ethylnitrosourea has been researched along with Klein Syndrome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cao, C; Chen, ZY; Guo, W; Hai, T; Hong, Q; Huang, J; Jia, Q; Jin, W; Li, Y; Luo, A; Meng, A; Qi, M; Qin, G; Shang, H; Wang, D; Wang, H; Wang, X; Wei, H; Yang, S; Yao, J; Zhang, H; Zhang, R; Zhang, T; Zhang, Y; Zhao, J; Zheng, Q; Zhou, Q | 1 |
| Beier, DR; Cockroft, JL; Goldowitz, D; Matera, I; Moran, JL; Pavan, WJ | 1 |
| Baxter, LL; Elliott, EC; Hou, L; Incao, A; Loftus, SK; Matera, I; Pavan, WJ; Rivas, C; Silver, DL; Watkins-Chow, DE | 1 |
3 other study(ies) available for ethylnitrosourea and Klein Syndrome
| Article | Year |
|---|---|
Creation of miniature pig model of human Waardenburg syndrome type 2A by ENU mutagenesis.
Topics: Amino Acid Sequence; Animals; Animals, Genetically Modified; Disease Models, Animal; Ethylnitrosourea; Female; Hearing Loss; Humans; Male; Microphthalmia-Associated Transcription Factor; Mutagenesis; Mutagens; Mutation; Sequence Homology; Swine; Swine, Miniature; Waardenburg Syndrome | 2017 |
A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3.
Topics: Animals; Arginine; Chromosome Mapping; Disease Models, Animal; Endothelin-3; Ethylnitrosourea; Gene Expression Regulation; Genetic Linkage; Histidine; Humans; Mice; Mutation; Pigmentation; Point Mutation; Waardenburg Syndrome | 2007 |
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy.
Topics: Animals; Base Sequence; Cell Differentiation; Chromosome Mapping; Codon, Nonsense; DNA-Binding Proteins; Embryo, Mammalian; Ethylnitrosourea; Female; Gene Expression Regulation, Developmental; Genetic Complementation Test; High Mobility Group Proteins; Humans; Kruppel-Like Transcription Factors; Male; Melanocytes; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mutagenesis; Mutagens; Nerve Tissue Proteins; Neural Crest; Pigmentation; Repressor Proteins; SOXE Transcription Factors; Transcription Factors; Waardenburg Syndrome; Zinc Finger Protein Gli3 | 2008 |