364 related articles for article (PubMed ID: 23552988)
1. 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]
2. 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]
3. 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]
4. 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]
5. Ethnic differences in ATP-binding cassette transporter, sub-family G, member 2 (ABCG2/BCRP): genotype combinations and estimated functions.
Sakiyama M; Matsuo H; Takada Y; Nakamura T; Nakayama A; Takada T; Kitajiri S; Wakai K; Suzuki H; Shinomiya N
Drug Metab Pharmacokinet; 2014; 29(6):490-2. PubMed ID: 24869748
[TBL] [Abstract][Full Text] [Related]
6. A strong role for the ABCG2 gene in susceptibility to gout in New Zealand Pacific Island and Caucasian, but not Māori, case and control sample sets.
Phipps-Green AJ; Hollis-Moffatt JE; Dalbeth N; Merriman ME; Topless R; Gow PJ; Harrison AA; Highton J; Jones PB; Stamp LK; Merriman TR
Hum Mol Genet; 2010 Dec; 19(24):4813-9. PubMed ID: 20858603
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Systematic genetic analysis of early-onset gout: ABCG2 is the only associated locus.
Zaidi F; Narang RK; Phipps-Green A; Gamble GG; Tausche AK; So A; Riches P; Andres M; Perez-Ruiz F; Doherty M; Janssen M; Joosten LAB; Jansen TL; Kurreeman F; Torres RJ; McCarthy GM; Miner JN; Stamp LK; Merriman TR; Dalbeth N
Rheumatology (Oxford); 2020 Sep; 59(9):2544-2549. PubMed ID: 31998961
[TBL] [Abstract][Full Text] [Related]
11. Association between ABCG2 Q141K polymorphism and gout risk affected by ethnicity and gender: a systematic review and meta-analysis.
Dong Z; Guo S; Yang Y; Wu J; Guan M; Zou H; Jin L; Wang J
Int J Rheum Dis; 2015 May; 18(4):382-91. PubMed ID: 25639607
[TBL] [Abstract][Full Text] [Related]
12. The association between the polymorphism rs2231142 in the ABCG2 gene and gout risk: a meta-analysis.
Lv X; Zhang Y; Zeng F; Yin A; Ye N; Ouyang H; Feng D; Li D; Ling W; Zhang X
Clin Rheumatol; 2014 Dec; 33(12):1801-5. PubMed ID: 24777469
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease.
Stark K; Reinhard W; Grassl M; Erdmann J; Schunkert H; Illig T; Hengstenberg C
PLoS One; 2009 Nov; 4(11):e7729. PubMed ID: 19890391
[TBL] [Abstract][Full Text] [Related]
15. Functional Characterization of Clinically-Relevant Rare Variants in
Toyoda Y; Mančíková A; Krylov V; Morimoto K; Pavelcová K; Bohatá J; Pavelka K; Pavlíková M; Suzuki H; Matsuo H; Takada T; Stiburkova B
Cells; 2019 Apr; 8(4):. PubMed ID: 31003562
[TBL] [Abstract][Full Text] [Related]
16. A meta-analysis of the associations between the Q141K and Q126X ABCG2 gene variants and gout risk.
Li R; Miao L; Qin L; Xiang Y; Zhang X; Peng H; Mailamuguli ; Sun Y; Yao H
Int J Clin Exp Pathol; 2015; 8(9):9812-23. PubMed ID: 26617691
[TBL] [Abstract][Full Text] [Related]
17. GLUT9 influences uric acid concentration in patients with Lesch-Nyhan disease.
Torres RJ; Puig JG
Int J Rheum Dis; 2018 Jun; 21(6):1270-1276. PubMed ID: 29879316
[TBL] [Abstract][Full Text] [Related]
18. Mediation analysis to understand genetic relationships between habitual coffee intake and gout.
Hutton J; Fatima T; Major TJ; Topless R; Stamp LK; Merriman TR; Dalbeth N
Arthritis Res Ther; 2018 Jul; 20(1):135. PubMed ID: 29976226
[TBL] [Abstract][Full Text] [Related]
19. Genetic analysis of ABCG2 and SLC2A9 gene polymorphisms in gouty arthritis in a Korean population.
Kim YS; Kim Y; Park G; Kim SK; Choe JY; Park BL; Kim HS
Korean J Intern Med; 2015 Nov; 30(6):913-20. PubMed ID: 26552468
[TBL] [Abstract][Full Text] [Related]
20. A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population.
Yang B; Mo Z; Wu C; Yang H; Yang X; He Y; Gui L; Zhou L; Guo H; Zhang X; Yuan J; Dai X; Li J; Qiu G; Huang S; Deng Q; Feng Y; Guan L; Hu D; Zhang X; Wang T; Zhu J; Min X; Lang M; Li D; Hu FB; Lin D; Wu T; He M
BMC Med Genomics; 2014 Feb; 7():10. PubMed ID: 24513273
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
