"Acyl-CoA Dehydrogenase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A flavoprotein oxidoreductase that has specificity for medium-chain fatty acids. It forms a complex with ELECTRON TRANSFERRING FLAVOPROTEINS and conveys reducing equivalents to UBIQUINONE.
- Acyl-CoA Dehydrogenase
- Acyl CoA Dehydrogenase
- Dehydrogenase, Acyl-CoA
- Fatty-acyl CoA Dehydrogenase
- CoA Dehydrogenase, Fatty-acyl
- Dehydrogenase, Fatty-acyl CoA
- Fatty acyl CoA Dehydrogenase
- MCACA Dehydrogenase
- Medium Chain Acyl-CoA Dehydrogenase
- Medium Chain Acyl CoA Dehydrogenase
- Medium-Chain Acyl-Coenzyme A Dehydrogenase
- Medium Chain Acyl Coenzyme A Dehydrogenase
- Octanoyl-CoA Dehydrogenase
- Dehydrogenase, Octanoyl-CoA
- Octanoyl CoA Dehydrogenase
- Palmitoyl-CoA Dehydrogenase
- Dehydrogenase, Palmitoyl-CoA
- Palmitoyl CoA Dehydrogenase
- Acyl-coenzyme A Dehydrogenase
- Acyl coenzyme A Dehydrogenase
- Dehydrogenase, Acyl-coenzyme A
- Medium-Chain Acyl-CoA Dehydrogenase
- Acyl-CoA Dehydrogenase, Medium-Chain
- Dehydrogenase, Medium-Chain Acyl-CoA
Below are MeSH descriptors whose meaning is more general than "Acyl-CoA Dehydrogenase".
Below are MeSH descriptors whose meaning is more specific than "Acyl-CoA Dehydrogenase".
This graph shows the total number of publications written about "Acyl-CoA Dehydrogenase" by people in this website by year, and whether "Acyl-CoA Dehydrogenase" was a major or minor topic of these publications.
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Below are the most recent publications written about "Acyl-CoA Dehydrogenase" by people in Profiles.
Yusupov R, Finegold DN, Naylor EW, Sahai I, Waisbren S, Levy HL. Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening. Mol Genet Metab. 2010 Sep; 101(1):33-9.
Sena S, Hu P, Zhang D, Wang X, Wayment B, Olsen C, Avelar E, Abel ED, Litwin SE. Impaired insulin signaling accelerates cardiac mitochondrial dysfunction after myocardial infarction. J Mol Cell Cardiol. 2009 Jun; 46(6):910-8.
Andresen BS, Dobrowolski SF, O'Reilly L, Muenzer J, McCandless SE, Frazier DM, Udvari S, Bross P, Knudsen I, Banas R, Chace DH, Engel P, Naylor EW, Gregersen N. Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency. Am J Hum Genet. 2001 Jun; 68(6):1408-18.
Wan YJ, Cai Y, Lungo W, Fu P, Locker J, French S, Sucov HM. Peroxisome proliferator-activated receptor alpha-mediated pathways are altered in hepatocyte-specific retinoid X receptor alpha-deficient mice. J Biol Chem. 2000 Sep 08; 275(36):28285-90.
Chace DH, Hillman SL, Van Hove JL, Naylor EW. Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometry. Clin Chem. 1997 Nov; 43(11):2106-13.
Ziadeh R, Hoffman EP, Finegold DN, Hoop RC, Brackett JC, Strauss AW, Naylor EW. Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies. Pediatr Res. 1995 May; 37(5):675-8.