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Journal Abstract Search

249 related items for PubMed ID: 30168273

  • 1. FOXP3 rs3761548 polymorphism is associated with knee osteoarthritis in a Turkish population.
    Cekin N, Pinarbasi E, Bildirici AE, Donmez G, Oztemur Z, Bulut O, Arslan S.
    Int J Rheum Dis; 2018 Oct; 21(10):1779-1786. PubMed ID: 30168273
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  • 2. Association of aplastic anemia and FoxP3 gene polymorphisms in Koreans.
    In JW, Lee N, Roh EY, Shin S, Park KU, Song EY.
    Hematology; 2017 Apr; 22(3):149-154. PubMed ID: 27702400
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  • 3. Significant association of interleukin-4 gene intron 3 VNTR polymorphism with susceptibility to knee osteoarthritis.
    Yigit S, Inanir A, Tekcan A, Tural E, Ozturk GT, Kismali G, Karakus N.
    Gene; 2014 Mar 01; 537(1):6-9. PubMed ID: 24406619
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  • 4. Single nucleotide polymorphisms in the FOXP3 gene are associated with increased risk of relapsing-remitting multiple sclerosis.
    Eftekharian MM, Sayad A, Omrani MD, Ghannad MS, Noroozi R, Mazdeh M, Mirfakhraie R, Movafagh A, Roshanaei G, Azimi T, Inoko H, Taheri M.
    Hum Antibodies; 2016 Mar 01; 24(3-4):85-90. PubMed ID: 27792007
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  • 5. The transcription factor Forkhead Box P3 gene variants affect idiopathic recurrent pregnancy loss.
    Saxena D, Misra MK, Parveen F, Phadke SR, Agrawal S.
    Placenta; 2015 Feb 01; 36(2):226-31. PubMed ID: 25499308
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  • 6. The role of two common FOXP3 gene promoter polymorphisms in preeclampsia in a Turkish population: a case-control study.
    Cekin N, Pinarbasi E, Esra Bildirici A, Okten H, Yanik A, Sonmez G.
    J Obstet Gynaecol; 2020 May 01; 40(4):495-499. PubMed ID: 32401107
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  • 7. [Association between single-nucleotide polymorphisms of key genes in T regulatory cells signaling pathways and the efficacy of allergic rhinitis immune therapy].
    Ruan Y, Zhang Y, Zhang L.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Jan 01; 51(1):34-42. PubMed ID: 26791767
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  • 11. The single-nucleotide polymorphism (SNP) of tumor necrosis factor α -308G/A gene is associated with early-onset primary knee osteoarthritis in an Egyptian female population.
    Abdel Galil SM, Ezzeldin N, Fawzy F, El-Boshy M.
    Clin Rheumatol; 2017 Nov 01; 36(11):2525-2530. PubMed ID: 28695434
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  • 14. Association of functional genetic variants of transcription factor Forkhead Box P3 and Nuclear Factor-κB with end-stage renal disease and renal allograft outcome.
    Misra MK, Mishra A, Pandey SK, Kapoor R, Sharma RK, Agrawal S.
    Gene; 2016 Apr 25; 581(1):57-65. PubMed ID: 26794449
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  • 15. 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 25; 184():105-111. PubMed ID: 28216259
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  • 16. Association of (-1,607) 1G/2G polymorphism of matrix metalloproteinase-1 gene with knee osteoarthritis in the Turkish population (knee osteoarthritis and MMPs gene polymorphisms).
    Barlas IO, Sezgin M, Erdal ME, Sahin G, Ankarali HC, Altintas ZM, Türkmen E.
    Rheumatol Int; 2009 Feb 25; 29(4):383-8. PubMed ID: 18802702
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  • 18. Genetic association of FOXP3 gene polymorphisms with allograft rejection in renal transplant patients.
    Qiu XY, Jiao Z, Zhang M, Chen JP, Shi XJ, Zhong MK.
    Nephrology (Carlton); 2012 May 25; 17(4):423-30. PubMed ID: 22239151
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  • 19. Association of FOXP3 and GAGE10 promoter polymorphisms and decreased FOXP3 expression in regulatory T cells with susceptibility to generalized vitiligo in Gujarat population.
    Giri PS, Patel S, Begum R, Dwivedi M.
    Gene; 2021 Feb 05; 768():145295. PubMed ID: 33181260
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