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Links from GEO DataSets

Items: 20

1.
Full record GDS3557

ERG transcription factor depletion effect on endothelial cell

Analysis of endothelial HUVEC cells depleted for the ETS-related gene (ERG) product. ERG is a member of the ETS family of transcription factors. Results provide insight into the role of ERG in the regulation of normal endothelial cell function.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 agent sets
Platform:
GPL570
Series:
GSE14801
6 Samples
Download data: CEL
2.

Expression data from ERG Si treated and Control HUVEC cells

(Submitter supplied) ERG (Ets Related Gene) is an ETS transcription factor that was originally described for its role in a number of human cancers. Our preliminary data demonstrate that ERG exhibits a highly EC restricted pattern of expression in cultured primary cells and several adult tissues including the heart, lung, and brain. In response to inflammatory stimuli, such as TNF-alpha, we observed a marked reduction of ERG expression in EC. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3557
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE14801
ID:
200014801
3.

Gene expression in HPAECs with ERG and FLI1 knockdown

(Submitter supplied) ERG and FLI1 were silenced in HPAECs using siRNA for 48h.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17889
2 Samples
Download data: CEL
Series
Accession:
GSE83641
ID:
200083641
4.

Gene expression profiling of Human Umbilical Vein Endothelial Cells (HUVEC) after treatment with Erg or control antisense (GeneBloc)

(Submitter supplied) The endothelial transcription factor Erg (Ets Related Gene) plays an important role in homeostasis and angiogenesis by regulating many endothelial functions including survival and junction stability. Here we show that Erg regulates endothelial cell migration. Transcriptome profiling of Erg-deficient endothelial cells (EC) identified 80 genes involved in cell migration as candidate Erg targets, including regulators of the Rho GTPases. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
15 Samples
Download data: CEL, CHP
Series
Accession:
GSE32984
ID:
200032984
5.

ERG and FLI1 in endothelial cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL570 GPL11154 GPL10999
20 Samples
Download data: BIGWIG, CEL
Series
Accession:
GSE109696
ID:
200109696
6.

Genome-wide analysis of ERG- and FLI1-binding in HUVECs, and histone modifications in HUVECs treated with siControl or siERG+siFLI1

(Submitter supplied) Endothelial-to-mesenchymal transition (EndMT) in which endothelial cells lose their characteristics and acquire mesenchymal property has recently been recognized as a driver of disease progression in wide range of pathologies. However, the regulatory mechanism of EndMT has not been fully understood. Here, we found that combined knockdown of two ETS family transcription factors, ERG and FLI1, induced EndMT. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL10999 GPL11154
12 Samples
Download data: BIGWIG
Series
Accession:
GSE109695
ID:
200109695
7.

Expression data in HUVECs treated with siERG, siFLI1, or both

(Submitter supplied) Endothelial-to-mesenchymal transition (EndMT) in which endothelial cells lose their characteristics and acquire mesenchymal property has recently been recognized as a driver of disease progression in wide range of pathologies. However, the regulatory mechanism of EndMT has not been fully understood. Here, we found that combined knockdown of two ETS family transcription factors, ERG and FLI1, induced EndMT. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE109662
ID:
200109662
8.

The transcription factor ERG regulates super-enhancers in endothelial cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18573 GPL11154
7 Samples
Download data: BEDGRAPH, BW
Series
Accession:
GSE124893
ID:
200124893
9.

The transcription factor ERG regulates super-enhancers in endothelial cells [ERG siRNA]

(Submitter supplied) We provide the functional and epigenomic evidence for ERG binding to super-enhancers in HUVEC and further show that loss of ERG results in inhibition of specific endothelial super-enhancers and associated target genes.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
5 Samples
Download data: BW
Series
Accession:
GSE124892
ID:
200124892
10.

The transcription factor ERG regulates super-enhancers in endothelial cells [ERG ChIP-seq]

(Submitter supplied) We provide the functional and epigenomic evidence for ERG binding to super-enhancers in HUVEC and further show that loss of ERG results in inhibition of specific endothelial super-enhancers and associated target genes.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: BEDGRAPH
Series
Accession:
GSE124891
ID:
200124891
11.

Analysis of ETS gene expression patterns uncovers novel ETS mediated gene silencing pathways in prostate cancers

(Submitter supplied) Deregulated expression of ETS transcription factors with oncogenic and tumor suppressor function occurs frequently in prostate cancer leading to profound alterations of the cancer transcriptome. By integrating genomic and functional studies we identified key targets of the aberrantly expressed ETS factors, ERG and ESE3. Altered expression of ETS factors led to the induction of the polycomb group protein EZH2 and silencing of the tumor suppressor Nkx3.1. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL887
67 Samples
Download data: TXT
Series
Accession:
GSE14206
ID:
200014206
12.

The oncofusion protein FUS-ERG targets key hematopoietic regulators and modulates the all-trans retinoic acid signaling pathway in t(16;21) acute myeloid leukemia

(Submitter supplied) Fusion proteins involving the ETS factor ERG have been associated with multiple cancers such as Ewing's sarcoma and prostate cancer. In acute myeloid leukemias harboring t(16;21) another ERG fusion protein is expressed, FUS-ERG. Here, we found that this FUS-ERG oncofusion protein acts in the context of a heptad of proteins (ERG, FLI1, GATA2, LYL1, LNMO2, RUNX1 and TAL1) central to proper expression of genes involved in maintaining a stem cell hematopoietic phenotype. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL11154 GPL10999
20 Samples
Download data: WIG
13.

Dysfunctional ERG signaling drives pulmonary vascular aging and persistent fibrosis

(Submitter supplied) We identified the transcription factor ETS-related gene (ERG) as a putative orchestrator of lung capillary homeostasis and repair following injury, and whose function was dysregulated in aging. Single-cell RNA-seq of ERG deficient mouse lungs revealed transcriptional abnormalities and fibrogenic features, resembling those associated with aging and IPF, including reduced number of lung progenitor ECs, known as general capillary (gCap) ECs.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: CSV
Series
Accession:
GSE187333
ID:
200187333
14.

Investigating the role of aging and lung fibrosis in Endothelial Cells with RNA sequencing

(Submitter supplied) In order to elucidate the contribute of the pulmonary vasculature to lung fibrosis, we injured young and aged mice with bleomycine, to create a model of resolving versus persistent lung fibrosis. The animals were sacrificed 30 days after the injury (time point in which we observed a divergent resolving vs persistent lung fibrosis in young vs aged mice). We found that lung fibrosis resolution in young mice was accompained by the activation of transcriptional programs promoting vascular repair and lung fibrosis resolution. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
16 Samples
Download data: TSV
Series
Accession:
GSE181508
ID:
200181508
15.

Investigating the role of aging and lung fibrosis in Endothelial Cells with ATAC sequencing

(Submitter supplied) In order to elucidate the contribute of the pulmonary vasculature to lung fibrosis, we injured young and aged mice with bleomycine, to create a model of resolving versus persistent lung fibrosis. The animals were sacrificed 30 days after the injury (time point in which we observed a divergent resolving vs persistent lung fibrosis in young vs aged mice).
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21103
18 Samples
Download data: TDF, TXT
Series
Accession:
GSE177055
ID:
200177055
16.

RNA-sequencing of human vascular endothelial cells after si-RNA mediated gene silencing of interleukin-6 (IL6)

(Submitter supplied) Purpose: To characterize the autocrine functions of IL6 in human endothelial cells Methods: Knockdown of interleukin-6 in cultured human umbilical vein endothelial cells were performed using stealth-siRNA and lipofectamine 2000. Total RNA was isolated 48h after siRNA introduction. RNA sequencing libraries were prepared using TruSeq stranded mRNA sample prep kit including poly-A selection. Sequencing was performed on a Illumina HiSeq2500 instrument. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
16 Samples
Download data: TAB
17.

Regulation of nuclear transcription by mitochondrial RNAs

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
22 Samples
Download data: MTX, TSV, TXT
Series
Accession:
GSE211971
ID:
200211971
18.

Regulation of nuclear transcription by mitochondrial RNAs [scRNA-seq/snRNA-seq]

(Submitter supplied) To understand the SncmtRNA-regulated endothelial gene expression. We performed single cell and single nuclear RNA-seq in endothelial cells with inhibition of SncmtRNA.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
8 Samples
Download data: MTX, TSV
Series
Accession:
GSE211970
ID:
200211970
19.

Regulation of nuclear transcription by mitochondrial RNAs [bulkRNA-seq]

(Submitter supplied) In order to understand the SncmtRNA-regulated endothelial transcriptome, we performed loss and gain of function of SncmtRNA and profiled transcriptome.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
14 Samples
Download data: TXT
Series
Accession:
GSE211969
ID:
200211969
20.

Stress-induced RNA–chromatin interactions promote endothelial dysfunction (scRNA-seq human vascular)

(Submitter supplied) Chromatin-associated RNA (caRNA) has been proposed as a type of epigenomic modifier. Here, we test whether environmental stress can induce cellular dysfunction through modulating RNA-chromatin interactions. We induce endothelial cell (EC) dysfunction with high glucose and TNFα (H + T), that mimic the common stress in diabetes mellitus. We characterize the H + T-induced changes in gene expression by single cell (sc)RNA-seq, DNA interactions by Hi-C, and RNA-chromatin interactions by iMARGI. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
10 Samples
Download data: MTX, TSV
Series
Accession:
GSE156341
ID:
200156341
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