ethylnitrosourea has been researched along with Craniofacial Abnormalities in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Andreeva, V; Burt, J; Cardarelli, J; Connolly, MH; Fraher, D; Stewart-Swift, C; Yelick, PC | 1 |
| Bhatt, S; Crawford, M; Dennis, JF; Inman, KE; Iulianella, A; Jones, NC; Leroux-Berger, M; Lynn, M; Melton, KR; Sandell, LL; Trainor, PA; Walker, M | 1 |
| Drake, TA; Lusis, AJ; Lyons, KM; Nadeau, JH; Nishimura, I; Zernik, J | 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 |
| Barbaric, I; Brown, SD; Cheeseman, M; Dear, TN; Hough, T; Hunter, AJ; Marusic, A; Perry, MJ; Rodrigues Da Costa, A; Salopek, D; Wells, S | 1 |
1 review(s) available for ethylnitrosourea and Craniofacial Abnormalities
| Article | Year |
|---|---|
ENU large-scale mutagenesis and quantitative trait linkage (QTL) analysis in mice: novel technologies for searching polygenetic determinants of craniofacial abnormalities.
Topics: Alkylating Agents; Animals; Cephalometry; Chromosome Mapping; Craniofacial Abnormalities; Ethylnitrosourea; Genetic Linkage; Humans; Maxillofacial Development; Mice; Models, Animal; Mutagenesis; Quantitative Trait Loci | 2003 |
4 other study(ies) available for ethylnitrosourea and Craniofacial Abnormalities
| Article | Year |
|---|---|
Identification of adult mineralized tissue zebrafish mutants.
Topics: Alcian Blue; Animals; Anthraquinones; Cartilage; Craniofacial Abnormalities; Disease Models, Animal; Ethylnitrosourea; Genes, Recessive; Mutagenesis; Phenotype; Zebrafish | 2011 |
A phenotype-driven ENU mutagenesis screen identifies novel alleles with functional roles in early mouse craniofacial development.
Topics: Animals; Cell Differentiation; Cell Movement; Craniofacial Abnormalities; Ethylnitrosourea; Fluorescence; Indoles; Maxillofacial Development; Mice; Mice, Mutant Strains; Mutagenesis; Neural Crest; Neural Tube Defects; Phenotype; Signal Transduction; Skull | 2011 |
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 |
An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda.
Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Animals; Bone Density; Bone Diseases, Metabolic; Conserved Sequence; Craniofacial Abnormalities; DNA-Binding Proteins; Ethylnitrosourea; Female; Genes, Lethal; Kyphosis; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Mutant Strains; Molecular Sequence Data; Mutagenesis; Mutation, Missense; Phenotype; Point Mutation; Repressor Proteins; Sequence Alignment; Sequence Homology, Amino Acid | 2008 |