ethylnitrosourea has been researched along with Proteinuria 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 | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bouriez-Jones, T; Bull, KR; Chaudhry, S; Cornall, RJ; Crockford, TL; Goodnow, CC; Hough, TA; Mason, T; Rimmer, AJ; Roberts, IS; Silver, KL | 1 |
| Arnold, CN; Beutler, B; Lin, P; Müller, U; Ross, C; Schwander, M; Smart, NG; Xia, Y | 1 |
| Aigner, B; Hrabé de Angelis, M; Klempt, M; Rathkolb, B; Tran, TV; Wanke, R; Wolf, E | 1 |
3 other study(ies) available for ethylnitrosourea and Proteinuria
| Article | Year |
|---|---|
Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome.
Topics: Abnormalities, Multiple; Animals; Disease Models, Animal; DNA Mutational Analysis; Ethylnitrosourea; Eye Abnormalities; Genetic Association Studies; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Kidney Tubules; Laminin; Mice; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Mutant Strains; Mutation; Myasthenic Syndromes, Congenital; Nephrotic Syndrome; Pedigree; Phenotype; Proteinuria; Pupil Disorders | 2014 |
Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis.
Topics: Alleles; Animals; Chromosome Mapping; Chromosome Segregation; Collagen Type IV; DNA Mutational Analysis; Ethylnitrosourea; Genome; Genome-Wide Association Study; Germ-Line Mutation; Glomerulosclerosis, Focal Segmental; Heterozygote; Homozygote; Mice; Mice, Inbred C57BL; Proteinuria; Renal Insufficiency; RNA Splice Sites | 2011 |
Large-scale albuminuria screen for nephropathy models in chemically induced mouse mutants.
Topics: Albuminuria; Alkylating Agents; Animals; Disease Models, Animal; Ethylnitrosourea; Female; Male; Mice; Mice, Inbred C3H; Mutagenesis; Pedigree; Phenotype; Proteinuria | 2005 |