Associated Papers
Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiency.
Abolhassani H et al.
Journal of Human Immunity, 2025
Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.
de Valles-Ibáñez G et al.
Frontiers in Immunology, 2018
29867916 (PubMed )
Supplement: data_sheet_1.PDF
Genetics of common variable immunodeficiency: role of transmembrane activator and calcium modulator and cyclophilin ligand interactor.
Sathkumara HD et al.
International Journal of Immunogenetics, 2015
Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations.
Freiberger T et al.
Human Immunology, 2012
Rare mutations in TNFRSF13B increase the risk of asthma symptoms in Swedish children.
Janzi M et al.
Genes and Immunity, 2012
Functional analysis of transmembrane activator and calcium-modulating cyclophilin ligand interactor (TACI) mutations associated with common variable immunodeficiency.
Fried AJ et al.
The Journal of Allergy and Clinical Immunology, 2011
Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiency.
Mohammadi J et al.
Journal of Clinical Immunology, 2009
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.
Salzer U et al.
Blood, 2009
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