基因位点

孕烷X受体基因位点与炎症性肠病的易感性相关

The Pregnane X Receptor Locus Is Associated with Susceptibility to Inflammatory Bowel Disease

它既受DNA上不同基因位点控制，又受不同等位基因控制。

It is controlled not only by different gene locus of DNA but also by different isolocus gene .

糖尿病线粒体DNA常见易感基因位点检测芯片的研制

Development of a chip for detecting the diabetes - associated common loci in mitochondrial genome

基因位点在B基因组或在D基因组上，Bar基因的转移有很大差别。

As to Bar gene transfer there was significant difference between the gene loci in B genome and in D genome .

人类第6号染色体NOTCH4基因位点多态性与精神分裂症的关系

Relationship Between the NOTCH_4 Locus of Chromosome 6 and Schizophrenia

确定了2个基因位点，ESTA和ESTB；

Two gene locus were determined .

LDH只有1个基因位点，为四聚体酶；

LDH , 1 locus and 2 alleles ;

关联分析结果表明，31个标记的42个等位基因位点与抽薹时间和开花时间相关（P0.05）。

Association analysis showed that forty two alleles from 31 markers were identified associations with bolting and flowering time ( P 0.05 ) .

目的检测安徽省1型糖尿病患者的抗原肽相关运载蛋白体（Transporterassociatedwithantigenprocessing，TAP）基因位点多态性。

Objective To understand the polymorphisms of transporter associated with antigen processing ( TAP ) genes in patients with Type 1 Diabetes mellitus in Anhui .

研究表明，抑癌基因位点附近常存在微卫星不稳定性（Microsatelliteinstability，MSI）。

Studies suggest that microsatellite instability ( MSI ) usually exist near the tumor suppressor gene loci .

HLA基因位点全相合和1～2个位点不合无血缘关系异基因骨髓移植的临床疗效比较

A comparison of clinical outcomes between HLA allele matched and 1 ~ 2 alleles mismatched unrelated allogeneic bone marrow transplantations

主要组织相容性复合物（majorhistocompatibilitycomplex，MHC）是由紧密连锁、高度多态的基因位点所组成的复合体，广泛存在于脊椎动物中。

Major histocompatibility complex ( major histocompatibility complex , MHC ) is tightly linked , highly polymorphic loci consisting of complex , widely distributed in vertebrates .

利用生物信息学软件预测，获得了2个候选的miRNA及4032个靶基因位点。

Two candidate new miRNA and 4032 target gene site were predicted with bioinformatics soft .

因此，可以将GH基因位点作为对牦牛产奶量等生产性能进行选择的分子遗传标记。

So it was expected to develop a molecular genetic marker for selection using PCR-PFLP at GH gene site .

EST由4个基因位点编码，具有多态性现象；

The number of EST isoenzyme bands was 15 EST , which was encoded by 4 loci , and had strong polymorphism .

同时，15个STR基因位点与相关的实验指标的变化存在一定相关性。

Meanwhile , the loci frequencies of STRs are correlated with the related indicators of changes in the experiment .

结果0～6岁汉族儿童a、T、b、F等位基因位点占优势，分别占75.0%、97.7%、97.4%、60.0%；

Results The alleles of a , T , b , F were predominant in Han children . The percentage is 75.0 % , 97.7 % , 97.4 % , and 60 % respectively .

小鼠p16~（INK4a）基因位点的结构和功能研究

Structure and Function of Mouse p16 ~ ( INK4a ) Locus

LDLR基因位点的RFLPs检测及其与FH的相关性

Direction of the Human LDLR Gene Sites by RFLPs and its relation to FH

对21种向日葵细胞质雄性不育（CMS）品系的线粒体基因组atpA基因位点处的DNA分子变异进行了分析和研究。

Molecular variation at atp A gene loci of mitochondrial genome was analised and characterized in 21 CMS lines of sunflower .

目的探讨雌激素受体α（ERα）第一内含子中两个基因位点变异的多态性与冠心病和冠心病发病危险因素的相关性。

Objective To investigate the relationship between estrogen receptor alpha gene polymorphism in intron 1 and the risk factors for the patients with coronary heart diease ( CHD ) .

我国汉族人群Eales病与HLA-B基因位点相关性的研究

Relationship between HLA-B allele and Eales disease in a Chinese Han population

目前已知6个基因位点突变可引起MBL浓度降低。

Six gene mutations , has been found to be responsible for the lower concentration of MBL .

健康成人和放射工作者体细胞HPRT基因位点突变率的检测和比较

Detection and comparison of mutant frequency of somatic HPRT locus between healthy adults and radiation workers

醋酸铅体外诱发人外周血淋巴细胞HPRT基因位点突变的研究

Study on Frequency of HPRT Locus Mutation in Human Peripheral Lymphocytes Induced by PbAc_2 in vitro

不同性状的部分主效QTLs位于相同区域表明同一基因位点可能同时控制着根形态的不同方面。这是首次有关根部膨大性状的基因定位。

Some of the main QTLs were common between traits showing that should be possible to modify several aspects of root morphology simultaneously .

选择9种STR基因位点和Amelogenin基因位点，以测序为基础，研究我国汉族人群STR遗传结构。

Genetic distributions for 9 STR loci and amelogenin locus were determined in Han nation population based on DNA sequencing .

结果该系统12个STR基因位点在汉族人群中均为高识别率位点，特别适合于陈旧血痕检验；

Results 12 STR loci system had high power of discrimination ( DP ) and it was suited for analysis of dated bloodstain especially .

晚期混合裂变产物内照射诱发体细胞HPRT基因位点突变率与剂量率关系的研究

Study on the relationship between dose-rates and somatic cell mutation at HPRT locus induced by late fission products

结果初步确定了大肠杆菌染色体上的lac操纵子结构基因位点适合外源基因的敲入和表达。

So we assured that the sites of structure genes in the lac operon of Escherichia coli chromosome were suitable for expressing foreign genes .