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Journal Abstract Search

125 related items for PubMed ID: 1376160

  • 1.
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  • 2. Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.
    Rich DP, Anderson MP, Gregory RJ, Cheng SH, Paul S, Jefferson DM, McCann JD, Klinger KW, Smith AE, Welsh MJ.
    Nature; 1990 Sep 27; 347(6291):358-63. PubMed ID: 1699126
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  • 5. Towards the biochemical defect in cystic fibrosis.
    Lancet; 1989 Dec 16; 2(8677):1433. PubMed ID: 2480500
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  • 7. Disease-associated mutations in cytoplasmic loops 1 and 2 of cystic fibrosis transmembrane conductance regulator impede processing or opening of the channel.
    Seibert FS, Jia Y, Mathews CJ, Hanrahan JW, Riordan JR, Loo TW, Clarke DM.
    Biochemistry; 1997 Sep 30; 36(39):11966-74. PubMed ID: 9305991
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  • 9. The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.
    Li C, Ramjeesingh M, Reyes E, Jensen T, Chang X, Rommens JM, Bear CE.
    Nat Genet; 1993 Apr 30; 3(4):311-6. PubMed ID: 7526932
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  • 11. Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites.
    Chang XB, Tabcharani JA, Hou YX, Jensen TJ, Kartner N, Alon N, Hanrahan JW, Riordan JR.
    J Biol Chem; 1993 May 25; 268(15):11304-11. PubMed ID: 7684377
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  • 15. Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive.
    Denning GM, Anderson MP, Amara JF, Marshall J, Smith AE, Welsh MJ.
    Nature; 1992 Aug 27; 358(6389):761-4. PubMed ID: 1380673
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  • 16. Dysfunction of CFTR bearing the delta F508 mutation.
    Welsh MJ, Denning GM, Ostedgaard LS, Anderson MP.
    J Cell Sci Suppl; 1993 Aug 27; 17():235-9. PubMed ID: 7511616
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  • 17. Cystic fibrosis transmembrane conductance regulator protein: what is its role in cystic fibrosis?
    Richardson PS, Alton EW.
    Eur Respir J; 1993 Feb 27; 6(2):160-2. PubMed ID: 7680321
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  • 18. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis.
    Welsh MJ, Smith AE.
    Cell; 1993 Jul 02; 73(7):1251-4. PubMed ID: 7686820
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  • 20. CFTR anion channel modulates expression of human transmembrane mucin MUC3 through the PDZ protein GOPC.
    Pelaseyed T, Hansson GC.
    J Cell Sci; 2011 Sep 15; 124(Pt 18):3074-83. PubMed ID: 21852426
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