Retinoschisin is linked to retinal Na/K-ATPase signaling and localization

Mutations in the RS1 gene cause X-linked juvenile retinoschisis (XLRS), a hereditary retinal dystrophy. We recently showed that retinoschisin, the protein encoded by RS1, regulates ERK signaling and apoptosis in retinal cells. In this study, we explored an influence of retinoschisin on the functiona...

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Detalles Bibliográficos
Autores principales: Plössl, Karolina, Royer, Melanie, Bernklau, Sarah, Tavraz, Neslihan N., Friedrich, Thomas, Wild, Jens, Weber, Bernhard H. F., Friedrich, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531734/
https://www.ncbi.nlm.nih.gov/pubmed/28615319
http://dx.doi.org/10.1091/mbc.E17-01-0064

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531734/
https://www.ncbi.nlm.nih.gov/pubmed/28615319
http://dx.doi.org/10.1091/mbc.E17-01-0064

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