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Cystic fibrosis airway epithelial cells

Schwiebert, E. M., N. Kizer, D. C. Gruenert, and B. A. Stanton. 1992. GTP-binding proteins inhibit cAMP activation of chloride channels in cystic fibrosis airway epithelial cells. Proc Natl Acad Sci USA 89(22) 10623-7. [Pg.635]

Gruenert, D. C., M. J. Yezzi, L. Chin, and A. L. Cozens. 1991. Characterization of normal and cystic fibrosis airway epithelial cells transformed with a temperature-sensitive SV40 plasmid. Ped Pulmonol Suppl 6 (Abstr) 137. [Pg.638]

Fajac, I., Briand, P., Monsigny, M. and Midoux, P. (1999) Sugar-mediated uptake of glycosylated polylysines and gene transfer into normal and cystic fibrosis airway epithelial cells. Hum. Gene Ther., 10, 395 106. [Pg.331]

Nanua, S., Sajjan, U., Keshavjee, S. and Hershenson, M.B. (2006) Absence of typical unfolded protein response in primary cultured cystic fibrosis airway epithelial cells. Biochem. Biophys. Res. Commun. 343, 135-143. [Pg.296]

Joseph, T., Look, D. Ferkol, T. NF-kappaB activation and sustained IL-8 gene expression in primary cultures of cystic fibrosis airway epithelial cells stimulated with Pseudomonas aeruginosa. Am J Physiol Lung Cell Mol Physiol 288 (2005) L471-9. [Pg.536]

Teramoto S, Bartlett JS, McCarty D, Xiao X, Samulski RJ, Boucher RC. Factors influencing adeno-associated vims-mediated gene transfer to human cystic fibrosis airway epithelial cells comparison with adenovims vectors. J Virol 1998 72 8904-8912. [Pg.91]

Rich DP, Anderson MP, Gregory RJ, Cheng SH, Paul S, Jefferson DM, McCaim JD, Klinger KW, Smith AE, Welsh MJ. Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells. Nature 1990 347 358-363. [Pg.349]

Kollen WJ, Schembri FM, Gerwig GJ, Vliegenthart JF, Glick MC, Scanlin TF. Enhanced efficiency of lactosylated poly-L-lysine-mediated gene transfer into cystic fibrosis airway epithelial cells. Am J Respir Cell Mol Biol 1999 20 1081-1086. [Pg.352]

KlinkDT, Chao S, GlickMC, Scanlin TF. Nuclear translation of lactosylated poly-1-lysine/cdna complex in cystic fibrosis airway epithelial cells. Mol Ther 2001 3 831-841. [Pg.364]

FIGURE 13-1. Electrolyte transport in the airway epithelial cell. Ca, calcium cAMP, cyclic-3, 5 -adenosine monophosphate Cl, chloride Na, sodium K potassium. (From Milavetz G, Smith JJ. Cystic fibrosis. In DiPiro JT, Talbert RL, Yee GC, et al, (eds.) Pharmacotherapy A Pathophysiologic Approach. 6th ed. New York McGraw-Hill 2005 592, with permission.)... [Pg.246]

Stutts MJ, Cotton CU, Yankaskas JR, Cheng E, Knowles MR, Gatzy JT, Boucher RC (1985) Chloride uptake into cultured airway epithelial cells from cystic fibrosis patients and normal individuals. Proc Natl Acad Sci USA 82(19) 6677-6681. [Pg.254]

Yankaskas, J. R., and R. C. Boucher. 1990. Transformation of airway epithelial cells with persistence of cystic fibrosis or normal ion transport phenotypes. Methods Enzymol 192 565-71. [Pg.635]

Cowley EA, Linsdell P (2002) Oxidant stress stimulates anion secretion from the human airway epithelial cell line Calu-3 implications for cystic fibrosis lung disease. J Physiol 543(Pt 1) 201-209... [Pg.116]

Wiszniewski L, Jornot L, Dudez T et al (2006) Long-term cultures of polarized airway epithelial cells from patients with cystic fibrosis. Am J Respir Cell Mol Biol 34(1) 39 8... [Pg.120]

Given that most adolescents and adults are chronically colonized with P. aeruginosa, attention has logically been focused on determining the role of this bacterium and its products in the production of pro-inflammatory cytokines and chemokines in normal and cystic fibrosis airway epithelia, and in epithelial cell lines established from patients with cystic fibrosis, or all lines which model the mutation of the CFTR. [Pg.124]


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See also in sourсe #XX -- [ Pg.122 , Pg.124 ]




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Cystic fibrosis

Cystic fibrosis epithelial cells

Epithelial

Epithelial cells

Epithelialization

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