1) mitochondrial diseases
线粒体疾病
1.
Nuclear genes and mitochondrial genes associated with mitochondrial diseases;
线粒体疾病与核基因-线粒体基因的表达调控
2.
MtDNA mutations were necessary for mitochondrial diseases that caused by mitochondrial dysfunction,but not sufficient to induce the pathology.
因线粒体功能缺陷导致的线粒体疾病,涉及线粒体基因组突变、核基因突变、及环境因素等复杂机制,深入阐明三者的相互作用关系具有重要的理论意义,进而指导线粒体疾病的诊断、预警、和治疗等,具有重要的潜在应用价值。
3) Mitochondria and Human Disease
线粒体与人类疾病
4) mitochondrial diseases
线粒体病
6) mitochondrial myopathy
线粒体肌病
1.
Chronic progressive external ophthalmoplegia type of mitochondrial myopathy(report of 3 families);
慢性进行性眼外肌瘫痪型线粒体肌病(附3个家系报告)
2.
Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy;
线粒体肌病患者线粒体DNA的突变分析
3.
Mitochondrial myopathy and mitochondrial encephalomyopathy;
线粒体肌病和脑肌病临床及预后的研究
补充资料：肾细胞线粒体
[图]
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条