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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

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

Archive ouverte | Pichon, Julien | CCSD

Pompe disease (glycogen storage disease type II) is a lysosomal storage disorder caused by the mutation of acid α-glucosidase (Gaa), the unique enzyme degrading glycogen in glucose into lysosomes. A massive glycogen overload is de...

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