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1425 related items for PubMed ID: 11591888

  • 1. Control of the proinflammatory state in cystic fibrosis lung epithelial cells by genes from the TNF-alphaR/NFkappaB pathway.
    Eidelman O, Srivastava M, Zhang J, Leighton X, Murtie J, Jozwik C, Jacobson K, Weinstein DL, Metcalf EL, Pollard HB.
    Mol Med; 2001 Aug; 7(8):523-34. PubMed ID: 11591888
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  • 3. Pharmacogenomics of the cystic fibrosis transmembrane conductance regulator (CFTR) and the cystic fibrosis drug CPX using genome microarray analysis.
    Srivastava M, Eidelman O, Pollard HB.
    Mol Med; 1999 Nov; 5(11):753-67. PubMed ID: 10656877
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  • 4. Inflammation in cystic fibrosis airways: relationship to increased bacterial adherence.
    Scheid P, Kempster L, Griesenbach U, Davies JC, Dewar A, Weber PP, Colledge WH, Evans MJ, Geddes DM, Alton EW.
    Eur Respir J; 2001 Jan; 17(1):27-35. PubMed ID: 11307750
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  • 5. IL-17 primes airway epithelial cells lacking functional Cystic Fibrosis Transmembrane conductance Regulator (CFTR) to increase NOD1 responses.
    Roussel L, Rousseau S.
    Biochem Biophys Res Commun; 2010 Jan 01; 391(1):505-9. PubMed ID: 19931506
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  • 7. 8-cyclopentyl-1,3-dipropylxanthine and other xanthines differentially bind to the wild-type and delta F508 first nucleotide binding fold (NBF-1) domains of the cystic fibrosis transmembrane conductance regulator.
    Cohen BE, Lee G, Jacobson KA, Kim YC, Huang Z, Sorscher EJ, Pollard HB.
    Biochemistry; 1997 May 27; 36(21):6455-61. PubMed ID: 9174362
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  • 8. Influence of cystic fibrosis transmembrane conductance regulator on gene expression in response to Pseudomonas aeruginosa infection of human bronchial epithelial cells.
    Reiniger N, Ichikawa JK, Pier GB.
    Infect Immun; 2005 Oct 27; 73(10):6822-30. PubMed ID: 16177360
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  • 10. Cellular heterogeneity of CFTR expression and function in the lung: implications for gene therapy of cystic fibrosis.
    Jiang Q, Engelhardt JF.
    Eur J Hum Genet; 1998 Jan 27; 6(1):12-31. PubMed ID: 9781011
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  • 12. Elevated miR-155 promotes inflammation in cystic fibrosis by driving hyperexpression of interleukin-8.
    Bhattacharyya S, Balakathiresan NS, Dalgard C, Gutti U, Armistead D, Jozwik C, Srivastava M, Pollard HB, Biswas R.
    J Biol Chem; 2011 Apr 01; 286(13):11604-15. PubMed ID: 21282106
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  • 15. miR-16 rescues F508del-CFTR function in native cystic fibrosis epithelial cells.
    Kumar P, Bhattacharyya S, Peters KW, Glover ML, Sen A, Cox RT, Kundu S, Caohuy H, Frizzell RA, Pollard HB, Biswas R.
    Gene Ther; 2015 Nov 01; 22(11):908-16. PubMed ID: 26133785
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  • 16. Transient receptor potential canonical channel 6 links Ca2+ mishandling to cystic fibrosis transmembrane conductance regulator channel dysfunction in cystic fibrosis.
    Antigny F, Norez C, Dannhoffer L, Bertrand J, Raveau D, Corbi P, Jayle C, Becq F, Vandebrouck C.
    Am J Respir Cell Mol Biol; 2011 Jan 01; 44(1):83-90. PubMed ID: 20203293
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  • 20. Differential regulation of inflammation by inflammatory mediators in cystic fibrosis lung epithelial cells.
    Tsuchiya M, Kumar P, Bhattacharyya S, Chattoraj S, Srivastava M, Pollard HB, Biswas R.
    J Interferon Cytokine Res; 2013 Mar 01; 33(3):121-9. PubMed ID: 23289731
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