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329 related items for PubMed ID: 7515571

  • 1. Hyperabsorption of Na+ and raised Ca(2+)-mediated Cl- secretion in nasal epithelia of CF mice.
    Grubb BR, Vick RN, Boucher RC.
    Am J Physiol; 1994 May; 266(5 Pt 1):C1478-83. PubMed ID: 7515571
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Increased contact time improves adenovirus-mediated CFTR gene transfer to nasal epithelium of CF mice.
    Jiang C, Akita GY, Colledge WH, Ratcliff RA, Evans MJ, Hehir KM, St George JA, Wadsworth SC, Cheng SH.
    Hum Gene Ther; 1997 Apr 10; 8(6):671-80. PubMed ID: 9113507
    [Abstract] [Full Text] [Related]

  • 4. cAMP- but not Ca(2+)-regulated Cl- conductance in the oviduct is defective in mouse model of cystic fibrosis.
    Leung AY, Wong PY, Gabriel SE, Yankaskas JR, Boucher RC.
    Am J Physiol; 1995 Mar 10; 268(3 Pt 1):C708-12. PubMed ID: 7534985
    [Abstract] [Full Text] [Related]

  • 5. Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.
    Boucher RC, Cotton CU, Gatzy JT, Knowles MR, Yankaskas JR.
    J Physiol; 1988 Nov 10; 405():77-103. PubMed ID: 3255805
    [Abstract] [Full Text] [Related]

  • 6. Minor role of Cl- secretion in non-cystic fibrosis and cystic fibrosis human nasal epithelium.
    Rückes-Nilges C, Weber U, Lindemann H, Münker G, Clauss W, Weber WM.
    Cell Physiol Biochem; 1999 Nov 10; 9(1):1-10. PubMed ID: 10352340
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 510 ( Pt 1)(Pt 1):237-47. PubMed ID: 9625880
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 6(4):445-55. PubMed ID: 7542031
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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 21; 257(5073):1125-8. PubMed ID: 1380724
    [Abstract] [Full Text] [Related]

  • 11. Activation of an apical Cl- conductance by Ca2+ ionophores in cystic fibrosis airway epithelia.
    Willumsen NJ, Boucher RC.
    Am J Physiol; 1989 Feb 21; 256(2 Pt 1):C226-33. PubMed ID: 2465689
    [Abstract] [Full Text] [Related]

  • 12. Anomalies in ion transport in CF mouse tracheal epithelium.
    Grubb BR, Paradiso AM, Boucher RC.
    Am J Physiol; 1994 Jul 21; 267(1 Pt 1):C293-300. PubMed ID: 8048488
    [Abstract] [Full Text] [Related]

  • 13. UTP inhibits Na+ absorption in wild-type and DeltaF508 CFTR-expressing human bronchial epithelia.
    Devor DC, Pilewski JM.
    Am J Physiol; 1999 Apr 21; 276(4):C827-37. PubMed ID: 10199813
    [Abstract] [Full Text] [Related]

  • 14. Transcellular sodium transport in cultured cystic fibrosis human nasal epithelium.
    Willumsen NJ, Boucher RC.
    Am J Physiol; 1991 Aug 21; 261(2 Pt 1):C332-41. PubMed ID: 1872375
    [Abstract] [Full Text] [Related]

  • 15. 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 21; 273(2 Pt 1):C734-40. PubMed ID: 9277371
    [Abstract] [Full Text] [Related]

  • 16. Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice.
    Clarke LL, Grubb BR, Yankaskas JR, Cotton CU, McKenzie A, Boucher RC.
    Proc Natl Acad Sci U S A; 1994 Jan 18; 91(2):479-83. PubMed ID: 7507247
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Isobutylmethylxanthine fails to stimulate chloride secretion in cystic fibrosis airway epithelia.
    Grubb B, Lazarowski E, Knowles M, Boucher R.
    Am J Respir Cell Mol Biol; 1993 Apr 01; 8(4):454-60. PubMed ID: 7682824
    [Abstract] [Full Text] [Related]

  • 19. Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia.
    Mall M, Gonska T, Thomas J, Schreiber R, Seydewitz HH, Kuehr J, Brandis M, Kunzelmann K.
    Pediatr Res; 2003 Apr 01; 53(4):608-18. PubMed ID: 12612194
    [Abstract] [Full Text] [Related]

  • 20. Ion transport across the jejunum in normal and cystic fibrosis mice.
    Grubb BR.
    Am J Physiol; 1995 Mar 01; 268(3 Pt 1):G505-13. PubMed ID: 7534995
    [Abstract] [Full Text] [Related]

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