Congenital muscular dystrophy-associated inflammatory chemokines provide axes for effective recruitment of therapeutic adult stem cell into muscles

BACKGROUND: Congenital muscular dystrophies (CMD) are a clinically and genetically heterogeneous group of neuromuscular disorders characterized by muscle weakness. The two most prevalent forms of CMD, collagen VI-related myopathies (COL6RM) and laminin α2 deficient CMD type 1A (MDC1A), are both caus...

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Detalles Bibliográficos
Autores principales: Alexeev, Vitali, Olavarria, Jacquelyn, Bonaldo, Paolo, Merlini, Luciano, Igoucheva, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607684/
https://www.ncbi.nlm.nih.gov/pubmed/33138863
http://dx.doi.org/10.1186/s13287-020-01979-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607684/
https://www.ncbi.nlm.nih.gov/pubmed/33138863
http://dx.doi.org/10.1186/s13287-020-01979-y

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