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Results 1 - 10 of 10 for Keto
  1. BCKDHB gene 
    ... group of enzymes called the branched-chain alpha-keto acid dehydrogenase (BCKD) enzyme complex. Two beta subunits ... dehydrogenase beta subunit BCKDH E1-beta branched chain keto acid dehydrogenase E1, beta polypeptide branched chain keto ...
    https://medlineplus.gov/genetics/gene/bckdhb - Genetics
  2. DBT gene 
    ... group of enzymes called the branched-chain alpha-keto acid dehydrogenase (BCKD) enzyme complex. Specifically, the protein ... branched chain transacylase (E2 component of branched chain keto acid dehydrogenase complex; maple syrup urine disease) E2 ...
    https://medlineplus.gov/genetics/gene/dbt - Genetics
  3. BCKDHA gene 
    ... group of enzymes called the branched-chain alpha-keto acid dehydrogenase (BCKD) enzyme complex. Two alpha subunits ... Health Condition BCKDE1A BCKDH E1-alpha branched chain keto acid dehydrogenase E1, alpha polypeptide (maple syrup urine ...
    https://medlineplus.gov/genetics/gene/bckdha - Genetics
  4. AKR1D1 gene 
    ... dehydrogenase 3o5bred 5-beta-reductase AK1D1_HUMAN aldo-keto reductase family 1, member D1 delta 4-3- ... 5-beta-reductase Tests of AKR1D1 PubMed ALDO-KETO REDUCTASE FAMILY 1, MEMBER D1; AKR1D1 NCBI Gene ...
    https://medlineplus.gov/genetics/gene/akr1d1 - Genetics
  5. Maple syrup urine disease 
    ... of the condition. BCKD deficiency Branched-chain alpha-keto acid dehydrogenase deficiency Branched-chain ketoaciduria Ketoacidemia MSUD ... novel regulatory defect in the branched-chain alpha-keto acid dehydrogenase complex due to a mutation in ...
    https://medlineplus.gov/genetics/condition/maple-syrup-urine-disease - Genetics
  6. DLD gene 
    ... to produce energy in cells.Branched-chain alpha-keto acid dehydrogenase, or BCKD, is one of the ... dehydrogenase complex, 2-oxo-glutarate complex, branched chain keto acid dehydrogenase complex) dihydrolipoyl dehydrogenase DLDH DLDH_HUMAN ...
    https://medlineplus.gov/genetics/gene/dld - Genetics
  7. Gyrate atrophy of the choroid and retina 
    ... OAT deficiency OKT deficiency Ornithine aminotransferase deficiency Ornithine keto acid aminotransferase deficiency Ornithine-delta-aminotransferase deficiency Ornithinemia ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  8. HSD17B4 gene 
    ... 24-enoyl-CoA hydratase beta-hydroxyacyl dehydrogenase beta-keto-reductase D-3-hydroxyacyl-CoA dehydratase D-bifunctional ...
    https://medlineplus.gov/genetics/gene/hsd17b4 - Genetics
  9. HADHB gene 
    ... of the enzymes, known as long-chain 3-keto-acyl-CoA thiolase. The alpha subunits contain the ... found to decrease only the long-chain 3-keto-acyl-CoA thiolase enzyme activity of mitochondrial trifunctional ...
    https://medlineplus.gov/genetics/gene/hadhb - Genetics
  10. Dihydrolipoamide dehydrogenase deficiency 
    ... that work together (enzyme complexes): branched-chain alpha-keto acid dehydrogenase (BCKD), pyruvate dehydrogenase (PDH), and alpha ( ...
    https://medlineplus.gov/...dihydrolipoamide-dehydrogenase-deficiency - Genetics