Clinical Associations of Biallelic and MonoallelicTNFRSF13BVariants in Italian Primary Antibody Deficiency Syndromes

The Impact of TACI Mutations: From Hypogammaglobulinemia in Infancy to Autoimmunity in Adulthood

(2017) A.B. Barroeta Seijas et al.   INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY

Decreased IgM, IgA, and IgG response to pneumococcal vaccine in children with transient hypogammaglobulinemia of infancy

(2016) Viviana Moschese et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

International Consensus Document (ICON): Common Variable Immunodeficiency Disorders

(2016) Francisco A. Bonilla et al.   Journal of Allergy and Clinical Immunology-In Practice

TNF receptor superfamily member 13b (TNFRSF13B) hemizygosity reveals transmembrane activator and CAML interactor haploinsufficiency at later stages of B-cell development

(2015) Neil Romberg et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Effect of TACI Signaling on Humoral Immunity and Autoimmune Diseases

(2015) Yi Zhang et al.   Journal of Immunology Research

The European Society for Immunodeficiencies (ESID) registry 2014

(2014) B. Grimbacher et al.   CLINICAL AND EXPERIMENTAL IMMUNOLOGY

Heterozygous Alterations ofTNFRSF13B/TACIin Tonsillar Hypertrophy and Sarcoidosis

(2013) Matthaios Speletas et al.   Clinical & Developmental Immunology

Efficient B Cell Responses to Borrelia hermsii Infection Depend on BAFF and BAFFR but Not TACI

(2013) Gregory S. Dickinson et al.   INFECTION AND IMMUNITY

Common variable immunodeficiency: two mutations are better than one

(2013) Antonio La Cava   JOURNAL OF CLINICAL INVESTIGATION

CVID-associated TACI mutations affect autoreactive B cell selection and activation

(2013) Neil Romberg et al.   JOURNAL OF CLINICAL INVESTIGATION

Malignancies are the major cause of death in patients with adult onset common variable immunodeficiency

(2012) I. Quinti et al.   BLOOD

Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations

(2012) T. Freiberger et al.   HUMAN IMMUNOLOGY

Quantification of IgM and IgA Anti-Pneumococcal Capsular Polysaccharides by a New ELISA Assay: a Valuable Diagnostic and Prognostic Tool for Common Variable Immunodeficiency

(2012) F. M. Cavaliere et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Three Different Classifications, B Lymphocyte Subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) Gene Mutations, CTLA-4 and ICOS Gene Polymorphisms in Turkish Patients with Common Variable Immunodeficiency

(2012) Necil Kutukculer et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Morbidity and mortality in common variable immune deficiency over 4 decades

(2011) E. S. Resnick et al.   BLOOD

TNFRSF13B/TACI Alterations in Greek Patients with Antibody Deficiencies

(2011) Matthaios Speletas et al.   JOURNAL OF CLINICAL IMMUNOLOGY

The C104R mutant impairs the function of transmembrane activator and calcium modulator and cyclophilin ligand interactor (TACI) through haploinsufficiency

(2010) John J. Lee et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88

(2010) Bing He et al.   NATURE IMMUNOLOGY

The murine equivalent of the A181E TACI mutation associated with common variable immunodeficiency severely impairs B-cell function

(2009) J. J. Lee et al.   BLOOD

Granulomatous-lymphocytic interstitial lung disease (GLILD) in common variable immunodeficiency (CVID)

(2009) Joon H. Park et al.   CLINICAL IMMUNOLOGY

Frequency of Treg Cells Is Reduced in CVID Patients with Autoimmunity and Splenomegaly and Is Associated with Expanded CD21lo B Lymphocytes

(2009) Gururaj Arumugakani et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Novel Mutations in TACI (TNFRSF13B) Causing Common Variable Immunodeficiency

(2009) Javad Mohammadi et al.   JOURNAL OF CLINICAL IMMUNOLOGY

Role of polymorphisms in theTNFRSF13B(TACI) gene in Spanish patients with immunoglobulin A deficiency

(2009) R. López-Mejías et al.   TISSUE ANTIGENS

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

(2008) U. Salzer et al.   BLOOD