gene mutation

Objective : To study the effects of propolis against gene mutation induced by powerful mutagens in mice.

目的: 探讨蜂胶对环磷酰胺等强诱变剂诱发基因突变的抑制作用.

Objective : To detect ED 1 gene mutation in three hypohidrotic ectodermal dysplasia ( HED ) nuclear families.

目的: 研究少汗性外胚叶发育不全引起先天缺牙的ED1基因突变.

Objective To study the biological significance of HBV preC/ C gene mutation.

目的研究WBV前C／C区基因变异的生物学意义。

Gene mutations in human gene can cause various diseases. The human autosomal dominant brachydactyly type B ( BDB) and autosomal dominant polycystic kidney disease ( PKD) are due to gene mutation on chromosome.

人类基因组上基因的突变可以引起各种各样疾病的发生，人的常染色体显性的B型短指和常染色体显性的多囊肾综合症就是由于染色体上的基因突变引起的。

How can a single gene mutation lead to a complex psychiatric phenotype?

点基因突变如何造成复杂的精神疾病表现型?

Mutation of DNA polymerase β gene in human nasopharyngeal cancer

DNA聚合酶β基因在鼻咽癌中的突变

Methods The peripheral lymphocytes from 20 workers exposed to mercury and 20 controls were measured with micronucleus test, comet assay, hprt gene mutation test and TCR gene mutation test.

方法选择荧光灯生产厂汞作业工人20名为接触组，无汞接触的其他从业人员20名为对照组，取外周血淋巴细胞，通过微核试验、彗星试验、hprt和TCR基因突变试验进行检测。

Methods Twenty-six cases of nasopharyngeal carcinoma tissues and control epithelial tissues were collected to study DNA pol β gene mutation with PT-PCR, PCR-SSCP and DNA sequence analyzing technique.

方法采用RT-PCR法（逆转录DNA聚合酶链反应）、PCR SSCP（聚合酶链单链构象多态性分析）、DNA序列分析法对26例鼻咽癌组织及癌旁组织标本进行polβ基因突变研究。

Objetive : To detect the gene mutation of a patient with anhidrotic ectodermal dysplasia.

目的: 检测无汗性外胚层发育不全患者的EDA基因 的突变.

Ras gene mutation in childhood AML was mainly found in M 2 , M 4 , M 5 subtypes.

AML患儿中ras基因突变多见于M2 、 M4及M5型.

Study on Mutation, Expression and Regulation of DNA Polymerase Beta Gene in Prostate Cancer

前列腺癌DNA聚合酶β基因突变、表达及其调控研究

The frequency of two CETP gene mutation had no significant difference in patients and controls.

心梗、脑卒中患者两种CETP基因突变频率与健康人无差别。

Cells with Ras gene mutation or transformed by Ras become resistant to p 53 dependent apoptosis.

Ras基因转染或突变的细胞能够对DNA损伤 引起的p53依赖性凋亡产生抗性.

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.

Low Density Lipoprotein Particle Size in Patients with CETP Gene Mutation Increases

胆固醇酯转运蛋白基因突变患者低密度脂蛋白亚组分颗粒直径增大

Variations of flower color are related to gene mutation and pollination pattern and so on.

研究认为,花色变异与基因突变、传粉机制等因素有关.

Study on DNA polymerase β gene mutation in human esophageal cancer tissues from high incidence area

食管癌高发区人食管癌组织中DNA聚合酶β基因突变检测

Objective To detect the activity of transglutaminase 1 ( TGM 1 ) and gene mutation in a family with lamellar ichthyosis.

目的检测一板层状鱼鳞病家系中患者转谷氨酰胺酶1的活性及其编码基因的突变.

Conclusion Abore point mutation is an inherited gene mutation.

结论表明该突变为一遗传性突变.

Relationship between M2 gene mutation and amantadine resistance in influenza virus

流感病毒M2基因变异与盐酸金刚烷胺耐药性的关系

The Ames test, Erythrocyte micronucleus assay, Spermatogonial chromosomal aberrations test and In vitro mammalian cell gene mutation test were used.

采用鼠伤寒沙门氏菌回复突变试验（Ames试验）、小鼠骨髓多染红细胞微核试验、小鼠睾丸精母细胞染色体畸变试验、V79细胞基因突变试验来检测有无致突变作用。

Conclusion There is K 14 1 A domain gene mutation in this DM-EBS pedigree.

结论本DM-EBS家系存在K14的基因突变.

Gene Mutation Analysis in Chinese Patients with Ectodermal Dysplasia

外胚层发育不良的基因突变研究

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.

If the suppressor gene mutation may lead to disorders and cancerous cell growth.

如果抑癌基因发生突变,也可导致细胞生长失调而发生癌变.

Objective To study the gene mutation in a pedigree with Dowling-Meara type epidermolysis bullosa simplex ( DM-EBS ).

目的研究Dowling-Meara亚型单纯型大疱性表皮松解症 ( DM -EBS ) 一家系的基因突变.

Occult Hepatitis B Virus Infection: Analysis of HBV Gene Mutation

隐匿性乙型肝炎病毒感染：HBV基因变异分析

HBV gene mutation along different types of TCM syndrome are detected by microarray assay.

基因芯片检测慢性乙型肝炎不同证候的HBV前 C区基因变异.

Mutation of p53 gene and human papillomavirus infection in cervical carcinoma

宫颈癌组织中乳头瘤病毒感染及抑癌基因p53突变的检测

Objective : To identify gene mutation in a family with Weber-Cockayne type epidermolysis bullosa simplex ( WC-EBS ).

鉴定单纯型大疱性表皮松解症Weber -Cockayne 亚型 一家系中的基因突变位点.