New clinical phenotype of branched-chain acyl-CoA oxidation defectBURLINA, A. B; ZACCHELLO, F; DIONISIS-VICI, C et al.Lancet (British edition). 1991, Num 8781, pp 1522-1523, issn 0140-6736Article

Short chain acyl-coenzyme A dehydrogenase (SCAD) deficiency: immunochemical demonstration of molecular heterogeneity due to variant SCAD with differing stabilityNAITO, E; INDO, Y; TANAKA, K et al.The Journal of clinical investigation. 1989, Vol 84, Num 5, pp 1671-1674, issn 0021-9738, 4 p.Article

Immunoprecipitation and electrophoretic analysis of four human acyl-CoA dehydrogenases and electron transfer flavoprotein using antibodies raised against the corresponding rat enzymesIKEDA, Y; TANAKA, K.Biochemical medicine and metabolic biology. 1987, Vol 37, Num 3, pp 329-334, issn 0885-4505Article

New evidence supporting a radical mechanism of the inactivation of general acyl-CoA dehydrogenase by a metabolite of hypoglycinMING-TAIN LAI; HUNG-WEN LIU.Journal of the American Chemical Society. 1992, Vol 114, Num 8, pp 3160-3162, issn 0002-7863Article

Studies of the inactivation of general acyl-CoA dehydrogenase by racemic (methylenecyclopropyl)acetyl-CoA: new evidence suggesting a radical mechanism of this enzyme-catalyzed reactionLENN, N. D; SHIH, Y; STANKOVICH, M. T et al.Journal of the American Chemical Society. 1989, Vol 111, Num 8, pp 3065-3067, issn 0002-7863, 3 p.Article

Perioperative management of a child with short-chain acyl-CoA dehydrogenase deficiencyTURPIN, Brian; TOBIAS, Joseph D.Paediatric anaesthesia (Paris). 2005, Vol 15, Num 9, pp 771-777, issn 1155-5645, 7 p.Article

Biochemical Correction of Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency After Portal Vein Injection of rAAV8-SCADBEATTIE, Stuart G; GOETZMAN, Eric; CONLON, Thomas et al.Human gene therapy. 2008, Vol 19, Num 6, pp 579-588, issn 1043-0342, 10 p.Article

Analysis of polymerase chain reaction-product by capillary electrophoresis with laser-induced fluorescence detection and its application to the diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiencyARAKAWA, H; UETANAKA, K; MAEDA, M et al.Journal of chromatography. A. 1994, Vol 680, Num 2, pp 517-523Conference Paper

Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiencyDAVIDSON-MUNDT, A; LUDER, A. S; GREENE, C. L et al.The Journal of pediatrics. 1992, Vol 120, Num 3, pp 444-446, issn 0022-3476Article

Impaired tetramer assembly of variant medium-chain acyl-coenzyme A dehydrogenase with a glutamate or aspartate substitution for lysine 304 causing instability of the proteinYOKOTA, I; SAIJO, T; VOCKLEY, J et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 36, pp 26004-26010, issn 0021-9258Article

A new simple screening method for the diagnosis of medium chain acyl-CoA dehydrogenase deficiencyBHUIYAN, A. K. M. J; WATMOUGH, N. J; TURNBULL, D. M et al.Clinica chimica acta. 1987, Vol 165, Num 1, pp 39-44, issn 0009-8981Article

Lethal multiple acyl-CoA dehydrogenation deficiency with dysmorphic featuresBENNETT, M. J; POLLITT, R. J; LAND, J. M et al.Journal of inherited metabolic disease. 1987, Vol 10, Num 1, pp 95-96, issn 0141-8955Article

Purification and properties of short chain acyl-CoA, medium chain acyl-CoA, and isovaleryl-CoA dehydrogenases from human liverFINOCCHIARO, G; ITO, M; TANAKA, K et al.The Journal of biological chemistry (Print). 1987, Vol 262, Num 17, pp 7982-7989, issn 0021-9258Article

The measurement of carnitine and acyl-carnitines : applications to the investigation of patients with suspected inherited disorders of mitochondrial fatty acid oxidationBHUIYAN, A. K. M. J; JACKSON, S; TURNBULL, D. M et al.Clinica chimica acta. 1992, Vol 207, Num 3, pp 185-204, issn 0009-8981Article

Frequency of the G985 MCAD mutation in the general populationBLAKEMORE, A. I. F; SINGLETON, H; POLLITT, R. J et al.Lancet (British edition). 1991, Vol 337, Num 8736, pp 298-299, issn 0140-6736, 2 p.Article

Molecular survey of a prevalent mutation, ⁹⁸⁵A-to-G transition, and identification of five infrequent mutations in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiencyYOKOTA, I; COATES, P. M; HALE, D. E et al.American journal of human genetics. 1991, Vol 49, Num 6, pp 1280-1291, issn 0002-9297Article

Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiencyVAN MALDEGEM, Bianca T; DURAN, Marinus; WANDERS, Ronald J. A et al.JAMA, the journal of the American Medical Association. 2006, Vol 296, Num 8, pp 943-952, issn 0098-7484, 10 p.Article

Identification of two variant short chain acyl-coenzyme a dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiencyNAITO, E; INDO, Y; TANAKA, K et al.The Journal of clinical investigation. 1990, Vol 85, Num 5, pp 1575-1582, issn 0021-9738Article

Inherited disorders of straight chain fatty acid oxidationPOLLITT, R. J.Archives of disease in childhood. 1987, Vol 62, Num 1, pp 6-7, issn 0003-9888Article

Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiencyHARPEY, J.-P; CHARPENTIER, C; COUDE, M et al.The Journal of pediatrics. 1987, Vol 110, Num 6, pp 881-884, issn 0022-3476Conference Paper

Mitochondrial short-chain acyl-CoA dehydrogenase of human liver and kidney can function as an oxidaseVANHOVE, G; VAN VELDHOVEN, P. P; EYSSEN, H. J et al.Biochemical journal (London. 1984). 1993, Vol 292, pp 23-30, issn 0264-6021, 1Article

Regulation of the redox potential of general acyl-CoA dehydrogenase by substrate bindingDONNELLY LENN, N; STANKOVICH, M. T; HUNG-WEN LIU et al.Biochemistry (Easton). 1990, Vol 29, Num 15, pp 3709-3715, issn 0006-2960, 7 p.Article

Functional characterization of rat glutaryl-CoA dehydrogenase and its comparison with straight-chain acyl-CoA dehydrogenaseLONG WU; YUQIN QIAO; JINBO GAO et al.Bioorganic & medicinal chemistry letters (Print). 2011, Vol 21, Num 22, pp 6667-6673, issn 0960-894X, 7 p.Article

A proteomic approach towards the identification of the matrix protein content of the two types of microbodies in Neurospora crassaMANAGADZE, David; WÜRTZ, Christian; WIESE, Sebastian et al.Proteomics (Weinheim. Print). 2010, Vol 10, Num 18, pp 3222-3234, issn 1615-9853, 13 p.Article

Enhanced production of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) via manipulating the fatty acid β-oxidation pathway in E. coliXIAOYUN LU; JINYU ZHANG; QIONG WU et al.FEMS microbiology letters. 2003, Vol 221, Num 1, pp 97-101, issn 0378-1097, 5 p.Article