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Summary Expression Gene Literature (16) GO Terms (0) Nucleotides (97) Proteins (27) Interactants (222) Wiki
XB--486248

Papers associated with ift88

Search for ift88 morpholinos using Textpresso

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6 paper(s) referencing morpholinos

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


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, Jin Z, Jiang K, Mitchell BJ, Jia J, Yang J., J Biol Chem. November 8, 2013; 288 (45): 32809-20.                


Nde1-mediated inhibition of ciliogenesis affects cell cycle re-entry., Kim S, Zaghloul NA, Bubenshchikova E, Oh EC, Rankin S, Katsanis N, Obara T, Tsiokas L., 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, 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.                


FGF signalling during embryo development regulates cilia length in diverse epithelia., Neugebauer JM, Amack JD, Peterson AG, Bisgrove BW, Yost HJ., Nature. April 2, 2009; 458 (7238): 651-4.      


Xenopus Bicaudal-C is required for the differentiation of the amphibian pronephros., Tran U, Pickney LM, Ozpolat BD, Wessely O., Dev Biol. July 1, 2007; 307 (1): 152-64.                  


Xenopus cDNA microarray identification of genes with endodermal organ expression., Park EC, Hayata T, Cho KW, Han JK., 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, Snarr BS, Emrazian A, Yost HJ., Dev Biol. November 15, 2005; 287 (2): 274-88.


Localization and loss-of-function implicates ciliary proteins in early, cytoplasmic roles in left-right asymmetry., Qiu D, Cheng SM, Wozniak L, McSweeney M, Perrone E, Levin M., Dev Dyn. September 1, 2005; 234 (1): 176-89.      


Orpk mouse model of polycystic kidney disease reveals essential role of primary cilia in pancreatic tissue organization., Cano DA, Murcia NS, Pazour GJ, Hebrok M., Development. July 1, 2004; 131 (14): 3457-67.


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, Swoboda P, Taulman PD, Thomas JH, Yoder BK., Development. May 1, 2001; 128 (9): 1493-505.


An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons., Qin H, Rosenbaum JL, Barr MM., Curr Biol. March 20, 2001; 11 (6): 457-61.


Expression of the orpk disease gene during kidney development and maturation., Nakanishi K, Sweeney WE, Avner ED, Murcia NS., Pediatr Nephrol. March 1, 2001; 16 (3): 219-26.


Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia., Taulman PD, Haycraft CJ, Balkovetz DF, Yoder BK., Mol Biol Cell. March 1, 2001; 12 (3): 589-99.


The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination., Murcia NS, Richards WG, Yoder BK, Mucenski ML, Dunlap JR, Woychik RP., Development. June 1, 2000; 127 (11): 2347-55.

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