HuGE Literature Finder
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| Diagnostic Rate of Autoinflammatory Diseases Evaluated by Fever Patterns in Pediatric- and Adult-Onset Patients. Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases 2020 Mar 26 (2): 60-62. Miyamae Takako, Hanaya Aki, Kawamoto Manabu, Tani Yumi, Kawaguchi Yasushi, Yamanaka Hisas |
| TNFAIP3, TNIP1, and MyD88 Polymorphisms Predict Septic-Shock-Related Death in Patients Who Underwent Major Surgery. Journal of clinical medicine 2019 Feb 8 (3): . Jiménez-Sousa Maria Ángeles, Fadrique Alejandra, Liu Pilar, Fernández-Rodríguez Amanda, Lorenzo-López Mario, Gómez-Sánchez Esther, Gómez-Sanz Alicia, Heredia-Rodríguez María, Gómez-Pesquera Estefanía, Martínez Isidoro, Tamayo Eduardo, Resino Salvad |
| SNP variations in IL10, TNFa and TNFAIP3 genes in patients with dry eye syndrome and Sjogren's syndrome. Journal of inflammation (London, England) 2019 16 6. Ben-Eli Hadas, Gomel Nir, Aframian Doron Jacob, Abu-Seir Rania, Perlman Riki, Ben-Chetrit Eldad, Mevorach Dror, Kleinstern Geffen, Paltiel Ora, Solomon Abrah |
| Genetics in Sjögren Syndrome. Rheumatic diseases clinics of North America 2016 Aug 42 (3): 435-47. Reksten Tove Ragna, Lessard Christopher J, Sivils Kathy |
| Downstream activation of NF-?B in the EDA-A1/EDAR signalling in Sjögren's syndrome and its regulation by the ubiquitin-editing enzyme A20. Clinical and experimental immunology 2016 Jan . Sisto Margherita, Barca Amilcare, Lofrumento Dario Domenico, Lisi Sabri |
| Germline variation of TNFAIP3 in primary Sjögren's syndrome-associated lymphoma. Annals of the rheumatic diseases 2015 Sep . Nocturne Gaetane, Tarn Jessica, Boudaoud Saida, Locke James, Miceli-Richard Corinne, Hachulla Eric, Dubost Jean-Jacques, Bowman Simon, Gottenberg Jacques-Eric, Criswell Lindsey A, Lessard Christopher J, Sivils Kathy L, Carapito Raphael, Bahram Siamak, Seror Raphaèle, Ng Wan-Fai, Mariette Xavi |
| Polymorphisms of TNFAIP3 gene in a Chinese Han population with fuchs heterochromic iridocyclitis. Ophthalmic genetics 2014 Jun 35 (2): 63-7. Li Hong, Hou Shengping, Du Liping, Zhou Qingyun, Kijlstra Aize, Liu Qi |
| Functional effect of polymorphisms in the promoter of TNFAIP3 (A20) in acute pancreatitis in the Han Chinese population. PloS one 2014 9 (7): e103104. Liu Yugang, Dan Gang, Wu Lijuan, Chen Guangyu, Wu Ailin, Zeng Ping, Xu Wanqi |
| Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease. PloS one 2014 9 (11): e112171. Cabrera Sonia, Sanchez Elena, Requena Teresa, Martinez-Bueno Manuel, Benitez Jesus, Perez Nicolas, Trinidad Gabriel, Soto-Varela Andrés, Santos-Perez Sofía, Martin-Sanz Eduardo, Fraile Jesus, Perez Paz, Alarcon-Riquelme Marta E, Batuecas Angel, Espinosa-Sanchez Juan M, Aran Ismael, Lopez-Escamez Jose |
| Germline and somatic genetic variations of TNFAIP3 in lymphoma complicating primary Sjogren's syndrome. Blood 2013 Dec 122 (25): 4068-76. Nocturne Gaetane, Boudaoud Saida, Miceli-Richard Corinne, Viengchareun Say, Lazure Thierry, Nititham Joanne, Taylor Kimberly E, Ma Averil, Busato Florence, Melki Judith, Lessard Christopher J, Sivils Kathy L, Dubost Jean-Jacques, Hachulla Eric, Gottenberg Jacques Eric, Lombès Marc, Tost Jorg, Criswell Lindsey A, Mariette Xavi |
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 genes in the NF-?B pathway with antibody-positive primary Sjögren's syndrome. Scandinavian journal of immunology 2013 Nov 78 (5): 447-54. Nordmark Gunnel, Wang Chuan, Vasaitis Lilian, Eriksson Per, Theander Elke, Kvarnström Marika, Forsblad-d'Elia Helena, Jazebi Helmi, Sjöwall Christopher, Reksten Tove Ragna, Brun Johan G, Jonsson Malin V, Johnsen Svein J, Wahren-Herlenius Marie, Omdal Roald, Jonsson Roland, Bowman Simon, Ng Wan-Fai, Eloranta Maija-Leena, Syvänen Ann-Christine, |
| 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 |
| Association studies of TNFSF4, TNFAIP3 and FAM167A-BLK polymorphisms with primary Sjogren's syndrome in Han Chinese. Journal of human genetics 2013 Jul 58 (7): 475-9. Sun Fei, Li Ping, Chen Hua, Wu Ziyan, Xu Juanjuan, Shen Min, Leng Xiaomei, Shi Qun, Zhang Wen, Tian Xinping, Li Yongzhe, Zhang Fengch |
| Multiple sclerosis risk genotypes correlate with an elevated cerebrospinal fluid level of the suggested prognostic marker CXCL13. Multiple sclerosis (Houndmills, Basingstoke, England) 2013 Jun 19 (7): 863-70. Lindén M, Khademi M, Lima Bomfim I, Piehl F, Jagodic M, Kockum I, Olsson |
| TNFAIP3 gene polymorphisms in a Chinese Han population with Vogt-Koyanagi-Harada syndrome. PloS one 2013 8 (3): e59515. Li Hong, Liu Qing, Hou Shengping, Du Liping, Zhou Qingyun, Zhou Yan, Kijlstra Aize, Yang Peize |
| Sequencing of TNFAIP3 and association of variants with multiple autoimmune diseases. Genes and immunity 2011 Apr 12 (3): 176-82. Musone S L, Taylor K E, Nititham J, Chu C, Poon A, Liao W, Lam E T, Ma A, Kwok P-Y, Criswell L |
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