mutation的例句大全

The Transcriptional Regulation Study on Human δ Globin Gene with CAAT Box C → T Point Mutation in Its Promoter

人δ珠蛋白基因启动子区CAAT盒C→T突变对其转录的影响

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This paper presents a technique for using mutation analysis to test the semantic correctness of XML-based component interactions.

本文提出一种变异分析技术来测试基于XML的网络异构组件交互的语义正确性。

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The results indicated that high mutation rates in STR loci should be considered when STR genotyping are applied to paternity test.

结果提示：用STR基因座进行亲子鉴定，必须考虑STR基因座突变因素。

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Dominant Lethal Mutation Test of Organic Sulfur

有机硫农药毒性试验显性致死突变试验

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Theeffect of dominant lethal mutation is higher than that of the aneuploid.

显性致死突变的效应比非整倍体胚胎的效应高。

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Dominant lethal mutation in mice induced by low dose tritiated water

低剂量氚水诱发雄性小鼠显性致死突变的研究

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Relationship between chromosomal aberration of germ cells and dominant lethal mutation in male mice after low dosage of X-irradiation

小剂量X射线诱发雄性小鼠生殖细胞染色体畸变与显性致死间关系

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The frequency of dominant lethal mutation induced by X-irradiation is 2.1995 × 10-3 gamete · 10mGy.

X射线在该期诱发的显性致死突变率是2.1995×10~（-3）/（配子·10mGy）。

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The study has provided theoretical basis in induced mutation medial lethal dose of different wheat varieties ( strains) to Ar+ implantation.

本项研究可为Ar+注入不同小麦品种（系）发生诱变的半致死剂量提供实验依据。

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A Study on UV Induced Screening of High Actinomycin X_2 Producing Strain by Lincomycin-resistant Lethal Mutation

放线菌素X2高产菌株的抗药性致死突变标志的诱变筛选研究

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Bovine leukocyte adhesion deficiency ( BLAD) is autosomal recessive disease. The pathogeny of BLAD is genic mutation of CD18-integrins on the leukocyte.

牛白细胞粘附缺陷病（BLAD）是一种常染色体单基因隐性遗传疾病，病因为白细胞表面整合素CD18亚单位基因突变所致。

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Molecular Cloning and Mutation Site Analysis of LPL Gene in Swine

猪LPL基因部分序列的克隆及多态性分析

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Conclusion LPL and β_3-AR mutation play role independently in the lipids metabolism of body.

结论LPL和β3-AR基因变异对机体脂质代谢的作用是相互独立的。

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The missense mutation between ADR nc-1and ADW or ayw is higher than between the different strains of adr.

不同亚型间的错义突变比同一亚型不同毒株间的错义突变多。

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CONCLUSION: GCH 1 gene mutation is only one of reasons to the DRD patients onset.

结论: GCH-1 基因突变只是部分DRD患者的发病原因.

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In this paper a modification of GA which introduces adaptive mutation is proposed to solve EAP.

鉴于此,提出一种信息素指导下的自适应变异方法求解专家分配问题.

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Meanwhile , chaos mutation adopted in order to increase the diversity of particles of PSO.

为有效保证PSO算法的粒子多样性, 在迭代过程中加入混沌变异.

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Conclusion The study on mutation of GFAP gene in Chinese patients with Alexander disease has never been reported previously.

结论此次发现为国内首例中国亚历山大病患者GFAP基因突变报告；

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Mutation Analysis of the IHH gene in two Chinese Families with Inherited Syndactyly and Adactylism

两个先天性并指缺指中国家系IHH基因的突变检测

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The results indicate that the mutation in coding region of IHH gene do not cause human Syndactyly and Adactylism disease in the two families.

研究认为这两个家系的致病原因并非IHH基因编码区的突变引起。

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