Functional consequences of mutations in the autophagy genes in the pathogenesis of Crohn's disease

Inflammatory Bowel Diseases

Volumn 18, Issue 4, 2012, Pages 778-781

  Brain, Oliver ^a   Cooney, Rachel ^b   Simmons, Alison ^a   Jewell, Derek ^c  

^a JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^b SANDWELL AND WEST BIRMINGHAM HOSPITALS NHS TRUST   (United Kingdom)

^c JRH   (United Kingdom)

Author keywords

Autophagy; Crohn's disease; Functional studies

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; HIGH MOBILITY GROUP B1 PROTEIN; INTERLEUKIN 18; INTERLEUKIN 1BETA;

ALLELE; AUTOPHAGOSOME; AUTOPHAGY; CHROMOSOME 5Q; CROHN DISEASE; GENE; GENE EXPRESSION; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; IRGM GENE; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM;

AUTOPHAGY; CARRIER PROTEINS; CROHN DISEASE; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GTP-BINDING PROTEINS; HUMANS; MALE; MUTATION; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84858699555     PISSN: 10780998     EISSN: 15364844     Source Type: Journal    
DOI: 10.1002/ibd.21832     Document Type: Review

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