NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE41872 Query DataSets for GSE41872
Status Public on Oct 27, 2012
Title Gene expression analysis after selective expression of tissue factor isoforms
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Analysis of TF isoform-induced breast cancer cell transformation at gene expression level. The hypothesis tested in the present study was that expression of TF isoforms upregulate genes involved in proliferation and transformation, while downregulating genes involved in cell cycle arrest and apoptosis. Results provide important information on the cellular response to TF expression with respect to pro-oncogenic programs .
 
Overall design Total RNA obtained from an MCF-7-based cell model (2A3-3) expressing full length tissue factor (2A3-3-flTF) or alternatvively spliced tissue factor (2A3-3-asTF) compared to cells expressing an empty vector control (2A3-3-pcDNA).
 
Contributor(s) Kocatürk B, Versteeg H
Citation(s) 23801760
Submission date Oct 26, 2012
Last update date Aug 13, 2018
Contact name Henri H Versteeg
E-mail(s) [email protected]
Phone +31-71-5263872
Organization name Leiden University Medical Center
Department Einthoven Lab for Experimental Vascular Medicine
Street address Albinusdreef 2
City Leiden
ZIP/Postal code 2333 ZA
Country Netherlands
 
Platforms (1)
GPL10558 Illumina HumanHT-12 V4.0 expression beadchip
Samples (10)
GSM1026834 2A3-3-pcDNA, replicate1
GSM1026835 2A3-3-pcDNA, replicate2
GSM1026836 2A3-3-pcDNA, replicate3
Relations
BioProject PRJNA178362

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
GSE41872_RAW.tar 26.2 Mb (http)(custom) TAR
GSE41872_non-normalized.txt.gz 3.0 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap