ethylnitrosourea has been researched along with Cochlear Hearing Loss in 4 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 | 4 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Irvin, DM; McNeill, RS; Miller, CR | 1 |
| Brown, SD; Hardisty-Hughes, RE; Joyce, S; Parker, A; Wisby, L | 1 |
| Bahlo, M; Dahl, HH; Manji, SS; Miller, KA; Mitchell, CA; Ooms, LM; Williams, LH | 1 |
| Andreasen, L; Bahlo, M; Dahl, HH; Kuiper, M; Manji, SS; Miller, KA; Rose, E; Siboe, M; Williams, LH | 1 |
4 other study(ies) available for ethylnitrosourea and Cochlear Hearing Loss
| Article | Year |
|---|---|
BRAF Mutations Open Doors for N-Ethyl-N-Nitrosourea-Induced Gliomagenesis.
Topics: Ethylnitrosourea; Glioma; Hearing Loss, Sensorineural; Humans; Mutation | 2016 |
Melody, an ENU mutation in Caspase 3, alters the catalytic cysteine residue and causes sensorineural hearing loss in mice.
Topics: Amino Acid Sequence; Animals; Caspase 3; Chromosome Mapping; Cochlea; Cysteine Proteases; Deafness; Ethylnitrosourea; Evoked Potentials, Auditory, Brain Stem; Female; Gene Expression Regulation; Hair Cells, Auditory; Hearing Loss, Sensorineural; Heterozygote; Homozygote; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Molecular Sequence Data; Mutagenesis; Point Mutation; Spiral Ganglion | 2010 |
A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain Mozart.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Behavior, Animal; Ethylnitrosourea; Hair Cells, Auditory; Hearing Loss, Sensorineural; Inositol Polyphosphate 5-Phosphatases; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Molecular Sequence Data; Mutagenesis; Mutation; Nerve Fibers; Nerve Tissue Proteins; Neural Conduction; Phosphoric Monoester Hydrolases; Spiral Ganglion; Vestibule, Labyrinth | 2011 |
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 |