生物
线粒体DNA
TFAM公司
肌病
线粒体
线粒体肌病
心肌病
遗传学
分子生物学
基因
内科学
医学
心力衰竭
出处
期刊:Humana Press eBooks
[Humana Press]
日期:2003-11-15
卷期号:: 003-054
被引量:95
标识
DOI:10.1385/1-59259-284-8:003
摘要
Although a variety of degenerative diseases are now known to be caused by two mutations in mitochondrial genes, the pathophysiology of these diseases remains poorly understood. As a consequence, relatively little progress has been made in developing new therapies for mitochondrial diseases. What has been needed are animal models for these diseases that are amenable to detailed biochemical, physiological, and molecular analysis, and on which promising therapies can be tested. In the past 5 yr, this deficiency has begun to be addressed by the construction of a number of mouse models of mitochondrial
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