Fixing frataxin: ‘ironing out’ the metabolic defect in Friedreich's ataxia-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Fixing frataxin: ‘ironing out’ the metabolic defect in Friedreich's ataxia

Published:2014-03-28 Issue:8 Volume:171 Page:2174-2190
ISSN:0007-1188
Container-title:British Journal of Pharmacology
language:en
Short-container-title:Br J Pharmacol

Author:

Anzovino A¹,Lane D J R¹,Huang M L-H¹,Richardson D R¹

Affiliation:

1. Molecular Pharmacology and Pathology Program; Department of Pathology and Bosch Institute; University of Sydney; Sydney NSW Australia

Funder

National Health and Medical Research Council

Muscular Dystrophy Association

Publisher

Wiley

Subject

Pharmacology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bph.12470/fullpdf

Reference179 articles.

1. Iron-dependent self-assembly of recombinant yeast frataxin: implications for Friedreich ataxia;Adamec;Am J Hum Genet,2000

2. A structural approach to understanding the iron-binding properties of phylogenetically different frataxins;Adinolfi;Hum Mol Genet,2002

3. Bacterial frataxin cyay is the gatekeeper of iron-sulfur cluster formation catalyzed by iscs;Adinolfi;Nat Struct Mol Biol,2009

4. The iron-binding function of transferrin in iron metabolism;Aisen;Semin Hematol,1977

5. Mutation of a putative mitochondrial iron transporter gene (abc7) in x-linked sideroblastic anemia and ataxia (xlsa/a);Allikmets;Hum Mol Genet,1999

Cited by 47 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. The Role of NRF2 in Trinucleotide Repeat Expansion Disorders;Antioxidants;2024-05-26

2. Frataxin deficiency shifts metabolism to promote reactive microglia via glucose catabolism;Life Science Alliance;2024-04-17

3. AAV8 gene therapy reverses cardiac pathology and prevents early mortality in a mouse model of Friedreich’s ataxia;Molecular Therapy - Methods & Clinical Development;2024-03

4. Mitochondria and the reactive species interactome: shaping the future of mitoredox medicine;Journal of Mitochondria, Plastids and Endosymbiosis;2024-01-31

5. Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think?;BMC Medical Genomics;2023-12-01

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