Hydroxyeicosatetraenoic acid oxidation in Chinese hamster ovary cells: a peroxisomal metabolic pathway.
暂无分享,去创建一个
[1] A. A. Spector,et al. Hydroxyeicosatetraenoic acid metabolism in cultured human skin fibroblasts. Evidence for peroxisomal beta-oxidation. , 1990, The Journal of clinical investigation.
[2] C. Raetz,et al. Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome. , 1989, The Journal of biological chemistry.
[3] M. Hart,et al. Murine cerebral microvascular endothelium incorporate and metabolize 12‐hydroxyeicosatetraenoic acid , 1988, Journal of cellular physiology.
[4] A. A. Spector,et al. Conversion of 15-hydroxyeicosatetraenoic acid to 11-hydroxyhexadecatrienoic acid by endothelial cells. , 1988, Biochemistry.
[5] H. Osmundsen,et al. Peroxisomal beta-oxidation of long-chain fatty acids possessing different extents of unsaturation. , 1987, The Biochemical journal.
[6] A. A. Spector,et al. Formation of 8-hydroxyhexadecatrienoic acid by vascular smooth muscle cells. , 1987, Prostaglandins.
[7] T. Hagve,et al. Mitochondrial and peroxisomal oxidation of arachidonic and eicosapentaenoic acid studied in isolated liver cells. , 1986, Biochimica et biophysica acta.
[8] H. Shio,et al. Zellwegar Syndrome: Biochemical and Morphological Studies on Two Patients Treated with Clofibrate , 1985, Pediatric Research.
[9] L. Peña,et al. Bile acid synthesis in rat liver peroxisomes: metabolism of 26-hydroxycholesterol to 3 beta-hydroxy-5-cholenoic acid. , 1985, Journal of lipid research.
[10] A. Poulos,et al. Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome? , 1984, Clinical genetics.
[11] R. Kelley. Review: the cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspects. , 1983, American journal of medical genetics.
[12] J. Berden,et al. Biochemical Studies in the Liver and Muscle of Patients with Zellweger Syndrome , 1983, Pediatric Research.
[13] J. Bremer,et al. Metabolism of very long-chain monounsaturated fatty acids (22:1) and the adaptation to their presence in the diet. , 1982, Journal of lipid research.
[14] K. Paigen,et al. A simple, rapid, and sensitive DNA assay procedure. , 1980, Analytical biochemistry.
[15] A. Hajra,et al. Subcellular localization of acyl coenzyme A: dihydroxyacetone phosphate acyltransferase in rat liver peroxisomes (microbodies). , 1979, The Journal of biological chemistry.
[16] P. Lazarow. Rat liver peroxisomes catalyze the beta oxidation of fatty acids. , 1978, The Journal of biological chemistry.
[17] M. M. Bradford. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.
[18] I. Rapin,et al. Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal Syndrome , 1973, Science.
[19] M. Lees,et al. Modification of the Lowry procedure for the analysis of proteolipid protein. , 1972, Analytical biochemistry.
[20] U. K. Laemmli,et al. Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.
[21] Seymour Geisser,et al. Statistical Principles in Experimental Design , 1963 .
[22] J. Folch,et al. A simple method for the isolation and purification of total lipides from animal tissues. , 1957, The Journal of biological chemistry.
[23] P. Srere,et al. [1] Citrate synthase. [EC 4.1.3.7. Citrate oxaloacetate-lyase (CoA-acetylating)] , 1969 .