Academic literature on the topic 'Foxp3[Forkhead box protein 3]'

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Journal articles on the topic "Foxp3[Forkhead box protein 3]"

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Utomo, Bambang Suprayogi Resi, Mochammad Hatta, Sutji Pratiwi, Muhammad Nasrum Massi, Lina Marlina, and Erica Gilda Minawati Simanjuntak. "Analysis of Forkhead Box Protein-3 (Foxp3) in Allergic Rhinitis Patients." International Journal of Otolaryngology and Head & Neck Surgery 07, no. 04 (2018): 228–36. http://dx.doi.org/10.4236/ijohns.2018.74024.

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Liu, X. Y., L. Z. Xu, X. Q. Luo, et al. "Forkhead box protein-3 (Foxp3)-producing dendritic cells suppress allergic response." Allergy 72, no. 6 (2017): 908–17. http://dx.doi.org/10.1111/all.13088.

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Yong, Fangfang, Hemei Wang, Chao Li, and Huiqun Jia. "Sevoflurane represses the migration and invasion of gastric cancer cells by regulating forkhead box protein 3." Journal of International Medical Research 49, no. 4 (2021): 030006052110059. http://dx.doi.org/10.1177/03000605211005936.

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Objective Previous studies suggested that sevoflurane exerts anti-proliferative, anti-migratory, and anti-invasive effects on cancer cells. To determine the role of sevoflurane on gastric cancer (GC) progression, we evaluated its effects on the proliferation, migration, and invasion of SGC7901, AGS, and MGC803 GC cells. Methods GC cells were exposed to different concentrations of sevoflurane (1.7, 3.4, or 5.1% v/v). Cell viability, migration, and invasion were evaluated using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and Transwell assays. Immunohistochemical staining and imm
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Chinn, I. K., J. D. Milner, P. Scheinberg, D. C. Douek, and M. L. Markert. "Thymus transplantation restores the repertoires of forkhead box protein 3 (FoxP3)+and FoxP3−T cells in complete DiGeorge anomaly." Clinical & Experimental Immunology 173, no. 1 (2013): 140–49. http://dx.doi.org/10.1111/cei.12088.

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Lin, Zewei, Xu Liu, Xiaoping Liu, and Jikui Liu. "DNA hypermethylation of the promoter attenuates forkhead box protein 3 (FOXP3) expression in hepatocellular carcinoma cells." Translational Cancer Research 8, no. 5 (2019): 2024–31. http://dx.doi.org/10.21037/tcr.2019.09.09.

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Wang, Meiqin, Ivana Yang, Elizabeth J. Davidson, et al. "Forkhead Box Protein 3 (FoxP3) Demethylation Is Associated with Tolerance Induction in Peanut-Induced Intestinal Allergy." Journal of Allergy and Clinical Immunology 137, no. 2 (2016): AB176. http://dx.doi.org/10.1016/j.jaci.2015.12.712.

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Brunst, Kelly J., Yuet-Kin Leung, Patrick H. Ryan, et al. "Forkhead box protein 3 (FOXP3) hypermethylation is associated with diesel exhaust exposure and risk for childhood asthma." Journal of Allergy and Clinical Immunology 131, no. 2 (2013): 592–94. http://dx.doi.org/10.1016/j.jaci.2012.10.042.

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Passerini, Laura, Sven Olek, Sara Di Nunzio, et al. "Forkhead box protein 3 (FOXP3) mutations lead to increased TH17 cell numbers and regulatory T-cell instability." Journal of Allergy and Clinical Immunology 128, no. 6 (2011): 1376–79. http://dx.doi.org/10.1016/j.jaci.2011.09.010.

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Lozano, Teresa, Noelia Casares, Celia Martil-Otal, et al. "Searching for Peptide Inhibitors of T Regulatory Cell Activity by Targeting Specific Domains of FOXP3 Transcription Factor." Biomedicines 9, no. 2 (2021): 197. http://dx.doi.org/10.3390/biomedicines9020197.

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(1) Background: The ability of cancer cells to evade the immune system is due in part to their capacity to induce and recruit T regulatory cells (Tregs) to the tumor microenvironment. Strategies proposed to improve antitumor immunity by depleting Tregs generally lack specificity and raise the possibility of autoimmunity. Therefore, we propose to control Tregs by their functional inactivation rather than depletion. Tregs are characterized by the expression of the Forkhead box protein 3 (FOXP3) transcription factor, which is considered their “master regulator”. Its interaction with DNA is assist
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North, Michelle, Sarah Mah, Lisa Steacy, Jeffrey Brook, Michael Kobor, and Anne K. Ellis. "Effects of Maternal Allergy On Umbilical Cord Blood Regulatory T Cell Forkhead Box Protein 3 (FOXP3) DNA Methylation." Journal of Allergy and Clinical Immunology 131, no. 2 (2013): AB53. http://dx.doi.org/10.1016/j.jaci.2012.12.872.

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Dissertations / Theses on the topic "Foxp3[Forkhead box protein 3]"

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Chappert, Pascal. "Homéostasie et mécanisme d'action in vivo des lymphocytes T régulateurs CD4+CD25+Foxp3+ chez la souris." Paris 6, 2007. http://www.theses.fr/2007PA066312.

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Homéostasie et mécanisme d’action in vivo des lymphocytes T régulateurs CD4+CD25+Foxp3+ chez la souris Parmi les différentes sous populations de cellules T, les cellules T régulatrices CD4+CD25+ (Tregs), gouvernées par le facteur de transcription Foxp3, représentent un lignage unique de cellules dédiées au maintien de la tolérance immune au soi. Des travaux préalables au sein du laboratoire avaient pu montrer leur potentialité dans le cadre de protocoles d’induction de tolérance à long terme en thérapie génique ou cellulaire vis-à-vis d’un antigène donné chez la souris. Les travaux présentés i
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Book chapters on the topic "Foxp3[Forkhead box protein 3]"

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Wang, Haitao, Philip Lazarovici, and Wenhua Zheng. "Forkhead Box Protein O." In Encyclopedia of Signaling Molecules. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101601.

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"Forkhead Box Protein O1." In Encyclopedia of Signaling Molecules. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101305.

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Conference papers on the topic "Foxp3[Forkhead box protein 3]"

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Cho, H., GH Han, DB Chay, S. Kim, and J.-H. Kim. "EP865 Forkhead box protein O1 and Paired box gene 3 overexpression is associated with poor prognosis in patients with epithelial ovarian cancer." In ESGO Annual Meeting Abstracts. BMJ Publishing Group Ltd, 2019. http://dx.doi.org/10.1136/ijgc-2019-esgo.914.

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Zheng, Ying, and Wilson S. Meng. "Polycation Coated Polymeric Particles as Vehicles of RNA Delivery Into Immune Cells." In ASME 2010 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. ASMEDC, 2010. http://dx.doi.org/10.1115/smasis2010-3714.

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The purpose of this work is to develop a carrier system for delivering RNA molecules aimed to downregulate specific functions in T cells. In many forms of cancer, T cells that express the protein Forkhead Box P3 (Foxp3) are associated with cancer progression. These cells can be identified by CD4 and CD25, molecules express on the cell surface. Studies have shown that downregulation of Foxp3 can increase the ability of other immune cells to destroy tumors. A class of RNA molecules, commonly referred to as “siRNA”, bind to and degrade specific messenger RNA (mRNA) in a sequence-dependent manner
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