317 related articles for article (PubMed ID: 1722350)
21. cAMP-stimulated ion currents in Xenopus oocytes expressing CFTR cRNA.
Cunningham SA; Worrell RT; Benos DJ; Frizzell RA
Am J Physiol; 1992 Mar; 262(3 Pt 1):C783-8. PubMed ID: 1372482
[TBL] [Abstract][Full Text] [Related]
22. Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl- channel is functional when retained in endoplasmic reticulum of mammalian cells.
Pasyk EA; Foskett JK
J Biol Chem; 1995 May; 270(21):12347-50. PubMed ID: 7539001
[TBL] [Abstract][Full Text] [Related]
23. Control of the cystic fibrosis transmembrane conductance regulator by alphaG(i) and RGS proteins.
Schreiber R; Kindle P; Benzing T; Walz G; Kunzelmann K
Biochem Biophys Res Commun; 2001 Mar; 281(4):917-23. PubMed ID: 11237748
[TBL] [Abstract][Full Text] [Related]
24. Protein kinase C activates chloride conductance in C127 cells stably expressing the cystic fibrosis gene.
Dechecchi MC; Tamanini A; Berton G; Cabrini G
J Biol Chem; 1993 May; 268(15):11321-5. PubMed ID: 7684379
[TBL] [Abstract][Full Text] [Related]
25. CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated state.
Wilkinson DJ; Mansoura MK; Watson PY; Smit LS; Collins FS; Dawson DC
J Gen Physiol; 1996 Jan; 107(1):103-19. PubMed ID: 8741733
[TBL] [Abstract][Full Text] [Related]
26. Radiotracer studies of cystic fibrosis transmembrane conductance regulator expressed in Xenopus oocytes.
Ohrui T; Skach W; Thompson M; Matsumoto-Pon J; Calayag C; Widdicombe JH
Am J Physiol; 1994 Jun; 266(6 Pt 1):C1586-93. PubMed ID: 7517633
[TBL] [Abstract][Full Text] [Related]
27. Molecular basis of defective anion transport in L cells expressing recombinant forms of CFTR.
Yang Y; Devor DC; Engelhardt JF; Ernst SA; Strong TV; Collins FS; Cohn JA; Frizzell RA; Wilson JM
Hum Mol Genet; 1993 Aug; 2(8):1253-61. PubMed ID: 7691345
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. GTP-binding proteins inhibit cAMP activation of chloride channels in cystic fibrosis airway epithelial cells.
Schwiebert EM; Kizer N; Gruenert DC; Stanton BA
Proc Natl Acad Sci U S A; 1992 Nov; 89(22):10623-7. PubMed ID: 1279687
[TBL] [Abstract][Full Text] [Related]
30. Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.
Rich DP; Anderson MP; Gregory RJ; Cheng SH; Paul S; Jefferson DM; McCann JD; Klinger KW; Smith AE; Welsh MJ
Nature; 1990 Sep; 347(6291):358-63. PubMed ID: 1699126
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Delta F508-CFTR channels: kinetics, activation by forskolin, and potentiation by xanthines.
Haws CM; Nepomuceno IB; Krouse ME; Wakelee H; Law T; Xia Y; Nguyen H; Wine JJ
Am J Physiol; 1996 May; 270(5 Pt 1):C1544-55. PubMed ID: 8967457
[TBL] [Abstract][Full Text] [Related]
33. The cystic fibrosis transmembrane conductance regulator. Overexpression, purification, and characterization of wild type and delta F508 mutant forms of the first nucleotide binding fold in fusion with the maltose-binding protein.
Ko YH; Thomas PJ; Delannoy MR; Pedersen PL
J Biol Chem; 1993 Nov; 268(32):24330-8. PubMed ID: 7693699
[TBL] [Abstract][Full Text] [Related]
34. Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding.
Logan J; Hiestand D; Daram P; Huang Z; Muccio DD; Hartman J; Haley B; Cook WJ; Sorscher EJ
J Clin Invest; 1994 Jul; 94(1):228-36. PubMed ID: 7518829
[TBL] [Abstract][Full Text] [Related]
35. Effect of deleting the R domain on CFTR-generated chloride channels.
Rich DP; Gregory RJ; Anderson MP; Manavalan P; Smith AE; Welsh MJ
Science; 1991 Jul; 253(5016):205-7. PubMed ID: 1712985
[TBL] [Abstract][Full Text] [Related]
36. Generation of cAMP-activated chloride currents by expression of CFTR.
Anderson MP; Rich DP; Gregory RJ; Smith AE; Welsh MJ
Science; 1991 Feb; 251(4994):679-82. PubMed ID: 1704151
[TBL] [Abstract][Full Text] [Related]
37. N-Acetyl-L-cysteine and its derivatives activate a Cl- conductance in epithelial cells.
Köttgen M; Busch AE; Hug MJ; Greger R; Kunzelmann K
Pflugers Arch; 1996 Feb; 431(4):549-55. PubMed ID: 8596698
[TBL] [Abstract][Full Text] [Related]
38. Intracellular cysteines of the cystic fibrosis transmembrane conductance regulator (CFTR) modulate channel gating.
Ketchum CJ; Yue H; Alessi KA; Devidas S; Guggino WB; Maloney PC
Cell Physiol Biochem; 2002; 12(1):1-8. PubMed ID: 11914543
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Possible regulation of CFTR-chloride channels by membrane-bound phosphatases in pancreatic duct cells.
Becq F; Fanjul M; Merten M; Figarella C; Hollande E; Gola M
FEBS Lett; 1993 Aug; 327(3):337-42. PubMed ID: 7688697
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
