Associated Papers
Re-evaluation of the contribution of TNFRSF13B variants to antibody deficiency.
Abolhassani H et al.
Journal of Human Immunity, 2025
Charge-based immunoreceptor signalling in health and disease.
Shi X et al.
Nature Reviews. Immunology, 2025
Genetics and clinical phenotypes in common variable immunodeficiency.
Cunningham-Rundles C et al.
Frontiers in Genetics, 2023
38274105 (PubMed )
Supplement: DataSheet1.PDF
TNFRSF13B genotypes control immune-mediated pathology by regulating the functions of innate B cells.
de Mattos Barbosa MG et al.
Jci Insight, 2021
TACI Mutations in Primary Antibody Deficiencies: A Nationwide Study in Greece.
Kakkas I et al.
Medicina (kaunas, Lithuania), 2021
Current genetic landscape in common variable immune deficiency.
Abolhassani H et al.
Blood, 2020
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
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
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
An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene.
Sazzini M et al.
Genes and Immunity, 2009
Select a paper to view details