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Showing results (151-160 of 393) with videos related to

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Progress in Clinical and Biological Research|January 1, 1990
Inborn errors of peroxisomal beta-oxidation: biochemical identification using enzymic and immunological methodsR J Wanders, C W van Roermund, A Schelen, et al.
Biochimica Et Biophysica Acta|December 14, 1987
Acid sphingomyelinase from human urine: purification and characterizationL E Quintern, G Weitz, H Nehrkorn, et al.
European Journal of Biochemistry|March 17, 1986
The malate/aspartate shuttle and pyruvate kinase as targets involved in the stimulation of gluconeogenesis by phenylephrineX M Leverve, A J Verhoeven, A K Groen, et al.
European Journal of Pediatrics|April 1, 1986
A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cellsR J Wanders, G Schrakamp, H van den Bosch, et al.
European Journal of Biochemistry|March 15, 1978
Intramitochondrial and extramitochondrial concentrations of adenine nucleotides and inorganic phosphate in isolated hepatocytes from fasted ratsT P Akerboom, H Bookelman, P F Zuurendonk, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysisR J Wanders, C W van Roermund, S Brul, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndromeC W van Roermund, S Brul, J M Tager, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Cytochrome c oxidase: organ-specific isoenzymes and deficienciesK M Sinjorgo, T B Hakvoort, A O Muijsers, et al.
The Journal of Allergy and Clinical Immunology|December 9, 2008
Contribution of CCR4 and CCR8 to antigen-specific T(H)2 cell trafficking in allergic pulmonary inflammationZamaneh Mikhak, Mieko Fukui, Alireza Farsidjani, et al.
Biochimica Et Biophysica Acta|July 20, 1990
Properties of the ATPase activity associated with peroxisome-enriched fractions from rat liver: comparison with mitochondrial F1F0-ATPaseE J Wolvetang, R J Wanders, R B Schutgens, et al.
Pageof 40

Showing results (151-160 of 393) with videos related to

Sort By:
Pageof 40
Progress in Clinical and Biological Research|January 1, 1990
Inborn errors of peroxisomal beta-oxidation: biochemical identification using enzymic and immunological methodsR J Wanders, C W van Roermund, A Schelen, et al.
Biochimica Et Biophysica Acta|December 14, 1987
Acid sphingomyelinase from human urine: purification and characterizationL E Quintern, G Weitz, H Nehrkorn, et al.
European Journal of Biochemistry|March 17, 1986
The malate/aspartate shuttle and pyruvate kinase as targets involved in the stimulation of gluconeogenesis by phenylephrineX M Leverve, A J Verhoeven, A K Groen, et al.
European Journal of Pediatrics|April 1, 1986
A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cellsR J Wanders, G Schrakamp, H van den Bosch, et al.
European Journal of Biochemistry|March 15, 1978
Intramitochondrial and extramitochondrial concentrations of adenine nucleotides and inorganic phosphate in isolated hepatocytes from fasted ratsT P Akerboom, H Bookelman, P F Zuurendonk, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysisR J Wanders, C W van Roermund, S Brul, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndromeC W van Roermund, S Brul, J M Tager, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Cytochrome c oxidase: organ-specific isoenzymes and deficienciesK M Sinjorgo, T B Hakvoort, A O Muijsers, et al.
The Journal of Allergy and Clinical Immunology|December 9, 2008
Contribution of CCR4 and CCR8 to antigen-specific T(H)2 cell trafficking in allergic pulmonary inflammationZamaneh Mikhak, Mieko Fukui, Alireza Farsidjani, et al.
Biochimica Et Biophysica Acta|July 20, 1990
Properties of the ATPase activity associated with peroxisome-enriched fractions from rat liver: comparison with mitochondrial F1F0-ATPaseE J Wolvetang, R J Wanders, R B Schutgens, et al.
Pageof 40