mutation的例句大全

Hence it is suggested that BCMA does not induce notable mutation on the cell.

该试验表明：BCMA无明显致细胞突变作用。

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The authors used technique of sister chromosome exchange ( SCE) to assess the effect on mutation with BCMA.

作者应用外周血姐妹染色单体交换率（SCE）技术估价多菌灵A的致突变作用。

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The process of human and other higher vertebrates' immune system produces antibodies using clonal selection mechanism is essentially a Darwinian selection and mutation process.

人体等高等脊椎动物的免疫系统利用克隆选择机制产生抗体的过程在本质上是一个达尔文式的选择和变异过程。

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Further analysis revealed that the shortened protein of the two bccp isoforms is arisen from a frame-shift mutation which is caused by an adenine insertion between intron 3 and intron 4 in the gene.

深入分析后发现导致bccp2、bccp3编码蛋白长度缩短的根源在于其内含子3与4之间存在一个由碱基A插入造成的移码突变。

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The disease is caused by a mutation of the ABCR gene which leads to the degeneration of photoreceptors in the retina and vision loss.

这种疾病是由基因的ABCR从而导致了在视网膜感光细胞退化和视力减退的突变。

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The incidence of the 1555 A → G mutation in AAID and matrilineal non syndromic deafness pedigrees is fairly high.

1555A→G突变在西南地区AAID及非综合征性耳聋家系均有较高发生率。

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Objective: The experiment was designed to research the relationship between mitochondrial DNA ( mtDNA) mutation and aminoglycoside antibiotic induced deafness ( AAID) and establish a gene diagnostic method.

目的：研究线粒体DNA突变与氨基糖甙类抗生素致聋（AAID）的关系，建立相应的基因诊断方法。

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Correlation between DNA Repair Gene XPD Polymorphism and p53 Mutation

非小细胞肺癌患者DNA修复基因XPD多态性与p53基因突变的相关性研究

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Objectice: To detect the mutation and polymorphism in exon 18 in Chinese Wilson's disease gene ( WND).

目的：检测中国人Wilson病（WD）基因的第18外显子（exon18）突变及多态。

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A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay

Werner综合征的一个新的复合杂合子突变导致WRN转录下降

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The full-length of THRSP α gene of ducks cloned by the author was used to detect the polymorphism in THRSP α intron. The association of mutation locus with growth and body compositions of 238 Pekin ducks at 6 wks was investigated by PCR-RFLP method.

根据克隆出的鸭THRSPα基因全长序列，采用PCR-RFLP法检测THRSPα内含子多态与238只6周龄北京鸭生长、屠体性状的关系。

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Preliminary studies on the HPRT gene mutation of human promyelocytic leukemia cells induced by THH

昆明山海棠诱导人白血病细胞HPRT基因突变的研究

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In this study we tried to localize bad~ mutation, clone bad~+ gene, and reveal the alternative mechanism through which UUA is translated instead of bldA tRNA when it is absent.

本研究试图定位bad~-突变，克隆bad~+基因，揭示替代bldA tRNA翻译UUA密码子的途径。

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A novel nonsense mutation in a β-thalassemia gene: β￣( 37) tgg → tag

一种新的β－地中海贫血基因&密码子37无义突变

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Detection of polymorphism mutation site of TBG gene from porcine

猪TBG基因多态性突变位点的检测

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The nature of all the three mutant alleles of this group is nonsense mutation disrupting the coding region of oxt gene.

该组的三个突变体等位基因的突变都是无义突变，它们都破坏了。Xt基因的编码区。

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Result: We had not point mutation in all subjects.

结果: 所有对象均未检测到点突变.

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Not every mutation causes a genetic disorder.

不是所有的基因突变都会导致重组.

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Keratin 17 gene mutation in patients with steatocystoma multiplex

多发性脂囊瘤患者角蛋白17基因突变的研究

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Spontaneous and induced mutation occur with animals viruses.

动物病毒的突变有自发突变和诱发突变.

词典精选例句