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Showing results (121-130 of 393) with videos related to

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Clinical and Experimental Immunology|February 1, 1993
Direct evidence that human follicular dendritic cells (FDC) rescue germinal centre B cells from death by apoptosisE Lindhout, M L Mevissen, J Kwekkeboom, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorderR J Wanders, H Schumacher, J Heikoop, et al.
European Journal of Biochemistry|March 15, 1978
Relationship between oxygen uptake of perifused rat-liver cells and the cytosolic phosphorylation state calculated from indicator metabolites and a redetermined equilibrium constantR van der Meer, T P Akerboom, A K Groen, et al.
The Journal of Biological Chemistry|December 10, 1983
Control of gluconeogenesis in rat liver cells. I. Kinetics of the individual enzymes and the effect of glucagonA K Groen, R C Vervoorn, R Van der Meer, et al.
Journal of Bioenergetics|September 1, 1971
Coupling mechanisms in anionic substrate transport across the inner membrane of rat-liver mitochondriaS Papa, N E Lofrumento, E Quagliariello, et al.
The Biochemical Journal|February 1, 1970
Effect of uncouplers on anion transport in rat liver mitochondriaS Papa, N E Lofrumento, A J Meijer, et al.
European Journal of Biochemistry|July 16, 1984
Factors determining the relative contribution of the adenine-nucleotide translocator and the ADP-regenerating system to the control of oxidative phosphorylation in isolated rat-liver mitochondriaR J Wanders, A K Groen, C W Van Roermund, et al.
The Journal of Clinical Investigation|June 1, 1987
Clinical diversity in glycogenosis type II. Biosynthesis and in situ localization of acid alpha-glucosidase in mutant fibroblastsA J Reuser, M Kroos, R Willemsen, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Pathogenesis of lysosomal storage disorders as illustrated by Gaucher diseaseJ M Aerts, S Van Weely, R Boot, et al.
The Journal of Biological Chemistry|March 15, 1991
Mannose 6-phosphate-independent membrane association of cathepsin D, glucocerebrosidase, and sphingolipid-activating protein in HepG2 cellsS Rijnboutt, H M Aerts, H J Geuze, et al.
Pageof 40

Showing results (121-130 of 393) with videos related to

Sort By:
Pageof 40
Clinical and Experimental Immunology|February 1, 1993
Direct evidence that human follicular dendritic cells (FDC) rescue germinal centre B cells from death by apoptosisE Lindhout, M L Mevissen, J Kwekkeboom, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorderR J Wanders, H Schumacher, J Heikoop, et al.
European Journal of Biochemistry|March 15, 1978
Relationship between oxygen uptake of perifused rat-liver cells and the cytosolic phosphorylation state calculated from indicator metabolites and a redetermined equilibrium constantR van der Meer, T P Akerboom, A K Groen, et al.
The Journal of Biological Chemistry|December 10, 1983
Control of gluconeogenesis in rat liver cells. I. Kinetics of the individual enzymes and the effect of glucagonA K Groen, R C Vervoorn, R Van der Meer, et al.
Journal of Bioenergetics|September 1, 1971
Coupling mechanisms in anionic substrate transport across the inner membrane of rat-liver mitochondriaS Papa, N E Lofrumento, E Quagliariello, et al.
The Biochemical Journal|February 1, 1970
Effect of uncouplers on anion transport in rat liver mitochondriaS Papa, N E Lofrumento, A J Meijer, et al.
European Journal of Biochemistry|July 16, 1984
Factors determining the relative contribution of the adenine-nucleotide translocator and the ADP-regenerating system to the control of oxidative phosphorylation in isolated rat-liver mitochondriaR J Wanders, A K Groen, C W Van Roermund, et al.
The Journal of Clinical Investigation|June 1, 1987
Clinical diversity in glycogenosis type II. Biosynthesis and in situ localization of acid alpha-glucosidase in mutant fibroblastsA J Reuser, M Kroos, R Willemsen, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Pathogenesis of lysosomal storage disorders as illustrated by Gaucher diseaseJ M Aerts, S Van Weely, R Boot, et al.
The Journal of Biological Chemistry|March 15, 1991
Mannose 6-phosphate-independent membrane association of cathepsin D, glucocerebrosidase, and sphingolipid-activating protein in HepG2 cellsS Rijnboutt, H M Aerts, H J Geuze, et al.
Pageof 40