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PacBio Sequencing and Its ApplicationsThe Role of Serine Proteases and Antiproteases in the Cystic Fibrosis LungReal-time imaging of exocytotic mucin release and swelling in Calu-3 cells using acridine orange.Respiratory epithelial cells orchestrate pulmonary innate immunity.Role for phospholipid acyl chains and cholesterol in pulmonary infections and inflammationDefective goblet cell exocytosis contributes to murine cystic fibrosis-associated intestinal disease.IFN-γ stimulates autophagy-mediated clearance of Burkholderia cenocepacia in human cystic fibrosis macrophagesLung function imaging methods in Cystic Fibrosis pulmonary diseaseUncovering Differences in Virulence Markers Associated with Achromobacter Species of CF and Non-CF Origin.Targeted proteomic quantitation of the absolute expression and turnover of cystic fibrosis transmembrane conductance regulator in the apical plasma membrane.Meconium ileus in cystic fibrosis is not linked to central repetitive region length variation in MUC1, MUC2, and MUC5AC.Salivary mucin 19 glycoproteins: innate immune functions in Streptococcus mutans-induced caries in mice and evidence for expression in human salivaCystic fibrosis mouse model-dependent intestinal structure and gut microbiomeBaseline Goblet Cell Mucin Secretion in the Airways Exceeds Stimulated Secretion over Extended Time Periods, and Is Sensitive to Shear Stress and Intracellular Mucin Stores.Cystic fibrosis: an inherited disease affecting mucin-producing organs.Iron Homeostasis and Inflammatory Status in Mice Deficient for the Cystic Fibrosis Transmembrane Regulator.Quantitative proteomics reveals an altered cystic fibrosis in vitro bronchial epithelial secretomeEvidence and Role for Bacterial Mucin Degradation in Cystic Fibrosis Airway Disease.Data Mining of Lung Microbiota in Cystic Fibrosis Patients.Hallmarks of therapeutic management of the cystic fibrosis functional landscape.Perspectives on mucus properties and formation--lessons from the biochemical worldThe human secretome atlas initiative: implications in health and disease conditions.Air trapping and airflow obstruction in newborn cystic fibrosis pigletsEukaryotic protein glycosylation: a primer for histochemists and cell biologistsIL-1β induction of MUC5AC gene expression is mediated by CREB and NF-κB and repressed by dexamethasone.Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airwaysCellular and molecular mechanisms of goblet cell metaplasia in the respiratory airways.Failure of respiratory defenses in the pathogenesis of bacterial pneumonia of cattle.Gaining the Upper Hand on Pulmonary Drug Delivery.Pseudomonas aeruginosa Diversification during Infection Development in Cystic Fibrosis Lungs-A Review.Proresolving Action of Docosahexaenoic Acid Monoglyceride in Lung Inflammatory Models Related to Cystic Fibrosis.Impaired TLR4 and HIF expression in cystic fibrosis bronchial epithelial cells downregulates hemeoxygenase-1 and alters iron homeostasis in vitro.Aspergillus fumigatus in cystic fibrosis: An update on immune interactions and molecular diagnostics in allergic bronchopulmonary aspergillosis.Genome-Wide Survey of Pseudomonas aeruginosa PA14 Reveals a Role for the Glyoxylate Pathway and Extracellular Proteases in the Utilization of Mucin.Constrictive Bronchiolitis in Cystic Fibrosis Adolescents with Refractory Pulmonary Decline.Mechanosensitive ATP release maintains proper mucus hydration of airwaysGene signature driving invasive mucinous adenocarcinoma of the lung.The emergence of multidrug-resistant Pseudomonas aeruginosa in cystic fibrosis patients on inhaled antibiotics.Recent progress in translational cystic fibrosis research using precision medicine strategies.Heated air humidification versus cold air nebulization in newly tracheostomized patients.
P2860
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P2860
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
CFTR, mucins, and mucus obstruction in cystic fibrosis.
@ast
CFTR, mucins, and mucus obstruction in cystic fibrosis.
@en
type
label
CFTR, mucins, and mucus obstruction in cystic fibrosis.
@ast
CFTR, mucins, and mucus obstruction in cystic fibrosis.
@en
prefLabel
CFTR, mucins, and mucus obstruction in cystic fibrosis.
@ast
CFTR, mucins, and mucus obstruction in cystic fibrosis.
@en
P2093
P2860
P1476
CFTR, mucins, and mucus obstruction in cystic fibrosis.
@en
P2093
C William Davis
Mary Callaghan Rose
Silvia M Kreda
P2860
P304
P356
10.1101/CSHPERSPECT.A009589
P577
2012-09-01T00:00:00Z