1.
The Relationship among HBV-associated Histopathological Indexes, X Gene Mutations and Prognosis in Patients with Chronic Hepatitis B Infection;
慢性乙型肝炎组织病理学指标及病毒X基因变异与患者预后的相关性研究
2.
The Functional Differences between Hepatitis B Virus X Proteins and Related Mutants with Genotype B and C;
B、C基因型乙型肝炎病毒X蛋白及其变异体的功能差别研究
3.
Association of X Gene C1485T Mutation with Hepatocellular Carcinoma in Chronic Hepatitis B Virus Infection
乙型肝炎病毒X基因C1485T变异与肝细胞癌发生相关性研究
4.
The mutation of hepatitis B virus X gene in the liver tissues of hepatocellular carcinoma patients
原发性肝细胞癌患者肝组织中乙型肝炎病毒X基因的变异
5.
Hepatitis B virus X gene mutation and hepatocellular carcinoma
乙型肝炎病毒X基因突变与肝细胞癌
6.
The study on the variance of HCV E protein gene and significance of the variance
HCV E蛋白基因的变异及变异的意义
7.
Heteroepitaxial growth of InP/GaAs using low-temperature In_xGa_(1-x)P graded buffers
基于低温In_xGa_(1-x)P组分渐变缓冲层的InP/GaAs异质外延
8.
Genomic Variation Induced by Polyploidization of Wheat;
小麦异源多倍体化诱导的基因组变异
9.
Variation in the PPARα Gene (V227A) Associates with Dyslipidemia;
PPARα V227A基因变异与血脂异常的关系
10.
The Association of C2528G Polymorphism of the PPAR Alpha Gene with Dyslipidemia;
PPARαC2528G基因变异与血脂异常的相关性
11.
The Association of -75bp/+83bp Polymorphism of the ApoA_1 Gene with Dyslipidemia
ApoA_1基因-75bp/+83bp变异与血脂异常的相关性
12.
Genetic Variation on LPL Gene and A-FABP Gene;
猪LPL基因和A-FABP基因遗传变异研究
13.
Analysis of four new variant alleles at FUT2 locus;
FUT2基因座4个新变异等位基因的分析
14.
Medical Research and Gene Detection in a Family with X-linked Liphoproliferative Disease;
X-连锁淋巴细胞异常增生症—家庭临床调查和基因检测
15.
Abnormal genes mutating is the pathogeny of cancer.
癌症的病因就是反常的基因变异。
16.
The Changes of Gene Expression of Potassium Channels Kv9.X and Effects of Different Medicines on Their Changes in Post-MI Rat Heart;
心肌梗死后大鼠钾通道Kv9.X基因表达变化及药物干预机制的研究
17.
Detection of EDA Gene Mutation in a Pedigree of Han Nationality in Xinjiang with X-linked Hypohidrotic Ectodermal Dysplasia (XLHED);
一新疆汉族X连锁少汗性外胚叶发育不全（XLHED）家系EDA基因突变检测
18.
Mutations of the SEDL Gene in X-linked Spondyloepiphyseal Dysplasia Tarda;
X-连锁迟发性脊椎骨骺发育不良SEDL基因突变研究