Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease

Inflammatory Bowel Diseases

Volumn 17, Issue 6, 2011, Pages 1392-1397

  Henckaerts, Liesbet ^a   Cleynen, Isabelle ^a   Brinar, Marko ^a   John, Jestinah Mahachie ^b   Van Steen, Kristel ^b   Rutgeerts, Paul ^a   Vermeire, Séverine ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b UNIVERSITY OF LIÈGE   (Belgium)

Author keywords

autophagy; Crohn's disease; pathogenesis; susceptibility

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; PEPTIDE; ULK1 PROTEIN; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; AUTOPHAGY; CONTROLLED STUDY; CROHN DISEASE; GENE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PHENOTYPE; PRIORITY JOURNAL; PROGENY; SINGLE NUCLEOTIDE POLYMORPHISM;

AUTOPHAGY; CASE-CONTROL STUDIES; CROHN DISEASE; GENETIC ASSOCIATION STUDIES; GENOTYPE; HAPLOTYPES; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN-SERINE-THREONINE KINASES; RISK FACTORS;

EID: 79955790354     PISSN: 10780998     EISSN: 15364844     Source Type: Journal    
DOI: 10.1002/ibd.21486     Document Type: Article

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