Loxhd1b inhibits the hair cell development in zebrafish: Possible relation to the BDNF/TrkB/ERK pathway

BACKGROUND: Mutations in lipoxygenase homology domain 1 (LOXHD1) cause autosomal recessive inheritance, leading to high-frequency and intermediate-frequency hearing losses in patients. To date, studies on the localization of LOXHD1 gene expression are limited. In this study, we aimed to observe the...

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Detalles Bibliográficos
Autores principales: Liu, Jingwen, Zhang, Xu, Zhang, Qingchen, Wang, Rongrong, Ma, Jingyu, Bai, Xiaohui, Wang, Dawei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729270/
https://www.ncbi.nlm.nih.gov/pubmed/36505516
http://dx.doi.org/10.3389/fncel.2022.1065309

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729270/
https://www.ncbi.nlm.nih.gov/pubmed/36505516
http://dx.doi.org/10.3389/fncel.2022.1065309

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