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358 related items for PubMed ID: 7544810

  • 1. CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium.
    Dupuit F, Kälin N, Brézillon S, Hinnrasky J, Tümmler B, Puchelle E.
    J Clin Invest; 1995 Sep; 96(3):1601-11. PubMed ID: 7544810
    [Abstract] [Full Text] [Related]

  • 2. Decreased expression of the CFTR protein in remodeled human nasal epithelium from non-cystic fibrosis patients.
    Brezillon S, Dupuit F, Hinnrasky J, Marchand V, Kälin N, Tümmler B, Puchelle E.
    Lab Invest; 1995 Feb; 72(2):191-200. PubMed ID: 7531792
    [Abstract] [Full Text] [Related]

  • 3. Nonsense mutation R1162X of the cystic fibrosis transmembrane conductance regulator gene does not reduce messenger RNA expression in nasal epithelial tissue.
    Rolfini R, Cabrini G.
    J Clin Invest; 1993 Dec; 92(6):2683-7. PubMed ID: 7504691
    [Abstract] [Full Text] [Related]

  • 4. Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis.
    Hamosh A, Trapnell BC, Zeitlin PL, Montrose-Rafizadeh C, Rosenstein BJ, Crystal RG, Cutting GR.
    J Clin Invest; 1991 Dec; 88(6):1880-5. PubMed ID: 1721624
    [Abstract] [Full Text] [Related]

  • 5. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.
    Dray-Charier N, Paul A, Scoazec JY, Veissière D, Mergey M, Capeau J, Soubrane O, Housset C.
    Hepatology; 1999 Jun; 29(6):1624-34. PubMed ID: 10347100
    [Abstract] [Full Text] [Related]

  • 6. Localization and up-regulation of mucin (MUC2) gene expression in human nasal biopsies of patients with cystic fibrosis.
    Li D, Wang D, Majumdar S, Jany B, Durham SR, Cottrell J, Caplen N, Geddes DM, Alton EW, Jeffery PK.
    J Pathol; 1997 Mar; 181(3):305-10. PubMed ID: 9155717
    [Abstract] [Full Text] [Related]

  • 7. Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF mice.
    Ostrowski LE, Yin W, Diggs PS, Rogers TD, O'Neal WK, Grubb BR.
    Gene Ther; 2007 Oct; 14(20):1492-501. PubMed ID: 17637798
    [Abstract] [Full Text] [Related]

  • 8. Transcript analysis of CFTR nonsense mutations in lymphocytes and nasal epithelial cells from cystic fibrosis patients.
    Will K, Dörk T, Stuhrmann M, von der Hardt H, Ellemunter H, Tümmler B, Schmidtke J.
    Hum Mutat; 1995 Oct; 5(3):210-20. PubMed ID: 7541274
    [Abstract] [Full Text] [Related]

  • 9. A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis.
    Gill DR, Southern KW, Mofford KA, Seddon T, Huang L, Sorgi F, Thomson A, MacVinish LJ, Ratcliff R, Bilton D, Lane DJ, Littlewood JM, Webb AK, Middleton PG, Colledge WH, Cuthbert AW, Evans MJ, Higgins CF, Hyde SC.
    Gene Ther; 1997 Mar; 4(3):199-209. PubMed ID: 9135733
    [Abstract] [Full Text] [Related]

  • 10. Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation.
    Sermet-Gaudelus I, Vallée B, Urbin I, Torossi T, Marianovski R, Fajac A, Feuillet MN, Bresson JL, Lenoir G, Bernaudin JF, Edelman A.
    Pediatr Res; 2002 Nov; 52(5):628-35. PubMed ID: 12409506
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium.
    Puchelle E, Gaillard D, Ploton D, Hinnrasky J, Fuchey C, Boutterin MC, Jacquot J, Dreyer D, Pavirani A, Dalemans W.
    Am J Respir Cell Mol Biol; 1992 Nov; 7(5):485-91. PubMed ID: 1384582
    [Abstract] [Full Text] [Related]

  • 13. Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosis.
    Noone PG, Hohneker KW, Zhou Z, Johnson LG, Foy C, Gipson C, Jones K, Noah TL, Leigh MW, Schwartzbach C, Efthimiou J, Pearlman R, Boucher RC, Knowles MR.
    Mol Ther; 2000 Jan; 1(1):105-14. PubMed ID: 10933918
    [Abstract] [Full Text] [Related]

  • 14. Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifestations of cystic fibrosis.
    Chu CS, Trapnell BC, Curristin SM, Cutting GR, Crystal RG.
    J Clin Invest; 1992 Sep; 90(3):785-90. PubMed ID: 1381723
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Repeat administration of DNA/liposomes to the nasal epithelium of patients with cystic fibrosis.
    Hyde SC, Southern KW, Gileadi U, Fitzjohn EM, Mofford KA, Waddell BE, Gooi HC, Goddard CA, Hannavy K, Smyth SE, Egan JJ, Sorgi FL, Huang L, Cuthbert AW, Evans MJ, Colledge WH, Higgins CF, Webb AK, Gill DR.
    Gene Ther; 2000 Jul; 7(13):1156-65. PubMed ID: 10918483
    [Abstract] [Full Text] [Related]

  • 17. An immunocytochemical assay to detect human CFTR expression following gene transfer.
    Davidson H, Wilson A, Gray RD, Horsley A, Pringle IA, McLachlan G, Nairn AC, Stearns C, Gibson J, Holder E, Jones L, Doherty A, Coles R, Sumner-Jones SG, Wasowicz M, Manvell M, Griesenbach U, Hyde SC, Gill DR, Davies J, Collie DD, Alton EW, Porteous DJ, Boyd AC.
    Mol Cell Probes; 2009 Dec; 23(6):272-80. PubMed ID: 19615439
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  • 19. Expression of cystic fibrosis transmembrane conductance regulator in liver tissue from patients with cystic fibrosis.
    Kinnman N, Lindblad A, Housset C, Buentke E, Scheynius A, Strandvik B, Hultcrantz R.
    Hepatology; 2000 Aug; 32(2):334-40. PubMed ID: 10915740
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