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The architecture of the animal fatty acid synthetase. III: Isolation and characterization of β-ketoacyl reductaseWONG, H; MATTICK, J. S; WAKIL, S. J et al.The Journal of biological chemistry (Print). 1983, Vol 258, Num 24, pp 15305-15311, issn 0021-9258Article

Structure of L-3-hydroxyacyl-coenzyme A dehydrogenase: preliminary chain tracing at 2.8 Å resolutionBIRKTOFT, J. J; HOLDEN, H. M; HAMLIN, R et al.Proceedings of the National Academy of Sciences of the United States of America. 1987, Vol 84, Num 23, pp 8262-8266, issn 0027-8424Article

Kinetics of coupled enzyme reactionsSONG-YU YANG; SCHULZ, H.Biochemistry (Easton). 1987, Vol 26, Num 17, pp 5579-5584, issn 0006-2960Article

Fatal outcome in a patient with long-chain 3-hydroxyacyl-CoA dhydrogenase deficiencyRIBES, A; RIUDOR, E; NAVARRO, C et al.Journal of inherited metabolic disease. 1992, Vol 15, Num 2, pp 278-279, issn 0141-8955Article

Skeletal muscle adaptation : training twice every second day vs. training once dailyHANSEN, Anne K; FISCHER, Christian P; PLOMGAARD, Peter et al.Journal of applied physiology (1985). 2005, Vol 98, Num 1, pp 93-99, issn 8750-7587, 7 p.Article

Long-chain 3-hydroxyacyl-CoA dehydrogenase in chorionic villi, fetal liver and fibroblasts and prenatal diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiencyVON DÖBELN, U; VENIZELOS, N; WESTGREN, M et al.Journal of inherited metabolic disease. 1994, Vol 17, Num 2, pp 185-188, issn 0141-8955Article

Calcineurin is not involved in some mitochondrial enzyme adaptations to endurance exercise training in rat skeletal muscleTERADA, Shin; NAKAGAWA, Hisashi; NAKAMURA, Yoshio et al.European journal of applied physiology. 2003, Vol 90, Num 1-2, pp 210-217, 8 p.Article

NEW BIOCHEMICAL METHODS OF DIFFERENTIATING BETWEEN FRESH MEAT AND THAWED, FROZEN MEAT = NOUVELLES METHODES BIOCHIMIQUES DE DIFFERENCIATION ENTRE LA VIANDE FRAICHE ET LA VIANDE CONGELEE, DECONGELEEGOTTESMANN P; HAMM R.1983; FLEISCHWIRTSCHAFT; ISSN 0015-363X; DEU; DA. 1983; VOL. 63; NO 2; PP. 219-221; BIBL. 11 REF.Article

A QUANTITATIVE CYTOCHEMICAL METHOD FOR THE MEASUREMENT OF BETA -HYDROXYACYL COA DEHYDROGENASE ACTIVITY IN RAT HEART MUSCLECHAMBERS DJ; BRAIMBRIDGE MV; FROST GTB et al.1982; HISTOCHEMISTRY (BERL.); ISSN 0301-5564; DEU; DA. 1982; VOL. 75; NO 1; PP. 67-76; BIBL. 13 REF.Article

THE EXISTENCE OF AN INNER-MEMBRANE-BOUND, LONG ACYL-CHAIN-SPECIFIC 3-HYDROXYACYL-COA DEHYDROGENASE IN MAMMALIAN MITOCHONDRIAMUSTAFA EL FAKHRI; MLDDLETON B.1982; BIOCHIM. BIOPHYS. ACTA; ISSN 0006-3002; NLD; DA. 1982; VOL. 713; NO 2; PP. 270-279; BIBL. 27 REF.Article

Purification, cloning, and overexpression of an alcohol dehydrogenase from Nocardia globerula reducing aliphatic ketones and bulky ketoestersPARKOT, Julia; GRÖGER, Harald; HUMMEL, Werner et al.Applied microbiology and biotechnology. 2010, Vol 86, Num 6, pp 1813-1820, issn 0175-7598, 8 p.Article

The HADHSC gene encoding short-chain L-3-hydroxyacyl-CoA dehydrogenase (SCHAD) and type 2 diabetes susceptibility : The damage studyVAN HOVE, Els C; HANSEN, Torben; MAASSEN, J. Antonie et al.Diabetes (New York, NY). 2006, Vol 55, Num 11, pp 3193-3196, issn 0012-1797, 4 p.Article

Evidence for fatty acid oxidation in human placenta, and the relationship of fatty acid oxidation enzyme activities with gestational ageRAKHEJA, D; BENNETT, M. J; FOSTER, B. M et al.Placenta (Eastbourne). 2002, Vol 23, Num 5, pp 447-450, issn 0143-4004Article

Structural organization of the gene for rat enoyl-CoA hydratase:3-hydroxyacyl-CoA dehydrogenase bifunctional enzymeISHII, N; HIJIKATA, M; OSUMI, T et al.The Journal of biological chemistry (Print). 1987, Vol 262, Num 17, pp 8144-8150, issn 0021-9258Article

Four weeks of speed endurance training reduces energy expenditure during exercise and maintains muscle oxidative capacity despite a reduction in training volumeMARCELLO IAIA, F; HELLSTEN, Ylva; JUNG NIELSEN, Jens et al.Journal of applied physiology (1985). 2009, Vol 106, Num 1, pp 73-80, issn 8750-7587, 8 p.Article

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Clinical presentation and follow-up of 50 patientsDEN BOER, Margarethe E. J; WANDERS, Ronald J. A; MORRIS, Andrew A. M et al.Pediatrics (Evanston). 2002, Vol 109, Num 1, pp 99-104, issn 0031-4005Article

Purification and identification of an Escherichia coli β-keto ester reductase as 2,5-diketo-D-gluconate reductase YqhEHABRYCH, Malgorzata; RODRIGUEZ, Sonia; STEWART, Jon D et al.Biotechnology progress. 2002, Vol 18, Num 2, pp 257-261, issn 8756-7938, 5 p.Article

Method for determining if a corpse has been frozen: measuring the activity of short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD)MIRAS, A; YAPO-ETTE, H; VIANCY-SABAN, C et al.Forensic science international. 2001, Vol 124, Num 1, pp 22-24, issn 0379-0738Article

Lack of quinone reductase activity suggests that amyloid-β peptide/ERAB induced lipid peroxidation is not directly related to production of reactive oxygen species by redoxcyclingSALIM, S; FILLING, C; MARTENSSON, E et al.Toxicology (Amsterdam). 2000, Vol 144, Num 1-3, pp 163-168, issn 0300-483XArticle

Differential diagnosis of hydroxydicarboxylic aciduria based on release of 3H2O from [9,10-3H]myristic and [9,10-3H]palmitic acids by intact cultured fibroblastsOLPIN, S. E; MANNING, N. J; CARPENTER, K et al.Journal of inherited metabolic disease. 1992, Vol 15, Num 6, pp 883-890, issn 0141-8955Article

Octanoate and palmitate β-oxidation in human leukocytes : implications for the rapid diagnosis of fatty acid β-oxidation disordersWANDERS, R. J. A; IJLST, L; VAN ELK, E et al.Journal of inherited metabolic disease. 1991, Vol 14, Num 3, pp 317-320, issn 0141-8955Article

Carnitine supplementation and depletion: tissue carnitines and enzymes in fatty acid oxidationNEGRAO, C. E; JI, L. L; SCHAUER, J. E et al.Journal of applied physiology (1985). 1987, Vol 63, Num 1, pp 315-321, issn 8750-7587Article

Relationship between enoyl-CoA hydratase and a peroxisomal bifunctional enzyme, enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase, from an n-alkane-utilizing yeast, Candida tropicalisUEDA, M; MORIKAWA, T; OKADA, H et al.Agricultural and biological chemistry. 1987, Vol 51, Num 8, pp 2197-2205, issn 0002-1369Article

Paternal Isodisomy of Chromosome 2 as a Cause of Long Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) DeficiencyBASKIN, Berivan; GERAGHTY, Michael; RAY, Peter N et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 7, pp 1808-1811, issn 1552-4825, 4 p.Article

Néovascularisation choroïdienne au cours d'un déficit en Long-Chain 3-Hydroxyacyl CoA Dehydrogenase (LCHAD) = Long-chain 3-hydroxyacyl CoA dehydrogenase deficiency and choroidal neovascularizationSTOPEK, D; GITTEAU LALA, E; LABARTHE, F et al.Journal français d'ophtalmologie. 2008, Vol 31, Num 10, pp 993-998, issn 0181-5512, 6 p.Article

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