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511 related items for PubMed ID: 17287432

  • 21. Rectal potential difference and the functional expression of CFTR in the gastrointestinal epithelia in cystic fibrosis mouse models.
    Weiner SA, Caputo C, Bruscia E, Ferreira EC, Price JE, Krause DS, Egan ME.
    Pediatr Res; 2008 Jan; 63(1):73-8. PubMed ID: 18043508
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. Small intestinal glucose absorption in cystic fibrosis: a study in human and transgenic DeltaF508 cystic fibrosis mouse tissues.
    Hardcastle J, Harwood MD, Taylor CJ.
    J Pharm Pharmacol; 2004 Mar 13; 56(3):329-38. PubMed ID: 15025858
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  • 25. Diabetic rats present higher urinary loss of proteins and lower renal expression of megalin, cubilin, ClC-5, and CFTR.
    Figueira MF, Castiglione RC, de Lemos Barbosa CM, Ornellas FM, da Silva Feltran G, Morales MM, da Fonseca RN, de Souza-Menezes J.
    Physiol Rep; 2017 Jul 13; 5(13):. PubMed ID: 28676554
    [Abstract] [Full Text] [Related]

  • 26. Cystic fibrosis transmembrane conductance regulator deficiency exacerbates islet cell dysfunction after beta-cell injury.
    Stalvey MS, Muller C, Schatz DA, Wasserfall CH, Campbell-Thompson ML, Theriaque DW, Flotte TR, Atkinson MA.
    Diabetes; 2006 Jul 13; 55(7):1939-45. PubMed ID: 16804061
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  • 27. Mild processing defect of porcine DeltaF508-CFTR suggests that DeltaF508 pigs may not develop cystic fibrosis disease.
    Liu Y, Wang Y, Jiang Y, Zhu N, Liang H, Xu L, Feng X, Yang H, Ma T.
    Biochem Biophys Res Commun; 2008 Aug 15; 373(1):113-8. PubMed ID: 18555011
    [Abstract] [Full Text] [Related]

  • 28. Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners.
    Li C, Naren AP.
    Pharmacol Ther; 2005 Nov 15; 108(2):208-23. PubMed ID: 15936089
    [Abstract] [Full Text] [Related]

  • 29. A mouse model for the delta F508 allele of cystic fibrosis.
    Zeiher BG, Eichwald E, Zabner J, Smith JJ, Puga AP, McCray PB, Capecchi MR, Welsh MJ, Thomas KR.
    J Clin Invest; 1995 Oct 15; 96(4):2051-64. PubMed ID: 7560099
    [Abstract] [Full Text] [Related]

  • 30. CFTR gene transfer to human cystic fibrosis pancreatic duct cells using a Sendai virus vector.
    Rakonczay Z, Hegyi P, Hasegawa M, Inoue M, You J, Iida A, Ignáth I, Alton EW, Griesenbach U, Ovári G, Vág J, Da Paula AC, Crawford RM, Varga G, Amaral MD, Mehta A, Lonovics J, Argent BE, Gray MA.
    J Cell Physiol; 2008 Feb 15; 214(2):442-55. PubMed ID: 17654517
    [Abstract] [Full Text] [Related]

  • 31. Cystic fibrosis and related diseases of the pancreas.
    Naruse S, Kitagawa M, Ishiguro H, Fujiki K, Hayakawa T.
    Best Pract Res Clin Gastroenterol; 2002 Jun 15; 16(3):511-26. PubMed ID: 12079272
    [Abstract] [Full Text] [Related]

  • 32. Cystic fibrosis transmembrane conductance regulator (CFTR) regulates the production of osteoprotegerin (OPG) and prostaglandin (PG) E2 in human bone.
    Le Heron L, Guillaume C, Velard F, Braux J, Touqui L, Moriceau S, Sermet-Gaudelus I, Laurent-Maquin D, Jacquot J.
    J Cyst Fibros; 2010 Jan 15; 9(1):69-72. PubMed ID: 20005786
    [Abstract] [Full Text] [Related]

  • 33. mGluR1 interacts with cystic fibrosis transmembrane conductance regulator and modulates the secretion of IL-10 in cystic fibrosis peripheral lymphocytes.
    Shanshiashvili LV, Dabrundashvili N, Natsvlishvili N, Kvaratskhelia E, Zhuravliova E, Barbakadze T, Koriauli S, Maisuradze E, Topuria T, Mikeladze DG.
    Mol Immunol; 2012 Jul 15; 51(3-4):310-5. PubMed ID: 22520513
    [Abstract] [Full Text] [Related]

  • 34. The CFTR-mediated protein secretion defect: pharmacological correction.
    McPherson MA, Pereira MM, Russell D, McNeilly CM, Morris RM, Stratford FL, Dormer RL.
    Pflugers Arch; 2001 Jul 15; 443 Suppl 1():S121-6. PubMed ID: 11845317
    [Abstract] [Full Text] [Related]

  • 35. 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
    [Abstract] [Full Text] [Related]

  • 36. Elevated hepatic SULT1E1 activity in mouse models of cystic fibrosis alters the regulation of estrogen responsive proteins.
    Li L, Falany CN.
    J Cyst Fibros; 2007 Jan 13; 6(1):23-30. PubMed ID: 16798114
    [Abstract] [Full Text] [Related]

  • 37. 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]

  • 38. Expression and function of CLC and cystic fibrosis transmembrane conductance regulator chloride channels in renal epithelial tubule cells: pathophysiological implications.
    Vandewalle A.
    Chang Gung Med J; 2007 Jun 13; 30(1):17-25. PubMed ID: 17477025
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  • 40. Expression of cystic fibrosis transmembrane conductance regulator in ganglion cells of the hearts.
    Pan P, Guo Y, Gu J.
    Neurosci Lett; 2008 Aug 15; 441(1):35-8. PubMed ID: 18584958
    [Abstract] [Full Text] [Related]

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