ethylnitrosourea has been researched along with Vestibular Diseases in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Andreasen, L; Bahlo, M; Dahl, HH; Kuiper, M; Manji, SS; Miller, KA; Rose, E; Siboe, M; Williams, LH | 1 |
| Alagramam, K; Davis, RR; Erway, LC; Pitts, D; Washington, JL; Wright, CG | 1 |
2 other study(ies) available for ethylnitrosourea and Vestibular Diseases
| Article | Year |
|---|---|
An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice.
Topics: Alleles; Amino Acid Sequence; Animals; Cadherins; DNA Mutational Analysis; Ethylnitrosourea; Hearing; Hearing Loss, Sensorineural; Humans; Mice; Mice, Transgenic; Models, Molecular; Molecular Sequence Data; Mutation; Protein Conformation; Sequence Homology, Amino Acid; Vestibular Diseases; Vestibule, Labyrinth | 2011 |
Characterization of a new allele of Ames waltzer generated by ENU mutagenesis.
Topics: Acoustic Stimulation; Adenine; Alleles; Animals; Auditory Threshold; Base Sequence; Cadherin Related Proteins; Cadherins; Deafness; DNA Mutational Analysis; Ethylnitrosourea; Evoked Potentials, Auditory, Brain Stem; Female; Guanine; Hair Cells, Auditory, Inner; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Microscopy, Electron, Scanning; Mutagens; Mutation; Organ of Corti; Phenotype; Protein Precursors; Vestibular Diseases | 2005 |