Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Arthritis and TNFSF13B[original query] |
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Analysis on the association of human BLYS (BAFF, TNFSF13B) polymorphisms with systemic lupus erythematosus and rheumatoid arthritis. Genes and immunity 2002 Nov 3 (7): 424-9. Kawasaki A, Tsuchiya N, Fukazawa T, Hashimoto H, Tokunaga |
Variants of genes implicated in type 1 interferon pathway and B-cell activation modulate the EULAR response to rituximab at 24 weeks in rheumatoid arthritis. RMD open 2017 10 3 (2): e000448. Juge Pierre-Antoine, Gazal Steven, Constantin Arnaud, Mariette Xavier, Combe Bernard, Tebib Jacques, Dougados Maxime, Sibilia Jean, Le Loet Xavier, Dieudé Philip |
Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus. Scientific reports 2018 May 8 (1): 8195. González-Serna David, Ortiz-Fernández Lourdes, Vargas Sofía, García Antonio, Raya Enrique, Fernández-Gutierrez Benjamín, López-Longo Francisco Javier, Balsa Alejandro, González-Álvaro Isidoro, Narvaez Javier, Gómez-Vaquero Carmen, Sabio José Mario, García-Portales Rosa, González-Escribano María Francisca, Tolosa Carles, Carreira Patricia, Kiemeney Lambertus, Coenen Marieke J H, Witte Torsten, Schneider Matthias, González-Gay Miguel Ángel, Martín Javi |
A TNFSF13B functional variant is not involved in systemic sclerosis and giant cell arteritis susceptibility. PloS one 2018 13 (12): e0209343. González-Serna David, Carmona Elio G, Ortego-Centeno Norberto, Simeón Carmen P, Solans Roser, Hernández-Rodríguez José, Tolosa Carlos, Castañeda Santos, Narváez Javier, Martinez-Valle Ferran, , , Witte Torsten, Neumann Thomas, Holle Julia, Beretta Lorenzo, Boiardi Luigi, Emmi Giacomo, Cimmino Marco A, Vaglio Augusto, Herrick Ariane L, Denton Christopher P, Salvarani Carlo, Cid María C, Morgan Ann W, Fonseca Carmen, González-Gay Miguel A, Martín Javier, Márquez A |
Analysis of TNFSF13B polymorphisms and BAFF expression in rheumatoid arthritis and primary Sjögren's syndrome patients. Molecular genetics & genomic medicine 2022 4 10 (6): e1950. Santillán-López Enrique, Muñoz-Valle José Francisco, Oregon-Romero Edith, Espinoza-García Noemí, Treviño-Talavera Beatriz Alejandra, Salazar-Camarena Diana Celeste, Marín-Rosales Miguel, Cruz Alvaro, Alvarez-Gómez Jhonatan Antonio, Sagrero-Fabela Nefertari, Cerpa-Cruz Sergio, Palafox-Sánchez Claudia Azuce |
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- Page last updated:Apr 22, 2024
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