Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations (Q57436454)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11425413%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

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

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8 November 2019

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8 November 2019

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8 November 2019

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8 November 2019

Christopher G. Mathew

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8 November 2019

A Cuthbert

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8 November 2019

P J Croucher

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8 November 2019

M M Mirza

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8 November 2019

S Mascheretti

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8 November 2019

S Fisher

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8 November 2019

H Frenzel

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8 November 2019

K King

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8 November 2019

A Hasselmeyer

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8 November 2019

A J MacPherson

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8 November 2019

S Bridger

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8 November 2019

S van Deventer

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8 November 2019

S Nikolaus

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8 November 2019

J E Lennard-Jones

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8 November 2019

U R Foelsch

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8 November 2019

M Krawczak

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8 November 2019

S Schreiber

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8 November 2019

language of work or name

English

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publication date

1 June 2001

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8 November 2019

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8 November 2019

volume

357

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8 November 2019

issue

9272

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8 November 2019

page(s)

1925-1928

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Familial occurrence of inflammatory bowel disease

8 November 2019

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Ulcerative colitis and Crohn's disease in an unselected population of monozygotic and dizygotic twins. A study of heritability and the influence of smoking

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Genetics versus environment in inflammatory bowel disease: results of a British twin study

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

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Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16.

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American families with Crohn's disease have strong evidence for linkage to chromosome 16 but not chromosome 12

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Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC study.

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Local administration of antisense phosphorothioate oligonucleotides to the p65 subunit of NF-kappa B abrogates established experimental colitis in mice

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Activation of nuclear factor kappa B inflammatory bowel disease

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

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A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort

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

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7 January 2021

Mechanisms in failure of infliximab for Crohn's disease

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7 January 2021

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

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7 January 2021

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

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7 January 2021

10.1016/S0140-6736(00)05063-7

Identifiers

DOI

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8 November 2019

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