研究人员对1492名平均年龄为48岁的加拿大女性进行了跟踪调查。 她们携带的BRCA1和BRCA2两种乳腺癌易感基因都没有发生突变。
The study tracked 1,492 Canadian women with an average age of 48 who did not have mutations in either of two breast cancer susceptibility genes - BRCA1 and BRCA2.
但是，与因继承了乳腺癌易感基因1和乳腺癌易感基因2中的某些基因突变而增加了5倍风险相比，这种冒险是小得多的。
But it's far smaller than the fivefold increased risk that comes from inheriting certain mutations in the BRCA1 and BRCA2 genes.
结论AGT基因M 235t突变具有明显的遗传倾向，可能是汉族人群易患高血压的候选基因(遗传标志)。
Conclusion M235T variant of AGT gene may be the candidate gene (genetic marker) responsible for the genetic predisposition to EH in Chinese Han population.
结论凝血酶原突变基因20210A可能增加了胃癌的遗传易感性。
Conclusion Prothrombin 20210a gene mutation may increase genetic susceptibility of gastric cancer.
在此次访问的最后部分我想请各位阐述以下如何才能最好的传达一幅引人注目的画面，说明易瑞沙是针对EGFR突变阳性的晚期NSCLC患者的一线治疗方法。
I would now like to focus for the remainder of our discussion on how best to convey a compelling picture for Iressa in advanced NSCLC as 1st line in EGFR mutation positive patients.
结论NAT 2 M位点的突变与胃癌易感性增加有关。
Conclusion NAT2 M1 mutation genotype was likely associated with the susceptibility to stomach cancer.
NOD2基因P 268s突变是中国人克罗恩病的易感基因吗？
Is P268S Mutation of NOD2 Gene the Susceptible Gene in ChinesePatients with Crohn's Disease?
结论：新的高分辨率熔解曲线分析法在检测KRAS基因突变时比直接测序法具有耗时短，易操作的优点，并且检测成本低廉，适合在临床开展。
Conclusions: The new high resolution melting curve analysis is more efficient, more convenient than direct sequencing. Moreover, it is a low-cost test, which is suitable for clinic test.
结论：新的高分辨率熔解曲线分析法在检测KRAS基因突变时比直接测序法具有耗时短，易操作的优点，并且检测成本低廉，适合在临床开展。
Conclusions: The new high resolution melting curve analysis is more efficient, more convenient than direct sequencing. Moreover, it is a low-cost test, which is suitable for clinic test.
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