The Burden of Non-Infectious Organ-Specific Immunopathology in Pediatric Common Variable Immunodeficiency., PMID:40141295
The Burden of Non-Infectious Organ-Specific Immunopathology in Pediatric Common Variable Immunodeficiency., PMID:40141295
Mutational Landscape of Bone Marrow CD19 and CD138 Cells in Waldenström Macroglobulinemia (WM) and IgM Monoclonal Gammopathy of Undetermined Significance (IgM MGUS)., PMID:39711167
Mutational Landscape of Bone Marrow CD19 and CD138 Cells in Waldenström Macroglobulinemia (WM) and IgM Monoclonal Gammopathy of Undetermined Significance (IgM MGUS)., PMID:39711167
NF-ΚB Activation as a Key Driver in Chronic Lymphocytic Leukemia Evolution to Richter's Syndrome: Unraveling the Influence of Immune Microenvironment Dynamics., PMID:39596634
NF-ΚB Activation as a Key Driver in Chronic Lymphocytic Leukemia Evolution to Richter's Syndrome: Unraveling the Influence of Immune Microenvironment Dynamics., PMID:39596634
A Novel Heterozygous NFKB2 Variant in a Multiplex Family with Common Variable Immune Deficiency and Autoantibodies Against Type I IFNs., PMID:39579251
A Novel Heterozygous NFKB2 Variant in a Multiplex Family with Common Variable Immune Deficiency and Autoantibodies Against Type I IFNs., PMID:39579251
Type-Specific Impacts of Protein Defects in Pathogenic NFKB2 Variants: Novel Clinical Findings From 138 Patients., PMID:39447838
Type-Specific Impacts of Protein Defects in Pathogenic NFKB2 Variants: Novel Clinical Findings From 138 Patients., PMID:39447838
Clinical, Immunological, and Genetic Features in Patients with NFKB1 and NFKB2 Mutations: a Systematic Review., PMID:38990428
Clinical, Immunological, and Genetic Features in Patients with NFKB1 and NFKB2 Mutations: a Systematic Review., PMID:38990428
The Scope and Impact of Viral Infections in Common Variable Immunodeficiency (CVID) and CVID-like Disorders: A Literature Review., PMID:38541942
The Scope and Impact of Viral Infections in Common Variable Immunodeficiency (CVID) and CVID-like Disorders: A Literature Review., PMID:38541942
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency., PMID:37938781
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency., PMID:37938781
TRIM55 promotes noncanonical NF-κB signaling and B cell-mediated immune responses by coordinating p100 ubiquitination and processing., PMID:37816088
TRIM55 promotes noncanonical NF-κB signaling and B cell-mediated immune responses by coordinating p100 ubiquitination and processing., PMID:37816088
Case Report: Mycosis fungoides as an exclusive manifestation of common variable immunodeficiency in a family with a NFKB2 gene mutation., PMID:37781189
Case Report: Mycosis fungoides as an exclusive manifestation of common variable immunodeficiency in a family with a NFKB2 gene mutation., PMID:37781189
Anti-complement 5 antibody ameliorates antibody-mediated rejection after liver transplantation in rats., PMID:37398677
Anti-complement 5 antibody ameliorates antibody-mediated rejection after liver transplantation in rats., PMID:37398677
Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports., PMID:37322808
Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports., PMID:37322808
Autoantibodies targeting type I interferons: Prevalence, mechanisms of induction, and association with viral disease susceptibility., PMID:37027328
Autoantibodies targeting type I interferons: Prevalence, mechanisms of induction, and association with viral disease susceptibility., PMID:37027328
NFKB2 haploinsufficiency identified via screening for IFN-α2 autoantibodies in children and adolescents hospitalized with SARS-CoV-2-related complications., PMID:36509151
NFKB2 haploinsufficiency identified via screening for IFN-α2 autoantibodies in children and adolescents hospitalized with SARS-CoV-2-related complications., PMID:36509151
Screening patients with autoimmune endocrine disorders for cytokine autoantibodies reveals monogenic immune deficiencies., PMID:36191466
Screening patients with autoimmune endocrine disorders for cytokine autoantibodies reveals monogenic immune deficiencies., PMID:36191466
Nfkb2 deficiency and its impact on plasma cells and immunoglobulin expression in murine small intestinal mucosa., PMID:35916405
Nfkb2 deficiency and its impact on plasma cells and immunoglobulin expression in murine small intestinal mucosa., PMID:35916405
Identifying predictive signalling networks for Vedolizumab response in ulcerative colitis., PMID:35543875
Identifying predictive signalling networks for Vedolizumab response in ulcerative colitis., PMID:35543875
Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study., PMID:34975878
Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study., PMID:34975878
Disseminated Coccidioidomycosis as the First Presentation of a C-Terminal NFKB2 Pathogenic Variant: A Case Report and Review of the Literature., PMID:34609106
Disseminated Coccidioidomycosis as the First Presentation of a C-Terminal NFKB2 Pathogenic Variant: A Case Report and Review of the Literature., PMID:34609106
Late-Onset Isolated Corticotrope Deficiency in a Woman with Down Syndrome., PMID:34007493
Late-Onset Isolated Corticotrope Deficiency in a Woman with Down Syndrome., PMID:34007493
T and B Lymphocyte Transcriptional States Differentiate between Sensitized and Unsensitized Individuals in Alpha-Gal Syndrome., PMID:33804792
T and B Lymphocyte Transcriptional States Differentiate between Sensitized and Unsensitized Individuals in Alpha-Gal Syndrome., PMID:33804792
Serum microRNAs as Tool to Predict Early Response to Benralizumab in Severe Eosinophilic Asthma., PMID:33525548
Serum microRNAs as Tool to Predict Early Response to Benralizumab in Severe Eosinophilic Asthma., PMID:33525548
Severe SARS-CoV-2 disease in the context of a NF-κB2 loss-of-function pathogenic variant., PMID:33007327
Severe SARS-CoV-2 disease in the context of a NF-κB2 loss-of-function pathogenic variant., PMID:33007327
Correction to: A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency., PMID:32901356
Correction to: A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency., PMID:32901356
A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency., PMID:32813180
A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency., PMID:32813180
TRAF3 Acts as a Checkpoint of B Cell Receptor Signaling to Control Antibody Class Switch Recombination and Anergy., PMID:32591397
TRAF3 Acts as a Checkpoint of B Cell Receptor Signaling to Control Antibody Class Switch Recombination and Anergy., PMID:32591397
Heterogeneity of Liver Disease in Common Variable Immunodeficiency Disorders., PMID:32184784
Heterogeneity of Liver Disease in Common Variable Immunodeficiency Disorders., PMID:32184784
NFKB2 polymorphisms associate with the risk of developing rheumatoid arthritis and response to TNF inhibitors: Results from the REPAIR consortium., PMID:32152480
NFKB2 polymorphisms associate with the risk of developing rheumatoid arthritis and response to TNF inhibitors: Results from the REPAIR consortium., PMID:32152480
Signature of genome wide gene expression in classical swine fever virus infected macrophages and PBMCs of indigenous vis-a-vis crossbred pigs., PMID:31935504
Signature of genome wide gene expression in classical swine fever virus infected macrophages and PBMCs of indigenous vis-a-vis crossbred pigs., PMID:31935504
Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies., PMID:31543881
Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies., PMID:31543881
Familial hypogammaglobulinemia with high RTE and naïve T lymphocytes., PMID:31468084
Familial hypogammaglobulinemia with high RTE and naïve T lymphocytes., PMID:31468084
Pathogenic NFKB2 variant in the ankyrin repeat domain (R635X) causes a variable antibody deficiency., PMID:30953794
Pathogenic NFKB2 variant in the ankyrin repeat domain (R635X) causes a variable antibody deficiency., PMID:30953794
Severe Facial Herpes Vegetans and Viremia in NFKB2-Deficient Common Variable Immunodeficiency., PMID:30941333
Severe Facial Herpes Vegetans and Viremia in NFKB2-Deficient Common Variable Immunodeficiency., PMID:30941333
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2., PMID:30941118
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2., PMID:30941118
Inherited Immunodeficiency: A New Association With Early-Onset Childhood Panniculitis., PMID:29610179
Inherited Immunodeficiency: A New Association With Early-Onset Childhood Panniculitis., PMID:29610179
Anticytokine autoantibodies in a patient with a heterozygous NFKB2 mutation., PMID:29225085
Anticytokine autoantibodies in a patient with a heterozygous NFKB2 mutation., PMID:29225085
MKK4 activates non-canonical NFκB signaling by promoting NFκB2-p100 processing., PMID:28733031
MKK4 activates non-canonical NFκB signaling by promoting NFκB2-p100 processing., PMID:28733031
A Case Report of Hypoglycemia and Hypogammaglobulinemia: DAVID Syndrome in a Patient With a Novel NFKB2 Mutation., PMID:28472507
A Case Report of Hypoglycemia and Hypogammaglobulinemia: DAVID Syndrome in a Patient With a Novel NFKB2 Mutation., PMID:28472507
Transcription factors of the alternative NF-κB pathway are required for germinal center B-cell development., PMID:27457956
Transcription factors of the alternative NF-κB pathway are required for germinal center B-cell development., PMID:27457956
Genes associated with common variable immunodeficiency: one diagnosis to rule them all?, PMID:27250108
Genes associated with common variable immunodeficiency: one diagnosis to rule them all?, PMID:27250108
RAG-mediated DNA double-strand breaks activate a cell type-specific checkpoint to inhibit pre-B cell receptor signals., PMID:26834154
RAG-mediated DNA double-strand breaks activate a cell type-specific checkpoint to inhibit pre-B cell receptor signals., PMID:26834154
Impact of loss of NF-κB1, NF-κB2 or c-REL on SLE-like autoimmune disease and lymphadenopathy in Fas(lpr/lpr) mutant mice., PMID:26084385
Impact of loss of NF-κB1, NF-κB2 or c-REL on SLE-like autoimmune disease and lymphadenopathy in Fas(lpr/lpr) mutant mice., PMID:26084385
Effects of Pholiota nameko polysaccharide on NF-κB pathway of murine bone marrow-derived dendritic cells., PMID:25812973
Effects of Pholiota nameko polysaccharide on NF-κB pathway of murine bone marrow-derived dendritic cells., PMID:25812973
Transcriptome analysis of medaka following epinecidin-1 and TH1-5 treatment of NNV infection., PMID:25449377
Transcriptome analysis of medaka following epinecidin-1 and TH1-5 treatment of NNV infection., PMID:25449377
Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100., PMID:25237204
Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessable p100., PMID:25237204
Transcription factors involved in prostate gland adaptation to androgen deprivation., PMID:24886974
Transcription factors involved in prostate gland adaptation to androgen deprivation., PMID:24886974
Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency., PMID:24140114
Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency., PMID:24140114
p53 mutants induce transcription of NF-κB2 in H1299 cells through CBP and STAT binding on the NF-κB2 promoter and gain of function activity., PMID:22198284
p53 mutants induce transcription of NF-κB2 in H1299 cells through CBP and STAT binding on the NF-κB2 promoter and gain of function activity., PMID:22198284
The nuclear-factor kappaB pathway is activated in pterygium., PMID:20811049
The nuclear-factor kappaB pathway is activated in pterygium., PMID:20811049
Promiscuous mutations activate the noncanonical NF-kappaB pathway in multiple myeloma., PMID:17692805
Promiscuous mutations activate the noncanonical NF-kappaB pathway in multiple myeloma., PMID:17692805
For research use only. Not for human or drug use.
