These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
1016 related articles for article (PubMed ID: 19506252)
1. Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout. Woodward OM; Köttgen A; Coresh J; Boerwinkle E; Guggino WB; Köttgen M Proc Natl Acad Sci U S A; 2009 Jun; 106(25):10338-42. PubMed ID: 19506252 [TBL] [Abstract][Full Text] [Related]
2. The rs2231142 variant of the ABCG2 gene is associated with uric acid levels and gout among Japanese people. Yamagishi K; Tanigawa T; Kitamura A; Köttgen A; Folsom AR; Iso H; Rheumatology (Oxford); 2010 Aug; 49(8):1461-5. PubMed ID: 20421215 [TBL] [Abstract][Full Text] [Related]
3. Identification of Two Dysfunctional Variants in the ABCG2 Urate Transporter Associated with Pediatric-Onset of Familial Hyperuricemia and Early-Onset Gout. Toyoda Y; Pavelcová K; Bohatá J; Ješina P; Kubota Y; Suzuki H; Takada T; Stiburkova B Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33669292 [TBL] [Abstract][Full Text] [Related]
4. ABCG2/BCRP dysfunction as a major cause of gout. Matsuo H; Takada T; Ichida K; Nakamura T; Nakayama A; Suzuki H; Hosoya T; Shinomiya N Nucleosides Nucleotides Nucleic Acids; 2011 Dec; 30(12):1117-28. PubMed ID: 22132966 [TBL] [Abstract][Full Text] [Related]
5. ABCG2 as a therapeutic target candidate for gout. Fujita K; Ichida K Expert Opin Ther Targets; 2018 Feb; 22(2):123-129. PubMed ID: 29264928 [TBL] [Abstract][Full Text] [Related]
6. Association of functional polymorphism rs2231142 (Q141K) in the ABCG2 gene with serum uric acid and gout in 4 US populations: the PAGE Study. Zhang L; Spencer KL; Voruganti VS; Jorgensen NW; Fornage M; Best LG; Brown-Gentry KD; Cole SA; Crawford DC; Deelman E; Franceschini N; Gaffo AL; Glenn KR; Heiss G; Jenny NS; Kottgen A; Li Q; Liu K; Matise TC; North KE; Umans JG; Kao WH Am J Epidemiol; 2013 May; 177(9):923-32. PubMed ID: 23552988 [TBL] [Abstract][Full Text] [Related]
7. The association between genetic polymorphisms in ABCG2 and SLC2A9 and urate: an updated systematic review and meta-analysis. Lukkunaprasit T; Rattanasiri S; Turongkaravee S; Suvannang N; Ingsathit A; Attia J; Thakkinstian A BMC Med Genet; 2020 Oct; 21(1):210. PubMed ID: 33087043 [TBL] [Abstract][Full Text] [Related]
8. Pleiotropic effect of the ABCG2 gene in gout: involvement in serum urate levels and progression from hyperuricemia to gout. Wrigley R; Phipps-Green AJ; Topless RK; Major TJ; Cadzow M; Riches P; Tausche AK; Janssen M; Joosten LAB; Jansen TL; So A; Harré Hindmarsh J; Stamp LK; Dalbeth N; Merriman TR Arthritis Res Ther; 2020 Mar; 22(1):45. PubMed ID: 32164793 [TBL] [Abstract][Full Text] [Related]
9. The ABCG2 Q141K hyperuricemia and gout associated variant illuminates the physiology of human urate excretion. Hoque KM; Dixon EE; Lewis RM; Allan J; Gamble GD; Phipps-Green AJ; Halperin Kuhns VL; Horne AM; Stamp LK; Merriman TR; Dalbeth N; Woodward OM Nat Commun; 2020 Jun; 11(1):2767. PubMed ID: 32488095 [TBL] [Abstract][Full Text] [Related]
10. Identification of ABCG2 dysfunction as a major factor contributing to gout. Matsuo H; Takada T; Ichida K; Nakamura T; Nakayama A; Takada Y; Okada C; Sakurai Y; Hosoya T; Kanai Y; Suzuki H; Shinomiya N Nucleosides Nucleotides Nucleic Acids; 2011 Dec; 30(12):1098-104. PubMed ID: 22132963 [TBL] [Abstract][Full Text] [Related]
11. Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects. Takei R; Cadzow M; Markie D; Bixley M; Phipps-Green A; Major TJ; Li C; Choi HK; Li Z; Hu H; ; Guo H; He M; Shi Y; Stamp LK; Dalbeth N; Merriman TR; Wei WH J Hum Genet; 2021 Feb; 66(2):161-169. PubMed ID: 32778763 [TBL] [Abstract][Full Text] [Related]
13. ABCG2 is a high-capacity urate transporter and its genetic impairment increases serum uric acid levels in humans. Nakayama A; Matsuo H; Takada T; Ichida K; Nakamura T; Ikebuchi Y; Ito K; Hosoya T; Kanai Y; Suzuki H; Shinomiya N Nucleosides Nucleotides Nucleic Acids; 2011 Dec; 30(12):1091-7. PubMed ID: 22132962 [TBL] [Abstract][Full Text] [Related]
14. Influence of the ABCG2 gout risk 141 K allele on urate metabolism during a fructose challenge. Dalbeth N; House ME; Gamble GD; Pool B; Horne A; Purvis L; Stewart A; Merriman M; Cadzow M; Phipps-Green A; Merriman TR Arthritis Res Ther; 2014 Jan; 16(1):R34. PubMed ID: 24476385 [TBL] [Abstract][Full Text] [Related]
15. The prevalence of the gout-associated polymorphism rs2231142 G>T in ABCG2 in a pregnant female Filipino cohort. Roman Y; Tiirikainen M; Prom-Wormley E Clin Rheumatol; 2020 Aug; 39(8):2387-2392. PubMed ID: 32107664 [TBL] [Abstract][Full Text] [Related]
16. Genetic polymorphisms and decreased protein expression of ABCG2 urate transporters are associated with susceptibility to gout, disease severity and renal-overload hyperuricemia. Pálinkás M; Szabó E; Kulin A; Mózner O; Rásonyi R; Juhász P; Nagy K; Várady G; Vörös D; Zámbó B; Sarkadi B; Poór G Clin Exp Med; 2023 Aug; 23(4):1277-1284. PubMed ID: 35939175 [TBL] [Abstract][Full Text] [Related]
17. The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients. Stiburkova B; Pavelcova K; Pavlikova M; Ješina P; Pavelka K Arthritis Res Ther; 2019 Mar; 21(1):77. PubMed ID: 30894219 [TBL] [Abstract][Full Text] [Related]
18. The Role of ABCG2 in the Pathogenesis of Primary Hyperuricemia and Gout-An Update. Eckenstaler R; Benndorf RA Int J Mol Sci; 2021 Jun; 22(13):. PubMed ID: 34206432 [TBL] [Abstract][Full Text] [Related]
19. Common defects of ABCG2, a high-capacity urate exporter, cause gout: a function-based genetic analysis in a Japanese population. Matsuo H; Takada T; Ichida K; Nakamura T; Nakayama A; Ikebuchi Y; Ito K; Kusanagi Y; Chiba T; Tadokoro S; Takada Y; Oikawa Y; Inoue H; Suzuki K; Okada R; Nishiyama J; Domoto H; Watanabe S; Fujita M; Morimoto Y; Naito M; Nishio K; Hishida A; Wakai K; Asai Y; Niwa K; Kamakura K; Nonoyama S; Sakurai Y; Hosoya T; Kanai Y; Suzuki H; Hamajima N; Shinomiya N Sci Transl Med; 2009 Nov; 1(5):5ra11. PubMed ID: 20368174 [TBL] [Abstract][Full Text] [Related]