Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (Q27860821)

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8 November 2019

title

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

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8 November 2019

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8 November 2019

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8 November 2019

Jean-Frédéric Colombel

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Colombel JF

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Zouali H

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Lesage S

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Cézard JP

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Belaiche J

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Tysk C

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O'Morain CA

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Gassull M

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Binder V

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Finkel Y

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Modigliani R

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Gower-Rousseau C

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Macry J

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Sahbatou M

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Thomas G

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language of work or name

English

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publication date

1 May 2001

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8 November 2019

volume

411

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8 November 2019

issue

6837

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8 November 2019

page(s)

599-603

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Etiology of the inflammatory bowel diseases

8 November 2019

cites work

1 reference

7 January 2021

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

1 reference

7 January 2021

Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease

1 reference

7 January 2021

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

1 reference

7 January 2021

The genetics of Crohn disease: complex segregation analysis of a family study with 265 patients with Crohn disease and 5,387 relatives

1 reference

7 January 2021

Investigation of inheritance of chronic inflammatory bowel diseases by complex segregation analysis

1 reference

7 January 2021

Clinical characteristics of Crohn's disease in 72 families

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Human Nod1 confers responsiveness to bacterial lipopolysaccharides

1 reference

7 January 2021

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

1 reference

7 January 2021

Human CARD4 protein is a novel CED-4/Apaf-1 cell death family member that activates NF-kappaB

1 reference

7 January 2021

Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene

1 reference

7 January 2021

Spontaneous, heritable colitis in a new substrain of C3H/HeJ mice

1 reference

7 January 2021

Intestinal inflammation and the gut microflora

1 reference

7 January 2021

Activation of nuclear factor kappa B inflammatory bowel disease

1 reference

7 January 2021

Immunosuppression by glucocorticoids: inhibition of NF-kappa B activity through induction of I kappa B synthesis

1 reference

7 January 2021

Sulfasalazine: a potent and specific inhibitor of nuclear factor kappa B

1 reference

7 January 2021

Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12

1 reference

7 January 2021

Linkage of inflammatory bowel disease to human chromosome 6p

1 reference

7 January 2021

Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease

1 reference

7 January 2021

High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12

1 reference

7 January 2021

Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci

1 reference

7 January 2021

Classification of inflammatory bowel disease

1 reference

7 January 2021

Identifiers

DOI

10.1038/35079107

2 references

Consolidated OpenCitations Corpus – April 2017

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Dimensions Publication ID

8 November 2019

1031360950

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017

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