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Laminin-111 Restores Regenerative Capacity in a Mouse Model for α7 Integrin Congenital Myopathy
Mutations in the α7 integrin gene cause congenital myopathy characterized by delayed developmental milestones and impaired mobility. Previous studies in dystrophic mice suggest the α7β1 integrin may be critical for muscle repair. To investigate the role that α7β1 integrin plays in muscle regeneratio...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Society for Investigative Pathology
2009
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2631338/ https://ncbi.nlm.nih.gov/pubmed/19074617 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2009.080522 |
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