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Deficiency of subunits of complex I or IV in mitochondrial myopathies: immunochemical and immunohistochemical study.

作者信息

Tanaka M, Nishikimi M, Suzuki H, Tada M, Ozawa T, Koga Y, Nonaka I

机构信息

Department of Biomedical Chemistry, Faculty of Medicine, University of Nagoya, Japan.

出版信息

J Inherit Metab Dis. 1987;10(3):284-8. doi: 10.1007/BF01800083.

DOI:10.1007/BF01800083
PMID:2828762
Abstract
摘要

相似文献

1
Deficiency of subunits of complex I or IV in mitochondrial myopathies: immunochemical and immunohistochemical study.线粒体肌病中复合物I或IV亚基的缺乏：免疫化学和免疫组织化学研究
J Inherit Metab Dis. 1987;10(3):284-8. doi: 10.1007/BF01800083.
2
Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies.线粒体肌病患者复合体I或复合体IV中亚基的部分缺陷。
Biochem Int. 1987 Mar;14(3):525-30.
3
Extensive defects of mitochondrial electron-transfer chain in muscular cytochrome c oxidase deficiency.肌肉细胞色素c氧化酶缺乏症中线粒体电子传递链的广泛缺陷。
Pediatr Res. 1988 Oct;24(4):447-54. doi: 10.1203/00006450-198810000-00006.
4
[Neurological approach to mitochondrial abnormalities].[线粒体异常的神经学研究方法]
No To Hattatsu. 1987 Mar;19(2):118-24.
5
[Muscle pathology in mitochondrial myopathy].[线粒体肌病中的肌肉病理学]
No To Hattatsu. 1987 Mar;19(2):110-7.
6
[Clinical and biochemical approach to mitochondrial cytopathy--defects of the respiratory chain].
No To Hattatsu. 1987 Mar;19(2):132-9.
7
Mitochondrial myopathies. Clinical, morphological and biochemical aspects.线粒体肌病。临床、形态学及生化方面
Eur J Pediatr. 1984 Feb;141(4):192-207. doi: 10.1007/BF00572761.
8
[A case of mitochondrial encephalomyopathy with a defect in electron transport at complex I and IV in skeletal muscle showing peripheral neuropathy].[一例线粒体脑肌病，骨骼肌中复合体I和IV的电子传递存在缺陷，伴有周围神经病变]
Rinsho Shinkeigaku. 1988 Jan;28(1):107-11.
9
[Kearns-Sayre syndrome: mitochondrial encephalomyopathy caused by deficiency of the respiratory chain].[卡恩斯-塞尔综合征：由呼吸链缺陷引起的线粒体脑肌病]
Rev Neurol (Paris). 1989;145(12):842-50.
10
Mitochondrial myopathies.线粒体肌病
J Inherit Metab Dis. 1987;10 Suppl 1:113-28. doi: 10.1007/BF01812852.

引用本文的文献

1
Purifying Selection against Pathogenic Mitochondrial DNA in Human T Cells.人 T 细胞中对致病性线粒体 DNA 的净化选择。
N Engl J Med. 2020 Oct 15;383(16):1556-1563. doi: 10.1056/NEJMoa2001265. Epub 2020 Aug 12.
2
NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findings.NADH-辅酶Q还原酶（复合体I）缺乏症：表型和生化检查结果的异质性
J Inherit Metab Dis. 1996;19(5):675-86. doi: 10.1007/BF01799845.
3
Muscle pathology in cytochrome c oxidase deficiency.细胞色素c氧化酶缺乏症中的肌肉病理学

本文引用的文献

1
Arrangement of proteins in the mitochondrial inner membrane.线粒体内膜中蛋白质的排列
Biochim Biophys Acta. 1982 Nov 30;694(3):291-306. doi: 10.1016/0304-4157(82)90009-0.
2
URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit.URF6，人类线粒体DNA的最后一个未鉴定阅读框，编码一种NADH脱氢酶亚基。
Science. 1986 Oct 31;234(4776):614-8. doi: 10.1126/science.3764430.
3
Variation in the levels of complex I subunits among tissues in a patient with mitochondrial encephalomyopathy and renal dysfunction.
Acta Neuropathol. 1988;77(2):152-60. doi: 10.1007/BF00687425.
4
Cytochrome c oxidase deficiency in infancy.婴儿期细胞色素c氧化酶缺乏症
Acta Neuropathol. 1989;77(3):267-75. doi: 10.1007/BF00687578.
5
Congenital deficiency of a 20-kDa subunit of mitochondrial complex I in fibroblasts.成纤维细胞中线粒体复合物I的20-kDa亚基先天性缺乏。
Am J Hum Genet. 1991 Jun;48(6):1121-6.
6
Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies.
Virchows Arch A Pathol Anat Histopathol. 1991;419(4):355-62. doi: 10.1007/BF01606527.
一名患有线粒体脑肌病和肾功能不全患者各组织中复合物I亚基水平的差异。
Biochem Int. 1987 Apr;14(4):735-9.
4
Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathy.
Biochem Biophys Res Commun. 1986 Oct 15;140(1):88-93. doi: 10.1016/0006-291x(86)91061-2.
5
Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies.线粒体肌病患者复合体I或复合体IV中亚基的部分缺陷。
Biochem Int. 1987 Mar;14(3):525-30.