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acyl-CoA dehydrogenase
Known as:
Medium-Chain Acyl-Coenzyme A Dehydrogenase
, Medium Chain Acyl Coenzyme A Dehydrogenase
, Dehydrogenase, Acyl-CoA
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A flavoprotein oxidoreductase that has specificity for medium-chain fatty acids. It forms a complex with ELECTRON TRANSFERRING FLAVOPROTEINS and…
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National Institutes of Health
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Related topics
Related topics
20 relations
ACAD10 gene
ACAD9 gene
ACADM gene
Acyl CoA Desaturases
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Broader (1)
Acyl CoA Dehydrogenases
Narrower (3)
Deficiency of butyryl-CoA dehydrogenase
Isobutyryl-CoA dehydrogenase deficiency
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2011
Review
2011
Asymmetric N-Heterocyclic Carbene (NHC) Catalyzed Acyl Anion Reactivity.
H. Vora
,
T. Rovis
Aldrichimica Acta
2011
Corpus ID: 3170035
The generation of acyl anion equivalents has been of interest to the synthetic community since the early 1960’s. Of the numerous…
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Highly Cited
1996
Highly Cited
1996
Regulatory Elements That Control Transcription Activation and Unsaturated Fatty Acid-mediated Repression of the Saccharomyces cerevisiae OLE1 Gene (*)
Jae-Yeon Choi
,
J. Stukey
,
Sue‐Yun Hwang
,
C. Martin
Journal of Biological Chemistry
1996
Corpus ID: 24519731
In Saccharomyces cerevisiae, unsaturated fatty acids are formed from saturated acyl-CoA precursors by Ole1p, a Δ-9 fatty acid…
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Highly Cited
1984
Highly Cited
1984
Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes.
N. Datta
,
Golder N Wilson
,
A. Hajra
New England Journal of Medicine
1984
Corpus ID: 30389053
The Zellweger cerebro-hepato-renal syndrome is a genetic disease characterized by the absence of peroxisomes and deficiency of…
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Highly Cited
1983
Highly Cited
1983
Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-CoA dehydrogenase in fibroblasts.
W. Rhead
,
B. Amendt
,
K. Fritchman
,
S. Felts
Science
1983
Corpus ID: 38922575
Dicarboxylic aciduria, an inborn error of metabolism in man, is thought to be caused by defective beta-oxidation of six-carbon to…
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Highly Cited
1982
Highly Cited
1982
Discovery of an arachidonoyl coenzyme A synthetase in human platelets.
D. Wilson
,
S. Prescott
,
P. Majerus
Journal of Biological Chemistry
1982
Corpus ID: 22726493
Highly Cited
1972
Highly Cited
1972
Effect of phospholipase C hydrolysis of membrane phospholipids on membranous enzymes.
R. Mavis
,
R. Bell
,
P. Vagelos
Journal of Biological Chemistry
1972
Corpus ID: 29586850
Highly Cited
1968
Highly Cited
1968
Activity and intracellular distribution of enzymes of ketone-body metabolism in rat liver.
D. Williamson
,
M. Bates
,
H. Krebs
Biochemical Journal
1968
Corpus ID: 6056537
1. The activities of hydroxymethylglutaryl-CoA synthase and lyase in rat liver were found to be two- to 15-fold greater than…
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Highly Cited
1964
Highly Cited
1964
PALMITYL-COA:CARNITINE PALMITYLTRANSFERASE. PURIFICATION FROM CALF-LIVER MITOCHONDRIA AND SOME PROPERTIES OF THE ENZYME.
K. Norum
Biochimica et Biophysica Acta
1964
Corpus ID: 43122975
Highly Cited
1961
Highly Cited
1961
The Enzymic Synthesis of Amino Acyl Derivatives of Ribonucleic Acid II. THE PREPARATION OF LEUCYL-, VALYL-, ISOLEUCYL-, AND METHIONYL RIBONUCLEIC ACID SYNTHETASES FROM ESCHERICHIA COLI
F. Bergmann
,
P. Berg
,
M. Dieckmann
1961
Corpus ID: 17611908
Highly Cited
1960
Highly Cited
1960
Biosynthesis of Fatty Acids I. STUDIES WITH ENZYMES OBTAINED FROM LIVER
R. Brady
,
R. Bradley
,
E. Trams
1960
Corpus ID: 8892590
The requirement for bicarbonate in the incubation medium for the conversion of octanoic acid to stearic acid by slices of liver…
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