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Series GSE60812 Query DataSets for GSE60812
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
Summary We evaluated the effect of caRAS/dnRAS expression and TGF-beta on p63 binding in HaCaT cells.
 
Overall design p63 binding sites in HaCaT cells were determined by ChIP-seq.
 
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
Submission date Aug 27, 2014
Last update date May 15, 2019
Contact name Daizo Koinuma
E-mail(s) d-koinuma@umin.ac.jp
Organization name University of Tokyo
Department Pathology
Street address Hongo 7-3-1, Bunkyo-ku
City Tokyo
ZIP/Postal code 113-0033
Country Japan
 
Platforms (1)
GPL10999 Illumina Genome Analyzer IIx (Homo sapiens)
Samples (5)
GSM1489260 p63 ChIP-seq, HaCaT, LacZ, without TGFB
GSM1489261 p63 ChIP-seq, HaCaT, LacZ, with TGFB
GSM1489262 p63 ChIP-seq, HaCaT, caRAS, with TGFB
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
Relations
BioProject PRJNA259609
SRA SRP045807

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
GSE60812_RAW.tar 754.9 Mb (http)(custom) TAR (of BED, WIG)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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