Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Tager

Showing results (251-260 of 393) with videos related to

Pageof 40
Sort By:
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.
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.
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.
Biochemical Society Transactions|December 1, 1984
Metabolic consequences of genetic defects in lysosomesJ M Tager, L V Jonsson, J M Aerts, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activitiesR J Wanders, C W van Roermund, A Schelen, et al.
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.
Pageof 40

Showing results (251-260 of 393) with videos related to

Sort By:
Pageof 40
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.
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.
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.
Biochemical Society Transactions|December 1, 1984
Metabolic consequences of genetic defects in lysosomesJ M Tager, L V Jonsson, J M Aerts, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activitiesR J Wanders, C W van Roermund, A Schelen, et al.
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.
Pageof 40