| 1 |
34785106 | Isoliquiritigenin-mediated miR-23a-3p inhibition activates PGC-1α to alleviate alcoholic liver injury. | 2022 Feb |
1 |
| 2 |
33549404 | Unexpected elevation in valproic acid concentration and agranulocytosis in a patient with short-chain acyl-CoA dehydrogenase deficiency. | 2021 May |
2 |
| 3 |
34790035 | Integrated Analysis of Expression and Prognostic Values of Acyl-CoA Dehydrogenase short-chain in Colorectal Cancer. | 2021 |
1 |
| 4 |
32540485 | Flavine adenine dinucleotide inhibits pathological cardiac hypertrophy and fibrosis through activating short chain acyl-CoA dehydrogenase. | 2020 Aug |
2 |
| 5 |
31120904 | Dynamic modelling of an ACADS genotype in fatty acid oxidation - Application of cellular models for the analysis of common genetic variants. | 2019 |
3 |
| 6 |
28507299 | The Fatty Acid β-Oxidation Pathway is Activated by Leucine Deprivation in HepG2 Cells: A Comparative Proteomics Study. | 2017 May 15 |
1 |
| 7 |
26989860 | Effects of short-chain acyl-CoA dehydrogenase on cardiomyocyte apoptosis. | 2016 Jul |
2 |
| 8 |
27051597 | Clinical relevance of short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Exploring the role of new variants including the first SCAD-disease-causing allele carrying a synonymous mutation. | 2016 Jun |
1 |
| 9 |
28018444 | Compound heterozygous mutations of ACADS gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures review. | 2016 Nov |
1 |
| 10 |
26045367 | Reveal genes functionally associated with ACADS by a network study. | 2015 Sep 15 |
2 |
| 11 |
24478438 | Forkhead box transcription factor regulation and lipid accumulation by hepatitis C virus. | 2014 Apr |
2 |
| 12 |
21211036 | The minor C-allele of rs2014355 in ACADS is associated with reduced insulin release following an oral glucose load. | 2011 Jan 6 |
2 |
| 13 |
21325261 | Mutations of ACADS gene associated with short-chain acyl-coenzyme A dehydrogenase deficiency. | 2011 Fall |
1 |
| 14 |
20376488 | Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency. | 2010 Jun |
2 |
| 15 |
20443061 | Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduria. | 2010 Jun |
1 |
| 16 |
19625492 | Diversity and dispersal of a ubiquitous protein family: acyl-CoA dehydrogenases. | 2009 Sep |
3 |
| 17 |
19639238 | Acyl-CoA dehydrogenases: Dynamic history of protein family evolution. | 2009 Aug |
2 |
| 18 |
18523805 | The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level. | 2008 Aug |
1 |
| 19 |
16020546 | Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids. | 2005 Sep 16 |
2 |
| 20 |
11231285 | Purification, characterization and cloning of isovaleryl-CoA dehydrogenase from higher plant mitochondria. | 2001 Mar |
1 |
| 21 |
11524729 | Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship. | 2001 Sep |
3 |
| 22 |
11216903 | Prevalent mutations in fatty acid oxidation disorders: diagnostic considerations. | 2000 Dec |
2 |