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J M Tager

Showing results (121-130 of 177) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1992
X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defectR J Wanders, C W van Roermund, W Lageweg, et al.
Progress in Clinical and Biological Research|January 1, 1988
Aberration in de novo ether lipid biosynthesis in peroxisomal disordersH van den Bosch, C G Schalkwijk, G Schrakamp, et al.
Biochimica Et Biophysica Acta|December 14, 1987
An improved procedure for the isolation of lamellar bodies from human lung. Lamellar bodies free of lysosomes contain a spectrum of lysosomal-type hydrolasesA C de Vries, A W Schram, M van den Berg, et al.
European Journal of Cell Biology|November 1, 1985
The subcellular localization of soluble and membrane-bound lysosomal enzymes in I-cell fibroblasts: a comparative immunocytochemical studyJ M van Dongen, R Willemsen, E I Ginns, et al.
European Journal of Cell Biology|April 1, 1992
Turnover of peroxisomal vesicles by autophagic proteolysis in cultured fibroblasts from Zellweger patientsJ C Heikoop, M van den Berg, A Strijland, et al.
Biochimica Et Biophysica Acta|May 10, 1979
Factors affecting the hydrolysis of ceramide-3 by alpha-galactosidase A from human liverA W Schram, M N Hamers, M R Samson, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23A Bout, J M Hoovers, E Bakker, et al.
Journal of Lipid Research|July 1, 1985
Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndromeG Schrakamp, C F Roosenboom, R B Schutgens, et al.
FEBS Letters|April 24, 1990
Demonstration of two isoforms of subunit VIIa of cytochrome c oxidase from human skeletal muscle. Implications for mitochondrial myopathiesJ J Van Beeumen, A B Van Kuilenburg, S Van Bun, et al.
Journal of the Neurological Sciences|February 1, 1987
Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblastsR J Wanders, R B Schutgens, G Schrakamp, et al.
Pageof 18

Showing results (121-130 of 177) with videos related to

Sort By:
Pageof 18
Journal of Inherited Metabolic Disease|January 1, 1992
X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defectR J Wanders, C W van Roermund, W Lageweg, et al.
Progress in Clinical and Biological Research|January 1, 1988
Aberration in de novo ether lipid biosynthesis in peroxisomal disordersH van den Bosch, C G Schalkwijk, G Schrakamp, et al.
Biochimica Et Biophysica Acta|December 14, 1987
An improved procedure for the isolation of lamellar bodies from human lung. Lamellar bodies free of lysosomes contain a spectrum of lysosomal-type hydrolasesA C de Vries, A W Schram, M van den Berg, et al.
European Journal of Cell Biology|November 1, 1985
The subcellular localization of soluble and membrane-bound lysosomal enzymes in I-cell fibroblasts: a comparative immunocytochemical studyJ M van Dongen, R Willemsen, E I Ginns, et al.
European Journal of Cell Biology|April 1, 1992
Turnover of peroxisomal vesicles by autophagic proteolysis in cultured fibroblasts from Zellweger patientsJ C Heikoop, M van den Berg, A Strijland, et al.
Biochimica Et Biophysica Acta|May 10, 1979
Factors affecting the hydrolysis of ceramide-3 by alpha-galactosidase A from human liverA W Schram, M N Hamers, M R Samson, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23A Bout, J M Hoovers, E Bakker, et al.
Journal of Lipid Research|July 1, 1985
Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndromeG Schrakamp, C F Roosenboom, R B Schutgens, et al.
FEBS Letters|April 24, 1990
Demonstration of two isoforms of subunit VIIa of cytochrome c oxidase from human skeletal muscle. Implications for mitochondrial myopathiesJ J Van Beeumen, A B Van Kuilenburg, S Van Bun, et al.
Journal of the Neurological Sciences|February 1, 1987
Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblastsR J Wanders, R B Schutgens, G Schrakamp, et al.
Pageof 18