ethylnitrosourea has been researched along with Labyrinth Diseases 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 | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alagramam, KN; Ball, G; Brown, SD; Chen, DH; Corey, DP; Furness, D; Gaudet, R; Geng, R; Gerka-Stuyt, J; Gopal, SR; Hardisty-Hughes, RE; Kinder, KJ; Parker, A; Sotomayor, M | 1 |
1 other study(ies) available for ethylnitrosourea and Labyrinth Diseases
| Article | Year |
|---|---|
Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells.
Topics: Age Factors; Animals; Animals, Newborn; Cadherin Related Proteins; Cadherins; Calcium; Cells, Cultured; Electroencephalography; Ethylnitrosourea; Evoked Potentials, Auditory, Brain Stem; Extracellular Matrix; Gene Expression Regulation; Genotype; Hair Cells, Auditory; Hearing Loss; Labyrinth Diseases; Mechanotransduction, Cellular; Mice; Mice, Transgenic; Microscopy, Atomic Force; Mutagens; Mutation, Missense; Phenotype; Polymorphism, Single Nucleotide; Protein Binding; Protein Precursors; Pyridinium Compounds; Quaternary Ammonium Compounds | 2013 |