Towards an in vitro model of cystic fibrosis small airway epithelium: characterisation of the human bronchial epithelial cell line CFBE41o-

[1]  L. Hagenfeldt,et al.  Heparin can improve the viability of transfected cystic fibrosis cell lines in vitro. , 2004, Life sciences.

[2]  J. Riordan,et al.  Purification and Crystallization of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)* , 2004, Journal of Biological Chemistry.

[3]  R. Müller,et al.  Transfection with different colloidal systems: comparison of solid lipid nanoparticles and liposomes. , 2004, Journal of controlled release : official journal of the Controlled Release Society.

[4]  D. Geddes,et al.  Update on gene therapy for cystic fibrosis. , 2003, Current opinion in molecular therapeutics.

[5]  G. Roomans,et al.  Activation of CFTR by genistein in human airway epithelial cell lines. , 2003, Biochemical and biophysical research communications.

[6]  D. Geddes,et al.  Pulmonary Gene Therapy , 2003 .

[7]  C. Ehrhardt,et al.  16HBE14o- Human Bronchial Epithelial Cell Layers Express P-Glycoprotein, Lung Resistance-Related Protein, and Caveolin-1 , 2003, Pharmaceutical Research.

[8]  Z. Bebők,et al.  Transient transfection of polarized epithelial monolayers with CFTR and reporter genes using efficacious lipids. , 2003, American journal of physiology. Cell physiology.

[9]  R. Boucher,et al.  An overview of the pathogenesis of cystic fibrosis lung disease. , 2002, Advanced drug delivery reviews.

[10]  D. Look,et al.  Inflammatory response in airway epithelial cells isolated from patients with cystic fibrosis. , 2002, American journal of respiratory and critical care medicine.

[11]  G. Novelli,et al.  In vitro correction of cystic fibrosis epithelial cell lines by small fragment homologous replacement (SFHR) technique , 2002, BMC Medical Genetics.

[12]  D. Clarke,et al.  Introduction of the Most Common Cystic Fibrosis Mutation (ΔF508) into Human P-glycoprotein Disrupts Packing of the Transmembrane Segments* , 2002, The Journal of Biological Chemistry.

[13]  G. Novelli,et al.  Isolation of CF cell lines corrected at ΔF508-CFTR locus by SFHR-mediated targeting , 2002, Gene Therapy.

[14]  Carsten Kneuer,et al.  Influence of apical fluid volume on the development of functional intercellular junctions in the human epithelial cell line 16HBE14o–: implications for the use of this cell line as an in vitro model for bronchial drug absorption studies , 2002, Cell and Tissue Research.

[15]  R. Kopito,et al.  A Principal Role for the Proteasome in Endoplasmic Reticulum-associated Degradation of Misfolded Intracellular Cystic Fibrosis Transmembrane Conductance Regulator* , 2002, The Journal of Biological Chemistry.

[16]  C. Wise Epithelial cell culture protocols , 2002 .

[17]  A. Bush,et al.  Cystic fibrosis: review of the decade. , 2001, Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace.

[18]  K. Audus,et al.  P-glycoprotein efflux pump expression and activity in Calu-3 cells. , 2001, Journal of pharmaceutical sciences.

[19]  S. Fang,et al.  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. , 1999, American journal of respiratory cell and molecular biology.

[20]  K. Rabe,et al.  Characterization of Cell Surface Lectin-binding Patterns of Human Airway Epithelium , 1999, The Histochemical Journal.

[21]  S. Randell,et al.  Evidence for Periciliary Liquid Layer Depletion, Not Abnormal Ion Composition, in the Pathogenesis of Cystic Fibrosis Airways Disease , 1998, Cell.

[22]  K. Kunzelmann,et al.  Targeted replacement of normal and mutant CFTR sequences in human airway epithelial cells using DNA fragments. , 1998, Human molecular genetics.

[23]  B. Milleron,et al.  MDR1-Pgp 170 expression in human bronchus. , 1997, The European respiratory journal.

[24]  B. Davidson,et al.  Complexes of Adenovirus with Polycationic Polymers and Cationic Lipids Increase the Efficiency of Gene Transfer in Vitro and in Vivo* , 1997, The Journal of Biological Chemistry.

[25]  J. Widdicombe,et al.  Culture and transformation of human airway epithelial cells. , 1995, The American journal of physiology.

[26]  L. Chin,et al.  Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[27]  R. Craig,et al.  A cystic fibrosis bronchial epithelial cell line: immortalization by adeno-12-SV40 infection. , 1991, American journal of respiratory cell and molecular biology.

[28]  K. Klinger,et al.  Expression of normal and cystic fibrosis phenotypes by continuous airway epithelial cell lines. , 1990, The American journal of physiology.

[29]  C. Basbaum,et al.  Long-term culture of normal and cystic fibrosis epithelial cells grown under serum-free conditions , 1990, In Vitro Cellular & Developmental Biology.

[30]  R. Jenkins,et al.  Pulmonary gene therapy. Realistic hope for the future, or false dawn in the promised land? , 2003, Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace.

[31]  G. Roomans Pharmacological Approaches to Correcting the Ion Transport Defect in Cystic Fibrosis , 2003, American journal of respiratory medicine : drugs, devices, and other interventions.

[32]  K. Roemer,et al.  Differentiation of human alveolar epithelial cells in primary culture: morphological characterization and synthesis of caveolin-1 and surfactant protein-C , 2002, Cell and Tissue Research.

[33]  M. Welsh,et al.  An in vitro model of differentiated human airway epithelia. Methods for establishing primary cultures. , 2002, Methods in molecular biology.

[34]  S. Rybárová,et al.  Immunohistochemical detection of LRP protein in the normal human lung. , 2001, Bratislavske lekarske listy.

[35]  B. Jasani,et al.  Caveolin and its cellular and subcellular immunolocalisation in lung alveolar epithelium: implications for alveolar epithelial type I cell function , 1999, Cell and Tissue Research.

[36]  L. Chin,et al.  CFTR expression and chloride secretion in polarized immortal human bronchial epithelial cells. , 1994, American journal of respiratory cell and molecular biology.