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Journal Abstract Search

113 related items for PubMed ID: 20005786

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  • 3. Osteoblast CFTR inactivation reduces differentiation and osteoprotegerin expression in a mouse model of cystic fibrosis-related bone disease.
    Stalvey MS, Clines KL, Havasi V, McKibbin CR, Dunn LK, Chung WJ, Clines GA.
    PLoS One; 2013; 8(11):e80098. PubMed ID: 24236172
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  • 6. Increased arylsulfatase B activity in cystic fibrosis cells following correction of CFTR.
    Bhattacharyya S, Look D, Tobacman JK.
    Clin Chim Acta; 2007 May 01; 380(1-2):122-7. PubMed ID: 17324393
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  • 7. 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 01; 18(3):707-18. PubMed ID: 17287432
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  • 9. 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 01; 29(6):1624-34. PubMed ID: 10347100
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  • 10. 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
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  • 11. 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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  • 12. Partial correction of endogenous DeltaF508 CFTR in human cystic fibrosis airway epithelia by spliceosome-mediated RNA trans-splicing.
    Liu X, Jiang Q, Mansfield SG, Puttaraju M, Zhang Y, Zhou W, Cohn JA, Garcia-Blanco MA, Mitchell LG, Engelhardt JF.
    Nat Biotechnol; 2002 Jan 15; 20(1):47-52. PubMed ID: 11753361
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  • 13. [Early bronchial inflammation in cystic fibrosis].
    Puchelle E.
    J Soc Biol; 2002 Jan 15; 196(1):29-35. PubMed ID: 12134630
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  • 14. Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances.
    Reddy MM, Quinton PM.
    JOP; 2001 Jul 15; 2(4 Suppl):212-8. PubMed ID: 11875262
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  • 15. Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF mice.
    Ostrowski LE, Yin W, Diggs PS, Rogers TD, O'Neal WK, Grubb BR.
    Gene Ther; 2007 Oct 15; 14(20):1492-501. PubMed ID: 17637798
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  • 16. 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
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  • 17. Modulation of cystic fibrosis transmembrane conductance regulator gene - expression by elevation of intracellular cyclic AMP.
    Bargon J, Loitsch S, Dauletbaev N, von Mallinckrodt C, Buhl R.
    Eur J Med Res; 1998 May 12; 3(5):256-62. PubMed ID: 9580572
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  • 18. The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.
    Sermet-Gaudelus I, Roussel D, Bui S, Deneuville E, Huet F, Reix P, Bellon G, Lenoir G, Edelman A.
    BMC Pediatr; 2006 Oct 03; 6():25. PubMed ID: 17018149
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  • 19. Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners.
    Li C, Naren AP.
    Pharmacol Ther; 2005 Nov 03; 108(2):208-23. PubMed ID: 15936089
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  • 20. Cl- absorption across the thick ascending limb is not altered in cystic fibrosis mice. A role for a pseudo-CFTR Cl- channel.
    Marvão P, De Jesus Ferreira MC, Bailly C, Paulais M, Bens M, Guinamard R, Moreau R, Vandewalle A, Teulon J.
    J Clin Invest; 1998 Dec 01; 102(11):1986-93. PubMed ID: 9835624
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