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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Detaylı Bibliyografya
Yayımlandı:Stem Cell Res Ther
Asıl Yazarlar: Alexeev, Vitali, Olavarria, Jacquelyn, Bonaldo, Paolo, Merlini, Luciano, Igoucheva, Olga
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7607684/
https://ncbi.nlm.nih.gov/pubmed/33138863
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13287-020-01979-y
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