3-Hydroxyacyl CoA Dehydrogenases
"3-Hydroxyacyl CoA Dehydrogenases" 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.
Enzymes that reversibly catalyze the oxidation of a 3-hydroxyacyl CoA to 3-ketoacyl CoA in the presence of NAD. They are key enzymes in the oxidation of fatty acids and in mitochondrial fatty acid synthesis.
| Descriptor ID |
D015094
|
| MeSH Number(s) |
D08.811.682.047.820.150
|
| Concept/Terms |
3-Hydroxyacyl CoA Dehydrogenases- 3-Hydroxyacyl CoA Dehydrogenases
- 3 Hydroxyacyl CoA Dehydrogenases
- CoA Dehydrogenases, 3-Hydroxyacyl
- Dehydrogenases, 3-Hydroxyacyl CoA
- beta-Hydroxyacyl Dehydrogenases
- Dehydrogenases, beta-Hydroxyacyl
- beta Hydroxyacyl Dehydrogenases
|
Below are MeSH descriptors whose meaning is more general than "3-Hydroxyacyl CoA Dehydrogenases".
Below are MeSH descriptors whose meaning is more specific than "3-Hydroxyacyl CoA Dehydrogenases".
This graph shows the total number of publications written about "3-Hydroxyacyl CoA Dehydrogenases" by people in this website by year, and whether "3-Hydroxyacyl CoA Dehydrogenases" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 1 | 1 | 2 |
| 2000 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 1 | 1 | 2 |
| 2009 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "3-Hydroxyacyl CoA Dehydrogenases" by people in Profiles.
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SIRT3 controls brown fat thermogenesis by deacetylation regulation of pathways upstream of UCP1. Mol Metab. 2019 07; 25:35-49.
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Transient central diabetes insipidus induced by ketamine infusion. Ann Pharmacother. 2014 Dec; 48(12):1642-5.
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HIV-1 Vpr enhances PPAR?/d-mediated transcription, increases PDK4 expression, and reduces PDC activity. Mol Endocrinol. 2013 Sep; 27(9):1564-76.
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Mental retardation linked to mutations in the HSD17B10 gene interfering with neurosteroid and isoleucine metabolism. Proc Natl Acad Sci U S A. 2009 Sep 01; 106(35):14820-4.
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Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation. Am J Hum Genet. 2008 Feb; 82(2):432-43.
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Expanded substrate screenings of human and Drosophila type 10 17beta-hydroxysteroid dehydrogenases (HSDs) reveal multiple specificities in bile acid and steroid hormone metabolism: characterization of multifunctional 3alpha/7alpha/7beta/17beta/20beta/21-HSD. Biochem J. 2003 Nov 15; 376(Pt 1):49-60.
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3-Hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency. J Inherit Metab Dis. 2003; 26(1):69-71.
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Absence of the G1528C (E474Q) mutation in the alpha-subunit of the mitochondrial trifunctional protein in women with acute fatty liver of pregnancy. Pediatr Res. 2002 May; 51(5):658-61.
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Early neonatal diagnosis of long-chain 3-hydroxyacyl coenzyme a dehydrogenase and mitochondrial trifunctional protein deficiencies. Mol Genet Metab. 2002 Feb; 75(2):120-7.
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Acylcarnitines in plasma and blood spots of patients with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase defiency. J Inherit Metab Dis. 2000 Sep; 23(6):571-82.