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Links from GEO DataSets

Items: 12

1.

Human umbilical vein endothelial cells (HUVECs): VEGF vs. ctrl, oxPAPC vs. ctrl

(Submitter supplied) MicroRNA profiling of human endothelial cells comparing VEGF and oxPAPC treated cells with their respective control-treated cells
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL15829
12 Samples
Download data: TXT
Series
Accession:
GSE102501
ID:
200102501
2.

NRF2 Controls Endothelial Plasticity with miR-93

(Submitter supplied) Here we studied the role of oxidized phospholipids in mediating phenotype switching of endothelial cells between quiescent and angiogenic states. Two oxPAPC datasets, a microRNA array and global run-on sequencing (GRO-seq), was combined with Nuclear factor erythroid 2-Related Factor 2 (NRF2) binding model to select candidate miRNAs for further studies. The pre-screening resulted in a selection of miR-106b~25 cluster for further studies. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL11154
2 Samples
Download data: BEDGRAPH
3.

miR-93 Targets in Human Endothelial Cells

(Submitter supplied) miR-93-5p controls endothelial glycolysis and proliferation
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
14 Samples
Download data: TXT
4.

NRF2 is a key regulator of endothelial miRNA expression under pro-atherogenic stimuli

(Submitter supplied) Regulation of coding and non-coding genes is studied from primary human aortic endothelial cells (HAECs), venous endothelial cells (HUVECs), aortic smooth muscle cells (HASMCs) and macrophages (CD14+) under pro-atherogenic stimuli (hypoxia, oxPAPC and hypoxia+oxPAPC) by integrating three different sequencing techinques: GRO-seq, miRNA-seq and RNA-seq
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing; Other
Platforms:
GPL16791 GPL18573 GPL11154
62 Samples
Download data: BEDGRAPH, TXT
5.

MicroRNA Profiling of Endothelial Cells

(Submitter supplied) In this study, the miRNA expression of human vascular endothelial cells from tissue-derived cells and cultured cells were profiled using miRNA sequencing. The data analysis revealed a striking switch in endothelial miRNA profile as the cells adapted from tissue to cell culture environment and the overall miRNA expression decreased significantly in cultured endothelial cells compared to tissue-derived endothelial cells. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18573
15 Samples
Download data: TXT
6.

Genome-wide microRNA analysis of reticulocytes isolated from patients with sickle cell disease

(Submitter supplied) MiRNAs are non-protein-coding small RNA molecules negatively regulating gene through inhibition of mRNA. The characteristics of microRNA expression patterns obtained from sickle cell diseases are not clearly elucidated. In this study, we recruited 12 children and adults suffering from sickle cells diseases with high HbF fetal hemoglobin (HbF) group (6 subjects) and lower HbF (6 subjects). The peripheral blood mononuclear cell (PBMN) were processed using a MACS column with magnetic anti-CD71 antibody to isolate reticulocytes according to the manufacturer’s instructions (Miltenyi Biotec, San Diego, CA). more...
Organism:
Rattus norvegicus; Homo sapiens; Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL17728
12 Samples
Download data: TXT
Series
Accession:
GSE111356
ID:
200111356
7.

UV- or oxidized lipid treated dermal skin fibroblasts

(Submitter supplied) Long wavelength Ultraviolet (UVA-1) radiation causes oxidative stress that leads to the formation of noxious substances within the skin. As a defensive mechanism skin cells produce detoxifying enzymes and antioxidants when they detect modified molecules. We have recently shown that UVA-1 irradiation oxidizes the abundant membrane phospholipid 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine (PAPC), which then induced the synthesis of the stress response protein heme oxygenase 1 (HO-1) in dermal fibroblasts. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE13606
ID:
200013606
8.

Expression data from iPSCs generated with Yamanaka factors and miR-302 cluster

(Submitter supplied) Baseline gene expression of adipose stem cell derived iPSCs generated by lentiviral Yamanaka 4 factors. We used microarrays to analyze the global gene expression of hACS derived iPSCs with KMOS and KMOS+miR-302.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE37896
ID:
200037896
9.

MicroRNA Regulation of Oxidative Stress, Proliferation, and Neural Tube Closure

(Submitter supplied) single-cell sequencing of the mouse cranial region at E8.25 (the start of neural tube closure, at E9.5 (the end of neural tube closure, and of a miR-302 knockout embryo at E9.5 (example of neural tube closure defrect).
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
3 Samples
Download data: RDS
Series
Accession:
GSE158449
ID:
200158449
10.

Reversal of high-glucose-induced transcriptional and epigenetic memories through NRF2 pathway activation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
29 Samples
Download data: BED
Series
Accession:
GSE241566
ID:
200241566
11.

Reversal of high-glucose-induced transcriptional and epigenetic memories through NRF2 pathway activation (RNA-seq).

(Submitter supplied) Aims: Evaluate the genome-wide gene expression and epigenomic alterations caused by transient high glucose (HG) in endothelial cells (ECs), and to assess NRF2 pathway activation as a potential treatment for the diabetes-associated transcriptional memory. Methods and results: We exposed human umbilical vein endothelial cells (HUVEC) to three different glucose treatments: control (5.5 mM for 8 days), HG (30 mM for 8 days) and memory (5.5 mM for 4 days followed by 30 mM for 4 days). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
21 Samples
Download data: TXT
Series
Accession:
GSE241565
ID:
200241565
12.

Reversal of high-glucose-induced transcriptional and epigenetic memories through NRF2 pathway activation (ATAC-seq).

(Submitter supplied) Aims: Evaluate the genome-wide gene expression and epigenomic alterations caused by transient high glucose (HG) in endothelial cells (ECs), and to assess NRF2 pathway activation as a potential treatment for the diabetes-associated transcriptional memory. Methods and results: We exposed human umbilical vein endothelial cells (HUVEC) to three different glucose treatments: control (5.5 mM for 8 days), HG (30 mM for 8 days) and memory (5.5 mM for 4 days followed by 30 mM for 4 days). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: BED
Series
Accession:
GSE241564
ID:
200241564
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