Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: IRAK2[original query] |
---|
The role of polymorphisms in Toll-like receptors and their associated intracellular signaling genes in measles vaccine immunity. Human genetics 2011 Oct 130 (4): 547-61. Ovsyannikova Inna G, Haralambieva Iana H, Vierkant Robert A, Pankratz V Shane, Jacobson Robert M, Poland Gregory |
Effects of endotoxin exposure on childhood asthma risk are modified by a genetic polymorphism in ACAA1. BMC medical genetics 2011 12 (1): 158. Sordillo Joanne E, Sharma Sunita, Poon Audrey, Lasky-Su Jessica, Belanger Kathleen, Milton Donald K, Bracken Michael B, Triche Elizabeth W, Leaderer Brian P, Gold Diane R, Litonjua Augusto |
Genetic polymorphisms associated with carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study. Physiological genomics 2013 Jan 45 (2): 79-88. Miller Virginia M, Petterson Tanya M, Jeavons Elysia N, Lnu Abhinita S, Rider David N, Heit John A, Cunningham Julie M, Huggins Gordon S, Hodis Howard N, Budoff Matthew J, Santoro Nanette, Hopkins Paul N, Lobo Rogerio A, Manson JoAnn E, Naftolin Frederick, Taylor Hugh S, Harman S Mitchell, de Andrade Mari |
A prominent role for the IL1 pathway and IL15 in susceptibility to chronic cavitary pulmonary aspergillosis. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 2014 Aug 20 (8): O480-8. Smith N L D, Hankinson J, Simpson A, Bowyer P, Denning D |
A coding IRAK2 protein variant compromises Toll-like receptor (TLR) signaling and is associated with colorectal cancer survival. The Journal of biological chemistry 2014 Aug 289 (33): 23123-31. Wang Hui, Flannery Sinead M, Dickhöfer Sabine, Huhn Stefanie, George Julie, Kubarenko Andriy V, Lascorz Jesus, Bevier Melanie, Willemsen Joschka, Pichulik Tica, Schafmayer Clemens, Binder Marco, Manoury Bénédicte, Paludan Søren R, Alarcon-Riquelme Marta, Bowie Andrew G, Försti Asta, Weber Alexander N |
Mutations in TLR/MYD88 pathway identify a subset of young chronic lymphocytic leukemia patients with favorable outcome. Blood 2014 Jun 123 (24): 3790-6. Martínez-Trillos Alejandra, Pinyol Magda, Navarro Alba, Aymerich Marta, Jares Pedro, Juan Manel, Rozman María, Colomer Dolors, Delgado Julio, Giné Eva, González-Díaz Marcos, Hernández-Rivas Jesús M, Colado Enrique, Rayón Consolación, Payer Angel R, Terol Maria José, Navarro Blanca, Quesada Victor, Puente Xosé S, Rozman Ciril, López-Otín Carlos, Campo Elías, López-Guillermo Armando, Villamor Ne |
Interleukin-1 receptor-associated kinase-2 genetic variant rs708035 increases NF-?B activity through promoting TRAF6 ubiquitination. The Journal of biological chemistry 2014 May 289 (18): 12507-19. Zhang Weina, He Tao, Wang Qiong, Li Xin, Wei Jianming, Hou Xiaoqiang, Zhang Bin, Huang Lei, Wang |
A frequent hypofunctional IRAK2 variant is associated with reduced spontaneous hepatitis C virus clearance. Hepatology (Baltimore, Md.) 2015 Aug . Wang Hui, El Maadidi Souhayla, Fischer Janett, Grabski Elena, Dickhöfer Sabine, Klimosch Sascha, Flannery Sinead M, Filomena Angela, Wolz Olaf-Oliver, Schneiderhan-Marra Nicole, Löffler Markus W, Wiese Manfred, Pichulik Tica, Müllhaupt Beat, Semela David, Dufour Jean-François, , Bochud Pierre-Yves, Bowie Andrew G, Kalinke Ulrich, Berg Thomas, Weber Alexander N |
Genome-wide association study of sepsis in extremely premature infants.
Archives of disease in childhood. Fetal and neonatal edition 2017 Mar . Srinivasan Lakshmi, Page Grier, Kirpalani Haresh, Murray Jeffrey C, Das Abhik, Higgins Rosemary D, Carlo Waldemar A, Bell Edward F, Goldberg Ronald N, Schibler Kurt, Sood Beena G, Stevenson David K, Stoll Barbara J, Van Meurs Krisa P, Johnson Karen J, Levy Joshua, McDonald Scott A, Zaterka-Baxter Kristin M, Kennedy Kathleen A, Sánchez Pablo J, Duara Shahnaz, Walsh Michele C, Shankaran Seetha, Wynn James L, Cotten C Michael, |
IRAK2 is associated with susceptibility to rheumatoid arthritis. Clinical rheumatology 2017 Nov . Hassine Hana Ben, Sghiri Rim, Chabchoub Elyes, Boumiza Asma, Slama Foued, Baccouche Khadija, Shakoor Zahid, Almogren Adel, Mariaselvam Christina, Tamouza Ryad, Bouajina Elyes, Zemni Ram |
Genetic variant of IRAK2 in the toll-like receptor signaling pathway and survival of non-small cell lung cancer. International journal of cancer 2018 Jul . Xu Yinghui, Liu Hongliang, Liu Shun, Wang Yanru, Xie Jichun, Stinchcombe Thomas E, Su Li, Zhang Ruyang, Christiani David C, Li Wei, Wei Qing |
IRAK2 and TLR10 confer risk of Hashimoto's disease: a genetic association study based on the Han Chinese population. Journal of human genetics 2019 May . Li Miao, Han Wei, Zhu Li, Jiang Jue, Qu Wei, Zhang Lei, Jia Liang, Zhou |
IRAK2 is associated with systemic lupus erythematosus risk. Clinical rheumatology 2019 Oct . Boumiza Asma, Zemni Ramzi, Sghiri Rim, Idriss Nadia, Hassine Hana Ben, Chabchoub Elyes, Mzabi Anis, Ghannouchi Neirouz, Bouajina Elyes, Ben Hadj Slama Fou |
Role of the Host Genetic Susceptibility to 2009 Pandemic Influenza A H1N1. Viruses 2021 3 13 (2): . Pérez-Rubio Gloria, Ponce-Gallegos Marco Antonio, Domínguez-Mazzocco Bruno André, Ponce-Gallegos Jaime, García-Ramírez Román Alejandro, Falfán-Valencia Ramc |
Polygenic Innate Immunity Score to Predict the Risk of Cytomegalovirus Infection in CMV D+/R- Transplant Recipients. A Prospective Multicenter Cohort Study. Frontiers in immunology 2022 13 897912. Bodro Marta, Cervera Carlos, Linares Laura, Suárez Belén, Llopis Jaume, Sanclemente Gemma, Casadó-Llombart Sergi, Fernández-Ruiz Mario, Fariñas María Carmen, Cantisan Sara, Montejo Miguel, Cordero Elisa, Oriol Isabel, Marcos María Angeles, Lozano Francisco, Moreno Asunción, |
Multi-locus SNP analyses of interleukin 1 receptor associated kinases 2 gene polymorphisms with the susceptibility to rheumatoid arthritis. PloS one 2022 17 (5): e0268496. Ghouri Maham, Ismail Muhammad, Zaidi Syeda Areesha, Rehman Shafique, Dahani Asadullah, Saleem Saima, Zehra Sitw |
Implication of genetic variants in primary microRNA processing sites in the risk of multiple sclerosis. EBioMedicine 2022 5 80 104052. Hecker Michael, Fitzner Brit, Putscher Elena, Schwartz Margit, Winkelmann Alexander, Meister Stefanie, Dudesek Ales, Koczan Dirk, Lorenz Peter, Boxberger Nina, Zettl Uwe Kla |
Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families. Scientific reports 2023 9 13 (1): 14978. Prashantha Hebbar, Rasheeba Nizam, Sumi Elsa John, Dinu Antony, Mohammad Dashti, Arshad Channanath, Azza Shaltout, Hessa Al-Khandari, Heikki A Koistinen, Jaakko Tuomilehto, Osama Alsmadi, Thangavel Alphonse Thanaraj, Fahd Al-Mul |
Hyperfunction variant rs708035 of interleukin 1 receptor-associated kinases 2 gene involved in the predisposition of leprosy infection. The journal of gene medicine 2023 1 e3473. Saleem Saima, Zia Mutaher, Siddiqui Farhatulain, Ghouri Maham, Kulsoom Ume, Kawal Sidra, Fatima Sehrish, Zehra Sitw |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: