Dystrophin Expressing Chimeric (DEC) Human Cells Provide a Potential Therapy for Duchenne Muscular Dystrophy

Duchenne Muscular Dystrophy (DMD) is a progressive and lethal disease caused by mutations of the dystrophin gene. Currently no cure exists. Stem cell therapies targeting DMD are challenged by limited engraftment and rejection despite the use of immunosuppression. There is an urgent need to introduce...

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Detalles Bibliográficos
Autores principales: Siemionow, Maria, Cwykiel, Joanna, Heydemann, Ahlke, Garcia, Jesus, Marchese, Enza, Siemionow, Krzysztof, Szilagyi, Erzsebet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960489/
https://www.ncbi.nlm.nih.gov/pubmed/29546607
http://dx.doi.org/10.1007/s12015-018-9807-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960489/
https://www.ncbi.nlm.nih.gov/pubmed/29546607
http://dx.doi.org/10.1007/s12015-018-9807-z

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