VNTR

Paternity testing by analysis of three VNTR genetic markers

VNTR遗传标记的亲权鉴定研究

Distribution of α 1 immunoglobulin gene VNTR polymorphisms in Chinese

我国汉族人群α1基因数目可变串联重复序列分布特征的研究

A Novel VNTR Polymorphisms of Human Rennin Gene and Essential Hypertension

肾素基因新的VNTR多态性与原发性高血压

Relationship between VNTR polymorphism of platelet glycoprotein ⅰ b gene and cerebral infarction

血小板膜糖蛋白GPⅠb基因VNTR多态性与脑梗死的关系

Detection of loss of heterozygosity of p53 gene by VNTR polymorphism analysis in human leukemia

以VNTR作为多态标记检测人类白血病p53基因杂合子性缺失

The VNTR regions are informative genetic markers for linkage mapping and individual identification .

VNTR区是连锁分析和个体鉴别的有效遗传标志。

Corpses identification using STR and VNTR loci system ; Probe Station Placement for Multiple Faults Localization

联合应用多个DNA位点进行尸源鉴定支持多故障定位的探测站点部署方法

Application of Multiple Loci VNTR in Survival Assay of Engraftment of Transplanted Allogeneic Bone Marrow

多位点VNTR用于异基因骨髓移植植入存活检定研究

Polymorphism analysis of the C ha RAS 3 ′ VNTR locus of Chinese Han population with AFLP page

中国汉族群体c-Ha-ras基因3′端-VNTR位点遗传多态性的初步研究

Genotyping of Mycobacterium tuberculosis in Jilin Province with VNTR

应用VNTR技术对吉林省结核分枝杆菌基因分型的研究

The action of detecting dynamic chimerism status by PCR - VNTR after CML allogeneic peripheral blood stem cell transplantation

用PCR-VNTR法检测CML异基因外周血干细胞移植后动态嵌合状态的作用

Comparative study of APOB gene 3 ′ VNTR polymorphisms between natural longevity and controls in Uighur nationality

APOB基因3′端短串联重复序列多态性与新疆维吾尔族自然长寿的关系

Parkinson 's disease sensitivity and the 40-bp VNTR polymorphism of DAT gene

多巴胺转运体基因可变数目串联重复多态在帕金森病易感性中的作用

The distribution of VNTR polymorphisms of the platelet membrane glycoprotein 1b α in Harbin Han nationality

哈尔滨地区汉族人群血小板膜糖蛋白GP1bα基因VNTR多态性分布状况

Polymorphism of the VNTR examination by FAM carboxyfluorescein modify to primer

FAM羧基荧光素修饰引物检测D1S80基因座遗传多态性

Conclusion We discovered a novel VNTR polymorphism in the rennin gene , and this polymorphism was not associated with EH .

结论本文发现的肾素基因新的VNTR多态性与原发性高血压无相关性。

We concluded that the genetic polymorphisms of apoB gene 3 ' - end VNTR in She Nationality follows the Mendelian Law .

实验证明：畲族人群apoB基因的多态性遵循孟德尔定律。

The importance of HWE-exact test in multiallelic system was emphasized , especially in the study of forensic VNTR and STR typing .

强调了精确检验在多等位基因标记系统，尤其是以VNTR、STR为代表的法医DNA分析研究中的重要性。

ABSTRACT : Objective To explore the association between monoamine oxidase A ( MAOA ) variable number tandem repeat ( VNTR ) polymorphism and major depression in Chinese Han population .

摘要：目的探讨单胺氧化酶A（MAOA）基因启动子可变数目重复序列（VNTR）多态性与重性抑郁症易感性的关系。

Objective : To investigate the association between polymorphism of VNTR in 5-HTT intron 2 and clinical phenotype in major depression and analysis the effect of VNTR polymorphisms on depression .

目的：分析5-HTT基因第二内含子上的VNTR多态性与抑郁症临床表型的关系，以探讨VNTR多态性对抑郁症发病的影响；

Objective To investigate the correlation between 3 ′ variable number of tandem repeats ( VNTR ) of apoB gene polymorphisms and coronary heart disease ( CHD ) in Han nationality .

目的探讨汉族人载脂蛋白（apo）B基因3′端可变数目串联重复序列（3′VNTR）多态性与冠心病的关系。

Objective To study the variable number of tandem repeat ( VNTR ) polymorphism of platelet glycoprotein ( GP ) Ib α gene in Han , Yi and Dai populations .

目的研究中国汉族人及云南省彝族、傣族人血小板膜糖蛋白（GP）Ibα基因可变数目串联重复序列（VNTR）的多态性特点。

Objective To access the application of spacer oligotyping ( Spoligotyping ) and Multiple Locus VNTR ( MLVA ) in epidemiological studies of Mycobacterium tuberculosis .

目的评价间隔区寡核苷酸分型（Spoligotyping）及多位点可变数量串联重复序列分析（MLVA）方法在结核分枝杆菌基因分型研究中的应用。

To examine the relationship of 5-HTT intron 2 VNTR polymorphism to antidepressant response and adverse effect of fluoxetine , in order to provide a biological predictive index of individual antidepressant treatment .

通过研究VNTR多态性与氟西汀治疗抑郁症疗效的关系，以及VNTR多态性与氟西汀副作用的关系，为抑郁症药物治疗的个体化提供生物学预测指标。

Objective To investigate the association of the 48 bp variable number tandem repeat ( VNTR ) polymorphism in the dopamine D4 receptor ( DRD4 ) gene exon III with schizophrenia in Chinese Han population .

目的在中国汉族人群中寻找散发精神分裂症与多巴胺D4受体（DRD4）基因第3外显子48bp片段可变数串联重复（VNTR）多态性的关系。

22 haemophilia A families were assayed by polymorphism sites BcL I , Xbal I and VNTR , and positive rate was respectively 55 % , 45 % and 36.4 % .

22例血友病甲家系采用BclⅠ，XbalⅠ多态位点和VNTR方法检测，检出率分别为55%，45%和36%。

AIM : To investigate the association of the polymorphism of 27 bp variable number of tandem repeats ( VNTR ) in endothelial nitric oxide synthase ( eNOS ) gene with restenosis after coronary stenting in Chinese population .

目的：探讨内皮型一氧化氮合酶（eNOS）基因27bp数目可变的串联重复序列（VNTR）多态性与中国汉族人群中冠状动脉支架置入后再狭窄的相关性。

Objective To find out the polymorphism distribution of St14 ( DXS52 ) variable number of tandem repeat ( VNTR ) in normal individuals in the northeastern regin of China and hence provide a proof for the gene diagnosis of hemophilia A.

目的探讨中国正常人群St14（DXS52）位点VNTR多态分布，为甲型血友病基因诊断提供依据。

Conclusions The 4a allele in VNTR polymorphism of intron 4 of eNOS gene is associated with portal hypertension occurence of liver cirrhosis , and 4a allele may be a marker for genetical predisposition of portal hypertension in Chinese Han population .

结论eNOS基因第4内含子的VNTR多态性与肝硬化门脉高压症形成相关，a等位基因可能是中国人群门脉高压症的遗传易感性的基因标志之一。

It was indicated that most of the immunogenicity , resided in a repeated increase in the amount of mucin present on cancer VNTR ( variable number of tandem repeats , VNTRs ) 20 amino acid peptide domain in the extracellular portion of the molecule .

MUC1的免疫原性区域主要位于该蛋白分子胞外段的20个氨基酸重复序列区域（VNTR）。