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The protective effects of systemic dexamethasone on sensory epithelial damage and hearing loss in targeted Cx26-null mice
Mutations in the GJB2 gene (encoding Connexin26(Cx26)) are the most common cause of hereditary deafness, accounting for about a quarter of all cases. Sensory epithelial damage is considered to be one of the main causes of deafness caused by GJB2 gene mutation. Dexamethasone (DEX) is widely used in t...
Autores principales: | Xu, Kai, Chen, Sen, Xie, Le, Qiu, Yue, Liu, Xiao-zhou, Bai, Xue, Jin, Yuan, Wang, Xiao-hui, Sun, Yu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9187686/ https://www.ncbi.nlm.nih.gov/pubmed/35688810 http://dx.doi.org/10.1038/s41419-022-04987-3 |
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