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Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers

The cystic fibrosis transmembrane conductance regulator (CFTR) is an integral membrane glycoprotein which functions as an anion channel and influences diverse cellular processes. We studied its role in the development of epithelial tightness by expressing wild-type (WT-CFTR) or mutant (ΔF508-CFTR) C...

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Detaylı Bibliyografya
Asıl Yazarlar: LeSimple, Pierre, Liao, Jie, Robert, Renaud, Gruenert, Dieter C, Hanrahan, John W
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Blackwell Science Inc 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2872727/
https://ncbi.nlm.nih.gov/pubmed/20156845
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2009.182246
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