Serine proteases degrade airway mucins in cystic fibrosis.
about
Secretion properties, clearance, and therapy in airway diseaseSecretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacumAspergillosis and the role of mucins in cystic fibrosisCystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.Neutrophil elastase enhances sputum solubilization in cystic fibrosis patients receiving DNase therapy.Neutrophil elastase causes tissue damage that decreases host tolerance to lung infection with burkholderia species.Characterization of biofilm-like structures formed by Pseudomonas aeruginosa in a synthetic mucus mediumBiogeochemical forces shape the composition and physiology of polymicrobial communities in the cystic fibrosis lung.KynR, a Lrp/AsnC-type transcriptional regulator, directly controls the kynurenine pathway in Pseudomonas aeruginosa.Cystic fibrosis: an inherited disease affecting mucin-producing organs.Altered protease and antiprotease balance during a COPD exacerbation contributes to mucus obstruction.Evidence and Role for Bacterial Mucin Degradation in Cystic Fibrosis Airway Disease.CFTR, mucins, and mucus obstruction in cystic fibrosis.Identification of essential genes of Pseudomonas aeruginosa for its growth in airway mucus.Nebulized thiocyanate improves lung infection outcomes in mice.Biochemical mechanisms and therapeutic potential of pseudohalide thiocyanate in human health.Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis.Impaired TLR4 and HIF expression in cystic fibrosis bronchial epithelial cells downregulates hemeoxygenase-1 and alters iron homeostasis in vitro.Biosynthesis of the polymeric gel-forming mucin MUC5BSialic acid-to-urea ratio as a measure of airway surface hydration.Asn347 Glycosylation of Corticosteroid-binding Globulin Fine-tunes the Host Immune Response by Modulating Proteolysis by Pseudomonas aeruginosa and Neutrophil Elastase.Investment in secreted enzymes during nutrient-limited growth is utility dependent.Mechanosensitive ATP release maintains proper mucus hydration of airwaysFaster, higher, stronger.Mucin acts as a nutrient source and a signal for the differential expression of genes coding for cellular processes and virulence factors in Acinetobacter baumannii.Infection is Not Required for Mucoinflammatory Lung Disease in CFTR-knockout Ferrets.Mucin Production and Hydration Responses to Mucopurulent Materials in Normal versus Cystic Fibrosis Airway Epithelia.Phospholipid transfer protein and alpha-1 antitrypsin regulate Hck kinase activity during neutrophil degranulation
P2860
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P2860
Serine proteases degrade airway mucins in cystic fibrosis.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Serine proteases degrade airway mucins in cystic fibrosis.
@ast
Serine proteases degrade airway mucins in cystic fibrosis.
@en
type
label
Serine proteases degrade airway mucins in cystic fibrosis.
@ast
Serine proteases degrade airway mucins in cystic fibrosis.
@en
prefLabel
Serine proteases degrade airway mucins in cystic fibrosis.
@ast
Serine proteases degrade airway mucins in cystic fibrosis.
@en
P2093
P2860
P356
P1476
Serine proteases degrade airway mucins in cystic fibrosis.
@en
P2093
Bruce K Rubin
Christina Rheineck
Gerrit John
Lutz Naehrlich
Markus O Henke
Shashi Chillappagari
P2860
P304
P356
10.1128/IAI.01252-10
P407
P577
2011-06-06T00:00:00Z