ethylnitrosourea has been researched along with Osteopetrosis in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Douni, E; Eliopoulos, E; Kollias, G; Makrinou, E; Penninger, JM; Rinotas, V; Schett, G; Zwerina, J | 1 |
| Bosman, EA; Estabel, J; Ismail, O; Podrini, C; Steel, KP; White, JK | 1 |
| Barnett, LB; Erickson, RP; Lewis, SE; Tashian, RE; Venta, PJ | 1 |
3 other study(ies) available for ethylnitrosourea and Osteopetrosis
| Article | Year |
|---|---|
A RANKL G278R mutation causing osteopetrosis identifies a functional amino acid essential for trimer assembly in RANKL and TNF.
Topics: Amino Acid Substitution; Animals; Disease Models, Animal; Ethylnitrosourea; Genes, Dominant; Mice; Mutation, Missense; Osteoclasts; Osteopetrosis; Point Mutation; Protein Binding; Protein Multimerization; RANK Ligand; Receptor Activator of Nuclear Factor-kappa B; Tumor Necrosis Factor-alpha | 2012 |
Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1.
Topics: Alleles; Animals; Chromosome Mapping; Chromosomes; Disease Models, Animal; Ethylnitrosourea; Female; Gene Expression Regulation; Genes, Lethal; Genes, Recessive; Male; Membrane Proteins; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Knockout; Mutagenesis; Mutation; Osteopetrosis; Phenotype | 2013 |
N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndrome.
Topics: Alleles; Animals; Carbonic Anhydrases; Chromosomes, Human, Pair 3; Disease Models, Animal; Ethylnitrosourea; Female; Genes; Humans; Immunodiffusion; Isoelectric Focusing; Male; Metabolism, Inborn Errors; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mutation; Osteopetrosis | 1988 |