Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Common Variable Immunodeficiency and ICOS[original query] |
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| The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency. Genes and immunity 2009 Mar 10 (2): 151-61. Haimila K, Einarsdottir E, de Kauwe A, Koskinen L L E, Pan-Hammarström Q, Kaartinen T, Kurppa K, Ziberna F, Not T, Vatta S, Ventura A, Korponay-Szabo I R, Adány R, Pocsai Z, Széles G, Dukes E, Kaukinen K, Mäki M, Koskinen S, Partanen J, Hammarström L, Saavalainen |
| Evaluation of CARMA1/CARD11 and Bob1 as candidate genes in common variable immunodeficiency. Journal of investigational allergology & clinical immunology 2011 21 (5): 348-53. Tampella G, Baronio M, Vitali M, Soresina A, Badolato R, Giliani S, Plebani A, Lougaris |
| Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency. Journal of clinical immunology 2012 Dec 32 (6): 1165-79. Kutukculer Necil, Gulez Nesrin, Karaca Neslihan E, Aksu Guzide, Berdeli Af |
| Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders. Clinical immunology (Orlando, Fla.) 2015 Oct 160 (2): 301-14. van Schouwenburg Pauline A, Davenport Emma E, Kienzler Anne-Kathrin, Marwah Ishita, Wright Benjamin, Lucas Mary, Malinauskas Tomas, Martin Hilary C, , Lockstone Helen E, Cazier Jean-Baptiste, Chapel Helen M, Knight Julian C, Patel Smita |
| The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID). Scientific reports 2021 Apr 11 (1): 8308. Bisgin Atil, Sonmezler Ozge, Boga Ibrahim, Yilmaz Musta |
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