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Genetic Polymorphisms in XRCC1, CD3EAP, PPP1R13L, XPB, XPC, and XPF and the Risk of Chronic Benzene Poisoning in a Chinese Occupational Population

机译:XRCC1,CD3EAP,PPP1R13L,XPB,XPC和XPF的遗传多态性与中国职业人群慢性苯中毒的风险

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摘要

ObjectivesIndividual variations in the capacity of DNA repair machinery to relieve benzene-induced DNA damage may be the key to developing chronic benzene poisoning (CBP), an increasingly prevalent occupational disease in China. ERCC1 (Excision repair cross complementation group 1) is located on chromosome 19q13.2–3 and participates in the crucial steps of Nucleotide Excision Repair (NER); moreover, we determined that one of its polymorphisms, ERCC1 rs11615, is a biomarker for CBP susceptibility in our previous report. Our aim is to further explore the deeper association between some genetic variations related to ERCC1 polymorphisms and CBP risk.
机译:目的改变DNA修复机制缓解苯诱导的DNA损伤的能力的个体差异可能是发展慢性苯中毒(CBP)的关键,慢性中毒在中国是一种日益普遍的职业病。 ERCC1(切除修复交叉互补组1)位于染色体19q13.2-3上,参与核苷酸切除修复(NER)的关键步骤。此外,我们在先前的报告中确定其多态性之一ERCC1 rs11615是CBP易感性的生物标记。我们的目的是进一步探索与ERCC1多态性有关的某些遗传变异与CBP风险之间的更深联系。

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