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Status |
Public on Aug 12, 2016 |
Title |
p63 binding regions in HaCaT epidermal keratinocyte infected with caRAS/dnRAS and treated with TGF-beta |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We evaluated the effect of caRAS/dnRAS expression and TGF-beta on p63 binding in HaCaT cells.
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Overall design |
p63 binding sites in HaCaT cells were determined by ChIP-seq.
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Contributor(s) |
Vasilaki E, Morikawa M, Koinuma D, Mizutani A, Hirano Y, Ehata S, Sundqvist A, Aburatani H, Moustakas A, Heldin C, Miyazono K |
Citation(s) |
27555661 |
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Submission date |
Aug 27, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Daizo Koinuma |
E-mail(s) |
d-koinuma@umin.ac.jp
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Organization name |
University of Tokyo
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Department |
Pathology
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Street address |
Hongo 7-3-1, Bunkyo-ku
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City |
Tokyo |
ZIP/Postal code |
113-0033 |
Country |
Japan |
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Platforms (1) |
GPL10999 |
Illumina Genome Analyzer IIx (Homo sapiens) |
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Samples (5)
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This SubSeries is part of SuperSeries: |
GSE60814 |
Ras and TGF-beta signaling aggravates the metastatic and invasive potential of cancer cells through activation of the deltaNp63 alpha transcriptional program |
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Relations |
BioProject |
PRJNA259609 |
SRA |
SRP045807 |
Supplementary file |
Size |
Download |
File type/resource |
GSE60812_RAW.tar |
754.9 Mb |
(http)(custom) |
TAR (of BED, WIG) |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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