UTR

The seem to the coding regions , the UTR of eukaryotic gene are also been spliced during gene transcription . However , these exons are not translated into protein during gene translation .

和编码区一样，真核基因的非翻译区在转录后期也进行了剪接，但是在翻译时并不被翻译成蛋白质。

Probable Existence of a Negative Regulation Region Within the 3 ′ UTR of Human Phosphoinositide 3-Kinase γ mRNA

PI3KγmRNA3′非翻译区可能存在基因表达负调控区

Sequence Analysis of 3 ′ - UTR of Myostatin Gene in Domestic Goose

家鹅Myostatin基因3-′UTR序列分析

Bioinformatics Analysis on 5 ′ UTR of IGF-I Gene in Red Steppes

草原红牛IGF-I基因5′调控区序列的生物信息学分析

Phylogenetic Tree Analysis of UTR and Transmembrane Structure Prediction of Proteins of Genus Bymovirus

大麦黄花叶病毒属成员UTR系统进化树分析及编码蛋白跨膜结构推测

PCR-RFLP Analysis of 3 ' - UTR of myogenin Gene in Pigs

猪肌细胞生成素基因3'端侧翼序列PCR-RFLP分析

The research on method for splice sites identification in eukaryotic gene untranslated coding regions ( UTR ) .

真核基因非翻译区剪接位点识别算法的研究。

Sequence and Polymorphism Analysis of Porcine Hormone-sensitive Lipase Gene 5 ′ - UTR and Exon ⅰ

不同品种猪HSL基因5′-UTR和外显子Ⅰ片段的克隆测序及多态性分析

The probes , 27 for 5 ′ UTR and 9 for C region , were designed in accordance with the data of sequence analysis .

根据序列分析数据设计了5′UTR27个探针和C区9个探针。

Enhancing hGH Expression Level in Insect Cells by Shortening the 5 ′ - UTR of hGH cDNA

缩短5′-UTR序列可以提高hGH基因在昆虫细胞中的表达

A Pilot Study on the Influence of HCV 5 ′ UTR and 3 ′ UTR on RNA Replication

HCVRNA复制过程中5'UTR与3'UTR作用的初步探讨

The phylogenetic tree based on the sequences of 3 ′ UTR is not the same as that based on the complete sequences .

基于3′端UTR序列的进化树与基于全基因序列的进化树不全相同。

Cloning and Sequencing of 5 ′ UTR of Enterovirus from Patients with HFMD in Shenzhen

深圳地区手足病肠道病毒5′端非编码区部分基因克隆和序列分析

That the inactivation of some antioncogenes came from the structural changes of their 3 ′ UTR ;

一些抗癌基因的失活来源于其3′UTR的结构变化；

It has been found that the 3 ′ UTR is involved in regulation of function of known oncogenes and antioncogenes ;

目前已经发现，3′UTR参与一些已知的癌基因和抗癌基因的功能调控；

The 3 ′ UTR sequence cannot be used for HEV genotyping for all HEV strains in place of the whole HEV genome sequence .

HEV3′端UTR序列不能完全代替全基因组序列进行基因型分型。

The nucleotide diversity value in the 3 ′ UTR was highest , lower in intron , the lowest in extron .

其中，3′端UTR区的核苷酸多样性最高，次之为内含子区，外显子区的核苷酸多态性最低。

The relationship of trinucleotide repeat sequence length polymorphism in 5 ' - utr of gstm_1 gene and genetic susceptibility to primary hepatocellular carcinoma

GSTM1基因内三核苷酸重复序列长度多态与肝癌遗传易感性的研究

Simultaneous detection of polymorphisms in the 3 ' - and 5 ' - UTR of thymidylate synthase gene using denaturing high-performance liquid chromatography

应用变性高效液相色谱技术建立胸苷酸合成酶基因多态检测平台

In recent years the research on the roles of eukaryotic mRNA 3 ′ UTR in suppression of malignant phenotype of tumor cells has achieved very exciting advances .

最近几年来，关于真核mRNA3′UTR在肿瘤细胞恶性表型抑制中作用的研究，取得了非常令人鼓舞的进展。

Objective : To analyze the partial sequences of 5 ′ UTR of Enterovirus from Patients with Hand Foot Mouth Disease ( HFMD ) in Shenzhen .

目的：分析深圳地区手足口病病人肠道病毒（EV）5′端非编码区（5′UTR）部分基因序列，了解本地区手足口病病人EV感染的基因型。

Objective : To investigate the C / T polymorphism in the 5 ′ - untranslated region ( UTR ) of the CD40 gene and its relationship with Graves'disease .

目的：探讨CD40基因5′非翻译区域C/T多态性和Graves病（GD）甲亢发病的相关性。

Results Seven SNPs in the exons , introns and 3 ′ untranslated region ( 3 ′ UTR ) of TGF β 3 gene were identified .

结果TGFβ3基因测序总长度5457bp，共发现7个SNP，位于内含子区5个、编码区和3′非翻译区各1个。

Objective ; To construct a promoter identifying plasmid with GFP as reporter gene , and then identify the promoter activity of HCV 5 ' - UTR with this construct .

目的：利用已有质粒构建带GFP报告基因的启动子鉴定质粒，并用此质粒鉴定丙型肝炎病毒5非翻译区（HCV5'-UTR）启动基因表达的活性。

The phylogenetic tree constructed by 3 ′ - UTR of Myostatin genes in these 13 species shows that 3 ′ - UTR sequence can offer certain information for animal 's evolution .

以13个物种Myostatin3-′UTR构建的分子进化树表明，3′UTR能够为动物进化提供一定信息，但适用于较低分类阶元。

VPg is served as the primer of duplication . One of researching focus is the study on Poly ( C ) and IRES in 5 ′ - UTR .

VPg可能充当RNA合成引物的作用，5′UTR内的Poly（C）和内部核糖体进入位点（internalribosomaentrysite，IRES）是当前研究的热点之一。

Results TTV DNA was identified by UTR PCR in 98.3 % of 22 7 volunteer blood donors , in 100 % both of 60 chronic hepatitis B patients and 80 chronic hepatitis C patients .

结果UTRPCR检测表明，健康献血员TTVDNA检出率为983%，而60例慢性乙型肝炎和80例慢性丙型肝炎患者血清中TTVDNA检出率均为100%；

Conclusion : The T / G polymorphism at position 3804 in 3 ′ - UTR of Fc receptor gene is rare in populations of southern China and this polymorphism has no relationship with SLE .

结论：Fc受体γ链基因3′-UTR3804位点T/G单碱基替换的多态性现象在中国南方汉族人群中少见，该位点的基因多态现象与SLE发病无关。

A new framework , named Information Entropy Model of Sliding Window ( IEMSW ), was proposed to effectively analyze the structural information contained in the 3 ' - UTR sequences around the polyadenylation site . 3 .

为有效地分析水稻3′-UTR序列剪切位点上下游序列中的信息结构，提出了一个新的分析框架，即DNA序列的滑动窗口信息熵模型。

Methods Genomic DNA was extracted from 368 healthy Chinese Han subjects , genotypes of the SNPs in Fc α R1 gene 5 ' - UTR and promoter region were determined by PCR and direct sequencing .

方法提取368例正常广东汉族人基因组，DNA扩增FcαR1基因5-UTR相关区域并直接测序鉴定基因型。