Acyl-CoA Dehydrogenase, Long-Chain
"Acyl-CoA Dehydrogenase, Long-Chain" 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 long-chain fatty acids. It forms a complex with ELECTRON-TRANSFERRING FLAVOPROTEINS and conveys reducing equivalents to UBIQUINONE.
| Descriptor ID |
D044942
|
| MeSH Number(s) |
D08.811.682.660.150.150 D12.776.331.102
|
| Concept/Terms |
Acyl-CoA Dehydrogenase, Long-Chain- Acyl-CoA Dehydrogenase, Long-Chain
- Acyl CoA Dehydrogenase, Long Chain
- Dehydrogenase, Long-Chain Acyl-CoA
- Long-Chain Acyl-CoA Dehydrogenase
- VLCAD
- Very-Long-Chain Acyl-CoA Dehydrogenase
- Acyl-CoA Dehydrogenase, Very-Long-Chain
- Dehydrogenase, Very-Long-Chain Acyl-CoA
- Very Long Chain Acyl CoA Dehydrogenase
- Long-Chain-Acyl-CoA Dehydrogenase
- Dehydrogenase, Long-Chain-Acyl-CoA
- Long Chain Acyl CoA Dehydrogenase
- Long-Chain-Acyl-Coenzyme A Dehydrogenase
- Dehydrogenase, Long-Chain-Acyl-Coenzyme A
- Long Chain Acyl Coenzyme A Dehydrogenase
Decanoyl CoA Dehydrogenase- Decanoyl CoA Dehydrogenase
- CoA Dehydrogenase, Decanoyl
- Dehydrogenase, Decanoyl CoA
- Decanoyl CoA-Dehydrogenase
- CoA-Dehydrogenase, Decanoyl
|
Below are MeSH descriptors whose meaning is more general than "Acyl-CoA Dehydrogenase, Long-Chain".
Below are MeSH descriptors whose meaning is more specific than "Acyl-CoA Dehydrogenase, Long-Chain".
This graph shows the total number of publications written about "Acyl-CoA Dehydrogenase, Long-Chain" by people in this website by year, and whether "Acyl-CoA Dehydrogenase, Long-Chain" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2014 | 0 | 1 | 1 |
| 2015 | 2 | 0 | 2 |
| 2020 | 1 | 1 | 2 |
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Below are the most recent publications written about "Acyl-CoA Dehydrogenase, Long-Chain" by people in Profiles.
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Mitochondrial energetic impairment in a patient with late-onset glutaric acidemia Type 2. Am J Med Genet A. 2020 10; 182(10):2426-2431.
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Accumulation of long-chain fatty acids in the tumor microenvironment drives dysfunction in intrapancreatic CD8+ T cells. J Exp Med. 2020 08 03; 217(8).
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Lipid metabolism in Rhodnius prolixus: Lessons from the genome. Gene. 2017 Jan 05; 596:27-44.
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Elevations of C14:1 and C14:2 Plasma Acylcarnitines in Fasted Children: A Diagnostic Dilemma. J Pediatr. 2016 Feb; 169:208-13.e2.
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Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States. Mol Genet Metab. 2015 Nov; 116(3):139-45.
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Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes. Am J Hum Genet. 2014 Nov 06; 95(5):565-78.
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Creatine supplementation prevents the accumulation of fat in the livers of rats fed a high-fat diet. J Nutr. 2011 Oct; 141(10):1799-804.
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Clinical and biochemical improvement of very long-chain acyl-CoA dehydrogenase deficiency in pregnancy. J Perinatol. 2010 Aug; 30(8):558-62.
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Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutation. Muscle Nerve. 2009 Mar; 39(3):374-82.
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Impaired long-chain fatty acid oxidation and contractile dysfunction in the obese Zucker rat heart. Diabetes. 2002 Aug; 51(8):2587-95.