141 related articles for article (PubMed ID: 2472008)
21. Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis.
Clarke LL; Grubb BR; Gabriel SE; Smithies O; Koller BH; Boucher RC
Science; 1992 Aug; 257(5073):1125-8. PubMed ID: 1380724
[TBL] [Abstract][Full Text] [Related]
22. Chloride secretory response of cystic fibrosis human airway epithelia. Preservation of calcium but not protein kinase C- and A-dependent mechanisms.
Boucher RC; Cheng EH; Paradiso AM; Stutts MJ; Knowles MR; Earp HS
J Clin Invest; 1989 Nov; 84(5):1424-31. PubMed ID: 2478586
[TBL] [Abstract][Full Text] [Related]
23. Cl- channels in CF: lack of activation by protein kinase C and cAMP-dependent protein kinase.
Hwang TC; Lu L; Zeitlin PL; Gruenert DC; Huganir R; Guggino WB
Science; 1989 Jun; 244(4910):1351-3. PubMed ID: 2472005
[TBL] [Abstract][Full Text] [Related]
24. Ketoconazole activates Cl- conductance and blocks Cl- and fluid absorption by cultured cystic fibrosis (CFPAC-1) cells.
Kersting U; Kersting D; Spring KR
Proc Natl Acad Sci U S A; 1993 May; 90(9):4047-51. PubMed ID: 7683418
[TBL] [Abstract][Full Text] [Related]
25. Nitric oxide has no beneficial effects on ion transport defects in cystic fibrosis human nasal epithelium.
Rückes-Nilges C; Lindemann H; Klimek T; Glanz H; Weber WM
Pflugers Arch; 2000 Nov; 441(1):133-7. PubMed ID: 11205052
[TBL] [Abstract][Full Text] [Related]
26. Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR.
Egan M; Flotte T; Afione S; Solow R; Zeitlin PL; Carter BJ; Guggino WB
Nature; 1992 Aug; 358(6387):581-4. PubMed ID: 1380129
[TBL] [Abstract][Full Text] [Related]
27. Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy.
Hyde SC; Gill DR; Higgins CF; Trezise AE; MacVinish LJ; Cuthbert AW; Ratcliff R; Evans MJ; Colledge WH
Nature; 1993 Mar; 362(6417):250-5. PubMed ID: 7681548
[TBL] [Abstract][Full Text] [Related]
28. Calu-3: a human airway epithelial cell line that shows cAMP-dependent Cl- secretion.
Shen BQ; Finkbeiner WE; Wine JJ; Mrsny RJ; Widdicombe JH
Am J Physiol; 1994 May; 266(5 Pt 1):L493-501. PubMed ID: 7515578
[TBL] [Abstract][Full Text] [Related]
29. Correction of the apical membrane chloride permeability defect in polarized cystic fibrosis airway epithelia following retroviral-mediated gene transfer.
Olsen JC; Johnson LG; Stutts MJ; Sarkadi B; Yankaskas JR; Swanstrom R; Boucher RC
Hum Gene Ther; 1992 Jun; 3(3):253-66. PubMed ID: 1379473
[TBL] [Abstract][Full Text] [Related]
30. In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis.
Knowles MR; Paradiso AM; Boucher RC
Hum Gene Ther; 1995 Apr; 6(4):445-55. PubMed ID: 7542031
[TBL] [Abstract][Full Text] [Related]
31. Regulation of chloride channels by protein kinase C in normal and cystic fibrosis airway epithelia.
Li M; McCann JD; Anderson MP; Clancy JP; Liedtke CM; Nairn AC; Greengard P; Welsch MJ
Science; 1989 Jun; 244(4910):1353-6. PubMed ID: 2472006
[TBL] [Abstract][Full Text] [Related]
32. Importance of basolateral K+ conductance in maintaining Cl- secretion in murine nasal and colonic epithelia.
MacVinish LJ; Hickman ME; Mufti DA; Durrington HJ; Cuthbert AW
J Physiol; 1998 Jul; 510 ( Pt 1)(Pt 1):237-47. PubMed ID: 9625880
[TBL] [Abstract][Full Text] [Related]
33. Activation of normal and cystic fibrosis Cl- channels by voltage, temperature, and trypsin.
Welsh MJ; Li M; McCann JD
J Clin Invest; 1989 Dec; 84(6):2002-7. PubMed ID: 2556452
[TBL] [Abstract][Full Text] [Related]
34. Cystic fibrosis transmembrane conductance regulator protein: what is its role in cystic fibrosis?
Richardson PS; Alton EW
Eur Respir J; 1993 Feb; 6(2):160-2. PubMed ID: 7680321
[No Abstract] [Full Text] [Related]
35. Quantitative fluorescence measurements of chloride secretion in native airway epithelium from CF and non-CF subjects.
Stern M; Munkonge FM; Caplen NJ; Sorgi F; Huang L; Geddes DM; Alton EW
Gene Ther; 1995 Dec; 2(10):766-74. PubMed ID: 8750017
[TBL] [Abstract][Full Text] [Related]
36. Mechanism of sodium hyperabsorption in cultured cystic fibrosis nasal epithelium: a patch-clamp study.
Chinet TC; Fullton JM; Yankaskas JR; Boucher RC; Stutts MJ
Am J Physiol; 1994 Apr; 266(4 Pt 1):C1061-8. PubMed ID: 7513953
[TBL] [Abstract][Full Text] [Related]
37. Reversed anion selectivity in cultured cystic fibrosis sweat duct cells.
Bell CL; Reddy MM; Quinton PM
Am J Physiol; 1992 Jan; 262(1 Pt 1):C32-8. PubMed ID: 1310214
[TBL] [Abstract][Full Text] [Related]
38. Noise analysis and single-channel observations of 4 pS chloride channels in human airway epithelia.
Duszyk M; French AS; Man SF
Biophys J; 1992 Feb; 61(2):583-7. PubMed ID: 1372182
[TBL] [Abstract][Full Text] [Related]
39. Localization of Cl- conductance in normal and Cl- impermeability in cystic fibrosis sweat duct epithelium.
Reddy MM; Quinton PM
Am J Physiol; 1989 Oct; 257(4 Pt 1):C727-35. PubMed ID: 2478027
[TBL] [Abstract][Full Text] [Related]
40. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.
Johnson LG; Boyles SE; Wilson J; Boucher RC
J Clin Invest; 1995 Mar; 95(3):1377-82. PubMed ID: 7533790
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
