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Showing results (201-210 of 393) with videos related to

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Journal of Lipid Research|March 1, 1988
Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursorsG Schrakamp, C G Schalkwijk, R B Schutgens, et al.
European Journal of Cell Biology|October 1, 1988
Immunocytochemical demonstration of the lysosomal enzyme alpha-glucosidase in the brush border of human intestinal epithelial cellsJ A Fransen, L A Ginsel, P H Cambier, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal and perinatal diagnosis of peroxisomal disordersR B Schutgens, G Schrakamp, R J Wanders, et al.
Biochimica Et Biophysica Acta|January 9, 1985
The cerebro-hepato-renal (Zellweger) syndrome. Impaired de novo biosynthesis of plasmalogens in cultured skin fibroblastsG Schrakamp, R B Schutgens, R J Wanders, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1974
Proceedings: Regulation of hepatic urea synthesisJ R Williamson, J A Gimpel, G J DeLeeuw, et al.
Molecular Immunology|October 1, 1987
Production of monoclonal antibodies to thyroglobulin by in vitro immunization with a free synthetic peptideM de Boer, F A Ossendorp, B J Al, et al.
Biochimica Et Biophysica Acta|April 12, 1979
Use of immobilized antibodies in investigating acid alpha-glucosidase in urine in relation to Pompe's diseaseA W Schram, B Brouwer-Kelder, W E Donker-Koopman, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 31, 1990
[Zellweger syndrome and other peroxisomal disorders: II. (Bio)chemical characteristics of a recently discovered group of diseases]R J Wanders, H S Heymans, R B Schutgens, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis of Zellweger syndrome by direct visualization of peroxisomes in chorionic villus fibroblasts by immunofluorescence microscopyR J Wanders, E A Wiemer, S Brul, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 30, 1986
Deficient activity of glucocerebrosidase in urine from patients with type 1 Gaucher diseaseJ M Aerts, W E Donker-Koopman, M Koot, et al.
Pageof 40

Showing results (201-210 of 393) with videos related to

Sort By:
Pageof 40
Journal of Lipid Research|March 1, 1988
Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursorsG Schrakamp, C G Schalkwijk, R B Schutgens, et al.
European Journal of Cell Biology|October 1, 1988
Immunocytochemical demonstration of the lysosomal enzyme alpha-glucosidase in the brush border of human intestinal epithelial cellsJ A Fransen, L A Ginsel, P H Cambier, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal and perinatal diagnosis of peroxisomal disordersR B Schutgens, G Schrakamp, R J Wanders, et al.
Biochimica Et Biophysica Acta|January 9, 1985
The cerebro-hepato-renal (Zellweger) syndrome. Impaired de novo biosynthesis of plasmalogens in cultured skin fibroblastsG Schrakamp, R B Schutgens, R J Wanders, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1974
Proceedings: Regulation of hepatic urea synthesisJ R Williamson, J A Gimpel, G J DeLeeuw, et al.
Molecular Immunology|October 1, 1987
Production of monoclonal antibodies to thyroglobulin by in vitro immunization with a free synthetic peptideM de Boer, F A Ossendorp, B J Al, et al.
Biochimica Et Biophysica Acta|April 12, 1979
Use of immobilized antibodies in investigating acid alpha-glucosidase in urine in relation to Pompe's diseaseA W Schram, B Brouwer-Kelder, W E Donker-Koopman, et al.
Nederlands Tijdschrift Voor Geneeskunde|March 31, 1990
[Zellweger syndrome and other peroxisomal disorders: II. (Bio)chemical characteristics of a recently discovered group of diseases]R J Wanders, H S Heymans, R B Schutgens, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis of Zellweger syndrome by direct visualization of peroxisomes in chorionic villus fibroblasts by immunofluorescence microscopyR J Wanders, E A Wiemer, S Brul, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 30, 1986
Deficient activity of glucocerebrosidase in urine from patients with type 1 Gaucher diseaseJ M Aerts, W E Donker-Koopman, M Koot, et al.
Pageof 40