Wolfram syndrome 1b mutation suppresses Mauthner-cell axon regeneration via ER stress signal pathway

Wolfram Syndrome (WS) is a fatal human inherited disease with symptoms of diabetes, vision decreasing, and neurodegeneration caused by mutations in the endoplasmic reticulum (ER)-resident protein WFS1. WFS1 has been reported to play an important role in glucose metabolism. However, the role of WFS1...

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Detalles Bibliográficos
Autores principales: Wang, Zongyi, Wang, Xinliang, Shi, Lingyu, Cai, Yuan, Hu, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9758940/
https://www.ncbi.nlm.nih.gov/pubmed/36527091
http://dx.doi.org/10.1186/s40478-022-01484-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9758940/
https://www.ncbi.nlm.nih.gov/pubmed/36527091
http://dx.doi.org/10.1186/s40478-022-01484-8

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