Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and TNFRSF21[original query] |
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| Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG. Neuroscience letters 2006 Mar 396 (2): 137-42. Norberg Anna, Forsgren Lars, Holmberg Dan, Holmberg Moni |
| Genetic analysis of atherosclerosis identifies a major susceptibility locus in the major histocompatibility complex of mice. Atherosclerosis 2016 Oct 254 124-132. Grainger Andrew T, Jones Michael B, Li Jing, Chen Mei-Hua, Manichaikul Ani, Shi Weib |
| Three Novel Players: PTK2B, SYK, and TNFRSF21 Were Identified to Be Involved in the Regulation of Bovine Mastitis Susceptibility via GWAS and Post-transcriptional Analysis. Frontiers in immunology 2019 8 10 1579. Yang Fan, Chen Fanghui, Li Lili, Yan Li, Badri Tarig, Lv Chenglong, Yu Daolun, Zhang Manling, Jang Xiaojun, Li Jie, Yuan Lu, Wang Genlin, Li Honglin, Li Jun, Cai Yaf |
| TNFRSF21 mutations cause high myopia. Journal of medical genetics 2019 6 56 (10): 671-677. Pan Hong, Wu Shijing, Wang Jing, Zhu Tian, Li Tengyan, Wan Bo, Liu Beihong, Luo Yan, Ma Xu, Sui Ruifang, Wang Binb |
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