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Series GSE55443 Query DataSets for GSE55443
Status Public on Aug 01, 2015
Title Candidates for bile acid-dependent PPARĪ±-target genes in mouse intestinal cells
Organism Mus musculus
Experiment type Expression profiling by array
Summary In addition to their role as a digestive detergent, bile acids have the ability to modulate the expression of genes. The intestinal content of cholic acids (CA) fluctuated in response to the daily feeding-fasting cycle; therefore, we hypothesized that the temporal accumulation of CA may affect the expression of genes in intestinal epithelial cells. To screen bile acid-regulated genes, we performed oligonucleotide microarray analyses using RNA isolated from the CA-treated intestinal cells of mice. Several types of genes were screened as candidates for bile acid-regulated genes. They included genes that encoded lipid metabolism-related proteins, receptors, transcriptional factors, and plasma-membrane transporters.
 
Overall design Total 2 samples were derived from [1] vehicle (0.05% DMSO and 0.25% ethanol)-treated intestinal epithelial cells of mice and [2] cholic acid (CA)-treated intestinal epithelial cells of mice.
 
Contributor(s) Koyanagi S, Okamura A, Dilxiat A, Kusunose N, Matsunaga N, Ohdo S
Citation(s) 25422143
Submission date Feb 27, 2014
Last update date Feb 02, 2018
Contact name Satoru Koyanagi
E-mail(s) skoyanagi@icloud.com
Organization name Kyushu University
Department Pharmaceutics
Street address 3-1-1 Maidashi, Higashi-ku
City Fukuoka
State/province Fukuoka
ZIP/Postal code 812-8582
Country Japan
 
Platforms (1)
GPL10787 Agilent-028005 SurePrint G3 Mouse GE 8x60K Microarray (Probe Name version)
Samples (2)
GSM1336903 S_I_Segment_Control
GSM1336904 S_I_Segment_CA
Relations
BioProject PRJNA239636

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
GSE55443_RAW.tar 21.8 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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