125 related articles for article (PubMed ID: 26124932)
1. Investigation of FOXP3 genetic variations at positions -2383 C/T and IVS9+459 T/C in southern Iranian patients with lung carcinoma.
Fazelzadeh Haghighi M; Ali Ghayumi M; Behzadnia F; Erfani N
Iran J Basic Med Sci; 2015 May; 18(5):465-71. PubMed ID: 26124932
[TBL] [Abstract][Full Text] [Related]
2. Crucial Role of
Birjan Z; Khashei Varnamkhasti K; Parhoudeh S; Naeimi L; Naeimi S
Diagnostics (Basel); 2023 Nov; 13(22):. PubMed ID: 37998578
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Genetic association study of promoter variation rs3761549 in the FOXP3 gene of Iranian patients diagnosed with brain tumour.
Moradi M; Naeimi S; Asadzade S; Rahi A
J Cell Biochem; 2019 Jul; 120(7):11915-11920. PubMed ID: 30802341
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. FOXP3 -3279 and IVS9+459 polymorphisms are associated with genetic susceptibility to myasthenia gravis.
Zhang J; Chen Y; Jia G; Chen X; Lu J; Yang H; Zhou W; Xiao B; Zhang N; Li J
Neurosci Lett; 2013 Feb; 534():274-8. PubMed ID: 23228687
[TBL] [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; 184():105-111. PubMed ID: 28216259
[TBL] [Abstract][Full Text] [Related]
8. 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; 204():16-22. PubMed ID: 30292536
[TBL] [Abstract][Full Text] [Related]
9. Interleukin-18 promoter polymorphism is associated with lung cancer: a case-control study.
Farjadfar A; Mojtahedi Z; Ghayumi MA; Erfani N; Haghshenas MR; Ghaderi A
Acta Oncol; 2009; 48(7):971-6. PubMed ID: 19642044
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The association of -330 interleukin-2 gene polymorphism and HLA-DR15 allele in Iranian patients with multiple sclerosis.
Sayad A
Int J Immunogenet; 2014 Aug; 41(4):330-4. PubMed ID: 24919928
[TBL] [Abstract][Full Text] [Related]
12. Multi-drug resistance-1 gene polymorphisms in nephrotic syndrome: impact on susceptibility and response to steroids.
Youssef DM; Attia TA; El-Shal AS; Abduelometty FA
Gene; 2013 Nov; 530(2):201-7. PubMed ID: 23994685
[TBL] [Abstract][Full Text] [Related]
13. Study of the association of forkhead box P3 (
Mishra S; Srivastava A; Mandal K; Phadke SR
J Genet; 2018 Jun; 97(2):405-410. PubMed ID: 29932060
[TBL] [Abstract][Full Text] [Related]
14. [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; 46(10):763-8. PubMed ID: 22321351
[TBL] [Abstract][Full Text] [Related]
15. Age-related changes in CD4+CD25+FOXP3+ regulatory T cells and their relationship with lung cancer.
Hou PF; Zhu LJ; Chen XY; Qiu ZQ
PLoS One; 2017; 12(3):e0173048. PubMed ID: 28253320
[TBL] [Abstract][Full Text] [Related]
16. CCL22 16C/a genetic variation is not associated with breast carcinoma in Southern Iranian population.
Erfani N; Moghaddasi-Sani F; Razmkhah M; Haghshenas MR; Talei A; Ghaderi A
Iran J Immunol; 2012 Dec; 9(4):226-33. PubMed ID: 23268288
[TBL] [Abstract][Full Text] [Related]
17. 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; 20(4):537-543. PubMed ID: 30229436
[TBL] [Abstract][Full Text] [Related]
18. Analysis of selected polymorphisms in FOXP3 gene in a cohort of Egyptian patients with schizophrenia.
Mostafa M; Fathy AA; Elwasify M; Abdelsalam M
J Genet Eng Biotechnol; 2022 May; 20(1):83. PubMed ID: 35641708
[TBL] [Abstract][Full Text] [Related]
19. Transcription factor FOXP3 gene variants affect epithelial ovarian carcinoma in the Han Chinese population.
Zhang Y; Xu L; Zhou B; Li Q; You D; Liu C; Song H; Wang Y; Song Y; Su M; Huang X; Yuan M; Lan Z; Wang W
Int J Clin Exp Pathol; 2018; 11(3):1684-1693. PubMed ID: 31938270
[TBL] [Abstract][Full Text] [Related]
20. Association and gene-gene interaction analyses for polymorphic variants in CTLA-4 and FOXP3 genes: role in susceptibility to autoimmune thyroid disease.
Fathima N; Narne P; Ishaq M
Endocrine; 2019 Jun; 64(3):591-604. PubMed ID: 30771152
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]