片语

coding starting region编码起始区

VP2-hydrophilic coding-regionVP2亲水性编码区

coding terminal region编码终止区

non-coding region非编码区

coding sequence region蛋白质编码区

coding g region编码区

VP1 coding-regionVP1蛋白编码区

VP2 coding-regionVP2蛋白编码区

英汉例句

• objective: to clone and analysis the coding region of mgb of ochotona princeps (pika).

  目的：克隆青藏高原高原鼠兔肌红蛋白（mgb）基因编码区，并分析其序列特征。

• objective to screen coding region of human renin gene to find new polymorphisms and investigate whether there are associations between new polymorphisms of renin gene and essential hypertension(eh).

  目的扫描肾素基因发现新的多态性，探讨肾素基因新多态性与原发性高血压的关联性。

• it is worth to note that snp in coding region of abca1 gene is important to mediate the expression of abca1 protein and different snp contribute differently to the presence of coronary heart disease.

  尤其值得注意的是，abca1基因编码区的snp对控制abca1的表达起着重要作用，不同的snp对冠心病事件的影响不同。在不同种族中同一snp分布频率不同，且对血脂水平和冠状动脉粥样硬化程度的影响也不尽相同。

• the evolutional regulation same as coding region are obtained for encoding region. a result that the evolutional level of encoding region is lower than coding region is presented.

  得到非编码区遵守与编码区一样的进化规律，非编码区进化水平低于编码区的结论。

• methods an eukaryotic expression vector encoding hantaan virus s gene coding region was constructed.

  方法利用基因重组技术，构建含汉滩病毒s片段编码区基因的真核表达质粒。

• firstly, the coding region of c1galt1c1 was amplified by pcr from genomic dna in peripheral blood and pcr products were directly sequenced.

  提取研究对象外周血基因组dna，扩增c1galt1c1基因的编码区，采用pcr产物直接测序的方法进行突变筛查。

• structurally, a gene is formed by three regions: a regulatory region called the promoter juxtaposed to the coding region containing the protein sequence, and a 「3’ tail」 sequence.

  从结构上来讲，基因包含三个区域：称为启动子的调节区域；与其并列的编码蛋白质的密码子区域；以及3「端尾部序列。

• 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.

  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。

• we find that the uneven distribution of bases in coding region is interrelated with the abundance distribution of amino acids and the synonymous codon usage;

  发现编码区堿基分布的非均匀性与氨基酸丰度的分布和同义密码子的非均匀使用紧密相关；

• direct dna sequencing of the whole coding region of gjb2 revealed that a common homozygous mutation 235delc was responsible for most of the affected members in the nshi family.

  对gjb2基因进行整个编码区域的测序，发现235堿基处发生了堿基c的纯合缺失， 这一突变可能是该家系中绝大多数患者致病的遗传基础。

• after more and more genome sequencing projects, like the 「human genome project」, the prediction of genes, including their coding region and their regulatory region, has received a lot of attention.

  在基因组测序工作完成后，利用计算工具进行基因识别以及基因结构预测受到了越来越多人的重视。

• the statistical characteristics of the coding region of nucleie acid sequences are reviewed.

  总结了序列编码区的统计特征。

• identification of characteristics single nucleotide polymorphisms (snps) existing in coding region of the gene, cyp4a11, may provide some new insights into the genetic mechanisms of hypertension.

  寻找人群中该酶基因之一的cyp4a11的编码区多态性位点分布情况，可以为研究高血压病的基因机制提供新的依据。

• 「we know how to interpret variations in the coding region much better than outside the coding region,」 he said.

  我们知道如何阐释编码区的变异，它比编码区外要好得多。

• objective: to search for mutations in the coding region of the gch1 gene in chinese patients with drd.

  目的：本实验旨在检测国人drd患者的gch1基因编码区的突变。

• objective:to examine mutation in the partial coding region of gjb2 gene in 43 cases of chinese patients with non syndromic hearing impairment (nshi).

  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。

• recognition for the coding region of dna sequences is the premise of t cell epitopes identification.

  準确地识别出dna序列的蛋白质编码区是开展t细胞表位筛选工作的前提。

• the results showed that the nucleotide composition in coding region of gene was significantly affected by the insertion of tes, but that was not the only factor in yielding mutational bias.

  结果表明：转座因子插入极显着地影响到基因编码区的同义密码子使用但并非唯一因素；

• it is reported that the expansion of cag in 5」 coding region of atxn2 gene is the characteristic of sca2.

  据报道，atxn2基因的5’端编码区域的三核苷酸cag重复的扩展是一脊髓小脑共济性失调2型（sca2）的特征突变。

• molecular genetic analysis of each proband was performed by direct dna sequencing of the entire coding region of kcnj2.

  通过直接dna测序，对先证者的kcnj2全部编码区进行分子遗传学分析，同时筛查对照受试者。

• thirdly, the expansion of cag in 5' coding region of atxn2 gene is detected in candidate gene region.

  最后，在患者基因组候选区域中，检测到了atxn2基因5’端编码区域的三核苷酸cag重复的扩展。

• conclusion that eukaryotic expression vectors containing coding region of nov gene was constructed can provide a strong molecular tool for the studies of effect of nov gene.

  结论本实验所构建的重组质粒为nov基因的作用研究提供了有利的分子工具。