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Diminution of Circulating CD4(+)CD25 (high) T Cells in Naïve Crohn's Disease

Digestive diseases and sciences, 2009-10, Vol.54, p.2084-2093

2009

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The role of toll‐like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease

Inflammatory bowel diseases, 2005-07, Vol.11 (7), p.645-652

2005

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Mutations in innate immune system NOD2/CARD 15 and TLR-4 (Thr399Ile) genes influence the risk for severe acute graft-versus-host disease in patients who underwent an allogeneic transplantation

Transplantation, 2006-01, Vol.81 (2), p.247-254

2006

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Predictive value of the CARD15 variant 1007fs for the diagnosis of intestinal stenoses and the need for surgery in Crohn's disease in clinical practice: Results of a Prospective Study

Inflammatory bowel diseases, 2006-12, Vol.12 (12), p.1114-1121

2006

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MEFV, TNF1rA, CARD15 and NLRP3 mutation analysis in PFAPA

Rheumatology international, 2010-03, Vol.30 (5), p.633-636

2010

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NOD2/CARD15 polymorphisms impair innate immunity and increase susceptibility to gastric cancer in an Italian population

Human immunology, 2009-09, Vol.70 (9), p.729-732

2009

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Biomarkers in inflammatory bowel disease

Current opinion in gastroenterology, 2004-07, Vol.20 (4), p.318-327

2004

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

Scandinavian journal of gastroenterology, 2003-12, Vol.38 (12), p.1235-1240

2003

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Familial case of Blau syndrome associated with a CARD15/NOD2 mutation

Ophthalmic genetics, 2010-09, Vol.31 (3), p.155-158

2010

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Association of polymorphisms in the interleukin‐18 gene in patients with Crohn's disease depending on the CARD15/NOD2 genotype

Inflammatory bowel diseases, 2005-12, Vol.11 (12), p.1031-1037

2005

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3020insC insertion in NOD2/CARD15 gene, a prevalent variant associated with anti-Saccharomyces cerevisiae antibodies and ileal location of Crohn’s disease in Tunisian population

Inflammation research, 2009-04, Vol.58 (4), p.218-223

2009

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CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins

Digestive and liver disease, 2005-10, Vol.37 (10), p.768-772

2005

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Distribution of common CARD15 variants in patients with sporadic crohn's disease : Cases from Turkey

Digestive diseases and sciences, 2006-04, Vol.51 (4), p.706-710

2006

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CARD15/NOD2 is not a predisposing factor for necrotizing enterocolitis

Digestive diseases and sciences, 2005-09, Vol.50 (9), p.1684-1687

2005

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NOD2/CARD15 gene mutation is not associated with susceptibility to Wegener's granulomatosis

Journal of rheumatology, 2003-02, Vol.30 (2), p.305

2003

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Identification of polymorphisms in bovine TLR2 and CARD15,associations between CARD15 polymorphisms and milk somatic cell score in Canadian Holsteins, and functional relevance of SNP c.3020A>T

Developments in biologicals, 2008, Vol.132, p.247

2008

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Genotype-phenotype correlations: how many disorders constitute inflammatory bowel disease?

European journal of gastroenterology & hepatology, 2003-06, Vol.15 (6), p.599-606

2003

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Alterations of the CARD15/NOD2 Gene and the Impact on Management and Treatment of Crohn’s Disease Patients

Digestive Diseases, 2003-01, Vol.21 (4), p.339-345

2003

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Inflammatory Bowel Diseases

Colitis, 2018, p.107-140

2018

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Nod2 Signaling Adaptor Protein
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Diminution of Circulating CD4(+)CD25 (high) T Cells in Naïve Crohn's Disease

The role of toll‐like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease

Mutations in innate immune system NOD2/CARD 15 and TLR-4 (Thr399Ile) genes influence the risk for severe acute graft-versus-host disease in patients who underwent an allogeneic transplantation

Predictive value of the CARD15 variant 1007fs for the diagnosis of intestinal stenoses and the need for surgery in Crohn's disease in clinical practice: Results of a Prospective Study

MEFV, TNF1rA, CARD15 and NLRP3 mutation analysis in PFAPA

NOD2/CARD15 polymorphisms impair innate immunity and increase susceptibility to gastric cancer in an Italian population

Biomarkers in inflammatory bowel disease

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

Familial case of Blau syndrome associated with a CARD15/NOD2 mutation

Association of polymorphisms in the interleukin‐18 gene in patients with Crohn's disease depending on the CARD15/NOD2 genotype

3020insC insertion in NOD2/CARD15 gene, a prevalent variant associated with anti-Saccharomyces cerevisiae antibodies and ileal location of Crohn’s disease in Tunisian population

CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins

Distribution of common CARD15 variants in patients with sporadic crohn's disease : Cases from Turkey

CARD15/NOD2 is not a predisposing factor for necrotizing enterocolitis

NOD2/CARD15 gene mutation is not associated with susceptibility to Wegener's granulomatosis

Identification of polymorphisms in bovine TLR2 and CARD15,associations between CARD15 polymorphisms and milk somatic cell score in Canadian Holsteins, and functional relevance of SNP c.3020A>T

Genotype-phenotype correlations: how many disorders constitute inflammatory bowel disease?

Alterations of the CARD15/NOD2 Gene and the Impact on Management and Treatment of Crohn’s Disease Patients

Inflammatory Bowel Diseases

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