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Status |
Public on Jun 12, 2018 |
Title |
Discovery of Selective Estrogen Receptor Covalent Antagonists (SERCAs) for the treatment of ERa(WT) and ERa(MUT) breast cancer. |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array Expression profiling by high throughput sequencing Genome binding/occupancy profiling by high throughput sequencing
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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 missing |
Has this study been published? Please login to update or notify GEO. |
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Submission date |
Jun 11, 2018 |
Last update date |
Mar 26, 2019 |
Contact name |
Zhenhua Wu |
E-mail(s) |
zhenhuawu75@gmail.com
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Phone |
6179592279
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Organization name |
H3 Biomedicine
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Street address |
300 Technology Square floor 5
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City |
Cambridge |
State/province |
MA |
ZIP/Postal code |
02139 |
Country |
USA |
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Platforms (3) |
GPL570 |
[HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
GPL20301 |
Illumina HiSeq 4000 (Homo sapiens) |
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Samples (85)
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This SuperSeries is composed of the following SubSeries:
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GSE115564 |
ESR1 mutations maintain higher ER pathway activity relative to vehicle and ERa-WT controls following treatment with Raloxifene or fulvestrant. |
GSE115607 |
ChIP-Seq analysis of estrogen deprived MCF7 cells treated with H3B-5942 and standards of care compounds |
GSE115608 |
Transcriptional profiling of Ishikawa cells treated with H3B-5942, E2, or standard of care compounds |
GSE115609 |
Transcriptional profiling of MCF7 cells treated with H3B05942, E2, or standard of care compounds |
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Relations |
BioProject |
PRJNA475560 |