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 |
|---|
| 2008 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2012 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
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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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Zieger M, Keeler AM, Flotte TR, ElMallah MK. AAV9 gene replacement therapy for respiratory insufficiency in very-long chain acyl-CoA dehydrogenase deficiency. J Inherit Metab Dis. 2019 09; 42(5):870-877.
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Keeler AM, Conlon T, Walter G, Zeng H, Shaffer SA, Dungtao F, Erger K, Cossette T, Tang Q, Mueller C, Flotte TR. Long-term correction of very long-chain acyl-coA dehydrogenase deficiency in mice using AAV9 gene therapy. Mol Ther. 2012 Jun; 20(6):1131-8.
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Sahai I, Bailey JC, Eaton RB, Zytkovicz T, Harris DJ. A near-miss: very long chain acyl-CoA dehydrogenase deficiency with normal primary markers in the initial well-timed newborn screening specimen. J Pediatr. 2011 Jan; 158(1):172; author reply 172-3.
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Beattie SG, Goetzman E, Tang Q, Conlon T, Campbell-Thompson M, Matern D, Vockley J, Flotte TR. Recombinant adeno-associated virus-mediated gene delivery of long chain acyl coenzyme A dehydrogenase (LCAD) into LCAD-deficient mice. J Gene Med. 2008 Oct; 10(10):1113-23.
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Spiekerkoetter U, Sun B, Zytkovicz T, Wanders R, Strauss AW, Wendel U. MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency. J Pediatr. 2003 Sep; 143(3):335-42.