(Q28245990)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

Association of DLG5 and inflammatory bowel disease across populations

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

Association of DLG5 R30Q variant with inflammatory bowel disease

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

Genetic variation in DLG5 is associated with inflammatory bowel disease

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

Dlg, Scribble and Lgl in cell polarity, cell proliferation and cancer

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

Interaction of lp-dlg/KIAA0583, a membrane-associated guanylate kinase family protein, with vinexin and beta-catenin at sites of cell-cell contact

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

DLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

Genotype-phenotype analysis of the Crohn's disease susceptibility haplotype on chromosome 5q31.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4087456

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.

29 September 2017

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

Further evidence of IBD5/CARD15 (NOD2) epistasis in the susceptibility to ulcerative colitis

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with Crohn disease in men

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

Association of Organic Cation Transporter Risk Haplotype With Perianal Penetrating Crohn’s Disease but Not With Susceptibility to IBD

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

DLG5 variants contribute to Crohn disease risk in a Canadian population

21 January 2018

1 reference

https://api.crossref.org/works/10.3748%2FWJG.V12.I23.3651

Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16773680

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16773680