Genomic organization of the human complex I 13-kDa subunit gene NDUFA5
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics,Molecular Biology
Cited by 6 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. Mancozeb induces nephrotoxicity by impairing the oxidative phosphorylation pathway: A transcriptome study;Ecotoxicology and Environmental Safety;2023-01
2. Hepatocyte miR-33a mediates mitochondrial dysfunction and hepatosteatosis by suppressing NDUFA5;Journal of Cellular and Molecular Medicine;2018-10-16
3. Evidence of Mitochondrial Dysfunction in Autism: Biochemical Links, Genetic-Based Associations, and Non-Energy-Related Mechanisms;Oxidative Medicine and Cellular Longevity;2017
4. Oxidized low-density lipoprotein and 15-deoxy-Δ12,14-PGJ2 increase mitochondrial complex I activity in endothelial cells;American Journal of Physiology-Heart and Circulatory Physiology;2003-12
5. Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain;Journal of Inherited Metabolic Disease;2001-02
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