Objective To explore the association of LPL gene polymorphisms with CHD.
目的探讨脂蛋白脂酶（LPL）基因多态性与冠心病的关系。
Objective: to investigate the distribution of cytokine gene polymorphisms.
目的探讨细胞因子基因多态性分布。
To investigate the possible relationship of C. albicans gene polymorphisms and its fluconazole-resistance.
探讨耐氟康唑白念珠菌基因多态性与其耐药性是否相关。
CONCLUSION: UGT1A7 gene polymorphisms may increase the genetic susceptibility of lung adenocarcinoma in Chinese.
结论：UGT1A7基因多态可能是中国人肺癌遗传易感性因素。
Objective To determine the distribution of cytochrome P450 1A1(CYP1A1) gene polymorphisms in Guangdong Hans women.
目的探讨广东汉族妇女细胞色素P45 01A1（CYP1A1）基因的多态性分布规律。
Objective: to assess the gene polymorphisms and concentration of vascular endothelial growth factor (VEGF) and the risk for stoke.
目的：探讨血管内皮细胞生长因子(VEGF)基因多态与血浆VEGF浓度以及脑卒中患病风险的关系。
Create a web-enabled script that given a locus link ID returns all the gene polymorphisms, OMIM citations associated with that gene.
建立一个web上使用的、一个地点链结的ID的脚本，可得到所有的基因多态、和那些基因相关的OM IM引文。
Objective:To clerify HLA DQA1 and DQB1 gene polymorphisms in a population of Tu and Sala nationalities from two areas in Qinghai province.
目的：检测青海土族和撒拉族健康个体HLADQA1和DQB1等位基因频率，了解和分析这两个民族的HLA DQA1和DQB1基因多态性。
ConclusionThe ARIX gene polymorphisms, especially the nucleotide change of G153A may be one of genetic risk factors for concomitant exotropia.
结论ARIX基因多态性，尤其是G153 A核苷酸突变可能是共同性外斜视的遗传风险因子。
Vitamin D, vitamin D binding protein gene polymorphisms, race and risk of incident stroke: the Atherosclerosis Risk in Communities (ARIC) study.
维生素D，维生素D结合蛋白基因多态性、种族与卒中发生风险：社区动脉粥样硬化风险研究（ARIC）。
The angiotensin (AGT) gene polymorphisms M235T and T174M are associated with mortality in heart failure (HF) patients, New Zealand researchers report.
新西兰科学家报道：他们发现血管紧张素（AGT）多基因型M235T和T174M与心力衰竭患者的死亡率有密切关系。
Objective To explore the relationship between gene polymorphisms of angiotensin converting enzyme (ACE) in the first wheezy children and wheeze relates.
目的探讨首次喘息患儿血管紧张素转换酶(ace)基因多态性表达及其与喘息再次发生的关系。
Study on the association of lecithin cholesterol acyltransferase gene polymorphisms with the lipid metabolism in coronary atherosclerotic heart disease;
卵磷脂胆固醇脂酰转移酶可促进组织、细胞内胆固醇的清除、维持细胞胆固醇稳态，在磷脂代谢中有重要的作用。
ObjectiveTo investigate the relationship of GSTM1 and GSTT1 gene polymorphisms with the development of noise induced hearing loss (NIHL) in Chinese workers.
目的探讨谷胱甘肽硫转移酶M1和T1（GSTM1和GSTT1）的基因多态性与噪声性听力损失易感性之间的关系。
To study TNF gene polymorphisms in gastric cancer may help discovering the susceptible population earlier, and providing prevention and treatment in gene level.
研究肿瘤坏死因子基因多态性有助于筛选发生胃癌的高危人群，在基因水平上为胃癌的早期防治提供理论基础。
Objective To investigate whether the angiotensinogen AGT(M235T) gene polymorphisms might be implicated in essential hypertension(EH) in Sichuan Hans population.
目的探讨血管紧张素原AGT（M2 35T）基因多态性与中国四川籍汉族人群原发性高血压（EH）的关系。
Recent epidemical study indicates that the incidence of AD in some populations is substantially influenced by the gene polymorphisms of the inflammation mediators.
近来流行病学研究显示炎症介质的基因多态性可以影响阿尔茨海默病在人群中的发病率。
Objective to investigate the relationship between the serum mannose-binding lectin (MBL) levels, gene polymorphisms and recurrent respiratory tract infection (RRTI).
目的探讨血清甘露聚糖结合凝集素(MBL)水平及基因多态性与儿童反复呼吸道感染(RRTI)的关系。
Objective To probe into the angiotensin converting enzyme(ACE)gene polymorphisms and the risk factors in coronary heart disease(CHD) in the Hainan Li and Han nationality.
目的探讨海南黎汉族冠心病（CHD）血管紧张素转换酶（ACE）基因多态性与危险因素的关系。
RESULTS: The genotype distributions and allele frequencies of MMP-9-1562C/T gene polymorphisms were similar in gastric upper gastrointestinal disease and healthy subjects.
结果：MMP-9基因-1562 C/T多态性位点的基因型和等位基因频率在病例组和对照组儿童中的分布无明显差别。
OBJECTIVE To investigate the association between valproic acid (VAP) plasma concentration at steady state (Css) and CYP2C19 gene polymorphisms for better individualized medication.
目的：寻找丙戊酸药物浓度与CYP2C19基因多态性的关系，以便临床根据患者的基因型进行个体化给药。
METHODS HLA-DQB1 gene polymorphisms were typed by sequence specific primer based polymerase chain reaction, in 42 patients with esophageal neoplasm and 136 normal control subjects.
方法运用序列特异性引物聚合酶链反应技术，检测无亲缘关系湖北汉族健康人136例、食管癌组42例患者的HLA-DQB1等位基因。
Methods: Gradient PCR was employed in analysis of aldosterone synthase (CYP11B2) gene polymorphisms, and gel Imaging Technology was used to determine the optimal annealing temperature.
方法：采用梯度PCR对醛固酮合酶基因(CYP11B2)进行扩增，通过凝胶呈像技术判断CYP11 B2基因最佳退火温度。
Methods TLR2 gene polymorphisms were analyzed by DNA sequencing in a small amount of samples. SNPs in TLR2 gene were detected by ligase detection technique in a large amount of samples.
方法在小样本中测序检测TLR2基因中可能存在的基因多态性，再用连接酶特异检测技术在大样本进行SNP分型，并通过统计学方法分析基因多态性与结核病易感性之间相关性。
Objective: To discuss mannose binding lectin (MBL) gene polymorphisms at 54 locus of Han population in Ningxia for further research on relationship of MBL gene mutation and HBV infection.
目的：探讨宁夏汉族人群中甘露糖结合凝集素(MBL)基因54位点多态性，为进一步研究MBL基因突变与乙型肝炎间的关联性提供依据。
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.
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 study the association between the polymorphisms of vitamin D receptor (VDR) gene and autoimmune liver diseases and (AIH) and primary biliary cirrhosis (PBC) in Chinese.
目的探讨维生素D受体（VDR）基因多态性与中国人自身免疫性肝炎（AIH）和原发性胆汁性肝硬化（PBC）发病的相关性。
Objective To investigate the association of cadherin 23 gene (CDH23) polymorphisms with the development of noise induced hearing loss (NIHL).
目的探讨钙粘蛋白23基因(CDH23)多态性与噪声性听力损失之间的关系。
Objective To analyze the relationship between polymorphisms of EDNRB gene and Hubei provincial patients of Han ethnicity with sporadic Hirschsprung disease (sHD).
目的研究中国湖北汉族人群内皮素受体- B (EDNRB)基因的多态性与散发性先天性巨结肠症发病的关系。
Objective To investigate the association of polymorphisms of CDT1 and GMNN gene, two important genes participating in DNA replication, with the risk of sporadic breast cancer.
目的探讨参与DNA复制的两个重要基因CDT1和GMNN基因多态性与我国人群散发乳腺癌的关联。
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