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Many genes, such as PKD1 and PKD2 which, when mutated, cause autosomal dominant polycystic kidney disease (ADPKD), have been found to localize to primary cilia. The cilium functions as a sensor to transmit extracellular signals into the cell. Abnormal cilia structure and function are associated with the development of polyscystic kidney disease (PKD). Cilia assembly includes centriole migration to the apical surface of the cell, ciliary vesicle docking and fusion with the cell membrane at the intended site of cilium outgrowth, and microtubule growth from the basal body. This review summarizes the most recent advances in cilia and PKD research, with special emphasis on the mechanisms of cytoplasmic and intraciliary protein transport during ciliogenesis.<jats:bold>Birth Defects Research (Part C) 102:174\u2013185, 2014<\/jats:bold>. \u00a9<jats:bold>2014 Wiley Periodicals, Inc<\/jats:bold>.<\/jats:p>","DOI":"10.1002\/bdrc.21066","type":"journal-article","created":{"date-parts":[[2014,6,5]],"date-time":"2014-06-05T06:50:44Z","timestamp":1401951044000},"page":"174-185","source":"Crossref","is-referenced-by-count":27,"title":["Cilia and polycystic kidney disease, kith and kin"],"prefix":"10.1002","volume":"102","author":[{"given":"Liwei","family":"Huang","sequence":"first","affiliation":[{"name":"Department of Medicine Eastern Virginia Medical School Norfolk Virginia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joshua H.","family":"Lipschutz","sequence":"additional","affiliation":[{"name":"Department of Medicine Philadelphia Veterans 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