intron的例句大全

Pedigree analysis of T53 → C in intron 1 and C59 → A in intron 4 mutations of apolipoprotein M gene expression

载脂蛋白M基因1号内含子T53→C和4号内含子C59→A突变的家系分析

Objective To analyze pedigree inheritance of T53 → C in intron 1 and C59 → A in intron 4 mutations of apolipoprotein M ( ApoM) gene expression in a Han nationality Chinese pedigree.

目的分析1个中国汉族家系的载脂蛋白M（ApoM）基因1号内含子T53→C、4号内含子C59→A突变的家系遗传。

Methods Long distance PCR ( LD-PCR) was used to detect intron 22 inversion among 22 HA patients and 14 members of two HA families to identify directly those with intron 22 inversion and its carriers.

方法对22例HA患者和两个家系的成员14人首先采用长距离DNA扩增（LD-PCR）技术，直接检测是否为基因倒位及其携带者；

Studies on Intron Length Polymorphism and EST Single Nucleotide Polymorphism in Brassica

芸薹属内含子长度多态性和EST单核苷酸多态性研究

To explore the variable number tandem repeats ( VNTR) of nucleotide sequence ATCT within intron 40 of von Willebrand factor gene in Han Chinese, polymerase chain reaction ( PCR) and polyacrylamide gel elec-trophoresis ( PAGE) were used to examine the VNTR in 71 individuals.

用聚合酶链反应（PCR）和聚丙烯酰胶凝胶电泳（PAGE）的方法，研究了71名中国汉族人142条染色体的vWF基因40号内含子的可变数目串联重复序列（VNTR）。

Objective To investigate the association between a 27 base pair ( bp) variable number of tandem repeats ( VNTRs, 4a/ 4b) polymorphism in intron 4 of the eNOS gene and diabetic nephropathy in type 2 diabetes mellitus of northern Chinese.

目的探讨内皮细胞型NO合成酶（eNOS）基因第4内含子一个27bp的可变数目串联重复序列多态性（VNTRs，4a/4b）与中国北方汉族人2型糖尿病（DM）合并肾病（DN）的相关性。

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 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；

A splice mutation were identified in interface of exon 5 and intron 5 ( 1875+ G? A).

通过对ALD基因研究发现一例患者ALD基因外显子5内含子5交界处发生了1875+G→A。

There are two important polymorphic sites in the SERT gene: variable number tandem repeats ( VNTRs) in the second intron, and SERT gene-linked polymorphic region [ 5-HTTLPR], which might influence the transcription efficiency of SERT gene and the stability of the mRNA transcripted.

SERT基因存在2个多态性区：VNTRs和5-HTTLPR，由此产生的不同基因型可影响SERT基因的转录效率及其mRNA的稳定性，从而影响SERT的数量、亲和力以及5-HT重吸收。

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。

Studies on the Splicing Ability of Wx Gene Intron 1 in Glutinous Rice

糯性水稻中蜡质基因第1内含子的剪接活性

One-Step PCR Method for Detecting the First Base of Splice Donor of Wx Intron 1 in Rice

PCR一步法检测水稻蜡质基因第一内含子剪接供体+1位碱基

Results F ⅷ: C of the proband and his daughter were 6. 9% and 3. 4%, respectively, each of them three had no intron 22 inversion. Double heterozygote mutation were detected in the female;

结果表型检测先证者（父亲）及其女儿的FⅧ：C分别为6.9%、3.4%；3人内含子22倒位为阴性；

application of mitochondrial nad 1 intron 2 sequences to molecular identification of some species of dendrobium sw.

线粒体nad1内含子2序列在石斛属植物分子鉴定中的应用。

in this study, based on the results the laboratory had, chicken oviduct ovalbumin gene upstream regulatory sequence and the first intron were selected as the research object, and its expression vector was constructed.

本研究根据实验室已有结果，选取鸡输卵管卵清蛋白基因上游调控序列和第一内含子作为研究对象，对其进行表达载体构建和优化研究。

base on the heterogeneity of bases distribution of exon on three codon sites, the heterogeneity index hi is introduced and used in the study of the sequence peculiarity of exon and intron in c elegans.

根据外显子在密码子三个位点上的分布不均匀性，引入非均匀指标HI，来研究线虫基因外显子与内含子的序列特征。

intron refers to the non-coding sequences in split gene and is removed before translation.

内含子是指断裂基因中的非编码区序列，在编码蛋白质前被去除。

conclusion the g allele may be a predisposing gene marker , hgr gene intron 4 polymorphism contributes to the development of ci in females.

结论对女性来说，等位基因G可能是脑梗死的易感基因标志。

the sequence analysis of the 3' end of intron 15 from human ldl receptor gene and its application in the study of gene diagnosis for familial hypercholesterolaemia

LDL受体基因内含子15结构分析及其在家族性高胆固醇血症基因诊断中的应用