Found: 8
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Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Deletion in Catna2, encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation.
- Published in:
- Nature Genetics, 2002, v. 31, n. 3, p. 279, doi. 10.1038/ng908
- By:
- Publication type:
- Article
Mutations of the Mouse ELMO Domain Containing 1 Gene (Elmod1) Link Small GTPase Signaling to Actin Cytoskeleton Dynamics in Hair Cell Stereocilia.
- Published in:
- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0036074
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- Publication type:
- Article
The R109H Variant of Fascin-2, a Developmentally Regulated Actin Crosslinker in Hair-Cell Stereocilia, Underlies Early-Onset Hearing Loss of DBA/2J Mice.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 29, p. 9683, doi. 10.1523/JNEUROSCI.1541-10.2010
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- Publication type:
- Article
The Chloride Intracellular Channel Protein CLIC5 Is Expressed at High Levels in Hair Cell Stereocilia and Is Essential for Normal Inner Ear Function.
- Published in:
- Journal of Neuroscience, 2006, v. 26, n. 40, p. 10188, doi. 10.1523/JNEUROSCI.2166-06.2006
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- Publication type:
- Article
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration.
- Published in:
- Nature, 2006, v. 443, n. 7107, p. 50, doi. 10.1038/nature05096
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- Publication type:
- Article
The harlequin mouse mutation downregulates apoptosis-inducing factor.
- Published in:
- Nature, 2002, v. 419, n. 6905, p. 367, doi. 10.1038/nature01034
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- Publication type:
- Article
Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice.
- Published in:
- Genetics, 2018, v. 208, n. 3, p. 1165, doi. 10.1534/genetics.117.300447
- By:
- Publication type:
- Article