ethylnitrosourea has been researched along with Deafness, Transitory in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 6 (85.71) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cao, C; Chen, ZY; Guo, W; Hai, T; Hong, Q; Huang, J; Jia, Q; Jin, W; Li, Y; Luo, A; Meng, A; Qi, M; Qin, G; Shang, H; Wang, D; Wang, H; Wang, X; Wei, H; Yang, S; Yao, J; Zhang, H; Zhang, R; Zhang, T; Zhang, Y; Zhao, J; Zheng, Q; Zhou, Q | 1 |
| Hernández-García, A; Justice, MJ; Kim, BJ; Lee, B; Oghalai, JS; Pereira, FA; Scott, DA; Seymour, ML; Shchelochkov, OA; Stockton, DW; Yu, Z; Zaveri, HP | 1 |
| 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 |
| Chen, J; Jia, Y; Li, J; Song, C; Xiong, W; Zhang, X | 1 |
| Abreu-Goodger, C; Dalmay, T; De Angelis, MH; Enright, AJ; Fuchs, H; Glazier, AM; Langford, C; Lewis, MA; Moreno-Pelayo, MA; Piipari, M; Quint, E; Redshaw, N; Steel, KP; van Dongen, S | 1 |
| Brown, SD; Hardisty-Hughes, RE; Parker, A | 1 |
| Gao, X; Gu, X; Wang, Z; Xiong, X; Xu, L | 1 |
7 other study(ies) available for ethylnitrosourea and Deafness, Transitory
| Article | Year |
|---|---|
Creation of miniature pig model of human Waardenburg syndrome type 2A by ENU mutagenesis.
Topics: Amino Acid Sequence; Animals; Animals, Genetically Modified; Disease Models, Animal; Ethylnitrosourea; Female; Hearing Loss; Humans; Male; Microphthalmia-Associated Transcription Factor; Mutagenesis; Mutagens; Mutation; Sequence Homology; Swine; Swine, Miniature; Waardenburg Syndrome | 2017 |
An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.
Topics: Abnormalities, Multiple; Alleles; Animals; Body Weight; Cardiovascular Diseases; Chromosome Deletion; Chromosome Disorders; Chromosomes; Chromosomes, Human, Pair 1; Embryonic Development; Ethylnitrosourea; Hearing Loss; Hippocampus; Male; Mice; Mice, Inbred C57BL; Nerve Tissue Proteins; Neurons; Phenotype; Repressor Proteins | 2013 |
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 |
Identification of a Novel ENU-Induced Mutation in Mouse
Topics: Animals; Auditory Perception; DiGeorge Syndrome; Ethylnitrosourea; Female; Genetic Linkage; Hearing Loss; Humans; Male; Mice; Mice, Inbred C57BL; Mutation; T-Box Domain Proteins | 2016 |
An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice.
Topics: Animals; Base Sequence; DNA Mutational Analysis; Ethylnitrosourea; Hair Cells, Auditory; Hearing Loss; Heterozygote; Mice; Mice, Inbred C57BL; Mice, Inbred Strains; MicroRNAs; Molecular Sequence Data; Mutation; Transfection | 2009 |
A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment.
Topics: Animals; Behavior, Animal; Breeding; Disease Models, Animal; Ear, Inner; Ethylnitrosourea; Genetic Testing; Hearing Loss; Mice; Mutation | 2010 |
Identification of a novel point mutation of mouse Atp2b2 induced by N-ethyl-N-nitrosourea mutagenesis.
Topics: Animals; Disease Models, Animal; Ear, Inner; Ethylnitrosourea; Evoked Potentials, Auditory, Brain Stem; Hearing Loss; Humans; Mice; Mice, Mutant Strains; Mutagenesis; Plasma Membrane Calcium-Transporting ATPases; Point Mutation | 2011 |