phosphoenolpyruvate has been researched along with Inborn Errors of Metabolism in 7 studies
Phosphoenolpyruvate: A monocarboxylic acid anion derived from selective deprotonation of the carboxy group of phosphoenolpyruvic acid. It is a metabolic intermediate in GLYCOLYSIS; GLUCONEOGENESIS; and other pathways.
phosphoenolpyruvate : A monocarboxylic acid anion resuting from selective deprotonation of the carboxy group of phosphoenolpyruvic acid.
phosphoenolpyruvic acid : A monocarboxylic acid that is acrylic acid substituted by a phosphonooxy group at position 2. It is a metabolic intermediate in pathways like glycolysis and gluconeogenesis.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (85.71) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lakomek, M | 1 |
| Neubauer, B | 1 |
| von der Lühe, A | 1 |
| Hoch, G | 1 |
| Winkler, H | 1 |
| Schröter, W | 1 |
| Buc, HA | 1 |
| Leroux, JP | 1 |
| Garreau, H | 1 |
| Marchand, JC | 1 |
| Cartier, P | 1 |
| Gherardi, M | 1 |
| Vergnes, H | 1 |
| Corberand, J | 1 |
| Régnier, C | 1 |
| Blume, KG | 1 |
| Arnold, H | 1 |
| Lohr, GW | 1 |
| Beutler, E | 1 |
| Koster, JF | 2 |
| Staal, GE | 1 |
| Niermeyer, MF | 1 |
| Staal, GJ | 1 |
| Nijessen, JG | 1 |
| Paglia, DE | 1 |
| Valentine, WN | 1 |
| Rucknagel, DL | 1 |
7 other studies available for phosphoenolpyruvate and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Erythrocyte pyruvate kinase deficiency: relations of residual enzyme activity, altered regulation of defective enzymes and concentrations of high-energy phosphates with the severity of clinical manifestation.
Topics: 2,3-Diphosphoglycerate; Adenosine Diphosphate; Adenosine Triphosphate; Anemia, Hemolytic, Congenital | 1992 |
Metabolic regulation in enzyme-deficient red cells.
Topics: Adenosine Triphosphate; Anemia, Hemolytic; Diphosphoglyceric Acids; Erythrocytes; Female; Fructoseph | 1974 |
[Erythrocytic pyruvate kinase deficiency accompanied by a severe neonatal hemolytic anemia. Family study and biochemical characterization of the enzyme].
Topics: Anemia, Hemolytic, Congenital; Erythrocytes; Female; Glucosephosphate Dehydrogenase; Glutathione Red | 1974 |
Additional diagnostic procedures for the detection of abnormal red cell pyruvate kinase.
Topics: Binding Sites; Drug Stability; Erythrocytes; Fructosephosphates; Hot Temperature; Humans; Metabolism | 1973 |
Pyruvate kinase in cultivated amniotic fluid cells.
Topics: Amniotic Fluid; Animals; Cells, Cultured; Female; Fibroblasts; Humans; Kinetics; Liver; Metabolism, | 1972 |
A new variant of red blood cell pyruvate kinase deficiency.
Topics: Allosteric Regulation; Drug Stability; Erythrocyte Aging; Erythrocytes; Hot Temperature; Humans; Kin | 1972 |
Defective erythrocyte pyruvate kinase with impaired kinetics and reduced optimal activity.
Topics: Adenine Nucleotides; Anemia, Hemolytic, Congenital; Child; Enzyme Activation; Erythrocytes; Fructose | 1972 |