• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defect.

作者信息

Lestienne P, Nelson J, Riederer P, Jellinger K, Reichmann H

机构信息

Department of Neurology, University of Würzburg, F.R.G.

出版信息

J Neurochem. 1990 Nov;55(5):1810-2. doi: 10.1111/j.1471-4159.1990.tb04973.x.

DOI:10.1111/j.1471-4159.1990.tb04973.x
PMID:2120389
Abstract

The mitochondrial genome codes for 13 proteins which are located in the respiratory chain. In postmortem brain of patients with Parkinson's disease, decreased activity of complex I of the respiratory chain could be demonstrated. Because seven subunits of complex I are coded by the mitochondrial genome, we analyzed the mitochondrial DNA of human postmortem substantia nigra, putamen, and frontal cortex by the Southern blot technique. No deletions of the mitochondrial genome could be demonstrated, thus indicating that either subunits which are encoded by the nuclear genome are decreased or enzyme activity is diminished by metabolites, toxins, or increase of Fe3+.

摘要

相似文献

1
Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defect.
J Neurochem. 1990 Nov;55(5):1810-2. doi: 10.1111/j.1471-4159.1990.tb04973.x.
2
Mitochondrial DNA and Parkinson's disease.线粒体DNA与帕金森病
Neurology. 1991 May;41(5 Suppl 2):38-42; discussion 42-3. doi: 10.1212/wnl.41.5_suppl_2.38.
3
Mitochondrial complex I deficiency in Parkinson's disease.帕金森病中的线粒体复合体I缺乏症。
J Neurochem. 1990 Mar;54(3):823-7. doi: 10.1111/j.1471-4159.1990.tb02325.x.
4
Abnormalities of the electron transport chain in idiopathic Parkinson's disease.特发性帕金森病中电子传递链的异常
Ann Neurol. 1989 Dec;26(6):719-23. doi: 10.1002/ana.410260606.
5
Mitochondrial DNA analysis in Parkinson's disease.帕金森病中的线粒体DNA分析。
Mov Disord. 1990;5(4):294-7. doi: 10.1002/mds.870050406.
6
Mitochondrial function in Parkinson's disease. The Royal Kings and Queens Parkinson's Disease Research Group.
Ann Neurol. 1992;32 Suppl:S116-24. doi: 10.1002/ana.410320720.
7
Mitochondrial complex I deficiency in Parkinson's disease.帕金森病中的线粒体复合体I缺陷
Adv Neurol. 1993;60:288-91.
8
Deficiencies in complex I subunits of the respiratory chain in Parkinson's disease.帕金森病中呼吸链复合体I亚基的缺陷。
Biochem Biophys Res Commun. 1989 Sep 29;163(3):1450-5. doi: 10.1016/0006-291x(89)91141-8.
9
Iron-dependent enzymes in Parkinson's disease.帕金森病中的铁依赖性酶。
J Neural Transm Suppl. 1995;46:157-64.
10
Unaltered respiratory chain enzyme activity and mitochondrial DNA in skeletal muscle from patients with idiopathic Parkinson's syndrome.特发性帕金森综合征患者骨骼肌中呼吸链酶活性及线粒体DNA未改变
Eur Neurol. 1994;34(5):263-7. doi: 10.1159/000117053.

引用本文的文献

1
Facets of movement disorders- a tribute to Heinz Reichmann.运动障碍的各个方面——向海因茨·赖希曼致敬。
J Neural Transm (Vienna). 2024 Dec;131(12):1363-1365. doi: 10.1007/s00702-024-02857-0. Epub 2024 Nov 5.
2
Revolutionizing our understanding of Parkinson's disease: Dr. Heinz Reichmann's pioneering research and future research direction.颠覆帕金森病认知的革命:海因茨·赖希曼博士的开拓性研究与未来研究方向。
J Neural Transm (Vienna). 2024 Dec;131(12):1367-1387. doi: 10.1007/s00702-024-02812-z. Epub 2024 Aug 7.
3
Mitochondrial dysfunction in Parkinson's disease - a key disease hallmark with therapeutic potential.
帕金森病中的线粒体功能障碍——具有治疗潜力的关键疾病标志。
Mol Neurodegener. 2023 Nov 11;18(1):83. doi: 10.1186/s13024-023-00676-7.
4
Selenium Effects on Oxidative Stress-Induced Calcium Signaling Pathways in Parkinson's Disease.硒对帕金森病中氧化应激诱导的钙信号通路的影响
Indian J Clin Biochem. 2022 Jul;37(3):257-266. doi: 10.1007/s12291-022-01031-1. Epub 2022 Apr 15.
5
Parkinson's Disease and Impairment in Mitochondrial Metabolism: A Pathognomic Signature.帕金森病与线粒体代谢障碍:一种病征特征。
Adv Exp Med Biol. 2021;1286:65-76. doi: 10.1007/978-3-030-55035-6_4.
6
The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer's Disease and Parkinson's Disease.线粒体在神经退行性疾病中的作用:阿尔茨海默病和帕金森病的启示。
Mol Neurobiol. 2020 Jul;57(7):2959-2980. doi: 10.1007/s12035-020-01926-1. Epub 2020 May 22.
7
Mitochondria, OxPhos, and neurodegeneration: cells are not just running out of gas.线粒体、氧化磷酸化和神经退行性变:细胞不只是“燃料”耗尽。
J Clin Invest. 2019 Jan 2;129(1):34-45. doi: 10.1172/JCI120848.
8
Aconitase causes iron toxicity in Drosophila pink1 mutants.乌头酸酶在果蝇pink1突变体中引发铁毒性。
PLoS Genet. 2013 Apr;9(4):e1003478. doi: 10.1371/journal.pgen.1003478. Epub 2013 Apr 25.
9
[Coenzyme Q10 in Parkinson's disease. Symptomatic or neuroprotective effects?].[帕金森病中的辅酶Q10。是对症治疗作用还是神经保护作用?]
Nervenarzt. 2007 Dec;78(12):1378-82. doi: 10.1007/s00115-007-2285-1.
10
The human nuclear-encoded acyl carrier subunit (NDUFAB1) of the mitochondrial complex I in human pathology.人类病理学中线粒体复合物I的人类核编码酰基载体亚基(NDUFAB1)
J Inherit Metab Dis. 1999 Apr;22(2):163-73. doi: 10.1023/a:1005402020569.