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Results 1 - 10 of 25 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. The PKLR gene is active (expressed) in the liver and in red blood cells, where it provides instructions for producing an enzyme called pyruvate kinase. This ...
  5. ... a large group of proteins known as the pyruvate dehydrogenase complex. This complex is made up of ...
  6. ... gene provides instructions for making a protein called pyruvate dehydrogenase phosphatase 1, which is part of a large group of proteins called the pyruvate dehydrogenase complex. The pyruvate dehydrogenase phosphatase 1 protein ...
  7. ... the E1 enzyme. This enzyme, also known as pyruvate dehydrogenase, is a component of a group of proteins called the pyruvate dehydrogenase complex.The pyruvate dehydrogenase complex plays an ...
  8. ... the E1 enzyme. This enzyme, also known as pyruvate dehydrogenase, is a component of a group of proteins called the pyruvate dehydrogenase complex.The pyruvate dehydrogenase complex plays an ...
  9. ... glyoxylate aminotransferase (oxalosis I; hyperoxaluria I; glycolicaciduria; serine-pyruvate aminotransferase) alanine-glyoxylate transaminase L-alanine: glyoxylate aminotransferase ...
  10. ... energy.Dihydrolipoamide dehydrogenase is also part of the pyruvate dehydrogenase (PDH) complex. This enzyme complex plays an ... energy for cells. It converts a molecule called pyruvate, which is formed from the breakdown of carbohydrates, ...
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