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Series GSE29647 Query DataSets for GSE29647
Status Public on Jun 01, 2011
Title Expression data from 9 and 13 weeks old TIFIAD1Cre mice
Organism Mus musculus
Experiment type Expression profiling by array
Summary We have investigated the p53-dependent stress response in medium spiny neurons (MSNs) that degenerate in Huntington’s disease. To induce p53 signaling cascade, we have genetically inactivated by the Cre/loxP system the essential RNA polymerase I (Pol I) transcription factor TIF-IA, leading to stabilization of p53 and induction of p53-dependent apoptosis.
In the present study, we selectively ablated the TIF-IA gene in MSNs by crossing TIF-IAflox/flox mice, homozygous for the floxed TIF-IA allele with transgenic mice expressing the Cre recombinase under the control of the D1 dopamine receptor (D1R) promoter.
 
Overall design To explore the molecular mechanisms underlying survival and death we profiled global gene expression in 9 and 13 week old control and TIF-IAD1RCre mutant mice (3 mice/each timepoint For each of the four conditions, five GeneChips were used each )
 
Contributor(s) Parkitna JR, Kreiner G, Schütz G, Parlato R
Citation(s) 23764776
Submission date Jun 01, 2011
Last update date May 04, 2018
Contact name Grzegorz Kreiner
E-mail(s) kreiner@if-pan.krakow.pl
Organization name Institute of Pharmacology
Department Dept. Brain Biochemistry
Street address Smetna 12
City Krakow
ZIP/Postal code 31-343
Country Poland
 
Platforms (1)
GPL8321 [Mouse430A_2] Affymetrix Mouse Genome 430A 2.0 Array
Samples (12)
GSM735013 9weeks, control, biol.rep1
GSM735014 9weeks, control, biol.rep2
GSM735015 9weeks, control, biol.rep3
Relations
BioProject PRJNA141231

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
GSE29647_RAW.tar 38.6 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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