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XB--486248
Papers associated with ift88 (and Disease Ontology)
Results 1 - 4 of 4 results
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Aquatic models of human ciliary diseases., Corkins ME, Krneta-Stankic V, Kloc M, Miller RK., Genesis. February 1, 2021; 59 (1-2): e23410.  |
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Divergent roles of the Wnt/PCP Formin Daam1 in renal ciliogenesis., Corkins ME, Krneta-Stankic V, Kloc M, McCrea PD, Gladden AB, Miller RK., PLoS One. August 30, 2019; 14 (8): e0221698.  |
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Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning., Fakhro KA, Choi M, Ware SM, Belmont JW, Towbin JA, Lifton RP, Khokha MK, Brueckner M., Proc Natl Acad Sci U S A. February 15, 2011; 108 (7): 2915-20.  |
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The hydrolethalus syndrome protein HYLS-1 links core centriole structure to cilia formation., Dammermann A, Pemble H, Mitchell BJ, McLeod I, Yates JR, Kintner C, Desai AB, Oegema K., Genes Dev. September 1, 2009; 23 (17): 2046-59.  |
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