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5. 4-bromotiglic acid, a novel inhibitor of thiolases and a tool for assessing the cooperation between the membrane-bound and soluble beta-oxidation systems of rat liver mitochondria. Liang X; Schulz H Biochemistry; 1998 Nov; 37(44):15548-54. PubMed ID: 9799519 [TBL] [Abstract][Full Text] [Related]
6. Heterogeneity of defects in mitochondrial acetoacetyl-CoA thiolase biosynthesis in fibroblasts from four patients with 3-ketothiolase deficiency. Nagasawa H; Yamaguchi S; Orii T; Schutgens RB; Sweetman L; Hashimoto T Pediatr Res; 1989 Aug; 26(2):145-9. PubMed ID: 2570398 [TBL] [Abstract][Full Text] [Related]
8. 3-Hydroxydicarboxylic and 3-ketodicarboxylic aciduria in three patients: evidence for a new defect in fatty acid oxidation at the level of 3-ketoacyl-CoA thiolase. Bennett MJ; Sherwood WG Clin Chem; 1993 May; 39(5):897-901. PubMed ID: 8485884 [TBL] [Abstract][Full Text] [Related]
9. Fatty acid oxidation in rat brain is limited by the low activity of 3-ketoacyl-coenzyme A thiolase. Yang SY; He XY; Schulz H J Biol Chem; 1987 Sep; 262(27):13027-32. PubMed ID: 3654601 [TBL] [Abstract][Full Text] [Related]
10. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes. Coates PM; Hale DE; Stanley CA; Corkey BE; Cortner JA Pediatr Res; 1985 Jul; 19(7):671-6. PubMed ID: 4022673 [TBL] [Abstract][Full Text] [Related]
11. Defect in biosynthesis of mitochondrial acetoacetyl-coenzyme A thiolase in cultured fibroblasts from a boy with 3-ketothiolase deficiency. Yamaguchi S; Orii T; Sakura N; Miyazawa S; Hashimoto T J Clin Invest; 1988 Mar; 81(3):813-7. PubMed ID: 2893809 [TBL] [Abstract][Full Text] [Related]
12. Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme. Heikoop JC; van Roermund CW; Just WW; Ofman R; Schutgens RB; Heymans HS; Wanders RJ; Tager JM J Clin Invest; 1990 Jul; 86(1):126-30. PubMed ID: 2365812 [TBL] [Abstract][Full Text] [Related]
13. 4-Bromo-2-octenoic acid specifically inactivates 3-ketoacyl-CoA thiolase and thereby fatty acid oxidation in rat liver mitochondria. Li JX; Schulz H Biochemistry; 1988 Aug; 27(16):5995-6000. PubMed ID: 3191104 [TBL] [Abstract][Full Text] [Related]
15. Expression and purification of His-tagged rat mitochondrial 3-ketoacyl-CoA thiolase wild-type and His352 mutant proteins. Zeng J; Li D Protein Expr Purif; 2004 Jun; 35(2):320-6. PubMed ID: 15135409 [TBL] [Abstract][Full Text] [Related]
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18. Biochemical and immunochemical study of seven families with 3-ketothiolase deficiency: diagnosis of heterozygotes using immunochemical determination of the ratio of mitochondrial acetoacetyl-CoA thiolase and 3-ketoacyl-CoA thiolase proteins. Yamaguchi S; Sakai A; Fukao T; Wakazono A; Kuwahara T; Orii T; Hashimoto T Pediatr Res; 1993 May; 33(5):429-32. PubMed ID: 8099727 [TBL] [Abstract][Full Text] [Related]
19. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids. Aubourg P; Kremser K; Roland MO; Rocchiccioli F; Singh I Pediatr Res; 1993 Sep; 34(3):270-6. PubMed ID: 7510868 [TBL] [Abstract][Full Text] [Related]
20. New insights in peroxisomal beta-oxidation. Implications for human peroxisomal disorders. Van Veldhoven PP Verh K Acad Geneeskd Belg; 1998; 60(3):195-214. PubMed ID: 9803880 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]