5,6-dihydroorotate has been researched along with Congenital Micrognathia in 2 studies
4,5-dihydroorotic acid: RN given refers to cpd without isomeric designation; structure
dihydroorotic acid : A pyrimidinemonocarboxylic acid that results from the base-catalysed cyclisation of N(alpha)-carbethoxyasparagine.
| 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Duley, JA | 1 |
| Henman, MG | 1 |
| Carpenter, KH | 1 |
| Bamshad, MJ | 1 |
| Marshall, GA | 1 |
| Ooi, CY | 1 |
| Wilcken, B | 1 |
| Pinner, JR | 1 |
| Rainger, J | 1 |
| Bengani, H | 1 |
| Campbell, L | 1 |
| Anderson, E | 1 |
| Sokhi, K | 1 |
| Lam, W | 1 |
| Riess, A | 1 |
| Ansari, M | 1 |
| Smithson, S | 1 |
| Lees, M | 1 |
| Mercer, C | 1 |
| McKenzie, K | 1 |
| Lengfeld, T | 1 |
| Gener Querol, B | 1 |
| Branney, P | 1 |
| McKay, S | 1 |
| Morrison, H | 1 |
| Medina, B | 1 |
| Robertson, M | 1 |
| Kohlhase, J | 1 |
| Gordon, C | 1 |
| Kirk, J | 1 |
| Wieczorek, D | 1 |
| Fitzpatrick, DR | 1 |
2 other studies available for 5,6-dihydroorotate and Congenital Micrognathia
| Article | Year |
|---|---|
Elevated plasma dihydroorotate in Miller syndrome: Biochemical, diagnostic and clinical implications, and treatment with uridine.
Topics: Abnormalities, Multiple; Child, Preschool; Dihydroorotate Dehydrogenase; Genotype; Humans; Limb Defo | 2016 |
Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH.
Topics: Abnormalities, Multiple; Animals; Base Sequence; Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing | 2012 |