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phosphoenolpyruvate and Metabolism, Inborn Errors

phosphoenolpyruvate has been researched along with Metabolism, Inborn Errors 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.

Metabolism, Inborn Errors: Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19906 (85.71)18.7374
1990's1 (14.29)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lakomek, M1
Neubauer, B1
von der Lühe, A1
Hoch, G1
Winkler, H1
Schröter, W1
Buc, HA1
Leroux, JP1
Garreau, H1
Marchand, JC1
Cartier, P1
Gherardi, M1
Vergnes, H1
Corberand, J1
Régnier, C1
Blume, KG1
Arnold, H1
Lohr, GW1
Beutler, E1
Koster, JF2
Staal, GE1
Niermeyer, MF1
Staal, GJ1
Nijessen, JG1
Paglia, DE1
Valentine, WN1
Rucknagel, DL1

Other Studies

7 other studies available for phosphoenolpyruvate and Metabolism, Inborn Errors

ArticleYear
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.
    European journal of haematology, 1992, Volume: 49, Issue:2

    Topics: 2,3-Diphosphoglycerate; Adenosine Diphosphate; Adenosine Triphosphate; Anemia, Hemolytic, Congenital

1992
Metabolic regulation in enzyme-deficient red cells.
    Enzyme, 1974, Volume: 18, Issue:1

    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].
    Acta haematologica, 1974, Volume: 52, Issue:4

    Topics: Anemia, Hemolytic, Congenital; Erythrocytes; Female; Glucosephosphate Dehydrogenase; Glutathione Red

1974
Additional diagnostic procedures for the detection of abnormal red cell pyruvate kinase.
    Clinica chimica acta; international journal of clinical chemistry, 1973, Feb-12, Volume: 43, Issue:3

    Topics: Binding Sites; Drug Stability; Erythrocytes; Fructosephosphates; Hot Temperature; Humans; Metabolism

1973
Pyruvate kinase in cultivated amniotic fluid cells.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 36, Issue:2

    Topics: Amniotic Fluid; Animals; Cells, Cultured; Female; Fibroblasts; Humans; Kinetics; Liver; Metabolism,

1972
A new variant of red blood cell pyruvate kinase deficiency.
    Biochimica et biophysica acta, 1972, Feb-28, Volume: 258, Issue:2

    Topics: Allosteric Regulation; Drug Stability; Erythrocyte Aging; Erythrocytes; Hot Temperature; Humans; Kin

1972
Defective erythrocyte pyruvate kinase with impaired kinetics and reduced optimal activity.
    British journal of haematology, 1972, Volume: 22, Issue:6

    Topics: Adenine Nucleotides; Anemia, Hemolytic, Congenital; Child; Enzyme Activation; Erythrocytes; Fructose

1972