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380 related items for PubMed ID: 1380724

  • 21. Cystic fibrosis transmembrane conductance regulator (CFTR) activity in nasal epithelial cells from cystic fibrosis patients with severe genotypes.
    Andersson C, Dragomir A, Hjelte L, Roomans GM.
    Clin Sci (Lond); 2002 Oct; 103(4):417-24. PubMed ID: 12241542
    [Abstract] [Full Text] [Related]

  • 22. Induction of a cAMP-stimulated chloride secretion in regenerating poorly differentiated airway epithelial cells by adenovirus-mediated CFTR gene transfer.
    Dupuit F, Chinet T, Zahm JM, Pierrot D, Hinnrasky J, Kaplan H, Bonnet N, Puchelle E.
    Hum Gene Ther; 1997 Aug 10; 8(12):1439-50. PubMed ID: 9287144
    [Abstract] [Full Text] [Related]

  • 23. The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon.
    Mall M, Kreda SM, Mengos A, Jensen TJ, Hirtz S, Seydewitz HH, Yankaskas J, Kunzelmann K, Riordan JR, Boucher RC.
    Gastroenterology; 2004 Jan 10; 126(1):32-41. PubMed ID: 14699484
    [Abstract] [Full Text] [Related]

  • 24. Porcine nasal epithelial cultures for studies of cystic fibrosis sinusitis.
    Dean N, Ranganath NK, Jones B, Zhang S, Skinner D, Rowe SM, Sorscher EJ, Woodworth BA.
    Int Forum Allergy Rhinol; 2014 Jul 10; 4(7):565-70. PubMed ID: 24733748
    [Abstract] [Full Text] [Related]

  • 25. Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis.
    Zabner J, Couture LA, Gregory RJ, Graham SM, Smith AE, Welsh MJ.
    Cell; 1993 Oct 22; 75(2):207-16. PubMed ID: 7691415
    [Abstract] [Full Text] [Related]

  • 26. Lubiprostone activates non-CFTR-dependent respiratory epithelial chloride secretion in cystic fibrosis mice.
    MacDonald KD, McKenzie KR, Henderson MJ, Hawkins CE, Vij N, Zeitlin PL.
    Am J Physiol Lung Cell Mol Physiol; 2008 Nov 22; 295(5):L933-40. PubMed ID: 18805957
    [Abstract] [Full Text] [Related]

  • 27. Calcium-activated chloride conductance is not increased in pancreatic duct cells of CF mice.
    Winpenny JP, Verdon B, McAlroy HL, Colledge WH, Ratcliff R, Evans MJ, Gray MA, Argent BE.
    Pflugers Arch; 1995 May 22; 430(1):26-33. PubMed ID: 7545279
    [Abstract] [Full Text] [Related]

  • 28. Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotype.
    Beck S, Kühr J, Schütz VV, Seydewitz HH, Brandis M, Greger R, Kunzelmann K.
    Pediatr Pulmonol; 1999 Apr 22; 27(4):251-9. PubMed ID: 10230924
    [Abstract] [Full Text] [Related]

  • 29. Correction of chloride transport and mislocalization of CFTR protein by vardenafil in the gastrointestinal tract of cystic fibrosis mice.
    Dhooghe B, Noël S, Bouzin C, Behets-Wydemans G, Leal T.
    PLoS One; 2013 Apr 22; 8(10):e77314. PubMed ID: 24204804
    [Abstract] [Full Text] [Related]

  • 30. Extracellular zinc and ATP restore chloride secretion across cystic fibrosis airway epithelia by triggering calcium entry.
    Zsembery A, Fortenberry JA, Liang L, Bebok Z, Tucker TA, Boyce AT, Braunstein GM, Welty E, Bell PD, Sorscher EJ, Clancy JP, Schwiebert EM.
    J Biol Chem; 2004 Mar 12; 279(11):10720-9. PubMed ID: 14701827
    [Abstract] [Full Text] [Related]

  • 31. Increasing expression of the normal human CFTR cDNA in cystic fibrosis epithelial cells results in a progressive increase in the level of CFTR protein expression, but a limit on the level of cAMP-stimulated chloride secretion.
    Rosenfeld MA, Rosenfeld SJ, Danel C, Banks TC, Crystal RG.
    Hum Gene Ther; 1994 Sep 12; 5(9):1121-9. PubMed ID: 7530494
    [Abstract] [Full Text] [Related]

  • 32. 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 12; 3(3):253-66. PubMed ID: 1379473
    [Abstract] [Full Text] [Related]

  • 33. 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 18; 362(6417):250-5. PubMed ID: 7681548
    [Abstract] [Full Text] [Related]

  • 34. cAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epithelia.
    Smith JJ, Welsh MJ.
    J Clin Invest; 1992 Apr 18; 89(4):1148-53. PubMed ID: 1313448
    [Abstract] [Full Text] [Related]

  • 35. Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model.
    Gabriel SE, Brigman KN, Koller BH, Boucher RC, Stutts MJ.
    Science; 1994 Oct 07; 266(5182):107-9. PubMed ID: 7524148
    [Abstract] [Full Text] [Related]

  • 36. Activation of intestinal Cl- secretion by lubiprostone requires the cystic fibrosis transmembrane conductance regulator.
    Bijvelds MJ, Bot AG, Escher JC, De Jonge HR.
    Gastroenterology; 2009 Sep 07; 137(3):976-85. PubMed ID: 19454284
    [Abstract] [Full Text] [Related]

  • 37. Loss of CFTR chloride channels alters salt absorption by cystic fibrosis airway epithelia in vitro.
    Zabner J, Smith JJ, Karp PH, Widdicombe JH, Welsh MJ.
    Mol Cell; 1998 Sep 07; 2(3):397-403. PubMed ID: 9774978
    [Abstract] [Full Text] [Related]

  • 38. Normalization of ion transport in murine cystic fibrosis nasal epithelium using gene transfer.
    MacVinish LJ, Goddard C, Colledge WH, Higgins CF, Evans MJ, Cuthbert AW.
    Am J Physiol; 1997 Aug 07; 273(2 Pt 1):C734-40. PubMed ID: 9277371
    [Abstract] [Full Text] [Related]

  • 39. Polarized distribution of HCO3- transport in human normal and cystic fibrosis nasal epithelia.
    Paradiso AM, Coakley RD, Boucher RC.
    J Physiol; 2003 Apr 01; 548(Pt 1):203-18. PubMed ID: 12562898
    [Abstract] [Full Text] [Related]

  • 40. 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 01; 441(1):133-7. PubMed ID: 11205052
    [Abstract] [Full Text] [Related]

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