AMPK Complex Activation Promotes Sarcolemmal Repair in Dysferlinopathy

Mutations in dysferlin are responsible for a group of progressive, recessively inherited muscular dystrophies known as dysferlinopathies. Using recombinant proteins and affinity purification methods combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS), we found that AMP-activated...

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Detalles Bibliográficos
Autores principales: Ono, Hiroya, Suzuki, Naoki, Kanno, Shin-ichiro, Kawahara, Genri, Izumi, Rumiko, Takahashi, Toshiaki, Kitajima, Yasuo, Osana, Shion, Nakamura, Naoko, Akiyama, Tetsuya, Ikeda, Kensuke, Shijo, Tomomi, Mitsuzawa, Shio, Nagatomi, Ryoichi, Araki, Nobukazu, Yasui, Akira, Warita, Hitoshi, Hayashi, Yukiko K., Miyake, Katsuya, Aoki, Masashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132631/
https://www.ncbi.nlm.nih.gov/pubmed/32087766
http://dx.doi.org/10.1016/j.ymthe.2020.02.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132631/
https://www.ncbi.nlm.nih.gov/pubmed/32087766
http://dx.doi.org/10.1016/j.ymthe.2020.02.006

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