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G Dacremont

Showing results (31-40 of 42) with videos related to

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Journal of Lipid Research|November 4, 2000
Subcellular localization and physiological role of alpha-methylacyl-CoA racemaseS Ferdinandusse, S Denis, L IJlst, et al.
The Veterinary Record|April 9, 1988
Mannosidosis in a litter of Persian catsT Maenhout, J A Kint, G Dacremont, et al.
Biochemical and Biophysical Research Communications|September 16, 1999
Molecular cloning and expression of human carnitine octanoyltransferase: evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acidsS Ferdinandusse, J Mulders, L IJlst, et al.
Journal of Lipid Research|March 15, 2002
Stereochemistry of the peroxisomal branched-chain fatty acid alpha- and beta-oxidation systems in patients suffering from different peroxisomal disordersS Ferdinandusse, H Rusch, A E M van Lint, et al.
Biochemical and Biophysical Research Communications|May 9, 2001
Identification of pristanal dehydrogenase activity in peroxisomes: conclusive evidence that the complete phytanic acid alpha-oxidation pathway is localized in peroxisomesG A Jansen, D M van den Brink, R Ofman, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1991
Peroxisomal localization of the immunoreactive beta-oxidation enzymes in a neonate with a beta-oxidation defect. Pathological observations in liver, adrenal cortex and kidneyM Espeel, F Roels, L Van Maldergem, et al.
The Journal of Biological Chemistry|December 25, 1991
Identification and purification of a peroxisomal branched chain fatty acyl-CoA oxidaseP P Van Veldhoven, G Vanhove, F Vanhoutte, et al.
Human Genetics|October 1, 1991
X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetusL Van Maldergem, M Espeel, F Roels, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Smith-Lemli-Opitz syndrome: deficient delta 7-reductase activity in cultured skin fibroblasts and chorionic villus fibroblasts and its application to pre- and postnatal detectionR J Wanders, G J Romeijn, F Wijburg, et al.
American Journal of Human Genetics|April 28, 2001
Dominant inheritance of sialuria, an inborn error of feedback inhibitionJ G Leroy, R Seppala, M Huizing, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Journal of Lipid Research|November 4, 2000
Subcellular localization and physiological role of alpha-methylacyl-CoA racemaseS Ferdinandusse, S Denis, L IJlst, et al.
The Veterinary Record|April 9, 1988
Mannosidosis in a litter of Persian catsT Maenhout, J A Kint, G Dacremont, et al.
Biochemical and Biophysical Research Communications|September 16, 1999
Molecular cloning and expression of human carnitine octanoyltransferase: evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acidsS Ferdinandusse, J Mulders, L IJlst, et al.
Journal of Lipid Research|March 15, 2002
Stereochemistry of the peroxisomal branched-chain fatty acid alpha- and beta-oxidation systems in patients suffering from different peroxisomal disordersS Ferdinandusse, H Rusch, A E M van Lint, et al.
Biochemical and Biophysical Research Communications|May 9, 2001
Identification of pristanal dehydrogenase activity in peroxisomes: conclusive evidence that the complete phytanic acid alpha-oxidation pathway is localized in peroxisomesG A Jansen, D M van den Brink, R Ofman, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1991
Peroxisomal localization of the immunoreactive beta-oxidation enzymes in a neonate with a beta-oxidation defect. Pathological observations in liver, adrenal cortex and kidneyM Espeel, F Roels, L Van Maldergem, et al.
The Journal of Biological Chemistry|December 25, 1991
Identification and purification of a peroxisomal branched chain fatty acyl-CoA oxidaseP P Van Veldhoven, G Vanhove, F Vanhoutte, et al.
Human Genetics|October 1, 1991
X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetusL Van Maldergem, M Espeel, F Roels, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Smith-Lemli-Opitz syndrome: deficient delta 7-reductase activity in cultured skin fibroblasts and chorionic villus fibroblasts and its application to pre- and postnatal detectionR J Wanders, G J Romeijn, F Wijburg, et al.
American Journal of Human Genetics|April 28, 2001
Dominant inheritance of sialuria, an inborn error of feedback inhibitionJ G Leroy, R Seppala, M Huizing, et al.
Pageof 5