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Long-chain-3-hydroxyacyl-CoA dehydrogenase

Known as: L-CHAD, Long Chain 3 Hydroxyacyl CoA Dehydrogenase, Long-Chain 3-Hydroxyacyl CoA Dehydrogenase 
An NAD-dependent 3-hydroxyacyl CoA dehydrogenase that has specificity for acyl chains containing 8 and 10 carbons.
National Institutes of Health

Related topics

Related topics

10 relations

Broader (1)

3-Hydroxyacyl CoA Dehydrogenases
3-Hydroxyacyl-CoA dehydrogenaseHADHA geneIn BloodProcess of secretion

Papers overview

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Highly Cited
2017
Highly Cited
2017
Adverse Childhood Experiences, Commitment Offense, and Race/Ethnicity: Are the Effects Crime-, Race-, and Ethnicity-Specific?
Adverse childhood experiences are associated with an array of health, psychiatric, and behavioral problems including antisocial… 
2017
2017
Rank And Response: A Field Experiment On Peer Information And Water Use Behavior
2010
2010
The association between overweight and school policies on physical activity: a multilevel analysis among elementary school youth in the PLAY-On study.
The objective is to examine school-level program and policy characteristics and student-level behavioural characteristics… 
2007
2007
Rv3389C from Mycobacterium tuberculosis, a member of the (R)-specific hydratase/dehydratase family.
2007
2007
Identification of novel mutations of the HADHA and HADHB genes in patients with mitochondrial trifunctional protein deficiency.
Patients with long-chain 3-hydroxyacyl coenzyme A dehydrogenase (LCHAD) deficiency manifest hypoketotic hypoglycemia… 
2006
2006
Isotope evidence of palaeorecharge and palaeoclimate in the deep confined aquifers of the Chad Basin, NE Nigeria.
2006
2006
Mechanical properties and the evolution of matrix molecules in PTFE upon irradiation with MeV alpha particles
2004
2004
Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Long-chain L-3-hydroxyacyl-CoA dehydrogenase (L-CHAD, EC 1.1.1.35) deficiency is a recently described inborn error of… 
1997
1997
Clinical, biochemical, and morphologic investigations of a case of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
We report the premortem and postmortem morphologic and histologic features and biochemical findings of a patient with long-chain… 
1994
1994
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (L-CHAD) deficiency in a patient with the Bannayan-Riley-Ruvalcaba syndrome.
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is an autosomal dominant condition of macrocephaly in combination with lipomas… 
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