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Journal Abstract Search

119 related items for PubMed ID: 23333728

  • 1. Alpha-defensin DEFA1A3 gene copy number variation in Asians and its genetic association study in Chinese systemic lupus erythematosus patients.
    Cheng FJ, Zhou XJ, Zhao YF, Zhao MH, Zhang H.
    Gene; 2013 Apr 01; 517(2):158-63. PubMed ID: 23333728
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  • 3. Alpha-defensin DEFA1A3 gene copy number elevation in Danish Crohn's disease patients.
    Jespersgaard C, Fode P, Dybdahl M, Vind I, Nielsen OH, Csillag C, Munkholm P, Vainer B, Riis L, Elkjaer M, Pedersen N, Knudsen E, Andersen PS.
    Dig Dis Sci; 2011 Dec 01; 56(12):3517-24. PubMed ID: 21701837
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  • 6. Polymorphisms in α-Defensin-Encoding DEFA1A3 Associate with Urinary Tract Infection Risk in Children with Vesicoureteral Reflux.
    Schwaderer AL, Wang H, Kim S, Kline JM, Liang D, Brophy PD, McHugh KM, Tseng GC, Saxena V, Barr-Beare E, Pierce KR, Shaikh N, Manak JR, Cohen DM, Becknell B, Spencer JD, Baker PB, Yu CY, Hains DS.
    J Am Soc Nephrol; 2016 Oct 01; 27(10):3175-3186. PubMed ID: 26940096
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  • 8. Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction.
    Ai Z, Li M, Liu W, Foo JN, Mansouri O, Yin P, Zhou Q, Tang X, Dong X, Feng S, Xu R, Zhong Z, Chen J, Wan J, Lou T, Yu J, Zhou Q, Fan J, Mao H, Gale D, Barratt J, Armour JA, Liu J, Yu X.
    Sci Transl Med; 2016 Jun 29; 8(345):345ra88. PubMed ID: 27358498
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  • 9. Runaway multi-allelic copy number variation at the α-defensin locus in African and Asian populations.
    Hughes T, Hansson L, Akkouh I, Hajdarevic R, Bringsli JS, Torsvik A, Inderhaug E, Steen VM, Djurovic S.
    Sci Rep; 2020 Jun 04; 10(1):9101. PubMed ID: 32499510
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  • 10. DEFA gene variants associated with IgA nephropathy in a Chinese population.
    Qi YY, Zhou XJ, Cheng FJ, Hou P, Zhu L, Shi SF, Liu LJ, Lv JC, Zhang H.
    Genes Immun; 2015 Jun 04; 16(3):231-7. PubMed ID: 25675412
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  • 12. Is FCGR2A a susceptibility gene to systemic lupus erythematosus in Chinese?
    Zhou XJ, Lv JC, Qin LX, Yang HZ, Yu F, Zhao MH, Zhang H.
    Lupus; 2011 Oct 04; 20(11):1198-202. PubMed ID: 21768177
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  • 13. Low copy numbers of complement C4 and homozygous deficiency of C4A may predispose to severe disease and earlier disease onset in patients with systemic lupus erythematosus.
    Jüptner M, Flachsbart F, Caliebe A, Lieb W, Schreiber S, Zeuner R, Franke A, Schröder JO.
    Lupus; 2018 Apr 04; 27(4):600-609. PubMed ID: 29050534
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  • 14. Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women.
    Kim JH, Jung SH, Bae JS, Lee HS, Yim SH, Park SY, Bang SY, Hu HJ, Shin HD, Bae SC, Chung YJ.
    Arthritis Rheum; 2013 Apr 04; 65(4):1055-63. PubMed ID: 23335107
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  • 15. Association of DYNC1H1 gene SNP/CNV with disease susceptibility, GCs efficacy, HRQOL, anxiety, and depression in Chinese SLE patients.
    Huang S, Zhang T, Wang Y, Wang L, Yan Z, Teng Y, Li Z, Lou Q, Liu S, Cai J, Chen Y, Li M, Huang H, Xu Z, Zou Y.
    J Clin Lab Anal; 2021 Aug 04; 35(8):e23892. PubMed ID: 34272765
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  • 18. Confirmation of C4 gene copy number variation and the association with systemic lupus erythematosus in Chinese Han population.
    Lv Y, He S, Zhang Z, Li Y, Hu D, Zhu K, Cheng H, Zhou F, Chen G, Zheng X, Li P, Ren Y, Yin X, Cui Y, Sun L, Yang S, Zhang X.
    Rheumatol Int; 2012 Oct 04; 32(10):3047-53. PubMed ID: 21904924
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  • 20. Role of STAT4 polymorphisms in systemic lupus erythematosus in a Japanese population: a case-control association study of the STAT1-STAT4 region.
    Kawasaki A, Ito I, Hikami K, Ohashi J, Hayashi T, Goto D, Matsumoto I, Ito S, Tsutsumi A, Koga M, Arinami T, Graham RR, Hom G, Takasaki Y, Hashimoto H, Behrens TW, Sumida T, Tsuchiya N.
    Arthritis Res Ther; 2008 Oct 04; 10(5):R113. PubMed ID: 18803832
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