MEF2A基因,MEF2A gene英语短句,例句大全

MEF2A基因,MEF2A gene
1)MEF2A geneMEF2A基因
1.Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease;中国冠状动脉粥样硬化性心脏病患者MEF2A基因的新突变研究
2.Objective To explore the variation of the exon 11 of MEF2A gene in patients with acute myocardial infarction(AMI).目的研究MEF2A基因第11外显子在普通急性心肌梗死(简称心梗)患者中的变异情况。
3.To understand the relationship between SNPs of MEF2A gene and carcass traits in chicken,three SNPs loci in MEF2A gene were detected by PCR-SSCP method in 240 Daheng quality meat chicken and its genetic effects on 9 carcass traits were also analyzed.为了解优质鸡MEF2A基因SNPs与屠体性状的相关性,以240只大恒优质肉鸡为材料,应用12对引物,采用PCR-SSCP技术对肌细胞特异性增强子因子2A(MEF2A)基因进行多态性检测。

英文短句/例句

1.Study on Cloning and Expression of Pig MEF2A Gene;猪MEF2A基因的克隆及表达规律的研究
2.Novel Mutaions and Polymorphisms Study of MEF2A in Chinese Patients with Coronary Artery Disease;中国冠心病患者MEF2A基因的新突变和基因多态性研究
3.Study on Association of Single Nucleotide Polymorphism of MEF2A Gene with Carcass Traits in Chicken优质鸡MEF2A基因的SNPs检测及其与屠体性状的相关研究
4.Research on Expression of MEF2 Gene in Muscle TissueMEF2a基因在肌肉组织中的表达研究
5.Role of Myocyte Specific-enhancer Factor 2A in Zebrafish Cardiac and Somite Development;肌肉细胞特异性增强因子2A（MEF2A）在斑马鱼心脏和体节发育中的作用
6.Biological function analysis of rarely found MEF2A mutations in exon 11MEF2A第11号外显子四个特殊变异位点的生物学活性研究
7.Association of CAG Repeat Length Variations in Exon11 of MEF2A with the Protein's Transcriptional Activation AbilityMEF2A第11号外显子CAG三联核苷酸重复序列的改变与其转录激活活性的相关性
8.extinguisher loci消失基因座，绝灭基因座
9.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
10.Genes are described as DOMINANT or RECESSIVE.基因分为显性基因和隐性基因。
11.hypomorphic allele次等位因素对偶基因
12.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
13.Research on Hte Microarray Based Gene Mining Algorithm;基于基因表达谱的基因挖掘算法研究
14.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
15.Genetic material produced by gene-splicing.重组基因材料基因分割而产生的基因材料
16.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。
17.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
18.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

相关短句/例句

predisposing gene MEF2A易感基因MEF2A
1.Some new factors is playing an important role in the genesis and development of this disease,which includes predisposing gene MEF2A,high fibrinogen,high homocysteine,adiponectin,leptin,infections,inflammation,character,heart rate and socioeconomic status and so on.一些新的危险因素如易感基因MEF2A、高纤维蛋白原、高同型半光氨酸、脂联素、瘦素、感染、炎症、性格、心率、社会经济地位在冠状动脉粥样硬化性心脏病的发生和发展中起重要的作用。
3)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
4)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
5)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。
6)AS geneAS基因