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- W2315149472 endingPage "548" @default.
- W2315149472 startingPage "541" @default.
- W2315149472 abstract "Cardiomyopathy is an inherited or acquired disease of the myocardium, which can result in severe ventricular dysfunction. Mitochondrial dysfunction is involved in the pathological process of cardiomyopathy. Many dysfunctions in cardiac mitochondria are consequences of mutations in nuclear or mitochondrial DNA followed by alterations in transcriptional regulation, mitochondrial protein function, and mitochondrial dynamics and energetics, presenting with associated multisystem mitochondrial disorders. To ensure correct diagnosis and optimal management of mitochondrial dysfunction in cardiomyopathy caused by multiple pathogenesis, multidisciplinary approaches are required, and to integrate between clinical and basic sciences, ideal translational models are needed. In this review, we will focus on experimental models to provide insights into basic mitochondrial physiology and detailed underlying mechanisms of cardiomyopathy and current mitochondria-targeted therapies for cardiomyopathy." @default.
- W2315149472 created "2016-06-24" @default.
- W2315149472 creator A5060322031 @default.
- W2315149472 creator A5064865297 @default.
- W2315149472 date "2015-10-31" @default.
- W2315149472 modified "2023-09-30" @default.
- W2315149472 title "An experimental approach to study the function of mitochondria in cardiomyopathy" @default.
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