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Critical contribution of mitochondria in the development of cardiomyopathy linked to desmin mutation

Archive ouverte | Hovhannisyan, Yeranuhi | CCSD

International audience. Abstract Background Beyond the observed alterations in cellular structure and mitochondria, the mechanisms linking rare genetic mutations to the development of heart failure in patients affec...

Absence of desmin results in impaired adaptive response to mechanical overloading of skeletal muscle

Archive ouverte | Joanne, Pierre | CCSD

International audience. Background: Desmin is a muscle-specific protein belonging to the intermediate filament family. Desmin mutations are linked to skeletal muscle defects, including inherited myopathies with seve...

Critical contribution of mitochondria in the development of cardiomyopathy linked to desminmutation

Archive ouverte | Hovhannisyan, Yeranuhi | CCSD

Beyond the observed alterations in cellular structure and mitochondria, the cellular mechanisms linking genetic mutations to the development of heart failure in patients affected by desmin defects remain unclear due, in part, to t...

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