1.
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
2.
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
3.
Another hot point mutation of Wilson disease gene in Chinese: exon 12
肝豆状核变性基因12号外显子突变特征的研究
4.
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。
5.
Emphasizing a display element or segment by modifying its visual attributes.
通过改变显示属性以突出某一显示单元或一段文字的方法。
6.
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
7.
Study on Mutation in Exon 8 of ATP7B Gene in Chinese Patients with Wilson Disease
中国人肝豆状核变性ATP7B基因8号外显子突变研究
8.
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。
9.
The dominant allele usually controls the normal form of the gene, while mutations are generally RECESSIVE.
显性基因通常控制基因的一般形式，而突变通常是隐性的。
10.
Dominant Dystrophic Epidermolysis Bullosa: Mutation Analysis;
显性营养不良型大疱性表皮松解症的基因突变研究
11.
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
12.
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
13.
BRCA1 Gene Exon2 and Exon20 Mutation Detection of Familial Breast Cancer and Early-onset Breastcancer from Qingdao in CHINA
青岛地区家族性及早发性乳腺癌BRCA1基因第2，20外显子突变研究
14.
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
15.
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
16.
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
17.
A STUDY ON MUTATION OF BRCA1 GENE EXON2 AND EXON20 OF FAMILIAL AND EARLY-ONSET BREAST CANCER
家族性及早发性乳癌病人BRCA1基因外显子2和20突变研究
18.
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