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Journal Abstract Search

294 related items for PubMed ID: 7541313

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  • 4. External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanism.
    Cantiello HF, Prat AG, Reisin IL, Ercole LB, Abraham EH, Amara JF, Gregory RJ, Ausiello DA.
    J Biol Chem; 1994 Apr 15; 269(15):11224-32. PubMed ID: 7512560
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  • 5. Pyrophosphate stimulates wild-type and mutant cystic fibrosis transmembrane conductance regulator Cl- channels.
    Carson MR, Winter MC, Travis SM, Welsh MJ.
    J Biol Chem; 1995 Sep 01; 270(35):20466-72. PubMed ID: 7544788
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  • 6. Apical and basolateral ATP stimulates tracheal epithelial chloride secretion via multiple purinergic receptors.
    Hwang TH, Schwiebert EM, Guggino WB.
    Am J Physiol; 1996 Jun 01; 270(6 Pt 1):C1611-23. PubMed ID: 8764143
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  • 8. CFTR in Calu-3 human airway cells: channel properties and role in cAMP-activated Cl- conductance.
    Haws C, Finkbeiner WE, Widdicombe JH, Wine JJ.
    Am J Physiol; 1994 May 01; 266(5 Pt 1):L502-12. PubMed ID: 7515579
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  • 9. Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR.
    Egan M, Flotte T, Afione S, Solow R, Zeitlin PL, Carter BJ, Guggino WB.
    Nature; 1992 Aug 13; 358(6387):581-4. PubMed ID: 1380129
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  • 10. 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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  • 13. CFTR channels expressed in CHO cells do not have detectable ATP conductance.
    Grygorczyk R, Tabcharani JA, Hanrahan JW.
    J Membr Biol; 1996 May 18; 151(2):139-48. PubMed ID: 8661502
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  • 14. Pyridine nucleotide redox potential modulates cystic fibrosis transmembrane conductance regulator Cl- conductance.
    Stutts MJ, Gabriel SE, Price EM, Sarkadi B, Olsen JC, Boucher RC.
    J Biol Chem; 1994 Mar 25; 269(12):8667-74. PubMed ID: 7510695
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  • 16. CFTR channels in immortalized human airway cells.
    Haws C, Krouse ME, Xia Y, Gruenert DC, Wine JJ.
    Am J Physiol; 1992 Dec 25; 263(6 Pt 1):L692-707. PubMed ID: 1282304
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  • 17. Cystic fibrosis transmembrane conductance regulator is required for protein kinase A activation of an outwardly rectified anion channel purified from bovine tracheal epithelia.
    Jovov B, Ismailov II, Benos DJ.
    J Biol Chem; 1995 Jan 27; 270(4):1521-8. PubMed ID: 7530244
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  • 18. Contribution of proline residues in the membrane-spanning domains of cystic fibrosis transmembrane conductance regulator to chloride channel function.
    Sheppard DN, Travis SM, Ishihara H, Welsh MJ.
    J Biol Chem; 1996 Jun 21; 271(25):14995-5001. PubMed ID: 8663008
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  • 19. Expression of cystic fibrosis transmembrane conductance regulator alters the responses to hypotonic cell swelling and ATP of Chinese hamster ovary cells.
    Thiele IE, Hug MJ, Hübner M, Greger R.
    Cell Physiol Biochem; 1998 Jun 21; 8(1-2):61-74. PubMed ID: 9547020
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  • 20. cAMP-activated Cl channels in CFTR-transfected cystic fibrosis pancreatic epithelial cells.
    Cliff WH, Schoumacher RA, Frizzell RA.
    Am J Physiol; 1992 May 21; 262(5 Pt 1):C1154-60. PubMed ID: 1375432
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