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J M Tager

Showing results (151-160 of 177) with videos related to

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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.
Prenatal Diagnosis|September 1, 1985
The cerebro-hepato-renal (Zellweger) syndrome: prenatal detection based on impaired biosynthesis of plasmalogensR B Schutgens, G Schrakamp, R J Wanders, et al.
Journal of the Neurological Sciences|April 1, 1988
Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's diseaseR J Wanders, H S Heymans, R B Schutgens, 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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987
Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disordersR J Wanders, M J van Wijland, C W van Roermund, 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 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.
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.
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.
Pageof 18

Showing results (151-160 of 177) with videos related to

Sort By:
Pageof 18
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.
Prenatal Diagnosis|September 1, 1985
The cerebro-hepato-renal (Zellweger) syndrome: prenatal detection based on impaired biosynthesis of plasmalogensR B Schutgens, G Schrakamp, R J Wanders, et al.
Journal of the Neurological Sciences|April 1, 1988
Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's diseaseR J Wanders, H S Heymans, R B Schutgens, 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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1987
Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disordersR J Wanders, M J van Wijland, C W van Roermund, 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 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.
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.
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.
Pageof 18