These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

59 related articles for article (PubMed ID: 7514292)

  • 1. [Mucoviscidosis--3 years after discovery of the gene].
    Bargon J
    Pneumologie; 1994 Feb; 48(2):63-72. PubMed ID: 7514292
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Episomal expression of wild-type CFTR corrects cAMP-dependent chloride transport in respiratory epithelial cells.
    Lei DC; Kunzelmann K; Koslowsky T; Yezzi MJ; Escobar LC; Xu Z; Ellison AR; Rommens JM; Tsui L-C ; Tykocinski M; Gruenert DC
    Gene Ther; 1996 May; 3(5):427-36. PubMed ID: 9156804
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Modulation of cystic fibrosis transmembrane conductance regulator gene - expression by elevation of intracellular cyclic AMP.
    Bargon J; Loitsch S; Dauletbaev N; von Mallinckrodt C; Buhl R
    Eur J Med Res; 1998 May; 3(5):256-62. PubMed ID: 9580572
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Antisense oligodeoxynucleotide to the cystic fibrosis transmembrane conductance regulator inhibits cyclic AMP-activated but not calcium-activated cell volume reduction in a human pancreatic duct cell line.
    Kopelman H; Gauthier C; Bornstein M
    J Clin Invest; 1993 Mar; 91(3):1253-7. PubMed ID: 7680666
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Defective regulatory volume decrease in human cystic fibrosis tracheal cells because of altered regulation of intermediate conductance Ca2+-dependent potassium channels.
    Vázquez E; Nobles M; Valverde MA
    Proc Natl Acad Sci U S A; 2001 Apr; 98(9):5329-34. PubMed ID: 11309505
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New perspectives and hope for cure-reflecting recent genetic developments in cystic fibrosis.
    Midro AT; Kulczycki LL
    Mater Med Pol; 1992; 24(4):253-5. PubMed ID: 1308055
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Gene therapy perspectives in cystic fibrosis].
    Midro AT; Kulczycki LL; Sledziewski A
    Postepy Hig Med Dosw; 1993; 47(4):221-30. PubMed ID: 8309849
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners.
    Li C; Naren AP
    Pharmacol Ther; 2005 Nov; 108(2):208-23. PubMed ID: 15936089
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances.
    Reddy MM; Quinton PM
    JOP; 2001 Jul; 2(4 Suppl):212-8. PubMed ID: 11875262
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [The cystic fibrosis gene, its product CFTR protein and its mutations].
    Goossens M; Fanen P; Costes B; Ghanem N
    Bull Acad Natl Med; 1993 Mar; 177(3):371-80; discussion 380-1. PubMed ID: 7689915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cystic fibrosis transmembrane conductance regulator (CFTR) and renal function.
    Stanton BA
    Wien Klin Wochenschr; 1997 Jun; 109(12-13):457-64. PubMed ID: 9261986
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Suitability of oligonucleotide-mediated cystic fibrosis gene repair in airway epithelial cells.
    de Semir D; Nadal M; González JR; Larriba S; Avinyó A; Nunes V; Casals T; Estivill X; Aran JM
    J Gene Med; 2003 Jul; 5(7):625-39. PubMed ID: 12825202
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cystic fibrosis and related diseases of the pancreas.
    Naruse S; Kitagawa M; Ishiguro H; Fujiki K; Hayakawa T
    Best Pract Res Clin Gastroenterol; 2002 Jun; 16(3):511-26. PubMed ID: 12079272
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CFTR and outward rectifying chloride channels are distinct proteins with a regulatory relationship.
    Gabriel SE; Clarke LL; Boucher RC; Stutts MJ
    Nature; 1993 May; 363(6426):263-8. PubMed ID: 7683773
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expression and maturation of Sendai virus vector-derived CFTR protein: functional and biochemical evidence using a GFP-CFTR fusion protein.
    Ban H; Inoue M; Griesenbach U; Munkonge F; Chan M; Iida A; Alton EW; Hasegawa M
    Gene Ther; 2007 Dec; 14(24):1688-94. PubMed ID: 17898794
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two steps closer to gene therapy for cystic fibrosis.
    Cutting GR
    Nat Genet; 1992 Sep; 2(1):4-5. PubMed ID: 1284643
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.