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Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease
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Human ADPKD primary cyst epithelial cells with a novel, single codon deletion in the PKD1 gene exhibit defective ciliary polycystin localization and loss of flow-induced Ca2+ signaling
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Loss of polycystin-1 in human cyst-lining epithelia leads to ciliary dysfunction
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Rhodopsin C terminus, the site of mutations causing retinal disease, regulates trafficking by binding to ADP-ribosylation factor 4 (ARF4)
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Co-assembly of polycystin-1 and-2 produces unique cation-permeable currents
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