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Links from GEO DataSets

Items: 20

1.
Full record GDS1372

Bone morphogenic protein 2 effect on idiopathic pulmonary arterial hypertension

Analysis of pulmonary artery smooth muscle cells (PASMC) from patients with idiopathic pulmonary arterial hypertension (IPAH). PASMC treated with 200 nM bone morphogenic protein 2 (BMP-2) for 24 hours. BMP signaling dysfunction has been implicated in IPAH.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 2 disease state sets
Platform:
GPL8300
Series:
GSE2559
7 Samples
Download data
2.

Effect of BMP-2 on Pulmonary Artery Smooth Muscle Cells from Patients with Idiopathic Pulmonary Arterial Hypertension

(Submitter supplied) Bone morphogenetic proteins (BMP) inhibit proliferation and induce apoptosis in pulmonary artery smooth muscle cells (PASMC) from normal subjects. Dysfunction of BMP signaling due to mutations in and/or downregulation of BMP receptors has been implicated in idiopathic pulmonary arterial hypertension (IPAH). We examined whether BMP differentially regulates gene expression in PASMC from normal subjects and IPAH patients using the Affymetrix microarray analysis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1372
Platform:
GPL8300
7 Samples
Download data
Series
Accession:
GSE2559
ID:
200002559
3.

Il13-stimulation of human paSMCs

(Submitter supplied) Idiopathic pulmonary arterial hypertension (IPAH) is characterized by medial hypertrophy due to pulmonary arterial smooth muscle cell (paSMC) hyperplasia. Interleukin (IL)-13 is a potent regulator of tissue fibrosis and remodelling, and its effects are dependent on the cell-type specific expression of the IL-13 receptor isotypes IL-4Rα, IL-13Rα1, and IL-13Rα2. In order to identify the possible mechanism how IL-13 can exert its antiproliferative effect on paSMC microarray analysis was performed. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1708
6 Samples
Download data: GPR
Series
Accession:
GSE15739
ID:
200015739
4.

RNA sequencing of healthy and diseased (idiopathic pulmonary hypertension) human pulmonary artery smooth muscle cells

(Submitter supplied) We performed RNA-seq to analyze gene expression in human PASMCs (Pulmonary arterial smooth muscle cells) isolated from subjects without disease and from subjects with IPAH (idiopathic pulmonary hypertension)
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
8 Samples
Download data: XLSX
5.

A critical role of microRNAs in human pulmonary arterial hypertension. miR-204: a novel therapeutic target

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by RT-PCR
Platforms:
GPL4133 GPL10305
8 Samples
Download data: TXT
Series
Accession:
GSE21284
ID:
200021284
6.

A critical role of microRNAs in human pulmonary arterial hypertension. miR-204: a novel therapeutic target (TaqMan qPCR)

(Submitter supplied) Pulmonary arterial hypertension (PAH) is a vascular remodeling disease characterized by enhanced pulmonary artery smooth muscle cell (PASMC) proliferation and suppressed apoptosis. Downregulation of the BMPR2 gene along with activation of the transcription factor NFAT have been implicated in the maintenance of pro-proliferative and anti-apoptotic stages of cells. Since an increasing number of microRNAs have been implicated in the regulation of genes specifically important for cell proliferation and apoptosis, we hypothesized that microRNAs might be associated with these cellular features in the etiology of PAH. more...
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL10305
4 Samples
Download data: TXT
Series
Accession:
GSE21281
ID:
200021281
7.

A critical role of microRNAs in human pulmonary arterial hypertension. miR-204: a novel therapeutic target (gene expression)

(Submitter supplied) Pulmonary arterial hypertension (PAH) is a vascular remodeling disease characterized by enhanced pulmonary artery smooth muscle cell (PASMC) proliferation and suppressed apoptosis. Downregulation of the BMPR2 gene along with activation of the transcription factor NFAT have been implicated in the maintenance of pro-proliferative and anti-apoptotic stages of cells. Since an increasing number of microRNAs have been implicated in the regulation of genes specifically important for cell proliferation and apoptosis, we hypothesized that microRNAs might be associated with these cellular features in the etiology of PAH. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
4 Samples
Download data: TXT
Series
Accession:
GSE21280
ID:
200021280
8.

Plasma microRNA profile in chronic thromboembolic pulmonary hypertension patients and healthy controls

(Submitter supplied) We aimed to identify the ebbrantly hypothesized that circulating miRNA profile might reflect the miRNAs involved in the pathogenesis of CTEPH more comprehensively, thus could be used as candidate biomarker and shed light on the recognition of CTEPH pathogenesis.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL18587
20 Samples
Download data: TXT
Series
Accession:
GSE56914
ID:
200056914
9.

SMAD1/5 binding regions of human pulmonary arterial smooth muscle cells (PASMCs) treated with BMP

(Submitter supplied) Smad1/5 are transcription factors that engage in BMP-induced transcription. We determined and analyzed Smad1/5 binding sites by ChIP-sequencing. We used expression microarrays to compare the Smad1/5 binding sites identified by ChIP-seq to BMP-induced gene expressions.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9115
2 Samples
Download data: BED, WIG
Series
Accession:
GSE28848
ID:
200028848
10.

Expression data of human pulmonary arterial smooth muscle cells (PASMCs) treated with BMP-4

(Submitter supplied) Smad1/5 are transcription factors that engage in BMP-induced transcription. We determined and analyzed Smad1/5 binding sites by ChIP-sequencing. We used expression microarrays to compare the Smad1/5 binding sites identified by ChIP-seq to BMP-induced gene expressions.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
3 Samples
Download data: CEL
Series
Accession:
GSE28847
ID:
200028847
11.

SMAD1/5 binding regions and expression data of human umbilical vein endothelial cells (HUVECs) and pulmonary arterial smooth muscle cells (PASMCs) treated with BMPs

(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:
GPL9115 GPL570
12 Samples
Download data: BED, CEL, WIG
Series
Accession:
GSE27661
ID:
200027661
12.

SMAD1/5 binding regions of human umbilical vein endothelial cells (HUVECs) treated with BMP.

(Submitter supplied) Smad1/5 binding regions were identified by ChIP-seq.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9115
2 Samples
Download data: BED, WIG
Series
Accession:
GSE27634
ID:
200027634
13.

Expression data of human umbilical vein endothelial cells (HUVECs) treated with BMP-6 and BMP-9

(Submitter supplied) Smad1/5 are transcription factors that engage in BMP-induced transcription. We determined and analyzed Smad1/5 binding sites by ChIP-sequencing. We used expression microarrays to compare the Smad1/5 binding sites identified by ChIP-seq to BMP-induced gene expressions.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
5 Samples
Download data: CEL
Series
Accession:
GSE27631
ID:
200027631
14.

Expression data analysis in lungs from mice induced for pulmonary arterial hypertension (PAH) by inhalation of Stachybotrys chartarum spores

(Submitter supplied) It has been reported that repeated intra-tracheal instillation of S. chartarum spores induced significant pulmonary arterial remodeling in mice, which resulted in pathological changes like human pulmonary arterial hypertension (PAH) and elevation right ventricle systolic pressure. Then, we used microarrays to know the complex molecular mechanisms that underlie pathogenesis of PAH.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE23178
ID:
200023178
15.

Digital Spatial Profiling identifies distinct molecular signatures of vascular lesions in Pulmonary Arterial Hypertension

(Submitter supplied) Idiopathic Pulmonary Arterial Hypertension (IPAH) is a severe human disease, characterized by extensive pulmonary vascular remodeling due to plexiform and obliterative lesions, media hypertrophy, and alterations of adventitia. The objective of the study was to test the hypothesis that microscopic IPAH vascular lesions express unique molecular profiles, which collectively are different from control pulmonary arteries. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL30991
220 Samples
Download data: DCC, TXT
Series
Accession:
GSE256539
ID:
200256539
16.

DNA methylation signatures of pulmonary arterial smooth muscle cells in chronic thromboembolic pulmonary hypertension

(Submitter supplied) DNA methylation signatures of pulmonary arterial smooth muscle cells in chronic thromboembolic pulmonary hypertension
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
8 Samples
Download data: IDAT, TXT
Series
Accession:
GSE113061
ID:
200113061
17.

Anti-proliferative effect of selexipag active metabolite MRE-269 on pulmonary arterial smooth muscle cells from patients with chronic thromboembolic pulmonary hypertension

(Submitter supplied) Chronic thromboembolic pulmonary hypertension (CTEPH) is a group 4 pulmonary hypertension (PH) characterized by non-resolving thromboembolism in the central pulmonary artery and vascular occlusion in the proximal and distal pulmonary artery. Medical therapy is chosen for patients who are ineligible for pulmonary endarterectomy or balloon pulmonary angioplasty or who have symptomatic residual PH after surgery or intervention. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
15 Samples
Download data: TXT
Series
Accession:
GSE221511
ID:
200221511
18.

Blood pulmonary arterial hypertension

(Submitter supplied) Microarray analysis of peripheral blood mononuclear (PBMC) cells in pulmonary arterial hypertension. Keywords = mononuclear cells Keywords = gene microarray Keywords = pulmonary arterial hypertension Keywords = Herpesvirus Keywords = biomarker Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS504
Platform:
GPL80
20 Samples
Download data
Series
Accession:
GSE703
ID:
200000703
19.
Full record GDS504

Pulmonary arterial hypertension and PBMC

Analysis of peripheral blood mononuclear (PBMC) cells in patients with pulmonary arterial hypertension (PAH). Altered gene expression patterns in PAH PBMCs may allow disease subgroup identification and prediction of treatment response.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL80
Series:
GSE703
20 Samples
Download data
DataSet
Accession:
GDS504
ID:
504
20.

Transcriptional profiling of lung cell populations in idiopathic pulmonary arterial hypertension

(Submitter supplied) Despite recent improvements in management of idiopathic pulmonary arterial hypertension, mortality remains high. Understanding the alterations in the transcriptome–phenotype of the key lung cells involved could provide insight into the drivers of pathogenesis. In this study, we examined differential gene expression of cell types implicated in idiopathic pulmonary arterial hypertension from lung explants of patients with idiopathic pulmonary arterial hypertension compared to control lungs. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL20795 GPL18573
11 Samples
Download data: H5
Series
Accession:
GSE169471
ID:
200169471
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