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...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Acta Neuropathol Commun
Main Authors: Lagalice, Lydie, Pichon, Julien, Gougeon, Eliot, Soussi, Salwa, Deniaud, Johan, Ledevin, Mireille, Maurier, Virginie, Leroux, Isabelle, Durand, Sylvie, Ciron, Carine, Franzoso, Francesca, Dubreil, Laurence, Larcher, Thibaut, Rouger, Karl, Colle, Marie-Anne
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2018
Teme:
Research
Online dostop: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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