Adenine nucleotide translocator deficiency in muscle: Potential therapeutic value of vitamin E-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Adenine nucleotide translocator deficiency in muscle: Potential therapeutic value of vitamin E

Published:1993-05 Issue:3 Volume:16 Page:548-552
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Bakker H. D.,Scholte H. R.,Van den Bogert C.,Jeneson J. A. L.,Ruitenbeek W.,Wanders R. J. A.,Abeling N. G. G. M.,van Gennip A. H.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00711678

Reference13 articles.

1. Arnold DL, Matthews PM, Radda GK (1984) Metabolic recovery after exercise and the assessment of mitochondrial function in vivo in human skeletal muscle by means of31P-NMR.Magn Reson Med 1: 307?315.

2. Bakker HD, Scholte HR, Van den Bogert C et al (1993) Deficiency of the adenine nucleotide translocator in muscle of a patient with myopathy and lactic acidosis: a new mitochondrial defect.Pediatr Res in press.

3. Chance B, Sies H, Boveris A (1979) Hydroperoxide metabolism in mammalian organs.Physiol Rev 59: 527?605.

4. Douglas CE, Chan AC, Choy PC (1986) Vitamin E inhibits platelet phospholipase A2.Biochim Biophys Acta 876: 639?645.

5. Linnane AW, Marzuki S, Ozawa T, Tanaka M (1989) Mitochondrial DNA mutations as an important contributor to ageing and degenerative disease.Lancet 1: 642?645.

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Computational studies of the mitochondrial carrier family SLC25. Present status and future perspectives;Bio-Algorithms and Med-Systems;2021-04-27

2. Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial Myopathy;JIMD Reports;2015

3. Fluorometric detection of ADP/ATP carrier deficiency in human muscle;Clinica Chimica Acta;2001-09

4. Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance;Science;2000-08-04

5. Physiology and Pathophysiology of the Mitochondrial ADP/ATP Carrier;Mitochondrial Diseases;1999

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3