Aberrant Protein Turn-Over Associated With Myofibrillar Disorganization in FHL1 Knockout Mice
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DOI: 10.3389/fgene.2018.00273
Abstract: Mutations in the FHL1 gene, and FHL1 protein deletion, are associated with rare hereditary myopathies and cardiomyopathies. FHL1-null mice develop age-dependent myopathy and increased autophagic activity. However, the molecular pathway involved in contractile function and… read more here.
Keywords: protein; myofibrillar disorganization; fhl1 mice; mice ... See more keywords