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Journal Abstract Search

115 related items for PubMed ID: 11518680

  • 1. Proliferation, not apoptosis, alters epithelial cell migration in small intestine of CFTR null mice.
    Gallagher AM, Gottlieb RA.
    Am J Physiol Gastrointest Liver Physiol; 2001 Sep; 281(3):G681-7. PubMed ID: 11518680
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  • 3. Defective CFTR promotes intestinal proliferation via inhibition of the hedgehog pathway during cystic fibrosis.
    Liu K, Wang X, Zou C, Zhang J, Chen H, Tsang L, Yu MK, Chung YW, Wang J, Dai Y, Liu Y, Zhang X.
    Cancer Lett; 2019 Apr 01; 446():15-24. PubMed ID: 30639531
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  • 5. Increased activity of epithelial Cdc42 Rho GTPase and tight junction permeability in the Cftr knockout intestine.
    Woode RA, Strubberg AM, Liu J, Walker NM, Clarke LL.
    Am J Physiol Gastrointest Liver Physiol; 2024 Oct 01; 327(4):G545-G557. PubMed ID: 39104325
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  • 6. 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 01; 26(5-6):222-34. PubMed ID: 25721416
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  • 7. 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; 2015 Jun 01; 70(2):89-97. PubMed ID: 12476034
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  • 8. CFTR Deletion Confers Mitochondrial Dysfunction and Disrupts Lipid Homeostasis in Intestinal Epithelial Cells.
    Kleme ML, Sané A, Garofalo C, Seidman E, Brochiero E, Berthiaume Y, Levy E.
    Nutrients; 2018 Jun 27; 10(7):. PubMed ID: 29954133
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  • 9. Eradication of small intestinal bacterial overgrowth in the cystic fibrosis mouse reduces mucus accumulation.
    De Lisle RC, Roach EA, Norkina O.
    J Pediatr Gastroenterol Nutr; 2006 Jan 27; 42(1):46-52. PubMed ID: 16385253
    [Abstract] [Full Text] [Related]

  • 10. Pseudomonas aeruginosa-induced apoptosis is defective in respiratory epithelial cells expressing mutant cystic fibrosis transmembrane conductance regulator.
    Cannon CL, Kowalski MP, Stopak KS, Pier GB.
    Am J Respir Cell Mol Biol; 2003 Aug 27; 29(2):188-97. PubMed ID: 12878584
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  • 11. Bacterial overgrowth in the cystic fibrosis transmembrane conductance regulator null mouse small intestine.
    Norkina O, Burnett TG, De Lisle RC.
    Infect Immun; 2004 Oct 27; 72(10):6040-9. PubMed ID: 15385508
    [Abstract] [Full Text] [Related]

  • 12. Defective CFTR- β-catenin interaction promotes NF-κB nuclear translocation and intestinal inflammation in cystic fibrosis.
    Liu K, Zhang X, Zhang JT, Tsang LL, Jiang X, Chan HC.
    Oncotarget; 2016 Sep 27; 7(39):64030-64042. PubMed ID: 27588407
    [Abstract] [Full Text] [Related]

  • 13. Reduced expression of Tis7/IFRD1 protein in murine and human cystic fibrosis airway epithelial cell models homozygous for the F508del-CFTR mutation.
    Blanchard E, Marie S, Riffault L, Bonora M, Tabary O, Clement A, Jacquot J.
    Biochem Biophys Res Commun; 2011 Aug 05; 411(3):471-6. PubMed ID: 21723850
    [Abstract] [Full Text] [Related]

  • 14. 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 Aug 05; 71(3):152-8. PubMed ID: 15051928
    [Abstract] [Full Text] [Related]

  • 15. Toll-like receptor-4 genotype influences the survival of cystic fibrosis mice.
    Canale-Zambrano JC, Auger ML, Haston CK.
    Am J Physiol Gastrointest Liver Physiol; 2010 Aug 05; 299(2):G381-90. PubMed ID: 20522639
    [Abstract] [Full Text] [Related]

  • 16. Impact of the cystic fibrosis mutation F508del-CFTR on renal cyst formation and growth.
    Li H, Yang W, Mendes F, Amaral MD, Sheppard DN.
    Am J Physiol Renal Physiol; 2012 Oct 15; 303(8):F1176-86. PubMed ID: 22874761
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 29(6):1624-34. PubMed ID: 10347100
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 44(1):83-90. PubMed ID: 20203293
    [Abstract] [Full Text] [Related]

  • 19. IGF binding protein-3 treatment alters intestinal cell proliferation but not body weight of adult cystic fibrosis transmembrane conductance regulator deficient mice.
    Canale-Zambrano JC, Haston CK.
    Pediatr Res; 2011 Feb 15; 69(2):129-34. PubMed ID: 21068693
    [Abstract] [Full Text] [Related]

  • 20. Generation of a conditional null allele for Cftr in mice.
    Hodges CA, Cotton CU, Palmert MR, Drumm ML.
    Genesis; 2008 Oct 15; 46(10):546-52. PubMed ID: 18802965
    [Abstract] [Full Text] [Related]

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