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thymine and Metabolism, Inborn Errors

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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Yokota, H1
Fernandez-Salguero, P1
Furuya, H1
Lin, K1
McBride, OW1
Podschun, B1
Schnackerz, KD1
Gonzalez, FJ1
Sumi, S1
Imaeda, M1
Kidouchi, K1
Ohba, S1
Hamajima, N1
Kodama, K1
Togari, H1
Wada, Y1
Jakobs, C1
Stellaard, F1
Smit, LM1
van Vugt, JM1
Duran, M1
Berger, R1
Rovers, P1

Other Studies

3 other studies available for thymine and Metabolism, Inborn Errors

ArticleYear
cDNA cloning and chromosome mapping of human dihydropyrimidine dehydrogenase, an enzyme associated with 5-fluorouracil toxicity and congenital thymine uraciluria.
    The Journal of biological chemistry, 1994, Sep-16, Volume: 269, Issue:37

    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.
    American journal of medical genetics, 1998, Jul-24, Volume: 78, Issue:4

    Topics: Adult; Amidohydrolases; Child; Child, Preschool; Female; Fluorouracil; Genes, Recessive; Homozygote;

1998
The first prenatal diagnosis of dihydropyrimidine dehydrogenase deficiency.
    European journal of pediatrics, 1991, Volume: 150, Issue:4

    Topics: Amniotic Fluid; Dihydrouracil Dehydrogenase (NADP); Female; Humans; Metabolism, Inborn Errors; Oxido

1991