Citations for
1IFT20, IFT88, MEIG1
MEIG1 determines the manchette localization of IFT20 and IFT88, two intraflagellar transport components in male germ cells
Yap YT, Shi L, Zhang D, Huang Q, Siddika F, Wang Z, Li W, Zhang Z.
Dev Biol. May;485:50-60. doi: 10.1016/j.ydbio.2022.03.001. Epub 2022 Mar 4. 2022
2IFT20, IFT57, IFT88
The T cell IFT20 interactome reveals new players in immune synapse assembly.
Galgano D, Onnis A, Pappalardo E, Galvagni F, Acuto O, Baldari CT.
J Cell Sci 130(6):1110-1121. doi: 10.1242/jcs.200006. Epub 2017 Feb 2. 2017
3IFT88
IFT88 influences chondrocyte actin organization and biomechanics.
Wang Z, Wann AK, Thompson CL, Hassen A, Wang W, Knight MM.
Osteoarthritis Cartilage 24(3):544-54. doi: 10.1016/j.joca.2015.10.003. Epub 2015 Oct 19. 2016
4IFT88, KIF3A
Heterotrimeric kinesin-2 (KIF3) mediates transition zone and axoneme formation of mouse photoreceptors.
Jiang L, Wei Y, Ronquillo CC, Marc RE, Yoder BK, Frederick JM, Baehr W.
J Biol Chem 290(20):12765-78. doi: 10.1074/jbc.M115.638437. Epub 2015 Mar 30. 2015
5IFT88
A Cilia Independent Role of Ift88/Polaris during Cell Migration.
Boehlke C, Janusch H, Hamann C, Powelske C, Mergen M, Herbst H, Kotsis F, Nitschke R, Kuehn EW.
PLoS One 10(10):e0140378. doi: 10.1371/journal.pone.0140378. eCollection 2015. 2015
6IFT88
Intraflagellar transport is essential for mammalian spermiogenesis but is absent in mature sperm.
San Agustin JT, Pazour GJ, Witman GB.
Mol Biol Cell 26(24):4358-72. doi: 10.1091/mbc.E15-08-0578. Epub 2015 Sep 30. 2015
7IFT88, TGFB1
TGF-β Suppresses Ift88 Expression in Chondrocytic ATDC5 Cells.
Kawasaki M, Ezura Y, Hayata T, Notomi T, Izu Y, Noda M.
J Cell Physiol 230(11):2788-95. doi: 10.1002/jcp.25005. 2015
8IFT88, MYH10
Myosin heavy chain 10 (MYH10) is required for centriole migration during the biogenesis of primary cilia.
Hong H, Kim J, Kim J.
Biochem Biophys Res Commun 461(1):180-5. doi: 10.1016/j.bbrc.2015.04.028. Epub 2015 Apr 13. 2015
9C2CD3, IFT52, IFT88
C2cd3 is critical for centriolar distal appendage assembly and ciliary vesicle docking in mammals.
Ye X, Zeng H, Ning G, Reiter JF, Liu A.
Proc Natl Acad Sci U S A 111(6):2164-9. doi: 10.1073/pnas.1318737111. Epub 2014 Jan 27. 2014
10IFT88, SFRP5
Ift88 regulates Hedgehog signaling, Sfrp5 expression, and β-catenin activity in post-natal growth plate.
Chang CF, Serra R.
J Orthop Res 31(3):350-6. doi: 10.1002/jor.22237. Epub 2012 Oct 3. 2013
11IFT88
Tg737 inhibition results in malignant transformation in fetal liver stem/progenitor cells by promoting cell-cycle progression and differentiation arrest.
You N, Liu W, Zhong X, Ji R, Zhang M, You H, Dou K, Tao K.
Mol Carcinog 51(8):659-73. doi: 10.1002/mc.20839. Epub 2011 Aug 11. Erratum in: Mol Carcinog. 2012 Oct;51(10):843. 2012
12IFT88
The cilia protein IFT88 is required for spindle orientation in mitosis.
Delaval B, Bright A, Lawson ND, Doxsey S.
Nat Cell Biol 13(4):461-8. doi: 10.1038/ncb2202. Epub 2011 Mar 27. 2011
13IFT88, TRIP11
GMAP210 and IFT88 are present in the spermatid golgi apparatus and participate in the development of the acrosome-acroplaxome complex, head-tail coupling apparatus and tail.
Kierszenbaum AL, Rivkin E, Tres LL, Yoder BK, Haycraft CJ, Bornens M, Rios RM.
Dev Dyn 240(3):723-36. doi: 10.1002/dvdy.22563. Epub 2011 Feb 10. 2011
14IFT46, IFT52, IFT88
Direct interactions of intraflagellar transport complex B proteins IFT88, IFT52, and IFT46.
Lucker BF, Miller MS, Dziedzic SA, Blackmarr PT, Cole DG.
J Biol Chem 285(28):21508-18. doi: 10.1074/jbc.M110.106997. Epub 2010 Apr 30. 2010
15IFT172, IFT57, IFT88
Zebrafish ift57, ift88, and ift172 intraflagellar transport mutants disrupt cilia but do not affect hedgehog signaling.
Lunt SC, Haynes T, Perkins BD.
Dev Dyn 238(7):1744-59. doi: 10.1002/dvdy.21999. 2009
16IFT88
Ciliary proteins link basal body polarization to planar cell polarity regulation.
Jones C, Roper VC, Foucher I, Qian D, Banizs B, Petit C, Yoder BK, Chen P.
Nat Genet 40(1):69-77. Epub 2007 Dec 9. 2008
17IFT88, RFX3
Distinct isoforms of the RFX transcription factor DAF-19 regulate ciliogenesis and maintenance of synaptic activity.
Senti G, Swoboda P.
Mol Biol Cell 19(12):5517-28. Epub 2008 Oct 8. 2008
18IFT88
The intraflagellar transport component IFT88/polaris is a centrosomal protein regulating G1-S transition in non-ciliated cells.
Robert A, Margall-Ducos G, Guidotti JE, Brégerie O, Celati C, Bréchot C, Desdouets C.
J Cell Sci 120(Pt 4):628-37. Epub 2007 Jan 30. Erratum in: J Cell Sci. 2007 Mar 1;120(Pt 5):918. 2007
19OFD1, IFT172, IFT88
Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification.
Ferrante MI, Zullo A, Barra A, Bimonte S, Messaddeq N, Studer M, Dolle P, Franco B.
Nat Genet 38(1):112-7. Epub 2005 Nov 27. 2006
20BTRC, CREBBP, CSRP2, FKBP8, GAS1, GSK3B, HHAT, HHIP, IFT88, KIF27, KIF3A, KIF7, RAB23, SHH, STIL, STK36, SUFU, VTN
Hedgehog signaling and congenital malformations.
Nieuwenhuis E, Hui CC.
Clin Genet 67(3):193-208. 2005
21TSG13D, LATS2, CRYL1, IFT88, GJB2
Molecular genetic evidence supporting a novel human hepatocellular carcinoma tumor suppressor locus at 13q12.11.
Chen CF, Yeh SH, Chen DS, Chen PJ, Jou YS.
Genes Chromosomes Cancer 44(3):320-8. 2005
22IFT88
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 12(3):589-99. 2001
23IFT88
Structure and expression of Tg737, a putative tumor suppressor gene, in human hepatocellular carcinomas.
Bonura C, Paterlini-Brechot P, Brechot C.
Hepatology 30(3):677-81 1999
24IFT88, TSG13D
The tetratricopeptide repeat containing Tg737 gene is a liver neoplasia tumor suppressor gene.
Isfort RJ, Cody DB, Doersen CJ, Richards WG, Yoder BK, Wilkinson JE, Kier LD, Jirtle RL, Isenberg JS, Klounig JE, Woychik RP.
Oncogene 15(15):1797-803. 1997
25IFT88
Characterization of the human homologue of the mouse Tg737 candidate polycystic kidney disease gene.
Schrick JJ, et al.
Hum Mol Genet 4 : 559-567. 1995
26IFT88
Sequence analysis of the human hTg737 gene and its polymorphic sites in patients with autosomal recessive polycystic kidney disease.
Onuchic LF, et al.
Mamm Genome 6 : 805-808. 1995
27ARPKD, IFT88
Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice.
Moyer JH, Lee-Tischler MJ, Kwon HY, Schrick JJ, Avner ED, Sweeney WE, Godfrey VL, Cacheiro NL, Wilkinson JE, Woychik RP.
Science 264(5163):1329-33. 1994