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Inhibiting autophagy reduces retinal degeneration caused by protein misfolding
Mutations in the genes necessary for the structure and function of vertebrate photoreceptor cells are associated with multiple forms of inherited retinal degeneration. Mutations in the gene encoding RHO (rhodopsin) are a common cause of autosomal dominant retinitis pigmentosa (adRP), with the Pro23H...
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| Vydáno v: | Autophagy |
|---|---|
| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Taylor & Francis
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6103695/ https://ncbi.nlm.nih.gov/pubmed/29940785 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15548627.2018.1463121 |
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