Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouse.
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Carnitine supplementation attenuates myocardial lipid accumulation in long-chain acyl-CoA dehydrogenase knockout micePantothenate kinase 1 is required to support the metabolic transition from the fed to the fasted stateProteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) genePioglitazone treatment restores in vivo muscle oxidative capacity in a rat model of diabetes.Mitochondrial fatty acid oxidation disorders: pathophysiological studies in mouse modelsAortic wall proteomic analysis in spontaneously hypertensive rats with a blood pressure decrease induced by 6-week load-free swimming.The absence of ABCD2 sensitizes mice to disruptions in lipid metabolism by dietary erucic acid.Peroxisomal L-bifunctional enzyme (Ehhadh) is essential for the production of medium-chain dicarboxylic acidsThe PPARalpha-PGC-1alpha Axis Controls Cardiac Energy Metabolism in Healthy and Diseased Myocardium.Evidence for Intramyocardial Disruption of Lipid Metabolism and Increased Myocardial Ketone Utilization in Advanced Human Heart Failure.Application of combined omics platforms to accelerate biomedical discovery in diabesity.Metabolic profiling of PPARalpha-/- mice reveals defects in carnitine and amino acid homeostasis that are partially reversed by oral carnitine supplementationOverexpression of carnitine palmitoyltransferase-1 in skeletal muscle is sufficient to enhance fatty acid oxidation and improve high-fat diet-induced insulin resistance.Carnitine supplementation induces acylcarnitine production in tissues of very long-chain acyl-CoA dehydrogenase-deficient mice, without replenishing low free carnitine.Contributions of carnitine acetyltransferases to intracellular acetyl unit transport in Candida albicans.Corresponding increase in long-chain acyl-CoA and acylcarnitine after exercise in muscle from VLCAD mice.Role of medium- and short-chain L-3-hydroxyacyl-CoA dehydrogenase in the regulation of body weight and thermogenesis.Peroxisomal fatty acid uptake mechanism in Saccharomyces cerevisiae.Normal rates of whole-body fat oxidation and gluconeogenesis after overnight fasting and moderate-intensity exercise in patients with medium-chain acyl-CoA dehydrogenase deficiency.Carnitine supplementation in high-fat diet-fed rats does not ameliorate lipid-induced skeletal muscle mitochondrial dysfunction in vivo.A novel mouse model of X-linked cardiac hypertrophy.The Effects of Long- or Medium-Chain Fat Diets on Glucose Tolerance and Myocellular Content of Lipid Intermediates in RatsAcetyl-l-carnitine deficiency in patients with major depressive disorder
P2860
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P2860
Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouse.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Characterization of carnitine ...... dehydrogenase-deficient mouse.
@en
Characterization of carnitine ...... dehydrogenase-deficient mouse.
@nl
type
label
Characterization of carnitine ...... dehydrogenase-deficient mouse.
@en
Characterization of carnitine ...... dehydrogenase-deficient mouse.
@nl
prefLabel
Characterization of carnitine ...... dehydrogenase-deficient mouse.
@en
Characterization of carnitine ...... dehydrogenase-deficient mouse.
@nl
P2093
P2860
P356
P1433
P1476
Characterization of carnitine ...... dehydrogenase-deficient mouse.
@en
P2093
Albert H Bootsma
Frédéric M Vaz
Henk Overmars
Liqun Tian
Naomi van Vlies
Philip A Wood
Willem Kulik
P2860
P304
P356
10.1042/BJ20041489
P407
P577
2005-04-01T00:00:00Z