Ribosomal Stalk Protein Silencing Partially Corrects the ΔF508-CFTR Functional Expression Defect

The most common cystic fibrosis (CF) causing mutation, deletion of phenylalanine 508 (ΔF508 or Phe508del), results in functional expression defect of the CF transmembrane conductance regulator (CFTR) at the apical plasma membrane (PM) of secretory epithelia, which is attributed to the degradation of...

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Detaylı Bibliyografya
Yayımlandı:PLoS Biol
Asıl Yazarlar: Veit, Guido, Oliver, Kathryn, Apaja, Pirjo M., Perdomo, Doranda, Bidaud-Meynard, Aurélien, Lin, Sheng-Ting, Guo, Jingyu, Icyuz, Mert, Sorscher, Eric J., Hartman, John L., Lukacs, Gergely L.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2016
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4864299/
https://ncbi.nlm.nih.gov/pubmed/27168400
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pbio.1002462
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