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Fuel utilization in subjects with carnitine palmitoyltransferase 2 gene mutationsØRNGREEN, Mette C; DUN, Morten; EJSTRUP, Rasmus et al.Annals of neurology. 2005, Vol 57, Num 1, pp 60-66, issn 0364-5134, 7 p.Article

Organization of the human liver carnitine palmitoyltransferase 1 gene (CPT1A) and identification of novel mutations in hypoketotic hypoglycaemiaGOBIN, Stéphanie; BONNEFONT, Jean-Paul; CEDERBAUM, Stephen et al.Human genetics. 2002, Vol 111, Num 2, pp 179-189, issn 0340-6717Article

Carnitine Palmitoyltransferase I and Acyl-CoA Dehydrogenase 9 in Retina : Insights of Retinopathy in Mitochondrial Trifunctional Protein DefectsROOMETS, Eva; KIVELÄ, Tero; TYNI, Tiina et al.Investigative ophthalmology & visual science. 2008, Vol 49, Num 4, pp 1660-1664, issn 0146-0404, 5 p.Article

Molecular assay for detection of the common carnitine palmitoyltransferase 1A 1436(C>T) mutationPARK, Jason Y; NARAYAN, Srinivas B; BENNETT, Michael J et al.Clinical chemistry and laboratory medicine. 2006, Vol 44, Num 9, pp 1090-1091, issn 1434-6621, 2 p.Article

A novel brain-expressed protein related to carnitine palmitoyltransferase IPRICE, Nigel T; VAN DER LEIJ, Feike R; JACKSON, Vicky N et al.Genomics (San Diego, Calif.). 2002, Vol 80, Num 4, pp 433-442, issn 0888-7543, 10 p.Article

Theophylline-induced changes in the activity of carnitine palmitoyltransferase in rat cardiac tissuesALHOMIDA, A. S.Toxicology (Amsterdam). 2000, Vol 145, Num 2-3, pp 185-193, issn 0300-483XArticle

Characterisation of carnitine palmitoyltransferases in patients with a carnitine palmitoyltransferase deficiency: implications for diagnosis and therapySCHAEFER, J; JACKSON, S; TARONI, F et al.Journal of neurology, neurosurgery and psychiatry. 1997, Vol 62, Num 2, pp 169-176, issn 0022-3050Article

Molecular analysis of carnitine palmitoyltransferase II deficiency with hepatocardiomuscular expressionBONNEFONT, J.-P; TARONI, F; CAVADINI, P et al.American journal of human genetics. 1996, Vol 58, Num 5, pp 971-978, issn 0002-9297Article

Involvement of carnitine acyltransferases in peroxisomal fatty acid metabolism by the yeast Pichia guilliermondiiPAGOT, Y; BELIN, J.-M.Applied and environmental microbiology (Print). 1996, Vol 62, Num 10, pp 3864-3867, issn 0099-2240Article

Mutations of carnitine palmitoyltransferase II (CPT II) in Japanese patients with CPT II deficiencyYASUNO, T; KANEOKA, H; SAITO, T et al.Clinical genetics. 2008, Vol 73, Num 5, pp 496-501, issn 0009-9163, 6 p.Article

Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutationsVLADUTIU, Georgirene D; QUACKENBUSH, Elizabeth J; HAINLINE, Bryan E et al.The Journal of pediatrics. 2002, Vol 141, Num 5, pp 734-736, issn 0022-3476, 3 p.Article

Functional characterization of mammalian Mitochondrial carnitine palmitoyltransferases I and II expressed in the yeast Pichia pastorisWOLDEGIORGIS, G; JIANYING SHI; HONGFA ZHU et al.The Journal of nutrition. 2000, Vol 130, Num 2, pp 310S-314S, issn 0022-3166, SUPConference Paper

Human skeletal muscle carnitine palmitoyltransferase I activity determined in isolated intact mitochondriaBERTHON, P. M; HOWLETT, R. A; HEIGENHAUSER, G. J. F et al.Journal of applied physiology (1985). 1998, Vol 85, Num 1, pp 148-153, issn 8750-7587Article

Enhancement of activities relative to fatty acid oxidation in the liver of rats depleted of L-carnitine by D-carnitine and a γ-butyrobetaine hydroxylase inhibitorTSOKO, M; BEAUSEIGNEUR, F; GRESTI, J et al.Biochemical pharmacology. 1995, Vol 49, Num 10, pp 1403-1410, issn 0006-2952Article

Carnitine palmitoyltransferase II deficiency : a new cause of recurrent pancreatitisTEIN, I; CHRISTODOULOU, J; DONNER, E et al.The Journal of pediatrics. 1994, Vol 124, Num 6, pp 938-940, issn 0022-3476Article

Interactive regulation of the pyruvate dehydrogenase complex and the carnitine palmitoyltransferase systemSUGDEN, M. C; HOLNESS, M. J.The FASEB journal. 1994, Vol 8, Num 1, pp 54-61, issn 0892-6638Article

Hypothalamic malonyl-CoA and the control of food intakeSU GAO; MORAN, Timothy H; LOPASCHUK, Gary D et al.Physiology & behavior. 2013, Vol 122, pp 17-24, issn 0031-9384, 8 p.Article

Recruitment of compensatory pathways to sustain oxidative flux with reduced carnitine palmitoyltransferase I activity characterizes inefficiency in energy metabolism in hypertrophied heartsSOROKINA, Natalia; O'DONNELL, J. Michael; MCKINNEY, Ronald D et al.Circulation (New York, N.Y.). 2007, Vol 115, Num 15, pp 2033-2041, issn 0009-7322, 9 p.Article

Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyOLPIN, S. E; AFIFI, A; MUNTONI, F et al.Journal of inherited metabolic disease. 2003, Vol 26, Num 6, pp 543-557, issn 0141-8955, 15 p.Article

Sensitivity of CPT I to malonyl-CoA in trained and untrained human skeletal muscleSTARRITT, E. C; HOWLETT, R. A; HEIGENHAUSER, G. J. F et al.American journal of physiology. Endocrinology and metabolism. 2000, Vol 41, Num 3, pp E462-E468, issn 0193-1849Article

Adult carnitine palmitoyltransferase II deficiency : Detection of characteristic carnitine esters in serum by tandem mass spectrometryGEMPEL, K; KOTTLORS, M; JAKSCH, M et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 8, pp 941-942, issn 0141-8955Article

Fine chromosome mapping of the genes for human liver and muscle carnitine palmitoyltransferase I (CPT1A and CPT1B)BRITTEN, C. H; MACKEY, D. W; ESSER, V et al.Genomics (San Diego, Calif.). 1997, Vol 40, Num 1, pp 209-211, issn 0888-7543Article

Lethal neonatal deficiency of carnitine palmitoyltransferase II associated with dysgenesis of the brain and kidneysNORTH, K. N; HOPPEL, C. L; DE GIROLAMI, U et al.The Journal of pediatrics. 1995, Vol 127, Num 3, pp 414-420, issn 0022-3476Article

Evidence against direct involvement of phosphorylation in the activation of carnitine palmitoyltransferase by okadaic acid in rat hepatocytesGUZMAN, M; KOLODZIEJ, M. P; CALDWELL, A et al.Biochemical journal (London. 1984). 1994, Vol 300, pp 693-699, issn 0264-6021, 3Article

Biochemical evidence for heterozygosity in muscular carnitine palmitoyltransferase deficiencyZIERZ, S; MUNDEGAR, R. R; JERUSALEM, F et al.The Clinical investigator. 1993, Vol 72, Num 1, pp 77-83, issn 0941-0198Article

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