ethylnitrosourea has been researched along with Deafness-Retinitis Pigmentosa Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Beynon, AJ; Croes, HJ; Cuppen, E; Fransen, JA; Guryev, V; Mul, JD; Peters, TA; Plasterk, RH; Smits, BM | 1 |
1 other study(ies) available for ethylnitrosourea and Deafness-Retinitis Pigmentosa Syndrome
Article | Year |
---|---|
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 |