他们发现三个单核苷酸多态性和妄想症有很大的关联，而且这三个单核苷酸多态性都位于Neuregulin3基因上。
They found three SNPs strongly associated with delusions, and all three SNPs are located in the neuregulin 3 gene.
有些单核苷酸多态性会出现于基因体本身，而其它一些则出现于基因体之间的脱氧核糖核酸之中。
Some SNPs occur in genes themselves. Others are found in the DNA between genes.
Quintana - Murci博士的数据来自人类基因组单体型计划图，旨在对单核苷酸多态性，即SNPs进行归类。
Dr Quintana-Murci's data were drawn from a project called HapMap, which catalogues what are known as single-nucleotide polymorphisms, or SNPs.
当前的基因检测分析了大约600,000个SNP(单核苷酸多态性)，只是整个基因组的千分之一。
Current genetic tests analyze about 600,000 SNPs (single nucleotide polymorphisms) or 0.1 percent of the entire genome.
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.
然而，当期《自然-遗传学》杂志报告sle与TNFSF4基因多态性有关。
However, the current Nature Genetics report associates SLE with a polymorphism at gene TNFSF4.
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.
直至最近，AD最重要的遗传易感基因，载脂蛋白e- e4的等位基因才被发现，但是其他基因遗传多态性也被发现。
Until recently, the most important genetic risk factor for AD was the presence of the allele E4 of the apolipoprotein e, but recently other genetic polymorphisms of risks have been identified.
单核苷酸多态性与变异基因拷贝数分别与近900和240个基因的活性改变有关。
SNP and CNV variation correlated with altered activity in almost 900 and 240 genes, respectively.
我们希望这种方法可以使我们了解在基因多态性中基因结构和基因调节的平衡。
We expect that this approach will get us closer to understanding the balance between gene content and gene regulation in the question of human-chimp diversity.
结论亚甲基四氢叶酸还原酶基因C677T基因多态性可能是我国大肠癌的遗传易感因素。
Conclusion These findings demonstrated that the genetic variation of MTHFR C677T should be a genetic susceptibility factor for colorectal cancer in a Chinese population.
目前，该技术已用于基因表达谱分析、新基因发现、基因突变、基因多态性分析、药物筛选和基因测序及疾病的诊断。
By the mean time, the technique have reported in the gene expression analysis, new gene discovery, gene mutation detection, SNP analysis, DNA re-sequence and diagnosis.
目的探讨HLADRB1基因多态性与肺结核（PTB）的遗传关联性及其与临床表现的关系。
Objective To assess the association of HLA DRB1 genes with pulmonary tuberculosis (PTB) and the correlation between HLA DRB1 alleles and clinical manifestations of patients with PTB.
目的探讨细胞因子基因多态性分布。
Objective: to investigate the distribution of cytokine gene polymorphisms.
表明载脂蛋白e基因多态性对绝经期妇女血脂的代谢有一定的影响。
Results showed that ApoE gene polymorphism have some effect on lipid metabolism in peripheral blood of postmenopausal women.
目的研究肾素-血管紧张素转换酶(ace)基因多态性与脑梗死的关系。
Objective To investigate the relationship between the polymorphism of the renin angiotensin converting enzyme (ACE) gene and cerebral infarction.
载脂蛋白基因多态性与血脂异常的关系备受人们关注。
The relationship of apolipoprotein gene and polymorphisms to dyslipidemia got people's highly attention.
肝脏药物转运体1B1基因多态性与他汀类药物致肌病有关；
The polymorphisms of liver drug transporter 1B1 genes are associated with myopathy induced by stating.
目的探讨血管紧张素转化酶(ace)基因缺失多态性与中国人脑梗死、高血压性脑出血的关系。
Objective To investigate the relationship between the angiotensin converting enzyme (ACE) gene deletion polymorphism and cerebral infarction, hypertensive cerebral hemorrhage in Chinese.
目的探讨脂蛋白脂酶（LPL）基因多态性与冠心病的关系。
Objective To explore the association of LPL gene polymorphisms with CHD.
MG患者的VDR基因多态性仍需进一步研究。
VDR gene polymorphism of MG patients still need for further study.
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.
对筛查出的多态性基因进行测序分析。
主要应用于新基因发现、基因表达分析、基因突变及多态性分析、基因测序等。
The main application is in discovering new genes, analysis of gene expression, gene mutation, polymorphism and genetic sequence test.
目的探讨抑郁症与G72基因多态性的关系，以及是否有混合家族史的抑郁症其g72基因多态性有无区别。
Objective to investigate the association between G72 gene polymorphisms and depression, and to probe the difference of G72 gene polymorphisms between depression with and without mixed family history.
结论：广西南宁地区多人群存在对氧磷酶2基因C311S多态性，该基因多态性可能存在一定的地域性差异。
CONCLUSION: Paraoxonase 2 gene C311S polymorphism exists in the population of Guangxi Nanning area, and this gene polymorphism may have certain differences in different areas.
了解不同种族人群间血管紧张素转换酶基因多态性的遗传特点，是研究血管紧张素转换酶基因I/D多态性与疾病相关性的基础和前提。
To know genetic features of ACE gene polymorphism of individuals of different nationalities is the basis and prerequisite to study the correlation of ACE gene I/D polymorphism with diseases.
了解不同种族人群间血管紧张素转换酶基因多态性的遗传特点，是研究血管紧张素转换酶基因I/D多态性与疾病相关性的基础和前提。
To know genetic features of ACE gene polymorphism of individuals of different nationalities is the basis and prerequisite to study the correlation of ACE gene I/D polymorphism with diseases.
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