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Status |
Public on May 05, 2022 |
Title |
TRIM33 is an oncogenic transcriptional coactivator stabilizing AR from Skp2-mediated ubiquitin-proteasomal degradation in prostate cancer |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing Expression 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
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Citation(s) |
35785414 |
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Submission date |
May 17, 2021 |
Last update date |
Aug 09, 2022 |
Contact name |
Edwin Chong Wing CHEUNG |
E-mail(s) |
ECheung@um.edu.mo
|
Organization name |
University of Macau
|
Department |
Faculty of Health Sciences
|
Lab |
Edwin CHEUNG`s lab
|
Street address |
Avenida da Universidade, Taipa
|
City |
Macau |
State/province |
Macau |
ZIP/Postal code |
999078 |
Country |
China |
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Platforms (1) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
|
Samples (17)
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This SuperSeries is composed of the following SubSeries: |
GSE174109 |
TRIM33 is an oncogenic transcriptional coactivator stabilizing AR from Skp2-mediated ubiquitin-proteasomal degradation in prostate cancer [ChIP-seq] |
GSE174589 |
TRIM33 is an oncogenic transcriptional coactivator stabilizing AR from Skp2-mediated ubiquitin-proteasomal degradation in prostate cancer [RNA-Seq] |
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Relations |
BioProject |
PRJNA730585 |