Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Multiple Sclerosis and FOXP3[original query] |
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The role of the CD58 locus in multiple sclerosis. Proceedings of the National Academy of Sciences of the United States of America 2009 Mar 106 (13): 5264-9. De Jager Philip L, Baecher-Allan Clare, Maier Lisa M, Arthur Ariel T, Ottoboni Linda, Barcellos Lisa, McCauley Jacob L, Sawcer Stephen, Goris An, Saarela Janna, Yelensky Roman, Price Alkes, Leppa Virpi, Patterson Nick, de Bakker Paul I W, Tran Dong, Aubin Cristin, Pobywajlo Susan, Rossin Elizabeth, Hu Xinli, Ashley Charles W, Choy Edwin, Rioux John D, Pericak-Vance Margaret A, Ivinson Adrian, Booth David R, Stewart Graeme J, Palotie Aarno, Peltonen Leena, Dubois Bénédicte, Haines Jonathan L, Weiner Howard L, Compston Alastair, Hauser Stephen L, Daly Mark J, Reich David, Oksenberg Jorge R, Hafler David |
Circulating levels of interleukin-35 in patients with multiple sclerosis: evaluation of the influences of FOXP3 gene polymorphism and treatment program. Journal of molecular neuroscience : MN 2015 Apr 55 (4): 891-7. Jafarzadeh A, Jamali M, Mahdavi R, Ebrahimi H A, Hajghani H, Khosravimashizi A, Nemati M, Najafipour H, Sheikhi A, Mohammadi M M, Daneshvar |
Increased THEMIS First Exon Usage in CD4+ T-Cells Is Associated with a Genotype that Is Protective against Multiple Sclerosis. PloS one 2016 11 (7): e0158327. Davies Jessica L, Thompson Sara, Kaur-Sandhu Harpreet, Sawcer Stephen, Coles Alasdair, Ban Maria, Jones Joan |
Single nucleotide polymorphisms in the FOXP3 gene are associated with increased risk of relapsing-remitting multiple sclerosis. Human antibodies 2016 Oct . Eftekharian Mohammad Mahdi, Sayad Arezou, Omrani Mir Davood, Ghannad Masoud Sabouri, Noroozi Rezvan, Mazdeh Mehrdokht, Mirfakhraie Reza, Movafagh Abolfazl, Roshanaei Ghodratollah, Azimi Tahereh, Inoko Hidetoshi, Taheri Mohamm |
The FOXP3 rs3761547 Gene Polymorphism in Multiple Sclerosis as a Male-Specific Risk Factor. Neuromolecular medicine 2018 9 20 (4): 537-543. Wawrusiewicz-Kurylonek Natalia, Chor??y Monika, Posmyk Renata, Zajkowska Olga, Zajkowska Agata, Kr?towski Adam Jacek, Tarasiuk Joanna, Kochanowicz Jan, Ku?akowska Ali |
Regulatory T Cells: From Discovery to Autoimmunity. Cold Spring Harbor perspectives in medicine 2018 1 8 (12): . Kitz Alexandra, Singer Emily, Hafler Dav |
The rs3761548 FOXP3 variant is associated with multiple sclerosis and transforming growth factor ß1 levels in female patients. Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2019 Aug . Flauzino Tamires, Alfieri Daniela Frizon, de Carvalho Jennings Pereira Wildea Lice, Oliveira Sayonara Rangel, Kallaur Ana Paula, Lozovoy Marcell Alysson Batisti, Kaimen-Maciel Damacio Ramón, de Oliveira Karen Brajão, Simão Andrea Name Colado, Reiche Edna Maria Visso |
Meta-analysis of FOXP3 gene rs3761548 and rs2232365 polymorphism and multiple sclerosis susceptibility. Medicine 2019 Sep 98 (38): e17224. Zhang Yijian, Zhang Junxin, Liu Hao, He Fan, Chen Angela, Yang Huilin, Pi B |
FOXP3rs3761548 gene variant and interleukin-35 serum levels as biomarkers in patients with multiple sclerosis. Revue neurologique 2020 9 177 (6): 647-654. Kamal A, Hosny M, Abd Elwahab A, Shawki Kamal Y, Shehata H S, Hassan |
FOXP3 and GATA3 Polymorphisms, Vitamin D3 and Multiple Sclerosis. Brain sciences 2021 Mar 11 (4): . Scazzone Concetta, Agnello Luisa, Lo Sasso Bruna, Salemi Giuseppe, Gambino Caterina Maria, Ragonese Paolo, Candore Giuseppina, Ciaccio Anna Maria, Giglio Rosaria Vincenza, Bivona Giulia, Vidali Matteo, Ciaccio Marcel |
A multiple sclerosis-protective coding variant reveals an essential role for HDAC7 in regulatory T cells. Science translational medicine 2022 12 14 (675): eabl3651. Axisa Pierre-Paul, Yoshida Tomomi M, Lucca Liliana E, Kasler Herbert G, Lincoln Matthew R, Pham Giang H, Del Priore Dante, Carpier Jean-Marie, Lucas Carrie L, Verdin Eric, Sumida Tomokazu S, Hafler David |
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- Page last updated:May 06, 2024
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