Search results
The page "Medium+chain+dehydrogenase" does not exist. You can create a draft and submit it for review or request that a redirect be created, but consider checking the search results below to see whether the topic is already covered.
Medium-chain acyl-CoA dehydrogenase deficiency (MCAD deficiency or MCADD) is a disorder of fatty acid oxidation that impairs the body's ability to break...15 KB (1,670 words) - 22:40, 29 December 2023- specificity for short-, medium-, or long-chain fatty acid acyl-CoA substrates. While different dehydrogenases target fatty acids of varying chain length, all types...17 KB (2,171 words) - 04:03, 25 March 2024
Medium-chain acyl-CoA dehydrogenase (EC 1.3.8.7, fatty acyl coenzyme A dehydrogenase (ambiguous), acyl coenzyme A dehydrogenase (ambiguous), acyl dehydrogenase...5 KB (558 words) - 23:43, 29 March 2024
ACADM (redirect from Medium-chain acyl-coenzyme A dehydrogenase)tissue. Medium-chain fatty acids are also produced when larger fatty acids are degraded. The acyl-coenzyme A dehydrogenase for medium-chain fatty acids...7 KB (955 words) - 09:28, 29 January 2023- Avoiding infant formulas with medium-chain triglycerides as the main fat source Long-chain hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is a mitochondrial...32 KB (3,362 words) - 15:08, 28 May 2024
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency is a rare autosomal recessive fatty acid oxidation disorder that prevents the body from converting...5 KB (399 words) - 20:41, 30 May 2024
Short-chain acyl-CoA dehydrogenase (EC 1.3.8.1, butyryl-CoA dehydrogenase, butanoyl-CoA dehydrogenase, butyryl dehydrogenase, unsaturated acyl-CoA reductase...4 KB (431 words) - 03:14, 30 March 2024- and short chain fatty acids; for this reason this disorder is sometimes called medium- and short-chain 3-hydroxyacyl-coenzyme A dehydrogenase (M/SCHAD)...4 KB (410 words) - 00:38, 2 August 2020
evolutionary relationship with alcohol dehydrogenase, which also belongs to the protein superfamily of medium-chain dehydrogenase/reductase enzymes (MDRs). Mammalian...7 KB (896 words) - 07:30, 3 June 2024
electron transport chain in the mitochondria. Older terms for glycerol-3-phosphate dehydrogenase include alpha glycerol-3-phosphate dehydrogenase (alphaGPDH)...23 KB (2,206 words) - 14:20, 26 August 2023
(December 2008). "Medium- and short-chain dehydrogenase/reductase gene and protein families : Dual functions of alcohol dehydrogenase 3: implications with...50 KB (5,566 words) - 06:06, 3 June 2024- ACADM or MCAD, a gene Medium-chain acyl-CoA dehydrogenase, an enzyme used in lipid metabolism Medium-chain acyl-coenzyme A dehydrogenase deficiency (MCAD deficiency...628 bytes (95 words) - 02:27, 24 October 2022
A dehydrogenase deficiency (LCHAD) - Long-chain 3-hydroxyacyl-coenzyme A Medium-chain acyl-coenzyme A dehydrogenase deficiency (MCAD) - Medium-chain acyl-coenzyme...4 KB (356 words) - 21:16, 7 December 2020
Fatty aldehyde dehydrogenase (or long-chain-aldehyde dehydrogenase) is an aldehyde dehydrogenase enzyme that in human is encoded in the ALDH3A2 gene on...5 KB (613 words) - 00:23, 4 April 2024- microsomal short-chain dehydrogenase/reductase and cytosolic medium-chain alcohol dehydrogenases. In Bovine, retinol dehydrogenase is found as a part...14 KB (1,491 words) - 22:48, 27 March 2024
HADHA (redirect from Long-chain 3-hydroxy acyl-coenzyme A dehydrogenase)associated with trifunctional protein deficiency or long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. HADHA is an 82.9 kDa protein composed of...12 KB (1,371 words) - 14:19, 16 June 2023- Fatty acid (redirect from Long chain fatty acid)2013. ISBN 978-1-118-16945-2. Roth, Karl S. (2013-12-19). "Medium-Chain Acyl-CoA Dehydrogenase Deficiency". Medscape. Beermann, C.; Jelinek, J.; Reinecker...54 KB (5,037 words) - 00:57, 30 March 2024
- fatty acid metabolism Long-chain hydroxyacyl-CoA dehydrogenase deficiency (LCHAD) > 1 in 75,000 Medium-chain acyl-CoA dehydrogenase deficiency (MCAD) > 1 in...7 KB (716 words) - 06:19, 9 June 2024
3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs...7 KB (959 words) - 02:18, 10 March 2024- and severe hypoglycemia. Disorders of fatty acid oxidation Medium chain acylCoA dehydrogenase deficiency (MCAD) Familial Leucine sensitive hypoglycemia...21 KB (1,265 words) - 01:46, 22 December 2023
- by the epithelium of decidual glands and inhibition of prostaglandin dehydrogenase (WHO 1997). Side‐effects of medical methods are heavy bleeding, pain
- Long chain/very long chain acyl CoA dehydrogenase deficiency LCAD VLCAD E71.311 Medium chain acyl CoA dehydrogenase deficiency MCAD E71.312 Short chain acyl
- Medium-chain acyl-coenzyme A dehydrogenase Deficiency Medium-chain acyl-coenzyme A dehydrogenase (MCAD) is an enzyme involved in mitochondrial fatty acid