Associated Papers
Crohn's Disease Susceptibility and Onset Are Strongly Related to Three NOD2 Gene Haplotypes.
Kaczmarek-Ryś M et al.
Journal of Clinical Medicine, 2021
Genetic deficiency of NOD2 confers resistance to invasive aspergillosis.
Gresnigt MS et al.
Nature Communications, 2018
Epistatic interaction between TLR4 and NOD2 in patients with Crohn's Disease: relation with risk and phenotype in a Spanish cohort.
Martinez-Chamorro A et al.
Immunobiology, 2016
Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project.
Cleynen I et al.
Gut, 2013
Ubiquitination and phosphorylation in the regulation of NOD2 signaling and NOD2-mediated disease.
Tigno-Aranjuez JT et al.
Biochimica Et Biophysica Acta, 2012
Perianal Crohn's disease: predictive factors and genotype-phenotype correlations.
Kanaan Z et al.
Digestive Surgery, 2012
Association analysis of the NOD2 gene with susceptibility to graft-versus-host disease in a Japanese population.
Tanabe T et al.
International Journal of Hematology, 2011
Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease.
Onnie CM et al.
European Journal of Gastroenterology & Hepatology, 2008
Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population.
Ernst A et al.
Scandinavian Journal of Gastroenterology, 2007
Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North Indians.
Juyal G et al.
Alimentary Pharmacology & Therapeutics, 2007
Role of discs large homolog 5.
Friedrichs F et al.
World Journal of Gastroenterology, 2006
Extreme heterogeneity in CARD15 and DLG5 Crohn disease-associated polymorphisms between German and Norwegian populations.
Medici V et al.
European Journal of Human Genetics : Ejhg, 2006
Genetic testing in Crohn disease: utility in individualizing patient management.
Mascheretti S et al.
American Journal of Pharmacogenomics : Genomics-related Research in Drug Development and Clinical Practice, 2005
NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe?
Arnott ID et al.
Genes and Immunity, 2004
NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype- phenotype analysis.
Heresbach D et al.
European Journal of Gastroenterology & Hepatology, 2004
Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.
Croucher PJ et al.
European Journal of Human Genetics : Ejhg, 2003
Variation at NOD2/CARD15 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population.
Zhou Z et al.
The American Journal of Gastroenterology, 2002