Pages that link to "Q53667090"
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The following pages link to Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans. (Q53667090):
Displaying 50 items.
- common variable immunodeficiency (Q1472818) (← links)
- Screening of functional and positional candidate genes in families with common variable immunodeficiency (Q21263125) (← links)
- The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88 (Q24293739) (← links)
- Role for Msh5 in the regulation of Ig class switch recombination (Q24681173) (← links)
- Hodgkin lymphoma cells express TACI and BCMA receptors and generate survival and proliferation signals in response to BAFF and APRIL (Q24681342) (← links)
- T and B lymphocyte subpopulations and activation/differentiation markers in patients with selective IgA deficiency (Q24683309) (← links)
- International Consensus Document (ICON): Common Variable Immunodeficiency Disorders (Q26777304) (← links)
- B-Cell Activating Factor as a Cancer Biomarker and Its Implications in Cancer-Related Cachexia (Q26784444) (← links)
- Humoral immunodeficiency : awareness for better support (Q26859051) (← links)
- Historical perspectives on tumor necrosis factor and its superfamily: 25 years later, a golden journey (Q26991848) (← links)
- Effect of TACI signaling on humoral immunity and autoimmune diseases (Q26995571) (← links)
- Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity (Q27183544) (← links)
- Unbalanced Immune System: Immunodeficiencies and Autoimmunity (Q28075911) (← links)
- Genetics of inflammatory bowel disease from multifactorial to monogenic forms (Q28081673) (← links)
- Educational paper: primary antibody deficiencies (Q28236790) (← links)
- Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions (Q28240370) (← links)
- Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum (Q28252393) (← links)
- To switch or not to switch--the opposing roles of TACI in terminal B cell differentiation (Q28279209) (← links)
- Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency (Q28300499) (← links)
- Toll-like receptor 9, transmembrane activator and calcium-modulating cyclophilin ligand interactor, and CD40 synergize in causing B-cell activation (Q30425171) (← links)
- Protective antiviral antibody responses in a mouse model of influenza virus infection require TACI (Q30430255) (← links)
- Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q (Q33228501) (← links)
- Interleukin-10 polymorphisms in Spanish IgA deficiency patients: a case-control and family study (Q33248070) (← links)
- Management of a young patient with combined autoimmunity: Evans syndrome: a case report (Q33373228) (← links)
- Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: clinical and immunologic outcomes in heterozygotes (Q33377299) (← links)
- Autoimmune manifestations in common variable immunodeficiency (Q33378880) (← links)
- Granulomatous disease in common variable immunodeficiency (Q33386034) (← links)
- Autoimmunity in primary immune deficiency: taking lessons from our patients (Q33394794) (← links)
- Autoimmune cytopenias in common variable immunodeficiency (Q33402558) (← links)
- Participation of B-cell-activating factor receptors in the pathogenesis of immune thrombocytopenia (Q33429051) (← links)
- Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8. (Q33506199) (← links)
- Airway epithelial cells produce B cell-activating factor of TNF family by an IFN-beta-dependent mechanism (Q33584291) (← links)
- Common variable immunodeficiency: etiological and treatment issues (Q33621805) (← links)
- Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID (Q33678784) (← links)
- IgA and IgG hypogammaglobulinemia in Waldenström's macroglobulinemia. (Q33707455) (← links)
- CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency (Q33755327) (← links)
- The many faces of common variable immunodeficiency (Q33790739) (← links)
- The clinical utility of molecular diagnostic testing for primary immune deficiency disorders: a case based review. (Q33992261) (← links)
- How I treat common variable immune deficiency (Q33997226) (← links)
- Why are there analogous disease mechanisms in chronic inflammatory diseases? (Q34005977) (← links)
- Toll-like receptor 7 and 9 defects in common variable immunodeficiency (Q34013669) (← links)
- Immunoglobulin responses at the mucosal interface. (Q34025272) (← links)
- Autoimmunity in common variable immunodeficiency (Q34056308) (← links)
- Role of B cells in common variable immune deficiency (Q34071102) (← links)
- Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency (Q34096958) (← links)
- Genome-wide association study of hematological and biochemical traits in a Japanese population (Q34097468) (← links)
- A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiency (Q34155993) (← links)
- Enhanced immunogenicity of HIV-1 envelope gp140 proteins fused to APRIL. (Q34232224) (← links)
- Morbidity and mortality in common variable immune deficiency over 4 decades (Q34241472) (← links)
- Use of combination chemotherapy for treatment of granulomatous and lymphocytic interstitial lung disease (GLILD) in patients with common variable immunodeficiency (CVID). (Q34296519) (← links)