ethylnitrosourea has been researched along with Deafness in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 3 (37.50) | 29.6817 |
| 2010's | 4 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dahl, HH; Manji, SS; Miller, KA; Williams, LH | 1 |
| Burt, RA; Carpinelli, MR; Kile, BT; Manning, MG; Rachel, AB | 1 |
| Brahmachary, M; Wong, EY; Xu, CY; Xu, PX | 1 |
| Brown, SD; Hardisty-Hughes, RE; Joyce, S; Parker, A; Wisby, L | 1 |
| Alagramam, K; Davis, RR; Erway, LC; Pitts, D; Washington, JL; Wright, CG | 1 |
| Avenarius, M; Bailey, JS; Banan, R; Federe, GC; Grabowski-Boase, L; Grillet, N; Hice, R; Housley, GD; Keithley, EM; Lagler, EA; Müller, U; Najmabadi, H; Ryan, AF; Schwander, M; Sczaniecka, A; Smith, RJ; Steffy, BM; Tarantino, LM; Wiltshire, T | 1 |
| Bergstrom, DE; Gagnon, LH; Johnson, KR; Longo-Guess, C | 1 |
| Brown, SD; Hardisty, RE; Mburu, P | 1 |
8 other study(ies) available for ethylnitrosourea and Deafness
| Article | Year |
|---|---|
Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction.
Topics: Amino Acid Sequence; Animals; Auditory Perception; Base Sequence; Cardiomyopathy, Hypertrophic; Cochlea; Deafness; Disease Models, Animal; Ethylnitrosourea; Genetic Predisposition to Disease; Hearing Tests; Homozygote; Immunohistochemistry; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Microscopy, Electron, Scanning; Molecular Sequence Data; Mutagens; Mutation; Myosin Heavy Chains; Phenotype; Vestibule, Labyrinth | 2013 |
Two ENU-induced alleles of Atp2b2 cause deafness in mice.
Topics: Alleles; Amino Acid Sequence; Animals; Chromosomes, Mammalian; Deafness; Ethylnitrosourea; Genetic Linkage; Hair Cells, Auditory; Male; Mice; Mice, Inbred BALB C; Molecular Sequence Data; Plasma Membrane Calcium-Transporting ATPases; Point Mutation | 2013 |
A Novel ENU-Induced Mutation in Myo6 Causes Vestibular Dysfunction and Deafness.
Topics: Animals; Auditory Threshold; Base Sequence; Behavior, Animal; Chromosomes, Mammalian; Deafness; Epithelium; Ethylnitrosourea; Evoked Potentials, Auditory, Brain Stem; Genes, Dominant; Hair Cells, Auditory; Male; Mice, Inbred C57BL; Mice, Mutant Strains; Mutation; Myosin Heavy Chains; Penetrance; Vestibule, Labyrinth | 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 |
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 |
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function.
Topics: Animals; Base Sequence; Chromosome Mapping; Deafness; Disease Models, Animal; Ethylnitrosourea; Female; Genes, Recessive; Genetic Testing; Hair Cells, Auditory, Outer; Humans; Male; Membrane Proteins; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mutagens; Neoplasm Proteins; Pedigree; Point Mutation; Psychomotor Agitation; Sequence Alignment | 2007 |
A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9.
Topics: Acoustic Stimulation; Amino Acid Motifs; Amino Acid Sequence; Animals; Behavior, Animal; Conserved Sequence; Deafness; Disease Models, Animal; Ethylnitrosourea; Evoked Potentials, Auditory, Brain Stem; Genotype; Hair Cells, Auditory; Heterozygote; Homozygote; Membrane Proteins; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Molecular Sequence Data; Mutagens; Mutation, Missense; Phenotype; Protein Denaturation; Protein Structure, Tertiary | 2007 |
ENU mutagenesis and the search for deafness genes.
Topics: Animals; Deafness; Disease Models, Animal; Ethylnitrosourea; Mice; Mutagenesis; Point Mutation | 1999 |