Metabolism and mitochondria in polycystic kidney disease research and therapy

Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common, potentially lethal, monogenic diseases and is caused predominantly by mutations in polycystic kidney disease 1 ( PKD1 ) and PKD2 , which encode polycystin 1 (PC1) and PC2, respectively. Over the decades-long course of th...

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Veröffentlicht in:	Nature reviews. Nephrology 2018-11, Vol.14 (11), p.678-687
Hauptverfasser:	Padovano, Valeria, Podrini, Christine, Boletta, Alessandra, Caplan, Michael J.
Format:	Artikel
Sprache:	eng
Schlagworte:	631/80/642/333/1465 692/4022/1585/1589 Care and treatment Development and progression Diagnosis Kidney diseases Kinases Medicine Medicine & Public Health Metabolism Mitochondria Mitochondrial DNA Mutation Nephrology Pathogenesis Phosphorylation Polycystic kidney disease Proteins Review Article
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