Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Inflammation and TRIO[original query] |
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| Polymorphisms in the interleukin-4 and IL-4 receptor genes and multiple sclerosis: a study in Spanish-Basque, Northern Irish and Belgian populations. International journal of immunogenetics 2005 Dec 32 (6): 383-8. Suppiah V, Goris A, Alloza I, Heggarty S, Dubois B, Carton H, Antigüedad A, Mendibe M, McDonnell G, Droogan A, Hawkins S, Graham C, Vandenbroeck |
| An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians. BMC medical genetics 2006 7 (): 64. Bugeja Matthew J, Booth David, Bennetts Bruce, Heard Robert, Rubio Justin, Stewart Grae |
| An association between asthma and TNF-308G/A polymorphism: meta-analysis. Journal of human genetics 2006 51 (8): 677-85. Aoki Takeshi, Hirota Tomomitsu, Tamari Mayumi, Ichikawa Kunio, Takeda Kazunori, Arinami Tadao, Shibasaki Masanao, Noguchi Emi |
| The neuropeptide genes TAC1, TAC3, TAC4, VIP and PACAP(ADCYAP1), and susceptibility to multiple sclerosis. Journal of neuroimmunology 2007 Feb 183 (1-2): 208-13. Cunningham Stephen, O'Doherty Catherine, Patterson Chris, McDonnell Gavin, Hawkins Stanley, Marrosu Marria G, Vandenbroeck Ko |
| An investigation of polymorphisms in the 4q1 3.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians. Multiple sclerosis (Houndmills, Basingstoke, England) 2006 Dec 12 (6): 710-22. Bugeja M J, Booth D R, Bennetts B H, Heard R N S, Stewart G |
| Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children. The American journal of gastroenterology 2008 Mar 103 (3): 615-20. Amre Devendra K, Mack David, Israel David, Morgan Kenneth, Lambrette Philippe, Law Liliane, Grimard Guy, Deslandres Colette, Krupoves Alfreda, Bucionis Vytautas, Costea Irina, Bissonauth Vishnee, Feguery Houda, D'Souza Savio, Levy Emile, Seidman Ernest |
| The Kruppel-like factor 6 genotype is associated with fibrosis in nonalcoholic fatty liver disease. Gastroenterology 2008 Jul 135 (1): 282-291.e1. Miele Luca, Beale Gary, Patman Gillian, Nobili Valerio, Leathart Julian, Grieco Antonio, Abate Marilena, Friedman Scott L, Narla Goutham, Bugianesi Elisabetta, Day Christopher P, Reeves Helen |
| Genes implicated in multiple sclerosis pathogenesis from consilience of genotyping and expression profiles in relapse and remission. BMC medical genetics 2008 9 (1): 17. Arthur Ariel T, Armati Patricia J, Bye Chris, , Heard Robert N S, Stewart Graeme J, Pollard John D, Booth David |
| The RETN gene rs1862513 polymorphism as a novel predisposing marker for familial Acne vulgaris in a Pakistani population. Iranian journal of basic medical sciences 2015 May 18 (5): 526-8. Hussain Sabir, Faraz Ahmad, Iqbal Tah |
| Nonalcoholic fatty liver disease risk and histologic severity are associated with genetic polymorphisms in children. Hepatology (Baltimore, Md.) 2022 5 77 (1): 197-212. Goyal Nidhi P, Rosenthal Sara B, Nasamran Chanod, Behling Cynthia A, Angeles Jorge E, Fishbein Mark H, Harlow Kathryn E, Jain Ajay K, Molleston Jean P, Newton Kimberly P, Ugalde-Nicalo Patricia, Xanthankos Stavra A, Yates Katherine, Schork Nicholas J, Fisch Kathleen M, Schwimmer Jeffrey B, |
| A novel pathogenesis concept of biliary atresia approached by combined molecular strategies. PloS one 2022 11 17 (11): e0277334. Laochareonsuk Wison, Surachat Komwit, Chiengkriwate Piyawan, Sangkhathat Suras |
| SEC16A Variants Predispose to Chronic Pancreatitis by Impairing ER-to-Golgi Transport and Inducing ER Stress. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 2024 8 e2402550. Min-Jun Wang, Yuan-Chen Wang, Emmanuelle Masson, Ya-Hui Wang, Dong Yu, Yang-Yang Qian, Xin-Ying Tang, Shun-Jiang Deng, Liang-Hao Hu, Lei Wang, Li-Juan Wang, Vinciane Rebours, David N Cooper, Claude Férec, Zhao-Shen Li, Jian-Min Chen, Wen-Bin Zou, Zhuan Li |
- Page last reviewed:Feb 1, 2024
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