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Satellite cells fail to contribute to muscle repair but are functional in Pompe disease (glycogenosis type II)
Pompe disease, which is due to acid alpha-glucosidase deficiency, is characterized by skeletal muscle dysfunction attributed to the accumulation of glycogen-filled lysosomes and autophagic buildup. Despite the extensive tissue damages, a failure of satellite cell (SC) activation and lack of muscle r...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Acta Neuropathol Commun |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2018
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6211565/ https://ncbi.nlm.nih.gov/pubmed/30382921 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-018-0609-y |
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