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Mitochondrial myopathies involving the respiratory chain: a biochemical analysis.

作者信息

Takamiya S, Yanamura W, Capaldi R A, Kennaway N G, Bart R, Sengers R C, Trijbels J M, Ruitenbeek W

出版信息

Ann N Y Acad Sci. 1986;488:33-43. doi: 10.1111/j.1749-6632.1986.tb46546.x.

DOI:10.1111/j.1749-6632.1986.tb46546.x
PMID:3034117
Abstract
摘要

相似文献

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Mitochondrial myopathies involving the respiratory chain: a biochemical analysis.涉及呼吸链的线粒体肌病：生化分析
Ann N Y Acad Sci. 1986;488:33-43. doi: 10.1111/j.1749-6632.1986.tb46546.x.
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Mitochondrial myopathies. Clinical, morphological and biochemical aspects.线粒体肌病。临床、形态学及生化方面
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Mitochondrial myopathies: disorders of the respiratory chain and oxidative phosphorylation.线粒体肌病：呼吸链与氧化磷酸化紊乱
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The mitochondrial myopathies. Defects of the mitochondrial respiratory chain and oxidative phosphorylation system.线粒体肌病。线粒体呼吸链和氧化磷酸化系统的缺陷。
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[A case of late-onset and slowly progressive mitochondrial myopathy with abnormalities of complexes in electron-transfer system].[一例伴有电子传递系统复合体异常的迟发性、缓慢进展性线粒体肌病]
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Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain.线粒体肌病：线粒体呼吸链复合体I和复合体III存在局部缺陷。
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Effect of chondrocyte mitochondrial dysfunction on cartilage degeneration: A possible pathway for osteoarthritis pathology at the subcellular level.软骨细胞线粒体功能障碍对软骨退变的影响：亚细胞水平骨关节炎病理的可能途径。
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Molecular defects in cytochrome oxidase in mitochondrial diseases.线粒体疾病中细胞色素氧化酶的分子缺陷
J Bioenerg Biomembr. 1988 Jun;20(3):353-64. doi: 10.1007/BF00769637.
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Defects in the cytochrome bc1 complex in mitochondrial diseases.
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Complexity and tissue specificity of the mitochondrial respiratory chain.线粒体呼吸链的复杂性与组织特异性
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Can J Vet Res. 1990 Jan;54(1):1-14.
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Mitochondrial encephalomyopathies and cytochrome c oxidase deficiency: muscle culture study.线粒体脑肌病与细胞色素c氧化酶缺乏症：肌肉培养研究
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Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies.
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Combined deficiencies of the pyruvate dehydrogenase complex and enzymes of the respiratory chain in mitochondrial myopathies.
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