Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 20, 2024. (Total: 231613Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 4 (of 4 Records)

Query Trace: Leiomyoma and XRCC1[original query]
DNA repair gene XRCC1 Arg399Gln polymorphism is associated with increased risk of uterine leiomyoma.
Human reproduction (Oxford, England) 2005 Jun 20 (6): 1586-9.
Jeon Yong-Tark, Kim Jae Weon, Park Noh-Hyun, Song Yong-Sang, Kang Soon-Beom, Lee Hyo-P
Genetic polymorphisms of DNA repair gene XRCC1 and risk of uterine leiomyoma.
Molecular and cellular biochemistry 2010 May 338 (1-2): 143-7.
Yang Yang, Zhai Xian Dun, Gao Lin Bo, Li Shi Liu, Wang Zheng, Chen Guo
The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma.
Fertility and sterility 2009 Mar 91 (3): 869-77.
Hsieh Yao-Yuan, Chang Chi-Chen, Bau Da-Tian, Tsai Fuu-Jen, Tsai Chang-Hai, Chen Chih-Pi
Association of XRCC1 Arg399GIn and Tp53 Arg72Pro polymorphisms and increased risk of uterine leiomyoma - A case-control study.
Genetics and molecular biology 2015 Dec 38 (4): 444-9.
Yaghmaei Minoo, Salimi Saeedeh, Namazi Lida, Farajian-Mashhadi Farzan
TOP