Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans

By U. Salzer, H. Chapel, A. Webster, Q. Pan-Hammarström, Annette Schmitt-Graeff, M. Schlesier, H. Peter, J. Rockstroh, P. Schneider, Alejandro A. Schäffer and 2 more. Nature Genetics, 2005

690 citations recorded by the source corpus.

Subfields: Cancer Research, Genetics, Immunology

View Paper: https://www.semanticscholar.org/paper/727edf03816518e0ebe482d7bd56ea59422d2c4f

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In Cancer Research

1. A. Cerutti

In Immunology

1. F. Mackay
2. A. Cerutti

Citations in the corpus

• Cracking the BAFF code (2009, background): “Because more than one receptor is required to transmit the signal, the system is susceptible to dominant effects of mutations, as is probably the case in patients with common variable immunodeficiency (CVID) harbouring heterozygous TACI mutation”
• The regulation of IgA class switching (2008, background): “TNFRSF13b mutations also cause common variable immunodeficiency, which is associated with pan-hypogammaglobulinaemi”