1.
Prevalence of cagA, cagE and cagT genes in cag pathogenicity island of Helicobacter pylori strains isolated from Shanghai patients and their clinical implications
上海地区幽门螺杆菌菌株cag致病岛基因cagA、cagE、cagT检出率及临床意义
2.
Identification and Characterization of hp0523 Gene from Cag Pathogenicity Island in Helicobacter Pylori
幽门螺杆菌Cag致病岛中hp0523基因功能的鉴定与分析
3.
Construction and identification of hp0527 gene mutant in Helicobacter pylori Cag-PAI
幽门螺杆菌Cag致病岛hp0527基因的缺失株构建和鉴定
4.
Construction of hp0523 gene mutant in Helicobacter pylori Cag-PAI and the influence on the ability of CagA protein translocation
幽门螺杆菌Cag致病岛hp0523基因的缺失及其对CagA蛋白转运能力的影响
5.
Predicting Disease Genes of Coronary Artery Disease Based on Functional Consistency
基于功能一致性预测冠心病致病基因
6.
Understanding of Underlying the Molecular Mechanism of Brachydactyly Type A-1;
A1型短指/趾症致病基因IHH的分子致病机理研究
7.
Proinsulin Gene Therapy for Diabetic Rats;
糖尿病大鼠胰岛素原基因治疗的研究
8.
The Study of Parkin and Pink1 Gene in Patients with Parkinson s Disease;
帕金森病致病基因parkin和PINK1的相关研究
9.
It occurs when a person's immune system, for unknown reaso, attacks the pancreas cells that make i ulin.
这一疾病是由于某种不确知的原因致使免疫系统损害产生胰岛素的胰岛细胞所致。
10.
Analyzing the Codon Usage Feature of Disease Genes and Predicting Disease-causative Genes;
疾病基因密码子使用特征分析及致病基因预测
11.
Molecular Genetic and Fuctional Studies of Human Diseases, Including Type Ⅱ Dentinogenesis Imperfecta (DGI)、Congenital Fibrosis of the Extraocular Muscles Type 1 (CFEOM1), Long QT Syndrome and Atrial Fibrillation;
几种单基因遗传病致病基因的突变和功能研究
12.
Molecular identification and homology analysis of genes clustered in a genomic glycosylation island of Xanthomonas oryzae pv.oryzae.
水稻白叶枯病菌糖基化岛GI基因的分子鉴定
13.
Pathogenic Gene and Mutation Site of Left Ventricular Noncompaction
左室心肌致密化不全的致病基因及突变位点
14.
Studies on the Mechanism of Directional Selection of Curvularia Lunata Virulence Differentiation and Virulence Gene Identification;
玉米弯孢叶斑病菌致病性分化定向选择机理与致病相关基因鉴定
15.
Pathogeniticy and Sequence Difference of GMK1 Gene in Gaeumannomyces Causing Wheat Take-All Disease;
小麦全蚀病菌致病性分化与致病基因GMK1核苷酸序列比较的研究
16.
Nowadays the pathogenesis of CFEOM has been studied in clinical pathology and molecular genetics fields, and researchers have found that it is a kind of primary neuropathy with secondary myopathic changes and that it has 3 genetic loci and 1 disease gene.
并发现3个遗传位点和1个致病基因。
17.
Detection of partial virulence determinants and phenotypes in Enterococci
肠球菌部分致病基因和表型的检测
18.
Mutation Analysis on the Pathogenic Gene for Van Der Woude Syndrome
范德伍兹综合征致病基因的突变检测