Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
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In vitro correction of cystic fibrosis epithelial cell lines by small fragment homologous replacement (SFHR) technique.The use of gene expression analysis and proteomic databases in the development of a screening system to determine the value of natural medicinal products.Airway Gland Structure and FunctionADAGE-Based Integration of Publicly Available Pseudomonas aeruginosa Gene Expression Data with Denoising Autoencoders Illuminates Microbe-Host Interactions.Unrestricted somatic stem cells from human umbilical cord blood grow in serum-free medium as spheres.TLR-4-mediated innate immunity is reduced in cystic fibrosis airway cells.Clinical and pharmacological experience with LJP-394.Pharmacological treatment of the ion transport defect in cystic fibrosis.Loss of the integrin-activating transmembrane protein Fam38A (Piezo1) promotes a switch to a reduced integrin-dependent mode of cell migration.New sequence-specific human ribonuclease: purification and propertiesDifferential sensitivity of normal and cystic fibrosis airway epithelial cells to epinephrine.Candida albicans ethanol stimulates Pseudomonas aeruginosa WspR-controlled biofilm formation as part of a cyclic relationship involving phenazines.Pharmacological approaches to correcting the ion transport defect in cystic fibrosis.Stimulation of chloride secretion by P1 purinoceptor agonists in cystic fibrosis phenotype airway epithelial cell line CFPEo-Caspases shutdown nonsense-mediated mRNA decay during apoptosis.Rescue of nonsense mutations by amlexanox in human cells.GTP-binding proteins inhibit cAMP activation of chloride channels in cystic fibrosis airway epithelial cells.Generation of SV40-transformed rabbit tracheal-epithelial-cell-derived blastocyst by somatic cell nuclear transfer.Activation of intestinal CFTR Cl- channel by heat-stable enterotoxin and guanylin via cAMP-dependent protein kinase.Phospholipase D1 is threonine-phosphorylated in human-airway epithelial cells stimulated by sphingosine-1-phosphate by a mechanism involving Src tyrosine kinase and protein kinase Cdelta.Effect of vaccine-elicited antibodies on colonization of Neisseria meningitidis serogroup B and C strains in a human bronchial epithelial cell culture model.Sensitivity of chloride efflux vs. transepithelial measurements in mixed CF and normal airway epithelial cell populations.Histamine stimulates a biphasic calcium response in the human tracheal epithelial cell line CF/T43.Effects of azithromycin on glutathione S-transferases in cystic fibrosis airway cells.Cl transport in complemented CF bronchial epithelial cells correlates with CFTR mRNA expression levels.Premature termination codon readthrough in human cells occurs in novel cytoplasmic foci and requires UPF proteins.Azithromycin selectively reduces tumor necrosis factor alpha levels in cystic fibrosis airway epithelial cells.The vacuolating toxin of Helicobacter pylori mimicks the CFTR-mediated chloride conductance.Expression of P2Y receptors in cell lines derived from the human lung.Restoration of cyclic adenosine monophosphate-stimulated chloride channel activity in human cystic fibrosis tracheobronchial submucosal gland cells by adenovirus-mediated and cationic lipid-mediated gene transfer.Intracellular calcium mobilization and phospholipid degradation in sphingosylphosphorylcholine-stimulated human airway epithelial cells.Immortalization of epithelial cells.Heterotrimeric G proteins, vesicle trafficking, and CFTR Cl- channels.An immortalized cystic fibrosis tracheal epithelial cell line homozygous for the delta F508 CFTR mutation.Oncogene-mediated propagation of tracheal epithelial cells from two cystic fibrosis fetuses with different mutations. Characterization of CFT-1 and CFT-2 cells in culture.Poly (D, L-lactide-co-glycolide)/DNA microspheres to facilitate prolonged transgene expression in airway epithelium in vitro, ex vivo and in vivo.Reverse transcription-polymerase chain reaction (RT-PCR) phenotypic analysis of cell cultures of human tracheal epithelium, tracheobronchial glands, and lung carcinomas.Zinc Deficiency via a Splice Switch in Zinc Importer ZIP2/SLC39A2 Causes Cystic Fibrosis-Associated MUC5AC Hypersecretion in Airway Epithelial Cells.
P2860
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P1343
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P2860
Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on June 1992
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
@en
Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
@nl
type
label
Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
@en
Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
@nl
prefLabel
Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
@en
Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
@nl
P2093
P2860
P4510
P356
P1476
Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
@en
P2093
A L Cozens
D C Gruenert
J A Wagner
W E Finkbeiner
P2860
P304
P356
10.1073/PNAS.89.11.5171
P407
P577
1992-06-01T00:00:00Z