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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...
Tallennettuna:
| Julkaisussa: | Mol Biol Cell |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The American Society for Cell Biology
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5531734/ https://ncbi.nlm.nih.gov/pubmed/28615319 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E17-01-0064 |
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