Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Syndrome and TREX1[original query] |
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| Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort. Genes and immunity 2011 Jun 12 (4): 270-9. Namjou B, Kothari P H, Kelly J A, Glenn S B, Ojwang J O, Adler A, Alarcón-Riquelme M E, Gallant C J, Boackle S A, Criswell L A, Kimberly R P, Brown E, Edberg J, Stevens A M, Jacob C O, Tsao B P, Gilkeson G S, Kamen D L, Merrill J T, Petri M, Goldman R R, Vila L M, Anaya J-M, Niewold T B, Martin J, Pons-Estel B A, Sabio J M, Callejas J L, Vyse T J, Bae S-C, Perrino F W, Freedman B I, Scofield R H, Moser K L, Gaffney P M, James J A, Langefeld C D, Kaufman K M, Harley J B, Atkinson J |
| Rare variants in the TREX1 gene and susceptibility to autoimmune diseases. BioMed research international 2013 2013 471703. Barizzone Nadia, Monti Sara, Mellone Simona, Godi Michela, Marchini Maurizio, Scorza Raffaella, Danieli Maria G, D'Alfonso Sand |
| Typing TREX1 gene in patients with systemic lupus erythematosus. Reumatismo 2015 67 (1): 1-7. Fredi M, Bianchi M, Andreoli L, Greco G, Olivieri I, Orcesi S, Fazzi E, Cereda C, Tincani |
| Genetic contributors and soluble mediators in prediction of autoimmune comorbidity. Journal of autoimmunity 2019 8 104 102317. Nezos Adrianos, Evangelopoulos Maria-Eleutheria, Mavragani Clio |
| TREX1 variants in Sjogren's syndrome related lymphomagenesis. Cytokine 2019 Jul 154781. Nezos Adrianos, Makri Panagiota, Gandolfo Saviana, De Vita Salvatore, Voulgarelis Michael, Crow Mary K, Mavragani Clio |
| Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review. Journal of clinical medicine 2019 5 8 (5): . Garau Jessica, Cavallera Vanessa, Valente Marialuisa, Tonduti Davide, Sproviero Daisy, Zucca Susanna, Battaglia Domenica, Battini Roberta, Bertini Enrico, Cappanera Silvia, Chiapparini Luisa, Crasà Camilla, Crichiutti Giovanni, Dalla Giustina Elvio, D'Arrigo Stefano, De Giorgis Valentina, De Simone Micaela, Galli Jessica, La Piana Roberta, Messana Tullio, Moroni Isabella, Nardocci Nardo, Panteghini Celeste, Parazzini Cecilia, Pichiecchio Anna, Pini Antonella, Ricci Federica, Saletti Veronica, Salvatici Elisabetta, Santorelli Filippo M, Sartori Stefano, Tinelli Francesca, Uggetti Carla, Veneselli Edvige, Zorzi Giovanna, Garavaglia Barbara, Fazzi Elisa, Orcesi Simona, Cereda Cristi |
| Genetic Study of Cerebral Small Vessel Disease in Chinese Han Population. Frontiers in neurology 2022 4 13 829438. Wang Yunchao, Shi Changhe, Li Yusheng, Yu Wenkai, Wei Sen, Fan Yu, Mao Chengyuan, Yang Zhihua, Yu Lulu, Zhao Zichen, Li Shanshan, Gao Yuan, Xu Yumi |
| New insights on familial colorectal cancer type X syndrome. Scientific reports 2022 2 12 (1): 2846. Garcia Felipe Antonio de Oliveira, de Andrade Edilene Santos, de Campos Reis Galvão Henrique, da Silva Sábato Cristina, Campacci Natália, de Paula Andre Escremin, Evangelista Adriane Feijó, Santana Iara Viana Vidigal, Melendez Matias Eliseo, Reis Rui Manuel, Palmero Edenir In |
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