F-Actin Dysplasia Involved in Organ of Corti Deformity in Gjb2 Knockdown Mouse Model

Mutations in the GJB2 gene encoding connexin26 (Cx26) protein are one of the most common causes of hereditary deafness. Previous studies have found that different Cx26-null mouse models have severe hearing loss and deformity of the organ of Corti (OC) as well as a reduction in microtubules in pillar...

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Detalles Bibliográficos
Autores principales: Liu, Xiao-zhou, Jin, Yuan, Chen, Sen, Xu, Kai, Xie, Le, Qiu, Yue, Wang, Xiao-hui, Sun, Yu, Kong, Wei-jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Molecular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957075/
https://www.ncbi.nlm.nih.gov/pubmed/35345836
http://dx.doi.org/10.3389/fnmol.2021.808553

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957075/
https://www.ncbi.nlm.nih.gov/pubmed/35345836
http://dx.doi.org/10.3389/fnmol.2021.808553

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