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Genetic basis for increased intestinal permeability in families with Crohn’s disease: role of CARD15 3020insC mutation?

Gut, 2006-03, Vol.55 (3), p.342-347

2006

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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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Frequency and Clinical Correlations of Granulomas in Children With Crohn Disease

Journal of pediatric gastroenterology and nutrition, 2008-04, Vol.46 (4), p.392-398

2008

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CARD15/NOD2, CD14 and toll-like 4 receptor gene polymorphisms in Saudi patients with Crohn's Disease

International journal of molecular sciences, 2012-04, Vol.13 (4), p.4268-4280

2012

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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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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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Crohn's Disease Is Associated with Polymorphism of CARD15/NOD2 Gene in a Hungarian Population

Annals of the New York Academy of Sciences, 2005-06, Vol.1051 (1), p.45-51

2005

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CARD15 Mutations Are Rare in Swedish Pediatric Crohn Disease

Journal of pediatric gastroenterology and nutrition, 2005-04, Vol.40 (4), p.456-460

2005

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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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Clinical features of Blau syndrome and early-onset sarcoidosis and associating CARD15/NOD2 gene mutations

Japanese Journal of Clinical Immunology, 2007, Vol.30(2), pp.123-132

KANAZAWA, Nobuo

2007

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Genetic basis for increased intestinal permeability in families with Crohn’s disease: role of CARD15 3020insC mutation?

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

Frequency and Clinical Correlations of Granulomas in Children With Crohn Disease

CARD15/NOD2, CD14 and toll-like 4 receptor gene polymorphisms in Saudi patients with Crohn's Disease

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

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

Crohn's Disease Is Associated with Polymorphism of CARD15/NOD2 Gene in a Hungarian Population

CARD15 Mutations Are Rare in Swedish Pediatric Crohn Disease

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

Clinical features of Blau syndrome and early-onset sarcoidosis and associating CARD15/NOD2 gene mutations

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