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PUBMED FOR HANDHELDS

Journal Abstract Search


219 related items for PubMed ID: 24784317

  • 21. Polymorphisms of endothelin 1 (G5665T and T-1370G) and endothelin receptor type A (C+70G and G-231A) in Graves' disease.
    Aydın AF, Develi-İş S, Doğru-Abbasoğlu S, Vural P, Ozderya A, Karadağ B, Uysal M.
    Int Immunopharmacol; 2014 Jan; 18(1):198-202. PubMed ID: 24291390
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  • 23. Prevalence of Selected Polymorphisms of Il7R, CD226, CAPSL, and CLEC16A Genes in Children and Adolescents with Autoimmune Thyroid Diseases.
    Borysewicz-Sańczyk H, Wawrusiewicz-Kurylonek N, Gościk J, Sawicka B, Bossowski F, Corica D, Aversa T, Waśniewska M, Bossowski A.
    Int J Mol Sci; 2024 Apr 04; 25(7):. PubMed ID: 38612837
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  • 24. Functional polymorphisms in TBX21 and HLX are associated with development and prognosis of Graves' disease.
    Morita M, Watanabe M, Inoue N, Inaoka C, Akamizu T, Tatsumi KI, Hidaka Y, Iwatani Y.
    Autoimmunity; 2012 Mar 04; 45(2):129-36. PubMed ID: 22014209
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  • 26. Association between functional SIRT1 polymorphisms and the clinical characteristics of patients with autoimmune thyroid disease.
    Sarumaru M, Watanabe M, Inoue N, Hisamoto Y, Morita E, Arakawa Y, Hidaka Y, Iwatani Y.
    Autoimmunity; 2016 Aug 04; 49(5):329-37. PubMed ID: 27245255
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  • 28. The MAGI2 gene polymorphism rs2160322 is associated with Graves' disease but not with Hashimoto's thyroiditis.
    Jia X, Zhai T, Wang B, Zhang J, Zhang F.
    J Endocrinol Invest; 2019 Jul 04; 42(7):843-850. PubMed ID: 30535759
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  • 30. Role of FOXP3 gene polymorphism in the susceptibility to Tunisian endemic Pemphigus Foliaceus.
    Ben Jmaa M, Abida O, Bahloul E, Toumi A, Khlif S, Fakhfakh R, Elloumi N, Sellami K, Masmoudi A, Turki H, Masmoudi H.
    Immunol Lett; 2017 Apr 04; 184():105-111. PubMed ID: 28216259
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  • 31. Association of CD58 Polymorphisms and its Protein Expression with the Development and Prognosis of Autoimmune Thyroid Diseases.
    Yamamoto M, Watanabe M, Inoue N, Watanabe A, Ozaki H, Ohsaki M, Hidaka Y, Iwatani Y.
    Immunol Invest; 2020 Feb 04; 49(1-2):106-119. PubMed ID: 31505972
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  • 32. Analysis of Associations of Human BAFF Gene Polymorphisms with Autoimmune Thyroid Diseases.
    Lin JD, Yang SF, Wang YH, Fang WF, Lin YC, Lin YF, Tang KT, Wu MY, Cheng CW.
    PLoS One; 2016 Feb 04; 11(5):e0154436. PubMed ID: 27136204
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  • 33. Foxp3 gene polymorphisms and haplotypes associate with susceptibility of Graves' disease in Chinese Han population.
    Zheng L, Wang X, Xu L, Wang N, Cai P, Liang T, Hu L.
    Int Immunopharmacol; 2015 Apr 04; 25(2):425-31. PubMed ID: 25708657
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  • 34. The FOXP3 rs3761547 Gene Polymorphism in Multiple Sclerosis as a Male-Specific Risk Factor.
    Wawrusiewicz-Kurylonek N, Chorąży M, Posmyk R, Zajkowska O, Zajkowska A, Krętowski AJ, Tarasiuk J, Kochanowicz J, Kułakowska A.
    Neuromolecular Med; 2018 Dec 04; 20(4):537-543. PubMed ID: 30229436
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  • 35. Clock gene PERIOD3 polymorphism is associated with susceptibility to Graves' disease but not to Hashimoto's thyroiditis.
    Helvaci N, Oguz SH, Kabacam S, Karabulut E, Akbiyik F, Alikasifoglu M, Gurlek A.
    Chronobiol Int; 2019 Oct 04; 36(10):1343-1350. PubMed ID: 31328557
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  • 36. Comprehensive analysis of cytokine gene polymorphisms defines the association of IL-12 gene with ophthalmopthy in Korean children with autoimmune thyroid disease.
    Jang JP, Cho WK, Baek IC, Choi EJ, Shin DH, Suh BK, Kim TG.
    Mol Cell Endocrinol; 2016 May 05; 426():43-9. PubMed ID: 26850223
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  • 38. Polymorphisms of ST2-IL18R1-IL18RAP gene cluster: a new risk for autoimmune thyroid diseases.
    Wang X, Zhu YF, Li DM, Qin Q, Wang Q, Muhali FS, Jiang WJ, Zhang JA.
    Int J Immunogenet; 2016 Feb 05; 43(1):18-24. PubMed ID: 26566691
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