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Summary Expression Gene Literature (17) GO Terms (0) Nucleotides (100) Proteins (29) Interactants (232) Wiki
XB--486248

Papers associated with ift88 (and Disease Ontology)

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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.          

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. January 1, 2019; 14 (8): e0221698.                      

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.                      

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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