Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders.

Clinical and experimental immunology - 1 Sept 2010

Packwood K, Drewe E, Staples E, Webster D, Witte T, Litzman J, Egner W, Sargur R, Sewell W, Lopez-Granados E, Seneviratne S L, Powell R J, Ferry B L, Chapel H M

Abstract excerpt

Common variable immunodeficiency disorders (CVIDs) are a heterogeneous group of diseases characterized by hypogammaglobulinaemia and consequent susceptibility to infection. CVID patients commonly develop a variety of additional manifestations for which the causative factors are not fully understood. Two such manifestations are granulomatous disease and enteropathy. Because the ability to predict complications...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cohort Studies
Share to Common Variable Immunodeficiency

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Crohn Disease

Share to Europe

Share to Gene Frequency

Share to Nod2 Signaling Adaptor Protein

Share to Polymorphism, Single Nucleotide

Share to United Kingdom

Source

Open in PubMed Open full text

Identifiers

PMID: 20646002
DOI: 10.1111/j.1365-2249.2010.04216.x
PMCID: PMC2962972

Genes

NOD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders.PMID 20646002Read ↗

Identification of Novel Genetic Variants in CVID Patients With Autoimmunity, Autoinflammation, or Malignancy.Semantic proximity Read ↗

High frequency of variants in genes associated with primary immunodeficiencies in patients with rheumatic diseases with secondary hypogammaglobulinaemia.Semantic proximity Read ↗

Inborn errors E778K and G908R in NOD2 gene increase risk of nontuberculous mycobacterial infection: a computational studySemantic proximity Read ↗

Quantitative and functional evaluation of innate immune responses in patients with common variable immunodeficiency.Semantic proximity Read ↗

NOD2-associated autoinflammatory disease: a large cohort study.Semantic proximity Read ↗

Consequence of functional Nod2 and Tlr4 mutations on gene transcription in Crohn's disease patients.Semantic proximity Read ↗

NOD2 gene mutations in ulcerative colitis: useless or misunderstood?Semantic proximity Read ↗

Implications of combined NOD2 and other gene mutations in autoinflammatory diseases.Semantic proximity Read ↗

Immune response and gene polymorphism profiles in Crohn's disease and ulcerative colitis.Semantic proximity Read ↗

Evaluation of cytokine genetic polymorphisms in adult patients with common variable immunodeficiency: A single-center study.Semantic proximity Read ↗

Nucleotide oligomerization domain polymorphism confers no risk to Guillain-Barré syndrome.Semantic proximity Read ↗

Pattern recognition receptor and autophagy gene variants are associated with development of antimicrobial antibodies in Crohn's disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.