1) MEF2A gene
MEF2A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。
2) 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][dʒi:n] [美][dʒin]
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][,pɔli'mɔ:fizəm] [美][,pɑlɪ'mɔrfɪzṃ]
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 gene
AS基因
补充资料：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。
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。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条