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Series GSE49428 Query DataSets for GSE49428
Status Public on Sep 01, 2013
Title Global analysis of NFATc1 binding and histone marks in VEGF-activated endothelial cells
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary We performed the newly mapping of genome-wide NFATc1 binding events in VEGF-stimulated primary cultured endothelial cells, by chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq). Combined NFATc1 ChIP-seq profile and the epigenetic histone marks revealed that predominant NFATc1-occupied peaks were overlapped with promoter marking but not silencer marking. DNA microarrays with NFATc1 expression or knockdown indicated the predominant NFATc1 binding targets were correlated with induced patterns.
 
Overall design Examination of NFATc1 and two different histone marks in HUVEC in the presence/absense of VEGF.
 
Contributor(s) Suehiro J, Kanki Y, Miura M, Manabe Y, Aburatani H, Kodama T, Minami T
Citation(s) 25157100
Submission date Jul 31, 2013
Last update date May 15, 2019
Contact name Jun-ichi Suehiro
Organization name Kyorin University School of Medicine
Department Department of Pharmacology and Toxicology
Street address 6-20-2, Shinkawa
City Mitaka
State/province Tokyo
ZIP/Postal code 181-8611
Country Japan
 
Platforms (1)
GPL10999 Illumina Genome Analyzer IIx (Homo sapiens)
Samples (6)
GSM1208343 HUVEC_H3K4me3 0h
GSM1208344 HUVEC_H3K4me3 VEGF_1h
GSM1208345 HUVEC_NFATc1_0h
This SubSeries is part of SuperSeries:
GSE49429 Genome-wide approaches reveal functional VEGF-inducible NFATc1 binding to the angiogenesis-related genes in endothelium
Relations
BioProject PRJNA215174
SRA SRP028803

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
GSE49428_RAW.tar 272.1 Mb (http)(custom) TAR (of WIG)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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