phosphoenolpyruvate has been researched along with Degenerative Disease, Nervous System, Hereditary in 1 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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abela, L | 1 |
| Spiegel, R | 1 |
| Crowther, LM | 1 |
| Klein, A | 1 |
| Steindl, K | 1 |
| Papuc, SM | 1 |
| Joset, P | 1 |
| Zehavi, Y | 1 |
| Rauch, A | 1 |
| Plecko, B | 1 |
| Simmons, TL | 1 |
1 other study available for phosphoenolpyruvate and Degenerative Disease, Nervous System, Hereditary
| Article | Year |
|---|---|
Plasma metabolomics reveals a diagnostic metabolic fingerprint for mitochondrial aconitase (ACO2) deficiency.
Topics: Aconitate Hydratase; Aconitic Acid; Adolescent; Biomarkers; Child; Child, Preschool; Female; Heredod | 2017 |