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Search Genes and Coding Regions. 巴斯德研究所提供的基因与编码区查找工具。
Specifies the start and end of a code region. 指定代码区域的开始和结束位置。
The carving gravure printed hand feeling lines includes over one coding region. 所述雕刻凹印手感线分为一个以上的编码区域。
The Script view provides color coding, parenthesis matching, auto-complete, and MDX code regions. 脚本视图提供了彩色编码、括号匹配、自动完成和MDX代码区域。
Using the regular expression of Perl, split the coding regions in two part according to which strand it locate, and throw off the annotation lines. 将细菌基因组编码区文件分成先导链编码区文件及滞后链编码区文件，并去除序列的注释行。
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。
There is terminate codon TAA of the whole ORF at the 3D coding region termination. 在3D编码区末端有整个ORF的终止密码子TAA。
Considering of the high mutative rate of the coding regions and the conservative heritance of the noncoding regions in human mitochondrial DNA (mtDNA). 针对人类mtDNA编码区突变率高和非编码区遗传保守的特点，对利用mtDNA分析人类母系血缘关系进行了初步的探索。
No mutation was found in the coding region, the intron-exon boundaries, or part of the promoter region of HOXD13. 我们对HOXD13基因的编码区，内含子-外显子交接区，和部分启动子区域进行序列分析未发现突变。
The human CYP2B6 gene is highly polymorphic,having many single nucleotide polymorphisms in promoters and coding regions. CYP2B6具有高度基因多态性,在基因编码区和非编码存在许多单碱基突变。
Furthermore, we found an important SNP (Single Nucleotide Polymorphism) at 725 position of the MC1R coding region. 另外发现牛MC1R基因编码区725处存在一重要的SNP(单核苷酸多态性)。
The coding region of Oedaleus asiaticus EPV spheroidin gene was obtained by PCR, and this fragment was subsequently cloned, sequenced and analyzed. 通过PCR扩增,获得OaEPV球状体蛋白基因编码区序列,并进行克隆、测序。
The results indicated that the complete length for coding region is 954bp, but Sus scrofa and Bos Taurus varies greatly, especially Sus scrofa. 结果表明,MSHR基因编码区长度为954bp,但猪和牛变异较大。
The sequence of the cDNA coding region was 1 197 bps, encoding a protein of 398 amino acids sharing 99% identical to CHS1 cDNA reported by Helariutta. 结果表明,克隆到的CHS基因全长为1197bps,编码一个由398个氨基酸残基组成的多肽,与Helariutta等发表的非洲菊查尔酮合酶CHS1基因的cDNA序列的CHS基因同源性高达99%25。
Methods 20 non-syndromic hearing loss (NSHL) cases were performed mutational analysis of the GJB2 coding region by PCR-direct sequencing. 方法采用PCR直接测序法对20个非综合征型遗传性聋家系的先证者（均为耳聋患者）进行GJB2基因的突变检测。
One of the foot-and-mouth disease virus(FMDV) type Asia 1 endemic strain nonstructural protein P3 coding region was amplified by RTPCR and sequenced. 经RT-PCR扩增得到一株口蹄疫亚洲1型流行毒株的非结构蛋白P3基因核苷酸序列,与其他代表性参考毒株的P3基因进行比较,分析该毒株P3区基因特征。
Abstract： To examine mutation in the partial coding region of GJB2 gene in 43 cases of Chinese patients with non-syndromic hearing impairment (NSHI). 摘要：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。
After complete sequence analysis of all coding regions within the locus, they found a single disease-segregating mutation, P222L, within the stress-response gene PRKRA. 他们对这些位置的所有基因编码之后的完整后续分析，发现一个单一疾病隔离突变-P222L，位置在压力反应基因PRKRA之内。
No mutation was found in the coding region, the intron-exon boundaries, or part of the promoter region of HOXD13. 我们对HOXD13基因的编码区，内含子-外显子交接区，和部分启动子区域进行序列分析未发现突变。
SPV pre-mRNAs contain three introns, compared to two found for B19: an additional intron was found within the capsid coding region. SPV RNA的第三个内含子位于核衣壳基因区内。