(Q75359720)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

title

Prevalence of mutations of the NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

1 reference

6

1 reference

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17 November 2019

author name string

J L Mendoza

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

L S Murillo

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

L Fernández

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

A S Peña

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

R Lana

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

D M Cruz-Santamaría

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

E G de la Concha

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

M Díaz-Rubio

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

J García-Paredes

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

publication date

1 December 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

Scandinavian Journal of Gastroenterology

17 November 2019

published in

1 reference

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17 November 2019

volume

38

1 reference

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17 November 2019

issue

12

1 reference

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17 November 2019

page(s)

1235-1240

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

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

17 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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/10.1080%2F00365520310006612

CARD15/NOD2 functions as an antibacterial factor in human intestinal epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

TNF-alpha and IFN-gamma regulate the expression of the NOD2 (CARD15) gene in human intestinal epithelial cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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/10.1080%2F00365520310006612

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

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)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

The genesis of IBD genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

Response to infliximab treatment in Crohn's disease is not associated with mutations in the CARD15 (NOD2) gene: an analysis in 534 patients from two multicenter, prospective GCP-level trials

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365520310006612

10.1080/00365520310006612

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14750643%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

1 reference