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J M Tager

Showing results (141-150 of 177) with videos related to

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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.
Biochimica Et Biophysica Acta|July 26, 1991
Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblastsJ C Heikoop, M Van den Berg, A Strijland, et al.
The Journal of Clinical Investigation|July 1, 1990
Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzymeJ C Heikoop, C W van Roermund, W W Just, 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|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.
European Journal of Biochemistry|March 15, 1984
Use of a monoclonal antibody to distinguish between precursor and mature forms of human lysosomal alpha-glucosidaseR P Oude Elferink, A Strijland, I Surya, et al.
Progress in Clinical and Biological Research|January 1, 1990
Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomesJ M Tager, S Brul, E A Wiemer, 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.
Pageof 18

Showing results (141-150 of 177) with videos related to

Sort By:
Pageof 18
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.
Biochimica Et Biophysica Acta|July 26, 1991
Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblastsJ C Heikoop, M Van den Berg, A Strijland, et al.
The Journal of Clinical Investigation|July 1, 1990
Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzymeJ C Heikoop, C W van Roermund, W W Just, 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|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.
European Journal of Biochemistry|March 15, 1984
Use of a monoclonal antibody to distinguish between precursor and mature forms of human lysosomal alpha-glucosidaseR P Oude Elferink, A Strijland, I Surya, et al.
Progress in Clinical and Biological Research|January 1, 1990
Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomesJ M Tager, S Brul, E A Wiemer, 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.
Pageof 18