| 1 | SPG80, UBAP1
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| Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
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| Farazi Fard MA, Rebelo AP, Buglo E, Nemati H, Dastsooz H, Gehweiler I, Reich S, Reichbauer J, Quintáns B, Ordóñez-Ugalde A, Cortese A, Courel S, Abreu L, Powell E, Danzi M, Martuscelli NB, Bis-Brewer DM, Tao F, Zarei F, Habibzadeh P, Yavarian M, Modarresi F, Silawi M, Tabatabaei Z, Yousefi M, Farpour HR, Kessler C, Mangold E, Kobeleva X, Mueller AJ, Haack TB, Tarnopolsky M, Gan-Or Z, Rouleau GA, Synofzik M, Sobrido MJ, Jordanova A, Schüle R, Zuchner S, Faghihi MA.
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| Am J Hum Genet 104(4):767-773. doi: 10.1016/j.ajhg.2019.03.001. Epub 2019 Mar 28.
2019
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| 2 | TGM7, UBAP1
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| Characterization of fusion genes in common and rare epithelial ovarian cancer histologic subtypes.
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| Earp MA, Raghavan R, Li Q, Dai J, Winham SJ, Cunningham JM, Natanzon Y, Kalli KR, Hou X, Weroha SJ, Haluska P, Lawrenson K, Gayther SA, Wang C, Goode EL, Fridley BL.
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| Oncotarget 8(29):46891-46899. doi: 10.18632/oncotarget.16781.
2017
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| 3 | PTPN23, UBAP1
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| Structural Basis for Selective Interaction between the ESCRT Regulator HD-PTP and UBAP1.
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| Gahloth D, Levy C, Heaven G, Stefani F, Wunderley L, Mould P, Cliff MJ, Bella J, Fielding AJ, Woodman P, Tabernero L.
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| Structure 24(12):2115-2126. doi: 10.1016/j.str.2016.10.006. Epub 2016 Nov 10.
2016
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| 4 | MVB12A, MVB12B, UBAP1
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| The molecular basis for selective assembly of the UBAP1-containing endosome-specific ESCRT-I complex
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| Wunderley L, Brownhill K, Stefani F, Tabernero L, Woodman P.
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| J Cell Sci. Feb 1;127(Pt 3):663-72. doi: 10.1242/jcs.140673. Epub 2013 Nov 27. 2014
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| 5 | TSG101, UBAP1, VPS28, VPS37A
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| The UBAP1 subunit of ESCRT-I interacts with ubiquitin via a SOUBA domain.
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| Agromayor M, Soler N, Caballe A, Kueck T, Freund SM, Allen MD, Bycroft M, Perisic O, Ye Y, McDonald B, Scheel H, Hofmann K, Neil SJ, Martin-Serrano J, Williams RL.
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| Structure 20(3):414-28. doi: 10.1016/j.str.2011.12.013.
2012
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| 6 | MVB12A, MVB12B, UBAP1, VPS37A
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| UBAP1 is a component of an endosome-specific ESCRT-I complex that is essential for MVB sorting.
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| Stefani F, Zhang L, Taylor S, Donovan J, Rollinson S, Doyotte A, Brownhill K, Bennion J, Pickering-Brown S, Woodman P.
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| Curr Biol 21(14):1245-50. doi: 10.1016/j.cub.2011.06.028. Epub 2011 Jul 14. 2011
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| 7 | KIF24, UBAP1, UBAP2
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| Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?
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| Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Scalabrini D, Cortini F, Fumagalli G, Cappa S, Binetti G, Franceschi M, Rainero I, Giordana MT, Mariani C, Bresolin N, Scarpini E, Galimberti D.
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| Neurosci Lett 482(3):240-4. doi: 10.1016/j.neulet.2010.07.047. Epub 2010 Jul 27.
2010
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| 8 | UBAP1
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| Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration.
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| Rollinson S, Rizzu P, Sikkink S, Baker M, Halliwell N, Snowden J, Traynor BJ, Ruano D, Cairns N, Rohrer JD, Mead S, Collinge J, Rossor M, Akay E, Guerreiro R, Rademakers R, Morrison KE, Pastor P, Alonso E, Martinez-Lage P, Graff-Radford N, Neary D, Heutink P, Mann DM, Van Swieten J, Pickering-Brown SM.
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| Neurobiol Aging 30(4):656-65. doi: 10.1016/j.neurobiolaging.2009.01.009. Epub 2009 Feb 12.
2009
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| 9 | UBAP1
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| Isolation and characterization of a novel cDNA, UBAP1, derived from the tumor suppressor locus in human chromosome 9p21-22.
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| Qian J, Yang J, Zhang X, Zhang B, Wang J, Zhou M, Tang K, Li W, Zeng Z, Zhao X, Shen S, Li G.
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| J Cancer Res Clin Oncol 127(10):613-8. 2001
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