Therapeutic targeting of mitochondria in muscular dystrophies. Editorial focus on: "Mitochondrial creatine sensitivity is lost in the D2.<i>mdx</i> model of Duchenne muscular dystrophy and rescued by the mitochondrial-enhancing compound Olesoxime".

Juracic, Emma S; Brahmbhatt, Aditya N; Hawke, Thomas J

Therapeutic targeting of mitochondria in muscular dystrophies. Editorial focus on: "Mitochondrial creatine sensitivity is lost in the D2.mdx model of Duchenne muscular dystrophy and rescued by the mitochondrial-enhancing compound Olesoxime".

Juracic, Emma S; Brahmbhatt, Aditya N; Hawke, Thomas J.

Afiliação

Juracic ES; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
Brahmbhatt AN; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
Hawke TJ; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.

Am J Physiol Cell Physiol ; 325(2): C563-C564, 2023 08 01.

Article em En | MEDLINE | ID: mdl-37458438

Assuntos

Distrofia Muscular de Duchenne; Humanos; Distrofia Muscular de Duchenne/tratamento farmacológico; Distrofia Muscular de Duchenne/genética; Creatina; Mitocôndrias; Colestenonas

Palavras-chave

PTP; dystrophy; mitochondria; oxidative stress

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofia Muscular de Duchenne Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Am J Physiol Cell Physiol Assunto da revista: FISIOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá

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