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Secretion properties, clearance, and therapy in airway diseaseGenes associated with MUC5AC expression in small airway epithelium of human smokers and non-smokersUpdate in Cystic Fibrosis 2014VAMP8 is a vesicle SNARE that regulates mucin secretion in airway goblet cellsMeasurements of Deposition, Lung Surface Area and Lung Fluid for Simulation of Inhaled CompoundsInhaled protein/peptide-based therapies for respiratory diseaseNovel Roles for Chloride Channels, Exchangers, and Regulators in Chronic Inflammatory Airway DiseasesMucociliary dysfunction in HIV and smoked substance abuseMechanisms of Bacterial Colonization of the Respiratory TractNotable Aspects of Glycan-Protein InteractionsThe Role of Serine Proteases and Antiproteases in the Cystic Fibrosis LungRole of epithelial mucins during airway infectionClinical issues of mucus accumulation in COPDInnate receptors and cellular defense against pulmonary infectionsThe cell biology of asthmaMucociliary clearance: pathophysiological aspectsCough and the transmission of tuberculosisMucociliary clearance defects in a murine in vitro model of pneumococcal airway infectionMucoadhesive nanoparticles may disrupt the protective human mucus barrier by altering its microstructureDelivery of RNAi Therapeutics to the Airways-From Bench to BedsideOrigins of cystic fibrosis lung diseaseAirway Gland Structure and FunctionAirway hydration and COPDClinical significance of airway mucus hypersecretion in chronic obstructive pulmonary diseaseAttenuation of cigarette smoke-induced airway mucus production by hydrogen-rich saline in ratsMunc18b is an essential gene in mice whose expression is limiting for secretion by airway epithelial and mast cellsMuc5b is required for airway defenceA pharmacologic approach to acquired cystic fibrosis transmembrane conductance regulator dysfunction in smoking related lung diseaseEvaluation of a novel technique in airway clearance therapy - Specific Cough Technique (SCT) in cystic fibrosis: A pilot study of a series of N-of-1 randomised controlled trials.Benefits and risks of manual hyperinflation in intubated and mechanically ventilated intensive care unit patients: a systematic review.Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigsOxidation increases mucin polymer cross-links to stiffen airway mucus gelsOvercoming the cystic fibrosis sputum barrier to leading adeno-associated virus gene therapy vectorsContinuous mucociliary transport by primary human airway epithelial cells in vitro.Microstructural alterations of sputum in cystic fibrosis lung disease.Intubation-free in vivo imaging of the tracheal mucosa using two-photon microscopy.Allergic asthma is distinguished by sensitivity of allergen-specific CD4+ T cells and airway structural cells to type 2 inflammation.Sodium tanshinone IIA sulfonate stimulated Cl- secretion in mouse trachea.Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.Gel-forming mucins form distinct morphologic structures in airways
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Airway mucus function and dysfunction.
@ast
Airway mucus function and dysfunction.
@en
type
label
Airway mucus function and dysfunction.
@ast
Airway mucus function and dysfunction.
@en
prefLabel
Airway mucus function and dysfunction.
@ast
Airway mucus function and dysfunction.
@en
P2860
P356
P1476
Airway mucus function and dysfunction.
@en
P2093
Burton F Dickey
John V Fahy
P2860
P304
P356
10.1056/NEJMRA0910061
P407
P5008
P577
2010-12-01T00:00:00Z