肿瘤易感性基因标志物项目或简称CGEMS是国家肿瘤研究所和哈佛大学的一个合作项目。
The Cancer Genetic Markers of Susceptibility or CGEMS is collaboration between National Cancer Institute and Harvard.
自然地，那些高压力、高(遗传)基因易感性的人患抑郁症的可能性最大。
Naturally, the people with both high stress and strong genetic predispositions are the most likely to have a depressive disorder.
这项研究表明，有些疾病是遗传基因易感性和病毒感染的共同作用引发的。
The research shows that some illnesses may require a combination of genetic predisposition and infection.
由于双胞胎拥有相同的基因，但可能受到的环境因素的影响不同，因此研究双胞胎可以“对基因易感性加以控制。”
Because twins share genes, but may have different exposures to environmental factors, studying twins allows an, "opportunity to control for genetic susceptibility."
而部分原因要归结为——遗传：有30种不同的基因可增高克罗恩病的易感性，但也并非每一个拥有这种基因的人就会得克罗恩病。
And heredity is partly to blame: some 30 different genes enhance susceptibility. But not everyone who has the genes gets Crohn's.
了解基因活性的遗传基础将有助于医学研究从而为个体提供有关他们自身对疾病易感性的信息。
The understanding of the genetic basis of gene activity will help medical research to provide individuals with information about their personal predisposition to disease.
而一个基因的多态性与疾病易感性及疾病表型都存在关联，是该基因直接参与发病的佐证。
A gene polymorphism and susceptibility to disease and disease phenotype correlation there is the gene directly involved in the pathogenesis of corroboration.
实际上基因在每种常见疾病风险也起到重要的作用，从而使我们有可能确定那些具有特异遗传易感性的个体。
Genes also play a major role in risk for virtually every common disease, affording the possibility of identifying persons who have a specific inherited predisposition.
DEFB基因产物是小分子抗菌肽，且拷贝数变化(CNV)可显著影响易感性及炎症反应。
DEFB gene products are small antimicrobial proinflammatory peptides, and copy number variation (CNV) could reasonably influence susceptibility to infection and inflammation.
这种变化将影响基因的活性，包括对疾病的易感性。
The changes can affect gene activity, including susceptibility to diseases.
结论EPHX1基因多态性可能与慢性苯中毒发生危险性相关，而EPHX2基因多态与慢性苯中毒易感性关系需进一步研究。
Conclusions genetic polymorphisms in EPHX1 may be associated with the risk of CBP, and further research is needed for the association between genetic polymorphisms in EPHX2 and susceptibility to CBP.
但是到现在为止，我们还没有发现与这种易感性相关的基因。
But until now, we hadn't identified any genes responsible for that susceptibility.
目的探讨XRCC1基因多态与儿童急性白血病遗传易感性的关系。
Objective To explore the association between genetic polymorphisms of XRCC1 and susceptibility to acute childhood leukemia.
HLA是迄今所知最为复杂的遗传多态性系统，是调控人体特异性免疫应答和决定疾病易感性个体差异的主要基因系统。
HLA is the most polymorphic gene complex of all human genetic systems, play a key role in specific immune response, determine the heterogeneity of individual associated with disease.
结论：HSF2基因多态性可能不是噪声性听力损失的遗传易感性因素。
Conclusion: Genetic polymorphism of the HSF2 gene might not be the susceptible factors of NIHL.
结论S SH技术是一种高效的筛选差异表达基因的方法，本实验结果为深入研究晕船易感性机制提供了重要的线索。
Conclusion SSH is an effective method for screening differentially expressed genes, the results of this study are helpful in exploring the mechanism of seasickness susceptibility.
目的：探讨XRCC1基因单核苷酸多态性与肺癌易感性的关系。
Objective: to investigate the correlation between XRCC1 genetic polymorphisms and susceptibility to human lung cancer.
目的探讨葡萄糖激酶（GCK）基因与妊娠糖尿病（GDM）易感性的关系。
Objective To evaluate the role of glucokinase(GCK) gene in the pathogenesis of gestational diabetes mellitus(GDM) in Chinese.
目的对原发性高血压患者进行HLA -DQA1等位基因的分型，分析高血压病患者的遗传易感性。
Objective To analyse the hereditary susceptibility by genotyping of HLA DQA1 alleles in essential hypertensives.
目的探讨谷胱甘肽s转移酶m 1 (GSTM 1)基因多态性与鼻咽癌(NPC)遗传易感性的关系。
Objective To study the relationship between the glutathione s transferase M1 (GSTM1) gene polymorphism and genetic susceptibility in nasopharyngeal carcinoma (NPC).
本实验旨在研究UGT1A7基因多态与肺癌易感性的关系。
This study was to examine the correlation of polymorphisms of UGT1A7 gene to genetic susceptibility of lung cancer.
致癌物代谢酶基因多态是肿瘤遗传易感性的一个重要方面。
Genetic polymorphism of carcinogen metabolizing enzymes is one of the important aspects of the genetic susceptibility to cancer.
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.
目的探讨谷胱甘肽转硫酶M1（GSTM1）、T1（GSTT1）基因多态性与胃癌遗传易感性的关系。
Objective In order to examine the relationship between glutathiones transferase M1, T1(GSTM1, GSTT1)genetic polymorphism and susceptibility to gastric cancer.
目的探讨N-乙酰转移酶2（NAT2）基因多态性与胃癌易感性的关系。
Objective To determine the association of N-acetyltransferases 2(NAT2)genetic polymorphisms and the susceptibility to stomach cancer.
本研究的目的是鉴定s100a14位点的功能性基因变异体，评价其与ESCC易感性的关系。
In this study, we sought to identify functional genetic variants in the S100A14 locus and assessed their associations with susceptibility to ESCC.
朊蛋白基因是单拷贝基因，高度保守，但在物种间可能存在易感性相关基因。
The prion-protein genes are single-copied and high conservative, but there might be related munity gene existing between animals.
朊蛋白基因是单拷贝基因，高度保守，但在物种间可能存在易感性相关基因。
The prion-protein genes are single-copied and high conservative, but there might be related munity gene existing between animals.
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