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Journal Abstract Search

197 related items for PubMed ID: 7510684

  • 61. Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents.
    Fulmer SB, Schwiebert EM, Morales MM, Guggino WB, Cutting GR.
    Proc Natl Acad Sci U S A; 1995 Jul 18; 92(15):6832-6. PubMed ID: 7542778
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  • 65. Cystic fibrosis transmembrane conductance regulator (CFTR).
    Higgins CF.
    Br Med Bull; 1992 Oct 18; 48(4):754-65. PubMed ID: 1281034
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  • 66. Regulation of recombinant cardiac cystic fibrosis transmembrane conductance regulator chloride channels by protein kinase C.
    Yamazaki J, Britton F, Collier ML, Horowitz B, Hume JR.
    Biophys J; 1999 Apr 18; 76(4):1972-87. PubMed ID: 10096895
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  • 67. Regulated trafficking of the CFTR chloride channel.
    Kleizen B, Braakman I, de Jonge HR.
    Eur J Cell Biol; 2000 Aug 18; 79(8):544-56. PubMed ID: 11001491
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  • 68. Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.
    Dalemans W, Barbry P, Champigny G, Jallat S, Dott K, Dreyer D, Crystal RG, Pavirani A, Lecocq JP, Lazdunski M.
    Nature; 2000 Aug 18; 354(6354):526-8. PubMed ID: 1722027
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  • 69. Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.
    Sheppard DN, Rich DP, Ostedgaard LS, Gregory RJ, Smith AE, Welsh MJ.
    Nature; 1993 Mar 11; 362(6416):160-4. PubMed ID: 7680769
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  • 72. cAMP-dependent protein kinase-mediated phosphorylation of cystic fibrosis transmembrane conductance regulator residue Ser-753 and its role in channel activation.
    Seibert FS, Tabcharani JA, Chang XB, Dulhanty AM, Mathews C, Hanrahan JW, Riordan JR.
    J Biol Chem; 1995 Feb 03; 270(5):2158-62. PubMed ID: 7530719
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  • 73. Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels.
    Wang F, Zeltwanger S, Hu S, Hwang TC.
    J Physiol; 2000 May 01; 524 Pt 3(Pt 3):637-48. PubMed ID: 10790148
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  • 74. Phosphate stimulates CFTR Cl- channels.
    Carson MR, Travis SM, Winter MC, Sheppard DN, Welsh MJ.
    Biophys J; 1994 Nov 01; 67(5):1867-75. PubMed ID: 7532021
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  • 76. The short apical membrane half-life of rescued {Delta}F508-cystic fibrosis transmembrane conductance regulator (CFTR) results from accelerated endocytosis of {Delta}F508-CFTR in polarized human airway epithelial cells.
    Swiatecka-Urban A, Brown A, Moreau-Marquis S, Renuka J, Coutermarsh B, Barnaby R, Karlson KH, Flotte TR, Fukuda M, Langford GM, Stanton BA.
    J Biol Chem; 2005 Nov 04; 280(44):36762-72. PubMed ID: 16131493
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  • 77. CFTR channels in immortalized human airway cells.
    Haws C, Krouse ME, Xia Y, Gruenert DC, Wine JJ.
    Am J Physiol; 1992 Dec 04; 263(6 Pt 1):L692-707. PubMed ID: 1282304
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