The apparent activity in vivo of the lysosomal pathway of glycogen catabolism in cultured human skin fibroblasts from patients with type III glycogen storage disease.
Open Access
- 1 July 1978
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 253 (14), 5005-5011
- https://doi.org/10.1016/s0021-9258(17)34648-3
Abstract
No abstract availableThis publication has 30 references indexed in Scilit:
- The permeability properties of the lysosomal membraneBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1977
- Cell culture in serum depleted of glycosidases by heatingExperimental Cell Research, 1977
- Physico-chemical and immunological properties of acid α-glucosidase from various human tissues in relation to glycogenosis type II (pompe's disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- The Lysosomal α-Glucosidases of Mammalian TissuesPublished by American Chemical Society (ACS) ,1975
- Rodent and Human Acid α‐GlucosidaseEuropean Journal of Biochemistry, 1972
- Amylo-1, 6-glucosidase in human fibroblasts: Studies in Type III glycogen storage diseaseBiochemical and Biophysical Research Communications, 1970
- Simultaneous absence of α-1,4-glucosidase and α-1,6-glucosidase activities (pH 4) in tissues of children with Type II glycogen storage diseaseBiochemistry, 1970
- Lysosomal α-glucosidase. II. Kinetics of action of the rat liver enzymeBiochemistry, 1970
- The Determination of Amylo-1,6-GlucosidaseEuropean Journal of Biochemistry, 1967
- Structure of Glycogen and Its Amylolytic DegradationPublished by Wiley ,1964