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Biochemical and Biophysical Research Communications|February 15, 1985
Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndromeJ M Tager, W A Van der Beek, R J Wanders, et al.
European Journal of Biochemistry|August 17, 1990
Function of oligosaccharide modification in glucocerebrosidase, a membrane-associated lysosomal hydrolaseS Van Weely, J M Aerts, M B Van Leeuwen, et al.
European Journal of Biochemistry|April 1, 1987
Biosynthesis and maturation of glucocerebrosidase in Gaucher fibroblastsL M Jonsson, G J Murray, S H Sorrell, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1986
Peroxisomal beta-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndromeR J Wanders, C W van Roermund, C T de Vries, et al.
The Journal of Clinical Investigation|December 1, 1987
Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disordersR J Wanders, C W van Roermund, M J van Wijland, et al.
European Journal of Pediatrics|August 1, 1986
Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteinsR J Wanders, R B Schutgens, G Schrakamp, et al.
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.
Biochemical and Biophysical Research Communications|May 16, 1988
Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disordersS Brul, E A Wiemer, A Westerveld, 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.
Clinical Genetics|January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)M C Loonen, A W Schram, J F Koster, et al.
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