检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]新乡医学院第一附属医院,河南卫辉453100
出 处:《医学信息(中旬刊)》2010年第3期470-472,共3页Medical Information Operations Sciences Fascicule
摘 要:目的:研究XRCC1单核苷酸多态性与豫北地区食管癌风险性的关系。方法:以PCR-RFL方法分析了食管癌病例(n=202)和按性别、年龄频数对照的正常对照者(n=317)XRCC1多态,并比较不同基因型与食管癌发生风险的关系。结果:Gln399Gln基因型在病例组和对照组中的频率分别为12.9%和6.3%,差异性显著(OR=2.117,95%CI=1.126~3.981;P<0.05)。结论:XRCC1Arg399Gln多态可能与豫北地区食管癌风险性有关。Objective : The current study was designed to investigate the polymorphisms of XRCC1 in Northern HeNan esophageal squamous cell carcinoma ( ESCC ) and test the hypothesis which these genetic variation may have impact on the risk of ESCC. Methods: A case - control study of 202 ESCC patients and 317 control subjects( matched for age,sex )was conducted to investigate the role of XRCC1 in ESCC. Genotyping was performed using PCRRFLP. Results:The Gln399Gln genotype frequency in ESCC patients is higher than that in controls( 12.9% &6. 3 % ), have significant difference between cases and controls ( OR = 2.117,95 % CI =1.126 - 3.981 ; P 〈 0.05 ). Conclusion : the polymerphisms in XRCC1 Arg399Gln may have significant impact on the risk of ESCC.
分 类 号:R394[医药卫生—医学遗传学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.30