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Biochimica Et Biophysica Acta|May 13, 1987
Studies on the peroxisomal oxidation of palmitate and lignocerate in rat liverR J Wanders, C W van Roermund, M J van Wijland, et al.
Journal of Neurology|January 1, 1987
Ultrastructural localization of glucocerebrosidase in cultured Gaucher's disease fibroblasts by immunocytochemistryR Willemsen, J M van Dongen, E I Ginns, et al.
Journal of General Internal Medicine|May 14, 2021
Association of Post-discharge Service Types and Timing with 30-Day Readmissions, Length of Stay, and CostsHyo Jung Tak, Andrew M Goldsweig, Fernando A Wilson, et al.
Biochemical and Biophysical Research Communications|December 15, 1986
Efficient routing of glucocerebrosidase to lysosomes requires complex oligosaccharide chain formationJ M Aerts, S Brul, W E Donker-Koopman, et al.
Biochemical and Biophysical Research Communications|June 16, 1988
Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acidsR J Wanders, C W van Roermund, M J van Wijland, et al.
Biochimica Et Biophysica Acta|July 26, 1985
The effect of detergents on immunoprecipitability of lysosomal sphingomyelinaseM Driessen, G Weitz, E M Brouwer-Kelder, et al.
Journal of Proteomics|October 23, 2012
Benchmarking stable isotope labeling based quantitative proteomicsA F Maarten Altelaar, Christian K Frese, Christian Preisinger, et al.
The Biochemical Journal|July 1, 1990
Comparative study on glucocerebrosidase in spleens from patients with Gaucher diseaseJ M Aerts, W E Donker-Koopman, S Brul, et al.
Bioscience Reports|December 1, 1984
Immunological studies on lysosomal sphingomyelinase: identification of a 28 000-Da component deficient in urine from patients with Niemann-Pick disease types A and BA W Schram, M Dreissen, J Bastiaannet, et al.
The Journal of Clinical Investigation|June 1, 1988
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysisS Brul, A Westerveld, A Strijland, et al.
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