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131 related items for PubMed ID: 14636063
21. Multiple independent functions of arrestins in the regulation of protease-activated receptor-2 signaling and trafficking. Stalheim L, Ding Y, Gullapalli A, Paing MM, Wolfe BL, Morris DR, Trejo J. Mol Pharmacol; 2005 Jan; 67(1):78-87. PubMed ID: 15475570 [Abstract] [Full Text] [Related]
22. Identification of the first germline mutation in the extracellular domain of the follitropin receptor responsible for spontaneous ovarian hyperstimulation syndrome. De Leener A, Caltabiano G, Erkan S, Idil M, Vassart G, Pardo L, Costagliola S. Hum Mutat; 2008 Jan; 29(1):91-8. PubMed ID: 17721928 [Abstract] [Full Text] [Related]
23. Extracellular loop 2 in the FSH receptor is crucial for ligand mediated receptor activation. Dupakuntla M, Pathak B, Roy BS, Mahale SD. Mol Cell Endocrinol; 2012 Oct 15; 362(1-2):60-8. PubMed ID: 22641019 [Abstract] [Full Text] [Related]
25. 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 15; 17(11):2162-76. PubMed ID: 12907758 [Abstract] [Full Text] [Related]
26. Inhibition of chemoattractant N-formyl peptide receptor trafficking by active arrestins. Key TA, Vines CM, Wagener BM, Gurevich VV, Sklar LA, Prossnitz ER. Traffic; 2005 Feb 15; 6(2):87-99. PubMed ID: 15634210 [Abstract] [Full Text] [Related]
27. Role of the rate of internalization of the agonist-receptor complex on the agonist-induced down-regulation of the lutropin/choriogonadotropin receptor. Nakamura K, Lazari MF, Li S, Korgaonkar C, Ascoli M. Mol Endocrinol; 1999 Aug 15; 13(8):1295-304. PubMed ID: 10446904 [Abstract] [Full Text] [Related]
28. [Mechanisms of polarized targeting of the FSH receptor]. Beau I, Groyer-Picard MT, Le Bivic A, Milgrom E, Misrahi M. J Soc Biol; 1999 Aug 15; 193(2):139-45. PubMed ID: 10451347 [Abstract] [Full Text] [Related]
29. Evidence that constitutively active luteinizing hormone/human chorionic gonadotropin receptors are rapidly internalized. Bradbury FA, Menon KM. Biochemistry; 1999 Jul 06; 38(27):8703-12. PubMed ID: 10393545 [Abstract] [Full Text] [Related]
30. Role of the intracellular domains of the human FSH receptor in G(alphaS) protein coupling and receptor expression. Ulloa-Aguirre A, Uribe A, Zariñán T, Bustos-Jaimes I, Pérez-Solis MA, Dias JA. Mol Cell Endocrinol; 2007 Jan 02; 260-262():153-62. PubMed ID: 17045734 [Abstract] [Full Text] [Related]
31. Internalization of gonadotropin-releasing hormone receptors (GnRHRs): does arrestin binding to the C-terminal tail target GnRHRs for dynamin-dependent internalization? Hislop JN, Caunt CJ, Sedgley KR, Kelly E, Mundell S, Green LD, McArdle CA. J Mol Endocrinol; 2005 Aug 02; 35(1):177-89. PubMed ID: 16087731 [Abstract] [Full Text] [Related]
32. Association of human follitropin (FSH) receptor with splicing variant of human lutropin/choriogonadotropin receptor negatively controls the expression of human FSH receptor. Yamashita S, Nakamura K, Omori Y, Tsunekawa K, Murakami M, Minegishi T. Mol Endocrinol; 2005 Aug 02; 19(8):2099-111. PubMed ID: 15890674 [Abstract] [Full Text] [Related]
33. Further studies of amino acids (268-304) in thyrotropin (TSH)--lutropin/chorionic gonadotropin (LH/CG) receptor chimeras: cysteine-301 is important in TSH binding and receptor tertiary structure. Akamizu T, Inoue D, Kosugi S, Kohn LD, Mori T. Thyroid; 1994 Aug 02; 4(1):43-8. PubMed ID: 8054860 [Abstract] [Full Text] [Related]
34. Effect of activating and inactivating mutations on the phosphorylation and trafficking of the human lutropin/choriogonadotropin receptor. Min L, Ascoli M. Mol Endocrinol; 2000 Nov 02; 14(11):1797-810. PubMed ID: 11075813 [Abstract] [Full Text] [Related]
35. An anionic residue at position 564 is important for maintaining the inactive conformation of the human lutropin/choriogonadotropin receptor. Kosugi S, Mori T, Shenker A. Mol Pharmacol; 1998 May 02; 53(5):894-901. PubMed ID: 9584216 [Abstract] [Full Text] [Related]
36. The third intracellular loop of the human somatostatin receptor 5 is crucial for arrestin binding and receptor internalization after somatostatin stimulation. Peverelli E, Mantovani G, Calebiro D, Doni A, Bondioni S, Lania A, Beck-Peccoz P, Spada A. Mol Endocrinol; 2008 Mar 02; 22(3):676-88. PubMed ID: 18096696 [Abstract] [Full Text] [Related]
37. The post-endocytotic fate of the gonadotropin receptors is an important determinant of the desensitization of gonadotropin responses. Bhaskaran RS, Ascoli M. J Mol Endocrinol; 2005 Apr 02; 34(2):447-57. PubMed ID: 15821109 [Abstract] [Full Text] [Related]