Similar articles for PMID: 18812316

Year	Number of Results
1994	1
1996	1
1997	5
1998	1
2000	3
2001	4
2002	1
2003	5
2004	16
2005	10
2006	8
2007	2
2008	6
2009	3
2010	2
2011	2
2012	4
2013	7
2014	5
2015	5
2016	4
2017	2
2018	2
2019	4
2020	5
2021	4
2022	6

1

The third intracellular loop stabilizes the inactive state of the neuropeptide Y1 receptor.

Chee MJ, Mörl K, Lindner D, Merten N, Zamponi GW, Light PE, Beck-Sickinger AG, Colmers WF. Chee MJ, et al. J Biol Chem. 2008 Nov 28;283(48):33337-46. doi: 10.1074/jbc.M804671200. Epub 2008 Sep 23. J Biol Chem. 2008. PMID: 18812316 Free PMC article.

2

Neuropeptide Y receptor mediates activation of ERK1/2 via transactivation of the IGF receptor.

Lecat S, Belemnaba L, Galzi JL, Bucher B. Lecat S, et al. Cell Signal. 2015 Jul;27(7):1297-304. doi: 10.1016/j.cellsig.2015.03.016. Epub 2015 Mar 25. Cell Signal. 2015. PMID: 25817573

3

The local environment at the cytoplasmic end of TM6 of the mu opioid receptor differs from those of rhodopsin and monoamine receptors: introduction of an ionic lock between the cytoplasmic ends of helices 3 and 6 by a L6.30(275)E mutation inactivates the mu opioid receptor and reduces the constitutive activity of its T6.34(279)K mutant.

Huang P, Visiers I, Weinstein H, Liu-Chen LY. Huang P, et al. Biochemistry. 2002 Oct 8;41(40):11972-80. doi: 10.1021/bi026067b. Biochemistry. 2002. PMID: 12356297

4

Role of G-protein beta gamma subunits in the augmentation of P2Y2 (P2U)receptor-stimulated responses by neuropeptide Y Y1 Gi/o-coupled receptors.

Selbie LA, King NV, Dickenson JM, Hill SJ. Selbie LA, et al. Biochem J. 1997 Nov 15;328 ( Pt 1)(Pt 1):153-8. doi: 10.1042/bj3280153. Biochem J. 1997. PMID: 9359846 Free PMC article.

5

Functional role of a conserved motif in TM6 of the rat mu opioid receptor: constitutively active and inactive receptors result from substitutions of Thr6.34(279) with Lys and Asp.

Huang P, Li J, Chen C, Visiers I, Weinstein H, Liu-Chen LY. Huang P, et al. Biochemistry. 2001 Nov 13;40(45):13501-9. doi: 10.1021/bi010917q. Biochemistry. 2001. PMID: 11695897

6

Structural determinants for G-protein activation and specificity in the third intracellular loop of the thyroid-stimulating hormone receptor.

Claus M, Neumann S, Kleinau G, Krause G, Paschke R. Claus M, et al. J Mol Med (Berl). 2006 Nov;84(11):943-54. doi: 10.1007/s00109-006-0087-8. Epub 2006 Sep 6. J Mol Med (Berl). 2006. PMID: 16955277

7

Leu128(3.43) (l128) and Val247(6.40) (V247) of CXCR1 are critical amino acid residues for g protein coupling and receptor activation.

Han X, Tachado SD, Koziel H, Boisvert WA. Han X, et al. PLoS One. 2012;7(8):e42765. doi: 10.1371/journal.pone.0042765. Epub 2012 Aug 24. PLoS One. 2012. PMID: 22936990 Free PMC article.

8

The third intracellular loop plays a critical role in bitter taste receptor activation.

Pydi SP, Singh N, Upadhyaya J, Bhullar RP, Chelikani P. Pydi SP, et al. Biochim Biophys Acta. 2014 Jan;1838(1 Pt B):231-6. doi: 10.1016/j.bbamem.2013.08.009. Epub 2013 Aug 29. Biochim Biophys Acta. 2014. PMID: 23994601 Free article.

9

Structural determinants for g protein activation and selectivity in the second intracellular loop of the thyrotropin receptor.

Neumann S, Krause G, Claus M, Paschke R. Neumann S, et al. Endocrinology. 2005 Jan;146(1):477-85. doi: 10.1210/en.2004-1045. Epub 2004 Oct 21. Endocrinology. 2005. PMID: 15498884

10

Constitutively active Gq/11-coupled receptors enable signaling by co-expressed G(i/o)-coupled receptors.

Bakker RA, Casarosa P, Timmerman H, Smit MJ, Leurs R. Bakker RA, et al. J Biol Chem. 2004 Feb 13;279(7):5152-61. doi: 10.1074/jbc.M309200200. Epub 2003 Nov 10. J Biol Chem. 2004. PMID: 14610092 Free article.

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