium in Autosomal Dominant Polycystic Kidney Disease

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is a ciliopathy caused by mutations in PKD1 and PKD2 that is characterized by renal tubular epithelial cell proliferation and progressive CKD. Although the molecular mechanisms involved in cystogenesis are not established, concurrent i...

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Vydáno v:J Am Soc Nephrol
Hlavní autoři: Tan, Adrian Y., Zhang, Tuo, Michaeel, Alber, Blumenfeld, Jon, Liu, Genyan, Zhang, Wanying, Zhang, Zhengmao, Zhu, Yi, Rennert, Lior, Martin, Che, Xiang, Jenny, Salvatore, Steven P., Robinson, Brian D., Kapur, Sandip, Donahue, Stephanie, Bobb, Warren O., Rennert, Hanna
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society of Nephrology 2018
Témata:
Basic Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6065086/
https://ncbi.nlm.nih.gov/pubmed/30042192
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2017080878
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