ethylnitrosourea has been researched along with Amelogenesis Imperfecta in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Açil, Y; Albers, HK; Fuchs, H; Grundner-Culemann, E; Hrabe de Angelis, M; Reis, A; Seedorf, H; Springer, IN | 1 |
| Fujimoto, N; Gondo, Y; Ishijima, J; Kaneda, H; Kawai, A; Kobayashi, K; Maeda, T; Masuya, H; Miura, I; Nagano, J; Noda, T; Sakuraba, Y; Sezutsu, H; Shimizu, A; Shimizu, K; Shiroishi, T; Wakana, S | 1 |
2 other study(ies) available for ethylnitrosourea and Amelogenesis Imperfecta
| Article | Year |
|---|---|
Amelogenesis imperfecta in a new animal model--a mutation in chromosome 5 (human 4q21).
Topics: Amelogenesis Imperfecta; Animals; Chromosome Mapping; Chromosomes, Human, Pair 4; Chromosomes, Human, Pair 5; Dental Enamel; Dental Enamel Proteins; Dentin; Disease Models, Animal; DNA Mutational Analysis; Ethylnitrosourea; Female; Genetic Testing; Humans; Male; Mice; Mice, Inbred C3H; Mice, Mutant Strains; Mutagenesis; Mutagens | 2004 |
Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI).
Topics: Amelogenesis; Amelogenesis Imperfecta; Amino Acid Sequence; Animals; Chromosome Mapping; Dental Enamel Proteins; Disease Models, Animal; Ethylnitrosourea; Humans; Mice; Molecular Sequence Data; Mutation; Phenotype; RNA, Messenger; Sequence Analysis, DNA | 2005 |