Recent advances and new perspectives in mitochondrial dysfunction

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作者
Cecilia Giulivi
Kezhong Zhang
Hirofumi Arakawa
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[1] University of California Davis,School of Veterinary Medicine, University of California at Davis and The MIND Institute
[2] Wayne State University School of Medicine,Center for Molecular Medicine and Genetics
[3] National Cancer Center Research Institute,Division of Cancer Biology
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In the last decade, there has been an increased appreciation for mitochondria as central hubs in diverse processes, such as cellular energy, immunity, and signal transduction. As such, we have become aware that mitochondrial dysfunction underlies many diseases, including primary (mutations in genes encoding mitochondrial proteins) and secondary mitochondrial diseases (mutations in non-mitochondrial genes critical for mitochondrial biology), as well as complex diseases with mitochondrial dysfunction (chronic or degenerative diseases). Evidence suggests that mitochondrial dysfunction may often precede other pathological signs in these disorders, further modulated by genetics, environment, and lifestyle.
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