| Published Application/Species/Sample/Dilution | Reference |
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- immunocytochemistry; human; 1:50; loading ...; fig 3C
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| Wang X, Sha Y, Wang W, Cui Y, Chen J, Yan W, et al. Novel IFT140 variants cause spermatogenic dysfunction in humans. Mol Genet Genomic Med. 2019;7:e920 pubmed publisher |
| Tao D, Xue H, Zhang C, Li G, Sun Y. The Role of IFT140 in Osteogenesis of Adult Mice Long Bone. J Histochem Cytochem. 2019;:22155419847188 pubmed publisher |
| Liu W, He X, Yang S, Zouari R, Wang J, Wu H, et al. Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice. Am J Hum Genet. 2019;104:738-748 pubmed publisher |
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| Bowie E, Norris R, Anderson K, Goetz S. Spinocerebellar ataxia type 11-associated alleles of Ttbk2 dominantly interfere with ciliogenesis and cilium stability. PLoS Genet. 2018;14:e1007844 pubmed publisher |
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| Vuolo L, Stevenson N, Heesom K, Stephens D. Dynein-2 intermediate chains play crucial but distinct roles in primary cilia formation and function. elife. 2018;7: pubmed publisher |
| Wang L, Failler M, Fu W, Dynlacht B. A distal centriolar protein network controls organelle maturation and asymmetry. Nat Commun. 2018;9:3938 pubmed publisher |
| Funabashi T, Katoh Y, Okazaki M, Sugawa M, Nakayama K. Interaction of heterotrimeric kinesin-II with IFT-B-connecting tetramer is crucial for ciliogenesis. J Cell Biol. 2018;217:2867-2876 pubmed publisher |
| Forbes T, Howden S, Lawlor K, Phipson B, Maksimovic J, Hale L, et al. Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms. Am J Hum Genet. 2018;102:816-831 pubmed publisher |
| Takei R, Katoh Y, Nakayama K. Robust interaction of IFT70 with IFT52-IFT88 in the IFT-B complex is required for ciliogenesis. Biol Open. 2018;7: pubmed publisher |
| Silva L, Jacobs D, Allard B, Fields T, Sharma M, Wallace D, et al. Inhibition of Hedgehog signaling suppresses proliferation and microcyst formation of human Autosomal Dominant Polycystic Kidney Disease cells. Sci Rep. 2018;8:4985 pubmed publisher |
| Ye F, Nager A, Nachury M. BBSome trains remove activated GPCRs from cilia by enabling passage through the transition zone. J Cell Biol. 2018;217:1847-1868 pubmed publisher |
| Li G, Liu M, Zhang S, Wan H, Zhang Q, Yue R, et al. Essential Role of IFT140 in Promoting Dentinogenesis. J Dent Res. 2018;97:423-431 pubmed publisher |
| Taulet N, Vitre B, Anguille C, Douanier A, Rocancourt M, Taschner M, et al. IFT proteins spatially control the geometry of cleavage furrow ingression and lumen positioning. Nat Commun. 2017;8:1928 pubmed publisher |
| Shimada H, Lu Q, Insinna Kettenhofen C, Nagashima K, English M, Semler E, et al. In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations. Cell Rep. 2017;20:384-396 pubmed publisher |
| Kanie T, Abbott K, Mooney N, Plowey E, Demeter J, JACKSON P. The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base. Dev Cell. 2017;42:22-36.e12 pubmed publisher |
| Phua S, Chiba S, Suzuki M, Su E, Roberson E, Pusapati G, et al. Dynamic Remodeling of Membrane Composition Drives Cell Cycle through Primary Cilia Excision. Cell. 2017;168:264-279.e15 pubmed publisher |
| Nozaki S, Katoh Y, Terada M, Michisaka S, Funabashi T, Takahashi S, et al. Regulation of ciliary retrograde protein trafficking by the Joubert syndrome proteins ARL13B and INPP5E. J Cell Sci. 2017;130:563-576 pubmed publisher |
| Fu W, Wang L, Kim S, Li J, Dynlacht B. Role for the IFT-A Complex in Selective Transport to the Primary Cilium. Cell Rep. 2016;17:1505-1517 pubmed publisher |
| Garcia Gonzalo F, Phua S, Roberson E, Garcia G, Abedin M, Schurmans S, et al. Phosphoinositides Regulate Ciliary Protein Trafficking to Modulate Hedgehog Signaling. Dev Cell. 2015;34:400-409 pubmed publisher |
| Siller S, Burke M, Li F, Takemaru K. Chibby functions to preserve normal ciliary morphology through the regulation of intraflagellar transport in airway ciliated cells. Cell Cycle. 2015;14:3163-72 pubmed publisher |
| Ran J, Yang Y, Li D, Liu M, Zhou J. Deacetylation of α-tubulin and cortactin is required for HDAC6 to trigger ciliary disassembly. Sci Rep. 2015;5:12917 pubmed publisher |
| Xu Y, Cao J, Huang S, Feng D, Zhang W, Zhu X, et al. Characterization of tetratricopeptide repeat-containing proteins critical for cilia formation and function. PLoS ONE. 2015;10:e0124378 pubmed publisher |
