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3-hydroxyacyl-CoA dehydrogenase
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51	Parent Fact Sheet Disorder Long Chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) Cause People with LCHADD have problems breaking down a fatty acid into energy for the body. LCHADD occurs when an enzyme called lo Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 10:55:30 Diabetes Hepatology Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hypoglycemia 3-hydroxyacyl-CoA dehydrogenase 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Blood sugar Very long-chain acyl-coenzyme A dehydrogenase deficiency Glycogen storage disease type I Medicine Health Biology
52	PARENT FACT SHEET Very long-chain acyl-CoA dehydrogenase deficiency (VLCAD) CAUSE VLCAD occurs when the very long chain acyl-CoA dehydrogenase enzyme is missing or not working properly. This enzyme’s job is to break do Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 10:28:56 Very long-chain acyl-coenzyme A dehydrogenase deficiency Rare diseases Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Carnitine Metabolism Acyl CoA dehydrogenase Acyl-CoA ACADVL Health Chemistry Medicine
53	Maine Newborn Screening Program List of Conditions Each baby born in Maine is screened for the conditions listed below. This list is correct as of July 1, 2008 but may change as conditions are added to or removed fro Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-12-13 06:47:38 Medical genetics Newborn screening Hyperammonemia 3-Methylcrotonyl-CoA carboxylase deficiency Isovaleric acidemia Glutaric acidemia type 2 Glutaric aciduria type 1 Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
54	Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:02:30 Hepatology Metabolism Fatty acids Fatty-acid metabolism disorder Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
55	The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Biology D-bifunctional protein deficiency HSD17B4 3-hydroxyacyl-CoA dehydrogenase Medical genetics Ataxia Mitochondrial disease Peroxisomal disorders Medicine Health
56	PDF Document Add to Reading List Source URL: www.jbc.org Language: English Biochemistry Crotonase family PECI Isomerase Thiolase Enoyl-CoA hydratase Acyl CoA dehydrogenase 3-hydroxyacyl-CoA dehydrogenase Acyl-CoA dehydrogenase Biology Chemistry Protein domains
57	PDF Document Add to Reading List Source URL: www.jbc.org Language: English - Date: 2001-06-10 13:02:06 Chemical kinetics Enoyl-CoA hydratase Acyl CoA dehydrogenase PECI Thiolase 3-hydroxyacyl-CoA dehydrogenase Acyl-CoA dehydrogenase Lipid Acyl-CoA oxidase Biology Chemistry Protein domains

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