Lutropin receptor

Angelova, K., Fanelli, F., and Puett, D. (2002) A model for constitutive lutropin receptor activation based on molecular simulation and engineered mutations in transmembrane helices 6 and 7. J. Biol. Chem. 211, 32202-32213. 

Li, S., Liu, X., Ascoli, M. p38JABl binds to the intracellular precursor of the lutropin/choriogonadotropin receptor and promotes its degradation. 

Liu, X., Davis, D., and Segaloff, D. L. (1993) Disruption of potential sites for N-hnked glyco-sylation does not impair hormone binding to the lutropin/choriogonadotropin receptor if Asn-173 is left intact. J. Biol. Chem. 268, 1513-1516. 

Min, L., and Ascoli, M. (2000) Effect of activating and inactivating mutations on the phosphorylation and trafficking of the human lutropin/choriogonadotropin receptor. Mol. Endocrinol. 14, 1797-1810. 

Lutrepulse gonadotrophin-releasing hormone, lutropin luteinizing hormone, luzindole (N-acetyl-2-benzyltryptamlne N 0774) is a melatonin receptor antagonist (with moderate selectivity for MeljB over the Meli subtype). It shows ANTIDEPressant-like activity in animal model. 

Fiete, D., Srivastava, V., Hindsgaul, O., Baenziger, J. U. (1991). A hepatic reticuloendothelial cell receptor specific for S04-4GalNAcpi, 4GlcNAcpi,2Mana that mediates rapid clearance of lutropin. Cell 67, 1103-1110. 

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