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9. Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein. Brown CR; Hong-Brown LQ; Biwersi J; Verkman AS; Welch WJ Cell Stress Chaperones; 1996 Jun; 1(2):117-25. PubMed ID: 9222597 [TBL] [Abstract][Full Text] [Related]
10. Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): slow degradation of wild-type and delta F508 CFTR in surface membrane preparations of immortalized airway epithelial cells. Wei X; Eisman R; Xu J; Harsch AD; Mulberg AE; Bevins CL; Glick MC; Scanlin TF J Cell Physiol; 1996 Aug; 168(2):373-84. PubMed ID: 8707873 [TBL] [Abstract][Full Text] [Related]
11. Functional activation of the cystic fibrosis trafficking mutant delta F508-CFTR by overexpression. Cheng SH; Fang SL; Zabner J; Marshall J; Piraino S; Schiavi SC; Jefferson DM; Welsh MJ; Smith AE Am J Physiol; 1995 Apr; 268(4 Pt 1):L615-24. PubMed ID: 7733303 [TBL] [Abstract][Full Text] [Related]
12. Limited proteolysis as a probe for arrested conformational maturation of delta F508 CFTR. Zhang F; Kartner N; Lukacs GL Nat Struct Biol; 1998 Mar; 5(3):180-3. PubMed ID: 9501909 [TBL] [Abstract][Full Text] [Related]
13. A novel natural product compound enhances cAMP-regulated chloride conductance of cells expressing CFTR[delta]F508. deCarvalho AC; Ndi CP; Tsopmo A; Tane P; Ayafor J; Connolly JD; Teem JL Mol Med; 2002 Feb; 8(2):75-87. PubMed ID: 12080183 [TBL] [Abstract][Full Text] [Related]
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15. PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator. Swiatecka-Urban A; Duhaime M; Coutermarsh B; Karlson KH; Collawn J; Milewski M; Cutting GR; Guggino WB; Langford G; Stanton BA J Biol Chem; 2002 Oct; 277(42):40099-105. PubMed ID: 12167629 [TBL] [Abstract][Full Text] [Related]
16. A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo. French PJ; van Doorninck JH; Peters RH; Verbeek E; Ameen NA; Marino CR; de Jonge HR; Bijman J; Scholte BJ J Clin Invest; 1996 Sep; 98(6):1304-12. PubMed ID: 8823295 [TBL] [Abstract][Full Text] [Related]
17. In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR. Rubenstein RC; Egan ME; Zeitlin PL J Clin Invest; 1997 Nov; 100(10):2457-65. PubMed ID: 9366560 [TBL] [Abstract][Full Text] [Related]
18. Endogenous surface expression of ΔF508-CFTR mediates cAMP-stimulated Cl(-) current in CFTR(ΔF508/ΔF508) pig thyroid epithelial cells. Li Y; Ganta S; Fong P Exp Physiol; 2012 Jan; 97(1):115-24. PubMed ID: 21948195 [TBL] [Abstract][Full Text] [Related]
19. Analysis of the localization of STE6/CFTR chimeras in a Saccharomyces cerevisiae model for the cystic fibrosis defect CFTR delta F508. Paddon C; Loayza D; Vangelista L; Solari R; Michaelis S Mol Microbiol; 1996 Mar; 19(5):1007-17. PubMed ID: 8830258 [TBL] [Abstract][Full Text] [Related]
20. Functional cystic fibrosis transmembrane conductance regulator tagged with an epitope of the vesicular stomatis virus glycoprotein can be addressed to the apical domain of polarized cells. Costa de Beauregard MA; Edelman A; Chesnoy-Marchais D; Tondelier D; Lapillonne A; El Marjou F; Robine S; Louvard D Eur J Cell Biol; 2000 Nov; 79(11):795-802. PubMed ID: 11139142 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]