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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

183 related items for PubMed ID: 12476034

  • 1. Residual cftr expression varies with age in cftr(tm1Hgu) cystic fibrosis mice: impact on morphology and physiology.
    Larbig M, Jansen S, Dorsch M, Bernhard W, Bellmann B, Dorin JR, Porteous DJ, Von Der Hardt H, Steinmetz I, Hedrich HJ, Tuemmler B, Tschernig T.
    Pathobiology; ; 70(2):89-97. PubMed ID: 12476034
    [Abstract] [Full Text] [Related]

  • 2. Molecular species compositions of lung and pancreas phospholipids in the cftr(tm1HGU/tm1HGU) cystic fibrosis mouse.
    Dombrowsky H, Clark GT, Rau GA, Bernhard W, Postle AD.
    Pediatr Res; 2003 Mar; 53(3):447-54. PubMed ID: 12595593
    [Abstract] [Full Text] [Related]

  • 3. Metabolism of surfactant phosphatidylcholine molecular species in cftr(tm1HGU/tm1HGU) mice compared to MF-1 mice.
    Bernhard W, Bertling A, Dombrowsky H, Vieten G, Rau G, von der Hardt H, Freihorst J.
    Exp Lung Res; 2001 Jun; 27(4):349-66. PubMed ID: 11400861
    [Abstract] [Full Text] [Related]

  • 4. 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; 18(3):707-18. PubMed ID: 17287432
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Lung pathology in response to repeated exposure to Staphylococcus aureus in congenic residual function cystic fibrosis mice does not increase in response to decreased CFTR levels or increased bacterial load.
    Davidson DJ, Webb S, Teague P, Govan JR, Dorin JR.
    Pathobiology; 2004 Mar; 71(3):152-8. PubMed ID: 15051928
    [Abstract] [Full Text] [Related]

  • 7. Lung surfactant in a cystic fibrosis animal model: increased alveolar phospholipid pool size without altered composition and surface tension function in cftrm1HGU/m1HGU mice.
    Bernhard W, Wang JY, Tschernig T, Tümmler B, Hedrich HJ, von der Hardt H.
    Thorax; 1997 Aug; 52(8):723-30. PubMed ID: 9337833
    [Abstract] [Full Text] [Related]

  • 8. Role of CFTR in airway disease.
    Pilewski JM, Frizzell RA.
    Physiol Rev; 1999 Jan; 79(1 Suppl):S215-55. PubMed ID: 9922383
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Strain-dependent pulmonary gene expression profiles of a cystic fibrosis mouse model.
    Haston CK, Cory S, Lafontaine L, Dorion G, Hallett MT.
    Physiol Genomics; 2006 Apr 13; 25(2):336-45. PubMed ID: 16614460
    [Abstract] [Full Text] [Related]

  • 11. [CFTR and transepithelial ionic transport abnormalities in cystic fibrosis].
    Becq F.
    Arch Pediatr; 2003 Sep 13; 10 Suppl 2():325s-332s. PubMed ID: 14671929
    [Abstract] [Full Text] [Related]

  • 12. Characteristic multiorgan pathology of cystic fibrosis in a long-living cystic fibrosis transmembrane regulator knockout murine model.
    Durie PR, Kent G, Phillips MJ, Ackerley CA.
    Am J Pathol; 2004 Apr 13; 164(4):1481-93. PubMed ID: 15039235
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. 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 13; 64(2):108-18. PubMed ID: 9705235
    [Abstract] [Full Text] [Related]

  • 16. Cystic fibrosis mouse model-dependent intestinal structure and gut microbiome.
    Bazett M, Honeyman L, Stefanov AN, Pope CE, Hoffman LR, Haston CK.
    Mamm Genome; 2015 Jun 13; 26(5-6):222-34. PubMed ID: 25721416
    [Abstract] [Full Text] [Related]

  • 17. Iron Homeostasis and Inflammatory Status in Mice Deficient for the Cystic Fibrosis Transmembrane Regulator.
    Deschemin JC, Allouche S, Brouillard F, Vaulont S.
    PLoS One; 2015 Jun 13; 10(12):e0145685. PubMed ID: 26709821
    [Abstract] [Full Text] [Related]

  • 18. Five percent of normal cystic fibrosis transmembrane conductance regulator mRNA ameliorates the severity of pulmonary disease in cystic fibrosis.
    Ramalho AS, Beck S, Meyer M, Penque D, Cutting GR, Amaral MD.
    Am J Respir Cell Mol Biol; 2002 Nov 13; 27(5):619-27. PubMed ID: 12397022
    [Abstract] [Full Text] [Related]

  • 19. Mucociliary clearance in cystic fibrosis knockout mice infected with Pseudomonas aeruginosa.
    Cowley EA, Wang CG, Gosselin D, Radzioch D, Eidelman DH.
    Eur Respir J; 1997 Oct 13; 10(10):2312-8. PubMed ID: 9387959
    [Abstract] [Full Text] [Related]

  • 20. In-frame elimination of exon 10 in Cftrtm1Unc CF mice.
    Xu Z, Gupta V, Lei D, Holmes A, Carlson E, Gruenert DC.
    Gene; 1998 Apr 28; 211(1):117-23. PubMed ID: 9573345
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.