BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

396 related articles for article (PubMed ID: 7531792)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. Localization of ZO-1 and E-cadherin in the nasal polyp epithelium.
    Jang YJ; Kim HG; Koo TW; Chung PS
    Eur Arch Otorhinolaryngol; 2002 Oct; 259(9):465-9. PubMed ID: 12386748
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Decreased expression of the cystic fibrosis transmembrane conductance regulator protein in remodeled airway epithelium from lung transplanted patients.
    Brézillon S; Hamm H; Heilmann M; Schäfers HJ; Hinnrasky J; Wagner TO; Puchelle E; Tümmler B
    Hum Pathol; 1997 Aug; 28(8):944-52. PubMed ID: 9269831
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Abnormal subcellular localization of mutated CFTR protein in a cystic fibrosis epithelial cell line.
    Demolombe S; Baró I; Laurent M; Hongre AS; Pavirani A; Escande D
    Eur J Cell Biol; 1994 Oct; 65(1):214-9. PubMed ID: 7534234
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations.
    Wilschanski M; Yahav Y; Yaacov Y; Blau H; Bentur L; Rivlin J; Aviram M; Bdolah-Abram T; Bebok Z; Shushi L; Kerem B; Kerem E
    N Engl J Med; 2003 Oct; 349(15):1433-41. PubMed ID: 14534336
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expression of cystic fibrosis transmembrane conductance regulator in the human distal lung.
    Regnier A; Dannhoffer L; Blouquit-Laye S; Bakari M; Naline E; Chinet T
    Hum Pathol; 2008 Mar; 39(3):368-76. PubMed ID: 18045644
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expression of cystic fibrosis transmembrane conductance regulator in human gallbladder epithelial cells.
    Dray-Charier N; Paul A; Veissiere D; Mergey M; Scoazec JY; Capeau J; Brahimi-Horn C; Housset C
    Lab Invest; 1995 Dec; 73(6):828-36. PubMed ID: 8558844
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A method for the rapid detection of recombinant CFTR during gene therapy in cystic fibrosis.
    Demolombe S; Baró I; Bebok Z; Clancy JP; Sorscher EJ; Thomas-Soumarmon A; Pavirani A; Escande D
    Gene Ther; 1996 Aug; 3(8):685-94. PubMed ID: 8854094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 16. Localisation of wild-type and DeltaF508-CFTR in nasal epithelial cells.
    Dormer RL; McNeilly CM; Morris MR; Pereira MM; Doull IJ; Becq F; Mettey Y; Vierfond JM; McPherson MA
    Pflugers Arch; 2001; 443 Suppl 1():S117-20. PubMed ID: 11845316
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expression and localization of CFTR in the rhesus monkey surface airway epithelium.
    Dupuit F; Bout A; Hinnrasky J; Fuchey C; Zahm JM; Imler JL; Pavirani A; Valerio D; Puchelle E
    Gene Ther; 1995 Mar; 2(2):156-63. PubMed ID: 7536618
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Retinoid status and the control of keratin expression and adhesion during the histogenesis of squamous metaplasia of tracheal epithelium.
    Lancillotti F; Darwiche N; Celli G; De Luca LM
    Cancer Res; 1992 Nov; 52(22):6144-52. PubMed ID: 1384955
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Submucosal glands are the predominant site of CFTR expression in the human bronchus.
    Engelhardt JF; Yankaskas JR; Ernst SA; Yang Y; Marino CR; Boucher RC; Cohn JA; Wilson JM
    Nat Genet; 1992 Nov; 2(3):240-8. PubMed ID: 1285365
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.