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M Tager

Showing results (211-220 of 393) with videos related to

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Circulation Research|April 28, 2001
Attenuation of hypoxic pulmonary vasoconstriction by endotoxemia requires 5-lipoxygenase in miceF Ichinose, W M Zapol, A Sapirstein, et al.
Biochimica Et Biophysica Acta|January 30, 1987
Determination of the structure of the carbohydrate chains of acid alpha-glucosidase from human placentaJ H Mutsaers, H Van Halbeek, J F Vliegenthart, et al.
Biochimica Et Biophysica Acta|November 18, 1981
Monoclonal antibodies against human acid alpha-glucosidaseJ Hilkens, J M Tager, F Buijs, et al.
Biochimica Et Biophysica Acta|January 28, 1985
Soluble sphingomyelinase from human urine as antigen for obtaining anti-sphingomyelinase antibodiesG Weitz, M Driessen, E M Brouwer-Kelder, et al.
The Journal of Biological Chemistry|February 25, 1991
Characterization of human glucocerebrosidase from different mutant allelesT Ohashi, C M Hong, S Weiler, et al.
Journal of the Neurological Sciences|December 1, 1988
Peroxisomal disorders in neurologyR J Wanders, H S Heymans, R B Schutgens, et al.
Analytical Biochemistry|May 1, 1986
A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodiesJ M Aerts, W E Donker-Koopman, G J Murray, et al.
Acta Biologica Et Medica Germanica|January 1, 1981
Control mechanisms of energy-dependent metabolic pathways in hepatocytesJ M Tager, R J Wanders, A K Groen, et al.
Enzyme|January 1, 1987
alpha-Glucosidase deficiency (Pompe's disease)J M Tager, R P Oude Elferink, A Reuser, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Human alkyldihydroxyacetonephosphate synthase deficiency: a new peroxisomal disorderR J Wanders, C Dekker, V A Hovarth, et al.
Pageof 40

Showing results (211-220 of 393) with videos related to

Sort By:
Pageof 40
Circulation Research|April 28, 2001
Attenuation of hypoxic pulmonary vasoconstriction by endotoxemia requires 5-lipoxygenase in miceF Ichinose, W M Zapol, A Sapirstein, et al.
Biochimica Et Biophysica Acta|January 30, 1987
Determination of the structure of the carbohydrate chains of acid alpha-glucosidase from human placentaJ H Mutsaers, H Van Halbeek, J F Vliegenthart, et al.
Biochimica Et Biophysica Acta|November 18, 1981
Monoclonal antibodies against human acid alpha-glucosidaseJ Hilkens, J M Tager, F Buijs, et al.
Biochimica Et Biophysica Acta|January 28, 1985
Soluble sphingomyelinase from human urine as antigen for obtaining anti-sphingomyelinase antibodiesG Weitz, M Driessen, E M Brouwer-Kelder, et al.
The Journal of Biological Chemistry|February 25, 1991
Characterization of human glucocerebrosidase from different mutant allelesT Ohashi, C M Hong, S Weiler, et al.
Journal of the Neurological Sciences|December 1, 1988
Peroxisomal disorders in neurologyR J Wanders, H S Heymans, R B Schutgens, et al.
Analytical Biochemistry|May 1, 1986
A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodiesJ M Aerts, W E Donker-Koopman, G J Murray, et al.
Acta Biologica Et Medica Germanica|January 1, 1981
Control mechanisms of energy-dependent metabolic pathways in hepatocytesJ M Tager, R J Wanders, A K Groen, et al.
Enzyme|January 1, 1987
alpha-Glucosidase deficiency (Pompe's disease)J M Tager, R P Oude Elferink, A Reuser, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Human alkyldihydroxyacetonephosphate synthase deficiency: a new peroxisomal disorderR J Wanders, C Dekker, V A Hovarth, et al.
Pageof 40