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Article

Genotype-phenotype analysis of the CXCL16 p.Ala181Val polymorphism in inflammatory bowel disease.

Clinical immunology (Orlando, Fla.) - 1 Apr 2008

Seiderer Julia, Dambacher Julia, Leistner Dorothea, Tillack Cornelia, Glas Jürgen, Niess Jan-Hendrik, Pfennig Simone, Jürgens Matthias, Müller-Myhsok Bertram, Göke Burkhard, Ochsenkühn Thomas, Lohse Peter, Reinecker Hans-Christian, Brand Stephan

Abstract excerpt

To identify if genetic determinants of CXCL16 modulate the susceptibility and phenotype of inflammatory bowel diseases (IBD), we analyzed genomic DNA from 574 individuals (365 IBD patients, 209 healthy controls) for the CXCL16 p.Ala181Val polymorphism. In this study, we demonstrate that in Crohn'...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18248772
DOI: 10.1016/j.clim.2007.11.016

Genes

CXCL16
NOD2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18248772-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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