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medium chain acyl CoA dehydrogenases
Summary
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Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
Livers of medium-chain acyl-coenzyme A dehydrgenase (MCAD) KO mice upon LPS treatment with fasting
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Literature
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MCAD deficiency caused by compound heterozygous pathogenic variants in ACADM.
Functional and structural impact of 10 ACADM missense mutations on human medium chain acyl-Coa dehyd…
Messenger RNA rescues medium-chain acyl-CoA dehydrogenase deficiency in fibroblasts from patients an…
MCAD activation by empagliflozin promotes fatty acid oxidation and reduces lipid deposition in NASH.
Genotype and residual enzyme activity in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: Are …
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Clinical Trials
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Fatty Acid Oxidation Defects and Insulin Sensitivity
Systemic Biomarkers of Brain Injury From Hyperammonemia
High Protein Diet in Patients With Long-chain Fatty Acid Oxidation Disorders
Triheptanoin Treatment Trial for Patients With Long-chain Fatty Acid Beta-oxidation Defects
An Open-label Phase 2 Study of UX007 (Triheptanoin) in Subjects With Long-Chain Fatty Acid Oxidation…
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