mutation的例句大全

ConclusionG 71 R gene mutation combined with G 6 PDdeficiency aggravates the degree of neonatal jaundice.

结论G6PD缺乏与G71R基因突变并存加重新生儿黄疸程度.

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As a state between root and affix , quasi-affixes has large mutation.

类词缀是一种词根向词缀过渡的状态, 具有很大的变异性.

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cells affected by mutation

受到突变影响的细胞

《牛津高阶英汉双解词典》

The aesthetical transmutation of the pan-media era is closely associated with the new media technology.

泛媒体时代出现的审美嬗变,与新媒介技术的影响紧密相关.

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Conclusbo : It'suggsts that ras gene aed p 53 gene mutation may be related with L-form infedtbo.

结合提示L型感染参与了ras原癌基因激活和p53抑癌基因的失活.

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Objective To study the method of the artificial thigh bone permutation perioperatively for advanced age.

目的探讨高龄人工股骨头置换术围手术期的治疗方法.

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Objective To analyse the mutation of ADAR gene in a pedigree with dyschromatosis symmetrical hereditaria.

目的探讨遗传性对称性色素异常症(DSH)一家系ADAR基因突变情况.

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Conclusion The model of Fgfr 3 Gly 374 Arg mutation causing achondroplasia in mice has been established successfully.

结论成功地建立了模拟人Fgfr3-Gly374Arg点突变所致软骨发育不全的小鼠模型.

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Chromosome aberrant and some gene mutations play an important role in male infertility.

染色体畸变和基因突变在男性不育中起着重要作用.

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Mutations of Axin have been identified previously in cerebellar medulloblastomas, hepatocellular carcinomas , brest carcinoma and hepatoblastomas.

已经在人髓母细胞瘤 、 肝细胞肝癌 、 肝母细胞瘤及乳腺癌中检测到了Axin基因的突变.

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In non-coding region It'shows mutation of single nucleotide deletion or substitution.

非编码区亦存在单个碱基缺失及置换突变.

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Genetics: Color mutation-The Hypo Boa is a Co-dominant or incomplete dominant trait.

遗传学: 彩色突变 - 该次宝儿是共同主导的或不完整的主要特征.

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Aerospace mutation could be used as to obtain new entomopathogenic strain for biological control.

航天诱变为选育生物防治优良菌株提供了新途径.

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Mutation was not detected in all patients indicating that other factors be attributable to hypospadias occurrence.

不是在所有病人中均发现了突变,提示还有别的因素参与了尿道下裂的发生.

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FvL mutation may be a underlying pathogenicity of familial BCS.

FvL突变可能是家族性BCS的内因.

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Duchene's muscular dystrophy and cystic fibrosis are examples of hereditary diseases that result from nonsense mutations.

无义突变能导致肌无力和囊肿纤维化等疾病.

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Objective : To construct enhanced cyan fluorescence protein ( ECFP ) lentiviral vector using the gene multipoint mutation.

目的: 通过多点突变构建增强型青色荧光蛋白 ( ECFP)慢病毒表达载体.

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Tree structure coding is utilized and crossover and mutation are uniquely designed in this algorithm.

利用树型结构编码,设计独特的杂交算子和变异算子.

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A decimal separated coding is used so crossover and mutation is separated also.

在编码方法上,设计了十进制分离编码方式,从而杂交和变异也分离同时进行.

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The probabilities of crossover and mutation adaptively determined according to fitnesses and fitness statistics of chromosomes.

采用自适应的方法,根据个体的适配值和种群的适配值统计特性确定交叉概率和变异概率.

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