| 1 | UBXN7, UFD1, VCP
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| Crystal structures of the UBX domain of human UBXD7 and its complex with p97 ATPase.
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| Li ZH, Wang Y, Xu M, Jiang T.
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| Biochem Biophys Res Commun. Apr 22;486(1):94-100. doi: 10.1016/j.bbrc.2017.03.005. Epub 2017 Mar 6. 2017
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| 2 | UFD1
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| Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis.
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| Giusti B, Sticchi E, De Cario R, Magi A, Nistri S, Pepe G.
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| Front Physiol. Aug 24;8:612. doi: 10.3389/fphys.2017.00612. eCollection 2017 2017
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| 3 | UFD1
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| Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome.
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| Napoli E, Tassone F, Wong S, Angkustsiri K, Simon TJ, Song G, Giulivi C.
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| J Biol Chem. Sep 18;290(38):23240-53. doi: 10.1074/jbc.M115.672360. Epub 2015 Jul 28 2015
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| 4 | NPLOC4, UFD1
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| Analysis of Npl4 deletion mutants in mammalian cells unravels new Ufd1-interacting motifs and suggests a regulatory role of Npl4 in ERAD.
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| Lass A, McConnell E, Fleck K, Palamarchuk A, Wójcik C.
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| Exp Cell Res 314(14):2715-23. Epub 2008 Jun 14. 2008
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| 5 | UFD1
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| A family- and population-based study of the UFD1L gene for schizophrenia.
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| Xie L, Ye L, Ju G, Xu Q, Zhang X, Liu S, Shi J, Yu Y, Wang Z, Shen Y, Wei J.
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| Am J Med Genet B Neuropsychiatr Genet 147B(7):1076-9. 2008
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| 6 | AMFR, NPLOC4, UFD1
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| Ufd1 is a cofactor of gp78 and plays a key role in cholesterol metabolism by regulating the stability of HMG-CoA reductase.
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| Cao J, Wang J, Qi W, Miao HH, Wang J, Ge L, DeBose-Boyd RA, Tang JJ, Li BL, Song BL.
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| Cell Metab 6(2):115-28. 2007
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| 7 | NPLOC4, UFD1
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| Ufd1-Npl4 is a negative regulator of cholera toxin retrotranslocation.
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| McConnell E, Lass A, Wójcik C.
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| Biochem Biophys Res Commun 355(4):1087-90. Epub 2007 Feb 22. 2007
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| 8 | UFD1
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| Expression profiling of adrenocortical neoplasms suggests a molecular signature of malignancy.
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| Velázquez-Fernández D, Laurell C, Geli J, Höög A, Odeberg J, Kjellman M, Lundeberg J, Hamberger B, Nilsson P, Bäckdahl M.
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| Surgery Dec;138(6):1087-94. doi: 10.1016/j.surg.2005.09.031 2005
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| 9 | CDC45, UFD1
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| Characterization of the bi-directional transcriptional control region between the human UFD1L and CDC45L genes.
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| Igaki H, Nakagawa K, Aoki Y, Ohtomo K, Kukimoto I, Kanda T.
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| Biochem Biophys Res Commun 283(3):569-76. 2001
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| 10 | NPLOC4, UFD1
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| Cloning and characterization of the gene encoding human NPL4, a protein interacting with the ubiquitin fusion-degradation protein (UFD1L).
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| Botta A, Tandoi C, Fini G, Calabrese G, Dallapiccola B, Novelli G.
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| Gene 275(1):39-46. 2001
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| 11 | DEL22Q11, UFD1
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| Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11.
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| Wadey R, et al.
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| Am J Hum Genet 65(1):247-249. No abstract available 1999
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| 12 | UFD1
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| Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L).
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| Novelli G, et al.
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| Biochim Biophys Acta 1396 : 158-162. 1998
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| 13 | UFD1
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| UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome.
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| Pizzuti A, et al.
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| Hum Mol Genet 6 : 259-265. 1997
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| 14 | UFD1
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| A proteolytic pathway that recognizes ubiquitin as a degradation signal.
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| Johnson ES, et al.
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| J Biol Chem 270 : 17442-17456. 1995
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