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
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| MeSH Number(s) |
D08.811.682.047.820.150
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| 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 |
|---|
| 2007 | 0 | 1 | 1 |
| 2016 | 2 | 0 | 2 |
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Below are the most recent publications written about "3-Hydroxyacyl CoA Dehydrogenases" by people in Profiles.
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Yonekawa Y, Thomas BJ, Capone A. Ultra-Wide-Field Autofluorescence in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Chorioretinopathy. JAMA Ophthalmol. 2016 Apr; 134(4):e155033.
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Falk MJ, Gai X, Shigematsu M, Vilardo E, Takase R, McCormick E, Christian T, Place E, Pierce EA, Consugar M, Gamper HB, Rossmanith W, Hou YM. A novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression. RNA Biol. 2016 05 03; 13(5):477-85.
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Pierce GL, Magyari PM, Aranda JM, Edwards DG, Hamlin SA, Hill JA, Braith RW. Effect of heart transplantation on skeletal muscle metabolic enzyme reserve and fiber type in end-stage heart failure patients. Clin Transplant. 2007 Jan-Feb; 21(1):94-100.
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Suzuki Y, Shimozawa N, Yajima S, Tomatsu S, Kondo N, Nakada Y, Akaboshi S, Lai M, Tanabe Y, Hashimoto T, et al. Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis. Am J Hum Genet. 1994 Jan; 54(1):36-43.