Mucins and their O-Glycans from human bronchial epithelial cell cultures. - Wikidata - wikimedia - TriplyDB

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

http://www.wikidata.org/entity/Q47351311

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Clinical Glycomics Employing Graphitized Carbon Liquid Chromatography-Mass Spectrometry Gene expression profiles reveal increased mClca3 (Gob5) expression and mucin production in a murine model of asbestos-induced fibrogenesis Comparable fitness and transmissibility between oseltamivir-resistant pandemic 2009 and seasonal H1N1 influenza viruses with the H275Y neuraminidase mutation.Human bronchial epithelial cells differentiate to 3D glandular acini on basement membrane matrix Mucin glycosylation and sulphation in airway epithelial cells is not influenced by cystic fibrosis transmembrane conductance regulator expression.New hyphenated methodologies in high-sensitivity glycoprotein analysis.The ER stress transducer IRE1β is required for airway epithelial mucin production Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.Localization of Burkholderia cepacia complex bacteria in cystic fibrosis lungs and interactions with Pseudomonas aeruginosa in hypoxic mucus.Glycomic analysis of human respiratory tract tissues and correlation with influenza virus infection.Human neutrophil elastase induces hypersecretion of mucin from well-differentiated human bronchial epithelial cells in vitro via a protein kinase C{delta}-mediated mechanism.Baseline Goblet Cell Mucin Secretion in the Airways Exceeds Stimulated Secretion over Extended Time Periods, and Is Sensitive to Shear Stress and Intracellular Mucin Stores.A physical linkage between cystic fibrosis airway surface dehydration and Pseudomonas aeruginosa biofilms.Blood Groups in Infection and Host Susceptibility.Mapping the protein domain structures of the respiratory mucins: a mucin proteome coverage study.CFTR, mucins, and mucus obstruction in cystic fibrosis.Airway mucus: From production to secretion.Effects of guaifenesin, N-acetylcysteine, and ambroxol on MUC5AC and mucociliary transport in primary differentiated human tracheal-bronchial cells.Acidic pH increases airway surface liquid viscosity in cystic fibrosis Molecular organization of the mucins and glycocalyx underlying mucus transport over mucosal surfaces of the airways Tracheobronchial air-liquid interface cell culture: a model for innate mucosal defense of the upper airways?Studying mucin secretion from human bronchial epithelial cell primary cultures.Directional secretomes reflect polarity-specific functions in an in vitro model of human bronchial epithelium.Eukaryotic protein glycosylation: a primer for histochemists and cell biologists High-sensitivity analytical approaches for the structural characterization of glycoproteins.Cellular and molecular biology of airway mucins.Host mucin glycosylation plays a role in bacterial adhesion in lungs of individuals with cystic fibrosis.Mucin glycosylation changes in cystic fibrosis lung disease are not manifest in submucosal gland secretions The Densely O-Glycosylated MUC2 Mucin Protects the Intestine and Provides Food for the Commensal Bacteria.TGF-β₂ decreases baseline and IL-13-stimulated mucin production by primary human bronchial epithelial cells.Biosynthesis of the polymeric gel-forming mucin MUC5B Cystic fibrosis and bacterial colonization define the sputum N-glycosylation phenotype.Synthetic tracheal mucus with native rheological and surface tension properties.Munc13-2-/- baseline secretion defect reveals source of oligomeric mucins in mouse airways.Physicochemical properties of mucus and their impact on transmucosal drug delivery.Statistical analysis of glycosylation profiles to compare tissue type and inflammatory disease state.Mucin Production and Hydration Responses to Mucopurulent Materials in Normal versus Cystic Fibrosis Airway Epithelia.

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P2860

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

http://www.wikidata.org/entity/Q47351311

description

2004 nî lūn-bûn

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年學術文章

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2004年學術文章

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name

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

@en

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

@nl

type

label

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

@en

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

@nl

prefLabel

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

@en

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

@nl

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AJPLUNG.00108.2004

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American Journal of Physiology - Lung Cellular and Molecular Physiology

P1476

Mucins and their O-Glycans from human bronchial epithelial cell cultures.

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P2093

C William Davis

http://www.w3.org/2001/XMLSchema#string

Gunnar C Hansson

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Jessica M Holmén

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John K Sheehan

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Lubna H Abdullah

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Niclas G Karlsson

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Scott H Randell

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P2860

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

Genomic organization of the human mucin gene MUC5B. cDNA and genomic sequences upstream of the large central exon

Mucous granule exocytosis and CFTR expression in gallbladder epithelium.

Terminal glycosylation in cystic fibrosis.

Small-scale analysis of O-linked oligosaccharides from glycoproteins and mucins separated by gel electrophoresis.

Mucus clearance as a primary innate defense mechanism for mammalian airways.

Increased sulfation of glycoconjugates by cultured nasal epithelial cells from patients with cystic fibrosis

Terminal glycosylation in cystic fibrosis (CF): a review emphasizing the airway epithelial cell.

Human airway mucin glycosylation: a combinatory of carbohydrate determinants which vary in cystic fibrosis.

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