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Dard, L.; Blanchard, W.; Hubert, C.; Lacombe, D.; Rossignol, R.
Molecular aspects of medicine, 02/2020, Letnik: 71Journal Article
Mitochondria are dynamic cellular organelles responsible for a large variety of biochemical processes as energy transduction, REDOX signaling, the biosynthesis of hormones and vitamins, inflammation or cell death execution. Cell biology studies established that 1158 human genes encode proteins localized to mitochondria, as registered in MITOCARTA. Clinical studies showed that a large number of these mitochondrial proteins can be altered in expression and function through genetic, epigenetic or biochemical mechanisms including the interaction with environmental toxics or iatrogenic medicine. As a result, pathogenic mitochondrial genetic and functional defects participate to the onset and the progression of a growing number of rare diseases. In this review we provide an exhaustive survey of the biochemical, genetic and clinical studies that demonstrated the implication of mitochondrial dysfunction in human rare diseases. We discuss the striking diversity of the symptoms caused by mitochondrial dysfunction and the strategies proposed for mitochondrial therapy, including a survey of ongoing clinical trials. •Mitochondria participate to variegated cellular functions.•Primary or secondary mitochondrial defects trigger rare diseases.•Environmental factors can induce mitochondrial dysfunction.•The molecular pathophysiology of mitochondrial diseases is very complex.•A too limited number of drugs is available to modulate mitochondrial function in human therapy.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Vir: Osebne bibliografije
in: SICRIS
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