1.
Construction of the eukaryotic vector carrying human dominant negative epidermal growth factor receptor,its expression and sub-cellular localization in COS-7 cells
人EGFR显性负性突变体真核表达载体的构建、蛋白表达及亚细胞结构定位
2.
Construction and validation of adenovirus expressing dominant negative TGF-β type Ⅰ receptors
显性负性突变型TGF-β Ⅰ型受体腺病毒的构建和功能验证
3.
DNA-negative mutant
ＤＮＡ－负性突变型
4.
Dominant-Negative Suppressor of Cytokine Signaling 1 Enhancement on Antiviral Activity of Interferon-Gamma against Coxsackie B_3 Virus in Vitro
负显突变体细胞因子信号转导抑制物-1增强干扰素-γ体外抗柯萨奇病毒活性
5.
Adenovirus-mediated Novel Dominant Negative Survivin D71A Inhibited Growth of Human Prostate Cancer Cells in Vitro and in Vivo;
新型Survivin显性负突变体D71A抑制前列腺肿瘤细胞体内外生长的实验研究
6.
A Study on Anti-wt-HBV Dominant Negative Mutants Constructed by Interfering Mutation in Replication;
利用复制干扰突变构建具有抗HBV作用的显性阴性突变体研究
7.
Theeffect of dominant lethal mutation is higher than that of the aneuploid.
显性致死突变的效应比非整倍体胚胎的效应高。
8.
Analysis of the mutations of rhodopsin gene in autosomal dominant retinitis pigmentosa family
常染色体显性遗传视网膜色素变性家系视紫红质基因突变分析
9.
Missense mutation in the βB1-crystallin gene caused autosomal dominant congenital cataract in China
晶状体蛋白βB1基因错义突变引起常染色体显性遗传性白内障
10.
Candidate Gene Screening for Autosomal Dominant Auditory Neuropathy in a Chinese Pedigree;
常染色体显性遗传性听神经病家系候选基因突变筛查
11.
Genetic Mapping and Mutation Analysis in Chinese Family with Congenital Cataract;
单纯常染色体显性遗传性白内障致病基因的定位及突变研究
12.
Screening Mutation of Related Genes in a Family with Autosomal Dominant Genetic Pulverulent Cataract
常染色体显性遗传性粉尘状白内障一家系的相关基因突变筛查
13.
The ultrastructure of the retina showed extensive and severe degeneration in the photoreceptors,parti cularly in outer segments and mitochondrias. Lipofuscin granules were accumulated in the cytoplasm.
感光细胞的超微结构有明显变性改变，尤以外节变性、线粒体变性、胞浆内脂褐素沉着为突出。
14.
Mutation Analysis of Retinitis Pigmentosa I Gene in Chinese Patients with Autosomal Dominant Retinitis Pigmentosa
常染色体显性遗传视网膜色素变性家系视网膜色素变性1基因（RP1）的突变分析
15.
Penetrance and mutations of mitochodrial DNA 11778 in Chinese Leber's hereditary optic neuropathy patients of Han nationality
中国汉族Leber遗传性视神经病线粒体DNA 11778位点突变与外显率分析
16.
Gene Localization and a Novel Mutation Identified for Non-syndromic Hearing Loss;
常染色体显性遗传非综合症型耳聋基因的定位与突变筛查
17.
Mutations in the Exon A of Androgen Receptor Gene in Males with Idiopathic Azoospermia and Severe Oligozoospermia;
雄激素受体基因外显子A突变与特发性无精及严重少精关系的研究
18.
A Pilot Study of HSF1(+) on the Prevention and Curation of Parkinson's Disease
热休克因子1正显性突变体对防治帕金森病的研究