gene mutation的例句大全

Background and Aim: Carcinoma is a type of multi-gene disease, and a complex process involved multi-factor, multi-stage and multi-gene mutation, which caused by activation of telomerase and cancer gene, devitalization of suppressor gene.

背景和目的：研究表明，肿瘤是一类多基因疾病，是由于端粒酶激活、癌基因激活或抑癌基因失活等引发的多因素、多阶段及多基因变异的综合病变过程。

Distribution of coagulation factor V gene mutation 1691 a in populations of different races

凝血因子V基因点突变1691A在不同种族人群中的分布

Analysis of Rb gene mutation in squamous cell carcinoma of larynx

喉鳞癌组织中Rb基因突变的分析

In 19 cases of TSCC with p53 gene mutation, the mutation was located in exon 5 in 12 cases, in exon 6 in 7, in exon 7 in 2 and in exon 8 in 15, respectively.

突变的19例舌癌，12例出现第5外显子突变，7例出现第6外显子突变，2例出现第7外显子突变，15例出现第8外显子突变。

Influence of individual radiation sensitivity on GPA gene mutation frequency in medical diagnostic X-ray workers

个体辐射敏感性对医用X射线工作者GPA基因突变频率的影响

Study and Analysis of Coagulation Factor V 1691G → A Gene Mutation

凝血因子V169G→A基因突变的研究分析

Conclusion The total of 11 types of gene mutation in β-thalassanemia carriers are multiple in Shenzhen area.

结论深圳地区β地中海贫血患儿珠蛋白基因缺陷类型共有11种，呈现多样性。

Objective: To detect and evaluate the TK gene mutation induced by genistein.

目的：用小鼠淋巴瘤细胞TK基因突变试验检测染料木素的诱变性。

Conclusion: RB gene mutation takes part in the development of laryngeal carcinoma.

结论：RB基因突变在喉癌的发生发展中起着一定的作用；

Studies on Gene Mutation Rate of Different Sex and Phylogeny of Sheep and Goats

绵山羊不同性别的基因突变率及其系统进化的研究

Conclusions FH is an euchromosome dominant genetic disease that is caused by the defective LDLR resulted from gene mutation.

结论：FH是一常染色体显性遗传性疾病，为基因突变导致LDLR缺陷所致的遗传性疾病。

The drinking water of photochemical disinfectant had no effect on gene mutation in Ames test, and didn ′ t make increase micronucleus formation of mice bone marrow and sperm deformity in the teratogenesis test of mice.

Ames试验结果是光化学消毒的饮用水无菌株基因突变作用，Ames试验结果阴性。在小鼠骨髓PCE微核试验中，光化学消毒水对小鼠无致骨髓PCE微核发生率升高的作用。

Gene Mutation Study of activating protein C resistance and Acv in arterial thrombosis

动脉血栓性疾病抗活化蛋白C和凝血因子Ⅴ基因突变的研究

aim: to investigate the point mutation at codon 54 of mannose binding lectin ( mbl) gene, detect the plasma mbl level, and analyze the correlation between the gene mutation frequency and plasma mbl concentration.

目的：初步调查健康蒙古族人甘露（聚）糖结合凝集素（MBL）基因54位密码子点突变的情况，检测其血浆MBL的含量，探讨两者的相关性。

Thymidine kinase gene mutation assay-comparison of microwell method and soft agar method

TK基因突变试验&琼脂平皿法与微孔平板法的比较

Discussion on Cloning Method for Detecting the HPRT Gene Mutation of Rats

克隆法检测大鼠体细胞HPRT基因突变探讨

Preliminary study of gene mutation in cytoplasmic loops of the thyroid stimulating hormone receptor among papillary thyroid cancer patients

促甲状腺激素受体胞内环基因突变与乳头状甲状腺癌发病的相关性研究

Objective To investigate the keratin 9 gene mutation in epidermolytic palmoplantar keratoderma ( EPPK) and its relationship with clinical manifestations.

目的探讨表皮松解性掌跖角化症家系的KRT9基因突变与临床表现的关系。

Relationship Between the ras Gene Mutation and Tissue Differentiation in the Invasive Hydatidiform Mole

ras基因突变与侵蚀性葡萄胎组织分化的关系研究

In 30 cases of thalassemia minor, there were 28 cases of gene mutation heterozygotes, 2 cases of which were dual gene mutations, and 5 cases of thalassemia major were all dual gene mutations.

30例轻型β地贫中，28例为基因突变杂合子，2例是双重基因突变子；5例重型β地贫中，均为基因双重突变子。