Found: 8
Select item for more details and to access through your institution.
The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Quiet as a mouse: dissecting the molecular and genetic basis of hearing.
- Published in:
- Nature Reviews Genetics, 2008, v. 9, n. 4, p. 277, doi. 10.1038/nrg2309
- By:
- Publication type:
- Article
A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 22, p. 3273, doi. 10.1093/hmg/ddl403
- By:
- Publication type:
- Article
Headbobber: A Combined Morphogenetic and Cochleosaccular Mouse Model to Study 10qter Deletions in Human Deafness.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056274
- By:
- Publication type:
- Article
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.
- Published in:
- Journal of Neuroscience, 2013, v. 33, n. 10, p. 4395, doi. 10.1523/JNEUROSCI.4514-12.2013
- By:
- Publication type:
- Article
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
- Published in:
- Nature Genetics, 2003, v. 34, n. 4, p. 421, doi. 10.1038/ng1208
- By:
- Publication type:
- Article
Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media.
- Published in:
- PLoS Genetics, 2006, v. 3, n. 4, p. 1556, doi. 10.1371/journal.pgen.0020149
- By:
- Publication type:
- Article
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.
- Published in:
- PLoS Genetics, 2017, v. 13, n. 8, p. 1, doi. 10.1371/journal.pgen.1006969
- By:
- Publication type:
- Article