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403 related items for PubMed ID: 8885249

  • 1. Determination of residues important in hormone binding to the extracellular domain of the luteinizing hormone/chorionic gonadotropin receptor by site-directed mutagenesis and modeling.
    Bhowmick N, Huang J, Puett D, Isaacs NW, Lapthorn AJ.
    Mol Endocrinol; 1996 Sep; 10(9):1147-59. PubMed ID: 8885249
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  • 2. Identification of two amino acid residues on the extracellular domain of the lutropin/choriogonadotropin receptor important in signaling.
    Huang J, Puett D.
    J Biol Chem; 1995 Dec 15; 270(50):30023-8. PubMed ID: 8530405
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  • 3. Identification of amino acid residues in transmembrane helices VI and VII of the lutropin/choriogonadotropin receptor involved in signaling.
    Fernandez LM, Puett D.
    Biochemistry; 1996 Apr 02; 35(13):3986-93. PubMed ID: 8672431
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  • 4. 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 02; 10(6):760-8. PubMed ID: 8776736
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  • 6. Intracellular retention of mutant gonadotropin receptors results in loss of hormone binding activity of the follitropin receptor but not of the lutropin/choriogonadotropin receptor.
    Rozzell TG, Wang H, Liu X, Segaloff DL.
    Mol Endocrinol; 1995 Dec 02; 9(12):1727-36. PubMed ID: 8614409
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  • 11. 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 02; 7(6):767-75. PubMed ID: 8395653
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  • 13. Expression of human luteinizing hormone (LH) receptor: interaction with LH and chorionic gonadotropin from human but not equine, rat, and ovine species.
    Jia XC, Oikawa M, Bo M, Tanaka T, Ny T, Boime I, Hsueh AJ.
    Mol Endocrinol; 1991 Jun 02; 5(6):759-68. PubMed ID: 1922095
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  • 14. 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 02; 19(5):1263-76. PubMed ID: 15677709
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  • 20. 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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