Papers associated with embryonic structure (and ift88)

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	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.
	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.
	Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning., Fakhro KA., Proc Natl Acad Sci U S A. February 15, 2011; 108 (7): 2915-20.
	Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros., Tran U., Dev Biol. July 1, 2007; 307 (1): 152-64.
	Xenopus cDNA microarray identification of genes with endodermal organ expression., Park EC., Dev Dyn. June 1, 2007; 236 (6): 1633-49.
	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.
	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 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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