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 *

117 related articles for article (PubMed ID: 8572248)

  • 1. CFTR gene transfer corrects defective glycoconjugate secretion in human CF epithelial tracheal cells.
    Mergey M; Lemnaouar M; Veissiere D; Perricaudet M; Gruenert DC; Picard J; Capeau J; Brahimi-Horn MC; Paul A
    Am J Physiol; 1995 Dec; 269(6 Pt 1):L855-64. PubMed ID: 8572248
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Cellular expression of CFTR in cystic fibrosis: defective cyclic AMP-dependent regulation of glycoconjugate secretion in cystic fibrosis fetal tracheal epithelial cells transfected by SV40 large T oncogene].
    Picard J; Lemnaouar M; Paul A
    Bull Acad Natl Med; 1993 Mar; 177(3):383-93; discussion 393-4. PubMed ID: 7689916
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 8(12):1439-50. PubMed ID: 9287144
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 5(9):1121-9. PubMed ID: 7530494
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A cystic fibrosis tracheal gland cell line, CF-KM4. Correction by adenovirus-mediated CFTR gene transfer.
    Kammouni W; Moreau B; Becq F; Saleh A; Pavirani A; Figarella C; Merten MD
    Am J Respir Cell Mol Biol; 1999 Apr; 20(4):684-91. PubMed ID: 10101000
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Correction of cAMP-stimulated fluid secretion in cystic fibrosis airway epithelia: efficiency of adenovirus-mediated gene transfer in vitro.
    Zabner J; Couture LA; Smith AE; Welsh MJ
    Hum Gene Ther; 1994 May; 5(5):585-93. PubMed ID: 7519884
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Restoration of cyclic adenosine monophosphate-stimulated chloride channel activity in human cystic fibrosis tracheobronchial submucosal gland cells by adenovirus-mediated and cationic lipid-mediated gene transfer.
    Jiang C; Finkbeiner WE; Widdicombe JH; Fang SL; Wang KX; Nietupski JB; Hehir KM; Cheng SH
    Am J Respir Cell Mol Biol; 1999 Jun; 20(6):1107-15. PubMed ID: 10340929
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Adenovirus-mediated generation of cAMP-stimulated Cl- transport in cystic fibrosis airway epithelia in vitro: effect of promoter and administration method.
    Zabner J; Wadsworth SC; Smith AE; Welsh MJ
    Gene Ther; 1996 May; 3(5):458-65. PubMed ID: 9156806
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Phosphorylation of vimentin is an intermediate step in protein kinase C-mediated glycoconjugate secretion.
    Bertrand F; Veissiere D; Hermelin B; Paul A; Capeau J; Picard J; Cherqui G
    Am J Physiol; 1994 Mar; 266(3 Pt 1):C611-21. PubMed ID: 7513122
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gene transfer to freshly isolated human respiratory epithelial cells in vitro using a replication-deficient adenovirus containing the human cystic fibrosis transmembrane conductance regulator cDNA.
    Rosenfeld MA; Chu CS; Seth P; Danel C; Banks T; Yoneyama K; Yoshimura K; Crystal RG
    Hum Gene Ther; 1994 Mar; 5(3):331-42. PubMed ID: 7517189
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Airway epithelial CFTR mRNA expression in cystic fibrosis patients after repetitive administration of a recombinant adenovirus.
    Harvey BG; Leopold PL; Hackett NR; Grasso TM; Williams PM; Tucker AL; Kaner RJ; Ferris B; Gonda I; Sweeney TD; Ramalingam R; Kovesdi I; Shak S; Crystal RG
    J Clin Invest; 1999 Nov; 104(9):1245-55. PubMed ID: 10545523
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. Adenovirus 5-fiber 35 chimeric vector mediates efficient apical correction of the cystic fibrosis transmembrane conductance regulator defect in cystic fibrosis primary airway epithelia.
    Granio O; Ashbourne Excoffon KJ; Henning P; Melin P; Norez C; Gonzalez G; Karp PH; Magnusson MK; Habib N; Lindholm L; Becq F; Boulanger P; Zabner J; Hong SS
    Hum Gene Ther; 2010 Mar; 21(3):251-69. PubMed ID: 19788389
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An immortalized cystic fibrosis tracheal epithelial cell line homozygous for the delta F508 CFTR mutation.
    Kunzelmann K; Schwiebert EM; Zeitlin PL; Kuo WL; Stanton BA; Gruenert DC
    Am J Respir Cell Mol Biol; 1993 May; 8(5):522-9. PubMed ID: 7683197
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Defective formation of PKA/CnA-dependent annexin 2-S100A10/CFTR complex in DeltaF508 cystic fibrosis cells.
    Borthwick LA; Riemen C; Goddard C; Colledge WH; Mehta A; Gerke V; Muimo R
    Cell Signal; 2008 Jun; 20(6):1073-83. PubMed ID: 18346874
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human lymphocytes transcribe the cystic fibrosis transmembrane conductance regulator gene and exhibit CF-defective cAMP-regulated chloride current.
    McDonald TV; Nghiem PT; Gardner P; Martens CL
    J Biol Chem; 1992 Feb; 267(5):3242-8. PubMed ID: 1371114
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Overexpression of R domain eliminates cAMP-stimulated Cl- secretion in 9/HTEo- cells in culture.
    Perez A; Risma KA; Eckman EA; Davis PB
    Am J Physiol; 1996 Jul; 271(1 Pt 1):L85-92. PubMed ID: 8760136
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Vector-specific complementation profiles of two independent primary defects in cystic fibrosis airways.
    Zhang Y; Jiang Q; Dudus L; Yankaskas JR; Engelhardt JF
    Hum Gene Ther; 1998 Mar; 9(5):635-48. PubMed ID: 9551612
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.