vanillic acid has been researched along with ubiquinone in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alam, SS; Brockman, D; Nambudiri, AM; Rudney, H | 1 |
| Fontecave, M; Lill, R; Mühlenhoff, U; Ozeir, M; Pierrel, F; Webert, H | 1 |
| Airik, R; Bergdoll, M; Doimo, M; Hildebrandt, F; Navas, P; Pierrel, F; Salviati, L; Santos-Ocaña, C; Trevisson, E | 1 |
3 other study(ies) available for vanillic acid and ubiquinone
| Article | Year |
|---|---|
Alternate routes for ubiquinone biosynthesis in rats.
Topics: Animals; Female; Hydroxybenzoates; Mitochondria, Liver; Mitochondria, Muscle; Myocardium; Rats; Ubiquinone; Vanillic Acid | 1976 |
Coenzyme Q biosynthesis: Coq6 is required for the C5-hydroxylation reaction and substrate analogs rescue Coq6 deficiency.
Topics: Adrenodoxin; Chromatography, High Pressure Liquid; Ferredoxin-NADP Reductase; Hydroxybenzoates; Hydroxylation; Membrane Proteins; Mutation; Parabens; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Ubiquinone; Vanillic Acid | 2011 |
Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency.
Topics: Amino Acid Sequence; Aminobenzoates; Ataxia; Gene Expression; Humans; Hydroxybenzoates; Mitochondria; Mitochondrial Diseases; Models, Molecular; Molecular Sequence Data; Muscle Weakness; Mutation; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Ubiquinone; Vanillic Acid | 2014 |