Connexin-43 reduction prevents muscle defects in a mouse model of manifesting Duchenne muscular dystrophy female carriers.

Nouet, Julie; Himelman, Eric; Lahey, Kevin C; Zhao, Qingshi; Fraidenraich, Diego

Nouet, Julie; Himelman, Eric; Lahey, Kevin C; Zhao, Qingshi; Fraidenraich, Diego.

Afiliação

Nouet J; Department of Cell Biology and Molecular Medicine, Rutgers Biomedical and Health Sciences, New Jersey Medical School, Newark, NJ, USA.
Himelman E; Department of Cell Biology and Molecular Medicine, Rutgers Biomedical and Health Sciences, New Jersey Medical School, Newark, NJ, USA.
Lahey KC; Department of Cell Biology and Molecular Medicine, Rutgers Biomedical and Health Sciences, New Jersey Medical School, Newark, NJ, USA.
Zhao Q; Department of Cell Biology and Molecular Medicine, Rutgers Biomedical and Health Sciences, New Jersey Medical School, Newark, NJ, USA.
Fraidenraich D; Department of Cell Biology and Molecular Medicine, Rutgers Biomedical and Health Sciences, New Jersey Medical School, Newark, NJ, USA. fraidedi@rutgers.edu.

Sci Rep ; 10(1): 5683, 2020 03 30.

Article em En | MEDLINE | ID: mdl-32231219

Assuntos

Conexina 43/metabolismo; Distrofia Muscular de Duchenne/genética; Distrofia Muscular de Duchenne/fisiopatologia; Animais; Cardiomiopatias/metabolismo; Conexina 43/genética; Modelos Animais de Doenças; Distrofina/genética; Feminino; Coração/fisiopatologia; Masculino; Camundongos; Camundongos Endogâmicos C57BL; Camundongos Endogâmicos mdx; Fibras Musculares Esqueléticas/metabolismo; Força Muscular; Músculo Esquelético/metabolismo; Distrofia Muscular Animal/metabolismo

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Conexina 43 / Distrofia Muscular de Duchenne Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

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