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