Crompton, Michael <br/><br/>
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.  [electronic resource] 

 -  PLoS genetics  Aug 2017 
 - e1006969 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1553-7404 
<br/><br/><label>Standard No.: </label>10.1371/journal.pgen.1006969  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Animals<br/>Chromosome Mapping<br/>Chronic Disease<br/>Disease Models, Animal<br/>Ear, Middle--metabolism<br/>Ethylnitrosourea--toxicity<br/>Female<br/>Genotyping Techniques<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Imidazoline Receptors<br/>Inflammation--genetics<br/>Integrin alpha6--genetics<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Lim Kinases--genetics<br/>Male<br/>Mice<br/>Mice, Knockout<br/>Mutation, Missense<br/>NF-kappa B--genetics<br/>Neuropeptides--genetics<br/>Otitis Media--genetics<br/>Penetrance<br/>Sequence Analysis, DNA<br/>Up-Regulation<br/>Vascular Endothelial Growth Factor A--genetics<br/>p21-Activated Kinases--genetics<br/>rac1 GTP-Binding Protein--genetics