FAQ

Short-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial

Known as: Butyryl-CoA Dehydrogenase, EC1.3.99.2, SCAD 
Short-chain specific acyl-CoA dehydrogenase, mitochondrial (412 aa, ~44 kDa) is encoded by the human ACADS gene. This protein plays a role in the… (More)

Topic mentions per year

Topic mentions per year

1981-2017
051019812017

Related topics

Related topics

9 relations
ACADS geneDeficiency of butyryl-CoA dehydrogenaseEnzyme GeneHomo sapiens
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Broader (2)

Butyryl-CoA dehydrogenaseOxidoreductase

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Short-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial
Oxidoreductase
Oxidation-Reduction
Homo sapiens
fatty acid metabolism
Deficiency of butyryl-CoA dehydrogenase

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Aberrant protein acylation is a common observation in inborn errors of acyl-CoA metabolism
Inherited disorders of acyl-CoA metabolism, such as defects in amino acid metabolism and fatty acid oxidation can present with… (More)
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2003
2003
Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder.
OBJECTIVE To understand the expanding clinical and biochemical spectrum of short-chain acyl-CoA dehydrogenase (SCAD) deficiency… (More)
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1998
1998
Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondria.
Most disease-causing missense mutations in short-chain acyl-CoA dehydrogenase (SCAD) and medium-chain acyl-CoA dehydrogenase are… (More)
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1998
1998
Structural characterization of the mouse long-chain acyl-CoA dehydrogenase gene and 5′ regulatory region
Long-chain acyl-CoA dehydrogenase (LCAD) is one of four enzymes involved in the initial step of mitochondrial β-oxidation of… (More)
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1997
1997
Functional correction of short-chain acyl-CoA dehydrogenase deficiency in transgenic mice: implications for gene therapy of human mitochondrial enzyme deficiencies.
We report the therapeutic effects of liver-specific expression of a short-chain acyl-CoA dehydrogenase (SCAD) transgene in the… (More)
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1996
1996
Recurrence of cervical artery dissection. A prospective study of 81 patients.
BACKGROUND AND PURPOSE Spontaneous cervical artery dissection (SCAD) is a common cause of stroke in the young; however, its… (More)
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1994
1994
Late-onset riboflavin-responsive myopathy with combined multiple acyl coenzyme A dehydrogenase and respiratory chain deficiency.
We studied the effect of riboflavin treatment on the clinical status and on the activities of beta-oxidation and respiratory… (More)
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1993
1993
Developmental, nutritional, and hormonal regulation of tissue-specific expression of the genes encoding various acyl-CoA dehydrogenases and alpha-subunit of electron transfer flavoprotein in rat.
Short chain (SCAD), medium chain (MCAD), and long chain acyl-CoA dehydrogenases (LCAD) catalyze the first step of fatty acid… (More)
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1989
1989
Molecular cloning and nucleotide sequence of cDNAs encoding the precursors of rat long chain acyl-coenzyme A, short chain acyl-coenzyme A, and isovaleryl-coenzyme A dehydrogenases. Sequence homology…
cDNAs encoding the entire coding regions of the precursors (p) of rat long chain acyl-CoA (LCAD), short chain acyl-CoA (SCAD) and… (More)
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1989
1989
Molecular cloning and nucleotide sequence of complementary DNAs encoding human short chain acyl-coenzyme A dehydrogenase and the study of the molecular basis of human short chain acyl-coenzyme A…
Complementary DNAs encoding the precursor of human placental short chain acyl-coenzyme A (CoA) dehydrogenase (SCAD) (EC 1.3.99.2… (More)
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