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• W109749587 abstract "mdx mice lack the protein dystrophin, the absence of which causes Duchenne muscular dystrophy in humans. To examine how mdx mice maintain muscle mass despite dystrophin deficiency, we measured protein turnover rates in muscles of mdx and wild-type (C57BL/10) mice in vivo. At all ages studied, rates of muscle protein synthesis and degradation were higher in mdx than in C57BL/10 mice." @default.
• W109749587 created "2016-06-24" @default.
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• W109749587 date "1990-06-15" @default.
• W109749587 modified "2023-09-23" @default.
• W109749587 title "Protein turnover is elevated in muscle of <i>mdx</i> mice <i>in vivo</i>" @default.
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• W109749587 doi "https://doi.org/10.1042/bj2680795" @default.
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