Acyl-CoA Dehydrogenases

"Acyl-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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Enzymes that catalyze the first step in the beta-oxidation of FATTY ACIDS.

Descriptor ID

D044944

MeSH Number(s)

D08.811.682.660.150

Concept/Terms

Acyl-CoA Dehydrogenases

Below are MeSH descriptors whose meaning is more general than "Acyl-CoA Dehydrogenases".

Chemicals and Drugs [D]
Enzymes and Coenzymes [D08]
Enzymes [D08.811]
Oxidoreductases [D08.811.682]
Oxidoreductases Acting on CH-CH Group Donors [D08.811.682.660]
Acyl-CoA Dehydrogenases [D08.811.682.660.150]

Below are MeSH descriptors whose meaning is related to "Acyl-CoA Dehydrogenases".

Below are MeSH descriptors whose meaning is more specific than "Acyl-CoA Dehydrogenases".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Acyl-CoA Dehydrogenases" by people in Harvard Catalyst Profiles by year, and whether "Acyl-CoA Dehydrogenases" was a major or minor topic of these publication.

Below are the most recent publications written about "Acyl-CoA Dehydrogenases" by people in Profiles.

Integrated changes in thermal stability and proteome abundance during altered nutrient states in Escherichia coli and human cells. Proteomics. 2022 10; 22(19-20):e2100254.

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Measurement of tissue acyl-CoAs using flow-injection tandem mass spectrometry: acyl-CoA profiles in short-chain fatty acid oxidation defects. Mol Genet Metab. 2012 Dec; 107(4):679-83.

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Short-chain acyl-coenzyme A dehydrogenase deficiency. Mol Genet Metab. 2008 Dec; 95(4):195-200.

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Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiency. Genet Med. 2007 Feb; 9(2):108-16.

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Coordinated and reversible reduction of enzymes involved in terminal oxidative metabolism in skeletal muscle mitochondria from a riboflavin-responsive, multiple acyl-CoA dehydrogenase deficiency patient. Electrophoresis. 2006 Mar; 27(5-6):1182-98.

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Anesthetic considerations for a patient with compound heterozygous medium-chain Acyl-CoA dehydrogenase deficiency. Anesth Analg. 2002 Jun; 94(6):1595-7, table of contents.

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Neonatal screening for medium--chain acyl-CoA dehydrogenase deficiency. Lancet. 2002 Feb 16; 359(9306):628.

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Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency. J Inherit Metab Dis. 2001 Jun; 24(3):417-8.

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Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy. Neurology. 1999 Jan 15; 52(2):366-72.

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Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria. Hum Mol Genet. 1998 Apr; 7(4):619-27.

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