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J M Tager

Showing results (111-120 of 177) with videos related to

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Biochimica Et Biophysica Acta|October 21, 1991
Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation groupE A Wiemer, M Out, A Schelen, et al.
Biochimica Et Biophysica Acta|August 8, 1989
Properties of acid ceramidase from human spleenB J Al, C W Tiffany, D S Gomes de Mesquita, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1986
Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum diseaseA W Schram, A Strijland, T Hashimoto, et al.
Journal of the Neurological Sciences|August 1, 1990
Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case reportR J Wanders, E Boltshauser, B Steinmann, et al.
European Journal of Biochemistry|March 15, 1984
Isolation and characterization of a precursor form of lysosomal alpha-glucosidase from human urineR P Oude Elferink, E M Brouwer-Kelder, I Surya, et al.
The Journal of Clinical Investigation|March 1, 1993
Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher diseaseS van Weely, M van den Berg, J A Barranger, et al.
Ultrastructural Pathology|September 1, 1988
An immunoelectron microscopic study of glucocerebrosidase in type 1 Gaucher's disease spleenR Willemsen, J M van Dongen, J M Aerts, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatmentR B Schutgens, R J Wanders, H S Heymans, et al.
Experimental Cell Research|August 1, 1988
Characterization of glucocerebrosidase in peripheral blood cells and cultured blastoid cellsJ M Aerts, J Heikoop, S van Weely, et al.
Biochimica Et Biophysica Acta|December 1, 1986
Comparison of the properties of a soluble form of glucocerebrosidase from human urine with those of the membrane-associated tissue enzymeJ M Aerts, W E Donker-Koopman, M Koot, et al.
Pageof 18

Showing results (111-120 of 177) with videos related to

Sort By:
Pageof 18
Biochimica Et Biophysica Acta|October 21, 1991
Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation groupE A Wiemer, M Out, A Schelen, et al.
Biochimica Et Biophysica Acta|August 8, 1989
Properties of acid ceramidase from human spleenB J Al, C W Tiffany, D S Gomes de Mesquita, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1986
Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum diseaseA W Schram, A Strijland, T Hashimoto, et al.
Journal of the Neurological Sciences|August 1, 1990
Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case reportR J Wanders, E Boltshauser, B Steinmann, et al.
European Journal of Biochemistry|March 15, 1984
Isolation and characterization of a precursor form of lysosomal alpha-glucosidase from human urineR P Oude Elferink, E M Brouwer-Kelder, I Surya, et al.
The Journal of Clinical Investigation|March 1, 1993
Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher diseaseS van Weely, M van den Berg, J A Barranger, et al.
Ultrastructural Pathology|September 1, 1988
An immunoelectron microscopic study of glucocerebrosidase in type 1 Gaucher's disease spleenR Willemsen, J M van Dongen, J M Aerts, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatmentR B Schutgens, R J Wanders, H S Heymans, et al.
Experimental Cell Research|August 1, 1988
Characterization of glucocerebrosidase in peripheral blood cells and cultured blastoid cellsJ M Aerts, J Heikoop, S van Weely, et al.
Biochimica Et Biophysica Acta|December 1, 1986
Comparison of the properties of a soluble form of glucocerebrosidase from human urine with those of the membrane-associated tissue enzymeJ M Aerts, W E Donker-Koopman, M Koot, et al.
Pageof 18