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CD133+ cells derived from skeletal muscles of Duchenne muscular dystrophy patients have a compromised myogenic and muscle regenerative capability

Cell-mediated gene therapy is a possible means to treat muscular dystrophies like Duchenne muscular dystrophy. Autologous patient stem cells can be genetically-corrected and transplanted back into the patient, without causing immunorejection problems. Regenerated muscle fibres derived from these cel...

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Detalhes bibliográficos
Publicado no:Stem Cell Res
Main Authors: Meng, Jinhong, Muntoni, Francesco, Morgan, Jennifer
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6048760/
https://ncbi.nlm.nih.gov/pubmed/29783100
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.scr.2018.05.004
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