Page last updated: 2024-08-21

ethylnitrosourea and Middle Ear Inflammation

ethylnitrosourea has been researched along with Middle Ear Inflammation in 2 studies

Research

Studies (2)

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	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ball, G; Bhutta, MF; Brown, SDM; Burton, MJ; Crompton, M; Dean, CH; Gale, R; Hardisty-Hughes, RE; Mallon, AM; Parker, A; Purnell, T; Simon, MM; Tateossian, H; Tyrer, HE; Wells, S; Williams, D	1
Adams, DJ; Grati, M; Hilton, JM; Ingham, N; Laskowski, RA; Lewis, MA; Pearson, S; Steel, KP	1

Other Studies

2 other study(ies) available for ethylnitrosourea and Middle Ear Inflammation

Article	Year
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways. PLoS genetics, 2017, Volume: 13, Issue:8 Topics: Alleles; Animals; Chromosome Mapping; Chronic Disease; Disease Models, Animal; Ear, Middle; Ethylnitrosourea; Female; Genotyping Techniques; Heterozygote; Homozygote; Humans; Imidazoline Receptors; Inflammation; Integrin alpha6; Intracellular Signaling Peptides and Proteins; Lim Kinases; Male; Mice; Mice, Knockout; Mutation, Missense; Neuropeptides; NF-kappa B; Otitis Media; p21-Activated Kinases; Penetrance; rac1 GTP-Binding Protein; Sequence Analysis, DNA; Up-Regulation; Vascular Endothelial Growth Factor A	2017
Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice. Genome biology, 2011, Sep-21, Volume: 12, Issue:9 Topics: Animals; Ear, Middle; Ethylnitrosourea; Evoked Potentials, Auditory, Brain Stem; Exome; Female; Genetic Predisposition to Disease; Immunohistochemistry; Inbreeding; LIM-Homeodomain Proteins; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mutation, Missense; Otitis Media; Pedigree; Penetrance; Point Mutation; Protein Structure, Secondary; Sequence Analysis, DNA; Transcription Factors	2011

Article

Year

A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.

PLoS genetics, 2017, Volume: 13, Issue:8

Topics: Alleles; Animals; Chromosome Mapping; Chronic Disease; Disease Models, Animal; Ear, Middle; Ethylnitrosourea; Female; Genotyping Techniques; Heterozygote; Homozygote; Humans; Imidazoline Receptors; Inflammation; Integrin alpha6; Intracellular Signaling Peptides and Proteins; Lim Kinases; Male; Mice; Mice, Knockout; Mutation, Missense; Neuropeptides; NF-kappa B; Otitis Media; p21-Activated Kinases; Penetrance; rac1 GTP-Binding Protein; Sequence Analysis, DNA; Up-Regulation; Vascular Endothelial Growth Factor A

2017

Exome sequencing identifies a missense mutation in Isl1 associated with low penetrance otitis media in dearisch mice.

Genome biology, 2011, Sep-21, Volume: 12, Issue:9

Topics: Animals; Ear, Middle; Ethylnitrosourea; Evoked Potentials, Auditory, Brain Stem; Exome; Female; Genetic Predisposition to Disease; Immunohistochemistry; Inbreeding; LIM-Homeodomain Proteins; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mutation, Missense; Otitis Media; Pedigree; Penetrance; Point Mutation; Protein Structure, Secondary; Sequence Analysis, DNA; Transcription Factors

2011