טוען...
The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control
Mutations in rhodopsin, the light-sensitive protein of rod cells, are the most common cause of autosomal dominant retinitis pigmentosa (ADRP). Many rod opsin mutations, such as P23H, lead to misfolding of rod opsin with detrimental effects on photoreceptor function and viability. Misfolded P23H rod...
שמור ב:
| הוצא לאור ב: | Hum Mol Genet |
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| Main Authors: | , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Oxford University Press
2014
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4240209/ https://ncbi.nlm.nih.gov/pubmed/25055872 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu385 |
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