Author:
Aerts J. M.,Hollak C.,Boot R.,Groener A.
Publisher
Springer Berlin Heidelberg
Reference57 articles.
1. Abe A, Gregory S, Lee L, Killen PD, Brady RO, Kulkarni A, Shayman JA (2000) Reduction of globotriaosylceramide in Fabry disease mice by substrate deprivation. J Clin Invest 105, 1563–1567
2. Aerts JM, van Weely S, Boot R, Hollak CE, Tager JM (1993) Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease. J Inherit Met Dis 16, 288–291
3. Aerts JMFG, Donker-Koopman WE, Murray GJ, Barranger JA, Tager JM, Schram AW (1986) A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodies. Anal Bio-chem 154, 655–663
4. Aerts JMFG, Schram AW, Strijland A, van Weely S, Jonsson LMV, Tager JM, Sorrell SH, Ginns EI, Barranger JA, Murray GJ (1988) Glucocerebrosidase, a lysosomal enzyme that does not undergo oligosaccharide phosphorylation. Biochem Biophys Acta 964, 303–308
5. Aerts JMFG, Hollak CEM (1997) Plasma and metabolic abnormalities in Gaucher’s disease. Baillieres Clin Haematol 10, 691–709
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