A morphometric study of mucins and small airway plugging in cystic fibrosis.
about
Targeting EGFR signalling in chronic lung disease: therapeutic challenges and opportunitiesAirway Gland Structure and FunctionRole of epithelial HCO3⁻ transport in mucin secretion: lessons from cystic fibrosisPseudomonas aeruginosa-mediated damage requires distinct receptors at the apical and basolateral surfaces of the polarized epithelium.Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.Harnessing Neutrophil Survival Mechanisms during Chronic Infection by Pseudomonas aeruginosa: Novel Therapeutic Targets to Dampen Inflammation in Cystic FibrosisEffects of Morus alba L. and Natural Products Including Morusin on In Vivo Secretion and In Vitro Production of Airway MUC5AC MucinBPIFB1 (LPLUNC1) is upregulated in cystic fibrosis lung diseaseLoss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children.Normal CFTR inhibits epidermal growth factor receptor-dependent pro-inflammatory chemokine production in human airway epithelial cells.Mucin production during prenatal and postnatal murine lung development.Patient-specific modeling of regional antibiotic concentration levels in airways of patients with cystic fibrosis: are we dosing high enough?Mucous solids and liquid secretion by airways: studies with normal pig, cystic fibrosis human, and non-cystic fibrosis human bronchi.Cystic fibrosis: an inherited disease affecting mucin-producing organs.Pro-resolving lipid mediator Resolvin D1 serves as a marker of lung disease in cystic fibrosis.Overexpressing mouse model demonstrates the protective role of Muc5ac in the lungs.Amphiregulin-dependent mucous cell metaplasia in a model of nonallergic lung injuryCystic fibrosis: a mucosal immunodeficiency syndrome.Haemophilus influenzae lysate induces aspects of the chronic obstructive pulmonary disease phenotypePyocyanin-induced mucin production is associated with redox modification of FOXA2.MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohortFibrinogen binding to ICAM-1 promotes EGFR-dependent mucin production in human airway epithelial cells.Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis.Physiological measurement of the small airways.Targeting cytosolic proliferating cell nuclear antigen in neutrophil-dominated inflammation.Putting lung function and physiology into perspective: cystic fibrosis in adults.The metabolomics of airway diseases, including COPD, asthma and cystic fibrosis.Neutrophil-Expressed p21/waf1 Favors Inflammation Resolution in Pseudomonas aeruginosa Infection.Chemokine expression of oral fibroblasts and epithelial cells in response to artificial saliva.EG-VEGF, BV8, and their receptor expression in human bronchi and their modification in cystic fibrosis: Impact of CFTR mutation (delF508).Pseudomonas aeruginosa pyocyanin causes airway goblet cell hyperplasia and metaplasia and mucus hypersecretion by inactivating the transcriptional factor FoxA2.Constrictive Bronchiolitis in Cystic Fibrosis Adolescents with Refractory Pulmonary Decline.Rhinovirus Delays Cell Repolarization in a Model of Injured/Regenerating Human Airway Epithelium.Morphometric Analysis of Explant Lungs in Cystic Fibrosis.Piggyback-the-Winner in host-associated microbial communitiesA new role for bicarbonate secretion in cervico-uterine mucus release.MUC5B promoter polymorphisms and risk of coal workers' pneumoconiosis in a Chinese population.Development of an airway mucus defect in the cystic fibrosis rat.Abnormal expression of Muc5b in Cftr-null mice and in mammary tumors of MMTV-ras mice.
P2860
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P2860
A morphometric study of mucins and small airway plugging in cystic fibrosis.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
A morphometric study of mucins and small airway plugging in cystic fibrosis.
@ast
A morphometric study of mucins and small airway plugging in cystic fibrosis.
@en
type
label
A morphometric study of mucins and small airway plugging in cystic fibrosis.
@ast
A morphometric study of mucins and small airway plugging in cystic fibrosis.
@en
prefLabel
A morphometric study of mucins and small airway plugging in cystic fibrosis.
@ast
A morphometric study of mucins and small airway plugging in cystic fibrosis.
@en
P2093
P2860
P356
P1433
P1476
A morphometric study of mucins and small airway plugging in cystic fibrosis
@en
P2093
Claire Danel
Daniel J Dusser
Jay A Nadel
P2860
P304
P356
10.1136/THX.2006.062190
P407
P577
2006-08-23T00:00:00Z