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Endothelin in Polycystic Kidney Disease
2011Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic kidney disease in man and is caused by germline mutations in PKD1 or PKD2. Affected patients develop progressively enlarged kidneys due to the growth of multiple renal epithelial cysts. Several studies have demonstrated marked intrafamilial phenotypic variability in PKD1 or
Ming-Yang, Chang, Albert C M, Ong
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[Diagnosis in Polycystic Kidney Disease].
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia, 2016The diagnosis of ADPKD should be based on a thorough assessment of the family history, radiological study and when indicated, genetic study. The anamnestic definition of 'negative family history' should be accepted only after a full clinical-instrumental assessment of close relatives of the subject .
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A methionine-Mettl3-N-methyladenosine axis promotes polycystic kidney disease
Cell Metabolism, 2021Harini Ramalingam +2 more
exaly
Polycystic Liver and Kidney Disease
Clinical Gastroenterology and Hepatology, 2022Kwabena Oware, Adu-Gyamfi +2 more
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The Structure of the Polycystic Kidney Disease Channel PKD2 in Lipid Nanodiscs
Cell, 2016Peter S Shen +2 more
exaly