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Influence of ageing on onset of mitochondrial disease.

作者信息

Miyabayashi S, Hayashi J I, Tada K

机构信息

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

出版信息

J Inherit Metab Dis. 1994;17(5):606-10. doi: 10.1007/BF00711599.

DOI:10.1007/BF00711599
PMID:7837768
Abstract
摘要

相似文献

1
Influence of ageing on onset of mitochondrial disease.
J Inherit Metab Dis. 1994;17(5):606-10. doi: 10.1007/BF00711599.
2
Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age.随着年龄增长，细胞色素c氧化酶缺陷细胞在海马体和脉络丛中积累。
Neurobiol Aging. 2001 Mar-Apr;22(2):265-72. doi: 10.1016/s0197-4580(00)00234-7.
3
Mitochondrial abnormalities in ageing macular photoreceptors.衰老黄斑区光感受器中的线粒体异常
Invest Ophthalmol Vis Sci. 2001 Nov;42(12):3016-22.
4
Aging research. Do mitochondrial mutations dim the fire of life?衰老研究。线粒体突变会熄灭生命之火吗？
Science. 1999 Oct 22;286(5440):664. doi: 10.1126/science.286.5440.664.
5
Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts.
J Inherit Metab Dis. 1992;15(3):323-6. doi: 10.1007/BF02435967.
6
Mitochondrial health, the epigenome and healthspan.线粒体健康、表观基因组与健康寿命。
Clin Sci (Lond). 2016 Aug 1;130(15):1285-305. doi: 10.1042/CS20160002.
7
The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy.线粒体DNA的m.13051G>A突变导致了不同的神经学症状和线粒体自噬激活。
Neurology. 2016 May 17;86(20):1921-3. doi: 10.1212/WNL.0000000000002688. Epub 2016 Apr 22.
8
SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiency.三例患有Leigh综合征和细胞色素c氧化酶缺乏症患者的SURF1基因突变
Neurology. 2003 Oct 14;61(7):991-3. doi: 10.1212/01.wnl.0000082391.98672.0a.
9
Diagnosis of fatal infantile defects of the mitochondrial respiratory chain: age dependence and postmortem analysis of enzyme activities.线粒体呼吸链致命性婴儿缺陷的诊断：年龄依赖性及酶活性的死后分析
J Neurol Sci. 1995 Dec;134(1-2):95-102. doi: 10.1016/0022-510x(95)00225-5.
10
An atypical case of cytochrome c oxidase deficiency with biochemical heterogeneity in fibroblasts.
Neurology. 1991 Dec;41(12):1957-60. doi: 10.1212/wnl.41.12.1957.

本文引用的文献

1
Nuclear but not mitochondrial genome involvement in human age-related mitochondrial dysfunction. Functional integrity of mitochondrial DNA from aged subjects.核基因组而非线粒体基因组参与人类与年龄相关的线粒体功能障碍。老年受试者线粒体DNA的功能完整性。
J Biol Chem. 1994 Mar 4;269(9):6878-83.
2
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.线粒体肌病患者肌肉线粒体DNA的缺失
Nature. 1988 Feb 25;331(6158):717-9. doi: 10.1038/331717a0.
3
Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy.
对三名患有细胞色素c氧化酶缺乏症并表现为 Leigh 型脑脊髓病的患者进行的免疫化学研究。
J Inherit Metab Dis. 1987;10(3):289-92. doi: 10.1007/BF01800084.
4
Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases.线粒体DNA突变是衰老和退行性疾病的一个重要促成因素。
Lancet. 1989 Mar 25;1(8639):642-5. doi: 10.1016/s0140-6736(89)92145-4.
5
Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy.
J Inherit Metab Dis. 1989;12(3):373-7. doi: 10.1007/BF01799245.
6
Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study.人类心脏中细胞色素c氧化酶缺乏的心肌细胞——一种与年龄相关的现象。一项组织化学超微细胞化学研究。
Am J Pathol. 1989 May;134(5):1167-73.
7
A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).线粒体肌病、脑病、乳酸酸中毒和卒中样发作（MELAS）中，线粒体tRNA（Leu）（UUR）基因的点突变
Biochem Biophys Res Commun. 1990 Dec 31;173(3):816-22. doi: 10.1016/s0006-291x(05)80860-5.
8
Detection of a specific mitochondrial DNA deletion in tissues of older humans.在老年人组织中检测特定的线粒体DNA缺失。
Nucleic Acids Res. 1990 Dec 11;18(23):6927-33. doi: 10.1093/nar/18.23.6927.
9
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.肌阵挛性癫痫伴蓬毛样红纤维病（MERRF）与线粒体DNA 赖氨酸转运RNA（tRNA<sup>Lys</sup>）突变有关。
Cell. 1990 Jun 15;61(6):931-7. doi: 10.1016/0092-8674(90)90059-n.
10
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.与线粒体脑肌病的MELAS亚组相关的tRNA（Leu）（UUR）基因突变。
Nature. 1990 Dec 13;348(6302):651-3. doi: 10.1038/348651a0.