A Comment on “Muscle Xenografts Reproduce Key Molecular Features of Facioscapulohumeral Muscular Dystrophy”: What Is New and What Has Already been Done and Reported but Was Not Quoted?

A study was recently published that sought to develop an in vivo model of facioscapulohumeral muscular dystrophy by transplanting muscle precursor cells from a patient into immunodeficient mice. The study largely applied the methodology used by our team in a study published more than two decades ago...

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Detalles Bibliográficos
Autores principales: Skuk, Daniel, Tremblay, Jacques P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Commentary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563933/
https://www.ncbi.nlm.nih.gov/pubmed/32830546
http://dx.doi.org/10.1177/0963689720939120

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563933/
https://www.ncbi.nlm.nih.gov/pubmed/32830546
http://dx.doi.org/10.1177/0963689720939120

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