(Q42934775)

11 November 2017

NOD2 (CARD15), the first susceptibility gene for Crohn's disease (English)

1 reference

11 November 2017

1 reference

2

1 reference

11 November 2017

1

McGovern DP

1 reference

11 November 2017

4

Jewell DP

1 reference

11 November 2017

Ahmad T

3

1 reference

PMC publication ID

1728539

11 November 2017

language of work or name

English

0 references

publication date

1 December 2001

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11 November 2017

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11 November 2017

49

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11 November 2017

6

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11 November 2017

752-754

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CARD15 mutations in Blau syndrome

11 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728539

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728539

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728539

International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728539

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728539

Nod1, an Apaf-1-like activator of caspase-9 and nuclear factor-kappaB

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728539

Mapping of a susceptibility locus for Crohn's disease on chromosome 16

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728539

Genetic dissection of complex traits

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1728539

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

27 May 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11709505

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/GUT.49.6.752

1 reference

11 November 2017

1 reference

PMC publication ID

1728539

11 November 2017

PubMed publication ID

11709505

1 reference

PMC publication ID

1728539