Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations (Q82627169)

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17 January 2020

title

Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations (English)

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17 January 2020

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17 January 2020

Bjorn Moum

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17 January 2020

Jorgen Jahnsen

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17 January 2020

Morten H Vatn

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17 January 2020

Valentina Medici

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17 January 2020

Silvia Mascheretti

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17 January 2020

Peter J P Croucher

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17 January 2020

Monika Stoll

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17 January 2020

Jochen Grebe

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17 January 2020

Giacomo C Sturniolo

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17 January 2020

Camilla Solberg

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17 January 2020

Stefan Schreiber

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17 January 2020

publication date

1 April 2006

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European Journal of Human Genetics

17 January 2020

published in

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17 January 2020

volume

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17 January 2020

issue

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17 January 2020

page(s)

459-468

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Incidence of Crohn's Disease in Four Counties in Southeastern Norway, 1990–93 A Prospective Population-Based Study

17 January 2020

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Incidence of ulcerative colitis and indeterminate colitis in four counties of southeastern Norway, 1990-93. A prospective population-based study. The Inflammatory Bowel South-Eastern Norway (IBSEN) Study Group of Gastroenterologists

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Incidence of inflammatory bowel disease across Europe: is there a difference between north and south? Results of the European Collaborative Study on Inflammatory Bowel Disease (EC-IBD)

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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 of inflammatory bowel disease: scientific and clinical implications

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

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

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

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Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for 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

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

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

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

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

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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

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

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7 January 2021

NOD2/CARD15 gene polymorphisms and Crohn's disease in the Chinese population.

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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

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

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NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?

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7 January 2021

Subclinical intestinal inflammation: an inherited abnormality in Crohn’s disease relatives?

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7 January 2021

Genetic variation in DLG5 is associated with inflammatory bowel disease

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7 January 2021

Identification of a novel human homolog of the Drosophila dlg, P-dlg, specifically expressed in the gland tissues and interacting with p55

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7 January 2021

Interaction of lp-dlg/KIAA0583, a membrane-associated guanylate kinase family protein, with vinexin and beta-catenin at sites of cell-cell contact

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

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The Nod2 gene in Crohn's disease: implications for future research into the genetics and immunology of Crohn's disease

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7 January 2021

Frequency of NOD2/CARD15 variants in both sporadic and familial cases of Crohn's disease across Italy. An Italian Group for Inflammatory Bowel Disease Study.

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7 January 2021

Prevalence of mutations of the NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn disease

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7 January 2021

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7 January 2021

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7 January 2021

Crohn's disease: ethnic variation in CARD15 genotypes

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7 January 2021

Association of DLG5 R30Q variant with inflammatory bowel disease

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7 January 2021

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7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201576

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17 January 2020

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