These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. [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 25; 46(10):763-8. PubMed ID: 22321351 [Abstract] [Full Text] [Related]
7. 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 25; 97(2):405-410. PubMed ID: 29932060 [Abstract] [Full Text] [Related]
8. Association study of forkhead box P3 gene polymorphisms with unexplained recurrent spontaneous abortion. Naderi-Mahabadi F, Zarei S, Fatemi R, Kamali K, Pahlavanzadeh Z, Jeddi-Tehrani M, Kazemi T, Idali F. J Reprod Immunol; 2015 Aug 25; 110():48-53. PubMed ID: 25989617 [Abstract] [Full Text] [Related]
9. Association of functional genetic variants of CTLA4 with reduced serum CTLA4 protein levels and increased risk of idiopathic recurrent miscarriages. Misra MK, Mishra A, Phadke SR, Agrawal S. Fertil Steril; 2016 Oct 25; 106(5):1115-1123.e6. PubMed ID: 27351445 [Abstract] [Full Text] [Related]
10. A genetic association study of NLRP2 and NLRP7 genes in idiopathic recurrent miscarriage. Huang JY, Su M, Lin SH, Kuo PL. Hum Reprod; 2013 Apr 25; 28(4):1127-34. PubMed ID: 23360675 [Abstract] [Full Text] [Related]
11. Co-stimulatory CD28 and transcription factor NFKB1 gene variants affect idiopathic recurrent miscarriages. Misra MK, Singh B, Mishra A, Agrawal S. J Hum Genet; 2016 Dec 25; 61(12):1035-1041. PubMed ID: 27488439 [Abstract] [Full Text] [Related]
12. Platelet-specific collagen receptor glycoprotein VI gene variants affect recurrent pregnancy loss. Siddesh A, Parveen F, Misra MK, Phadke SR, Agrawal S. Fertil Steril; 2014 Oct 25; 102(4):1078-1084.e3. PubMed ID: 25086789 [Abstract] [Full Text] [Related]
13. 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 25; 69(2):262-6. PubMed ID: 23498308 [Abstract] [Full Text] [Related]
14. The role of FOXP3 rs3761548 and rs2294021 polymorphisms in pediatrics acute lymphoblastic leukemia: association with risk and response to therapy. Ghasemi Z, Kalantar K, Amirghofran Z. Mol Biol Rep; 2021 Feb 25; 48(2):1139-1150. PubMed ID: 33517519 [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 25; 184():105-111. PubMed ID: 28216259 [Abstract] [Full Text] [Related]
16. Meta-analysis of FOXP3 polymorphisms and recurrent spontaneous abortion susceptibility. Shuai R, Li D, Xu X, Yang X, Liu D. Am J Reprod Immunol; 2024 Mar 25; 91(3):e13827. PubMed ID: 38433312 [Abstract] [Full Text] [Related]
17. Association of FOXP3 rs3761548 polymorphism and its reduced expression with unexplained recurrent spontaneous abortions: A South Indian study. Dirsipam K, Ponnala D, Madduru D, Bonu R, Jahan P. Am J Reprod Immunol; 2021 Sep 25; 86(3):e13431. PubMed ID: 33882185 [Abstract] [Full Text] [Related]
18. The serum level of transforming growth factor beta1 and its association with Foxp3 gene polymorphism in Iranian women with recurrent spontaneous abortion. Hadinedoushan H, Abbasirad N, Aflatoonian A, Eslami G. Hum Fertil (Camb); 2015 Mar 25; 18(1):54-9. PubMed ID: 25019584 [Abstract] [Full Text] [Related]
19. [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 25; 51(1):34-42. PubMed ID: 26791767 [Abstract] [Full Text] [Related]
20. FOXP3 Gene Variants in Patients with Systemic Lupus Erythematosus: Association with Disease Susceptibility in Men and Relationship with Abortion in Women. Heydarinejad P, Gholijani N, Habibagahi Z, Malekmakan MR, Amirghofran Z. Iran J Immunol; 2022 Jun 25; 19(2):172-183. PubMed ID: 35767890 [Abstract] [Full Text] [Related] Page: [Next] [New Search]