Contribution of dysferlin deficiency to skeletal muscle pathology in asymptomatic and severe dystroglycanopathy models: generation of a new model for Fukuyama congenital muscular dystrophy.

Kanagawa, Motoi; Lu, Zhongpeng; Ito, Chiyomi; Matsuda, Chie; Miyake, Katsuya; Toda, Tatsushi

Kanagawa, Motoi; Lu, Zhongpeng; Ito, Chiyomi; Matsuda, Chie; Miyake, Katsuya; Toda, Tatsushi.

Afiliação

Kanagawa M; Division of Neurology/Molecular Brain Science, Kobe University Graduate School of Medicine, Kobe, Japan.
Lu Z; Division of Neurology/Molecular Brain Science, Kobe University Graduate School of Medicine, Kobe, Japan.
Ito C; Division of Neurology/Molecular Brain Science, Kobe University Graduate School of Medicine, Kobe, Japan.
Matsuda C; Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan.
Miyake K; Department of Histology and Cell Biology, School of Medicine, Kagawa University, Ikenobe, Miki, Kagawa, Japan.
Toda T; Division of Neurology/Molecular Brain Science, Kobe University Graduate School of Medicine, Kobe, Japan.

PLoS One ; 9(9): e106721, 2014.

Article em En | MEDLINE | ID: mdl-25198651

Assuntos

Distroglicanas/metabolismo; Proteínas de Membrana/genética; Modelos Biológicos; Proteínas Musculares/genética; Músculo Esquelético/patologia; Síndrome de Walker-Warburg/genética; Animais; Disferlina; Humanos; Camundongos; Camundongos Transgênicos; Síndrome de Walker-Warburg/metabolismo

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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Músculo Esquelético / Distroglicanas / Síndrome de Walker-Warburg / Proteínas de Membrana / Modelos Biológicos / Proteínas Musculares Limite: Animals / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Japão

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