國家衛生研究院 NHRI:Item 3990099045/14692
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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/14692


    Title: Mitochondrial dysfunction as an underlying cause of skeletal muscle disorders
    Authors: Chen, TH;Koh, KY;Lin, KMC;Chou, CK
    Contributors: Institute of Biomedical Engineering and Nanomedicine
    Abstract: Mitochondria are an important energy source in skeletal muscle. A main function of mitochondria is the generation of ATP for energy through oxidative phosphorylation (OXPHOS). Mitochondrial defects or abnormalities can lead to muscle disease or multisystem disease. Mitochondrial dysfunction can be caused by defective mitochondrial OXPHOS, mtDNA mutations, Ca2+ imbalances, mitochondrial-related proteins, mitochondrial chaperone proteins, and ultrastructural defects. In addition, an imbalance between mitochondrial fusion and fission, lysosomal dysfunction due to insufficient biosynthesis, and/or defects in mitophagy can result in mitochondrial damage. In this review, we explore the association between impaired mitochondrial function and skeletal muscle disorders. Furthermore, we emphasize the need for more research to determine the specific clinical benefits of mitochondrial therapy in the treatment of skeletal muscle disorders.
    Date: 2022-11
    Relation: International Journal of Molecular Sciences. 2022 Nov;23(21):Article number 12926.
    Link to: http://dx.doi.org/10.3390/ijms232112926
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1422-0067&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000881234300001
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85141550791
    Appears in Collections:[Kurt Ming-Chao Lin] Periodical Articles

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