Cystic Fibrosis Transmembrane Conductance Regulator Folding Mutations Reveal Differences in Corrector Efficacy Linked to Increases in Immature Cystic Fibrosis Transmembrane Conductance Regulator Expression

Background: Most cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene that lead to protein misfolding and degradation by the ubiquitin–proteasome system. Previous studies demonstrated that PIAS4 facilitates the modification of wild-type (WT) a...

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Detalles Bibliográficos
Autores principales: Peters, Kathryn W., Gong, Xiaoyan, Frizzell, Raymond A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8576290/
https://www.ncbi.nlm.nih.gov/pubmed/34764878
http://dx.doi.org/10.3389/fphys.2021.695767

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8576290/
https://www.ncbi.nlm.nih.gov/pubmed/34764878
http://dx.doi.org/10.3389/fphys.2021.695767

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