Cystic fibrosis transmembrane conductance regulator is expressed in mucin granules from Calu-3 and primary human airway epithelial cells.
about
Real-time imaging of exocytotic mucin release and swelling in Calu-3 cells using acridine orange.Airway Gland Structure and FunctionDefective goblet cell exocytosis contributes to murine cystic fibrosis-associated intestinal disease.Junctional abnormalities in human airway epithelial cells expressing F508del CFTR.Quantitative proteomics reveals an altered cystic fibrosis in vitro bronchial epithelial secretomeRegulated mucin secretion from airway epithelial cellsDefective postsecretory maturation of MUC5B mucin in cystic fibrosis airwaysThe buffer capacity of airway epithelial secretions.Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin Release.
P2860
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P2860
Cystic fibrosis transmembrane conductance regulator is expressed in mucin granules from Calu-3 and primary human airway epithelial cells.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Cystic fibrosis transmembrane ...... human airway epithelial cells.
@en
Cystic fibrosis transmembrane ...... human airway epithelial cells.
@nl
type
label
Cystic fibrosis transmembrane ...... human airway epithelial cells.
@en
Cystic fibrosis transmembrane ...... human airway epithelial cells.
@nl
prefLabel
Cystic fibrosis transmembrane ...... human airway epithelial cells.
@en
Cystic fibrosis transmembrane ...... human airway epithelial cells.
@nl
P2093
P2860
P356
P1476
Cystic fibrosis transmembrane ...... human airway epithelial cells.
@en
P2093
John W Hanrahan
Julie Goepp
Melissa L Palmer
Pasquale Ferraro
Pierre LeSimple
Renaud Robert
Scott C Fahrenkrug
Scott M O'Grady
P2860
P304
P356
10.1165/RCMB.2012-0419RC
P577
2013-10-01T00:00:00Z