Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Memory and TNFRSF13B[original query] |
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| Lymphocyte characteristics in children with common variable immunodeficiency. Clinical immunology (Orlando, Fla.) 2010 Apr 135 (1): 63-71. van de Ven Annick A J M, van de Corput Lisette, van Tilburg Cornelis M, Tesselaar Kiki, van Gent Rogier, Sanders Elisabeth A M, Boes Marianne, Bloem Andries C, van Montfrans Joris |
| Phenotypic and clinical heterogeneity associated with monoallelic TNFRSF13B-A181E mutations in common variable immunodeficiency. Human immunology 2010 May 71 (5): 505-11. Dong Xiangyang, Hoeltzle Michelle V, Hagan John B, Park Miguel A, Li James T, Abraham Roshini |
| 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 |
| TNF receptor superfamily member 13b (TNFRSF13B) hemizygosity reveals transmembrane activator and CAML interactor haploinsufficiency at later stages of B-cell development. The Journal of allergy and clinical immunology 2015 Jun . Romberg Neil, Virdee Manmeet, Chamberlain Nicolas, Oe Tyler, Schickel Jean-Nicolas, Perkins Tiffany, Cantaert Tineke, Rachid Rima, Rosengren Sally, Palazzo Regina, Geha Raif, Cunningham-Rundles Charlotte, Meffre Er |
| Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes. Journal of immunology research 2016 2016 8390356. Pulvirenti Federica, Zuntini Roberta, Milito Cinzia, Specchia Fernando, Spadaro Giuseppe, Danieli Maria Giovanna, Pession Andrea, Quinti Isabella, Ferrari Simo |
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- Page last updated:Jun 02, 2023
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