نتایج جستجو برای: xrcc3 gene

تعداد نتایج: 1141511  

Journal: :Cancer research 2004
Jiali Han Graham A Colditz Leona D Samson David J Hunter

UV can cause a wide range of DNA lesions. UVA-induced oxidative DNA damage and blocked DNA replication by UVB-induced photoproducts can lead to double-strand breaks (DSBs). We selected 11 haplotype-tagging single nucleotide polymorphisms in three DSB repair genes XRCC2, XRCC3, and LigaseIV and evaluated their associations with skin cancer risk in a nested case-control study within the Nurses' H...

2014
Claudia Bănescu Adrian P. Trifa Smaranda Demian Erzsebeth Benedek Lazar Delia Dima Carmen Duicu Minodora Dobreanu

The genetic polymorphisms of X-ray repair cross complementing group 1 (XRCC1), X-ray repair cross complementing group 3 (XRCC3), and xeroderma pigmentosum complementation group D (XPD) repair genes may lead to genetic instability and leukemogenesis. The purpose of the study was to evaluate the association between XRCC1 Arg399Gln, Arg280His and Arg194Trp, XRCC3 Thr241Met, and XPD Lys751Gln polym...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2003
Tasha R Smith Edward A Levine Nancy D Perrier Mark Steven Miller Rita I Freimanis Kurt Lohman L Douglas Case Jianfeng Xu Harvey W Mohrenweiser Jennifer J Hu

Mammalian cells are constantly exposed to genotoxic agents from both endogenous and exogenous sources. Genetic variability in DNA repair contributes to deficient repair and breast cancer risk. Using samples collected in an ongoing, clinic-based, case-control study (253 cases and 268 controls), we tested whether breast cancer risk is associated with four amino acid substitution variants in three...

2013
Guohua Huang Shaoxi Cai Wei Wang Qing Zhang Aihua Liu

Many studies have reported the association of X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, Arg194Trp, Arg280His, -77T>C, and X-ray repair cross-complementing group 3 (XRCC3) T241M polymorphisms with lung cancer risk, but the results remained controversial. Hence, we performed a meta-analysis to investigate the association between lung cancer risk and XRCC1 Arg399Gln (14,156 cases...

2011
Jessica Clague Greg Wilhoite Aaron Adamson Adam Bailis Jeffrey N. Weitzel Susan L. Neuhausen

BRCA1 and BRCA2 are the most well-known breast cancer susceptibility genes. Additional genes involved in DNA repair have been identified as predisposing to breast cancer. One such gene, RAD51C, is essential for homologous recombination repair. Several likely pathogenic RAD51C mutations have been identified in BRCA1- and BRCA2-negative breast and ovarian cancer families. We performed complete se...

Journal: :The EMBO journal 2006
Amélie Rodrigue Matthieu Lafrance Marie-Christine Gauthier Darin McDonald Michael Hendzel Stephen C West Maria Jasin Jean-Yves Masson

DNA repair by homologous recombination is essential for preserving genomic integrity. The RAD51 paralogs (RAD51B, RAD51C, RAD51D, XRCC2 and XRCC3) play important roles in this process. In this study, we show that human RAD51 interacts with RAD51C-XRCC3 or RAD51B-C-D-XRCC2. In addition to being critical for RAD51 focus formation, RAD51C localizes to DNA damage sites. Inhibition of RAD51C results...

Journal: :Nucleic Acids Research 2005
Yasukazu Yonetani Helfrid Hochegger Eiichiro Sonoda Sayoko Shinya Hideki Yoshikawa Shunichi Takeda Mistuyoshi Yamazoe

Metazoan Rad51 plays a central role in homologous DNA recombination, and its activity is controlled by a number of Rad51 cofactors. These include five Rad51 paralogs, Rad51B, Rad51C, Rad51D, XRCC2 and XRCC3. We previously hypothesized that all five paralogs participate collaboratively in repair. However, this idea was challenged by the biochemical identification of two independent complexes com...

Journal: :Environmental Health Perspectives 2003
William W Au Salama A Salama Carlos H Sierra-Torres

A major barrier to understanding the role of polymorphic DNA repair genes for environmental cancer is that the functions of variant genotypes are largely unknown. Using our cytogenetic challenge assays, we conducted an investigation to address the deficiency. Using X-rays or ultraviolet (UV) light, we irradiated blood lymphocytes from 80 nonsmoking donors to challenge the cells to repair the in...

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