1.
Study on Mutation of Mitochondrial DNA of in Patients of Mitochondrial Myopathy and Encephalomyopathy
线粒体肌病/脑肌病的线粒体DNA突变研究
2.
Mutational Analysis of Mitochondrial DNA in Familes with Maternally Inherited Hearing Loss;
母系遗传性耳聋线粒体DNA突变分析
3.
Detection and Analysis of Mitochondrial DNA Mutation in Colorectal Carcinoma;
大肠癌线粒体DNA突变的检测与分析
4.
The New Development of the Research on the Sudden Change in Mitochondria DNA in Physiology;
生理学“线粒体DNA突变”研究的新进展
5.
Study on Mitochondrial DNA Mutations and Alteration of Copy Numbers in Breast Cancer;
乳腺癌线粒体DNA突变和拷贝数改变的研究
6.
The Study of mtDNA Mutation in Leber Hereditary Optic Neuropathy;
Leber遗传性视神经病变线粒体DNA突变的研究
7.
Development of Oligonucleotide Biochips for Detection of Mitochondrial DNA Mutations in Chinese Pedigree
线粒体DNA突变体寡核苷酸芯片的建立与运用
8.
Study of Mitochondrial DNA Point Mutation in Patients with Basal Ganglia Calcification on Cranial CT
脑CT示基底节钙化者的线粒体DNA突变研究
9.
The Study of Molecular Mechanism in Mitochondrial DNA Mutations Related Hearing Loss;
线粒体DNA突变相关的耳聋分子机制的研究
10.
The Effect of Mitochondrial DNA Mutation on the Penetrance and Visual Acuity of Leber Hereditary Optic Neuropathy;
LHON家系线粒体DNA突变与发病和预后的关系
11.
Analysis of Mitochondrial DNA Mutation in Leber Hereditary Optic Neuropathy (LHON) in Two Chinese Pedigrees;
2个Leber视神经萎缩（LHON）家系线粒体DNA突变的分析
12.
The research progress of the association of mitochondrial DNA mutation with cardiomyopathy;
线粒体DNA突变与心肌病关系的研究进展
13.
The Detection of Mutation on Mitochondrial DNA and Clinical Analysis in Leber Hereditary Optic Neuropathy--A Pedigree of 18 Person;
Leber遗传性视神经病变线粒体DNA突变检测及临床分析——一家系18人
14.
Studies on Detection of Deletion Mutation of Human Mtiochondrial DNA;
人线粒体DNA缺失突变检测的研究
15.
Study on mitochondrial DNA deletion in aging mice
衰老小鼠线粒体DNA缺失突变的研究
16.
Study of Mutations in the D-LOOP Region of Mitochondrial DNA in Acute Leukaemia;
急性白血病线粒体DNA D-LOOP区突变的研究
17.
The Research of Transfecting Mutated mtDNA of Colorectal Carcinoma Cell Line into NIH3T3 Cell Line and LST Cell Line;
突变大肠癌线粒体DNA转染NIH3T3及LST细胞的研究
18.
Mitochondrial DNA Point Mutations Studies in Hereditary Ataxia;
遗传性共济失调线粒体DNA部分点突变的研究