• 2,6-Dimethylheptanoyl-CoA is a specific substrate for long-chain acyl-CoA dehydrogenase (LCAD): evidence for a major role of LCAD in branched-chain fatty acid oxidation
• A mitochondrial long-chain fatty acid oxidation defect leads to transfer RNA uncharging and activation of the integrated stress response in the mouse heart
• A new, simple assay for long-chain acyl-CoA dehydrogenase in cultured skin fibroblasts using stable isotopes and GC-MS
• A simple spectrophotometric assay for long-chain acyl-CoA dehydrogenase activity measurements in human skin fibroblasts
• Ablation of smooth muscle caldesmon affects the relaxation kinetics of arterial muscle
• Acadl-SNP based genotyping assay for long-chain acyl-CoA dehydrogenase deficient mice
• Adenosine induces dilation of epicardial coronary arteries in mice: relationship between coronary flow velocity reserve and coronary flow reserve in vivo using transthoracic echocardiography
• Berberine alleviates nonalcoholic fatty liver induced by a high-fat diet in mice by activating SIRT3
• Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liver
• Cardiac hypertrophy in mice with long-chain acyl-CoA dehydrogenase or very long-chain acyl-CoA dehydrogenase deficiency
• Carnitine supplementation attenuates myocardial lipid accumulation in long-chain acyl-CoA dehydrogenase knockout mice
• Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouse
• Creatine supplementation prevents fatty liver in rats fed choline-deficient diet: a burden of one-carbon and fatty acid metabolism
• Deficiency of the mitochondrial electron transport chain in muscle does not cause insulin resistance
• Dietary phytoestrogens increase metabolic resistance (cold tolerance) in long-chain acyl-CoA dehydrogenase-deficient mice
• Differential induction of genes in liver and brown adipose tissue regulated by peroxisome proliferator-activated receptor-alpha during fasting and cold exposure in acyl-CoA dehydrogenase-deficient mice
• Disrupted blastocoele formation reveals a critical developmental role for long-chain acyl-CoA dehydrogenase
• Dynamic simulations on the mitochondrial fatty acid beta-oxidation network
• Exploring urine biomarkers of early health effects for occupational exposure to titanium dioxide nanoparticles using metabolomics
• Fasting-induced myocardial lipid accumulation in long-chain acyl-CoA dehydrogenase knockout mice is accompanied by impaired left ventricular function
• Food withdrawal lowers energy expenditure and induces inactivity in long-chain fatty acid oxidation-deficient mouse models
• Gasdermin D plays a key role as a pyroptosis executor of non-alcoholic steatohepatitis in humans and mice
• Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse
• Human long chain, very long chain and medium chain acyl-CoA dehydrogenases are specific for the S-enantiomer of 2- methylpentadecanoyl-CoA
• Identification of very-long-chain acyl-CoA dehydrogenase deficiency in three patients previously diagnosed with long-chain acyl-CoA dehydrogenase deficiency
• Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiency
• Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defects
• Influence of dietary fatty acid chain-length on metabolic tolerance in mouse models of inherited defects in mitochondrial fatty acid beta-oxidation
• Is autism a disorder of fatty acid metabolism? Possible dysfunction of mitochondrial beta-oxidation by long chain acyl-CoA dehydrogenase
• L-carnitine supplementation as a potential antioxidant therapy for inherited neurometabolic disorders
• Late-onset riboflavin-responsive myopathy with combined multiple acyl coenzyme A dehydrogenase and respiratory chain deficiency
• Long-chain acyl-CoA dehydrogenase deficiency as a cause of pulmonary surfactant dysfunction
• Management of fatty acid oxidation disorders: a survey of current treatment strategies
• Metabolic dysregulation and emerging therapeutical targets for hepatocellular carcinoma
• Metabolic myopathies
• Mitochondrial acyl-CoA dehydrogenases (VLCAD, LCAD, MCAD, SCAD)
• Mitochondrial dysfunction due to long-chain Acyl-CoA dehydrogenase deficiency causes hepatic steatosis and hepatic insulin resistance
• Mitochondrial long chain fatty acid beta-oxidation in man and mouse
• Mitochondrial transcription factor A is increased but expression of ATP synthase beta subunit and medium-chain acyl-CoA dehydrogenase genes are decreased in hearts of copper-deficient rats
• Myocardial energy shortage and unmet anaplerotic needs in the fasted long-chain acyl-CoA dehydrogenase knockout mouse
• New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency
• Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts
• Recombinant adeno-associated virus-mediated gene delivery of long chain acyl coenzyme A dehydrogenase (LCAD) into LCAD-deficient mice
• Role of peroxisomal oxidation in the conversion of arachidonic acid to eicosatrienoic acid in human skin fibroblasts
• SIRT3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation
• Slc22a5 haploinsufficiency does not aggravate the phenotype of the long-chain acyl-CoA dehydrogenase KO mouse
• Synergistic heterozygosity in mice with inherited enzyme deficiencies of mitochondrial fatty acid beta-oxidation
• Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation
• Tissue-specific strategies of the very-long chain acyl-CoA dehydrogenase-deficient (VLCAD-/-) mouse to compensate a defective fatty acid beta-oxidation
• Tissue-specific strategies of the very-long chain acyl-CoA dehydrogenase-deficient (VLCAD-/-) mouse to compensate a defective fatty acid β-oxidation
• Transcriptome analysis suggests a compensatory role of the cofactors coenzyme A and NAD⁺ in medium-chain acyl-CoA dehydrogenase knockout mice
• Vitamin D Insufficiency Exacerbates Adipose Tissue Macrophage Infiltration and Decreases AMPK/SIRT1 Activity in Obese Rats
• Wuzhi capsule (Schisandra Sphenanthera extract) attenuates liver steatosis and inflammation during non-alcoholic fatty liver disease development