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Series GSE17594 Query DataSets for GSE17594
Status Public on Jan 01, 2010
Title NOD2 and human ileal gene expression
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Profiling of ileal mucosal gene expression in Chron's disease patients with and without NOD2 risk alleles; through microarray analyses it was discovered that 18 genes related to lymphocyte and phagocyte activation recuitment were upregulated in affected ileum in NOD2R patients as compared to ileum in NOD2s (no risk alleles) patients, thus supporting the concept that NOD2 risk alleles contribute to impaired regulation of inflammation in the ileum.
 
Overall design Mucosal biopsies of resected ileum were collected from 8 Crohn's disease patients at risk for NOD2R alleles. The patients were genotyped for the three major NOD2 risk alleles (Arg702Trp, Gly908Arg, Leu1007fs). Microarray analysis was performed in samples from NOD2R (at least one risk allele) Crohn’s disease patients, NOD2S (no risk alleles) Crohn’s disease patients and NOD2S controls.
 
Contributor(s) Li E, Hunt S
Citation(s) 20155851
Submission date Aug 11, 2009
Last update date Feb 22, 2018
Contact name Rekha Meyer
E-mail(s) rmeyer@pathbox.wustl.edu
Phone 314 362 8853
Organization name Washington University School of Medicine
Street address 4320 Forest Park Av
City St Louis
State/province MO
ZIP/Postal code 63128
Country USA
 
Platforms (2)
GPL4133 Agilent-014850 Whole Human Genome Microarray 4x44K G4112F (Feature Number version)
GPL6848 Agilent-012391 Whole Human Genome Oligo Microarray G4112A (Probe Name version)
Samples (20)
GSM438281 Unaffected ileum subject CD-124 N1
GSM438282 Affected ileum subject CD-124 II
GSM438283 Affected ileum subject CD-15 II
Relations
BioProject PRJNA118503

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE17594_RAW.tar 128.9 Mb (http)(custom) TAR (of GPR)
Processed data included within Sample table

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