Rap2b基因,Rap2b gene英语短句,例句大全

Rap2b基因,Rap2b gene
1)Rap2b geneRap2b基因
1.1-Rap2b eukaryotic expression vector, to understand the effects on AKT,ERK,JNK and P38 signaling pathway of NIH3T3 cells Through transfecting Rap2b gene into NIH3T3 cells.结论Rap2b基因外源性高表达可能对P38通路有活化作用,对JNK、ERK、AKT通路无活化作用。
2.The aim of this study is to explore the roles of RAP2B gene in carcinogenesis.作为具有保守结构域的Ras超家族成员,RAP2B基因在肿瘤发生发展中的作用仍属未知。

英文短句/例句

1.Construction of eukaryotic expression vector of Rap2b and its effects on the pathway of NIH3T3 cellsRap2b基因真核表达载体构建及其对NIH3T3细胞P38通路的影响
2.Identification and Functional Analysis of A Novel Candidate Oncogene RAP2B in Lung Cancer新的肺癌候选癌基因RAP2B的鉴定和功能研究初探
3.Bioinformatic analysis on the Rap2B-like gene from Clonorchis sinnensis and its cloning and expression华支睾吸虫Rap2B样基因的生物信息学分析及其克隆、表达
4.Study on the Expression of rap2b in Lung Carcinoma;rap2b在肺癌中的表达及其意义
5.extinguisher loci消失基因座，绝灭基因座
6.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
7.Genes are described as DOMINANT or RECESSIVE.基因分为显性基因和隐性基因。
8.hypomorphic allele次等位因素对偶基因
9.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
10.Research on Hte Microarray Based Gene Mining Algorithm;基于基因表达谱的基因挖掘算法研究
11.Human Genome Project,Post-genome Research and Gene Medicine --New Century of Diagnosis,Pharmaceutics and Therapy with Gene Technique;人类基因组计划、后基因组研究与基因医学——基因诊断、基因制药与基因治疗的新世纪
12.Genetic material produced by gene-splicing.重组基因材料基因分割而产生的基因材料
13.Gene distribution was out of balance. Dominant genes were more than recessive ones.基因的分布是不对称的,显性基因多于隐性基因。
14.Association of apoE Gene, A2M Gene and ACE Gene Polymorphism with Alzheimer s Disease;apoE基因、A2M基因、ACE基因与汉人Alzheimer病的相关性研究
15.Study on Inheritance of the Quality Transgenes Over-expressed in Transgenic Wheat;转基因小麦外源基因品质基因表达的遗传研究
16.Legal Research on Gene Science and Technology--Does Gene Belong to Invention or Discovery;基因科技的法律问题研究——“发明”基因?“发现”基因?
17.Mapping of Genetic Modifiers of Eyal~(bor/bor) Mice定位Eyal~(bor/bor)基因型小鼠Eyal基因的遗传修饰基因
18.Analyses of Genome-wide Disease Resistance Genes and Their Expansion in Medicago truncatula蒺藜苜蓿全基因组抗病基因和基因扩张分析

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。