Role of NOD2 gene in Crohn's disease;Rôle du gène NOD2 dans la maladie de Crohn

Gastroenterologie Clinique et Biologique

Volumn 26, Issue 1, 2002, Pages 13-15

  Hugot, Jean Pierre ^a,b  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b Fondation Jean Dausset   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; GENE PRODUCT; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; UNCLASSIFIED DRUG;

APOPTOSIS; CROHN DISEASE; EDITORIAL; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; IMMUNITY;

CARRIER PROTEINS; CROHN DISEASE; GENOTYPE; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; NOD2 SIGNALING ADAPTOR PROTEIN;

EID: 0036190966     PISSN: 03998320     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Editorial

References (9)

1. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
2. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
3. Nod2, a Nod1/Apaf-I family member that is restricted to monocytes and activates NF-kappaB
4. Mapping of a susceptibility locus for Crohn's disease on chromosome 16
5. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
6. Human Nod1 confers responsiveness to bacterial lipopolysaccharides
7. CARD15 mutations in Blau syndrome
8. Structure-function analysis of the tobacco mosaic virus resistance gene N
9. Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations