148 related articles for article (PubMed ID: 22037268)
1. Single nucleotide polymorphism WRN Leu1074Phe is associated with prostate cancer susceptibility in Chinese subjects.
Wang L; Kaku H; Huang P; Xu K; Yang K; Zhang J; Li M; Xie L; Wang X; Sakai A; Watanabe M; Nasu Y; Shimizu K; Kumon H; Na Y
Acta Med Okayama; 2011 Oct; 65(5):315-23. PubMed ID: 22037268
[TBL] [Abstract][Full Text] [Related]
2. A polymorphism in Werner syndrome gene is associated with breast cancer susceptibility in Chinese women.
Wang Z; Xu Y; Tang J; Ma H; Qin J; Lu C; Wang X; Hu Z; Wang X; Shen H
Breast Cancer Res Treat; 2009 Nov; 118(1):169-75. PubMed ID: 19205873
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 22173703
[TBL] [Abstract][Full Text] [Related]
4. A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population.
Zhou H; Mori S; Tanaka M; Sawabe M; Arai T; Muramatsu M; Mieno MN; Shinkai S; Yamada Y; Miyachi M; Murakami H; Sanada K; Ito H
J Bone Miner Metab; 2015 Nov; 33(6):694-700. PubMed ID: 25637295
[TBL] [Abstract][Full Text] [Related]
5. Association of the rs1346044 Polymorphism of the Werner Syndrome Gene RECQL2 with Increased Risk and Premature Onset of Breast Cancer.
Zins K; Frech B; Taubenschuss E; Schneeberger C; Abraham D; Schreiber M
Int J Mol Sci; 2015 Dec; 16(12):29643-53. PubMed ID: 26690424
[TBL] [Abstract][Full Text] [Related]
6. 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; 54(2):1201-7. PubMed ID: 23322570
[TBL] [Abstract][Full Text] [Related]
7. Polymorphisms of the WRN gene and DNA damage of peripheral lymphocytes in age-related cataract in a Han Chinese population.
Jiang S; Hu N; Zhou J; Zhang J; Gao R; Hu J; Guan H
Age (Dordr); 2013 Dec; 35(6):2435-44. PubMed ID: 23334603
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 19945966
[TBL] [Abstract][Full Text] [Related]
9. Association Between WRN Cys1367Arg (T>C) and Cancer Risk: A Meta-analysis.
Wang B; Li G; Sun F; Dong N; Sun Z; Jiang D
Technol Cancer Res Treat; 2016 Feb; 15(1):20-7. PubMed ID: 25468760
[TBL] [Abstract][Full Text] [Related]
10. The Werner's Syndrome RecQ helicase/exonuclease at the nexus of cancer and aging.
Chun SG; Shaeffer DS; Bryant-Greenwood PK
Hawaii Med J; 2011 Mar; 70(3):52-5. PubMed ID: 21365542
[TBL] [Abstract][Full Text] [Related]
11. Werner syndrome as a hereditary risk factor for exocrine pancreatic cancer: potential role of WRN in pancreatic tumorigenesis and patient-tailored therapy.
Chun SG; Yee NS
Cancer Biol Ther; 2010 Sep; 10(5):430-7. PubMed ID: 20657174
[TBL] [Abstract][Full Text] [Related]
12. Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseases.
Lebel M; Monnat RJ
Ageing Res Rev; 2018 Jan; 41():82-97. PubMed ID: 29146545
[TBL] [Abstract][Full Text] [Related]
13. Lack of association of the WRN C1367T polymorphism with senile cataract in the Israeli population.
Ehrenberg M; Dratviman-Storobinsky O; Avraham-Lubin BR; Goldenberg-Cohen N
Mol Vis; 2010 Aug; 16():1771-5. PubMed ID: 20808731
[TBL] [Abstract][Full Text] [Related]
14. WRN helicase defective in the premature aging disorder Werner syndrome genetically interacts with topoisomerase 3 and restores the top3 slow growth phenotype of sgs1 top3.
Aggarwal M; Brosh RM
Aging (Albany NY); 2009 Feb; 1(2):219-33. PubMed ID: 20157511
[TBL] [Abstract][Full Text] [Related]
15. Genetic variation in the premature aging gene WRN: a case-control study on breast cancer susceptibility.
Ding SL; Yu JC; Chen ST; Hsu GC; Shen CY
Cancer Epidemiol Biomarkers Prev; 2007 Feb; 16(2):263-9. PubMed ID: 17301258
[TBL] [Abstract][Full Text] [Related]
16. WRN polymorphisms affect expression levels of plasminogen activator inhibitor type 1 in cultured fibroblasts.
Castro E; Oviedo-Rodríguez V; Angel-Chávez LI
BMC Cardiovasc Disord; 2008 Feb; 8():5. PubMed ID: 18312663
[TBL] [Abstract][Full Text] [Related]
17. A novel mutation of the WRN gene in a Chinese patient with Werner syndrome.
Zhao N; Hao F; Qu T; Zuo YG; Wang BX
Clin Exp Dermatol; 2008 May; 33(3):278-81. PubMed ID: 18205852
[TBL] [Abstract][Full Text] [Related]
18. Copy number variations of DNA repair genes and the age-related cataract: Jiangsu Eye Study.
Jiang J; Zhou J; Yao Y; Zhu R; Liang C; Jiang S; Yang M; Lu Y; Xing Q; Guan H
Invest Ophthalmol Vis Sci; 2013 Feb; 54(2):932-8. PubMed ID: 23329665
[TBL] [Abstract][Full Text] [Related]
19. [The role of Werner's syndrome gene in the genetic susceptibility to the type 2 diabetes in Chinese population].
Luo Y; Ji L; Han X
Zhonghua Yi Xue Za Zhi; 2000 May; 80(5):360-1. PubMed ID: 11798788
[TBL] [Abstract][Full Text] [Related]
20. Influence of a single-nucleotide polymorphism of the DNA mismatch repair-related gene exonuclease-1 (rs9350) with prostate cancer risk among Chinese people.
Zhang Y; Li P; Xu A; Chen J; Ma C; Sakai A; Xie L; Wang L; Na Y; Kaku H; Xu P; Jin Z; Li X; Guo K; Shen H; Zheng S; Kumon H; Liu C; Huang P
Tumour Biol; 2016 May; 37(5):6653-9. PubMed ID: 26646562
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]