1) TBX1 gene
TBX1基因
1.
Association analysis between TBX1 gene and human conotruncal defects.;
TBX1基因与人类圆锥动脉干畸形相关性的研究
2.
Objective To investigate the mutations of TBX1 gene in Chinese patients with congenital heart defects(CHD),and study the relationship between mutations of TBX1 gene and nonsyndromic CHD.
目的检测中国先天性心脏病患者TBX1基因突变以探讨TBX1基因突变与非综合征心脏畸形发生的相关性。
2) TBX1
TBX1基因
1.
TBX1 Gene and Chromosome 22q11.2 Microdeletion Syndrome;
TBX1基因与染色体22q11.2微缺失综合征
2.
Objective To explore the regulatory mechanism of retioic acid induced by Shh and Fgf8 on the TBX1 expression in myocardial cells in the chromosome 22q11.
2微缺失综合征中心肌细胞TBX1基因的调节机制。
3.
Objective To study the regulatory mechanism of retinoic acid(RA) on the Tbx1 expression in cardiomyocytes.
目的研究视黄酸(RA)对心肌细胞Tbx1基因表达的影响。
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