PubMed for id: 2660

Year	Number of Results
1996	1
1999	3
2000	3
2002	4
2003	4
2004	1
2005	13
2006	13
2007	8
2008	15
2009	8
2010	17
2011	15
2012	14
2013	9
2024	0

1

Cullin 4B is a novel prognostic marker that correlates with colon cancer progression and pathogenesis.

Jiang T, Tang HM, Wu ZH, Chen J, Lu S, Zhou CZ, Yan DW, Peng ZH. Jiang T, et al. Med Oncol. 2013;30(2):534. doi: 10.1007/s12032-013-0534-7. Epub 2013 May 7. Med Oncol. 2013. PMID: 23649548

2

Cul4B regulates neural progenitor cell growth.

Liu HC, Enikolopov G, Chen Y. Liu HC, et al. BMC Neurosci. 2012 Sep 19;13:112. doi: 10.1186/1471-2202-13-112. BMC Neurosci. 2012. PMID: 22992378 Free PMC article.

3

Rescue of the genetically engineered Cul4b mutant mouse as a potential model for human X-linked mental retardation.

Chen CY, Tsai MS, Lin CY, Yu IS, Chen YT, Lin SR, Juan LW, Chen YT, Hsu HM, Lee LJ, Lin SW. Chen CY, et al. Hum Mol Genet. 2012 Oct 1;21(19):4270-85. doi: 10.1093/hmg/dds261. Epub 2012 Jul 3. Hum Mol Genet. 2012. PMID: 22763239

4

CUL4B ubiquitin ligase in mouse development: a model for human X-linked mental retardation syndrome?

Zhao Y, Sun Y. Zhao Y, et al. Cell Res. 2012 Aug;22(8):1224-6. doi: 10.1038/cr.2012.79. Epub 2012 May 15. Cell Res. 2012. PMID: 22584258 Free PMC article.

5

Deletion of CUL4B leads to concordant phenotype in a monozygotic twin pair.

Ravn K, Lindquist SG, Nielsen K, Dahm TL, Tümer Z. Ravn K, et al. Clin Genet. 2012 Sep;82(3):292-4. doi: 10.1111/j.1399-0004.2011.01839.x. Epub 2012 Jan 11. Clin Genet. 2012. PMID: 22182342 No abstract available.

6

CUL4B-deficiency in humans: understanding the clinical consequences of impaired Cullin 4-RING E3 ubiquitin ligase function.

Kerzendorfer C, Hart L, Colnaghi R, Carpenter G, Alcantara D, Outwin E, Carr AM, O'Driscoll M. Kerzendorfer C, et al. Mech Ageing Dev. 2011 Aug;132(8-9):366-73. doi: 10.1016/j.mad.2011.02.003. Epub 2011 Feb 23. Mech Ageing Dev. 2011. PMID: 21352845 Review.

7

Cullin 4-ring finger-ligase plays a key role in the control of endoreplication cycles in Arabidopsis trichomes.

Roodbarkelari F, Bramsiepe J, Weinl C, Marquardt S, Novák B, Jakoby MJ, Lechner E, Genschik P, Schnittger A. Roodbarkelari F, et al. Proc Natl Acad Sci U S A. 2010 Aug 24;107(34):15275-80. doi: 10.1073/pnas.1006941107. Epub 2010 Aug 9. Proc Natl Acad Sci U S A. 2010. PMID: 20696906 Free PMC article.

8

A novel nonsense mutation in CUL4B gene in three brothers with X-linked mental retardation syndrome.

Badura-Stronka M, Jamsheer A, Materna-Kiryluk A, Sowińska A, Kiryluk K, Budny B, Latos-Bieleńska A. Badura-Stronka M, et al. Clin Genet. 2010 Feb;77(2):141-4. doi: 10.1111/j.1399-0004.2009.01331.x. Epub 2009 Dec 10. Clin Genet. 2010. PMID: 20002452

9

Mutation in CUL4B, which encodes a member of cullin-RING ubiquitin ligase complex, causes X-linked mental retardation.

Zou Y, Liu Q, Chen B, Zhang X, Guo C, Zhou H, Li J, Gao G, Guo Y, Yan C, Wei J, Shao C, Gong Y. Zou Y, et al. Am J Hum Genet. 2007 Mar;80(3):561-6. doi: 10.1086/512489. Epub 2007 Jan 25. Am J Hum Genet. 2007. PMID: 17273978 Free PMC article.

10

Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.

Tarpey PS, Raymond FL, O'Meara S, Edkins S, Teague J, Butler A, Dicks E, Stevens C, Tofts C, Avis T, Barthorpe S, Buck G, Cole J, Gray K, Halliday K, Harrison R, Hills K, Jenkinson A, Jones D, Menzies A, Mironenko T, Perry J, Raine K, Richardson D, Shepherd R, Small A, Varian J, West S, Widaa S, Mallya U, Moon J, Luo Y, Holder S, Smithson SF, Hurst JA, Clayton-Smith J, Kerr B, Boyle J, Shaw M, Vandeleur L, Rodriguez J, Slaugh R, Easton DF, Wooster R, Bobrow M, Srivastava AK, Stevenson RE, Schwartz CE, Turner G, Gecz J, Futreal PA, Stratton MR, Partington M. Tarpey PS, et al. Am J Hum Genet. 2007 Feb;80(2):345-52. doi: 10.1086/511134. Epub 2007 Jan 4. Am J Hum Genet. 2007. PMID: 17236139 Free PMC article.

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