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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1

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8 November 2019

Alastair Forbes

13

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8 November 2019

Cathryn Lewis

18

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8 November 2019

Christopher G. Mathew

20

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8 November 2019

author name string

A Cuthbert

2

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8 November 2019

P J Croucher

3

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8 November 2019

M M Mirza

4

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8 November 2019

S Mascheretti

5

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8 November 2019

S Fisher

6

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8 November 2019

H Frenzel

7

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8 November 2019

K King

8

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8 November 2019

A Hasselmeyer

9

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8 November 2019

A J MacPherson

10

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8 November 2019

S Bridger

11

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8 November 2019

S van Deventer

12

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8 November 2019

S Nikolaus

14

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8 November 2019

J E Lennard-Jones

15

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8 November 2019

U R Foelsch

16

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8 November 2019

M Krawczak

17

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8 November 2019

S Schreiber

19

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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

page(s)

1925-1928

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8 November 2019

issue

9272

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Familial occurrence of inflammatory bowel disease

8 November 2019

cites work

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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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7 January 2021

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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7 January 2021

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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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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

1 reference

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8 November 2019

1 reference