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Journal Abstract Search


384 related items for PubMed ID: 33181260

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Altered expression of nuclear factor of activated T cells, forkhead box P3, and immune-suppressive genes in regulatory T cells of generalized vitiligo patients.
    Giri PS, Dwivedi M, Laddha NC, Begum R, Bharti AH.
    Pigment Cell Melanoma Res; 2020 Jul 05; 33(4):566-578. PubMed ID: 31917889
    [Abstract] [Full Text] [Related]

  • 3. Genetic association of nuclear factor of activated T cells' 3'UTR and structural polymorphisms with susceptibility to generalized vitiligo in Gujarat population.
    Giri P, Bhimani R, Patil S, Dwivedi M.
    Gene; 2023 Sep 05; 880():147629. PubMed ID: 37429370
    [Abstract] [Full Text] [Related]

  • 4. Association of NLRP1 genetic variants and mRNA overexpression with generalized vitiligo and disease activity in a Gujarat population.
    Dwivedi M, Laddha NC, Mansuri MS, Marfatia YS, Begum R.
    Br J Dermatol; 2013 Nov 05; 169(5):1114-25. PubMed ID: 23773036
    [Abstract] [Full Text] [Related]

  • 5. Association of FOXP3 (rs3761548) promoter polymorphism with nondermatomal vitiligo: A study from India.
    Jahan P, Cheruvu R, Tippisetty S, Komaravalli PL, Valluri V, Ishaq M.
    J Am Acad Dermatol; 2013 Aug 05; 69(2):262-6. PubMed ID: 23498308
    [Abstract] [Full Text] [Related]

  • 6. Interleukin-4 genetic variants correlate with its transcript and protein levels in patients with vitiligo.
    Imran M, Laddha NC, Dwivedi M, Mansuri MS, Singh J, Rani R, Gokhale RS, Sharma VK, Marfatia YS, Begum R.
    Br J Dermatol; 2012 Aug 05; 167(2):314-23. PubMed ID: 22512783
    [Abstract] [Full Text] [Related]

  • 7. 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 05; 184():105-111. PubMed ID: 28216259
    [Abstract] [Full Text] [Related]

  • 8. Association between FOXP3 polymorphisms and vitiligo in a Han Chinese population.
    Song P, Wang XW, Li HX, Li K, Liu L, Wei C, Jian Z, Yi XL, Li Q, Wang G, Li CY, Gao TW.
    Br J Dermatol; 2013 Sep 05; 169(3):571-8. PubMed ID: 23582052
    [Abstract] [Full Text] [Related]

  • 9. Decreased suppression of CD8+ and CD4+ T cells by peripheral regulatory T cells in generalized vitiligo due to reduced NFATC1 and FOXP3 proteins.
    Giri PS, Dwivedi M, Begum R.
    Exp Dermatol; 2020 Aug 05; 29(8):759-775. PubMed ID: 32682346
    [Abstract] [Full Text] [Related]

  • 10. 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 05; 22(3):149-154. PubMed ID: 27702400
    [Abstract] [Full Text] [Related]

  • 11. 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 Apr 05; 24(3-4):85-90. PubMed ID: 27792007
    [Abstract] [Full Text] [Related]

  • 12. G allele at -924 A > G position of FoxP3 gene promoter as a risk factor for tuberculosis.
    Beiranvand E, Abediankenari S, Khani S, Hosseini HM, Zeinali S, Beiranvand B, Goudarzi M, Seyedjavadi SS.
    BMC Infect Dis; 2017 Oct 11; 17(1):673. PubMed ID: 29020928
    [Abstract] [Full Text] [Related]

  • 13. Study of the association of forkhead box P3 (FOXP3) gene polymorphisms with unexplained recurrent spontaneous abortions in Indian population.
    Mishra S, Srivastava A, Mandal K, Phadke SR.
    J Genet; 2018 Jun 11; 97(2):405-410. PubMed ID: 29932060
    [Abstract] [Full Text] [Related]

  • 14. Polymorphism of Foxp3 gene affects the frequency of regulatory T cells and disease activity in patients with rheumatoid arthritis in Iranian population.
    Hashemi V, Farrokhi AS, Tanomand A, Babaloo Z, Hojjat-Farsangi M, Anvari E, Tahoori MT, Ezzeddini R, Hosseini A, Gharibi T, Ghalamfarsa G, Jadidi-Niaragh F.
    Immunol Lett; 2018 Dec 11; 204():16-22. PubMed ID: 30292536
    [Abstract] [Full Text] [Related]

  • 15. Correlation of increased MYG1 expression and its promoter polymorphism with disease progression and higher susceptibility in vitiligo patients.
    Dwivedi M, Laddha NC, Begum R.
    J Dermatol Sci; 2013 Sep 11; 71(3):195-202. PubMed ID: 23706493
    [Abstract] [Full Text] [Related]

  • 16. Association of Crohn's disease with Foxp3 gene polymorphisms and its colonic expression in Chinese patients.
    Xia S, Zhang D, Zheng S, Wu C, Lin Q, Ying S, Shao X, Jiang Y.
    J Clin Lab Anal; 2019 May 11; 33(4):e22835. PubMed ID: 30710380
    [Abstract] [Full Text] [Related]

  • 17. An association study of single nucleotide polymorphisms of the FOXP3 intron-1 and the risk of Psoriasis vulgaris.
    Song QH, Shen Z, Xing XJ, Yin R, Wu YZ, You Y, Guo H, Chen L, Hao F, Bai Y.
    Indian J Biochem Biophys; 2012 Feb 11; 49(1):25-35. PubMed ID: 22435141
    [Abstract] [Full Text] [Related]

  • 18. Association of elevated homocysteine levels and Methylenetetrahydrofolate reductase (MTHFR) 1298 A > C polymorphism with Vitiligo susceptibility in Gujarat.
    Jadeja SD, Mansuri MS, Singh M, Patel H, Marfatia YS, Begum R.
    J Dermatol Sci; 2018 May 11; 90(2):112-122. PubMed ID: 29395581
    [Abstract] [Full Text] [Related]

  • 19. Human forkhead box protein 3 gene variants associated with altered susceptibility to idiopathic recurrent pregnancy loss: A retrospective case-control study.
    Bahia W, Zitouni H, Kanabekova P, Bauyrzhanova Z, Shaimardanova M, Finan RR, Aimagambetova G, Almawi WY.
    Am J Reprod Immunol; 2022 Aug 11; 88(2):e13551. PubMed ID: 35452532
    [Abstract] [Full Text] [Related]

  • 20. Genetic polymorphisms in IL-2, IL-10 and FOXP3 are associated with autoimmune neutropenia in early childhood and autoantibody specificity in a Danish cohort.
    Kløve-Mogensen K, Steffensen R, Masmas TN, Glenthøj A, Jensen CF, Ratcliffe P, Höglund P, Hasle H, Nielsen KR, Haunstrup TM.
    Scand J Immunol; 2024 Aug 11; 100(2):e13374. PubMed ID: 38750640
    [Abstract] [Full Text] [Related]


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