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583 related items for PubMed ID: 10098515

  • 21. Deletions of portions of the extracellular loops of the lutropin/choriogonadotropin receptor decrease the binding affinity for ovine luteinizing hormone, but not human choriogonadotropin, by preventing the formation of mature cell surface receptor.
    Abell A, Liu X, Segaloff DL.
    J Biol Chem; 1996 Feb 23; 271(8):4518-27. PubMed ID: 8626807
    [Abstract] [Full Text] [Related]

  • 22. The differential binding affinities of the luteinizing hormone (LH)/choriogonadotropin receptor for LH and choriogonadotropin are dictated by different extracellular domain residues.
    Galet C, Ascoli M.
    Mol Endocrinol; 2005 May 23; 19(5):1263-76. PubMed ID: 15677709
    [Abstract] [Full Text] [Related]

  • 23. The hinge region of the TSH receptor stabilizes ligand binding and determines different signaling profiles of human and bovine TSH.
    Jaeschke H, Schaarschmidt J, Günther R, Mueller S.
    Endocrinology; 2011 Oct 23; 152(10):3986-96. PubMed ID: 21846801
    [Abstract] [Full Text] [Related]

  • 24. Mutational analyses of the extracellular domain of the full-length lutropin/choriogonadotropin receptor suggest leucine-rich repeats 1-6 are involved in hormone binding.
    Thomas D, Rozell TG, Liu X, Segaloff DL.
    Mol Endocrinol; 1996 Jun 23; 10(6):760-8. PubMed ID: 8776736
    [Abstract] [Full Text] [Related]

  • 25. Mutation of a highly conserved acidic residue present in the second intracellular loop of G-protein-coupled receptors does not impair hormone binding or signal transduction of the luteinizing hormone/chorionic gonadotropin receptor.
    Wang Z, Wang H, Ascoli M.
    Mol Endocrinol; 1993 Jan 23; 7(1):85-93. PubMed ID: 8383288
    [Abstract] [Full Text] [Related]

  • 26. Role of the intracellular domains of the human FSH receptor in G(alphaS) protein coupling and receptor expression.
    Ulloa-Aguirre A, Uribe A, Zariñán T, Bustos-Jaimes I, Pérez-Solis MA, Dias JA.
    Mol Cell Endocrinol; 2007 Jan 02; 260-262():153-62. PubMed ID: 17045734
    [Abstract] [Full Text] [Related]

  • 27. Characterization of two fly LGR (leucine-rich repeat-containing, G protein-coupled receptor) proteins homologous to vertebrate glycoprotein hormone receptors: constitutive activation of wild-type fly LGR1 but not LGR2 in transfected mammalian cells.
    Nishi S, Hsu SY, Zell K, Hsueh AJ.
    Endocrinology; 2000 Nov 02; 141(11):4081-90. PubMed ID: 11089539
    [Abstract] [Full Text] [Related]

  • 28. Temperature sensitivity of some mutants of the lutropin/choriogonadotropin receptor.
    Jaquette J, Segaloff DL.
    Endocrinology; 1997 Jan 02; 138(1):85-91. PubMed ID: 8977389
    [Abstract] [Full Text] [Related]

  • 29. An anionic residue at position 564 is important for maintaining the inactive conformation of the human lutropin/choriogonadotropin receptor.
    Kosugi S, Mori T, Shenker A.
    Mol Pharmacol; 1998 May 02; 53(5):894-901. PubMed ID: 9584216
    [Abstract] [Full Text] [Related]

  • 30. Leutropin/beta-adrenergic receptor chimeras bind choriogonadotropin and adrenergic ligands but are not expressed at the cell surface.
    Moyle WR, Bernard MP, Myers RV, Marko OM, Strader CD.
    J Biol Chem; 1991 Jun 15; 266(17):10807-12. PubMed ID: 1645710
    [Abstract] [Full Text] [Related]

  • 31. Surface retention of an inactivating lutropin receptor mutant in exoloop 3.
    Bhowmick N, Narayan P, Puett D.
    Mol Cell Biochem; 1998 Oct 15; 187(1-2):221-7. PubMed ID: 9788760
    [Abstract] [Full Text] [Related]

  • 32. Follitropin receptors contain cryptic ligand binding sites.
    Lin W, Bernard MP, Cao D, Myers RV, Kerrigan JE, Moyle WR.
    Mol Cell Endocrinol; 2007 Jan 02; 260-262():83-92. PubMed ID: 17059863
    [Abstract] [Full Text] [Related]

  • 33. Structural predictions for the ligand-binding region of glycoprotein hormone receptors and the nature of hormone-receptor interactions.
    Jiang X, Dreano M, Buckler DR, Cheng S, Ythier A, Wu H, Hendrickson WA, el Tayar N.
    Structure; 1995 Dec 15; 3(12):1341-53. PubMed ID: 8747461
    [Abstract] [Full Text] [Related]

  • 34.
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  • 35. Interaction, signal generation, signal divergence, and signal transduction of LH/CG and the receptor.
    Ji TH, Ryu KS, Gilchrist R, Ji I.
    Recent Prog Horm Res; 1997 Dec 15; 52():431-53; discussion 454. PubMed ID: 9238862
    [Abstract] [Full Text] [Related]

  • 36. Contributions of intracellular loops 2 and 3 of the lutropin receptor in Gs coupling.
    Angelova K, Fanelli F, Puett D.
    Mol Endocrinol; 2008 Jan 15; 22(1):126-38. PubMed ID: 17872379
    [Abstract] [Full Text] [Related]

  • 37. Identification of hormone-binding regions of the luteinizing hormone/human chorionic gonadotropin receptor using synthetic peptides.
    Roche PC, Ryan RJ, McCormick DJ.
    Endocrinology; 1992 Jul 15; 131(1):268-74. PubMed ID: 1612004
    [Abstract] [Full Text] [Related]

  • 38. hCG-receptor binding and transmembrane signaling.
    Puett D, Bhowmick N, Fernandez LM, Huang J, Wu C, Narayan P.
    Mol Cell Endocrinol; 1996 Dec 20; 125(1-2):55-64. PubMed ID: 9027343
    [Abstract] [Full Text] [Related]

  • 39. The regulation of the binding affinity of the luteinizing hormone/choriogonadotropin receptor by sodium ions is mediated by a highly conserved aspartate located in the second transmembrane domain of G protein-coupled receptors.
    Quintana J, Wang H, Ascoli M.
    Mol Endocrinol; 1993 Jun 20; 7(6):767-75. PubMed ID: 8395653
    [Abstract] [Full Text] [Related]

  • 40. Influence of the hinge region and its adjacent domains on binding and signaling patterns of the thyrotropin and follitropin receptor.
    Schaarschmidt J, Huth S, Meier R, Paschke R, Jaeschke H.
    PLoS One; 2014 Jun 20; 9(10):e111570. PubMed ID: 25340405
    [Abstract] [Full Text] [Related]

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