Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Syndrome and TNIP1[original query] |
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| 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 of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese. PloS one 2014 9 (5): e95573. Shi Yanyun, Jia Yading, Hou Shengping, Fang Jing, Zhou Yan, Kijlstra Aize, Yang Peize |
| 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 |
| 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 |
| Genetics in Sjögren Syndrome. Rheumatic diseases clinics of North America 2016 Aug 42 (3): 435-47. Reksten Tove Ragna, Lessard Christopher J, Sivils Kathy |
| 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 |
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