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Exon相关的网络例句
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Moreover, we illustrated the method by examining similarity or dissimilarity of exon-1 ofβ-globin gene of 11 species, and compared our results with some existing results of other methods.

以11种生物的β-globin基因的第一外显子为例分析了序列间的相似性,并同其它文献中的相似性分析的结果进行了比较。

Moreover, we illustrate these methods by examining dissimilarity of exon-1 of β-globin gene of 11 species, and compare our results with some existing numerical methods.

根据向量之间的欧氏距离,我们分析了11种生物的β-globin基因的第一外显子序列的相似性,并同其它文献中的相似性分析的结果进行了比较。

Methods The total RNA of leucocyte was extracted 43 allergic vasculitis patients and 24 normal subjects before and after treatment with Trizol reagent and the integrity and concentrations of HLA-DRw53 gene mRNA were determined by agarose gel electrophoresis and UV spectrophotometer after denatured with 1% formaldehyde, the product was transcribed into complementary retroviral synthetic deoxyribonucleic acid, and sequence-specific primers were designed based on the sequences of second HLA-DRw53 gene exon and housekeeping gene glyceraldehyde phosphate-dehydrogenase cDNA.

利用随机引物逆转录合成互补脱氧核糖核酸,根据HLA-DRw53基因第二外显子序列和管家基因人磷酸甘油醛脱氢酶的cDNA序列设计序列特异性引物。检测43例变应性血管炎患者治疗前后与24名正常人HLA-DRw53基因mRNA表达量的变化。

Objective: To study the relationship between the exon 1 A/G polymorphism of the CTLA-4 gene and the response to antithyroid drugs in Graves' disease.

目的:对Graves病患者CTLA-4基因外显子1第17密码子49位点A/G多态性与GD患者的临床特点及其对抗甲状腺药物的疗效关系进行研究,为临床治疗的决策提供依据。

The primers of exon 1 and 2 of hircine GDF9 gene were designed on base of the sequence of ovine GDF9 gene.

本研究根据绵羊GDF9基因序列设计引物扩增山羊GDF9基因的外显子1和外显子2。

The products amplified by primer 2 had polymorphism. The sequencing results indicated that there were two nucleotide mutations( C→A and C→T )at exon 1183bp and 336bp of hircine GDF9 gene, but the two mutations did not cause amino acid change. The products amplified by primer 3 had polymorphism.

所设计的6对引物扩增产物中共有3对发现了多态,引物1经SSCP分析虽然没有发现多态但经克隆测序却在外显子1编码区前-4bp处检测到A→C的突变。

Especially, in the second exon two base substitutions had been found at positions +368 and +456. At position +368, the first result was in substitution of glutamine for arginine. While the second was homonymy substitution at position +456.

在第2外显子有2处碱基取代,分别是+368处的G→A,导致精氨酸→谷氨酰胺,及+456处的T→C,为同义取代,仍为丙氨酸;第5外显子+1572处的A→G,导致组氨酸→精氨酸。

Results Homozygosity of C→T transition at position 11514 in exon 8 resulting in Thr359Met was identified in the proband, and heterozygosity for Thr359Met ...

该遗传性FⅦ缺乏症家系为纯合子错义突变Thr35 9Met;推测此突变影响了蛋白质分子的空间构型,从而产生异常FⅦ蛋白的功能。

Results: Tyr486Asp missense mutation in Exon 5 of UGT1A1 gene was found and homozygote of the mutation was confirmed in the proband.

结果:该先证者UGT1A1基因的第5外显子第486密码子发生了T→G碱基的错义突变,导致了酪氨酸变成了天门冬氨酸(Tyr486Asp)。

Ormazabal C, Hurtado C, Aranaz P, et al. Low frequency of JAK2 exon 12 mutations in classic and atypical CMPDs.

本研究建立的多重位点特异性PCR方法可同时检测JAK2 V617F突变和4种常见的JAK2 exon12突变,具有检测灵敏度高、应用方便的特点。

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然而,正如其名字所指出的那样,CD盘不能写,也不能用任何方式改变其内容。

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