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ketone body catabolic process
Known as:
ketone body breakdown
, ketone body catabolism
, ketone body degradation
The chemical reactions and pathways resulting in the breakdown of ketone bodies, any one of the three substances: acetoacetate, D-3-hydroxybutyrate…
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National Institutes of Health
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2006
2006
Dietary medium chain triglycerides increase endurance capacity in rats - increased ketone body catabolism and decreased mitochondrial uncoupling
N. S. Knight
,
A. Murray
,
S. Bullock
,
S. Little
,
K. Clarke
2006
Corpus ID: 57468525
2002
2002
Purification and Properties of a Pig Heart Thiolase with Broad Chain Length Specificity and Comparison of Thiolases from Pig Heart and Escherichia COG *
Harold
,
Staack
,
J. Binstock
,
Horst
,
SchulzS
2002
Corpus ID: 30041621
A thiolase (acetyl CoA acyltransferase, EC 2.3.1.16) which acts on substrates of various chain lengths (thiolase I) has been…
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1998
1998
Practical assay method of cytosolic acetoacetyl-CoA thiolase by rapid release of cytosolic enzymes from cultured lymphocytes using digitonin.
H. Watanabe
,
S. Yamaguchi
,
+5 authors
T. Hashimoto
Tohoku journal of experimental medicine
1998
Corpus ID: 28899593
We designed a simple approach to determine cytosolic acetoacetyl-CoA thiolase (CT) activity for differential diagnosis of ketone…
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1996
1996
PRENATAL DIAGNOSIS OF SUCCINYL‐COENZYME A:3‐KETOACID COENZYME A TRANSFERASE DEFICIENCY
T. Fukao
,
Xiang-qian Song
,
+6 authors
N. Kondo
Prenatal Diagnosis
1996
Corpus ID: 6059901
Succinyl‐CoA:3‐ketoacid CoA transferase (SCOT) deficiency is a rare disorder of ketone body catabolism. In the present study, we…
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1996
1996
Mild form of beta‐ketothiolase deficiency (mitochondrial acetoacetyl‐CoA thiolase deficiency) in two Japanese siblings: identification of detectable residual activity and cross‐reactive material in…
T. Fukao
,
A. Kodama
,
+8 authors
N. Kondo
Clinical Genetics
1996
Corpus ID: 19101086
Mitochondrial acetoacetyl‐CoA thiolase (T2) deficiency is an inherited metabolic disorder of isoleucine and ketone body…
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1995
1995
Prenatal diagnosis in a family with mitochondrial acetoacetyl‐coenzyme a thiolase deficiency with the use of the polymerase chain reaction followed by the heteroduplex detection method
T. Fukao
,
A. Wakazono
,
+4 authors
T. Orii
Prenatal Diagnosis
1995
Corpus ID: 31695501
Mitochondrial acetoacetyl‐coenzyme A (CoA) thiolase deficiency is an organic aciduria which affects isoleucine and ketone body…
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1992
1992
Sequence of a cDNA clone encoding pig heart mitochondrial CoA transferase.
T. Lin
,
W. A. Bridger
Journal of Biological Chemistry
1992
Corpus ID: 24131335
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