hOGG1基因,hOGG1 gene
1)hOGG1 genehOGG1基因
英文短句/例句

1.Exploring of Down-regulated Expression of hOGG1 Gene in Pathogenesis and Therapeutic Mechanism of Lung Cancer;hOGG1基因低表达在肺癌发病及治疗机制中的探索
2.Study on Relationship between hOGG1 Genetic Polymorphism and Susceptibility of Esophageal Carcinoma in Kazakh and Han in XinjianghOGG1基因多态性与新疆哈、汉民族食管癌易感性的研究
3.Study on in Vitro Cleavage Activity and Transient Effects on A549 Cells of Hammerhead Ribozyme Targeting to Base Excision Repair Gene hOGG1;hOGG1基因特异性锤头状核酶体外切割活性及其在A549细胞内瞬时效应的研究
4.Genetic Polymorphism in HOGG1 and Susceptibility to Chronic Atrophic Gastritis, Gastric Cancer;HOGG1在萎缩性胃炎及胃癌中基因多态性分析
5.Study on the Relationship between the Genetic Polymorphism in hOGG1, p53 and Susceptibility to Lung Cancer;hOGG1、p53基因多态性与肺癌遗传易感性关系研究
6.Primary research on the association between the polymorphism of hOGG1 gene and the infection susceptibility of HIV-1DNA修复基因hOGG1多态性与HIV-1易感性的关系研究
7.Effect Potassium Dichromate Exposure on hOGG1 and hMTH1 Gene Expression in Human Lung Epithelial Cell;重铬酸钾对人肺上皮细胞hOGG1及hMTH1基因表达的影响
8.The Study of the Relationship between the Polymorphism of hOGG1 Genes and XPD Genes and Susceptibility to Lung CancerhOGG1、XPD基因多态性与宣威肺癌遗传易感性的关系研究
9.Relationship between hOGG1 gene polymorphism and the susceptibility of esophageal cancer in Kazakh nationalityDNA修复基因hOGG1多态性与新疆哈萨克族食管癌易感性的研究
10.Association of hOGG1 Polymorphism Ser326Cys between the Susceptibility of Esophageal Cancer and Its Clinicopathological CharacteristicshOGG1 Ser326Cys基因多态性与食管癌及其临床病理特性的关系
11.Single-Nucleotide Polymorphisms in DNA Repair Gene hOGG1 and APE1 and Susceptibility to Hepatocellular CarcinomaDNA修复基因hOGG1和APE1单核苷酸多态性与肝细胞癌遗传易感性关系的研究
12.The implications of hOGG1 expression in hepatocellular carcinoma and cirrhosis tissueshOGG1在原发性肝癌和肝硬化组织中的表达及意义
13.extinguisher loci消失基因座,绝灭基因座
14.Of, relating to, produced by, or being genes or a gene.基因的基因的,与基因有关的,基因产生的
15.Genes are described as DOMINANT or RECESSIVE.基因分为显性基因和隐性基因。
16.hypomorphic allele次等位因素对偶基因
17.Studies on Polymorphism of Prolactin Receptor Gene and Follicle-Stimulating Hormone Beta Subunit Gene in Swine;猪PRLR基因和FSHβ亚基基因多态性研究
18.Research on Hte Microarray Based Gene Mining Algorithm;基于基因表达谱的基因挖掘算法研究
相关短句/例句

gene[英][d?i:n][美][d?in]基因
1.Study of the Preparation and the Characteristics of pRc/CMV-BChE Gene-chitosan nanoparticles ①;丁酰胆碱酯酶基因-壳聚糖纳米粒初步研究
2.Correlation between traditional Chinese medicine syndromes in primary immunoglobulin A nephropathy and A267G in 5'-untranslated region within exonal of megsin gene;Megsin基因E1-5’UTR区A267G与免疫球蛋白A型肾病阴虚证的相关性
3.Study on gene chip of leiomyoma of uterus;子宫肌瘤基因芯片的研究
3)Genes基因
1.Study on Apoptosis of Human Leukemia Cells and Its Related Genes Regulation Induced by ~(235) U;浓缩铀诱发细胞凋亡的形态及基因调控
2.Screening of lymphatic metastasis-associated genes in esophageal squamous cell carcinoma;食管癌淋巴结转移相关基因筛选的研究
3.Study on the Genotyping of Aminoglycoside Modifying Enzymes Genes from Pan-drug Resistant Acinetobacter Baumannii.;泛耐药鲍曼不动杆菌氨基糖苷类修饰酶基因研究
4)Polymorphism[英][,p?li'm?:fiz?m][美][,pɑl?'m?rf?zm?]基因
1.The Study on Apolipoprotein E Gene Polymorphism Characteristics of Cerebral Infarction and Intracerebral Hemorrhage;脑梗死与脑出血apoE-基因多态性特点研究
2.The Relations of Gene Polymorphisms of eNOS and FⅦ with Coronary Heart Disease in Henan Han Population;河南汉族人群一氧化氮合酶和凝血因子Ⅶ基因多态性与冠心病相关性分析
3.Methods:Polymorphism of the 677th site C/T of MTHFR gene and the 66th site A/G of MTRR gene were detected by polymerase chain reaction-restrction fragment length polymorphism in disease group(n=64) and normal controls(n=104).目的:研究同型半胱氨酸相关酶中亚甲基四氢叶酸还原酶(MTHFR)及蛋氨酸合成酶还原酶(MTRR)基因的多态性与先天神经管缺陷的关系。
5)AS geneAS基因
6)Genetic[英][d??'net?k][美][d??'n?t?k]基因
1.Antigenic and genetic characterization of A/Shenzhen/1/99(H3N2) virus;A/深圳/1/99(H3N2)病毒抗原性及基因特性研究
2.Relationship between the genetic polymorphisms of VDR and susceptibility to pulmonary tuberculosis among the Chinese Han population维生素D受体基因多态性与汉族人肺结核发病的关系
3.MTHER genetic C677T polymorphisms were determined by PCR-RFLP.N5, 10 亚甲基四氢叶酸还原酶(MTHFR)是参与甲硫氨酸-叶酸代谢的关键酶,其基因677位点C→T错义突变可造成此酶活性降低,导致高同型半胱氨酸血症,现已证明高同型半胱氨酸是诱发胎儿出生缺陷和心血管疾病的一个独立危险因素。
延伸阅读

J基因分子式:CAS号:性质:为免疫球蛋白V区与C区之间的连接区(J区)编码的基因。