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Long chain acyl-CoA dehydrogenase deficiency

Known as: Long-chain acyl-CoA dehydrogenase deficiency, Acyl-Coa Dehydrogenase, Long-Chain, Deficiency of, Acyl-CoA Dehydrogenase, Long-Chain Deficiency 
A genetic disorder characterized by deficiency of the enzyme long-chain acyl-coenzyme A dehydrogenase that metabolizes long-chain fatty acids. Signs… Expand
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Hypoxia-inducible factor 1 (HIF-1) mediates a metabolic switch that blocks the conversion of pyruvate to acetyl-CoA in cancer… Expand
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Review
2014
Review
2014
CoA (coenzyme A) and its derivatives have a critical role in regulating cardiac energy metabolism. This includes a key role as a… Expand
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2013
2013
AIMS The aim of this animal study is to assess fasting-induced changes in myocardial substrate metabolism and energy status as a… Expand
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2013
2013
Physiological hyperglycaemia and hyperinsulinaemia are strong modulators of gene expression, which underpins some of their well… Expand
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2010
2010
OBJECTIVE The role of angiotensin converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism in early onset coronary… Expand
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Highly Cited
2005
Highly Cited
2005
In the present paper, we describe a novel method which enables the analysis of tissue acylcarnitines and carnitine biosynthesis… Expand
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Highly Cited
2003
Highly Cited
2003
Fatty acid oxidation (FAO) defects are inborn errors of metabolism clinically associated with cardiomyopathy and sudden infant… Expand
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2002
2002
Very-long-chain acyl-coenzyme A dehydrogenase deficiency is an inborn error of fatty acid metabolism. The clinical presentation… Expand
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1989
1989
cDNAs encoding the entire coding regions of the precursors (p) of rat long chain acyl-CoA (LCAD), short chain acyl-CoA (SCAD) and… Expand
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Review
1987
Review
1987
There are now nine inherited diseases that have been identified in the pathway of mitochondrial fatty acid oxidation, including… Expand
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