Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Common Variable Immunodeficiency and TNFRSF13C[original query] |
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Mutational analysis of human BAFF receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency. Journal of clinical immunology 2005 Sep 25 (5): 496-502. Losi Claretta Gioia, Silini Antonietta, Fiorini Claudia, Soresina Annarosa, Meini Antonella, Ferrari Simona, Notarangelo Luigi D, Lougaris Vassilios, Plebani Alessand |
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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