Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Syndrome and MYD88[original query] |
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| TIRAP (MAL) S180L polymorphism is a common protective factor against developing tuberculosis and systemic lupus erythematosus. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2008 Sep 8 (5): 541-4. Castiblanco John, Varela Diana-Cristina, Castaño-Rodríguez Natalia, Rojas-Villarraga Adriana, Hincapié María-Eugenia, Anaya Juan-Manu |
| Absence of somatic MYD88 L265P mutations in patients with primary Sjogren's syndrome. Genes and immunity 2014 Jan 15 (1): 54-6. Voulgarelis M, Mavragani C P, Xu L, Treon S P, Moutsopoulos H |
| Somatic mutations in MYD88 and CXCR4 are determinants of clinical presentation and overall survival in Waldenstrom macroglobulinemia. Blood 2014 May 123 (18): 2791-6. Treon Steven P, Cao Yang, Xu Lian, Yang Guang, Liu Xia, Hunter Zachary |
| Association of Polymorphisms in IRAK1, IRAK4 and MyD88, and Severe Invasive Pneumococcal Disease. The Pediatric infectious disease journal 2015 Sep 34 (9): 1008-13. Carrasco-Colom Jaume, Jordan Iolanda, Alsina Laia, Garcia-Garcia Juan-José, Cambra-Lasaosa Francisco José, Martín-Mateos María Anunciación, Juan Manel, Muñoz-Almagro Carm |
| Paediatric obstructive sleep apnoea syndrome (OSAS) is associated with tonsil colonisation by Streptococcus pyogenes. Scientific reports 2016 6 20609. Viciani Elisa, Montagnani Francesca, Tavarini Simona, Tordini Giacinta, Maccari Silvia, Morandi Matteo, Faenzi Elisa, Biagini Cesare, Romano Antonio, Salerni Lorenzo, Finco Oretta, Lazzi Stefano, Ruggiero Paolo, De Luca Andrea, Barocchi Michèle A, Manetti Andrea G |
| Two Genetic Variations in the IRF8 region are associated with Behçet's disease in Han Chinese. Scientific reports 2016 6 19651. Jiang Yanni, Wang Hong, Yu Hongsong, Li Lin, Xu Dengfeng, Hou Shengping, Kijlstra Aize, Yang Peize |
| MYD88 mutation status does not impact overall survival in Waldenström macroglobulinemia. American journal of hematology 2017 10 93 (2): 187-194. Abeykoon Jithma P, Paludo Jonas, King Rebecca L, Ansell Stephen M, Gertz Morie A, LaPlant Betsy R, Halvorson Alese E, Gonsalves Wilson I, Dingli David, Fang Hong, Rajkumar S Vincent, Lacy Martha Q, He Rong, Kourelis Taxiarchis, Reeder Craig B, Novak Anne J, McPhail Ellen D, Viswanatha David S, Witzig Thomas E, Go Ronald S, Habermann Thomas M, Buadi Francis K, Dispenzieri Angela, Leung Nelson, Lin Yi, Thompson Carrie A, Hayman Suzanne R, Kyle Robert A, Kumar Shaji K, Kapoor Prasha |
| Polymorphisms in the myeloid differentiation primary response 88 pathway do not explain low expression levels in sudden infant death syndrome. Acta paediatrica (Oslo, Norway : 1992) 2019 Jul 108 (7): 1262-1266. Bjørnvall Christina Dybdrodt, Opdal Siri H, Rognum Torleiv O, Ferrante Lin |
| Exploratory Study of MYD88 L265P, Rare NLRP3 Variants, and Clonal Hematopoiesis Prevalence in Patients With Schnitzler Syndrome. Arthritis & rheumatology (Hoboken, N.J.) 2019 7 71 (12): 2121-2125. Pathak Shelly, Rowczenio Dorota M, Owen Roger G, Doody Gina M, Newton Darren J, Taylor Claire, Taylor Jan, Cargo Catherine, Hawkins Philip N, Krause Karoline, Lachmann Helen J, Savic Sini |
| TLR4/NF-?B signaling pathway gene single nucleotide polymorphisms alter gene expression levels and affect ARDS occurrence and prognosis outcomes. Medicine 2019 Jun 98 (26): e16029. Ding Yueping, Feng Qijia, Chen Jianshi, Song J |
| 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 |
| Variations within Toll-like receptor (TLR) and TLR signaling pathway-related genes and their synergistic effects on the risk of Guillain-Barré syndrome. Journal of the peripheral nervous system : JPNS 2022 Feb . Dutta Debprasad, Nagappa Madhu, Sreekumaran Nair Binu V, Das Sumit Kumar, Wahatule Rahul, Sinha Sanjib, Vasanthapuram Ravi, Taly Arun B, Debnath Monoj |
| Liquid Biopsies for Circulating Tumor DNA Detection May Reveal Occult Hematologic Malignancies in Patients With Solid Tumors. JCO precision oncology 2023 3 7 e2200583. Aldea Mihaela, Tagliamento Marco, Bayle Arnaud, Vasseur Damien, Vergé Véronique, Marinello Arianna, Danlos François-Xavier, Blanc-Durand Felix, Bernard Elsa, Cerbone Luigi, Mosele Maria Fernanda, Renneville Aline, Hadoux Julien, Loriot Yohann, Sakkal Madona, Vozy Aurore, Sarkozy Clementine, Smolenschi Cristina, Nicotra Claudio, Martin-Romano Patricia, Boccon-Gibod Clementine, Habza Wafikaamira, Lazarovici Julien, Ponce Santiago, Hollebecque Antoine, Marzac Christophe, Lacroix Ludovic, Barlesi Fabrice, André Fabrice, Besse Benjamin, Rouleau Etienne, Italiano Antoine, Micol Jean-Baptis |
| Ibrutinib and venetoclax as primary therapy in symptomatic treatment naïve Waldenström macroglobulinemia. Blood 2023 11 . Jorge J Castillo, Andrew R Branagan, David Sermer, Catherine Flynn, Kirsten E Meid, Megan Little, Katherine Stockman, Timothy P White, Alexa G Canning, Maria Luisa Guerrera, Amanda Kofides, Shirong Liu, Xia Liu, Kris Richardson, Nicholas Tsakmaklis, Christopher J Patterson, Zachary R Hunter, Steven P Treon, Shayna Sarosi |
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