trimethylamine has been researched along with Genetic Diseases in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "We have previously shown that primary trimethylaminuria, or fish-odour syndrome, is caused by an inherited defect in the flavin-containing monooxygenase 3 (FMO3) catalysed N-oxidation of the dietary-derived malodorous amine, trimethylamine (TMA)." | 3.70 | A novel mutation in the flavin-containing monooxygenase 3 gene, FM03, that causes fish-odour syndrome: activity of the mutant enzyme assessed by proton NMR spectroscopy. ( Chalmers, RA; Dolphin, CT; Holmes, HC; Iles, RA; Janmohamed, A; Michelakakis, H; Murphy, HC; Phillips, IR; Shephard, EA, 2000) |
| 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 |
|---|---|
| Eugène, M | 1 |
| Murphy, HC | 1 |
| Dolphin, CT | 1 |
| Janmohamed, A | 1 |
| Holmes, HC | 1 |
| Michelakakis, H | 1 |
| Shephard, EA | 1 |
| Chalmers, RA | 1 |
| Phillips, IR | 1 |
| Iles, RA | 1 |
2 other studies available for trimethylamine and Genetic Diseases
| Article | Year |
|---|---|
[Diagnosis of "fish odor syndrome" by urine nuclear magnetic resonance proton spectrometry].
Topics: Genetic Carrier Screening; Genetic Diseases, Inborn; Humans; Magnetic Resonance Spectroscopy; Methyl | 1998 |
A novel mutation in the flavin-containing monooxygenase 3 gene, FM03, that causes fish-odour syndrome: activity of the mutant enzyme assessed by proton NMR spectroscopy.
Topics: Adult; Alleles; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Child, Preschool; Femal | 2000 |