| 1 | MTNR1B
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| The rs10830963 variant of melatonin receptor MTNR1B is associated with increased risk for gestational diabetes mellitus in a Greek population.
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| Vlassi M, Gazouli M, Paltoglou G, Christopoulos P, Florentin L, Kassi G, Mastorakos G.
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| Hormones (Athens) 11(1):70-6.
2012
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| 2 | MTNR1B
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| Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes.
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| Bonnefond A, Clément N, Fawcett K, Yengo L, Vaillant E, Guillaume JL, Dechaume A, Payne F, Roussel R, Czernichow S, Hercberg S, Hadjadj S, Balkau B, Marre M, Lantieri O, Langenberg C, Bouatia-Naji N; Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC), Charpentier G, Vaxillaire M, Rocheleau G, Wareham NJ, Sladek R, McCarthy MI, Dina C, Barroso I, Jockers R, Froguel P.
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| Nat Genet 44(3):297-301. doi: 10.1038/ng.1053.
2012
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| 3 | MTNR1B
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| Melatonin receptor 1 B polymorphisms associated with the risk of gestational diabetes mellitus.
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| Kim JY, Cheong HS, Park BL, Baik SH, Park S, Lee SW, Kim MH, Chung JH, Choi JS, Kim MY, Yang JH, Cho DH, Shin HD, Kim SH.
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| BMC Med Genet 12:82. doi: 10.1186/1471-2350-12-82.
2011
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| 4 | G6PC2, MTNR1B
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| Effects of GCK, GCKR, G6PC2 and MTNR1B variants on glucose metabolism and insulin secretion.
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| Hu C, Zhang R, Wang C, Yu W, Lu J, Ma X, Wang J, Jiang F, Tang S, Bao Y, Xiang K, Jia W.
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| PLoS One 5(7):e11761. 2010
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| 5 | MTNR1A, MTNR1B
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| Mutation screening of melatonin-related genes in patients with autism spectrum disorders.
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| Jonsson L, Ljunggren E, Bremer A, Pedersen C, Landén M, Thuresson K, Giacobini M, Melke J.
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| BMC Med Genomics 3:10. 2010
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| 6 | MTNR1B
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| Genetic variants in MTNR1B affecting insulin secretion.
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| Müssig K, Staiger H, Machicao F, Häring HU, Fritsche A.
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| Ann Med 42(6):387-93. doi: 10.3109/07853890.2010.502125. Review.
2010
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| 7 | MTNR1B
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| Variants in MTNR1B influence fasting glucose levels.
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| Prokopenko I, Langenberg C, Florez JC, Saxena R, Soranzo N, Thorleifsson G, Loos RJ, Manning AK, Jackson AU, Aulchenko Y, Potter SC, Erdos MR, Sanna S, Hottenga JJ, Wheeler E, Kaakinen M, Lyssenko V, Chen WM, Ahmadi K, Beckmann JS, Bergman RN, Bochud M, Bonnycastle LL, Buchanan TA, Cao A, Cervino A, Coin L, Collins FS, Crisponi L, de Geus EJ, Dehghan A, Deloukas P, Doney AS, Elliott P, Freimer N, Gateva V, Herder C, Hofman A, Hughes TE, Hunt S, Illig T, Inouye M, Isomaa B, Johnson T, Kong A, Krestyaninova M, Kuusisto J, Laakso M, Lim N, Lindblad U, Lindgren CM, McCann OT, Mohlke KL, Morris AD, Naitza S, Orrù M, Palmer CN, Pouta A, Randall J, Rathmann W, Saramies J, Scheet P, Scott LJ, Scuteri A, Sharp S, Sijbrands E, Smit JH, Song K, Steinthorsdottir V, Stringham HM, Tuomi T, Tuomilehto J, Uitterlinden AG, Voight BF, Waterworth D, Wichmann HE, Willemsen G, Witteman JC, Yuan X, Zhao JH, Zeggini E, Schlessinger D, Sandhu M, Boomsma DI, Uda M, Spector TD, Penninx BW, Altshuler D, Vollenweider P, Jarvelin MR, Lakatta E, Waeber G, Fox CS, Peltonen L, Groop LC, Mooser V, Cupples LA, Thorsteinsdottir U, Boehnke M, Barroso I, Van Duijn C, Dupuis J, Watanabe RM, Stefansson K, McCarthy MI, Wareham NJ, Meigs JB, Abecasis GR.
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| Nat Genet 41(1):77-81. Epub 2008 Dec 7.
2009
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| 8 | MTNR1B
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| Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion.
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| Lyssenko V, Nagorny CL, Erdos MR, Wierup N, Jonsson A, Spégel P, Bugliani M, Saxena R, Fex M, Pulizzi N, Isomaa B, Tuomi T, Nilsson P, Kuusisto J, Tuomilehto J, Boehnke M, Altshuler D, Sundler F, Eriksson JG, Jackson AU, Laakso M, Marchetti P, Watanabe RM, Mulder H, Groop L.
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| Nat Genet 41(1):82-8. Epub 2008 Dec 7.
2009
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| 9 | MTNR1B
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| A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.
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| Bouatia-Naji N, Bonnefond A, Cavalcanti-Proença C, Sparsø T, Holmkvist J, Marchand M, Delplanque J, Lobbens S, Rocheleau G, Durand E, De Graeve F, Chèvre JC, Borch-Johnsen K, Hartikainen AL, Ruokonen A, Tichet J, Marre M, Weill J, Heude B, Tauber M, Lemaire K, Schuit F, Elliott P, Jørgensen T, Charpentier G, Hadjadj S, Cauchi S, Vaxillaire M, Sladek R, Visvikis-Siest S, Balkau B, Lévy-Marchal C, Pattou F, Meyre D, Blakemore AI, Jarvelin MR, Walley AJ, Hansen T, Dina C, Pedersen O, Froguel P.
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| Nat Genet 41(1):89-94. Epub 2008 Dec 7.
2009
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| 10 | MTNR1A, MTNR1B
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| Gene structures, biochemical characterization and distribution of rat melatonin receptors.
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| Ishii H, Tanaka N, Kobayashi M, Kato M, Sakuma Y.
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| J Physiol Sci 59(1):37-47. Epub 2008 Dec 6.
2009
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| 11 | MTNR1A, MTNR1B
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| C-terminal domains within human MT1 and MT2 melatonin receptors are involved in internalization processes.
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| Sethi S, Adams W, Pollock J, Witt-Enderby PA.
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| J Pineal Res 45(2):212-8. Epub 2008 Mar 14.
2008
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| 12 | MTNR1B
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| The MT2 melatonin receptor subtype is present in human retina and decreases in Alzheimer's disease.
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| Savaskan E, Jockers R, Ayoub M, Angeloni D, Fraschini F, Flammer J, Eckert A, Muller-Spahn F, Meyer P.
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| Curr Alzheimer Res 4(1):47-51. 2007
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| 13 | GPR50, MTNR1A, MTNR1B
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| The orphan GPR50 receptor specifically inhibits MT1 melatonin receptor function through heterodimerization.
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| Levoye A, Dam J, Ayoub MA, Guillaume JL, Couturier C, Delagrange P, Jockers R.
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| EMBO J 25(13):3012-23. Epub 2006 Jun 15. 2006
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| 14 | MTNR1B
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| A role of melatonin in neuroectodermal-mesodermal interactions: the hair follicle synthesizes melatonin and expresses functional melatonin receptors.
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| Kobayashi H, Kromminga A, Dunlop TW, Tychsen B, Conrad F, Suzuki N, Memezawa A, Bettermann A, Aiba S, Carlberg C, Paus R.
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| FASEB J 19(12):1710-2. Epub 2005 Jul 19. 2005
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| 15 | MTNR1B
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| Genetic polymorphisms of human melatonin 1b receptor gene in circadian rhythm sleep disorders and controls.
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| Ebisawa T, Uchiyama M, Kajimura N, Kamei Y, Shibui K, Kim K, Kudo Y, Iwase T, Sugishita M, Jodoi T, Ikeda M, Ozeki Y, Watanabe T, Sekimoto M, Katoh M, Yamada N, Toyoshima R, Okawa M, Takahashi K, Yamauchi T.
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| Neurosci Lett 280(1):29-32. 2000
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| 16 | MTNR1B
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| Molecular characterization of a second melatonin receptor expressed in human retina and brain : The Mel1b melatonin receptor.
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| Reppert SM, et al.
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| Proc Natl Acad Sci U S A 92 : 8734-8738. 1995
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