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121 related items for PubMed ID: 3778684
1. Mitochondrial acetoacetyl-CoA thiolase deficiency. Hartlage P, Eller G, Carter L, Roesel A, Hommes F. Biochem Med Metab Biol; 1986 Oct; 36(2):198-206. PubMed ID: 3778684 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
4. The oxoacyl-coenzyme A thiolases of animal tissues. Middleton B. Biochem J; 1973 Apr; 132(4):717-30. PubMed ID: 4721607 [Abstract] [Full Text] [Related]
5. Regulation of thiolases from pig heart. Control of fatty acid oxidation in heart. Olowe Y, Schulz H. Eur J Biochem; 1980 Aug; 109(2):425-9. PubMed ID: 6105961 [Abstract] [Full Text] [Related]
6. [Ketoacidotic coma in an infant as the form of onset of a mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency]. Yeste Fernández D, Castelló Girona F, Mora Graupera J, Riudor Taravila E, Arranz Amo J, Ribes Rubió A, Pérez Cerdá C. An Esp Pediatr; 1996 Jun; 44(6):620-2. PubMed ID: 8849116 [No Abstract] [Full Text] [Related]
7. Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency. Schram AW, Goldfischer S, van Roermund CW, Brouwer-Kelder EM, Collins J, Hashimoto T, Heymans HS, van den Bosch H, Schutgens RB, Tager JM. Proc Natl Acad Sci U S A; 1987 Apr; 84(8):2494-6. PubMed ID: 2882519 [Abstract] [Full Text] [Related]
8. 3-Ketothiolase deficiency: heterogeneity in a defect of mitochondrial acetoacetyl-CoA thiolase biosynthesis in fibroblasts from four patients. Nagasawa H, Yamaguchi S, Orii T, Schutgens RB, Sweetman L, Hashimoto T. J Inherit Metab Dis; 1989 Apr; 12(3):368-72. PubMed ID: 2575689 [No Abstract] [Full Text] [Related]
9. The presence of a new 3-oxoacyl-CoA thiolase in rat liver peroxisomes. Miyazawa S, Osumi T, Hashimoto T. Eur J Biochem; 1980 Feb; 103(3):589-96. PubMed ID: 6766863 [Abstract] [Full Text] [Related]
10. [Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency in Argentina]. de Kremer RD, de Boldini CD, Kelley RI, Civallero GE. Medicina (B Aires); 1997 Feb; 57(1):52-8. PubMed ID: 9435370 [Abstract] [Full Text] [Related]
11. Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency: an inborn error of isoleucine and ketone body metabolism. Søvik O. J Inherit Metab Dis; 1993 Feb; 16(1):46-54. PubMed ID: 8487503 [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 [Abstract] [Full Text] [Related]
13. cDNA-derived amino acid sequence of rat mitochondrial 3-oxoacyl-CoA thiolase with no transient presequence: structural relationship with peroxisomal isozyme. Arakawa H, Takiguchi M, Amaya Y, Nagata S, Hayashi H, Mori M. EMBO J; 1987 May; 6(5):1361-6. PubMed ID: 3038520 [Abstract] [Full Text] [Related]
14. Molecular cloning of cDNA for rat mitochondrial 3-oxoacyl-CoA thiolase. Miura S, Takiguchi M, Matsue H, Amaya Y, Tatibana M, Shigesada K, Osumi T, Hashimoto T, Mori M. Eur J Biochem; 1986 Jan 15; 154(2):479-84. PubMed ID: 3753682 [Abstract] [Full Text] [Related]
15. Beta-ketothiolase deficiency in a Malaysian infant. Rajan D, Constance LSL, Brandon P. Med J Malaysia; 2019 Apr 15; 74(2):174-175. PubMed ID: 31079130 [Abstract] [Full Text] [Related]
16. The NH2-terminal 14-16 amino acids of mitochondrial and bacterial thiolases can direct mature ornithine carbamoyltransferase into mitochondria. Arakawa H, Amaya Y, Mori M. J Biochem; 1990 Jan 15; 107(1):160-4. PubMed ID: 2332418 [Abstract] [Full Text] [Related]
17. Mitochondrial acetoacetyl-CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosis. Paquay S, Bourillon A, Pichard S, Benoist JF, de Lonlay P, Dobbelaere D, Fouilhoux A, Guffon N, Rouvet I, Labarthe F, Mention K, Touati G, Valayannopoulos V, Ogier de Baulny H, Elmaleh-Bergès M, Acquaviva-Bourdain C, Vianey-Saban C, Schiff M. J Inherit Metab Dis; 2017 May 15; 40(3):415-422. PubMed ID: 28255778 [Abstract] [Full Text] [Related]
18. Properties of peroxisomal 3-ketoacyl-coA thiolase from rat liver. Miyazawa S, Furuta S, Osumi T, Hashimoto T, Ui N. J Biochem; 1981 Aug 15; 90(2):511-9. PubMed ID: 6117552 [Abstract] [Full Text] [Related]
19. 6-Methyluracil excretion in 2-methylacetoacetyl-CoA thiolase deficiency and in two children with an unexplained recurrent ketoacidaemia. Cromby CH, Manning NJ, Pollitt RJ, Powell S, Bennett MJ. J Inherit Metab Dis; 1994 Aug 15; 17(1):81-4. PubMed ID: 7914250 [Abstract] [Full Text] [Related]
20. 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 15; 33(5):429-32. PubMed ID: 8099727 [Abstract] [Full Text] [Related] Page: [Next] [New Search]