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European Journal of Biochemistry|March 15, 1984
Isolation and characterization of a precursor form of lysosomal alpha-glucosidase from human urineR P Oude Elferink, E M Brouwer-Kelder, I Surya, et al.
Ultrastructural Pathology|September 1, 1988
An immunoelectron microscopic study of glucocerebrosidase in type 1 Gaucher's disease spleenR Willemsen, J M van Dongen, J M Aerts, et al.
Ultrastructural Pathology|September 1, 1993
Synthesis and in situ localization of lysosomal alpha-glucosidase in muscle of an unusual variant of glycogen storage disease type IIR Willemsen, A T van der Ploeg, H F Busch, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1980
Introduction of a viral thymidine kinase gene and the human beta-globin gene into developmentally multipotential mouse teratocarcinoma cellsA Pellicer, E F Wagner, A el-Kareh, et al.
Human Mutation|April 1, 1998
Glycogen Storage Disease type II: genetic and biochemical analysis of novel mutations in infantile patients from Turkish ancestryM M Hermans, M A Kroos, J A Smeitink, et al.
Neurology|January 1, 1987
Ganglioside storage, hexosaminidase lability, and urinary oligosaccharides in adult Sandhoff's diseaseP A Bolhuis, J G Oonk, P E Kamp, et al.
The Biochemical Journal|February 1, 1993
The conservative substitution Asp-645-->Glu in lysosomal alpha-glucosidase affects transport and phosphorylation of the enzyme in an adult patient with glycogen-storage disease type IIM M Hermans, E de Graaff, M A Kroos, et al.
The Journal of Biological Chemistry|March 29, 2000
Allosteric activation of acid alpha-glucosidase by the human papillomavirus E7 proteinW Zwerschke, B Mannhardt, P Massimi, et al.
The Histochemical Journal|October 1, 1991
A quantitative immunoelectronmicroscopic study on soluble, membrane-associated and membrane-bound lysosomal enzymes in human intestinal epithelial cellsR Willemsen, R Brünken, C W Sorber, et al.
American Journal of Human Genetics|January 1, 1990
Adult and infantile glycogenosis type II in one family, explained by allelic diversityL H Hoefsloot, A T van der Ploeg, M A Kroos, et al.
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