A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways. [electronic resource]
Producer: 20170913Description: e1006969 p. digitalISSN:- 1553-7404
- Alleles
- Animals
- Chromosome Mapping
- Chronic Disease
- Disease Models, Animal
- Ear, Middle -- metabolism
- Ethylnitrosourea -- toxicity
- Female
- Genotyping Techniques
- Heterozygote
- Homozygote
- Humans
- Imidazoline Receptors
- Inflammation -- genetics
- Integrin alpha6 -- genetics
- Intracellular Signaling Peptides and Proteins -- genetics
- Lim Kinases -- genetics
- Male
- Mice
- Mice, Knockout
- Mutation, Missense
- NF-kappa B -- genetics
- Neuropeptides -- genetics
- Otitis Media -- genetics
- Penetrance
- Sequence Analysis, DNA
- Up-Regulation
- Vascular Endothelial Growth Factor A -- genetics
- p21-Activated Kinases -- genetics
- rac1 GTP-Binding Protein -- genetics
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Publication Type: Journal Article
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