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

Single nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease.

World journal of gastroenterology - 21 Dec 2005

Gazouli Maria, Mantzaris Gerassimos, Archimandritis Athanassios J, Nasioulas George, Anagnou Nicholas P

Abstract excerpt

AIM: To validate novel single nucleotide polymorphisms (SNPs) in Greek patients with Crohn's disease (CD). METHODS: A total of 120 patients with CD, 85 patients with UC, and 100 unrelated healthy controls were genotyped. Genotyping was performed by allele-specific PCR or by PCR-RFLP analysis. RESULTS: Our results showed that the 1672T and -207C alleles were obviously over-represented in CD patients only (P<0.01...

Read the complete abstract on PubMed

Topics

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

Share to Crohn Disease
Share to Greece

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Membrane Proteins

Share to Organic Cation Transport Proteins

Share to Risk Factors

Share to Solute Carrier Family 22 Member 5

Share to Symporters

Share to Tumor Suppressor Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 16437728
DOI: 10.3748/wjg.v11.i47.7525
PMCID: PMC4725165

Genes

NOD2
DLG5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Single nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease.PMID 16437728Read ↗

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.Semantic proximity Read ↗

Role of CARD15, DLG5 and OCTN genes polymorphisms in children with inflammatory bowel diseases.Semantic proximity Read ↗

Variants of OCTN1-2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis.Semantic proximity Read ↗

OCTN and CARD15 gene polymorphism in Chinese patients with inflammatory bowel disease.Semantic proximity Read ↗

Association of the organic cation transporter OCTN genes with Crohn's disease in the Spanish population.Semantic proximity Read ↗

Association between OCTN1/2 gene polymorphisms (1672C-T, 207G-C) and susceptibility of Crohn's disease: a meta-analysis.Semantic proximity Read ↗

OCTN1 variant L503F is associated with familial and sporadic inflammatory bowel disease.Semantic proximity Read ↗

The contribution of OCTN1/2 variants within the IBD5 locus to disease susceptibility and severity in Crohn's disease.Semantic proximity Read ↗

Evidence for association of OCTN genes and IBD5 with ulcerative colitis.Semantic proximity Read ↗

Frequency of CARD15 polymorphisms in patients with Crohn's disease from Toledo, Spain: genotype-phenotype correlation.Semantic proximity Read ↗

Functional variants of OCTN cation transporter genes are associated with Crohn disease.Semantic proximity Read ↗

Polymorphisms in the organic cation transporter genes SLC22A4 and SLC22A5 and Crohn's disease in a New Zealand Caucasian cohort.Semantic proximity Read ↗

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