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European Journal of Biochemistry|March 16, 1987
Relationship between the two immunologically distinguishable forms of glucocerebrosidase in tissue extractsJ M Aerts, W E Donker-Koopman, C van Laar, et al.
European Journal of Biochemistry|August 15, 1983
Monoclonal antibodies against human beta-glucocerebrosidaseR A Barneveld, F P Tegelaers, E I Ginns, et al.
European Journal of Biochemistry|June 1, 1987
Signal sequence and DNA-mediated expression of human lysosomal alpha-galactosidase AS Tsuji, B M Martin, D C Kaslow, et al.
Biochimica Et Biophysica Acta|March 17, 1988
Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylationJ M Aerts, A W Schram, A Strijland, et al.
Bailliere'S Clinical Haematology|March 14, 1998
Gaucher's disease: studies of gene transfer to haematopoietic cellsJ A Barranger, E O Rice, J Dunigan, et al.
European Journal of Biochemistry|August 1, 1985
The occurrence of two immunologically distinguishable beta-glucocerebrosidases in human spleenJ M Aerts, W E Donker-Koopman, M K van der Vliet, et al.
Human Genetics|January 1, 1983
Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodiesR A Barneveld, W Keijzer, F P Tegelaers, et al.
Biochimica Et Biophysica Acta|June 5, 1991
Clinical phenotype of Gaucher disease in relation to properties of mutant glucocerebrosidase in cultured fibroblastsS Van Weely, M B Van Leeuwen, I D Jansen, et al.
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