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Journal Abstract Search

316 related items for PubMed ID: 9027343

  • 21.
    ; . PubMed ID:
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  • 22. 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
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  • 23.
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  • 25. 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 15; 7(6):767-75. PubMed ID: 8395653
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  • 26. Opposite contribution of two ligand-selective determinants in the N-terminal hormone-binding exodomain of human gonadotropin receptors.
    Vischer HF, Granneman JC, Bogerd J.
    Mol Endocrinol; 2003 Oct 15; 17(10):1972-81. PubMed ID: 12869592
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  • 27. 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 15; 7(1):85-93. PubMed ID: 8383288
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  • 28. 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
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  • 29. The amino-terminal region of the luteinizing hormone/choriogonadotropin receptor contacts both subunits of human choriogonadotropin. II. Photoaffinity labeling.
    Phang T, Kundu G, Hong S, Ji I, Ji TH.
    J Biol Chem; 1998 May 29; 273(22):13841-7. PubMed ID: 9593729
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  • 30. Lutropins appear to contact two independent sites in the extracellular domain of their receptors.
    Bernard MP, Myers RV, Moyle WR.
    Biochem J; 1998 Nov 01; 335 ( Pt 3)(Pt 3):611-7. PubMed ID: 9794802
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  • 31. Co-evolution of ligand-receptor pairs.
    Moyle WR, Campbell RK, Myers RV, Bernard MP, Han Y, Wang X.
    Nature; 1994 Mar 17; 368(6468):251-5. PubMed ID: 8145825
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  • 32. Lysine residues 2 and 104 of the human chorionic gonadotrophin beta subunit influence receptor binding.
    Xia H, Huang J, Chen TM, Puett D.
    J Mol Endocrinol; 1993 Jun 17; 10(3):337-43. PubMed ID: 8373517
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  • 33.
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  • 34. Structural analysis of yoked chorionic gonadotropin-luteinizing hormone receptor ectodomain complexes by circular dichroic spectroscopy.
    Fralish GB, Dattilo B, Puett D.
    Mol Endocrinol; 2003 Jul 17; 17(7):1192-202. PubMed ID: 12677007
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  • 35. Exoloop 3 of the luteinizing hormone/choriogonadotropin receptor. Lys583 is essential and irreplaceable for human choriogonadotropin (hCG)-dependent receptor activation but not for high affinity hCG binding.
    Ryu KS, Gilchrist RL, Ji I, Kim SJ, Ji TH.
    J Biol Chem; 1996 Mar 29; 271(13):7301-4. PubMed ID: 8631747
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  • 36. The carboxy-terminal region of the glycoprotein hormone alpha-subunit: contributions to receptor binding and signaling in human chorionic gonadotropin.
    Chen F, Wang Y, Puett D.
    Mol Endocrinol; 1992 Jun 29; 6(6):914-9. PubMed ID: 1379673
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  • 37. Thyrotropin-luteinizing hormone/chorionic gonadotropin receptor extracellular domain chimeras as probes for thyrotropin receptor function.
    Nagayama Y, Wadsworth HL, Chazenbalk GD, Russo D, Seto P, Rapoport B.
    Proc Natl Acad Sci U S A; 1991 Feb 01; 88(3):902-5. PubMed ID: 1992482
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  • 38. Pleiotropic effects of substitutions of a highly conserved leucine in transmembrane helix III of the human lutropin/choriogonadotropin receptor with respect to constitutive activation and hormone responsiveness.
    Shinozaki H, Fanelli F, Liu X, Jaquette J, Nakamura K, Segaloff DL.
    Mol Endocrinol; 2001 Jun 01; 15(6):972-84. PubMed ID: 11376115
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  • 39. Specificity of cognate ligand-receptor interactions: fusion proteins of human chorionic gonadotropin and the heptahelical receptors for human luteinizing hormone, thyroid-stimulating hormone, and follicle-stimulating hormone.
    Schubert RL, Narayan P, Puett D.
    Endocrinology; 2003 Jan 01; 144(1):129-37. PubMed ID: 12488338
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  • 40. Fusing the carboxy-terminal peptide of the chorionic gonadotropin (CG) beta-subunit to the common alpha-subunit: retention of O-linked glycosylation and enhanced in vivo bioactivity of chimeric human CG.
    Furuhashi M, Shikone T, Fares FA, Sugahara T, Hsueh AJ, Boime I.
    Mol Endocrinol; 1995 Jan 01; 9(1):54-63. PubMed ID: 7539107
    [Abstract] [Full Text] [Related]

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