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ACATAcyl CoA (Coenzyme A): Cholesterol Acyltransferase
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References in periodicals archive ?
Ladha et al., "Increased insulin and leptin sensitivity in mice lacking acyl CoA:diacylglycerol acyltransferase 1," Journal of Clinical Investigation, vol.
Plasma and hepatic cholesterol and hepatic activities of 3-hydroxy-3-methylglutaryl-CoA reductase and acyl CoA: cholesterol transferase are lower in rats fed citrus peel extract or a mixture of citrus bioflavonoids.
ACS therefore catalyzes the terminal step of peptide fermentation, the conversion of acyl CoA derivatives to the corresponding acid with concomitant synthesis of ATP (1).
Caciotti et al., "Sudden unexpected infant death (SUDI) in a newborn due to medium chain acyl CoA dehydrogenase (MCAD) deficiency with an unusual severe genotype," The Italian Journal of Pediatrics, vol.
Albumin fraction V, fatty acid free (10% solution for tissue culture), TOFA (5-tetradecyloxy-2-furancarboxylic acid), C75 (4-methylene-2-octyl-5-oxotetrahydrofuran-3-carboxylic acid), oleic acid, oleoyl-CoA, D (+) glucose, dexamethasone, insulin, and acyl CoA synthase from Pseudomonas sp.
The decreased CE synthesis was associated with significantly decreased acyl CoA:cholesterol acyltransferase gene expression and activity.
TMS tests: Phenylketonuria, Isovaleric Acidemia, Type 1 Glutaric Aciduria, Medium Chain Acyl CoA Dehydrogenase (MCAD) deficiency, HMG CoA lyase deficiency.
The enzymes located within the mitochondrial matrix are responsible for [beta]-oxidation ofthe medium- to shortchain acyl-CoA intermediates, including long-chain, medium-chain, and short-chain acyl-CoA dehydrogenases; a short-chain hydratase, also named crotonase; a medium-/short-chain 3-hydroxyacyl-CoA-dehydrogenase; and both medium-chain and short-chain 3-keto acyl CoA thiolases (17).