Nalaganje...

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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: LeSimple, Pierre, Liao, Jie, Robert, Renaud, Gruenert, Dieter C, Hanrahan, John W
Format: Artigo
Jezik:Inglês
Izdano: Blackwell Science Inc 2010
Teme:
Online dostop: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
Oznake: Označite
Brez oznak, prvi označite!