Disease on EC 1.1.1.35 - 3-hydroxyacyl-CoA dehydrogenase
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3-hydroxyacyl-coa dehydrogenase deficiency
3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency and Hyperinsulinaemic Hypoglycaemia: Characterization of a Novel Mutation and Severe Dietary Protein Sensitivity.
3-hydroxyacyl-coa dehydrogenase deficiency
3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrations.
3-hydroxyacyl-coa dehydrogenase deficiency
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment.
3-hydroxyacyl-coa dehydrogenase deficiency
A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women.
3-hydroxyacyl-coa dehydrogenase deficiency
A novel HPLC-based method to diagnose peroxisomal D-bifunctional protein enoyl-CoA hydratase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Biochemical characterization and crystal structure determination of human heart short chain L-3-hydroxyacyl-CoA dehydrogenase provide insights into catalytic mechanism.
3-hydroxyacyl-coa dehydrogenase deficiency
Clinical and image-guided chorioretinal findings in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone.
3-hydroxyacyl-coa dehydrogenase deficiency
Clinical course and cardiovascular outcomes in patients with the long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Clinical outcomes in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Diagnosis of a patient with a kinetic variant of medium and short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency by newborn screening.
3-hydroxyacyl-coa dehydrogenase deficiency
Disorders of mitochondrial long-chain fatty acid oxidation.
3-hydroxyacyl-coa dehydrogenase deficiency
Evidence that 3-hydroxyisobutyric acid inhibits key enzymes of energy metabolism in cerebral cortex of young rats.
3-hydroxyacyl-coa dehydrogenase deficiency
Fatty acid transport and mitochondrial oxidation disorders.
3-hydroxyacyl-coa dehydrogenase deficiency
Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management.
3-hydroxyacyl-coa dehydrogenase deficiency
Heterozygosity for long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency and deterioration in liver function in a newborn infant infected with human immunodeficiency virus.
3-hydroxyacyl-coa dehydrogenase deficiency
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion.
3-hydroxyacyl-coa dehydrogenase deficiency
Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation.
3-hydroxyacyl-coa dehydrogenase deficiency
Impaired Fat Oxidation During Exercise in Long-Chain Acyl-CoA Dehydrogenase Deficiency Patients and Effect of IV-Glucose.
3-hydroxyacyl-coa dehydrogenase deficiency
Inherited metabolic diseases affecting the carrier.
3-hydroxyacyl-coa dehydrogenase deficiency
L-3-hydroxyacyl-CoA dehydrogenase deficiency: two cases with pigmentary retinopathy.
3-hydroxyacyl-coa dehydrogenase deficiency
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings.
3-hydroxyacyl-coa dehydrogenase deficiency
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a severe fatty acid oxidation disorder.
3-hydroxyacyl-coa dehydrogenase deficiency
Long-chain 3-hydroxyacyl-CoA dehydrogenase in chorionic villi, fetal liver and fibroblasts and prenatal diagnosis of 3-hydroxyacyl-CoA dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency and cardiogenic shock.
3-hydroxyacyl-coa dehydrogenase deficiency
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.
3-hydroxyacyl-coa dehydrogenase deficiency
Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase.
3-hydroxyacyl-coa dehydrogenase deficiency
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Ochrobactrum anthropi bacteremia in a child with inborn error of mitochondrial fatty acid oxidation.
3-hydroxyacyl-coa dehydrogenase deficiency
Pigmentary retinopathy in long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Prospective screening for pediatric mitochondrial trifunctional protein defects in pregnancies complicated by liver disease.
3-hydroxyacyl-coa dehydrogenase deficiency
Quantitative measurement of total and free 3-hydroxy fatty acids in serum or plasma samples: short-chain 3-hydroxy fatty acids are not esterified.
3-hydroxyacyl-coa dehydrogenase deficiency
Role of short-chain hydroxyacyl CoA dehydrogenases in SCHAD deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with hyperinsulinism: a novel glucose-fatty acid cycle?
3-hydroxyacyl-coa dehydrogenase deficiency
Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: the clinical relevance of an early diagnosis and report of four new cases.
3-hydroxyacyl-coa dehydrogenase deficiency
Short-chain 3-hydroxyacyl-CoA dehydrogenase is a negative regulator of insulin secretion in response to fuel and non-fuel stimuli in INS832/13 ?-cells.
3-hydroxyacyl-coa dehydrogenase deficiency
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy.
3-hydroxyacyl-coa dehydrogenase deficiency
Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders.
3-hydroxyacyl-coa dehydrogenase deficiency
Stability of long-chain and short-chain 3-hydroxyacyl-CoA dehydrogenase activity in postmortem liver.
3-hydroxyacyl-coa dehydrogenase deficiency
Stable pigmentary retinopathy in a child with 3-hydroxyacyl-CoA dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
Structural organization of the human short-chain L-3-hydroxyacyl-CoA dehydrogenase gene.
3-hydroxyacyl-coa dehydrogenase deficiency
Ten year follow up of pigmentary retinopathy associated with 3-hydroxyacyl-CoA dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
The L-3-hydroxyacyl-CoA dehydrogenase deficiency.
3-hydroxyacyl-coa dehydrogenase deficiency
[Long chain 3-hydroxyacyl-coA dehydrogenase deficiency, asociation with HELLP and magnetic resonance spectroscopy findings].
3-hydroxyacyl-coa dehydrogenase deficiency
[Long-chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency and cardiomyopathy]
Alzheimer Disease
Human brain short chain L-3-hydroxyacyl coenzyme A dehydrogenase is a single-domain multifunctional enzyme. Characterization of a novel 17beta-hydroxysteroid dehydrogenase.
Alzheimer Disease
Role of type 10 17beta-hydroxysteroid dehydrogenase in the pathogenesis of Alzheimer's disease.
Bacteremia
Ochrobactrum anthropi bacteremia in a child with inborn error of mitochondrial fatty acid oxidation.
Brain Diseases
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy.
Breast Neoplasms
Impact of 17?-HSD12, the 3-ketoacyl-CoA reductase of long-chain fatty acid synthesis, on breast cancer cell proliferation and migration.
Carcinogenesis
Increased EHHADH Expression Predicting Poor Survival of Osteosarcoma by Integrating Weighted Gene Coexpression Network Analysis and Experimental Validation.
Carcinoma, Embryonal
Isolation of a cDNA clone encoding mouse 3-hydroxyacyl CoA dehydrogenase.
Cardiomyopathies
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Cardiomyopathies
[Long-chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency and cardiomyopathy]
Cardiomyopathy, Dilated
Medium-Chain Acyl-CoA Dehydrogenase Deficiency in an Infant with Dilated Cardiomyopathy.
Cholestasis
Maternal susceptibility locus for obstetric cholestasis maps to chromosome region 2p13 in Finnish patients.
Confusion
The effect of respiratory chain impairment of beta-oxidation in rat heart mitochondria.
Congenital Hyperinsulinism
Functional genomics of the beta-cell: short-chain 3-hydroxyacyl-coenzyme A dehydrogenase regulates insulin secretion independent of K+ currents.
Congenital Hyperinsulinism
Hyperinsulinism in infancy and childhood: when an insulin level is not always enough.
Congenital Hyperinsulinism
Mechanisms of amino acid-stimulated insulin secretion in congenital hyperinsulinism.
Congenital Hyperinsulinism
Mechanisms of Disease: advances in diagnosis and treatment of hyperinsulinism in neonates.
Congenital Hyperinsulinism
The Hypoglycemic Phenotype is Islet Cell-Autonomous in Short-chain Hydroxyacyl-CoA Dehydrogenase (SCHAD) Deficient Mice.
Congenital Hyperinsulinism
[Hyperinsulinism in infancy and childhood: when an insulin level is not always enough.]
Cytochrome-c Oxidase Deficiency
Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders.
Dehydration
Characterization of a {beta}-hydroxybutyryl-CoA dehydrogenase from Mycobacterium tuberculosis.
Diabetes Mellitus, Type 2
Rat heart fatty acid-binding protein content is increased in experimental diabetes.
Diabetes Mellitus, Type 2
The HADHSC gene encoding short-chain L-3-hydroxyacyl-CoA dehydrogenase (SCHAD) and type 2 diabetes susceptibility: the DAMAGE study.
enoyl-coa hydratase deficiency
A novel HPLC-based method to diagnose peroxisomal D-bifunctional protein enoyl-CoA hydratase deficiency.
Fatty Liver
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Fatty Liver
Acute fatty liver of pregnancy and neonatal long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency.
Fatty Liver
Acute fatty liver of pregnancy associated with short-chain acyl-coenzyme A dehydrogenase deficiency.
Fatty Liver
Acute fatty liver of pregnancy in a woman with ulcerative colitis and familial hidradenitis suppurativa.
Fatty Liver
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Fatty Liver
Maternal acute fatty liver of pregnancy and the associated risk for long-chain 3-hydroxyacyl-coenzyme a dehydrogenase (LCHAD) deficiency in infants.
Fatty Liver, Alcoholic
beta-Oxidation in human alcoholic and non-alcoholic hepatic steatosis.
Fetal Death
Acute fatty liver of pregnancy and neonatal long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency.
Glycogen Storage Disease
Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency.
Glycogen Storage Disease Type V
Increased muscular beta-hydroxyacyl CoA dehydrogenase with McArdle's disease.
Hamartoma Syndrome, Multiple
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (L-CHAD) deficiency in a patient with the Bannayan-Riley-Ruvalcaba syndrome.
Hamartoma Syndrome, Multiple
Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS).
Heart Failure
Contribution of intrinsic skeletal muscle changes to 31P NMR skeletal muscle metabolic abnormalities in patients with chronic heart failure.
Hepatomegaly
Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase cDNA.
Hyperinsulinism
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion.
Hyperinsulinism
Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene.
Hyperinsulinism
Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase.
Hyperinsulinism
Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with hyperinsulinism: a novel glucose-fatty acid cycle?
Hyperinsulinism
Short-chain 3-hydroxyacyl-CoA dehydrogenase is a negative regulator of insulin secretion in response to fuel and non-fuel stimuli in INS832/13 ?-cells.
Hyperinsulinism
Short-chain 3-hydroxyacyl-coenzyme A dehydrogenase associates with a protein super-complex integrating multiple metabolic pathways.
Hypoglycemia
3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrations.
Hypoglycemia
Acute fatty liver of pregnancy and neonatal long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency.
Hypoglycemia
Genome-Wide Homozygosity Analysis Reveals HADH Mutations as a Common Cause of Diazoxide-Responsive Hyperinsulinemic-Hypoglycemia in Consanguineous Pedigrees.
Hypoglycemia
Novel insights into fatty acid oxidation, amino acid metabolism, and insulin secretion from studying patients with loss of function mutations in 3-hydroxyacyl-CoA dehydrogenase.
Hypoglycemia
Short-chain 3-hydroxyacyl-CoA dehydrogenase is a negative regulator of insulin secretion in response to fuel and non-fuel stimuli in INS832/13 ?-cells.
Hypoglycemia
Specificity in beta cell expression of L-3-hydroxyacyl-CoA dehydrogenase, short chain, and potential role in down-regulating insulin release.
Hypokinesia
Effect of spontaneous recovery or retraining after hindlimb suspension on aerobic capacity.
Hypoparathyroidism
Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation.
Insulin Resistance
GLUT4 and Glycogen Synthase Are Key Players in Bed Rest-Induced Insulin Resistance.
Insulin Resistance
Muscle oxidative capacity is a better predictor of insulin sensitivity than lipid status.
Insulinoma
Functional genomics of the beta-cell: short-chain 3-hydroxyacyl-coenzyme A dehydrogenase regulates insulin secretion independent of K+ currents.
Intermittent Claudication
Muscle enzyme adaptation in patients with peripheral arterial insufficiency: spontaneous adaptation, effect of different treatments and consequences on walking performance.
Iron Deficiencies
Perturbation of mitochondrial composition in muscle by iron deficiency. Implications regarding regulation of mitochondrial assembly.
Leptospirosis
Leptospiral 3-hydroxyacyl-CoA dehydrogenase as an early urinary biomarker of leptospirosis.
Liver Cirrhosis
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings.
Liver Diseases
Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancy.
Liver Failure
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
long-chain-3-hydroxyacyl-coa dehydrogenase deficiency
Accumulation of 3-hydroxy-fatty acids in the culture medium of long-chain L-3-hydroxyacyl CoA dehydrogenase (LCHAD) and mitochondrial trifunctional protein-deficient skin fibroblasts: implications for medium chain triglyceride dietary treatment of LCHAD deficiency.
long-chain-3-hydroxyacyl-coa dehydrogenase deficiency
Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients.
long-chain-3-hydroxyacyl-coa dehydrogenase deficiency
Mutations in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase are Associated with Placental Maternal Floor Infarction/Massive Perivillous Fibrin Deposition.
Malnutrition
Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency.
Metabolic Diseases
Biochemical characterization and crystal structure determination of human heart short chain L-3-hydroxyacyl-CoA dehydrogenase provide insights into catalytic mechanism.
Metabolic Diseases
Evidence that 3-hydroxyisobutyric acid inhibits key enzymes of energy metabolism in cerebral cortex of young rats.
Muscle Hypotonia
Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase cDNA.
Muscular Diseases
Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone.
Muscular Diseases
Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS).
Myocardial Infarction
[Adaptation in properties of skeletal muscle to coronary artery occlusion/reperfusion in rats]
Myoglobinuria
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Myoglobinuria
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy.
nadh:ubiquinone reductase (h+-translocating) deficiency
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Neoplasms
Glucose tolerance in relation to skeletal muscle enzyme activities in cancer patients.
Neoplasms
Increased EHHADH Expression Predicting Poor Survival of Osteosarcoma by Integrating Weighted Gene Coexpression Network Analysis and Experimental Validation.
Obesity
Adipocyte differentiation is regulated by mitochondrial trifunctional protein ?-subunit via sirtuin 1.
ornithine carbamoyltransferase deficiency
Inherited metabolic diseases affecting the carrier.
Ornithine Carbamoyltransferase Deficiency Disease
Inherited metabolic diseases affecting the carrier.
Parkinson Disease
L-3-hydroxyacyl-CoA dehydrogenase II protects in a model of Parkinson's disease.
Perinatal Death
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment.
Peripheral Nervous System Diseases
Disorders of mitochondrial long-chain fatty acid oxidation.
Pregnancy Complications
Acute fatty liver of pregnancy associated with short-chain acyl-coenzyme A dehydrogenase deficiency.
Pregnancy Complications
Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management.
Pregnancy Complications
Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Protein Deficiency
D-bifunctional protein deficiency: a cause of neonatal onset seizures and hypotonia.
Protein Deficiency
Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management.
Retinitis Pigmentosa
L-3-hydroxyacyl-CoA dehydrogenase deficiency: two cases with pigmentary retinopathy.
Retinitis Pigmentosa
Pigmentary retinopathy in long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
Retinitis Pigmentosa
Stable pigmentary retinopathy in a child with 3-hydroxyacyl-CoA dehydrogenase deficiency.
Retinitis Pigmentosa
Ten year follow up of pigmentary retinopathy associated with 3-hydroxyacyl-CoA dehydrogenase deficiency.
Rhabdomyolysis
Impaired Fat Oxidation During Exercise in Long-Chain Acyl-CoA Dehydrogenase Deficiency Patients and Effect of IV-Glucose.
Seizures
Seizure-induced impairment in neuronal ketogenesis: Role of zinc-?2-glycoprotein in mitochondria.
Shock, Cardiogenic
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency and cardiogenic shock.
Starvation
Metabolic changes in the African fruit beetle, Pachnoda sinuata, during starvation.
Tuberculosis
Characterization of a {beta}-hydroxybutyryl-CoA dehydrogenase from Mycobacterium tuberculosis.
Tuberculosis
Crystal structure of Mycobacterium tuberculosis FadB2 implicated in mycobacterial ?-oxidation.
Zellweger Syndrome
Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase cDNA.
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