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See Latest ArticlesSrc Inhibition Ameliorates Polycystic Kidney Disease
Journal of the American Society of Nephrology, 04/07/08
Sweeney WE et al. - Despite identification of the genes responsible for autosomal dominant polycystic kidney disease (PKD) and autosomal recessive PKD (ARPKD), the precise functions of their cystoprotein products remain unknown. Recent data suggested that multimeric cystoprotein complexes initiate aberrant signaling cascades in PKD, and common components of these signaling pathways may be therapeutic targets.
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Today in Basic Science/Genetics...keeping you current
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Conditionally immortalized human podocyte cell lines established from urine
American Journal of Physiology: Renal Physiology, 12/04/09
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Today in Cystic Dz...keeping you current
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Echocardiographic findings in kidney transplant patients with autosomal dominant polycystic kidney disease
Scandinavian Journal of Urology and Nephrology, 12/04/09
Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease
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Cystin Localizes to Primary Cilia via Membrane Microdomains and a Targeting Motif
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