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Syntaxin 8 and the Endoplasmic Reticulum Processing of ΔF508-CFTR
BACKGROUND/AIMS: Cystic fibrosis (CF) is a lethal recessive disorder caused by mutations in the CF transmembrane conductance regulator (CFTR). ΔF508, the most common mutation, is a misfolded protein that is retained in the endoplasmic reticulum and degraded, precluding delivery to the cell surface [...
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| Publicado en: | Cell Physiol Biochem |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6482459/ https://ncbi.nlm.nih.gov/pubmed/30485852 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000495596 |
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