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Items: 1 to 20 of 86

1.

Polymorphisms in genes involved in DNA double-strand break repair pathway and susceptibility to benzene-induced hematotoxicity.

Shen M, Lan Q, Zhang L, Chanock S, Li G, Vermeulen R, Rappaport SM, Guo W, Hayes RB, Linet M, Yin S, Yeager M, Welch R, Forrest MS, Rothman N, Smith MT.

Carcinogenesis. 2006 Oct;27(10):2083-9. Epub 2006 May 25.

PMID:
16728435
2.

Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity.

Lan Q, Zhang L, Shen M, Jo WJ, Vermeulen R, Li G, Vulpe C, Lim S, Ren X, Rappaport SM, Berndt SI, Yeager M, Yuenger J, Hayes RB, Linet M, Yin S, Chanock S, Smith MT, Rothman N.

Carcinogenesis. 2009 Jan;30(1):50-8. doi: 10.1093/carcin/bgn249. Epub 2008 Oct 31.

3.

The associations between single nucleotide polymorphisms of DNA repair genes, DNA damage, and age-related cataract: Jiangsu Eye Study.

Su S, Yao Y, Zhu R, Liang C, Jiang S, Hu N, Zhou J, Yang M, Xing Q, Guan H.

Invest Ophthalmol Vis Sci. 2013 Feb 1;54(2):1201-7. doi: 10.1167/iovs.12-10940.

PMID:
23322570
4.

Microsomal epoxide hydrolase (EPHX1) polymorphisms are associated with aberrant promoter methylation of ERCC3 and hematotoxicity in benzene-exposed workers.

Xing C, Chen Q, Li G, Zhang L, Zheng M, Zou Z, Hou L, Wang QF, Liu X, Guo X.

Environ Mol Mutagen. 2013 Jul;54(6):397-405. doi: 10.1002/em.21786. Epub 2013 Jun 25.

PMID:
23797950
5.

Depletion of WRN enhances DNA damage in HeLa cells exposed to the benzene metabolite, hydroquinone.

Galván N, Lim S, Zmugg S, Smith MT, Zhang L.

Mutat Res. 2008 Jan 8;649(1-2):54-61. Epub 2007 Aug 7.

6.

Esophageal cancer risk is associated with polymorphisms of DNA repair genes MSH2 and WRN in Chinese population.

Li T, Suo Q, He D, Du W, Yang M, Fan X, Liu J.

J Thorac Oncol. 2012 Feb;7(2):448-52. doi: 10.1097/JTO.0b013e31823c487a.

7.

Polymorphisms in cytokine and cellular adhesion molecule genes and susceptibility to hematotoxicity among workers exposed to benzene.

Lan Q, Zhang L, Shen M, Smith MT, Li G, Vermeulen R, Rappaport SM, Forrest MS, Hayes RB, Linet M, Dosemeci M, Alter BP, Weinberg RS, Yin S, Yeager M, Welch R, Waidyanatha S, Kim S, Chanock S, Rothman N.

Cancer Res. 2005 Oct 15;65(20):9574-81.

8.

Werner syndrome protein, WRN, protects cells from DNA damage induced by the benzene metabolite hydroquinone.

Ren X, Lim S, Smith MT, Zhang L.

Toxicol Sci. 2009 Feb;107(2):367-75. doi: 10.1093/toxsci/kfn254. Epub 2008 Dec 8.

9.

Polymorphisms in genes involved in innate immunity and susceptibility to benzene-induced hematotoxicity.

Shen M, Zhang L, Lee KM, Vermeulen R, Hosgood HD, Li G, Yin S, Rothman N, Chanock S, Smith MT, Lan Q.

Exp Mol Med. 2011 Jun 30;43(6):374-8.

10.

Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity.

Hosgood HD 3rd, Zhang L, Shen M, Berndt SI, Vermeulen R, Li G, Yin S, Yeager M, Yuenger J, Rothman N, Chanock S, Smith M, Lan Q.

Occup Environ Med. 2009 Dec;66(12):848-53. doi: 10.1136/oem.2008.044024. Epub 2009 Sep 22.

11.

Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma.

Khayat AS, Lobo Gatti L, Moura Lima E, de Assumpção PP, Nascimento Motta FJ, Harada ML, Casartelli C, Marques Payão SL, Cardoso Smith MA, Burbano RR.

Clin Exp Med. 2005 Dec;5(4):161-8.

PMID:
16362795
12.

Colorectal cancer and polymorphisms in DNA repair genes WRN, RMI1 and BLM.

Frank B, Hoffmeister M, Klopp N, Illig T, Chang-Claude J, Brenner H.

Carcinogenesis. 2010 Mar;31(3):442-5. doi: 10.1093/carcin/bgp293. Epub 2009 Nov 27.

PMID:
19945966
13.

Accumulation of Werner protein at DNA double-strand breaks in human cells.

Lan L, Nakajima S, Komatsu K, Nussenzweig A, Shimamoto A, Oshima J, Yasui A.

J Cell Sci. 2005 Sep 15;118(Pt 18):4153-62. Epub 2005 Sep 1.

14.

Genetic polymorphisms of DNA double-strand break repair pathway genes and glioma susceptibility.

Zhao P, Zou P, Zhao L, Yan W, Kang C, Jiang T, You Y.

BMC Cancer. 2013 May 10;13:234. doi: 10.1186/1471-2407-13-234.

15.

Genetic Variants That Predispose to DNA Double-Strand Breaks in Lymphocytes From a Subset of Patients With Familial Colorectal Carcinomas.

Arora S, Yan H, Cho I, Fan HY, Luo B, Gai X, Bodian DL, Vockley JG, Zhou Y, Handorf EA, Egleston BL, Andrake MD, Nicolas E, Serebriiskii IG, Yen TJ, Hall MJ, Golemis EA, Enders GH.

Gastroenterology. 2015 Dec;149(7):1872-1883.e9. doi: 10.1053/j.gastro.2015.08.052. Epub 2015 Sep 5.

16.

Genetic polymorphisms in XRCC1, APE1, ADPRT, XRCC2, and XRCC3 and risk of chronic benzene poisoning in a Chinese occupational population.

Zhang Z, Wan J, Jin X, Jin T, Shen H, Lu D, Xia Z.

Cancer Epidemiol Biomarkers Prev. 2005 Nov;14(11 Pt 1):2614-9.

17.

BCR/ABL stimulates WRN to promote survival and genomic instability.

Slupianek A, Poplawski T, Jozwiakowski SK, Cramer K, Pytel D, Stoczynska E, Nowicki MO, Blasiak J, Skorski T.

Cancer Res. 2011 Feb 1;71(3):842-51. doi: 10.1158/0008-5472.CAN-10-1066. Epub 2010 Dec 1.

18.

Polymorphisms in DNA repair genes, hair dye use, and the risk of non-Hodgkin lymphoma.

Guo H, Bassig BA, Lan Q, Zhu Y, Zhang Y, Holford TR, Leaderer B, Boyle P, Qin Q, Zhu C, Li N, Rothman N, Zheng T.

Cancer Causes Control. 2014 Oct;25(10):1261-70. doi: 10.1007/s10552-014-0423-1. Epub 2014 Sep 2.

19.

Distinct functions for WRN and TP53 in a shared pathway of cellular response to 1-beta-D-arabinofuranosylcytosine and bleomycin.

Poot M, Jin X, Hill JP, Gollahon KA, Rabinovitch PS.

Exp Cell Res. 2004 Jun 10;296(2):327-36.

PMID:
15149862
20.

Breast cancer risk associated with genotypic polymorphism of the nonhomologous end-joining genes: a multigenic study on cancer susceptibility.

Fu YP, Yu JC, Cheng TC, Lou MA, Hsu GC, Wu CY, Chen ST, Wu HS, Wu PE, Shen CY.

Cancer Res. 2003 May 15;63(10):2440-6.

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