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

Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease.

Immunogenetics - 1 Apr 2006

Schnitzler Fabian, Brand Stephan, Staudinger Tanja, Pfennig Simone, Hofbauer Katrin, Seiderer Julia, Tillack Cornelia, Göke Burkhard, Ochsenkühn Thomas, Lohse Peter

Abstract excerpt

We performed a limited DNA sequence analysis of the CARD15 gene in 89 patients with Crohn's disease (CD), 19 patients with ulcerative colitis (UC), and three patients with indeterminate colitis (IC), who were heterozygous carriers of one of the common CARD15 mutations [c.2104C>T (p.R702W), c.2722G>C (p.G908R), or c.3019_3020insC (p.Leu1007fsX1008)], the c.2462+10A>C variant, or of a new amino acid substitution in...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Amino Acid Substitution

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Genetic Predisposition to Disease

Share to Inflammatory Bowel Diseases

Share to Intracellular Signaling Peptides and Proteins

Share to Nod2 Signaling Adaptor Protein

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 16485124
DOI: 10.1007/s00251-005-0073-2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease.PMID 16485124Read ↗

Frequency of three common mutations of CARD15/NOD2 gene in Iranian IBD patients.Semantic proximity Read ↗

Rapid detection of common CARD15 variants in patients with inflammatory bowel disease.Semantic proximity Read ↗

Distribution of common CARD15 variants in patients with sporadic Crohn's disease: cases from Turkey.Semantic proximity Read ↗

Analysis of the three common mutations in the CARD15 gene (R702W, G908R and 1007fs) in South African colored patients with inflammatory bowel disease.Semantic proximity Read ↗

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.Semantic proximity Read ↗

CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies.Semantic proximity Read ↗

CARD15 gene polymorphisms in Serbian patients with Crohn's disease: genotype-phenotype analysis.Semantic proximity Read ↗

Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease.Semantic proximity Read ↗

NOD2/CARD15 mutations in Croatian patients with Crohn's disease: prevalence and genotype-phenotype relationship.Semantic proximity Read ↗

Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis.Semantic proximity Read ↗

Card15 and Crohn's disease: healthy homozygous carriers of the 3020insC frameshift mutation.Semantic proximity Read ↗

CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure.Semantic proximity Read ↗

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