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Correction: Muscle health in a mouse model of Duchenne muscular dystrophy can be partially improved by restoring mitochondrial creatine metabolism.
Bellissimo CA, Delfinis LJ, Hughes MC, Turnbull PC, Gandhi S, DiBenedetto SN, Rahman F, Tadi P, Amaral C, Dehghani A, Quadrilatero J, Schlattner U, Perry CGR. Bellissimo CA, et al. Appl Physiol Nutr Metab. 2021 Feb;46(2):190. doi: 10.1139/apnm-2020-1066. Epub 2020 Dec 23. Appl Physiol Nutr Metab. 2021. PMID: 33356880 No abstract available.
Mitochondrial creatine sensitivity is lost in the D2.mdx model of Duchenne muscular dystrophy and rescued by the mitochondrial-enhancing compound Olesoxime.
Bellissimo CA, Delfinis LJ, Hughes MC, Turnbull PC, Gandhi S, DiBenedetto SN, Rahman FA, Tadi P, Amaral CA, Dehghani A, Cobley JN, Quadrilatero J, Schlattner U, Perry CGR. Bellissimo CA, et al. Among authors: rahman fa. Am J Physiol Cell Physiol. 2023 May 1;324(5):C1141-C1157. doi: 10.1152/ajpcell.00377.2022. Epub 2023 Jan 23. Am J Physiol Cell Physiol. 2023. PMID: 36689672 Free article.
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