ethylnitrosourea has been researched along with Hyperkyphosis 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 |
---|---|
Brown, MA; Brown, SD; Cox, RD; Croucher, PI; Esapa, CT; Loh, NY; Nesbit, MA; Piret, SE; Thakker, RV; Thomas, G | 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 |
2 other study(ies) available for ethylnitrosourea and Hyperkyphosis
Article | Year |
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Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway.
Topics: Animals; Bone Density; Chlorocebus aethiops; COS Cells; Disease Models, Animal; Ethylnitrosourea; Female; Glycosylation; Kyphosis; Male; MAP Kinase Signaling System; Mice; Mice, Inbred BALB C; Mutation, Missense; Protein Processing, Post-Translational; Receptors, Atrial Natriuretic Factor; Spine; Tibia | 2016 |
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 |