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1.The first ATG rule for recognizing the start codon of gene coding sequences is given.
提出了一个识别基因起始密码子的第一ATG规则.收藏指正
2.In human cDNA sequencing projecs, it is vital to know whether the first ATG codon is a real start codon or an in frame Met codon without initiation function.
在人类cDNA序列确定全长基因的过程中 ,必须判断第一个ATG密码子是真正的起始密码子还是框内的非起始作用的甲硫氨酸密码子 .收藏指正
3.Furthermore, a fragment of 150bp from start codon ATG to 150nt showed the most variation.
从ATG至第150bp区段的核苷酸序列变异频率最高。收藏指正
4.DNA sequencing revealed that the IPNS gene of S. cattleya consists of 963 bp encoding a protein of 321 amino acids with ATG as start codon, TGA as stop codon.
经基因序列分析表明牲畜链霉菌中IPNS基因,由963bp组成,起始密码子为ATG,终止密码子为TGA,共编码321个氨基酸,所克隆的牲畜链霉菌IPNS基因编码蛋白与已知的S.收藏指正
5.This fragment three flanking end location is in the first translation start codon ATG (+1) up stream 128 bp.
这段片段的3’端起始点在第一个外显子里第一个翻译密码子ATG(+l)上游128 bp处。收藏指正
6.Investigation pointed out the presence of HNF3β, C/EBP, and NF-κB regulatory element binding sites located upstream of the first start codon.
研究表明,Hepcidin属于II型急性时相反应蛋白,其启动子区域存在HNF3β(肝核因子)、C/EBP(CCAAT/增强子结合蛋白)、NF-κB(核因子κB)等转录因子结合位点。收藏指正
7.The detection rates of pre-S2 start codon mutation were significantly different in different groups: from 50.00% (HCC), 39.47% (LC), 8.00% (CH), to ASC (0).
前S2起始码变异在HCC、LC组的检出率分别为50．00％、39．47％,明显高于慢性肝炎组的8．00％、慢性无症状乙型肝炎表面抗原携带者组的0(P值均<0．05)。收藏指正
8.Allelic Variants of Human Calcitonin Receptor, Vitamin D Receptor Start Codon and SP1 Binding Site of COL1A1: Distribution and Association with Bone Mineral Density in Adults of Han Nationality in Beijing Area
北京地区汉族人群降钙素受体基因、维生素D受体基因起始密码子和Ⅰ型胶原基因SP1转录结合位点多态性与骨密度关系的研究收藏指正
9.The distance and the composition between the Shine-Dalgarno(SD)sequence and the start codon have, profound effect on the expression of prochymosin gene causing a 15fold difference.
Shine-Dalgarno序列与起始密码子之间的距离与组成对凝乳酸原基因表达有明显的影响,可导致其表达水平有15倍之差。收藏指正
10.The detected ratios of pre-S2 start codon and pre-S deletion mutations were significantly higher in genotype C than in genotype B (43.04% vs 1.23%, 36.71% vs 19.75%, P < 0.05, respectively).
C基因型前S2起始码变异的检出率为43．04％,高于B型的1．23％(P<0．05)。 前S区缺失变异在C基因型中的检出率也高于B型(36．71％与19．75％,P<0．05)。收藏指正
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