Regulation of normal and cystic fibrosis airway surface liquid volume by phasic shear stress.
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Secretion properties, clearance, and therapy in airway disease17beta-Estradiol inhibits Ca2+-dependent homeostasis of airway surface liquid volume in human cystic fibrosis airway epithelia.Myosin Vb is required for trafficking of the cystic fibrosis transmembrane conductance regulator in Rab11a-specific apical recycling endosomes in polarized human airway epithelial cellsBestrophin-1 enables Ca2+-activated Cl- conductance in epitheliaRescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770Epithelial Sodium and Chloride Channels and AsthmaClaudins: Gatekeepers of lung epithelial functionAirway hydration and COPDDeletion of the ubiquitin ligase Nedd4L in lung epithelia causes cystic fibrosis-like diseaseTowards a virtual lung: multi-scale, multi-physics modelling of the pulmonary system.17β-Estradiol inhibits phosphorylation of stromal interaction molecule 1 (STIM1) protein: implication for store-operated calcium entry and chronic lung diseases.LMTK2-mediated phosphorylation regulates CFTR endocytosis in human airway epithelial cells.Vocal fold surface hydration: a review.Continuous mucociliary transport by primary human airway epithelial cells in vitro.Model demonstrates functional purpose of the nasal cycle.Differential inhibitory effects of CysLT(1) receptor antagonists on P2Y(6) receptor-mediated signaling and ion transport in human bronchial epithelia.Expression cloning of TMEM16A as a calcium-activated chloride channel subunit.Effect of epithelium ATP release on cyclic pressure-induced airway mucus secretion.Immunohistochemical localization of the aquaporins AQP1, AQP3, AQP4, and AQP5 in the mouse respiratory system.Airway mucus function and dysfunction.An EGFR autocrine loop encodes a slow-reacting but dominant mode of mechanotransduction in a polarized epithelium.c-Cbl facilitates endocytosis and lysosomal degradation of cystic fibrosis transmembrane conductance regulator in human airway epithelial cellsA functional anatomic defect of the cystic fibrosis airway.Tgf-β1 inhibits Cftr biogenesis and prevents functional rescue of ΔF508-Cftr in primary differentiated human bronchial epithelial cells.Linking increased airway hydration, ciliary beating, and mucociliary clearance through ENaC inhibitionA2B adenosine receptor signaling attenuates acute lung injury by enhancing alveolar fluid clearance in miceRegulator of G-protein signaling 4 suppresses LPS-induced MUC5AC overproduction in the airway.Functional apical large conductance, Ca2+-activated, and voltage-dependent K+ channels are required for maintenance of airway surface liquid volume.Rho signaling regulates pannexin 1-mediated ATP release from airway epithelia.Patient-specific modeling of regional antibiotic concentration levels in airways of patients with cystic fibrosis: are we dosing high enough?Defective adenosine-stimulated cAMP production in cystic fibrosis airway epithelia: a novel role for CFTR in cell signaling.Progression of pulmonary hyperinflation and trapped gas associated with genetic and environmental factors in children with cystic fibrosis.Tgf-beta downregulation of distinct chloride channels in cystic fibrosis-affected epithelia.Cigarette smoke exposure reveals a novel role for the MEK/ERK1/2 MAPK pathway in regulation of CFTRGenetic variation of αENaC influences lung diffusion during exercise in humans.Automated acquisition and analysis of airway surface liquid height by confocal microscopyBaseline Goblet Cell Mucin Secretion in the Airways Exceeds Stimulated Secretion over Extended Time Periods, and Is Sensitive to Shear Stress and Intracellular Mucin Stores.H5N1 Virus Hemagglutinin Inhibition of cAMP-Dependent CFTR via TLR4-Mediated Janus Tyrosine Kinase 3 Activation Exacerbates Lung Inflammation.Disabled-2 protein facilitates assembly polypeptide-2-independent recruitment of cystic fibrosis transmembrane conductance regulator to endocytic vesicles in polarized human airway epithelial cellsArsenic promotes ubiquitinylation and lysosomal degradation of cystic fibrosis transmembrane conductance regulator (CFTR) chloride channels in human airway epithelial cells
P2860
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P2860
Regulation of normal and cystic fibrosis airway surface liquid volume by phasic shear stress.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Regulation of normal and cysti ...... volume by phasic shear stress.
@ast
Regulation of normal and cysti ...... volume by phasic shear stress.
@en
type
label
Regulation of normal and cysti ...... volume by phasic shear stress.
@ast
Regulation of normal and cysti ...... volume by phasic shear stress.
@en
prefLabel
Regulation of normal and cysti ...... volume by phasic shear stress.
@ast
Regulation of normal and cysti ...... volume by phasic shear stress.
@en
P2093
P1476
Regulation of normal and cysti ...... volume by phasic shear stress.
@en
P2093
Brian Button
Richard C Boucher
Robert Tarran
P304
P356
10.1146/ANNUREV.PHYSIOL.68.072304.112754
P577
2006-01-01T00:00:00Z