Glutaryl-CoA dehydrogenase

Known as: Glutaryl-CoA Dehydrogenase [Chemical/Ingredient], Glutaryl-Coenzyme A Dehydrogenase, Dehydrogenase, Glutaryl-CoA 
A flavoprotein enzyme that is responsible for the catabolism of LYSINE; HYDROXYLYSINE; and TRYPTOPHAN. It catalyzes the oxidation of GLUTARYL-CoA to… (More)
National Institutes of Health

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Highly Cited
2006
Highly Cited
2006
Glutaryl-CoA dehydrogenase (GCDH) deficiency is a rare inborn disorder of l-lysine, l-hydroxylysine, and l-tryptophan metabolism… (More)
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2006
2006
We report here riboflavin responsiveness in a patient with glutaryl CoA dehydrogenase (GCDH) deficiency, compound heterozygous… (More)
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2006
2006
Glutaryl-CoA dehydrogenase (GCD) is a homotetrameric enzyme containing one noncovalently bound FAD per monomer that oxidatively… (More)
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2005
2005
Neurologic disease in glutaryl-CoA dehydrogenase (GCDH) deficiency usually presents with acute encephalopathic crises before 2… (More)
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Review
2004
Review
2004
Summary: Acute encephalopathic crisis in glutaryl-CoA dehydrogenase deficiency results in an unfavourable disease course and poor… (More)
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Review
2004
Review
2004
Summary: This paper summarizes the published experience as well as results of the 3rd International Workshop on Glutaryl-CoA… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Therapeutic neovascularization may constitute an important strategy to salvage tissue from critical ischemia… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND Prospective studies indicate that baseline levels of C-reactive protein (CRP), the prototypic marker of inflammation… (More)
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Highly Cited
1996
Highly Cited
1996
BACKGROUND Glutaryl-CoA dehydrogenase deficiency (GDD) is a recessively inherited neurometabolic disorder associated with… (More)
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1981
1981
Glutaryl-CoA dehydrogenase, a flavoprotein, catalyzes the reaction -OOCCH3CH2--CH2COSR (FAD leads to FADH2) leads to CH3CH… (More)
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