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Summary Anatomy Item Literature (826) Expression Attributions Wiki
XB-ANAT-1514

Papers associated with process (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.                    

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.                

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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