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Results 1 - 8 of 8 for pyruvate
  1. Pyruvate carboxylase deficiency is an inherited disorder that causes lactic acid and other potentially toxic compounds to accumulate in the blood. High levels ...
  2. Pyruvate dehydrogenase deficiency is characterized by the buildup of a chemical called lactic acid in the body and a variety of neurological problems. Signs and ...
  3. Pyruvate kinase deficiency is an inherited disorder that affects red blood cells, which carry oxygen to the ...
  4. ... complexes): branched-chain alpha-keto acid dehydrogenase (BCKD), pyruvate dehydrogenase (PDH), and alpha (α)-ketoglutarate dehydrogenase (αKGDH). ... syrup urine disease, type III Genetic Testing Registry: Pyruvate dehydrogenase E3 deficiency Pyruvate dehydrogenase E3 deficiency National ...
  5. ... aid in energy production in mitochondria, including the pyruvate dehydrogenase complex and the alpha-ketoglutarate dehydrogenase complex ( ... Reduced activity of complex I, II, or III, pyruvate dehydrogenase, or alpha-ketoglutarate dehydrogenase leads to potentially ...
  6. ... glycogen breakdown, lactate dehydrogenase converts a molecule called pyruvate to a similar molecule called lactate.Mutations in ... In cardiac muscle, lactate dehydrogenase converts lactate to pyruvate, which can participate in other chemical reactions to ...
  7. ... caused by variants in genes that form the pyruvate dehydrogenase complex or coenzyme Q10, both of which ...
  8. ... Citation on PubMed Lakomek M, Winkler H. Erythrocyte pyruvate kinase- and glucose phosphate isomerase deficiency: perturbation of ...