Similar articles for PMID: 24438591

Year	Number of Results
1987	1
1988	1
1991	3
1993	6
1994	4
1995	5
1996	11
1997	6
1998	11
1999	3
2000	8
2001	4
2002	8
2003	12
2004	4
2005	4
2006	3
2007	5
2008	2
2009	2
2010	1
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2013	2
2014	2
2015	1
2018	1
2020	1
2021	2
2022	1
2024	0

1

Differences between lutropin-mediated and choriogonadotropin-mediated receptor activation.

Grzesik P, Teichmann A, Furkert J, Rutz C, Wiesner B, Kleinau G, Schülein R, Gromoll J, Krause G. Grzesik P, et al. FEBS J. 2014 Mar;281(5):1479-1492. doi: 10.1111/febs.12718. Epub 2014 Feb 10. FEBS J. 2014. PMID: 24438591 Free article.

2

A splice variant of the human luteinizing hormone (LH) receptor modulates the expression of wild-type human LH receptor.

Nakamura K, Yamashita S, Omori Y, Minegishi T. Nakamura K, et al. Mol Endocrinol. 2004 Jun;18(6):1461-70. doi: 10.1210/me.2003-0489. Epub 2004 Mar 18. Mol Endocrinol. 2004. PMID: 15031322

3

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. Zhang M, et al. Cell Signal. 2009 Nov;21(11):1663-71. doi: 10.1016/j.cellsig.2009.07.003. Epub 2009 Jul 16. Cell Signal. 2009. PMID: 19616090 Free PMC article.

4

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. Shinozaki H, et al. Mol Endocrinol. 2001 Jun;15(6):972-84. doi: 10.1210/mend.15.6.0661. Mol Endocrinol. 2001. PMID: 11376115

5

A constitutively active mutant of the human lutropin receptor (hLHR-L457R) escapes lysosomal targeting and degradation.

Galet C, Ascoli M. Galet C, et al. Mol Endocrinol. 2006 Nov;20(11):2931-45. doi: 10.1210/me.2006-0138. Epub 2006 Jun 27. Mol Endocrinol. 2006. PMID: 16803865 Free PMC article.

6

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. Abell A, et al. J Biol Chem. 1996 Feb 23;271(8):4518-27. doi: 10.1074/jbc.271.8.4518. J Biol Chem. 1996. PMID: 8626807 Free article.

7

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 Jr, Pereira MA, Lemos Marini SH, Baptista MT, Arnhold IJ, Fanelli F, Mendonca BB, Segaloff DL. Latronico AC, et al. J Clin Endocrinol Metab. 2000 Dec;85(12):4799-805. doi: 10.1210/jcem.85.12.7071. J Clin Endocrinol Metab. 2000. PMID: 11134146

8

Effect of activating and inactivating mutations on the phosphorylation and trafficking of the human lutropin/choriogonadotropin receptor.

Min L, Ascoli M. Min L, et al. Mol Endocrinol. 2000 Nov;14(11):1797-810. doi: 10.1210/mend.14.11.0555. Mol Endocrinol. 2000. PMID: 11075813

9

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. Hirakawa T, et al. J Biol Chem. 2003 Dec 5;278(49):49348-57. doi: 10.1074/jbc.M306557200. Epub 2003 Sep 24. J Biol Chem. 2003. PMID: 14507927 Free article.

10

Identification of Key Receptor Residues Discriminating Human Chorionic Gonadotropin (hCG)- and Luteinizing Hormone (LH)-Specific Signaling.

Lazzaretti C, Secco V, Paradiso E, Sperduti S, Rutz C, Kreuchwig A, Krause G, Simoni M, Casarini L. Lazzaretti C, et al. Int J Mol Sci. 2020 Dec 25;22(1):151. doi: 10.3390/ijms22010151. Int J Mol Sci. 2020. PMID: 33375708 Free PMC article.

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