ethylnitrosourea has been researched along with Autosomal Chromosome Disorders 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 | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hernández-García, A; Justice, MJ; Kim, BJ; Lee, B; Oghalai, JS; Pereira, FA; Scott, DA; Seymour, ML; Shchelochkov, OA; Stockton, DW; Yu, Z; Zaveri, HP | 1 |
| Beynon, AJ; Croes, HJ; Cuppen, E; Fransen, JA; Guryev, V; Mul, JD; Peters, TA; Plasterk, RH; Smits, BM | 1 |
| Haag, MM; Soukup, SW | 1 |
3 other study(ies) available for ethylnitrosourea and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.
Topics: Abnormalities, Multiple; Alleles; Animals; Body Weight; Cardiovascular Diseases; Chromosome Deletion; Chromosome Disorders; Chromosomes; Chromosomes, Human, Pair 1; Embryonic Development; Ethylnitrosourea; Hearing Loss; Hippocampus; Male; Mice; Mice, Inbred C57BL; Nerve Tissue Proteins; Neurons; Phenotype; Repressor Proteins | 2013 |
Identification of a rat model for usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward genetics.
Topics: Animals; Chromosome Disorders; Codon, Terminator; Disease Models, Animal; Dyneins; Ethylnitrosourea; Genes, Recessive; Genetic Linkage; Humans; Male; Mutagenesis; Mutagens; Myosin VIIa; Myosins; Point Mutation; Polymorphism, Single Nucleotide; Rats; Rats, Wistar; Usher Syndromes | 2005 |
Association of chromosome 4 abnormalities with ethylnitrosourea-induced neuro-oncogenesis in the rat.
Topics: Animals; Cell Line; Cell Transformation, Viral; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Ethylnitrosourea; Karyotyping; Nervous System Neoplasms; Nitrosourea Compounds; Rats | 1984 |