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Human Genome Epidemiology Literature Finder

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Query Trace: Multiple Sclerosis and TBX21[original query]
The low EOMES/TBX21 molecular phenotype in multiple sclerosis reflects CD56+ cell dysregulation and is affected by immunomodulatory therapies. Clinical immunology (Orlando, Fla.) 2016 Jan . McKay Fiona C, Gatt Prudence N, Fewings Nicole, Parnell Grant P, Schibeci Stephen D, Basuki Monica A I, Powell Joseph E, Goldinger Anita, Fabis-Pedrini Marzena J, Kermode Allan G, Burke Therese, Vucic Steve, Stewart Graeme J, Booth David Similar articles in PubMed
The protective role of TBX21-1514T>C polymorphism in susceptibility to multiple sclerosis. Iranian journal of neurology 2019 3 17 (3): 111-116. Akbarian Fatemeh, Ataei Mitra, Salehi Zivar, Nabavi Masoud, Sanati Mohammad Hosse Similar articles in PubMed
Myelin oligodendrocyte glycoprotein-associated disease is associated with BANK1, RNASET2 and TNIP1 polymorphisms. Journal of neuroimmunology 2022 Aug 372 577937. Shu Yaqing, Ma Xiaoyu, Chen Chen, Wang Yuge, Sun Xiaobo, Zhang Liang, Lu Zhengqi, Petersen Frank, Qiu Wei, Yu Xinh Similar articles in PubMed
ABCB1 gene polymorphisms impact the effect of high-dose intravenous methylprednisolone therapy on optic neuritis associated with AQP4-IgG-positive neuromyelitis optica spectrum disorder. Journal of clinical pharmacy and therapeutics 2022 4 47 (9): 1379-1387. Dai Yuyang, Ni Siyang, Wu Feng, Guo Shaojie, Zhao Xiuli, Wang Jiaw Similar articles in PubMed