Proteomic analysis of AQP11-null kidney: Proximal tubular type polycystic kidney disease

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is caused by the mutation of polycystins (PC-1 or PC-2), in which cysts start from the collecting duct to extend to all nephron segments with eventual end stage renal failure. The cyst development is attenuated by a vasopressin V2 receptor antagon...

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Detalles Bibliográficos
Autores principales: Saito, Tatsuya, Tanaka, Yasuko, Morishita, Yoshiyuki, Ishibashi, Kenichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709289/
https://www.ncbi.nlm.nih.gov/pubmed/29204517
http://dx.doi.org/10.1016/j.bbrep.2017.11.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709289/
https://www.ncbi.nlm.nih.gov/pubmed/29204517
http://dx.doi.org/10.1016/j.bbrep.2017.11.003

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