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Journal of Lipid Research|April 10, 2009
Bile acids: the role of peroxisomesSacha Ferdinandusse, Simone Denis, Phyllis L Faust, et al.
Journal of Inherited Metabolic Disease|April 30, 2010
Clinical aspects of short-chain acyl-CoA dehydrogenase deficiencyBianca T van Maldegem, Ronald J A Wanders, Frits A Wijburg
Cancer Chemotherapy and Pharmacology|January 27, 2000
Phase I trial with weekly EO9, a novel bioreductive alkylating indoloquinone, by the EORTC Early Clinical Study Group (ECSG)S Aamdal, B Lund, I Koier, et al.
Biochimica Et Biophysica Acta|June 5, 1992
Subcellular localization of squalene synthase in human hepatoma cell line Hep G2L H Cohen, M Griffioen, C W van Roermund, et al.
European Journal of Biochemistry|March 15, 1983
Measurement of binding of adenine nucleotides and phosphate to cytosolic proteins in permeabilized rat-liver cellsH S Gankema, A K Groen, R J Wanders, et al.
Orphanet Journal of Rare Diseases|March 12, 2011
Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 geneCaroline Sevin, Sacha Ferdinandusse, Hans R Waterham, et al.
European Journal of Biochemistry|May 17, 1982
Transport of N-acetylglutamate in rat-liver mitochondriaA J Meijer, G M Van Woerkom, R J Wanders, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1992
Infantile refsum disease: gastrointestinal presentation of a peroxisomal disorderH Mandel, D Meiron, R B Schutgens, et al.
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