BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

248 related articles for article (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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 537(1):6-9. PubMed ID: 24406619
    [TBL] [Abstract][Full Text] [Related]  

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

  • 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; 36(2):226-31. PubMed ID: 25499308
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The role of two common
    Cekin N; Pinarbasi E; Esra Bildirici A; Okten H; Yanik A; Sonmez G
    J Obstet Gynaecol; 2020 May; 40(4):495-499. PubMed ID: 32401107
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 51(1):34-42. PubMed ID: 26791767
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 69(2):262-6. PubMed ID: 23498308
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 42(2):170-80. PubMed ID: 25448791
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FOXP3 gene is associated with susceptibility to ischemic stroke in the Chinese population.
    Wang Y; Shan T; Mao P; Jiang Y; Wang Z
    Clin Neurol Neurosurg; 2024 Jul; 242():108313. PubMed ID: 38754303
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 36(11):2525-2530. PubMed ID: 28695434
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Role of
    Yaylacıoğlu Tuncay F; Serbest Ceylanoğlu K; Güntekin Ergün S; Ergün G; Konuk O
    Turk J Ophthalmol; 2024 Apr; 54(2):69-75. PubMed ID: 38645270
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 17(1):673. PubMed ID: 29020928
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 581(1):57-65. PubMed ID: 26794449
    [TBL] [Abstract][Full Text] [Related]  

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

  • 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; 29(4):383-8. PubMed ID: 18802702
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Tumour necrosis factor alpha -308G/A gene polymorphism: lack of association with knee osteoarthritis in a Turkish population.
    Sezgin M; Barlas IO; Ankarali HC; Altintaş ZM; Türkmen E; Gökdoğan T; Sahin G; Erdal ME
    Clin Exp Rheumatol; 2008; 26(5):763-8. PubMed ID: 19032806
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 17(4):423-30. PubMed ID: 22239151
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 768():145295. PubMed ID: 33181260
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FoxP3 genetic variants and risk of non-small cell lung cancer in the Chinese Han population.
    He YQ; Bo Q; Yong W; Qiu ZX; Li YL; Li WM
    Gene; 2013 Dec; 531(2):422-5. PubMed ID: 24035934
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.