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Retinoschisin and Cardiac Glycoside Crosstalk at the Retinal Na/K-ATPase
PURPOSE: Mutations in the RS1 gene, which encodes retinoschisin, cause X-linked juvenile retinoschisis, a retinal dystrophy in males. Retinoschisin specifically interacts with the retinal sodium–potassium adenosine triphosphatase (Na/K-ATPase), a transmembrane ion pump. Na/K-ATPases also bind cardia...
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| Gepubliceerd in: | Invest Ophthalmol Vis Sci |
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| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The Association for Research in Vision and Ophthalmology
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7405613/ https://ncbi.nlm.nih.gov/pubmed/32392309 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.61.5.1 |
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