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PUBMED FOR HANDHELDS

Journal Abstract Search


140 related items for PubMed ID: 2254302

  • 1. Extracellular domain of lutropin/choriogonadotropin receptor expressed in transfected cells binds choriogonadotropin with high affinity.
    Xie YB, Wang H, Segaloff DL.
    J Biol Chem; 1990 Dec 15; 265(35):21411-4. PubMed ID: 2254302
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  • 2. 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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  • 3. 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
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  • 4. 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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  • 6. Human choriogonadotropin binds to a lutropin receptor with essentially no N-terminal extension and stimulates cAMP synthesis.
    Ji IH, Ji TH.
    J Biol Chem; 1991 Jul 15; 266(20):13076-9. PubMed ID: 1649176
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  • 7. 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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  • 12. 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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  • 15. 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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  • 16. 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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