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Journal Abstract Search

123 related items for PubMed ID: 7542477

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  • 23. Long-term cAMP activation of Na(+)-K(+)-2Cl- cotransporter activity in HT-29 human adenocarcinoma cells.
    Slotki IN, Breuer WV, Greger R, Cabantchik ZI.
    Am J Physiol; 1993 Apr; 264(4 Pt 1):C857-65. PubMed ID: 7682775
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  • 24.
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  • 25. The adenosine A(2A) antagonistic properties of selected C8-substituted xanthines.
    Van der Walt MM, Terre'Blanche G, Petzer A, Lourens AC, Petzer JP.
    Bioorg Chem; 2013 Aug; 49():49-58. PubMed ID: 23892098
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  • 28. Synthesis and biological evaluation of the enantiomers of the potent and selective A1-adenosine antagonist 1,3-dipropyl-8-[2-(5,6-epoxynorbonyl)]-xanthine.
    Pfister JR, Belardinelli L, Lee G, Lum RT, Milner P, Stanley WC, Linden J, Baker SP, Schreiner G.
    J Med Chem; 1997 Jun 06; 40(12):1773-8. PubMed ID: 9191953
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  • 29. Xanthine derivatives as antagonists at A1 and A2 adenosine receptors.
    Schwabe U, Ukena D, Lohse MJ.
    Naunyn Schmiedebergs Arch Pharmacol; 1985 Sep 06; 330(3):212-21. PubMed ID: 2997628
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  • 30. ATP and A1 adenosine receptor agonists mobilize intracellular calcium and activate K+ and Cl- currents in normal and cystic fibrosis airway epithelial cells.
    Rugolo M, Mastrocola T, Whörle C, Rasola A, Gruenert DC, Romeo G, Galietta LJ.
    J Biol Chem; 1993 Nov 25; 268(33):24779-84. PubMed ID: 8227038
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  • 31. 8-(Sulfostyryl)xanthines: water-soluble A2A-selective adenosine receptor antagonists.
    Müller CE, Sandoval-Ramírez J, Schobert U, Geis U, Frobenius W, Klotz KN.
    Bioorg Med Chem; 1998 Jun 25; 6(6):707-19. PubMed ID: 9681137
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  • 32. Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance.
    Strong TV, Wilkinson DJ, Mansoura MK, Devor DC, Henze K, Yang Y, Wilson JM, Cohn JA, Dawson DC, Frizzell RA.
    Hum Mol Genet; 1993 Mar 25; 2(3):225-30. PubMed ID: 7684641
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  • 33. Effect of trifluoromethyl and other substituents on activity of xanthines at adenosine receptors.
    Jacobson KA, Shi D, Gallo-Rodriguez C, Manning M, Müller C, Daly JW, Neumeyer JL, Kiriasis L, Pfleiderer W.
    J Med Chem; 1993 Sep 03; 36(18):2639-44. PubMed ID: 8410976
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  • 34. Substituted 1,3-dipropylxanthines as irreversible antagonists of A1 adenosine receptors.
    Scammells PJ, Baker SP, Belardinelli L, Olsson RA.
    J Med Chem; 1994 Aug 19; 37(17):2704-12. PubMed ID: 8064798
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  • 35. 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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  • 36. Aza-analogs of 8-styrylxanthines as A2A-adenosine receptor antagonists.
    Müller CE, Sauer R, Geis U, Frobenius W, Talik P, Pawlowski M.
    Arch Pharm (Weinheim); 1997 Jun 27; 330(6):181-9. PubMed ID: 9264243
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  • 37. A nonolfactory shark adenosine receptor activates CFTR with unique pharmacology and structural features.
    Bhanot S, Hemminger G, Martin CL, Aller SG, Forrest JN.
    Am J Physiol Cell Physiol; 2021 May 01; 320(5):C892-C901. PubMed ID: 33689481
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  • 38. Binding of [3H]MSX-2 (3-(3-hydroxypropyl)-7-methyl-8-(m-methoxystyryl)-1-propargylxanthine) to rat striatal membranes--a new, selective antagonist radioligand for A(2A) adenosine receptors.
    Müller CE, Maurinsh J, Sauer R.
    Eur J Pharm Sci; 2000 May 01; 10(4):259-65. PubMed ID: 10838015
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  • 39. Binding thermodynamics of adenosine A2a receptor ligands.
    Borea PA, Dalpiaz A, Varani K, Guerra L, Gilli G.
    Biochem Pharmacol; 1995 Feb 14; 49(4):461-9. PubMed ID: 7532939
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  • 40. Competition of adenine nucleotides for a 1,3-[3H]-dipropyl-8-cyclopentylxanthine binding site in rat vas deferens.
    Smith AD, Cheek DJ, Buxton IL, Westfall DP.
    Clin Exp Pharmacol Physiol; 1997 Jul 14; 24(7):492-7. PubMed ID: 9248666
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