Associated Papers
Common Variable Immunodeficiency Clinical Manifestations Are Shaped by Presence and Type of Heterozygous NFKB1 Variants.
Yin J et al.
The Journal of Allergy and Clinical Immunology. in Practice, 2025
Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50.
Fliegauf M et al.
Frontiers in Immunology, 2022
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
Li J et al.
The Journal of Experimental Medicine, 2021
34473196 (PubMed )
Supplement: JEM_20210566_TableS1.xlsx › Table_S1
Histaminergic transmission slows progression of amyotrophic lateral sclerosis.
Apolloni S et al.
Journal of Cachexia, Sarcopenia and Muscle, 2019
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.
Tuijnenburg P et al.
The Journal of Allergy and Clinical Immunology, 2018
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