1.
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
2.
Heteroplasmy of Leber's hereditary optic neuropathy families with 11778 mutation
Leber遗传性视神经病变11778突变家系异质性的研究
3.
Extremely mutable sites are called 'hot spots'.
极端可突变的位置称为“热点”。
4.
The Genetic Analysis of Leber s Hereditary Optic Neuropathy in Chinese Pedigrees with Mitochondrial DNA Mutations;
Leber遗传性视神经病突变位点的研究
5.
Advance in research on mutations associated with HIV-1 drug resistance
HIV-1耐药性突变位点研究进展
6.
Detection of polymorphism mutation site of TBG gene from porcine
猪TBG基因多态性突变位点的检测
7.
Screening of CYP21 gene P459H mutation by PCR-ACRS
PCR-ACRS方法筛查CYP21基因P459H的突变位点
8.
Using SSR Marker to Map the Mutant Sites of the Wheat Salt-Tolerant Mutant and the Study on the Difference of Its mtDNA;
小麦耐盐突变体突变位点的SSR标记定位及其线粒体DNA差异的研究
9.
Studies on the Active Site of Arginine Kinase from Sea Cucumber Stichopus Japonicus by Site Mutagenesis;
点突变研究海参精氨酸激酶的活性位点
10.
Study on OPTN Gene Mutation in Glaucoma Family with MYOC Gene T455K Mutation;
MYOC基因T455K位点突变青光眼家系OPTN基因突变的研究
11.
Furthermore,it's same to the Homo sapiens apolipoprotein J(CLU) gene sequence in GenBank(DQ012938).
检出一个突变位点并与GenBank(DQ012938)发表序列一致。
12.
Screen of CYP21 Gene P459H Mutation in Adult Han Ethnic Group by PCR-ACRS;
PCR-ACRS法筛查成年汉族人CYP21基因P459H的突变位点
13.
Development of a DNA Biochip for Detection of Known DNA Mutations Associated with MODY2 and MODY3
MODY2和MODY3相关DNA突变位点检测集成芯片的建立
14.
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
15.
Construction of Calmodulin-binding site mutant of myosin light chain kinase
肌球蛋白轻链激酶CaM结合位点突变体的构建
16.
Rapid detection of high frequency mutational sites of Chinese Wilson's disease gene
中国人Wilson病患者基因高频突变位点的快速检测
17.
Construction of N-linked glycosylation site mutants of envelope glycoprotein genes of hantavirus
汉坦病毒包膜糖蛋白糖基化位点突变体的构建
18.
Spotting the Positions on the Genome for 4 Pathogenicity-related Mutagenic Sites of Magnaporthe Grisea and Analyzing on a Peg Deficiency Mutant;
稻瘟菌四个致病相关突变位点的定位及侵染钉缺陷突变体的初步研究