407 related articles for article (PubMed ID: 30621105)
21. A comprehensive analysis of the association of common variants of ABCG2 with gout.
Yu KH; Chang PY; Chang SC; Wu-Chou YH; Wu LA; Chen DP; Lo FS; Lu JJ
Sci Rep; 2017 Aug; 7(1):9988. PubMed ID: 28855613
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. 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]
25. Complex analysis of urate transporters SLC2A9, SLC22A12 and functional characterization of non-synonymous allelic variants of GLUT9 in the Czech population: no evidence of effect on hyperuricemia and gout.
Hurba O; Mancikova A; Krylov V; Pavlikova M; Pavelka K; Stibůrková B
PLoS One; 2014; 9(9):e107902. PubMed ID: 25268603
[TBL] [Abstract][Full Text] [Related]
26. The genetics of hyperuricaemia and gout.
Reginato AM; Mount DB; Yang I; Choi HK
Nat Rev Rheumatol; 2012 Oct; 8(10):610-21. PubMed ID: 22945592
[TBL] [Abstract][Full Text] [Related]
27. Polymorphisms of uric transporter proteins in the pathogenesis of gout in a Chinese Han population.
Wan W; Xu X; Zhao DB; Pang YF; Wang YX
Genet Mol Res; 2015 Mar; 14(1):2546-50. PubMed ID: 25867401
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Associations between the SLC22A12 gene and gout susceptibility: a meta-analysis.
Zou Y; Du J; Zhu Y; Xie X; Chen J; Ling G
Clin Exp Rheumatol; 2018; 36(3):442-447. PubMed ID: 29352852
[TBL] [Abstract][Full Text] [Related]
30. Association between serum uric acid related genetic loci and diabetic kidney disease in the Chinese type 2 diabetes patients.
Yan D; Wang J; Jiang F; Zhang R; Sun X; Wang T; Wang S; Peng D; He Z; Bao Y; Hu C; Jia W
J Diabetes Complications; 2016 Jul; 30(5):798-802. PubMed ID: 26993665
[TBL] [Abstract][Full Text] [Related]
31. Substantial anti-gout effect conferred by common and rare dysfunctional variants of URAT1/SLC22A12.
Toyoda Y; Kawamura Y; Nakayama A; Nakaoka H; Higashino T; Shimizu S; Ooyama H; Morimoto K; Uchida N; Shigesawa R; Takeuchi K; Inoue I; Ichida K; Suzuki H; Shinomiya N; Takada T; Matsuo H
Rheumatology (Oxford); 2021 Nov; 60(11):5224-5232. PubMed ID: 33821957
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Polymorphisms in GCKR, SLC17A1 and SLC22A12 were associated with phenotype gout in Han Chinese males: a case-control study.
Zhou ZW; Cui LL; Han L; Wang C; Song ZJ; Shen JW; Li ZQ; Chen JH; Wen ZJ; Wang XM; Shi YY; Li CG
BMC Med Genet; 2015 Aug; 16():66. PubMed ID: 26290326
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Functional polymorphisms of the ABCG2 gene are associated with gout disease in the Chinese Han male population.
Zhou D; Liu Y; Zhang X; Gu X; Wang H; Luo X; Zhang J; Zou H; Guan M
Int J Mol Sci; 2014 May; 15(5):9149-59. PubMed ID: 24857923
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Association between intronic SNP in urate-anion exchanger gene, SLC22A12, and serum uric acid levels in Japanese.
Shima Y; Teruya K; Ohta H
Life Sci; 2006 Nov; 79(23):2234-7. PubMed ID: 16920156
[TBL] [Abstract][Full Text] [Related]
39. T6092C polymorphism of SLC22A12 gene is associated with serum uric acid concentrations in Korean male subjects.
Jang WC; Nam YH; Park SM; Ahn YC; Park SH; Choe JY; Shin IH; Kim SK
Clin Chim Acta; 2008 Dec; 398(1-2):140-4. PubMed ID: 18824160
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
