| 1 |
34437764 | Altered mitochondrial metabolism in peripheral blood cells from patients with inborn errors of β-oxidation. | 2022 Jan |
1 |
| 2 |
35001339 | VLCAD inhibits the proliferation and invasion of hepatocellular cancer cells through regulating PI3K/AKT axis. | 2022 May |
2 |
| 3 |
33725513 | Mitochondrial morphology, bioenergetics and proteomic responses in fatty acid oxidation disorders. | 2021 May |
2 |
| 4 |
34245263 | Fetal Cardiac Lipid Sensing Triggers an Early and Sex-related Metabolic Energy Switch in Intrauterine Growth Restriction. | 2021 Oct 21 |
1 |
| 5 |
34465376 | A novel mutation in ACADVL causing very long-chain acyl-coenzyme-A dehydrogenase deficiency in a South Asian pediatric patient: a case report and review of the literature. | 2021 Sep 1 |
1 |
| 6 |
34740033 | Alterations in hepatic fatty acids reveal depletion of total polyunsaturated fatty acids following irinotecan plus 5-fluorouracil treatment in an animal model of colorectal cancer. | 2021 Nov |
1 |
| 7 |
32669490 | Adult-onset Repeat Rhabdomyolysis with a Very Long-chain Acyl-CoA Dehydrogenase Deficiency Due to Compound Heterozygous ACADVL Mutations. | 2020 Nov 1 |
2 |
| 8 |
33597881 | Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation. | 2020 |
1 |
| 9 |
30401918 | Management and diagnosis of mitochondrial fatty acid oxidation disorders: focus on very-long-chain acyl-CoA dehydrogenase deficiency. | 2019 Feb |
2 |
| 10 |
28980192 | Clinical, Biochemical, and Molecular Features in 37 Saudi Patients with Very Long Chain Acyl CoA Dehydrogenase Deficiency. | 2018 |
1 |
| 11 |
29459657 | Very long-/ and long Chain-3-Hydroxy Acyl CoA Dehydrogenase Deficiency correlates with deregulation of the mitochondrial fusion/fission machinery. | 2018 Feb 19 |
1 |
| 12 |
29499131 | Dynamic Regulation of Long-Chain Fatty Acid Oxidation by a Noncanonical Interaction between the MCL-1 BH3 Helix and VLCAD. | 2018 Mar 1 |
2 |
| 13 |
27076444 | The Regulation of Fatty Acid Oxidation in Human Preeclampsia. | 2016 Oct |
2 |
| 14 |
27644403 | Activation of PPARα by Fatty Acid Accumulation Enhances Fatty Acid Degradation and Sulfatide Synthesis. | 2016 Oct |
2 |
| 15 |
25737446 | Strategies for correcting very long chain acyl-CoA dehydrogenase deficiency. | 2015 Apr 17 |
1 |
| 16 |
25811481 | SIRT3 and SIRT5 regulate the enzyme activity and cardiolipin binding of very long-chain acyl-CoA dehydrogenase. | 2015 |
3 |
| 17 |
25843429 | A heterozygous missense mutation in adolescent-onset very long-chain acyl-CoA dehydrogenase deficiency with exercise-induced rhabdomyolysis. | 2015 Apr |
1 |
| 18 |
26051273 | Nickel inhibits mitochondrial fatty acid oxidation. | 2015 Aug 7 |
2 |
| 19 |
26147000 | Energy Metabolism Disorder as a Contributing Factor of Rheumatoid Arthritis: A Comparative Proteomic and Metabolomic Study. | 2015 |
1 |
| 20 |
23185754 | [Study on gene differential expressions of substance and energy metabolism in chronic superficial gastritis patients of Pi deficiency syndrome and of pi-wei hygropyrexia syndrome]. | 2012 Sep |
1 |
| 21 |
22093833 | Role of suppressor of cytokine signaling 3 in lipid metabolism: analysis based on a phage-display human liver cDNA library. | 2011 Dec 9 |
3 |
| 22 |
19889959 | Dysregulation of very long chain acyl-CoA dehydrogenase coupled with lipid peroxidation. | 2010 Jan |
1 |
| 23 |
20480395 | High-resolution melting analysis, a simple and effective method for reliable mutation scanning and frequency studies in the ACADVL gene. | 2010 Jun |
1 |
| 24 |
20816094 | Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I. | 2010 Sep 8 |
1 |
| 25 |
19156135 | Biochemical correction of very long-chain acyl-CoA dehydrogenase deficiency following adeno-associated virus gene therapy. | 2009 Mar |
1 |
| 26 |
19535822 | An overview of beta-oxidation disorders. | 2009 Jun 8 |
1 |
| 27 |
19649258 | A novel tandem mass spectrometry method for rapid confirmation of medium- and very long-chain acyl-CoA dehydrogenase deficiency in newborns. | 2009 Jul 30 |
1 |
| 28 |
17374501 | Expression and characterization of mutations in human very long-chain acyl-CoA dehydrogenase using a prokaryotic system. | 2007 Jun |
2 |
| 29 |
11524729 | Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship. | 2001 Sep |
2 |
| 30 |
10700700 | Death caused by perioperative fasting and sedation in a child with unrecognized very long chain acyl-coenzyme A dehydrogenase deficiency. | 2000 Mar |
1 |
| 31 |
9973285 | Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency. | 1999 Feb |
2 |
| 32 |
10077518 | Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death. | 1999 Mar 16 |
2 |
| 33 |
10607478 | Characterization of the human very-long-chain acyl-CoA dehydrogenase gene promoter region: a role for activator protein 2. | 1999 Dec |
2 |
| 34 |
9498103 | Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients. | 1998 Jan 12 |
2 |
| 35 |
8650121 | Prenatal diagnosis of mitochondrial fatty acid oxidation defects. | 1996 Feb |
2 |
| 36 |
8845838 | Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene. | 1996 Apr |
2 |