Page last updated: 2024-08-21

ethylnitrosourea and Inner Ear Disease

ethylnitrosourea has been researched along with Inner Ear Disease in 1 studies

Research

Studies (1)

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

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

Other Studies

1 other study(ies) available for ethylnitrosourea and Inner Ear Disease

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. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013, Mar-06, Volume: 33, Issue:10 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

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.

The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013, Mar-06, Volume: 33, Issue:10

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