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Journal Abstract Search

157 related items for PubMed ID: 11714890

  • 1. Similar apparent constitutive activity of human histamine H(2)-receptor fused to long and short splice variants of G(salpha).
    Wenzel-Seifert K, Kelley MT, Buschauer A, Seifert R.
    J Pharmacol Exp Ther; 2001 Dec; 299(3):1013-20. PubMed ID: 11714890
    [Abstract] [Full Text] [Related]

  • 2. Constitutive activity and ligand selectivity of human, guinea pig, rat, and canine histamine H2 receptors.
    Preuss H, Ghorai P, Kraus A, Dove S, Buschauer A, Seifert R.
    J Pharmacol Exp Ther; 2007 Jun; 321(3):983-95. PubMed ID: 17332265
    [Abstract] [Full Text] [Related]

  • 3. Mutations of Cys-17 and Ala-271 in the human histamine H2 receptor determine the species selectivity of guanidine-type agonists and increase constitutive activity.
    Preuss H, Ghorai P, Kraus A, Dove S, Buschauer A, Seifert R.
    J Pharmacol Exp Ther; 2007 Jun; 321(3):975-82. PubMed ID: 17347323
    [Abstract] [Full Text] [Related]

  • 4. Co-expression of the beta2-adrenoceptor and dopamine D1-receptor with Gsalpha proteins in Sf9 insect cells: limitations in comparison with fusion proteins.
    Gille A, Seifert R.
    Biochim Biophys Acta; 2003 Jun 27; 1613(1-2):101-14. PubMed ID: 12832091
    [Abstract] [Full Text] [Related]

  • 5. Functional differences between full and partial agonists: evidence for ligand-specific receptor conformations.
    Seifert R, Wenzel-Seifert K, Gether U, Kobilka BK.
    J Pharmacol Exp Ther; 2001 Jun 27; 297(3):1218-26. PubMed ID: 11356949
    [Abstract] [Full Text] [Related]

  • 6. Distinct interaction of human and guinea pig histamine H2-receptor with guanidine-type agonists.
    Kelley MT, Bürckstümmer T, Wenzel-Seifert K, Dove S, Buschauer A, Seifert R.
    Mol Pharmacol; 2001 Dec 27; 60(6):1210-25. PubMed ID: 11723228
    [Abstract] [Full Text] [Related]

  • 7. Monovalent anions differentially modulate coupling of the beta2-adrenoceptor to G(s)alpha splice variants.
    Seifert R.
    J Pharmacol Exp Ther; 2001 Aug 27; 298(2):840-7. PubMed ID: 11454950
    [Abstract] [Full Text] [Related]

  • 8. The olfactory G protein G(alphaolf) possesses a lower GDP-affinity and deactivates more rapidly than G(salphashort): consequences for receptor-coupling and adenylyl cyclase activation.
    Liu HY, Wenzel-Seifert K, Seifert R.
    J Neurochem; 2001 Jul 27; 78(2):325-38. PubMed ID: 11461968
    [Abstract] [Full Text] [Related]

  • 9. Molecular analysis of beta(2)-adrenoceptor coupling to G(s)-, G(i)-, and G(q)-proteins.
    Wenzel-Seifert K, Seifert R.
    Mol Pharmacol; 2000 Nov 27; 58(5):954-66. PubMed ID: 11040042
    [Abstract] [Full Text] [Related]

  • 10. Probing ligand-specific histamine H1- and H2-receptor conformations with NG-acylated Imidazolylpropylguanidines.
    Xie SX, Ghorai P, Ye QZ, Buschauer A, Seifert R.
    J Pharmacol Exp Ther; 2006 Apr 27; 317(1):139-46. PubMed ID: 16394198
    [Abstract] [Full Text] [Related]

  • 11. Effects of impromidine- and arpromidine-derived guanidines on recombinant human and guinea pig histamine H1 and H2 receptors.
    Xie SX, Schalkhausser F, Ye QZ, Seifert R, Buschauer A.
    Arch Pharm (Weinheim); 2007 Jan 27; 340(1):9-16. PubMed ID: 17206612
    [Abstract] [Full Text] [Related]

  • 12. Distinct interactions of G(salpha-long), G(salpha-short), and G(alphaolf) with GTP, ITP, and XTP.
    Liu HY, Seifert R.
    Biochem Pharmacol; 2002 Aug 15; 64(4):583-93. PubMed ID: 12167477
    [Abstract] [Full Text] [Related]

  • 13. Point mutations in the second extracellular loop of the histamine H2 receptor do not affect the species-selective activity of guanidine-type agonists.
    Preuss H, Ghorai P, Kraus A, Dove S, Buschauer A, Seifert R.
    Naunyn Schmiedebergs Arch Pharmacol; 2007 Dec 15; 376(4):253-64. PubMed ID: 17999052
    [Abstract] [Full Text] [Related]

  • 14. Differential coupling of the human cannabinoid receptors hCB1R and hCB2R to the G-protein G(alpha)i2beta1gamma2.
    Nickl K, Gardner EE, Geiger S, Heilmann J, Seifert R.
    Neurosci Lett; 2008 Dec 05; 447(1):68-72. PubMed ID: 18845226
    [Abstract] [Full Text] [Related]

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  • 18. N1-(3-cyclohexylbutanoyl)-N2-[3-(1H-imidazol-4-yl)propyl]guanidine (UR-AK57), a potent partial agonist for the human histamine H1- and H2-receptors.
    Xie SX, Kraus A, Ghorai P, Ye QZ, Elz S, Buschauer A, Seifert R.
    J Pharmacol Exp Ther; 2006 Jun 05; 317(3):1262-8. PubMed ID: 16554355
    [Abstract] [Full Text] [Related]

  • 19. No evidence for functional selectivity of proxyfan at the human histamine H3 receptor coupled to defined Gi/Go protein heterotrimers.
    Schnell D, Burleigh K, Trick J, Seifert R.
    J Pharmacol Exp Ther; 2010 Mar 05; 332(3):996-1005. PubMed ID: 19959746
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