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Mitochondrial disease: a historical, biochemical, and London perspective.

机译:线粒体疾病:历史、生化和伦敦视角。

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摘要

Roland Luft is credited with describing the first truly mitochondrial disorder in the late 1950s and early 1960s. Cases such as his have proven to be exceptionally rare. Some years later, methods of mitochondrial analysis--enzymatic, polarographic, and spectroscopic, which had been developed primarily by groups in Philadelphia--were applied to the study of mitochondria isolated from skeletal muscle biopsies of patients thought to have defects of oxidative phosphorylation. In the vanguard of these investigations were groups in New York and London. John Clark led the latter group. Application of biochemical studies, more recently supplemented by molecular mtDNA and nuclear DNA studies, have revealed that mitochondrial disorders are among the most common of all metabolic disorders.
机译:Roland Luft 因在 1950 年代末和 1960 年代初描述了第一个真正的线粒体疾病而受到赞誉。事实证明,像他这样的案例非常罕见。几年后,线粒体分析方法——酶学、极谱法和光谱学,主要由费城的小组开发——被应用于研究从被认为具有氧化磷酸化缺陷的患者的骨骼肌活检中分离出的线粒体。这些调查的先锋是纽约和伦敦的团体。约翰·克拉克(John Clark)领导了后者。生化研究的应用,最近辅以分子mtDNA和核DNA研究,表明线粒体疾病是所有代谢疾病中最常见的疾病之一。

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