ethylnitrosourea has been researched along with Polysyndactyly 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 | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Askew, GN; Charbit, A; Cheeseman, M; Chia, R; Dear, TN; Denny, P; Fisher, EM; Gheryani, N; Holt, N; Lalanne, Z; Miller, G; Neilan, M; Tucci, V; Wells, S | 1 |
| Adamson, SL; Anderson, N; Aubin, JE; Bai, D; Bruneau, BG; Ciliberti, N; Fleming, C; Flenniken, AM; Gittens, JE; Gong, XQ; Grynpas, M; Henderson, JE; Henkelman, RM; Kelsey, LB; Kidder, GM; Laird, DW; Lounsbury, C; McKerlie, C; Moreno, L; Nieman, BJ; Osborne, LR; Peterson, K; Qu, D; Roscoe, W; Rossant, J; Shao, Q; Sled, JG; Stanford, WL; Tong, D; Veitch, GI; Voronina, I; Vukobradovic, I; Wood, GA; Zhu, Y; Zirngibl, RA | 1 |
2 other study(ies) available for ethylnitrosourea and Polysyndactyly
| Article | Year |
|---|---|
ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2.
Topics: Alleles; Animals; Base Sequence; DNA Mutational Analysis; Ethylnitrosourea; Female; Fibrillin-1; Fibrillin-2; Fibrillins; Genotype; Hindlimb; Humans; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Knockout; Microfilament Proteins; Muscle Weakness; Muscle, Skeletal; Mutagenesis; Mutation; Phenotype; Syndactyly | 2010 |
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
Topics: Abnormalities, Multiple; Animals; Biomechanical Phenomena; Bone and Bones; Bone Density; Connexin 43; Craniofacial Abnormalities; Dental Enamel Hypoplasia; Disease Models, Animal; Ethylnitrosourea; Eye Abnormalities; Gap Junctions; Heart Defects, Congenital; Humans; Mice; Penetrance; Point Mutation; Stem Cells; Syndactyly | 2005 |