Papers associated with cilium (and ift88)

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	TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B., JCI Insight. November 8, 2023; 8 (21):
	GJA1 depletion causes ciliary defects by affecting Rab11 trafficking to the ciliary base., Jang DG., Elife. August 25, 2022; 11
	The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus., Beckers A., Sci Rep. June 25, 2021; 11 (1): 13333.
	Aquatic models of human ciliary diseases., Corkins ME., Genesis. February 1, 2021; 59 (1-2): e23410.
	Divergent roles of the Wnt/PCP Formin Daam1 in renal ciliogenesis., Corkins ME., PLoS One. January 1, 2019; 14 (8): e0221698.
	Stabilization of speckle-type POZ protein (Spop) by Daz interacting protein 1 (Dzip1) is essential for Gli turnover and the proper output of Hedgehog signaling., Schwend T., J Biol Chem. November 8, 2013; 288 (45): 32809-32820.
	Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry., Kim S., Nat Cell Biol. April 1, 2011; 13 (4): 351-60.
	The hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formation., Dammermann A., Genes Dev. September 1, 2009; 23 (17): 2046-59.
	FGF signalling during embryo development regulates cilia length in diverse epithelia., Neugebauer JM., Nature. April 2, 2009; 458 (7238): 651-4.
	Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros., Tran U., Dev Biol. July 1, 2007; 307 (1): 152-64.
	Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer's vesicle are required for specification of the zebrafish left-right axis., Bisgrove BW., Dev Biol. November 15, 2005; 287 (2): 274-88.
	Localization and loss-of-function implicates ciliary proteins in early, cytoplasmic roles in left-right asymmetry., Qiu D., Dev Dyn. September 1, 2005; 234 (1): 176-89.
	Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization., Cano DA., Development. July 1, 2004; 131 (14): 3457-67.
	The C. elegans homolog of the murine cystic kidney disease gene Tg737 functions in a ciliogenic pathway and is disrupted in osm-5 mutant worms., Haycraft CJ., Development. May 1, 2001; 128 (9): 1493-505.
	An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons., Qin H., Curr Biol. March 20, 2001; 11 (6): 457-61.
	Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia., Taulman PD., Mol Biol Cell. March 1, 2001; 12 (3): 589-99.
	The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination., Murcia NS., Development. June 1, 2000; 127 (11): 2347-55.

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