PubMed (OMIM) for id: 7314

Year	Number of Results
1985	1
1987	2
1988	1
1989	2
1990	1
1998	1
1999	1
2002	1
2004	1
2006	1
2007	1
2008	1
2009	1
2010	1
2024	0

1

Glutamine deamidation and dysfunction of ubiquitin/NEDD8 induced by a bacterial effector family.

Cui J, Yao Q, Li S, Ding X, Lu Q, Mao H, Liu L, Zheng N, Chen S, Shao F. Cui J, et al. Science. 2010 Sep 3;329(5996):1215-8. doi: 10.1126/science.1193844. Epub 2010 Aug 5. Science. 2010. PMID: 20688984 Free PMC article.

2

Disease-associated mutant ubiquitin causes proteasomal impairment and enhances the toxicity of protein aggregates.

Tank EM, True HL. Tank EM, et al. PLoS Genet. 2009 Feb;5(2):e1000382. doi: 10.1371/journal.pgen.1000382. Epub 2009 Feb 13. PLoS Genet. 2009. PMID: 19214209 Free PMC article.

3

Hypothalamic neurodegeneration and adult-onset obesity in mice lacking the Ubb polyubiquitin gene.

Ryu KY, Garza JC, Lu XY, Barsh GS, Kopito RR. Ryu KY, et al. Proc Natl Acad Sci U S A. 2008 Mar 11;105(10):4016-21. doi: 10.1073/pnas.0800096105. Epub 2008 Feb 25. Proc Natl Acad Sci U S A. 2008. PMID: 18299572 Free PMC article.

4

Genotype phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletions.

Andrieux J, Villenet C, Quief S, Lignon S, Geffroy S, Roumier C, de Leersnyder H, de Blois MC, Manouvrier S, Delobel B, Benzacken B, Bitoun P, Attie-Bitach T, Thomas S, Lyonnet S, Vekemans M, Kerckaert JP. Andrieux J, et al. J Med Genet. 2007 Aug;44(8):537-40. doi: 10.1136/jmg.2006.048736. Epub 2007 Apr 27. J Med Genet. 2007. PMID: 17468296 Free PMC article.

5

Frameshift proteins in autosomal dominant forms of Alzheimer disease and other tauopathies.

van Leeuwen FW, van Tijn P, Sonnemans MA, Hobo B, Mann DM, Van Broeckhoven C, Kumar-Singh S, Cras P, Leuba G, Savioz A, Maat-Schieman ML, Yamaguchi H, Kros JM, Kamphorst W, Hol EM, de Vos RA, Fischer DF. van Leeuwen FW, et al. Neurology. 2006 Jan 24;66(2 Suppl 1):S86-92. doi: 10.1212/01.wnl.0000193882.46003.6d. Neurology. 2006. PMID: 16432153

6

Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis muscle fibers.

Fratta P, Engel WK, Van Leeuwen FW, Hol EM, Vattemi G, Askanas V. Fratta P, et al. Neurology. 2004 Sep 28;63(6):1114-7. doi: 10.1212/01.wnl.0000138574.56908.5d. Neurology. 2004. PMID: 15452314

7

Emerging roles of ubiquitin in transcription regulation.

Conaway RC, Brower CS, Conaway JW. Conaway RC, et al. Science. 2002 May 17;296(5571):1254-8. doi: 10.1126/science.1067466. Science. 2002. PMID: 12016299 Review.

8

Ubiquitin tag for sperm mitochondria.

Sutovsky P, Moreno RD, Ramalho-Santos J, Dominko T, Simerly C, Schatten G. Sutovsky P, et al. Nature. 1999 Nov 25;402(6760):371-2. doi: 10.1038/46466. Nature. 1999. PMID: 10586873 No abstract available.

9

Frameshift mutants of beta amyloid precursor protein and ubiquitin-B in Alzheimer's and Down patients.

van Leeuwen FW, de Kleijn DP, van den Hurk HH, Neubauer A, Sonnemans MA, Sluijs JA, Köycü S, Ramdjielal RD, Salehi A, Martens GJ, Grosveld FG, Peter J, Burbach H, Hol EM. van Leeuwen FW, et al. Science. 1998 Jan 9;279(5348):242-7. doi: 10.1126/science.279.5348.242. Science. 1998. PMID: 9422699

10

The human ubiquitin gene family: structure of a gene and pseudogenes from the Ub B subfamily.

Baker RT, Board PG. Baker RT, et al. Nucleic Acids Res. 1987 Jan 26;15(2):443-63. doi: 10.1093/nar/15.2.443. Nucleic Acids Res. 1987. PMID: 3029682 Free PMC article.

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