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Research Article

Analysis of chosen polymorphisms in FoxP3 gene in children and adolescents with autoimmune thyroid diseases

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Pages 395-400 | Received 21 Jul 2013, Accepted 30 Mar 2014, Published online: 01 May 2014

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Marta Rydzewska, Aleksandra Góralczyk, Joanna Gościk, Natalia Wawrusiewicz-Kurylonek, Anna Bossowska, Adam Krętowski & Artur Bossowski. (2018) Analysis of chosen polymorphisms rs2476601 a/G – PTPN22, rs1990760 C/T – IFIH1, rs179247 a/G – TSHR in pathogenesis of autoimmune thyroid diseases in children. Autoimmunity 51:4, pages 183-190.
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Shuyuan Chu, Xiaoning Zhong, Jianquan Zhang, Xiaoying Lai, Jiajun Xie & Yu Li. (2016) Four SNPs and Systemic Level of FOXP3 in Smokers and Patients with Chronic Obstructive Pulmonary Disease. COPD: Journal of Chronic Obstructive Pulmonary Disease 13:6, pages 760-766.
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Artur Bossowski, Marcin Moniuszko, Ewelina Idźkowska, Kamil Grubczak, Paulina Singh, Anna Bossowska, Tanja Diana & George J. Kahaly. (2016) Decreased proportions of CD4 + IL17+/CD4 + CD25 + CD127− and CD4 + IL17+/CD4 + CD25 + CD127 − FoxP3+ T cells in children with autoimmune thyroid diseases. Autoimmunity 49:5, pages 320-328.
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Min-Gu Lee, Sang-Cheol Bae & Young Ho Lee. (2015) Association between FOXP3 polymorphisms and susceptibility to autoimmune diseases: A meta-analysis. Autoimmunity 48:7, pages 445-452.
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WenJuan Xiao, ZeLin Liu, JiangHai Lin, JingBo Li, KeJing Wu, Yun Ma, YingXue Gong & ZeHuan Liu. (2015) Polymorphisms in TLR1, TLR6 and TLR10 genes and the risk of Graves’ disease. Autoimmunity 48:1, pages 13-18.
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Articles from other publishers (31)

Guiqin Tan, Guangbing Zheng, Jiang Li, Yingping Zhu, Zhongzhi Liang, Hua Li, Hongsong Yu & Xin Wang. (2023) Association of genetic variations in FoxP3 gene with Graves' disease in a Southwest Chinese Han population . Immunity, Inflammation and Disease 11:10.
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Mikołaj Radziszewski, Aleksander Kuś & Tomasz Bednarczuk. (2023) Genotype-phenotype correlations in Graves’ disease. Best Practice & Research Clinical Endocrinology & Metabolism 37:2, pages 101745.
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Maged Mostafa, Aya Ahmed Fathy, Mohamed Elwasify & Maha Abdelsalam. (2022) Analysis of selected polymorphisms in FOXP3 gene in a cohort of Egyptian patients with schizophrenia. Journal of Genetic Engineering and Biotechnology 20:1.
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Fangyu Zhou, Xin Wang, Lingjun Wang, Xin Sun, Guiqin Tan, Wenwen Wei, Guangbing Zheng, Xiaomin Ma, Dan Tian & Hongsong Yu. (2022) Genetics, Epigenetics, Cellular Immunology, and Gut Microbiota: Emerging Links With Graves’ Disease. Frontiers in Cell and Developmental Biology 9.
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Artur Bossowski & Karolina Stożek. 2021. Graves' Disease. Graves' Disease.
Huiyong Peng, Xiangmei Ding, Juan Xu, Yue Han, Jun Yang, Xinyi Tang, Shengjun Wang & Yingzhao Liu. (2021) Elevated Expression of the Long Noncoding RNA MAFTRR in Patients with Hashimoto’s Thyroiditis. Journal of Immunology Research 2021, pages 1-11.
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Guiqin Tan, Xin Wang, Guangbing Zheng, Juan Du, Fangyu Zhou, Zhongzhi Liang, Wenwen Wei & Hongsong Yu. (2021) Meta-analysis reveals significant association between FOXP3 polymorphisms and susceptibility to Graves’ disease . Journal of International Medical Research 49:4, pages 030006052110041.
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S. I. Zhukova, I. D. Kanner, T. M. Mamontova, E. M. Shelomentceva & M. L. Maximov. (2021) The role of regulatory T cells in autoimmune thyroiditis. Meditsinskiy sovet = Medical Council:21, pages 152-159.
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Beata Sawicka, Hanna Borysewicz-Sańczyk, Natalia Wawrusiewicz-Kurylonek, Tommaso Aversa, Domenico Corica, Joanna Gościk, Adam Krętowski, Małgorzata Waśniewska & Artur Bossowski. (2020) Analysis of Polymorphisms rs7093069-IL-2RA, rs7138803-FAIM2, and rs1748033-PADI4 in the Group of Adolescents With Autoimmune Thyroid Diseases. Frontiers in Endocrinology 11.
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Hanna Borysewicz-Sańczyk, Beata Sawicka, Natalia Wawrusiewicz-Kurylonek, Barbara Głowińska-Olszewska, Anna Kadłubiska, Joanna Gościk, Agnieszka Szadkowska, Aleksandra Łosiewicz, Wojciech Młynarski, Adam Kretowski & Artur Bossowski. (2020) Genetic Association Study of IL2RA, IFIH1, and CTLA-4 Polymorphisms With Autoimmune Thyroid Diseases and Type 1 Diabetes. Frontiers in Pediatrics 8.
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Han-ning Li, Xing-rui Li, Ya-ying Du, Zhi-fang Yang & Zheng-tao Lv. (2020) The Association Between Foxp3 Polymorphisms and Risk of Graves' Disease: A Systematic Review and Meta-Analysis of Observational Studies. Frontiers in Endocrinology 11.
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Ersin Akgöllü. (2020) Evaluation of Forkhead Box P3 gene polymorphisms in chronic HBV infection . The Journal of Gene Medicine 22:6.
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Saeed Hosseini Teshnizi, Mohammad Ali‐Hassanzadeh, Behrouz Gharesi‐Fard, Dieter Kabelitz & Kurosh Kalantar. (2019) Influence of forkhead box protein 3 polymorphisms (rs2232365, rs3761548) with the outcome of pregnancy: A meta‐analysis. Journal of Cellular Physiology 234:9, pages 16573-16581.
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Nusrath Fathima, Parimala Narne & Mohammed Ishaq. (2019) Association and gene–gene interaction analyses for polymorphic variants in CTLA-4 and FOXP3 genes: role in susceptibility to autoimmune thyroid disease. Endocrine 64:3, pages 591-604.
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Aleksander Kuś, Mikołaj Radziszewski, Aleksandra Glina, Konrad Szymański, Beata Jurecka‐Lubieniecka, Edyta Pawlak‐Adamska, Dorota Kula, Natalia Wawrusiewicz‐Kurylonek, Joanna Kuś, Piotr Miśkiewicz, Rafał Płoski, Marek Bolanowski, Jacek Daroszewski, Barbara Jarząb, Artur Bossowski & Tomasz Bednarczuk. (2018) Paediatric‐onset and adult‐onset Graves' disease share multiple genetic risk factors. Clinical Endocrinology 90:2, pages 320-327.
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Natalia Wawrusiewicz-Kurylonek, Monika Chorąży, Renata Posmyk, Olga Zajkowska, Agata Zajkowska, Adam Jacek Krętowski, Joanna Tarasiuk, Jan Kochanowicz & Alina Kułakowska. (2018) The FOXP3 rs3761547 Gene Polymorphism in Multiple Sclerosis as a Male-Specific Risk Factor. NeuroMolecular Medicine 20:4, pages 537-543.
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D. VEJRAZKOVA, J. VCELAK, E. VACLAVIKOVA, M. VANKOVA, K. ZAJICKOVA, M. DUSKOVA, J. VRBIKOVA & B. BENDLOVA. (2018) Genetic Predictors of the Development and Recurrence of Graves' Disease. Physiological Research, pages S431-S439.
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Minjeong Nam, Sue Shin, Kyoung Un Park, Inho Kim, Sung-Soo Yoon, Tack-Kyun Kwon & Eun Young Song. (2018) Association of FOXP3 Single Nucleotide Polymorphisms With Clinical Outcomes After Allogenic Hematopoietic Stem Cell Transplantation . Annals of Laboratory Medicine 38:6, pages 591-598.
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Faheem Shehjar, Dil Afroze, Raiz A. Misgar, Sajad A. Malik & Bashir A. Laway. (2018) Association of FoxP3 promoter polymorphisms with the risk of Graves' disease in ethnic Kashmiri population. Gene 672, pages 88-92.
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Jianyu Yao, Tianze Zhang, Lili Zhang, Kaiyu Han & Linyou Zhang. (2017) FOXP3 polymorphisms in interstitial lung disease among Chinese Han population: A genetic association study . The Clinical Respiratory Journal 12:3, pages 1182-1190.
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Qin-xia Xu, Xiao-yan Qiu, Zheng Jiao, Ming Zhang & Ming-kang Zhong. (2018) FOXP3 rs3761549 polymorphism predicts long-term renal allograft function in patients receiving cyclosporine-based immunosuppressive regimen. Gene 644, pages 93-100.
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F.-F. Yuan, X.-P. Ye, W. Liu, L.-Q. Xue, Y.-R. Ma, L.-L. Zhang, M.-M. Zhang, F. Sun, Y.-Y. Wan, Q.-Y. Zhang, S.-X. Zhao & H.-D. Song. (2018) Genetic study of early-onset Graves’ disease in the Chinese Han population. Clinical Genetics 93:1, pages 103-110.
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Mei Yu, Xueying Tan & Yongmin Huang. (2017) Foxp-3 variants are associated with susceptibility to Graves’ disease in Chinese population. European Journal of Inflammation 15:2, pages 113-119.
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Cadiele Oliana Reichert, Joel da Cunha, Débora Levy, Luciana Morganti Ferreira Maselli, Sérgio Paulo Bydlowski & Celso Spada. 2017. Lymphocyte Updates - Cancer, Autoimmunity and Infection. Lymphocyte Updates - Cancer, Autoimmunity and Infection.
Leonn Mendes Soares Pereira, Samara Tatielle Monteiro Gomes, Ricardo Ishak & Antonio Carlos Rosário Vallinoto. (2017) Regulatory T Cell and Forkhead Box Protein 3 as Modulators of Immune Homeostasis. Frontiers in Immunology 8.
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Aleksander Kuś, Konrad Szymański, Beata Jurecka-Lubieniecka, Edyta Pawlak-Adamska, Dorota Kula, Piotr Miśkiewicz, Marek Bolanowski, Rafał Płoski, Artur Bossowski, Jacek Daroszewski, Barbara Jarząb & Tomasz Bednarczuk. (2016) Gender-dependent and age-of-onset-specific association of the rs11675434 single-nucleotide polymorphism near TPO with susceptibility to Graves’ ophthalmopathy. Journal of Human Genetics 62:3, pages 373-377.
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Maneesh Kumar Misra, Aditi Mishra, Shashi Kant Pandey, Rakesh Kapoor, Raj Kumar Sharma & Suraksha Agrawal. (2016) Association of functional genetic variants of transcription factor Forkhead Box P3 and Nuclear Factor-κB with end-stage renal disease and renal allograft outcome. Gene 581:1, pages 57-65.
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Zhe Piao, Hyung Joon Kim, Jung Yoon Choi, Che Ry Hong, Ji Won Lee, Hyoung Jin Kang, Kyung Duk Park & Hee Young Shin. (2016) Effect of FOXP3 polymorphism on the clinical outcomes after allogeneic hematopoietic stem cell transplantation in pediatric acute leukemia patients. International Immunopharmacology 31, pages 132-139.
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Lei Zheng, XiaoBei Wang, Lijuan Xu, Ning Wang, Pengcheng Cai, Tao Liang & LiHua Hu. (2015) Foxp3 gene polymorphisms and haplotypes associate with susceptibility of Graves' disease in Chinese Han population. International Immunopharmacology 25:2, pages 425-431.
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D. Saxena, M.K. Misra, F. Parveen, S.R. Phadke & S. Agrawal. (2015) The transcription factor Forkhead Box P3 gene variants affect idiopathic recurrent pregnancy loss. Placenta 36:2, pages 226-231.
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Lei Chen, Qiming Yu, Bixia Liu & Liming Zhu. (2014) Association of FoxP3 rs3761548 polymorphism with susceptibility to colorectal cancer in the Chinese population. Medical Oncology 31:12.
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