ACAD8 gene

Known as: ACAD8, ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 8, acyl-CoA dehydrogenase family member 8 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2017
0120042017

Papers overview

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2017
2017
Isobutyryl-CoA Dehydrogenase Deficiency (IBDD) is an inherited disorder of valine metabolism caused by mutations in ACAD8. Most… (More)
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Review
2015
Review
2015
To the Editor : Isobutyryl-CoA dehydrogenase (IBD) deficiency is a very rare autosomal recessive metabolic disorder that is… (More)
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Review
2014
Review
2014
Inherited diseases are the result of DNA sequence changes. In recessive diseases, the clinical phenotype results from the… (More)
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2013
2013
The study of the genetic regulation of metabolism in human serum samples can contribute to a better understanding of the… (More)
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2007
2007
Alzheimer’s disease (AD) is a genetically complex disorder, and several genes related to cholesterol metabolism have been… (More)
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2007
2007
Purpose: Isobutyryl-CoA dehydrogenase deficiency is a defect in valine metabolism and was first reported in a child with… (More)
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2006
2006
The isobutyryl-CoA dehydrogenase (IBD) enzyme is involved in the degradation of valine. IBD deficiency was first reported in 1998… (More)
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2004
2004
Mitochondrial fatty acid β-oxidation is an important energy resource for many mammal tissues. Acyl-CoA dehydrogenases (ACADs) are… (More)
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