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Journal Abstract Search

115 related items for PubMed ID: 14605099

  • 1. The postendocytotic trafficking of the human lutropin receptor is mediated by a transferable motif consisting of the C-terminal cysteine and an upstream leucine.
    Galet C, Hirakawa T, Ascoli M.
    Mol Endocrinol; 2004 Feb; 18(2):434-46. PubMed ID: 14605099
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  • 2. Identification of a transferable two-amino-acid motif (GT) present in the C-terminal tail of the human lutropin receptor that redirects internalized G protein-coupled receptors from a degradation to a recycling pathway.
    Galet C, Min L, Narayanan R, Kishi M, Weigel NL, Ascoli M.
    Mol Endocrinol; 2003 Mar; 17(3):411-22. PubMed ID: 12554787
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  • 3. A constitutively active mutant of the human lutropin receptor (hLHR-L457R) escapes lysosomal targeting and degradation.
    Galet C, Ascoli M.
    Mol Endocrinol; 2006 Nov; 20(11):2931-45. PubMed ID: 16803865
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  • 6. GIPC binds to the human lutropin receptor (hLHR) through an unusual PDZ domain binding motif, and it regulates the sorting of the internalized human choriogonadotropin and the density of cell surface hLHR.
    Hirakawa T, Galet C, Kishi M, Ascoli M.
    J Biol Chem; 2003 Dec 05; 278(49):49348-57. PubMed ID: 14507927
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  • 7. Seven non-contiguous intracellular residues of the lutropin/choriogonadotropin receptor dictate the rate of agonist-induced internalization and its sensitivity to non-visual arrestins.
    Nakamura K, Liu X, Ascoli M.
    J Biol Chem; 2000 Jan 07; 275(1):241-7. PubMed ID: 10617611
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  • 8. 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 07; 10(6):760-8. PubMed ID: 8776736
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  • 9. Postendocytotic trafficking of the follicle-stimulating hormone (FSH)-FSH receptor complex.
    Krishnamurthy H, Kishi H, Shi M, Galet C, Bhaskaran RS, Hirakawa T, Ascoli M.
    Mol Endocrinol; 2003 Nov 07; 17(11):2162-76. PubMed ID: 12907758
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  • 13. 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 07; 19(5):1263-76. PubMed ID: 15677709
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  • 15. Effects of truncations of the cytoplasmic tail of the luteinizing hormone/chorionic gonadotropin receptor on receptor-mediated hormone internalization.
    Rodriguez MC, Xie YB, Wang H, Collison K, Segaloff DL.
    Mol Endocrinol; 1992 Mar 07; 6(3):327-36. PubMed ID: 1316539
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  • 16. A cell surface inactive mutant of the human lutropin receptor (hLHR) attenuates signaling of wild-type or constitutively active receptors via heterodimerization.
    Zhang M, Feng X, Guan R, Hébert TE, Segaloff DL.
    Cell Signal; 2009 Nov 07; 21(11):1663-71. PubMed ID: 19616090
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  • 17. A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptor.
    Latronico AC, Chai Y, Arnhold IJ, Liu X, Mendonca BB, Segaloff DL.
    Mol Endocrinol; 1998 Mar 07; 12(3):442-50. PubMed ID: 9514160
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  • 18. Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: a novel constitutively activating mutation in the first transmembrane helix.
    Latronico AC, Shinozaki H, Guerra G, Pereira MA, Lemos Marini SH, Baptista MT, Arnhold IJ, Fanelli F, Mendonca BB, Segaloff DL.
    J Clin Endocrinol Metab; 2000 Dec 07; 85(12):4799-805. PubMed ID: 11134146
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  • 20. Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasia.
    Wu SM, Hallermeier KM, Laue L, Brain C, Berry AC, Grant DB, Griffin JE, Wilson JD, Cutler GB, Chan WY.
    Mol Endocrinol; 1998 Nov 07; 12(11):1651-60. PubMed ID: 9817592
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