thymine has been researched along with Inborn Errors of Metabolism in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yokota, H | 1 |
| Fernandez-Salguero, P | 1 |
| Furuya, H | 1 |
| Lin, K | 1 |
| McBride, OW | 1 |
| Podschun, B | 1 |
| Schnackerz, KD | 1 |
| Gonzalez, FJ | 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 |
| Jakobs, C | 1 |
| Stellaard, F | 1 |
| Smit, LM | 1 |
| van Vugt, JM | 1 |
| Duran, M | 1 |
| Berger, R | 1 |
| Rovers, P | 1 |
3 other studies available for thymine and Inborn Errors of Metabolism
| Article | Year |
|---|---|
cDNA cloning and chromosome mapping of human dihydropyrimidine dehydrogenase, an enzyme associated with 5-fluorouracil toxicity and congenital thymine uraciluria.
Topics: Amino Acid Sequence; Animals; Base Sequence; Chromosome Mapping; Chromosomes, Human, Pair 1; Criceti | 1994 |
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 |
The first prenatal diagnosis of dihydropyrimidine dehydrogenase deficiency.
Topics: Amniotic Fluid; Dihydrouracil Dehydrogenase (NADP); Female; Humans; Metabolism, Inborn Errors; Oxido | 1991 |