References
- Miao Z, Li C, Chen Y, Zhao S, Wang Y, Wang Z, Dietary and lifestyle changes associated with high prevalence of hyperuricemia and gout in the Shandong coastal cities of Eastern China. J Rheumatol 2008;35:1859–64.
- Hediger MA, Johnson RJ, Miyazaki H, Endou H. Molecular physiology of urate transport. Physiology (Bethesda) 2005;20:125–33.
- Enomoto A, Kimura H, Chairoungdua A, Shigeta Y, Jutabha P, Cha SH, Molecular identification of a renal urate anion exchanger that regulates blood urate levels. Nature 2002;417:447–52.
- Hediger MA. Kidney function: gateway to a long life? Nature 2002;417:393, 395.
- Ichida K, Hosoyamada M, Hisatome I, Enomoto A, Hikita M, Endou H, Clinical and molecular analysis of patients with renal hypouricemia in Japan – influence of URAT1 gene on urinary urate excretion. J Am Soc Nephrol 2004;15:164–73.
- Komoda F, Sekine T, Inatomi J, Enomoto A, Endou H, Ota T, The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia. Pediatr Nephrol 2004;19:728–33.
- Graessler J, Graessler A, Unger S, Kopprasch S, Tausche AK, Kuhlisch E, Association of the human urate transporter 1 with reduced renal uric acid excretion and hyperuricemia in a German Caucasian population. Arthritis Rheum 2006;54:292–300.
- Shima Y, Teruya K, Ohta H. Association between intronic SNP in urate-anion exchanger gene, SLC22A12, and serum uric acid levels in Japanese. Life Sci 2006;79:2234–7.
- Vazquez-Mellado J, Jimenez-Vaca AL, Cuevas-Covarrubias S, Alvarado-Romano V, Pozo-Molina G, Burgos-Vargas R. Molecular analysis of the SLC22A12 (URAT1) gene in patients with primary gout. Rheumatology (Oxford) 2007;46:215–19.
- Li C, Han L, Levin AM, Song H, Yan S, Wang Y, Multiple single nucleotide polymorphisms in the human urate transporter 1 (hURAT1) gene are associated with hyperuricaemia in Han Chinese. J Med Genet 2010;47:204–10.
- Li T, Walsh JR, Ghishan FK, Bai L. Molecular cloning and characterization of a human urate transporter (hURAT1) gene promoter. Biochim Biophys Acta 2004;1681:53–8.
- Zhang H, Gelernter J, Gruen JR, Kranzler HR, Herman AI, Simen AA. Functional impact of a single-nucleotide polymorphism in the OPRD1 promoter region. J Hum Genet 2010;55:278–84.
- Ogasawara K, Terada T, Asaka J, Katsura T, Inui K. Human organic anion transporter 3 gene is regulated constitutively and inducibly via a cAMP-response element. J Pharmacol Exp Ther 2006;319:317–22.
- Segard-Maurel I, Rajkowski K, Jibard N, Schweizer-Groyer G, Baulieu EE, Cadepond F. Glucocorticosteroid receptor dimerization investigated by analysis of receptor binding to glucocorticosteroid responsive elements using a monomer-dimer equilibrium model. Biochemistry 1996;35:1634–42.
- Woodward OM, Kottgen A, Coresh J, Boerwinkle E, Guggino WB, Kottgen M. Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout. Proc Natl Acad Sci USA 2009;106:10338–42.
- Li S, Sanna S, Maschio A, Busonero F, Usala G, Mulas A, The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts. PLoS Genet 2007;3:e194.
- Charles BA, Shriner D, Doumatey A, Chen G, Zhou J, Huang H, A genome-wide association study of serum uric acid in African Americans. BMC Med Genomics 2011;4:17.
- Piret SE, Danoy P, Dahan K, Reed AA, Pryce K, Wong W, Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21. Hum Genet 2011;129:51–8.
- Guan M, Zhang J, Chen Y, Liu W, Kong N, Zou H. High-resolution melting analysis for the rapid detection of an intronic single nucleotide polymorphism in SLC22A12 in male patients with primary gout in China. Scand J Rheumatol 2009;38:276–81.
- De Kloet ER, Vreugdenhil E, Oitzl MS, Joels M. Brain corticosteroid receptor balance in health and disease. Endocr Rev 1998;19:269–301.
- Guardiola-Diaz HM, Kolinske JS, Gates LH, Seasholtz AF. Negative glucocorticoid regulation of cyclic adenosine 3′,5′-monophosphate-stimulated corticotropin-releasing hormone-reporter expression in AtT-20 cells. Mol Endocrinol 1996;10:317–29.
- Ray A, Prefontaine KE. Physical association and functional antagonism between the p65 subunit of transcription factor NF-kappa B and the glucocorticoid receptor. Proc Natl Acad Sci USA 1994;91:752–6.
- Pfahl M. Nuclear receptor/AP-1 interaction. Endocr Rev 1993;14:651–8.