Found: 15
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Ototoxicity of polystyrene nanoplastics in mice, HEI-OC1 cells and zebrafish.
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- Frontiers in Molecular Neuroscience, 2024, p. 1, doi. 10.3389/fnmol.2024.1345536
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- Article
Ferroptosis is involved in PGPS-induced otitis media in C57BL/6 mice.
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- Cell Death Discovery, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41420-022-01025-1
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- Article
Autophagy Contributes to the Rapamycin-Induced Improvement of Otitis Media.
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- Frontiers in Cellular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fncel.2021.753369
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- Article
Phenotypic differences in the inner ears of CBA/CaJ and C57BL/6J mice carrying missense and single base pair deletion mutations in the Cdh23 gene.
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- Journal of Neuroscience Research, 2021, v. 99, n. 10, p. 2743, doi. 10.1002/jnr.24905
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- Article
Autophagy impairment as a key feature for acetaminophen-induced ototoxicity.
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- Cell Death & Disease, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41419-020-03328-6
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- Article
Current Understanding of Host Genetics of Otitis Media.
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- Frontiers in Genetics, 2020, p. 1, doi. 10.3389/fgene.2019.01395
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- Article
The microRNA-183/96/182 Cluster is Essential for Stereociliary Bundle Formation and Function of Cochlear Sensory Hair Cells.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-36894-z
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- Article
Comprehensive Expression of Wnt Signaling Pathway Genes during Development and Maturation of the Mouse Cochlea.
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- PLoS ONE, 2016, v. 11, n. 2, p. 1, doi. 10.1371/journal.pone.0148339
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- Article
ACF7 Is a Hair-Bundle Antecedent, Positioned to Integrate Cuticular Plate Actin and Somatic Tubulin.
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- Journal of Neuroscience, 2014, v. 34, n. 1, p. 305, doi. 10.1523/JNEUROSCI.1880-13.2014
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- 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.
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- Journal of Neuroscience, 2013, v. 33, n. 10, p. 4395, doi. 10.1523/JNEUROSCI.4514-12.2013
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- Article
The Mechanosensory Structure of the Hair Cell Requires Clarin-1, a Protein Encoded by Usher Syndrome III Causative Gene.
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- Journal of Neuroscience, 2012, v. 32, n. 28, p. 9485, doi. 10.1523/JNEUROSCI.0311-12.2012
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- Article
Mutations in Protocadherin 15 and Cadherin 23 Affect Tip Links and Mechanotransduction in Mammalian Sensory Hair Cells.
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- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0019183
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- Article
Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in usher syndrome type 1F.
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- Human Molecular Genetics, 2010, v. 19, n. 8, p. 1515, doi. 10.1093/hmg/ddq025
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- Article
A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia.
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- Human Genetics, 2010, v. 127, n. 1, p. 83, doi. 10.1007/s00439-009-0749-z
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- Article
Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation†.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2748, doi. 10.1093/hmg/ddp210
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- Article