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Journal Abstract Search

345 related items for PubMed ID: 27792007

  • 1. 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; 24(3-4):85-90. PubMed ID: 27792007
    [Abstract] [Full Text] [Related]

  • 2. 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; 184():105-111. PubMed ID: 28216259
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. [Study on association of functional polymorphisms in Foxp3 gene with the susceptibility to unexplained recurrent spontaneous abortion].
    Wu ZG, You ZS, Zhang C, Li ZY, Su XM, Zhang XM, Li YG.
    Zhonghua Fu Chan Ke Za Zhi; 2011 Oct 05; 46(10):763-8. PubMed ID: 22321351
    [Abstract] [Full Text] [Related]

  • 5. 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 05; 20(4):537-543. PubMed ID: 30229436
    [Abstract] [Full Text] [Related]

  • 6. 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
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  • 8. Secondary progressive in contrast to relapsing-remitting multiple sclerosis patients show a normal CD4+CD25+ regulatory T-cell function and FOXP3 expression.
    Venken K, Hellings N, Hensen K, Rummens JL, Medaer R, D'hooghe MB, Dubois B, Raus J, Stinissen P.
    J Neurosci Res; 2006 Jun 05; 83(8):1432-46. PubMed ID: 16583400
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  • 9. Genetic polymorphisms of Foxp3 in patients with rheumatoid arthritis.
    Paradowska-Gorycka A, Jurkowska M, Felis-Giemza A, Romanowska-Próchnicka K, Manczak M, Maslinski S, Olesinska M.
    J Rheumatol; 2015 Feb 05; 42(2):170-80. PubMed ID: 25448791
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  • 10. 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 05; 21(10):1779-1786. PubMed ID: 30168273
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  • 12. Some polymorphisms in Epstein-Barr virus-induced gene 3 modify the risk for chronic rhinosinusitis.
    Zhang Y, Wang C, Zhao Y, Zhang L.
    Am J Rhinol Allergy; 2013 Oct 05; 27(2):91-7. PubMed ID: 23562195
    [Abstract] [Full Text] [Related]

  • 13. Compromised CD4+ CD25(high) regulatory T-cell function in patients with relapsing-remitting multiple sclerosis is correlated with a reduced frequency of FOXP3-positive cells and reduced FOXP3 expression at the single-cell level.
    Venken K, Hellings N, Thewissen M, Somers V, Hensen K, Rummens JL, Medaer R, Hupperts R, Stinissen P.
    Immunology; 2008 Jan 05; 123(1):79-89. PubMed ID: 17897326
    [Abstract] [Full Text] [Related]

  • 14. 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 05; 36(2):226-31. PubMed ID: 25499308
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  • 16. Transcriptional characteristics of CD4+ T cells in multiple sclerosis: relative lack of suppressive populations in blood.
    Edström M, Mellergård J, Mjösberg J, Jenmalm M, Vrethem M, Press R, Dahle C, Ernerudh J.
    Mult Scler; 2011 Jan 05; 17(1):57-66. PubMed ID: 20847001
    [Abstract] [Full Text] [Related]

  • 17. 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 05; 25(2):425-31. PubMed ID: 25708657
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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 05; 33(4):e22835. PubMed ID: 30710380
    [Abstract] [Full Text] [Related]

  • 20. Association of SHMT1, MAZ, ERG, and L3MBTL3 Gene Polymorphisms with Susceptibility to Multiple Sclerosis.
    Nazari Mehrabani SZ, Shushizadeh MH, Abazari MF, Nouri Aleagha M, Ardalan A, Abdollahzadeh R, Azarnezhad A.
    Biochem Genet; 2019 Jun 05; 57(3):355-370. PubMed ID: 30456721
    [Abstract] [Full Text] [Related]

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