Induced Fetal Human Muscle Stem Cells with High Therapeutic Potential in a Mouse Muscular Dystrophy Model

Duchenne muscular dystrophy (DMD) is a progressive and fatal muscle-wasting disease caused by DYSTROPHIN deficiency. Cell therapy using muscle stem cells (MuSCs) is a potential cure. Here, we report a differentiation method to generate fetal MuSCs from human induced pluripotent stem cells (iPSCs) by...

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Detalles Bibliográficos
Autores principales: Zhao, Mingming, Tazumi, Atsutoshi, Takayama, Satoru, Takenaka-Ninagawa, Nana, Nalbandian, Minas, Nagai, Miki, Nakamura, Yumi, Nakasa, Masanori, Watanabe, Akira, Ikeya, Makoto, Hotta, Akitsu, Ito, Yuta, Sato, Takahiko, Sakurai, Hidetoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363940/
https://www.ncbi.nlm.nih.gov/pubmed/32619494
http://dx.doi.org/10.1016/j.stemcr.2020.06.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363940/
https://www.ncbi.nlm.nih.gov/pubmed/32619494
http://dx.doi.org/10.1016/j.stemcr.2020.06.004

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