Genetics of hypogammaglobulinemia: what do we really know? - Wikidata - awgldk - TriplyDB

Genetics of hypogammaglobulinemia: what do we really know?

Genetics of hypogammaglobulinemia: what do we really know?

http://www.wikidata.org/entity/Q37571008

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Application of Flow Cytometry in the Evaluation of Primary Immunodeficiencies Primary B-cell deficiencies reveal a link between human IL-17-producing CD4 T-cell homeostasis and B-cell differentiation.TLR signaling and effector functions are intact in XLA neutrophils.Toll-like receptor 4-, 7-, and 8-activated myeloid cells from patients with X-linked agammaglobulinemia produce enhanced inflammatory cytokines.Common Variable Immunodeficiency and Circulating TFH Respiratory Health and Related Quality of Life in Patients with Congenital Agammaglobulinemia in the Northern Region of the UK.T cell-B cell interactions in primary immunodeficiencies.Common variable immunodeficiency (CVID): exploring the multiple dimensions of a heterogeneous disease.Bruton's tyrosine kinase--an integral protein of B cell development that also has an essential role in the innate immune system.ICON: the early diagnosis of congenital immunodeficiencies.Gastrointestinal Manifestations in X-linked Agammaglobulinemia.Delayed diagnosis in X-linked agammaglobulinemia and its relationship to the occurrence of mutations in BTK non-kinase domains.Mutations in Bruton's tyrosine kinase impair IgA responses.Parental Consanguinity is Associated with a Severe Phenotype in Common Variable Immunodeficiency

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Genetics of hypogammaglobulinemia: what do we really know?

http://www.wikidata.org/entity/Q37571008

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 03 August 2009

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Genetics of hypogammaglobulinemia: what do we really know?

@en

Genetics of hypogammaglobulinemia: what do we really know?

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type

label

Genetics of hypogammaglobulinemia: what do we really know?

@en

Genetics of hypogammaglobulinemia: what do we really know?

@nl

prefLabel

Genetics of hypogammaglobulinemia: what do we really know?

@en

Genetics of hypogammaglobulinemia: what do we really know?

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J.COI.2009.07.003

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Current Opinion in Immunology

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Genetics of hypogammaglobulinemia: what do we really know?

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Mary Ellen Conley

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P2860

Bruton's tyrosine kinase (Btk): function, regulation, and transformation with special emphasis on the PH domain

Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes

Role for Msh5 in the regulation of Ig class switch recombination

Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency

An antibody-deficiency syndrome due to mutations in the CD19 gene

TACI is mutant in common variable immunodeficiency and IgA deficiency

Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia.

Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: clinical and immunologic outcomes in heterozygotes.

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

Humoral immunodeficiency with facial dysmorphology and limb anomalies: a new syndrome.

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466-471

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10.1016/J.COI.2009.07.003

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26713795

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19651503

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