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Satellite cells fail to contribute to muscle repair but are functional in Pompe disease (glycogenosis type II).

Archive ouverte | Lagalice, Lydie | CCSD

International audience. 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 bu...

FoxO3a overexpression prevents both glycogen overload and autophagic buildup in skeletal muscle of Pompe disease

Archive ouverte | Pichon, Julien | CCSD

FoxO3a overexpression prevents both glycogen overload and autophagic buildup in skeletal muscle of Pompe disease. 6eme congrès international de Myologie

FoxO3a overexpression prevents both glycogen overload and autophagic buildup in skeletal muscle of Pompe disease.

Archive ouverte | Pichon, Julien | CCSD

International audience

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