Towards an in vitro model of cystic fibrosis small airway epithelium: characterisation of the human bronchial epithelial cell line CFBE41o-
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C. Ehrhardt | C. Lehr | M. Laue | Kwang-Jin Kim | C. Baldes | E. Collnot | Ulrich Becker | Christiane Baldes
[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.