Joseph M. Tager

Affiliations: 
University of Amsterdam, Amsterdam, Netherlands 
Area:
biochemistry
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"Joseph Tager"
Bio:

Prof. dr. J.M. Tager, 1925 - 2011 at the Album Academicum of the University of Amsterdam

Mean distance: 15.52
 

Parents

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Sidney Herbert Cameron grad student 1952 UCLA
 (Enzymatic changes during senescence in the banana)

Children

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Jan B. Hoek grad student 1972 Amsterdam
Dirk Roos grad student 1973 Amsterdam (Cell Biology Tree)
Phillip G. de Groot grad student 1981 Amsterdam
Stanley Brul grad student 1991 Amsterdam
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Publications

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Wanders RJ, Tager JM. (1998) Lipid metabolism in peroxisomes in relation to human disease. Molecular Aspects of Medicine. 19: 69-154
van Weely S, Brandsma M, Strijland A, et al. (1993) Demonstration of the existence of a second, non-lysosomal glucocerebrosidase that is not deficient in Gaucher disease. Biochimica Et Biophysica Acta. 1181: 55-62
Middelkoop E, Wiemer EA, Schoenmaker DE, et al. (1993) Topology of catalase assembly in human skin fibroblasts. Biochimica Et Biophysica Acta. 1220: 15-20
Heikoop JC, Wanders RJ, Strijland A, et al. (1992) Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata--a complementation study. Human Genetics. 89: 439-44
Wanders RJ, van Roermund CW, Brul S, et al. (1992) Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis. Journal of Inherited Metabolic Disease. 15: 385-8
Lombardo MC, van der Zwaan JW, Brul S, et al. (1992) A procedure for selecting mammalian cells with an impairment in oxidative phosphorylation. Biochimica Et Biophysica Acta. 1138: 275-81
Lageweg W, Wanders RJ, Tager JM. (1991) Long-chain-acyl-CoA synthetase and very-long-chain-acyl-CoA synthetase activities in peroxisomes and microsomes from rat liver. An enzymological study. European Journal of Biochemistry / Febs. 196: 519-23
Middelkoop E, Strijland A, Tager JM. (1991) Does aminotriazole inhibit import of catalase into peroxisomes by retarding unfolding? Febs Letters. 279: 79-82
Van Weely S, Van Leeuwen MB, Jansen IDC, et al. (1991) Clinical phenotype of Gaucher disease in relation to properties of mutant glucocerebrosidase in cultured fibroblasts Bba - Molecular Basis of Disease. 1096: 301-311
Lageweg W, Steen I, Tager JM, et al. (1991) A fluorimetric assay for acyl-CoA synthetase activities. Analytical Biochemistry. 197: 384-8
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