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Journal Abstract Search


165 related items for PubMed ID: 9705235

  • 1. Molecular pathophysiology of cystic fibrosis based on the rescued knockout mouse model.
    Cohen JC, Morrow SL, Cork RJ, Delcarpio JB, Larson JE.
    Mol Genet Metab; 1998 Jun; 64(2):108-18. PubMed ID: 9705235
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  • 2. Cystic fibrosis transmembrane conductance regulator (CFTR) dependent cytoskeletal tension during lung organogenesis.
    Cohen JC, Larson JE.
    Dev Dyn; 2006 Oct; 235(10):2736-48. PubMed ID: 16906518
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  • 3. Glycoconjugate metabolism in a cystic fibrosis knockout mouse model.
    Mailleau C, Paul A, Colin M, Xing PX, Guernier C, Bernaudin JF, Capeau J, Brahimi-Horn MC.
    Mol Genet Metab; 2001 Feb; 72(2):122-31. PubMed ID: 11161838
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  • 4. Lung disease in mice with cystic fibrosis.
    Kent G, Iles R, Bear CE, Huan LJ, Griesenbach U, McKerlie C, Frndova H, Ackerley C, Gosselin D, Radzioch D, O'Brodovich H, Tsui LC, Buchwald M, Tanswell AK.
    J Clin Invest; 1997 Dec 15; 100(12):3060-9. PubMed ID: 9399953
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  • 6. A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.
    French PJ, van Doorninck JH, Peters RH, Verbeek E, Ameen NA, Marino CR, de Jonge HR, Bijman J, Scholte BJ.
    J Clin Invest; 1996 Sep 15; 98(6):1304-12. PubMed ID: 8823295
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  • 8. Pathophysiologic consequences following inhibition of a CFTR-dependent developmental cascade in the lung.
    Cohen JC, Larson JE.
    BMC Dev Biol; 2005 Feb 04; 5():2. PubMed ID: 15694001
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  • 10. Intestinal phenotype of variable-weight cystic fibrosis knockout mice.
    Canale-Zambrano JC, Poffenberger MC, Cory SM, Humes DG, Haston CK.
    Am J Physiol Gastrointest Liver Physiol; 2007 Jul 04; 293(1):G222-9. PubMed ID: 17615178
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  • 12. Distinct pattern of lung gene expression in the Cftr-KO mice developing spontaneous lung disease compared with their littermate controls.
    Guilbault C, Novak JP, Martin P, Boghdady ML, Saeed Z, Guiot MC, Hudson TJ, Radzioch D.
    Physiol Genomics; 2006 Apr 13; 25(2):179-93. PubMed ID: 16418321
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  • 14. A second dose of a CFTR cDNA-liposome complex is as effective as the first dose in restoring cAMP-dependent chloride secretion to null CF mice trachea.
    Goddard CA, Ratcliff R, Anderson JR, Glenn E, Brown S, Gill DR, Hyde SC, MacVinish LJ, Huang L, Higgins CF, Cuthbert AW, Evans MJ, Colledge WH.
    Gene Ther; 1997 Nov 13; 4(11):1231-6. PubMed ID: 9425447
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  • 16. Decreased peroxisome proliferator activated receptor alpha is associated with bile duct injury in cystic fibrosis transmembrane conductance regulator-/- mice.
    Pall H, Zaman MM, Andersson C, Freedman SD.
    J Pediatr Gastroenterol Nutr; 2006 Mar 13; 42(3):275-81. PubMed ID: 16540796
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  • 17. Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice.
    Mall M, Grubb BR, Harkema JR, O'Neal WK, Boucher RC.
    Nat Med; 2004 May 13; 10(5):487-93. PubMed ID: 15077107
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  • 18. Cystic fibrosis is associated with a defect in apical receptor-mediated endocytosis in mouse and human kidney.
    Jouret F, Bernard A, Hermans C, Dom G, Terryn S, Leal T, Lebecque P, Cassiman JJ, Scholte BJ, de Jonge HR, Courtoy PJ, Devuyst O.
    J Am Soc Nephrol; 2007 Mar 13; 18(3):707-18. PubMed ID: 17287432
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