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Links from GEO DataSets

Items: 12

1.

Inhibition of EB3 activates the Meis2-Pax6 regenerative program in wet AMD [scRNA-seq]

(Submitter supplied) Wet age-related macular degeneration (AMD), characterized by leaky neovessels emanating from the choroid, is a main cause of blindness. As current treatments for wet AMD require regular intravitreal injections of anti-VEGF biologics, there is a need for the novel development of less invasive treatments. Here, we developed a novel inhibitor of microtubule-associated End Binding 3 protein (EB3), herein termed EBIN, which blocked pathological Ca2+ signaling in activated endothelial cells and suppressed leakage of choroidal neovessels. more...
Organism:
Chlorocebus sabaeus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28895
6 Samples
Download data: MTX, TSV, TXT
Series
Accession:
GSE228273
ID:
200228273
2.

Inhibition of EB3 activates the Meis2-Pax6 regenerative program in wet AMD

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Chlorocebus sabaeus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL28895 GPL21566 GPL20301
20 Samples
Download data: MTX, TSV
Series
Accession:
GSE228276
ID:
200228276
3.

Inhibition of EB3 activates the Meis2-Pax6 regenerative program in wet AMD [scATAC-seq]

(Submitter supplied) Wet age-related macular degeneration (AMD), characterized by leaky neovessels emanating from the choroid, is a main cause of blindness. As current treatments for wet AMD require regular intravitreal injections of anti-VEGF biologics, there is a need for the novel development of less invasive treatments. Here, we developed a novel inhibitor of microtubule-associated End Binding 3 protein (EB3), herein termed EBIN, which blocked pathological Ca2+ signaling in activated endothelial cells and suppressed leakage of choroidal neovessels. more...
Organism:
Chlorocebus sabaeus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21566 GPL28895
4 Samples
Download data: BED, MTX, TSV, TXT
Series
Accession:
GSE228270
ID:
200228270
4.

Inhibition of EB3 activates the Meis2-Pax6 regenerative program in wet AMD [RNA-seq]

(Submitter supplied) Wet age-related macular degeneration (AMD), characterized by leaky neovessels emanating from the choroid, is a main cause of blindness. As current treatments for wet AMD require regular intravitreal injections of anti-VEGF biologics, there is a need for the novel development of less invasive treatments. Here, we developed a novel inhibitor of microtubule-associated End Binding 3 protein (EB3), herein termed EBIN, which blocked pathological Ca2+ signaling in activated endothelial cells and suppressed leakage of choroidal neovessels. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
10 Samples
Download data: TXT
Series
Accession:
GSE228269
ID:
200228269
5.

Single-cell transcriptome of wet AMD patient-derived endothelial cells in angiogenic sprouting

(Submitter supplied) Age-related macular degeneration (AMD) is a global leading cause of visual impairment in older populations. ‘Wet’ AMD, the most common subtype of this disease, occurs when pathological angiogenesis infiltrates the subretinal space (choroidal neovascularization), causing hemorrhage and retinal damage. Gold standard anti-vascular endothelial growth factor (VEGF) treatment is an effective therapy, but the long-term prevention of visual decline has not been as successful. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
6 Samples
Download data: MTX, TSV
Series
Accession:
GSE213933
ID:
200213933
6.

An angiogenic role for the aryl hydrocarbon receptor in choroidal neovascularization

(Submitter supplied) We report that decreased expression and activity of AhR exacerbates murine neovascular age-related macular degeneration, and increases cell migration and tube formation. The mechanism involves increased expression of pro-angiogenic mediators and altered matrix degradation. The results of our study suggest that the AhR signaling pathway may be important in multiple AMD related pathways.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: TXT
Series
Accession:
GSE56983
ID:
200056983
7.

RNA-seq of CYR61-treated THP1 human monocytes

(Submitter supplied) We assess the effects of CYR61 treatment on the transcriptome of human THP1 monocytes.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
20 Samples
Download data: TSV
Series
Accession:
GSE233125
ID:
200233125
8.

scRNAseq of peripheral blood mononuclear cells in age-related macular degeneration

(Submitter supplied) We profiled using single cell RNA sequencing the peripheral blood mononuclear cells from control patients and patients with age-related macular degeneration (AMD).
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
65 Samples
Download data: CSV, MTX, TSV
Series
Accession:
GSE222647
ID:
200222647
9.

Bulk RNA-seq of: HUVECs co-incubated with CYR61-treated mouse bone marrow-derived macrophages; CYR61-treated murine bone marrow-derived macrophages; CYR61-treated HUVECs; and CYR61-treated human THP1 monocytes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24676 GPL24247
69 Samples
Download data
Series
Accession:
GSE222102
ID:
200222102
10.

RNA-seq of CYR61-treated human umbilical vein endothelial cells

(Submitter supplied) We assess the effect of CYR61 treatment on the transcriptome of human umbilical vein endothelial cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
20 Samples
Download data: TSV
Series
Accession:
GSE222101
ID:
200222101
11.

RNA-seq of CYR61-treated murine bone marrow-derived macrophages

(Submitter supplied) We assess the effect of CYR61 treatment on the transcriptome of mouse bone marrow-derived macrophages.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
11 Samples
Download data: TSV
Series
Accession:
GSE222100
ID:
200222100
12.

RNA-seq of human umbilical vein endothelial cells co-incubated with CYR61-treated mouse bone marrow-derived macrophages

(Submitter supplied) We assess the transcriptional changes when human umbilical vein endothelial cells are co-incubated with naïve or CYR61-activated mouse bone marrow-derived macrophages.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
18 Samples
Download data: TSV
Series
Accession:
GSE222099
ID:
200222099
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