thymine has been researched along with Metabolism, Inborn Errors in 3 studies
Metabolism, Inborn Errors: Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.
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 Metabolism, Inborn Errors
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 |