(Q62717246)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14747834%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

title

Analysis of the CARD15 variants R702W, G908R and L1007fs in Italian IBD patients (English)

1 reference

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17 November 2019

1

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17 November 2019

Dario Gregori

4

1 reference

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17 November 2019

author name string

Marjan Maria van Duist

2

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17 November 2019

Silvia Regazzoni

3

1 reference

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17 November 2019

Marco Bardessono

5

1 reference

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17 November 2019

Paola Salacone

6

1 reference

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17 November 2019

Nadia Scaglione

7

1 reference

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17 November 2019

Raffaello Sostegni

8

1 reference

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17 November 2019

Nicoletta Sapone

9

1 reference

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17 November 2019

Francesca Bresso

10

1 reference

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17 November 2019

Angela Sambataro

11

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17 November 2019

Ezio Gaia

12

1 reference

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17 November 2019

Angelo Pera

13

1 reference

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17 November 2019

Marco Astegiano

14

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17 November 2019

M De Marchi

15

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17 November 2019

publication date

1 March 2004

1 reference

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European Journal of Human Genetics

17 November 2019

published in

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17 November 2019

volume

12

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17 November 2019

issue

3

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17 November 2019

page(s)

206-212

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201130

17 November 2019

exact match

0 references

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7 January 2021

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7 January 2021

Intestinal epithelial cells and innate immunity in the intestine: is CARD15/Nod2 another player?

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7 January 2021

3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population

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7 January 2021

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Association of NOD2 with Crohn's Disease in a homogenous Irish population

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7 January 2021

NOD2 insertion mutation in a cretan Crohn's disease population

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7 January 2021

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7 January 2021

Problems of reporting genetic associations with complex outcomes

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7 January 2021

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

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7 January 2021

CARD15/NOD2 mutational analysis in Japanese patients with Crohn's disease

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7 January 2021

Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease

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7 January 2021

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.

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7 January 2021

A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews

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7 January 2021

Detecting marker-disease association by testing for Hardy-Weinberg disequilibrium at a marker locus

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases.

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7 January 2021

Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for Crohn's disease

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7 January 2021

Crohn's disease: influence of age at diagnosis on site and clinical type of disease

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7 January 2021

The molecular classification of the clinical manifestations of Crohn's disease

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7 January 2021

Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease

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7 January 2021

Early development of stricturing or penetrating pattern in Crohn's disease is influenced by disease location, number of flares, and smoking but not by NOD2/CARD15 genotype

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7 January 2021

Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p.

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7 January 2021

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7 January 2021

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7 January 2021

CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.

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7 January 2021

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7 January 2021

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

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7 January 2021