The Reduction in Microtubule Arrays Caused by the Dysplasia of the Non-Centrosomal Microtubule-Organizing Center Leads to a Malformed Organ of Corti in the Cx26-Null Mouse

Mutations in the GJB2 gene account for approximately 20–50% of all non-syndromic hereditary deafness cases. The malformed organ of Corti (OC) was observed in different Cx26-null mouse models, which was mainly caused by the developmental arrest of pillar cells (PCs). However, the mechanism of develop...

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Detalles Bibliográficos
Autores principales: Qiu, Yue, Xu, Kai, Xie, Le, Chen, Sen, Sun, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219875/
https://www.ncbi.nlm.nih.gov/pubmed/35740388
http://dx.doi.org/10.3390/biomedicines10061364

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219875/
https://www.ncbi.nlm.nih.gov/pubmed/35740388
http://dx.doi.org/10.3390/biomedicines10061364

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