|
Status |
Public on Mar 05, 2012 |
Title |
Whole-genome study reveals distinct mechanisms used by p53 to regulate activated and repressed genes in embryonic stem cells |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
This SuperSeries is composed of the SubSeries listed below.
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|
|
Overall design |
Refer to individual Series
|
|
|
Contributor(s) |
Huang J |
Citation(s) |
22387025 |
|
Submission date |
Dec 29, 2010 |
Last update date |
May 15, 2019 |
Contact name |
Jing Huang |
E-mail(s) |
[email protected]
|
Organization name |
National Cancer Institute
|
Lab |
Cancer Biology and Genetics
|
Street address |
37 Convent Dr. 37/3140
|
City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
MD 20892 |
Country |
USA |
|
|
Platforms (2) |
GPL6246 |
[MoGene-1_0-st] Affymetrix Mouse Gene 1.0 ST Array [transcript (gene) version] |
GPL9250 |
Illumina Genome Analyzer II (Mus musculus) |
|
Samples (24)
|
GSM412778 |
R1E Mock 4 |
GSM412779 |
R1E Adriamycin 1 |
GSM412780 |
R1E Adriamycin 2 |
GSM412781 |
R1E Adriamycin 3 |
GSM412782 |
R1E Adriamycin 4 |
GSM412783 |
R1E UV 1 |
GSM412784 |
R1E UV 2 |
GSM412785 |
R1E UV 3 |
GSM412786 |
R1E UV 4 |
GSM647216 |
mES, p53-/-, Ctr, rep1 |
GSM647217 |
mES, p53-/-, Ctr, rep2 |
GSM647218 |
mES, p53-/-, Ctr, rep3 |
GSM647219 |
mES, p53-/-, Adr, rep1 |
GSM647220 |
mES, p53-/-, Adr, rep2 |
GSM647221 |
mES, p53-/-, Adr, rep3 |
GSM647222 |
Input_seq_untreated |
GSM647223 |
Input_seq_Adr8h |
GSM647224 |
p53_ChIP_seq_untreated |
GSM647225 |
p53_ChIP_seq_Adr8h |
GSM647226 |
p53S18P_ChIP_seq_untreated |
GSM647227 |
p53S18P_ChIP_seq_Adr8h |
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This SuperSeries is composed of the following SubSeries: |
GSE26360 |
Genome-wide analysis revealed a crosstalk between p53 and the pluripotent gene networks in mouse embryonic stem cells (expression) |
GSE26361 |
Genome-wide analysis revealed a crosstalk between p53 and the pluripotent gene networks in mouse embryonic stem cells (ChIP-Seq) |
|
Relations |
BioProject |
PRJNA136879 |