目的克隆人神经生长因子基因编码区。
Objective Molecular cloning and sequencing of the human nerve growth factor gene.
本研究扩增得到的基因片段与报道的猪ghrh基因编码区序列完全一致。
Homogenious analysis showed that it was consistent with the reported porcine GHRH gene sequence.
根据基因编码区的周期性质，设计了具有窄带选通特性的FIR数字滤波器和自适应滤波器。
According to the periodicity of the coding regions, the FIR filter and the adaptive filters with narrow pass-band are developed.
研究南阳牛HCRTR1基因编码区单核苷酸多态性，为利用遗传标记进行肉牛选育奠定基础。
One hundred and twenty two Nanyang cattle were used for SNPs discovery in the complete coding region of HCRTR1 gene using PCR-SSCP and sequencing methods.
结果从活化的人白细胞中克隆到IDO基因编码区全长，并构建了IDOEGFP融合蛋白表达载体。
Results The full-length coding sequence of IDO was cloned from activated human leukocytes and the expression vector for IDO-EGFP fusion protein was constructed.
本文采用PCR-SSCP及PCR产物直接测序等技术，对15例肺癌患者的组织标本及8例正常对照个体血细胞SOX4基因编码区进行了突变分析。
Using PCR-SSCP and PCR product direct sequencing techniques, we analysed the ORF region of SOX4 gene encoding in 15 lung cancer tissues and 8 normal controls.
就此，15号染色体上成为研究热点的这一区域存在另外两种编码尼古丁受体的基因，提示实际情况将更为复杂。
That, and the fact that the region of chromosome 15 under scrutiny has two other nicotine-receptor genes in it, suggests the situation may indeed be more complex.
蛋白质编码区仅1.5％的基因组入账。
Protein-coding regions accounted for just 1.5% of the genome.
我们的研究表明，只有对基因组编码区的深入分析，这些核心通路和调节过程的基因改变才能被发现。
Our data indicate that genetically altered core pathways and regulatory processes only become evident once the coding regions of the genome are analyzed in depth.
再经重叠pcr技术将这两段DNA连接在一起，构成完整的ZP3基因的编码区。
Then with overlapping PCR technology to link this two DNA together to form a complete ZP 3 gene encoding.
目的研究中国江西庚型肝炎病毒5非编码区(5- NCR)基因结构特征。
To study the genic characteristics of 5 'non - coding region (5' NCR) of HGV in Jiangxi, China.
经d NA序列分析表明所获基因含有全部前导序列，其成熟蛋白编码部分与从第一骨架区引物所克隆的序列相符。
DNA sequences analysis indicated that the cloned genes included the whole leader sequences and the mature Ig protein encoding regions.
目的：克隆人牙本质基质蛋白1 (DMP1)成熟肽编码区基因片段。
Aim: Cloning and partially sequencing of human dentin matrix protein 1 (DMP1) encoding mature protein.
目的：克隆小鼠牙本质涎蛋白(DSP)成熟肽编码区基因。
Aim: Cloning and partially sequencing of mouse dentin sialoprotein (DSP) encoding mature protein.
目的：克隆小鼠牙胚组织中釉基质丝氨酸蛋白酶(EMSP1)成熟肽编码区基因。
Objective: To clone cDNA of enamel matrix serine proteinase (EMSP1) encoding mature protein from mouse dental germs.
目的：克隆成骨蛋白-1（OP-1）成熟蛋白编码区基因。
Aim: Cloning and sequencing of hOP-1 cDNA encoding mature protein.
目的：分析43例中国人非综合征性听力减退（NSHI）患者的GJB2基因部分编码区的突变的情况。
Objective:To examine mutation in the partial coding region of GJB2 gene in 43 cases of Chinese patients with non syndromic hearing impairment (NSHI).
对分离到的HEV71阳性分离株进行VP1编码区基因扩增，核苷酸序列测定和同源进化分析。
And identified HEV71 isolates were performed by gene amplification of VP1 coding region, nucleotide sequencing and homology analysis of evolution.
这些突变分布于atm基因整个编码区，每个外显子都存在基因变异位点，没有发现明显的突变热点。
These gene mutation distributing in all over the whole coding section of ATM gene. Every Exon exist the gene mutated site and no obvious hot mutated site be discovered.
目的获得人甘露聚糖结合凝集素相关丝氨酸蛋白酶-2（MASP-2）编码区基因。
Objective To obtain the gene fragment encoding human mannan-binding lectin (MBL)-associated serine protease-2 (MASP-2).
同时，采用同源序列分离法，获得了小麦PSY基因的完整编码区序列。
Otherwise, the complete coding sequence of phytoene synthase gene (PSY) was isolated from the same wheat variety by using homologous sequence separation.
目的：对不同粘附力变形链球菌临床分离株表面蛋白V区、P区编码基因进行序列测定。
Objective: To sequence V-region and P-region gene of surface protein of serotype c Streptococcus mutans clinical isolates with different adherent abilities.
分别设计MSX1、PAX9基因特异性引物，聚合酶链反应扩增全部外显子编码区和内含子-外显子剪接序列，产物纯化后直接测序。
Specific primers were designed for MSX1 and PAX9 respectively. Mutation analysis was performed by direct sequencing of all the coding exons and intron-exon boundaries.
在已经有注释的4 732个基因中，861个基因的编码区中有ssr。
Among 4 732 annotated genes up to now, SSRs were found in 861 genes.
研究背景：组织特异的基因表达是由基因组非编码区中的调控模块和对应的蛋白反式因子共同决定的。
BACKGROUNDTissue specific pattern of gene expression is probably determined by regulatory modules encoded in the genome DNA and trans-regulatory apparatus.
方法1。根据HSP70全长基因序列设计针对其编码区的引物，在下游引物的宁端加人MG7模拟表位的核昔酸序列。
Methods (1) The coding sequence of MG7 mimotope (GC23) was included in the reverse primer, and by PCR incorporated with HSP70 gene at the 3 terminus.
在HCV的编码基因中，核心区(C区)序列具有高度遗传保守性，c基因表达产物具有良好的抗原稳定性。
Among HCV encoding gene, core region shows greater sequence conservation. Core gene expression has favorable antigen stability.
在HCV的编码基因中，核心区(C区)序列具有高度遗传保守性，c基因表达产物具有良好的抗原稳定性。
Among HCV encoding gene, core region shows greater sequence conservation. Core gene expression has favorable antigen stability.
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