1.
Study of Activation of BTAK Expression in Primary Ovarian Surface Epithelial Cells Carrying Heterozygous BRCA Mutation and Tumorigenesis of Ovarian Carcinoma;
携带BRCA杂合性突变的卵巢表面上皮细胞BTAK的表达和卵巢癌发生机制的研究
2.
Expression, Mutation and LOH of Gene ING1 in Sporadic Colorectal Carcinoma;
散发性结直肠癌中ING1基因的表达、突变及杂合性缺失研究
3.
Identifying 1p LOH in Oligodendroglioma with Denaturing High Performance Liquid Chromatography
变性高效液相色谱检测少突胶质细胞瘤1p杂合性缺失
4.
Refinement of High Heterozygosity Loss on Chromosome in Sporadic Colorectal Cancer;
散发性结直肠癌高频杂合缺失精细定位及SMAD4基因突变的初步研究
5.
Expression, Mutation, and Deletion of S100A2 Gene in Gastric Carcinoma;
胃癌组织中S100A2基因的表达及突变、杂合性缺失研究
6.
Study on 10q23 LOH and Both Mutation and Expression of PTEN Gene of the Oesophageal Squamous Cell Carcinomas in Chinese Population;
中国人食管癌10q23杂合性缺失和PTEN基因突变及表达研究
7.
An Analysis of HCCS1 Gene Mutation and Loss of Hetrozygosity in Hepatocellular Carcinoma
肝细胞癌HCCS1基因突变和杂合缺失分析
8.
Research on Brittleness of Complex System Based on Catastrophe Theory;
基于突变理论的复杂系统的脆性研究
9.
Familial Hypercholesterolemia due to Mutation of Low Density Liporotein Receptor Gene
家族性高胆固醇血症患者低密度脂蛋白受体基因复合杂合突变分析
10.
Compound Heterozygosis Mutation of Low Density Lipoprotein Receptor Gene in Familial Hypercholestero-lemia Family
家族性高胆固醇血症一家系成员低密度脂蛋白受体基因复合杂合突变分析
11.
Doe to its exceeding sterility, the mutation was maintained by heterozygotes, and it was also inherited stably after five generations of self-pollination.
由于其高度不育，突变性状采用杂合体保存，经5代连续自交，均表现稳定遗传特性。
12.
The Expression of uPAR and BRCA-1 in Tissue of Epithelial Ovarian Tumour and Its Significance;
UPAR、BRCA-1在卵巢上皮性肿瘤组织中的表达及意义
13.
Research on Brittleness of Complex System Based on Cusp Catastrophe Model
基于尖点突变模型对复杂系统脆性问题的研究
14.
The Application of Catastrophe Theory in the Research of Complex System Brittleness Theory;
突变理论在复杂系统脆性理论研究中的应用
15.
Trait Investigation and Genetic Analysis of Mutant Gray-black Moth Hybrids of Silkworm
家蚕突变型灰黑蛾杂交性状调查与遗传分析
16.
Study on the Hotspot Mutations of the Wilson Disease Gene in Hunan and Multiplex PCR Reverse Hybridization Technology;
湖南地区肝豆状核变性基因突变热点和多重PCR反向杂交技术研究
17.
KCNJ5 Gly387Arg Mutation Responsible for Familial Long QT Syndrome;
KCNJ5基因Gly387Arg突变导致家族性长QT综合征
18.
Characteristics of Photosynthesis in Two Leaf Color Mutants of Rice
两个水稻叶色突变体的光合特性研究