ethylnitrosourea has been researched along with Hyperdactyly 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 | 1 (33.33) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Chang, TC; Chen, RZ; Cheng, X; Jia, Y; Lv, H; Tan, Y | 1 |
Chen, B; Chen, DY; Chen, L; Mi, T; Xue, ZF; Yin, J; Zhou, Y | 1 |
Bach, A; Blanc, I; Guénet, JL; Lallemand, Y; Perrin-Schmitt, F; Robert, B | 1 |
3 other study(ies) available for ethylnitrosourea and Hyperdactyly
Article | Year |
---|---|
An ENU-induced mutation in Twist1 transactivation domain causes hindlimb polydactyly with complete penetrance and dominant-negatively impairs E2A-dependent transcription.
Topics: Animals; Basic Helix-Loop-Helix Transcription Factors; Ethylnitrosourea; Female; HEK293 Cells; Humans; Male; Mice; Mice, Inbred C57BL; Mutagens; Mutation; Penetrance; Polydactyly; Protein Domains; Twist-Related Protein 1 | 2020 |
Multiple abnormalities due to a nonsense mutation in the Alx4 gene.
Topics: Animals; Chromosomes, Mammalian; Codon, Nonsense; Ethylnitrosourea; Genetic Loci; Hernia, Umbilical; Heterozygote; Homeodomain Proteins; Mice; Mice, Inbred C57BL; Mutagenesis; Polydactyly; Teratogenesis | 2013 |
A new mouse limb mutation identifies a Twist allele that requires interacting loci on chromosome 4 for its phenotypic expression.
Topics: Alleles; Animals; Chromosome Mapping; Chromosomes, Mammalian; Crosses, Genetic; DNA Primers; Ethylnitrosourea; Genes, Dominant; In Situ Hybridization; Membrane Proteins; Mice; Mice, Inbred C57BL; Microsatellite Repeats; Mutation; Myogenic Regulatory Factors; Nuclear Proteins; Patched Receptors; Phenotype; Polydactyly; Receptors, Cell Surface; Sequence Analysis, DNA; Twist-Related Protein 1 | 2003 |