Distribution of common CARD15 variants in patients with sporadic Crohn's disease: cases from Turkey. (Q54608705)

1 June 2018

title

Distribution of common CARD15 variants in patients with sporadic Crohn's disease: cases from Turkey. (English)

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1 June 2018

Güher Saruhan-Direskeneli

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6

object named as

Güher Saruhan-Direskeneli

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1 June 2018

author name string

F Aytül Uyar

1

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1 June 2018

Hülya Over-Hamzaoğlu

2

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1 June 2018

Filiz Türe

3

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1 June 2018

Ahmet Gül

4

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1 June 2018

Nurdan Tözün

5

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1 June 2018

publication date

1 April 2006

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1 June 2018

Digestive Diseases and Sciences

published in

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1 June 2018

volume

51

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issue

4

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1 June 2018

page(s)

706-710

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1 June 2018

https://scigraph.springernature.com/pub.10.1007/s10620-006-3195-y

exact match

0 references

cites work

Association between polymorphisms in the Toll-like receptor 4, CD14, and CARD15/NOD2 and inflammatory bowel disease in the Greek population

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Crossref

https://api.crossref.org/works/10.1007%2FS10620-006-3195-Y

NOD2/CARD15 gene polymorphism in patients with inflammatory bowel disease: is Hungary different?

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10620-006-3195-Y

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

21 January 2018

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Nod2 is a general sensor of peptidoglycan through muramyl dipeptide (MDP) detection

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CARD15 mutations in patients with Crohn's disease in a homogeneous Spanish population.

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

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

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Etiology of the inflammatory bowel diseases

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

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

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

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12 December 2020

CARD15/NOD2 mutational analysis in Japanese patients with Crohn's 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 frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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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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12 December 2020

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

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

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Crohn disease: frequency and nature of CARD15 mutations in Ashkenazi and Sephardi/Oriental Jewish families

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Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study

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Card15 gene overexpression in mononuclear and epithelial cells of the inflamed Crohn's disease colon

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

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

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12 December 2020

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

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12 December 2020

Human leukocyte antigen-A, -B and -C alleles and human leukocyte antigen haplotypes in Turkey: relationship to other populations

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

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CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population.

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Crohn's disease and the NOD2 gene: a role for paneth cells

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12 December 2020

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

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

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12 December 2020

Variation at NOD2/CARD15 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population.

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12 December 2020

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

1 reference

12 December 2020

10.1007/S10620-006-3195-Y

Identifiers

DOI

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1 June 2018

PubMed ID

16614992

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1 June 2018