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Autosomal-dominant polycystic kidney disease in infancy and childhood: Progression and outcome
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The non-selective cation-permeable channel TRPC3 is a tetrahedron with a cap on the large cytoplasmic end
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A polycystin-1 multiprotein complex is disrupted in polycystic kidney disease cells
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PKD2 interacts and co-localizes with mDia1 to mitotic spindles of dividing cells - Role of mDia1 in PKD2 localization to mitotic spindles
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Pkd2 haploinsufficiency alters intracellular calcium regulation in vascular smooth muscle cells
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TRPC3 mediates T-cell receptor-dependent calcium entry in human T-lymphocytes
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BRITISH JOURNAL OF PHARMACOLOGY (2000)
Location of mutations within the PKD2 gene influences clinical outcome
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