dihydrouracil has been researched along with Inborn Errors of Metabolism in 3 studies
hexahydropyrimidine-2,4-dione: structure in first source
5,6-dihydrouracil : A pyrimidine obtained by formal addition of hydrogen across the 5,6-position of uracil.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 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 |
|---|---|
| Nakajima, Y | 1 |
| Meijer, J | 1 |
| Dobritzsch, D | 1 |
| Ito, T | 1 |
| Zhang, C | 1 |
| Wang, X | 1 |
| Watanabe, Y | 1 |
| Tashiro, K | 1 |
| Meinsma, R | 1 |
| Roelofsen, J | 1 |
| Zoetekouw, L | 1 |
| van Kuilenburg, ABP | 1 |
| Yeung, CW | 1 |
| Yau, MM | 1 |
| Ma, CK | 1 |
| Siu, TS | 1 |
| Tam, S | 1 |
| Lam, CW | 1 |
| Sumi, S | 1 |
| Imaeda, M | 1 |
| Kidouchi, K | 1 |
| Ohba, S | 1 |
| Hamajima, N | 1 |
| Kodama, K | 1 |
| Togari, H | 1 |
| Wada, Y | 1 |
3 other studies available for dihydrouracil and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Dihydropyrimidinase deficiency in four East Asian patients due to novel and rare DPYS mutations affecting protein structural integrity and catalytic activity.
Topics: Amidohydrolases; Asian People; Brain; Catalytic Domain; Child; Child, Preschool; Crystallization; Fe | 2017 |
Diagnosis of dihydropyrimidinase deficiency in a Chinese boy with dihydropyrimidinuria.
Topics: Child, Preschool; China; Dihydropyrimidine Dehydrogenase Deficiency; Hong Kong; Humans; Male; Metabo | 2013 |
Population and family studies of dihydropyrimidinuria: prevalence, inheritance mode, and risk of fluorouracil toxicity.
Topics: Adult; Amidohydrolases; Child; Child, Preschool; Female; Fluorouracil; Genes, Recessive; Homozygote; | 1998 |