| 1 |
34437764 | Altered mitochondrial metabolism in peripheral blood cells from patients with inborn errors of β-oxidation. | 2022 Jan |
1 |
| 2 |
33975883 | Suppression of ACADM-Mediated Fatty Acid Oxidation Promotes Hepatocellular Carcinoma via Aberrant CAV1/SREBP1 Signaling. | 2021 Jul 1 |
5 |
| 3 |
31560547 | Quantitative Proteomics of Th-MYCN Transgenic Mice Reveals Aurora Kinase Inhibitor Altered Metabolic Pathways and Enhanced ACADM To Suppress Neuroblastoma Progression. | 2019 Nov 1 |
1 |
| 4 |
29317722 | Loss of the Mitochondrial Fatty Acid β-Oxidation Protein Medium-Chain Acyl-Coenzyme A Dehydrogenase Disrupts Oxidative Phosphorylation Protein Complex Stability and Function. | 2018 Jan 9 |
3 |
| 5 |
28753542 | MRI in medium-chain acyl-coenzyme a dehydrogenase deficiency: neuroimaging during the first month. | 2017 Aug 28 |
2 |
| 6 |
29018241 | Eugenol inhibits oxidative phosphorylation and fatty acid oxidation via downregulation of c-Myc/PGC-1β/ERRα signaling pathway in MCF10A-ras cells. | 2017 Oct 10 |
1 |
| 7 |
26992026 | Insights into Medium-chain Acyl-CoA Dehydrogenase Structure by Molecular Dynamics Simulations. | 2016 Aug |
2 |
| 8 |
25503862 | First case report of medium-chain acyl-coenzyme A dehydrogenase deficiency in China. | 2015 May |
1 |
| 9 |
25743752 | Aspirin regulates hepatocellular lipid metabolism by activating AMPK signaling pathway. | 2015 Feb |
2 |
| 10 |
26798524 | Intermediate MCAD Deficiency Associated with a Novel Mutation of the ACADM Gene: c.1052C>T. | 2015 |
1 |
| 11 |
24478438 | Forkhead box transcription factor regulation and lipid accumulation by hepatitis C virus. | 2014 Apr |
2 |
| 12 |
23509891 | In vitro and in vivo consequences of variant medium-chain acyl-CoA dehydrogenase genotypes. | 2013 Mar 20 |
1 |
| 13 |
23633211 | Production and release of acylcarnitines by primary myotubes reflect the differences in fasting fat oxidation of the donors. | 2013 Jun |
2 |
| 14 |
23810226 | A synonymous polymorphic variation in ACADM exon 11 affects splicing efficiency and may affect fatty acid oxidation. | 2013 Sep-Oct |
1 |
| 15 |
23095120 | Sudden unexpected infant death (SUDI) in a newborn due to medium chain acyl CoA dehydrogenase (MCAD) deficiency with an unusual severe genotype. | 2012 Oct 24 |
1 |
| 16 |
21211036 | The minor C-allele of rs2014355 in ACADS is associated with reduced insulin release following an oral glucose load. | 2011 Jan 6 |
2 |
| 17 |
20434892 | [Infant coma in the emergency department: 2 cases of MCAD deficiency]. | 2010 Jul |
1 |
| 18 |
20567907 | Medium-chain acyl-CoA dehydrogenase deficiency in Saudi Arabia: incidence, genotype, and preventive implications. | 2010 Dec |
1 |
| 19 |
19493551 | Increased lipid metabolism and cell turnover of MiaPaCa2 cells induced by high-fat diet in an orthotopic system. | 2009 Aug |
2 |
| 20 |
18061544 | Mutation of Tyr375 to Lys375 allows medium-chain acyl-CoA dehydrogenase to acquire acyl-CoA oxidase activity. | 2007 Dec |
2 |
| 21 |
16291504 | Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations. | 2006 Jan |
1 |
| 22 |
16365837 | Fluoromorphic substrates for fatty acid metabolism: highly sensitive probes for mammalian medium-chain acyl-CoA dehydrogenase. | 2006 Jan 16 |
1 |
| 23 |
15817096 | The Brugada ECG pattern in a neonate. | 2005 Mar |
1 |
| 24 |
15855325 | Pioglitazone induces mitochondrial biogenesis in human subcutaneous adipose tissue in vivo. | 2005 May |
1 |
| 25 |
15337167 | Thermal unfolding of medium-chain acyl-CoA dehydrogenase and iso(3)valeryl-CoA dehydrogenase: study of the effect of genetic defects on enzyme stability. | 2004 Sep 6 |
1 |
| 26 |
15466077 | The sudden infant death syndrome gene: does it exist? | 2004 Oct |
2 |
| 27 |
15559414 | [Deficiency of the fatty-acid oxidising enzyme medium-chain acyl-CoA dehydrogenase (MCAD) in an adult, detected during a neonatal screening programme]. | 2004 Oct 30 |
2 |
| 28 |
12522104 | The transcriptional coactivator PGC-1 regulates the expression and activity of the orphan nuclear receptor estrogen-related receptor alpha (ERRalpha). | 2003 Mar 14 |
2 |
| 29 |
14692513 | Binding of the human "electron transferring flavoprotein" (ETF) to the medium chain acyl-CoA dehydrogenase (MCAD) involves an arginine and histidine residue. | 2003 Oct |
2 |
| 30 |
12181319 | Peroxisome proliferator-activated receptor coactivator-1alpha (PGC-1alpha) coactivates the cardiac-enriched nuclear receptors estrogen-related receptor-alpha and -gamma. Identification of novel leucine-rich interaction motif within PGC-1alpha. | 2002 Oct 25 |
2 |
| 31 |
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 |
| 32 |
10679947 | Mutation 985A>G in the MCAD gene shows low incidence in Estonian population. | 2000 Mar |
2 |
| 33 |
10913960 | A successful strategy for preimplantation diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. | 2000 Jul |
1 |
| 34 |
11216903 | Prevalent mutations in fatty acid oxidation disorders: diagnostic considerations. | 2000 Dec |
2 |
| 35 |
9477967 | Elimination reactions in the medium-chain acyl-CoA dehydrogenase: bioactivation of cytotoxic 4-thiaalkanoic acids. | 1998 Feb 3 |
1 |
| 36 |
9090694 | Medium chain acyl-CoA dehydrogenase deficiency and fatal valproate toxicity. | 1997 Feb |
1 |
| 37 |
8666240 | Structure and chromosomal location of the mouse medium-chain acyl-CoA dehydrogenase-encoding gene and its promoter. | 1996 May 8 |
1 |
| 38 |
8840534 | Frequency of 985A-to-G mutation in medium-chain acyl-CoA dehydrogenase gene among patients with sudden infant death syndrome, Reye syndrome, severe motor and intellectual disabilities and healthy newborns in Japan. | 1996 Aug |
2 |
| 39 |
7586519 | Identification and quantification of intermediates of unsaturated fatty acid metabolism in plasma of patients with fatty acid oxidation disorders. | 1995 Oct |
1 |
| 40 |
7603790 | Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies. | 1995 May |
1 |
| 41 |
20301597 | Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency | 1993 |
2 |
| 42 |
24242229 | Medium-chain acyl CoA dehydrogenase deficiency: Its relationship to SIDS and the impact on genetic counseling. | 1993 Mar |
1 |
| 43 |
1288265 | Fatty liver, encephalopathy, and sudden unexpected death in early childhood due to medium-chain acyl-coenzyme A dehydrogenase deficiency. | 1992 Dec |
1 |
| 44 |
1731887 | Structural organization and regulatory regions of the human medium-chain acyl-CoA dehydrogenase gene. | 1992 Jan 14 |
2 |
| 45 |
1756601 | Heterogeneity for mutations in medium chain acyl-CoA dehydrogenase deficiency in the UK population. | 1991 Oct |
1 |
| 46 |
2000272 | Hypoglycemia, hypotonia, and cardiomyopathy: the evolving clinical picture of long-chain acyl-CoA dehydrogenase deficiency. | 1991 Mar |
1 |
| 47 |
3035565 | Nucleotide sequence of medium-chain acyl-CoA dehydrogenase mRNA and its expression in enzyme-deficient human tissue. | 1987 Jun |
2 |
| 48 |
3318304 | New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency. | 1987 |
2 |
| 49 |
6646897 | Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels. | 1983 Nov |
1 |