Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: Syndrome and STAT4[original query] |
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Variant form of STAT4 is associated with primary Sjögren's syndrome. Genes and immunity 2008 Apr 9 (3): 267-70. Korman B D, Alba M I, Le J M, Alevizos I, Smith J A, Nikolov N P, Kastner D L, Remmers E F, Illei G |
Additive effects of the major risk alleles of IRF5 and STAT4 in primary Sjögren's syndrome. Genes and immunity 2009 Jan 10 (1): 68-76. Nordmark G, Kristjansdottir G, Theander E, Eriksson P, Brun J G, Wang C, Padyukov L, Truedsson L, Alm G, Eloranta M-L, Jonsson R, Rönnblom L, Syvänen A |
Association of STAT4 and BLK, but not BANK1 or IRF5, with primary antiphospholipid syndrome. Arthritis and rheumatism 2009 Aug 60 (8): 2468-71. Yin Hong, Borghi Maria Orietta, Delgado-Vega Angélica M, Tincani Angela, Meroni Pier-Luigi, Alarcón-Riquelme Marta |
STAT4 single nucleotide polymorphism, rs7574865 G/T, as a risk for antiphospholipid syndrome. Annals of the rheumatic diseases 2009 Aug 68 (8): 1366-7. Horita T, Atsumi T, Yoshida N, Nakagawa H, Kataoka H, Yasuda S, Koike |
STAT4 gene polymorphism is associated with psoriasis in the genetically homogeneous population of Crete, Greece. Human immunology 2009 Sep 70 (9): 738-41. Zervou Maria I, Goulielmos George N, Castro-Giner Francesc, Tosca Androniki D, Krueger-Krasagakis Sabi |
Association of STAT4 polymorphism with rheumatoid arthritis and systemic lupus erythematosus: a meta-analysis. Molecular biology reports 2010 Jan 37 (1): 141-7. Ji Jong Dae, Lee Won Jin, Kong Kyoung Ae, Woo Jin Hyun, Choi Seong Jae, Lee Young Ho, Song Gwan G |
Association of EBF1, FAM167A(C8orf13)-BLK and TNFSF4 gene variants with primary Sjögren's syndrome. Genes and immunity 2011 Mar 12 (2): 100-9. Nordmark G, Kristjansdottir G, Theander E, Appel S, Eriksson P, Vasaitis L, Kvarnström M, Delaleu N, Lundmark P, Lundmark A, Sjöwall C, Brun J G, Jonsson M V, Harboe E, Gøransson L G, Johnsen S J, Söderkvist P, Eloranta M-L, Alm G, Baecklund E, Wahren-Herlenius M, Omdal R, Rönnblom L, Jonsson R, Syvänen A |
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 |
STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behçet's disease. Human immunology 2010 Jul 71 (7): 723-6. Hu Ke, Yang Peizeng, Jiang Zhengxuan, Hou Shengping, Du Liping, Li Fuzh |
Influence of STAT4 polymorphism in primary Sjögren's syndrome. The Journal of rheumatology 2010 May 37 (5): 1016-9. Palomino-Morales Rogelio J, Diaz-Gallo Lina-Marcela, Witte Torsten, Anaya Juan-Manuel, Martín Javi |
Association of STAT4 polymorphisms with susceptibility to primary membranous glomerulonephritis and renal failure. Clinica chimica acta; international journal of clinical chemistry 2011 Oct 412 (21-22): 1899-904. Chen Shih-Yin, Chen Cheng-Hsu, Huang Yu-Chuen, Chan Chia-Jung, Hsieh Yao-Yuan, Yu Min-Chien, Tsai Chang-Hai, Tsai Fuu-J |
Association of STAT4 rs7574865 polymorphism with autoimmune diseases: a meta-analysis. Molecular biology reports 2012 Sep 39 (9): 8873-82. Liang Ya-Ling, Wu Hua, Shen Xi, Li Pei-Qiang, Yang Xiao-Qing, Liang Li, Tian Wei-Hua, Zhang Li-Feng, Xie Xiao-Do |
Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients. Human immunology 2012 Jul 73 (7): 740-6. Fourati Hajer, Bouzid Dorra, Abida Olfa, Kharrat Najla, Mnif Fatma, Haddouk Samy, Fesel Constantin, Costa João, Ben Ayed Mourad, Abid Mohamed, Rebai Ahmed, Penha-Gonçalves Carlos, Masmoudi Hat |
Meta-analysis reveals an association of STAT4 polymorphisms with systemic autoimmune disorders and anti-dsDNA antibody. Human immunology 2013 Aug 74 (8): 986-92. Zheng Junfeng, Yin Junping, Huang Renliang, Petersen Frank, Yu Xinh |
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome.
Nature genetics 2013 Nov 45 (11): 1284-92. Lessard Christopher J, Li He, Adrianto Indra, Ice John A, Rasmussen Astrid, Grundahl Kiely M, Kelly Jennifer A, Dozmorov Mikhail G, Miceli-Richard Corinne, Bowman Simon, Lester Sue, Eriksson Per, Eloranta Maija-Leena, Brun Johan G, Gøransson Lasse G, Harboe Erna, Guthridge Joel M, Kaufman Kenneth M, Kvarnström Marika, Jazebi Helmi, Cunninghame Graham Deborah S, Grandits Martha E, Nazmul-Hossain Abu N M, Patel Ketan, Adler Adam J, Maier-Moore Jacen S, Farris A Darise, Brennan Michael T, Lessard James A, Chodosh James, Gopalakrishnan Rajaram, Hefner Kimberly S, Houston Glen D, Huang Andrew J W, Hughes Pamela J, Lewis David M, Radfar Lida, Rohrer Michael D, Stone Donald U, Wren Jonathan D, Vyse Timothy J, Gaffney Patrick M, James Judith A, Omdal Roald, Wahren-Herlenius Marie, Illei Gabor G, Witte Torsten, Jonsson Roland, Rischmueller Maureen, Rönnblom Lars, Nordmark Gunnel, Ng Wan-Fai, , Mariette Xavier, Anaya Juan-Manuel, Rhodus Nelson L, Segal Barbara M, Scofield R Hal, Montgomery Courtney G, Harley John B, Sivils Kathy |
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23.
Nature genetics 2013 Nov 45 (11): 1361-5. Li Yongzhe, Zhang Kunlin, Chen Hua, Sun Fei, Xu Juanjuan, Wu Ziyan, Li Ping, Zhang Liuyan, Du Yang, Luan Haixia, Li Xi, Wu Lijun, Li Hongbin, Wu Huaxiang, Li Xiangpei, Li Xiaomei, Zhang Xiao, Gong Lu, Dai Lie, Sun Lingyun, Zuo Xiaoxia, Xu Jianhua, Gong Huiping, Li Zhijun, Tong Shengquan, Wu Min, Li Xiaofeng, Xiao Weiguo, Wang Guochun, Zhu Ping, Shen Min, Liu Shengyun, Zhao Dongbao, Liu Wei, Wang Yi, Huang Cibo, Jiang Quan, Liu Guijian, Liu Bin, Hu Shaoxian, Zhang Wen, Zhang Zhuoli, You Xin, Li Mengtao, Hao Weixin, Zhao Cheng, Leng Xiaomei, Bi Liqi, Wang Yongfu, Zhang Fengxiao, Shi Qun, Qi Wencheng, Zhang Xuewu, Jia Yuan, Su Jinmei, Li Qin, Hou Yong, Wu Qingjun, Xu Dong, Zheng Wenjie, Zhang Miaojia, Wang Qian, Fei Yunyun, Zhang Xuan, Li Jing, Jiang Ying, Tian Xinping, Zhao Lidan, Wang Li, Zhou Bin, Li Yang, Zhao Yan, Zeng Xiaofeng, Ott Jurg, Wang Jing, Zhang Fengch |
Association of GTF2I and GTF2IRD1 polymorphisms with systemic lupus erythematosus in a Chinese Han population. Clinical and experimental rheumatology 2015 Aug . Li Yuan, Li Ping, Chen Si, Wu Ziyan, Li Jing, Zhang Shulan, Cao Chunwei, Wang Li, Liu Bin, Zhang Fengchun, Li Yong Z |
Molecular Genetic Advances in Uveitis. Progress in molecular biology and translational science 2015 134 283-98. Hou Shengping, Kijlstra Aize, Yang Peize |
From Genetic Predisposition to Molecular Mechanisms of Autoimmune Primary Adrenal Insufficiency. Frontiers of hormone research 2016 46 115-32. Falorni Alberto, Brozzetti Annalisa, Perniola Rober |
Meta-analysis of STAT4 and IFIH1 polymorphisms in type 1 diabetes mellitus patients with autoimmune polyglandular syndrome type III. Genetics and molecular research : GMR 2015 14 (4): 17730-8. de Azevêdo Silva J, Tavares N A C, Santos M M S, Moura R, Guimarães R L, Araújo J, Crovella S, Brandão L A |
Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry.
Arthritis & rheumatology (Hoboken, N.J.) 2017 Jan . Taylor Kimberly E, Wong Quenna, Levine David M, McHugh Caitlin, Laurie Cathy, Doheny Kimberly, Lam Mi Y, Baer Alan N, Challacombe Stephen, Lanfranchi Hector, Schiødt Morten, Srinivasan M, Umehara Hisanori, Vivino Frederick B, Zhao Yan, Shiboski Stephen C, Daniels Troy E, Greenspan John S, Shiboski Caroline H, Criswell Lindsey |
Antiphospholipid syndrome's genetic and epigenetic aspects. Autoimmunity reviews 2019 7 18 (9): 102352. Iuliano Annamaria, Galeazzi Mauro, Sebastiani Gian Domeni |
STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren's Syndrome: Association with Disease Susceptibility and Clinical Aspects. Journal of immunology research 2019 2019 7682827. Colafrancesco Serena, Ciccacci Cinzia, Priori Roberta, Latini Andrea, Picarelli Giovanna, Arienzo Francesca, Novelli Giuseppe, Valesini Guido, Perricone Carlo, Borgiani Pao |
Constitutive Activation of Natural Killer Cells in Primary Biliary Cholangitis. Frontiers in immunology 2019 12 10 2633. Hydes Theresa J, Blunt Matthew D, Naftel Jennifer, Vallejo Andres F, Seumois Grégory, Wang Alice, Vijayanand Pandurangan, Polak Marta E, Khakoo Salim |
Common genetic susceptibility loci link PFAPA syndrome, Behçet's disease, and recurrent aphthous stomatitis. Proceedings of the National Academy of Sciences of the United States of America 2020 6 117 (25): 14405-14411. Manthiram Kalpana, Preite Silvia, Dedeoglu Fatma, Demir Selcan, Ozen Seza, Edwards Kathryn M, Lapidus Sivia, Katz Alexander E, , Feder Henry M, Lawton Maranda, Licameli Greg R, Wright Peter F, Le Julie, Barron Karyl S, Ombrello Amanda K, Barham Beverly, Romeo Tina, Jones Anne, Srinivasalu Hemalatha, Mudd Pamela A, DeBiasi Roberta L, Gül Ahmet, Marshall Gary S, Jones Olcay Y, Chandrasekharappa Settara C, Stepanovskiy Yuriy, Ferguson Polly J, Schwartzberg Pamela L, Remmers Elaine F, Kastner Daniel |
A First Step for the Molecular Characterization of Neurological Involvement of Behçet Syndrome: an Italian Pivotal Study. Journal of molecular neuroscience : MN 2020 11 71 (6): 1284-1289. Padula Maria Carmela, Leccese Pietro, Lascaro Nancy, Padula Angela Anna, Carbone Teresa, Martelli Giuseppe, D'Angelo Salvato |
[Predictive significance of genetic analysis of the development of dry eye disease of different origin]. Vestnik oftalmologii 2024 1 139 (6): 13-18. T N Safonova, G V Zaitseva, V I Loginov, A M Burdenn |
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- Page last updated:Apr 22, 2024
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