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

World journal of gastroenterology : WJG, 2005-02, Vol.11 (5), p.681

2005

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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

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

Gut, 2003-06, Vol.52 (6), p.840-846

2003

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Mucosal integrity and barrier function in the pathogenesis of early lesions in Crohn’s disease

Journal of Clinical Pathology, 2005-06, Vol.58 (6), p.568-572

Sanders, D S A

2005

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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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Polymorphisms of CARD15/NOD2 and CD14 genes in New Zealand Crohn's disease patients

Immunology and cell biology, 2005-10, Vol.83 (5), p.498-503

2005

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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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Slipping the barrier: how variants in CARD15 could alter permeability of the intestinal wall and population health

Gut, 2006-03, Vol.55 (3), p.308-309

Schreiber, S

2006

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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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Identification of Card15/Nod2 mRNA in Intestinal Tissue of Experimentally Induced Colitis in Rats

Journal of Veterinary Medical Science, 2006, Vol.68(7), pp.701-708

2006

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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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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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Blau症候群と若年発症サルコイドーシスの臨床像とCARD15/NOD2遺伝子異常

日本臨床免疫学会会誌, 2007, Vol.30(2), pp.123-132

金澤, 伸雄

2007

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

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

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

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

Mucosal integrity and barrier function in the pathogenesis of early lesions in Crohn’s 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

Polymorphisms of CARD15/NOD2 and CD14 genes in New Zealand Crohn's disease patients

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

Slipping the barrier: how variants in CARD15 could alter permeability of the intestinal wall and population health

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

Identification of Card15/Nod2 mRNA in Intestinal Tissue of Experimentally Induced Colitis in Rats

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

Inflammatory Bowel Diseases

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

Blau症候群と若年発症サルコイドーシスの臨床像とCARD15/NOD2遺伝子異常

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