Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers.
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Emerging role of cystic fibrosis transmembrane conductance regulator - an epithelial chloride channel in gastrointestinal cancersClaudins: Gatekeepers of lung epithelial functionAirway epithelial homeostasis and planar cell polarity signaling depend on multiciliated cell differentiationCryptorchidism-induced CFTR down-regulation results in disruption of testicular tight junctions through up-regulation of NF-κB/COX-2/PGE2Validation of normal human bronchial epithelial cells as a model for influenza A infections in human distal tracheaParacellular transport through healthy and cystic fibrosis bronchial epithelial cell lines--do we have a proper model?Breaking barriers. New insights into airway epithelial barrier function in health and disease.Mimicking the host and its microenvironment in vitro for studying mucosal infections by Pseudomonas aeruginosa.Quantitative imaging of airway liquid absorption in cystic fibrosis.Interleukin-4 and interleukin-13 compromise the sinonasal epithelial barrier and perturb intercellular junction protein expression.Regulation of male fertility by CFTR and implications in male infertility.CFTR interacts with ZO-1 to regulate tight junction assembly and epithelial differentiation through the ZONAB pathway.Altered ion transport by thyroid epithelia from CFTR(-/-) pigs suggests mechanisms for hypothyroidism in cystic fibrosis.Ets homologous factor regulates pathways controlling response to injury in airway epithelial cellsTransforming growth factor-β1 and cigarette smoke inhibit the ability of β2-agonists to enhance epithelial permeability.Direct interactions between ENaC gamma subunit and ClCN2 in cystic fibrosis epithelial cells.Endogenous surface expression of ΔF508-CFTR mediates cAMP-stimulated Cl(-) current in CFTR(ΔF508/ΔF508) pig thyroid epithelial cellsH5N1 Virus Hemagglutinin Inhibition of cAMP-Dependent CFTR via TLR4-Mediated Janus Tyrosine Kinase 3 Activation Exacerbates Lung Inflammation.Influenza virus M2 targets cystic fibrosis transmembrane conductance regulator for lysosomal degradation during viral infectionUsing Drugs to Probe the Variability of Trans-Epithelial Airway Resistance.Junctional abnormalities in human airway epithelial cells expressing F508del CFTR.Matrix Metalloproteinase-9 Mediates RSV Infection in Vitro and in VivoEpithelial permeability alterations in an in vitro air-liquid interface model of allergic fungal rhinosinusitis.Liquid hyper-absorption as a cause of increased DTPA clearance in the cystic fibrosis airwayChanges in microRNA and mRNA expression with differentiation of human bronchial epithelial cells.Anchored PDE4 regulates chloride conductance in wild-type and ΔF508-CFTR human airway epithelia.Ion channels in asthma.Regulation of paracellular permeability: factors and mechanisms.In Vitro Models to Study Human Lung Development, Disease and Homeostasis.Insulin signaling via the PI3-kinase/Akt pathway regulates airway glucose uptake and barrier function in a CFTR-dependent manner.The role of stretch-activated ion channels in acute respiratory distress syndrome: finally a new target?Differentiation between human ClC-2 and CFTR Cl- channels with pharmacological agents.Respiratory syncytial virus infection disrupts monolayer integrity and function in cystic fibrosis airway cells.Sensitivity of chloride efflux vs. transepithelial measurements in mixed CF and normal airway epithelial cell populations.NHERF1 and CFTR restore tight junction organisation and function in cystic fibrosis airway epithelial cells: role of ezrin and the RhoA/ROCK pathway.Recovery of ΔF508-CFTR function by analogs of hyaluronan disaccharide.Influenza virus infection alters ion channel function of Airway and alveolar cells: Mechanisms and physiological sequelae.Loss of cystic fibrosis transmembrane conductance regulator impairs lung endothelial cell barrier function and increases susceptibility to microvascular damage from cigarette smoke.Extracellular oxidation in Cystic Fibrosis airway epithelium causes enhanced EGFR/ADAM17 activity.Gap Junctions Are Involved in the Rescue of CFTR-Dependent Chloride Efflux by Amniotic Mesenchymal Stem Cells in Coculture with Cystic Fibrosis CFBE41o- Cells.
P2860
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P2860
Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh
2010年學術文章
@zh-hant
name
Cystic fibrosis transmembrane ...... ay epithelial cell monolayers.
@en
Cystic fibrosis transmembrane ...... ay epithelial cell monolayers.
@nl
type
label
Cystic fibrosis transmembrane ...... ay epithelial cell monolayers.
@en
Cystic fibrosis transmembrane ...... ay epithelial cell monolayers.
@nl
prefLabel
Cystic fibrosis transmembrane ...... ay epithelial cell monolayers.
@en
Cystic fibrosis transmembrane ...... ay epithelial cell monolayers.
@nl
P2093
P2860
P1476
Cystic fibrosis transmembrane ...... ay epithelial cell monolayers.
@en
P2093
Dieter C Gruenert
John W Hanrahan
Pierre LeSimple
Renaud Robert
P2860
P304
P356
10.1113/JPHYSIOL.2009.182246
P407
P577
2010-02-15T00:00:00Z