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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
 
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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
Johannes Maria Franciscus Gerardus (Hans) Aerts grad student 1988 Amsterdam
Stanley Brul grad student 1991 Amsterdam

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Publications

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Tager JM, Aerts JM, van den Bogert C, et al. (1994) Signals on proteins, intracellular targeting and inborn errors of organellar metabolism. Journal of Inherited Metabolic Disease. 17: 459-69
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
van Weely S, van den Berg M, Barranger JA, et al. (1993) Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher disease. The Journal of Clinical Investigation. 91: 1167-75
Aerts JM, Van Weely S, Boot R, et al. (1993) Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease. Journal of Inherited Metabolic Disease. 16: 288-91
Middelkoop E, Wiemer EA, Schoenmaker DE, et al. (1993) Topology of catalase assembly in human skin fibroblasts. Biochimica Et Biophysica Acta. 1220: 15-20
Wiemer EA, Ofman R, Middelkoop E, et al. (1992) Production and characterisation of monoclonal antibodies against native and disassembled human catalase. Journal of Immunological Methods. 151: 165-75
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
Kwekkeboom J, de Groot C, Tager JM. (1992) Efficient electric field-induced generation of hybridomas from human B lymphocytes without prior activation in vitro. Human Antibodies and Hybridomas. 3: 48-53
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
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