Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency. - Wikidata - awgldk - TriplyDB

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.

http://www.wikidata.org/entity/Q34096958

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The transmembrane activator TACI triggers immunoglobulin class switching by activating B cells through the adaptor MyD88 International Consensus Document (ICON): Common Variable Immunodeficiency Disorders Comparison of diagnostic criteria for common variable immunodeficiency disorder Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: clinical and immunologic outcomes in heterozygotes.Autoimmune manifestations in common variable immunodeficiency.Granulomatous disease in common variable immunodeficiency.Autoimmunity in primary immune deficiency: taking lessons from our patients.Autoimmune cytopenias in common variable immunodeficiency.Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8.Common variable immunodeficiency: etiological and treatment issues.Selective IgA deficiency.Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID The many faces of common variable immunodeficiency.How I treat common variable immune deficiency.Autoimmunity in common variable immunodeficiency.Role of B cells in common variable immune deficiency.Morbidity and mortality in common variable immune deficiency over 4 decades Comparisons of CVID and IgGSD: referring physicians, autoimmune conditions, pneumovax reactivity, immunoglobulin levels, blood lymphocyte subsets, and HLA-A and -B typing in 432 adult index patients.The C104R mutant impairs the function of transmembrane activator and calcium modulator and cyclophilin ligand interactor (TACI) through haploinsufficiency Clinical and technical phosphoproteomic research.TACI deficiency enhances antibody avidity and clearance of an intestinal pathogen Rare variants at 16p11.2 are associated with common variable immunodeficiency Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions.Bone marrow transcriptome and epigenome profiles of equine common variable immunodeficiency patients unveil block of B lymphocyte differentiation.IgH sequences in common variable immune deficiency reveal altered B cell development and selection.Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.Perspectives on common variable immune deficiency.Toll-like receptor function in primary B cell defects.Transmembrane activator and CAML interactor (TACI) haploinsufficiency results in B-cell dysfunction in patients with Smith-Magenis syndrome.Chipping away at a mountain: genomic studies in common variable immunodeficiency.Common Variable Immunodeficiency and Circulating TFH Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes.TACI mutations and impaired B-cell function in subjects with CVID and healthy heterozygotes.Genome-wide association identifies diverse causes of common variable immunodeficiency Translational mini-review series on immunodeficiency: molecular defects in common variable immunodeficiency.Genetic Diagnosis Using Whole Exome Sequencing in Common Variable Immunodeficiency.Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

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Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.

http://www.wikidata.org/entity/Q34096958

description

2007 nî lūn-bûn

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2007 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2007 թվականի ապրիլին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Reexamining the role of TACI c ...... and selective IgA deficiency.

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Reexamining the role of TACI c ...... and selective IgA deficiency.

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Reexamining the role of TACI c ...... and selective IgA deficiency.

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Reexamining the role of TACI c ...... and selective IgA deficiency.

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Reexamining the role of TACI c ...... and selective IgA deficiency.

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Reexamining the role of TACI c ...... and selective IgA deficiency.

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Reexamining the role of TACI c ...... and selective IgA deficiency.

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Reexamining the role of TACI c ...... and selective IgA deficiency.

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Reexamining the role of TACI c ...... and selective IgA deficiency.

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Nature Genetics

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Reexamining the role of TACI c ...... and selective IgA deficiency.

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Bodo Grimbacher

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Chiara Bacchelli

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David L Nelson

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H Bobby Gaspar

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Janne Björkander

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Lennart Hammarström

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Likun Du

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Qiang Pan-Hammarström

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Steven Offer

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Timothy W Behrens

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P2860

Impaired IgA class switching in APRIL-deficient mice

TACI is mutant in common variable immunodeficiency and IgA deficiency

The New York Cancer Project: rationale, organization, design, and baseline characteristics

TACI and BAFF-R mediate isotype switching in B cells

Phenylketonuria screening registry as a resource for population genetic studies.

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

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429-430

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scholarly article

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10.1038/NG0407-429

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4

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39

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Charlotte Cunningham-Rundles

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2007-04-01T00:00:00Z

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6416987

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17392797

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2931279

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