2-methylhexadecanoic acid has been researched along with pristanic acid in 2 studies
Studies (2-methylhexadecanoic acid) | Trials (2-methylhexadecanoic acid) | Recent Studies (post-2010) (2-methylhexadecanoic acid) | Studies (pristanic acid) | Trials (pristanic acid) | Recent Studies (post-2010) (pristanic acid) |
---|---|---|---|---|---|
11 | 0 | 0 | 103 | 2 | 17 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Asselberghs, S; Dieuaide-Noubhani, M; Mannaerts, GP; Van Veldhoven, PP | 1 |
Bennett, MJ; Brys, V; Fournier, B; Fransen, M; Mannaerts, GP; Meyhi, E; Squires, RH; Van Veldhoven, PP | 1 |
2 other study(ies) available for 2-methylhexadecanoic acid and pristanic acid
Article | Year |
---|---|
Evidence that multifunctional protein 2, and not multifunctional protein 1, is involved in the peroxisomal beta-oxidation of pristanic acid.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Animals; Chromatography, Gas; Chromatography, High Pressure Liquid; Enoyl-CoA Hydratase; Fatty Acids; Isomerases; Liver; Microbodies; Multienzyme Complexes; Oxidation-Reduction; Palmitic Acids; Palmitoyl Coenzyme A; Peroxisomal Bifunctional Enzyme; Rats; Stereoisomerism | 1997 |
Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency.
Topics: Cells, Cultured; Fatty Acids; Female; Fibroblasts; Humans; Infant, Newborn; Isomerism; Malabsorption Syndromes; Oxidation-Reduction; Palmitic Acids; Peroxisomal Disorders; Peroxisomes; Racemases and Epimerases; Skin; Vitamin K Deficiency | 2001 |