tryptophan has been researched along with Genetic Diseases in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Avitabile, T; Choragiewicz, T; Fiedorowicz, M; Grieb, P; Kamińska, A; Kocki, T; Nowakowska, D; Rejdak, R; Toro, MD; Turski, WA; Wertejuk, K; Wełniak-Kaminska, M; Zweifel, S | 1 |
| Caldovic, L; Cheng, SF; Morizono, H; Packman, S; Panglao, MG; Tuchman, M | 1 |
2 other study(ies) available for tryptophan and Genetic Diseases
| Article | Year |
|---|---|
Tryptophan Pathway Abnormalities in a Murine Model of Hereditary Glaucoma.
Topics: Animals; Biomarkers; Disease Models, Animal; Disease Susceptibility; Genetic Diseases, Inborn; Glaucoma; Kynurenic Acid; Kynurenine; Magnetic Resonance Imaging; Metabolic Networks and Pathways; Mice; Retina; Species Specificity; Tryptophan | 2021 |
Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia.
Topics: Acetyltransferases; Adenine; Amino-Acid N-Acetyltransferase; Base Sequence; Denmark; Female; Genetic Diseases, Inborn; Guanine; Hispanic or Latino; Homozygote; Humans; Hyperammonemia; Infant; Infant, Newborn; Male; Molecular Sequence Data; Mutation; Polymorphism, Restriction Fragment Length; Sequence Analysis, DNA; Tryptophan; White People | 2003 |