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XB-ANAT-3662
Papers associated with ciliary axoneme (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 |
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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. |
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Aquatic models of human ciliary diseases., Corkins ME., Genesis. February 1, 2021; 59 (1-2): e23410. |
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The hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formation., Dammermann A., Genes Dev. September 1, 2009; 23 (17): 2046-59. |
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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. |
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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. |
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