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Lateral transport of Smoothened from the plasma membrane to the membrane of the cilium
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Nephronophthisis: Disease Mechanisms of a Ciliopathy
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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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A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
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A role for rhodopsin in a signal transduction cascade that regulates membrane trafficking and photoreceptor polarity
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The intraflagellar transport protein IFT20 is associated with the Golgi complex and is required for cilia assembly
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Loss of polycystin-1 in human cyst-lining epithelia leads to ciliary dysfunction
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A BAR domain in the N terminus of the Arf GAP ASAP1 affects membrane structure and trafficking of epidermal growth factor receptor
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Odf2-deficient mother centrioles lack distal/subdistal appendages and the ability to generate primary cilia
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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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Multiple signals axe required for α2,6-sialyltransferase (ST6Gal I) oligomerization and Golgi localization
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The Rab8 GTPase selectively regulates AP-1B-dependent basolateral transport in polarized Madin!Darby canine kidney cells
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The AP-1A and AP-1B clathrin adaptor complexes define biochemically and functionally distinct membrane domains
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Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells
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The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia
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Distinct subcellular expression of endogenous polycystin-2 in the plasma membrane and Golgi apparatus of MDCK cells
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Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium
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The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway
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Myosin Vb is associated with plasma membrane recycling systems
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Polycystin-2 is a novel cation channel implicated in defective intracellular Ca2+ homeostasis in polycystic kidney disease
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Co-assembly of polycystin-1 and-2 produces unique cation-permeable currents
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Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene Tg737, are required for assembly of cilia and flagella
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ADPKD: A human disease altering Golgi function and basolateral exocytosis in renal epithelia
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Compromised cytoarchitecture and polarized trafficking in autosomal dominant polycystic kidney disease cells
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