(Q47845454)

6 February 2018

title

CARD15 mutations in patients with Crohn's disease in a homogeneous Spanish population (English)

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6 February 2018

J. Enrique Domínguez Muñoz

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3

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6 February 2018

author name string

Concepción Núñez

1

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6 February 2018

Manuel Barreiro

2

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6 February 2018

Aurelio Lorenzo

4

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6 February 2018

Carlos Zapata

5

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6 February 2018

A Salvador Peña

6

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6 February 2018

language of work or name

English

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publication date

1 March 2004

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6 February 2018

The American Journal of Gastroenterology

published in

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6 February 2018

volume

99

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6 February 2018

issue

3

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6 February 2018

page(s)

450-456

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6 February 2018

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

cites work

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

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

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

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

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

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

21 January 2018

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CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population.

21 January 2018

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Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-kappaB

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

Card15 gene overexpression in mononuclear and epithelial cells of the inflamed Crohn's disease colon

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

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

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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Behaviour of Crohn's disease according to the Vienna classification: changing pattern over the course of the disease

21 January 2018

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

21 January 2018

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Role ofNOD2 variants in spondylarthritis

21 January 2018

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3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

CARD15 gene and the classification of Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

The genetics of inflammatory bowel disease

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1572-0241.2004.04066.X

NOD2 insertion mutation in a cretan Crohn's disease population

21 January 2018

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10.1111/J.1572-0241.2004.04066.X

21 January 2018

Identifiers

DOI

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6 February 2018

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6 February 2018