(Q34382325)

1 August 2017

title

NOD2/CARD15 gene polymorphism in patients with inflammatory bowel disease: is Hungary different? (English)

1 reference

inflammatory bowel diseases

1 August 2017

main subject

0 references

Janos Lonovics

1 reference

1 August 2017

Herbert Lochs

1 reference

1 August 2017

Carsten Büning

1 reference

1 August 2017

Tomas Molnar

1 reference

1 August 2017

Ferenc Nagy

1 reference

1 August 2017

Renita Weltrich

1 reference

1 August 2017

Bettina Bochow

1 reference

1 August 2017

Janine Genschel

1 reference

1 August 2017

Hartmut Schmidt

1 reference

1 August 2017

language of work or name

English

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publication date

1 January 2005

1 reference

World Journal of Gastroenterology

1 August 2017

published in

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1 August 2017

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1 August 2017

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1 August 2017

page(s)

407-411

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Striking elevation in incidence and prevalence of inflammatory bowel disease in a province of western Hungary between 1977-2001

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

Lack of common NOD2 variants in Japanese patients with Crohn's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

The molecular classification of the clinical manifestations of Crohn's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

The epidemiology and the pathogenesis of inflammatory bowel disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

A simple classification of Crohn's disease: report of the Working Party for the World Congresses of Gastroenterology, Vienna 1998.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

Incidence of inflammatory bowel disease across Europe: is there a difference between north and south? Results of the European Collaborative Study on Inflammatory Bowel Disease (EC-IBD)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

NOD2/CARD15 gene polymorphisms and Crohn's disease in the Chinese population.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4205349

The genetics of inflammatory bowel disease

27 October 2018

1 reference

12 December 2020

The c-insertion mutation of the NOD2 gene is associated with fistulizing and fibrostenotic phenotypes in Crohn's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

European Cooperative Crohn's Disease Study (ECCDS): results of drug treatment

1 reference

12 December 2020

CARD15 gene and the classification of Crohn's disease

1 reference

12 December 2020

Identifiers

DOI

10.3748/WJG.V11.I3.407

1 reference

release_yqonz3bd6jg2zld5xmg6vhrk44

1 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/yqonz3bd6jg2zld5xmg6vhrk44

24 November 2022

mapped directly with Wikidata item

PMC publication ID

4205349

1 reference

1 August 2017

1 reference