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Links from GEO DataSets

Items: 18

1.
Full record GDS1922

Angiopoietin-1 and vascular endothelial growth factor angiogenic effect on aortic rings (RAE230A)

Analysis of aortic rings treated with angiopoietin-1 (Ang-1) or vascular endothelial growth factor (VEGF). Aortic rings can generate neovessels ex vivo after angiogenic factor stimulation. Results identify transcriptional events associated with angiogenesis in VEGF and Ang-1 stimulated aortic rings.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 3 agent sets
Platform:
GPL341
Series:
GSE3355
9 Samples
Download data
DataSet
Accession:
GDS1922
ID:
1922
2.

Genes associated with angiogenic response to Ang-1 or VEGF

(Submitter supplied) Specific Aims To identify novel transcriptional events associated with angiogenesis in VEGF and Ang-1 stimulated rat aortic rings. Our studies take advantage of the capacity of rat aortic rings to generate new vessels in collagen gels. Rat aortic rings embedded in collagen gel immediately after excision from the animal produce a self-limited angiogenic response under serum-free conditions and in the absence of exogenous stimuli. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Datasets:
GDS1922 GDS1923
Platforms:
GPL341 GPL342
18 Samples
Download data
Series
Accession:
GSE3355
ID:
200003355
3.
Full record GDS1923

Angiopoietin-1 and vascular endothelial growth factor angiogenic effect on aortic rings (RAE230B)

Analysis of aortic rings treated with angiopoietin-1 (Ang-1) or vascular endothelial growth factor (VEGF). Aortic rings can generate neovessels ex vivo after angiogenic factor stimulation. Results identify transcriptional events associated with angiogenesis in VEGF and Ang-1 stimulated aortic rings.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 3 agent sets
Platform:
GPL342
Series:
GSE3355
8 Samples
Download data
DataSet
Accession:
GDS1923
ID:
1923
4.

Gene expression in TNF treated rat aortic rings cultured in collagen or fibrin gels.

(Submitter supplied) Angiogenesis in cultures of rat aorta begins with neovessels sprouting from the aortic explant within the first three days of culture. We used microarrys to examine the effects of TNF-alpha on gene expression in both fibrin and collagen gels during the first 48 hours or culture.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6247
12 Samples
Download data: CEL
Series
Accession:
GSE23153
ID:
200023153
5.

Gene expression during first day of collagen gel culture of rat aortic rings

(Submitter supplied) Angiogenesis in collagen gel cultures of rat aorta begins with neovessels sprouting from the aortic explant within the first three days of culture. We used microarrays to detail the pattern of gene expression underlying initial 24 hours of growth, prior to the sprouting of visible neovessles, and identified distinct classes of up-regulated genes during this process.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6247
6 Samples
Download data: CEL
Series
Accession:
GSE23152
ID:
200023152
6.

Genes regulated by inflammatory cytokines in five primary endothelial cell types

(Submitter supplied) Genes regulated by inflammatory cytokines in five primary endothelial cell types Keywords: ordered
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS498 GDS499 GDS501 GDS502
Platform:
GPL371
15 Samples
Download data
Series
Accession:
GSE569
ID:
200000569
7.
Full record GDS502

Inflammatory cytokine effect on primary colon endothelial cells

Examination of gene expression induced by interferon gamma (IFNg), tumor necrosis factor alpha (TNFa) and interleukin 4 (IL4) inflammatory cytokines on primary colon endothelial cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, log ratio, 3 agent sets
Platform:
GPL371
Series:
GSE569
3 Samples
Download data
DataSet
Accession:
GDS502
ID:
502
8.
Full record GDS501

Inflammatory cytokine effect on primary dermal endothelial cells

Examination of gene expression induced by interferon gamma (IFNg), tumor necrosis factor alpha (TNFa) and interleukin 4 (IL4) inflammatory cytokines on primary dermal endothelial cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, log ratio, 3 agent sets
Platform:
GPL371
Series:
GSE569
3 Samples
Download data
DataSet
Accession:
GDS501
ID:
501
9.
Full record GDS499

Inflammatory cytokine effect on primary aortic endothelial cells

Examination of gene expression induced by interferon gamma (IFNg), tumor necrosis factor alpha (TNFa) and interleukin 4 (IL4) inflammatory cytokines on primary aortic endothelial cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, log ratio, 3 agent sets
Platform:
GPL371
Series:
GSE569
3 Samples
Download data
DataSet
Accession:
GDS499
ID:
499
10.
Full record GDS498

Inflammatory cytokine effect on primary lung endothelial cells

Examination of gene expression induced by interferon gamma (IFNg), tumor necrosis factor alpha (TNFa) and interleukin 4 (IL4) inflammatory cytokines on primary lung endothelial cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, log ratio, 3 agent sets
Platform:
GPL371
Series:
GSE569
3 Samples
Download data
DataSet
Accession:
GDS498
ID:
498
11.

Comparison between aortic and endocardial endothelial cells expression profiles

(Submitter supplied) Endocardial (EE) and Aortic (AE) endothelial cells were isolated from the same two rats, pooled (EE and AE kept separately) and cultured for 2 passages. Culture conditions and confluence of EE and AE cell cultures were kept as identical as possible. RNA was isolated and the expression profile of both endothelial cell types was compared using the Affymetrix rat genome U34A array. Keywords: parallel sample
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS695
Platform:
GPL85
2 Samples
Download data: CEL, EXP, RPT
Series
Accession:
GSE1478
ID:
200001478
12.
Full record GDS695

Cardiac and aortic endothelial cells

Gene expression profiles of endocardial (EE) and aortic (AE) endothelial cells. EE and AE genetic diversity in culture reflects in vivo physiological diversity.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 cell type sets
Platform:
GPL85
Series:
GSE1478
2 Samples
Download data: CEL, EXP, RPT
DataSet
Accession:
GDS695
ID:
695
13.

VEGF induction of HUVEC

(Submitter supplied) Angiogenesis, the formation of new capillaries by sprouting from preexisting vessels, is mainly induced by VEGF-A. To identify genes which are induced by VEGF-A in endothelial cells, HUVEC were starved and induced by VEGF-A165 for 30, 60 and 150min. RNA of induced and uninduced cells was isolated and subjected to microarray analysis using Affymetrix microarray.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3567
Platform:
GPL570
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE15464
ID:
200015464
14.

Comparison of VEGF versus EGF gene expression in HUVEC

(Submitter supplied) Angiogenesis is defined as the formation of new capillaries by sprouting from preexisting vessels. It is mainly triggered by vascular endothelial growth factor (VEGF) and occurs in the adult primarily in wound healing processes or in pathologic tumor vessel growth. To identify genes specifically triggered by VEGF and involved in the process of angiogenesis, we utilized Affymetrix microarrays hybridized with cRNA of human umbilical vein endothelial cells (HUVEC) stimulated with either the main trigger of angiogenesis, VEGF or a more general mitogenic growth factor, EGF. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS3568 GDS3570
Platforms:
GPL97 GPL96
14 Samples
Download data: CEL, CHP
Series
Accession:
GSE10778
ID:
200010778
15.
Full record GDS3570

VEGF-A effect on endothelial cell line: time course (HG-U133B)

Analysis of umbilical vein endothelial cells (HUVEC) treated with VEGF-A for up to 6 hours in vitro. VEGF-A is a major trigger of vasculogenesis and physiologic angiogenesis. Results provide insight into the molecular mechanisms underlying the vasculogenic and angiogenic activity of VEGF-A.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 5 time sets
Platform:
GPL97
Series:
GSE10778
5 Samples
Download data: CEL, CHP
16.
Full record GDS3568

VEGF-A effect on endothelial cell line: time course (HG-U133A)

Analysis of umbilical vein endothelial cells (HUVEC) treated with VEGF-A or EGF for up to 6 hours. VEGF-A is a major trigger of vasculogenesis and angiogenesis. EGF is a general growth factor. Results provide insight into the mechanisms underlying the vasculogenic and angiogenic activity of VEGF-A.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 agent, 5 time sets
Platform:
GPL96
Series:
GSE10778
9 Samples
Download data: CEL, CHP
17.
Full record GDS3567

VEGF-A effect on endothelial cell line: time course (HG-U133 Plus 2.0)

Analysis of umbilical vein endothelial cells (HUVEC) treated with VEGF-A for up to 150 minutes in vitro. VEGF-A is a major trigger of vasculogenesis and physiologic angiogenesis. Results provide insight into the molecular mechanisms underlying the vasculogenic and angiogenic activity of VEGF-A.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 4 time sets
Platform:
GPL570
Series:
GSE15464
4 Samples
Download data: CEL, CHP
18.

Correlating global gene regulation to morphogenesis and maturation in the chick extra-embryonic vascular system

(Submitter supplied) Formation of blood vessels requires the concerted regulation of an unknown number of genes in a spatial-, time- and dosage-dependent manner. We investigated vascular development in vivo by determining global gene regulation throughout the formation of the chick chorio-allantoic membrane (CAM). Our study provides a comprehensive molecular map of vascular maturation during developmental angiogenesis and might thus be a valuable resource to streamline further research of candidates susceptible to mediate pathological angiogenesis.
Organism:
Gallus gallus
Type:
Expression profiling by array
Platform:
GPL3213
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE11636
ID:
200011636
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