Quantitative Evaluation of Exon Skipping in Urine-Derived Cells for Duchenne Muscular Dystrophy.

Kunitake, Katsuhiko; Sathyaprakash, Chaitra; Motohashi, Norio; Aoki, Yoshitsugu

Kunitake, Katsuhiko; Sathyaprakash, Chaitra; Motohashi, Norio; Aoki, Yoshitsugu.

Afiliação

Kunitake K; Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
Sathyaprakash C; Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
Motohashi N; Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
Aoki Y; Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan. tsugu56@ncnp.go.jp.

Methods Mol Biol ; 2587: 153-164, 2023.

Article em En | MEDLINE | ID: mdl-36401029

Assuntos

Distrofia Muscular de Duchenne; Humanos; Distrofia Muscular de Duchenne/genética; Distrofia Muscular de Duchenne/terapia; Distrofia Muscular de Duchenne/metabolismo; Distrofina/genética; Distrofina/metabolismo; Éxons; Mioblastos/metabolismo; Fenótipo

Palavras-chave

Duchenne muscular dystrophy (DMD); Exon skipping; Immunocytochemistry; MYOD1; RT-PCR; Urine-derived cells (UDCs); Western blotting

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofia Muscular de Duchenne Limite: Humans Idioma: En Revista: Methods Mol Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google