טוען...
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...
שמור ב:
| הוצא לאור ב: | Biochem Biophys Rep |
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| Main Authors: | , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Elsevier
2017
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5709289/ https://ncbi.nlm.nih.gov/pubmed/29204517 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbrep.2017.11.003 |
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