NOD2/CARD15 gene polymorphisms and Crohn's disease in the Chinese population
暂无分享,去创建一个
D. Jewell | J. Sung | Tariq Ahmad | R. Leong | A. Armuzzi | M. Wong | P. Tse | Rupert Leong
[1] Judy H. Cho,et al. Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan. , 2003, Gastroenterology.
[2] M. Daly,et al. CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure. , 2002, American journal of human genetics.
[3] T. Hibi,et al. Lack of common NOD2 variants in Japanese patients with Crohn's disease. , 2002, Gastroenterology.
[4] Alastair Forbes,et al. The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease. , 2002, Gastroenterology.
[5] T. Ahmad,et al. The molecular classification of the clinical manifestations of Crohn's disease. , 2002, Gastroenterology.
[6] S. Targan,et al. Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease. , 2002, Gastroenterology.
[7] K. Huse,et al. Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[8] S. Fisher,et al. Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations , 2001, The Lancet.
[9] Mourad Sahbatou,et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease , 2001, Nature.
[10] Judy H. Cho,et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease , 2001, Nature.
[11] J. Cavanaugh,et al. International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16. , 2001, American journal of human genetics.
[12] S. Yamaoka,et al. Nod2, a Nod1/Apaf-1 Family Member That Is Restricted to Monocytes and Activates NF-κB* , 2001, The Journal of Biological Chemistry.
[13] C. Khor,et al. Racial differences in the prevalence of ulcerative colitis and Crohn's disease in Singapore. , 1998, Journal of gastroenterology and hepatology.
[14] T. Shimosegawa,et al. Crohn's disease is associated with novel polymorphisms in the 5'-flanking region of the tumor necrosis factor gene. , 1999, Gastroenterology.
[15] E. Rappaport,et al. Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus – A GISC study , 1999, European Journal of Human Genetics.
[16] E. Jabs,et al. American families with Crohn's disease have strong evidence for linkage to chromosome 16 but not chromosome 12. , 1998, Gastroenterology.
[17] J. Weber,et al. Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[18] Jean Weissenbach,et al. Mapping of a susceptibility locus for Crohn's disease on chromosome 16 , 1996, Nature.
[19] T. Kodama,et al. HLA-linked susceptibility and resistance genes in Crohn's disease. , 1995, Gastroenterology.
[20] T. Sørensen,et al. Familial occurrence of inflammatory bowel disease. , 1991, The New England journal of medicine.
[21] J. Lennard-jones,et al. Classification of inflammatory bowel disease. , 1989, Scandinavian journal of gastroenterology. Supplement.