B cell expansion with NF-κB and T cell anergy (BENTA) is a rare primary immunodeficiency disorder caused by gain-of-function (GOF) mutations in the CARD11 gene. Affected patients present with persistent B cell lymphocytosis in early childhood paired with lymphadenopathy and splenomegaly. Until now only six activating mutations from 14 patients have been reported in CARD11. Here we report a patient from China with polyclonal B cell lymphocytosis and frequent infections in early life. A heterozygous mutation (c.377G>A, G126D) in exon 5 of CARD11 gene (NM_032415) was identified by whole exome sequencing. In vitro functional studies showed that the G126D mutation is associated with increased expression of CARD11 and NF-κB activation in Hela ...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
B cell expansion with NF-κB and T cell anergy (BENTA) is a rare primary immunodeficiency disorder ca...
Germline gain-of-function mutations in CARD11 lead to the primary immunodeficiency, B cell expansion...
CARD11 is a lymphocyte-specific scaffold molecule required for proper activation of B- and T-cells i...
CARD11 is a lymphocyte-specific scaffold molecule required for proper activation of B- and T-cells i...
The antigen receptors of lymphocytes are coupled to signaling pathways which are essential for B cel...
Thesis (Ph.D.)--University of Washington, 2018Gain of function mutations in key signaling molecules ...
CARD11 encodes a scaffold protein in lymphocytes that links antigen receptor engagement with downstr...
Tight regulation of lymphocytes is critical for sustaining human health and prevention of infectious...
Background Caspase activation and recruitment domain 11 (CARD11) encodes a scaffold protein in ly...
BACKGROUND: Profound combined immunodeficiency can present with normal numbers of T and B cells, and...
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by antibody defici...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
B cell expansion with NF-κB and T cell anergy (BENTA) is a rare primary immunodeficiency disorder ca...
Germline gain-of-function mutations in CARD11 lead to the primary immunodeficiency, B cell expansion...
CARD11 is a lymphocyte-specific scaffold molecule required for proper activation of B- and T-cells i...
CARD11 is a lymphocyte-specific scaffold molecule required for proper activation of B- and T-cells i...
The antigen receptors of lymphocytes are coupled to signaling pathways which are essential for B cel...
Thesis (Ph.D.)--University of Washington, 2018Gain of function mutations in key signaling molecules ...
CARD11 encodes a scaffold protein in lymphocytes that links antigen receptor engagement with downstr...
Tight regulation of lymphocytes is critical for sustaining human health and prevention of infectious...
Background Caspase activation and recruitment domain 11 (CARD11) encodes a scaffold protein in ly...
BACKGROUND: Profound combined immunodeficiency can present with normal numbers of T and B cells, and...
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by antibody defici...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely ...