dihydrouracil has been researched along with flavin-adenine dinucleotide in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bertone, M; Goettig, P; Gross, E; Haas, D; Kiechle, M; Magdolen, V; Meindl, A; van Kuilenburg, AB; Weidensee, S | 1 |
1 other study(ies) available for dihydrouracil and flavin-adenine dinucleotide
Article | Year |
---|---|
A mild phenotype of dihydropyrimidine dehydrogenase deficiency and developmental retardation associated with a missense mutation affecting cofactor binding.
Topics: Amino Acid Sequence; Child; Creatinine; Dihydropyrimidine Dehydrogenase Deficiency; Dihydrouracil Dehydrogenase (NADP); Flavin-Adenine Dinucleotide; Genotype; Humans; Male; Molecular Sequence Data; Mutation, Missense; Protein Binding; Sequence Homology, Amino Acid; Thymine; Uracil | 2011 |