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Series GSE37917 Query DataSets for GSE37917
Status Public on Aug 28, 2012
Title Sirt1, p53 and p38MAPK are crucial regulators of detrimental phenotypes of ESCs with Max expression ablation
Organism Mus musculus
Experiment type Expression profiling by array
Summary Ablation of expression of the Max gene encoding a Myc protein partner in ES cells provoked two major phenomena, i.e. loss of pluripotency and apoptotic cell death. We found that nicotinamide (Nam) significantly alleviates these Max expression ablation-coupled phenotypes in ES cells. To see the alleviation effect of Nam on the overall expression profile of Max-null ES cells whose Max expression is controlled by the tet-off system, we eliminated Max expression by adding doxycycline (Dox) in the presence of Nam.
 
Overall design DNA microarray analyses were performed using total RNAs from Nam (4 mM)-treated Max-null ES cells that were cultured in the presence or absence of doxycycline for 6 days.
 
Contributor(s) Hishida T, Nakachi Y, Mizuno Y, Okazaki Y, Okuda A
Citation(s) 22696478
Submission date May 10, 2012
Last update date Feb 11, 2019
Contact name Akihiko Okuda
E-mail(s) akiokuda@saitama-med.ac.jp
Phone 81-42-984-4787
Organization name Saitama Medical University
Department Research Center for Genomic Medicine
Lab Division of Biomedical Sciences
Street address 1397-1 Yamane
City Hidaka
State/province Saitama
ZIP/Postal code 3501241
Country Japan
 
Platforms (1)
GPL1261 [Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array
Samples (4)
GSM688705 Max-null ES Dox untreated ver2
GSM688706 Max-null ES Dox-treated (6 day)
GSM929906 Max-null ES cells (Nam+)(Dox-)
Relations
BioProject PRJNA165155

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
GSE37917_RAW.tar 13.8 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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