Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and MX1[original query] |
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The CGGGG insertion/deletion polymorphism of the IRF5 promoter is a strong risk factor for primary Sjögren's syndrome. Arthritis and rheumatism 2009 Jun 60 (7): 7. Miceli-Richard C, Gestermann N, Ittah M, Comets E, Loiseau P, Puechal X, Hachulla E, Gottenberg JE, Lebon P, Becquemont L, Mariette X |
STAT4 is a confirmed genetic risk factor for Sjögren's syndrome and could be involved in type 1 interferon pathway signaling. Genes and immunity 2010 Jul 11 (5): 432-8. Gestermann N, Mekinian A, Comets E, Loiseau P, Puechal X, Hachulla E, Gottenberg J-E, Mariette X, Miceli-Richard |
Circulating plasmablasts contribute to antiphospholipid antibody production, associated with type I interferon upregulation. Journal of thrombosis and haemostasis : JTH 2019 Mar . Hisada Ryo, Kato Masaru, Sugawara Eri, Kanda Masatoshi, Fujieda Yuichiro, Oku Kenji, Bohgaki Toshiyuki, Amengual Olga, Horita Tetsuya, Yasuda Shinsuke, Atsumi Tatsu |
Association of single nucleotide polymorphisms in the CD209, MMP9, TNFA and IFNG genes with susceptibility to Japanese encephalitis in children from North India. Gene 2021 9 808 145962. Deval Hirawati, Alagarasu Kalichamy, Srivastava Neha, Bachal Rupali, Mittal Mahima, Agrawal Apoorv, Bote Minal, Gondhalekar Aniket, Bondre Vijay P, Kant Raj |
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