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Journal Abstract Search

268 related items for PubMed ID: 15051928

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  • 3. 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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  • 4. Expression of S100A8 correlates with inflammatory lung disease in congenic mice deficient of the cystic fibrosis transmembrane conductance regulator.
    Tirkos S, Newbigging S, Nguyen V, Keet M, Ackerley C, Kent G, Rozmahel RF.
    Respir Res; 2006 Mar 29; 7(1):51. PubMed ID: 16571124
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  • 11. Acute Pseudomonas challenge in cystic fibrosis mice causes prolonged nuclear factor-kappa B activation, cytokine secretion, and persistent lung inflammation.
    Saadane A, Soltys J, Berger M.
    J Allergy Clin Immunol; 2006 May 29; 117(5):1163-9. PubMed ID: 16675347
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  • 14. 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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  • 15. Severe osteopenia in CFTR-null mice.
    Dif F, Marty C, Baudoin C, de Vernejoul MC, Levi G.
    Bone; 2004 Sep 13; 35(3):595-603. PubMed ID: 15336594
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  • 16. A proinflammatory, antiapoptotic phenotype underlies the susceptibility to acute pancreatitis in cystic fibrosis transmembrane regulator (-/-) mice.
    Dimagno MJ, Lee SH, Hao Y, Zhou SY, McKenna BJ, Owyang C.
    Gastroenterology; 2005 Aug 13; 129(2):665-81. PubMed ID: 16083720
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  • 17. Very mild disease phenotype of congenic CftrTgH(neoim)Hgu cystic fibrosis mice.
    Tóth B, Wilke M, Stanke F, Dorsch M, Jansen S, Wedekind D, Charizopoulou N, Bot A, Burmester M, Leonhard-Marek S, de Jonge HR, Hedrich HJ, Breves G, Tümmler B.
    BMC Genet; 2008 Apr 09; 9():28. PubMed ID: 18400105
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