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Links from GEO DataSets

Items: 20

1.

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
2.

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
3.

Apelin/APJ targeted microRNAs in pulmonary artery endothelial cells

(Submitter supplied) Evaluation of microRNAs that are downstream of apelin/APJ signaling in the pulmonary artery endothelial cells.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL8179
12 Samples
Download data: TXT
Series
Accession:
GSE42343
ID:
200042343
4.

Single cell RNA sequencing of distal thrombus tissue from CTEPH patients

(Submitter supplied) Our current understanding of CTEPH pathobiology is primarily derived from cell-based studies limited by the use of specific cell markers or phenotypic modulation in cell culture. Therefore, our main objective is to identify the multiple cell types that comprise the CTEPH thrombus and to study their dysfunction. Here we used single cell RNA sequencing (scRNAseq) of tissue removed at the time of pulmonary endarterectomy (PEA) surgery from five patients to identify the multiple cell types. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
5 Samples
Download data: MTX, TSV
Series
Accession:
GSE224143
ID:
200224143
5.

Let-7b regulates skeletal muscle growth, development and fat deposition in deletion-type dwarf chickens

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Gallus gallus
Type:
Non-coding RNA profiling by array
Platform:
GPL15455
6 Samples
Download data: TXT
Series
Accession:
GSE37368
ID:
200037368
6.

Let-7b regulates skeletal muscle growth, development and fat deposition in deletion-type dwarf chickens (7-week-old chickens)

(Submitter supplied) A deletion mutation in the growth hormone receptor (GHR) gene results in the inhibition of skeletal muscle growth and fat deposition in dwarf chickens. In this study, microarray techniques were used to detect the miRNA and mRNA expression profiles of 14-day-old embryo and 7-week-old chicken skeletal muscle of deletion-type dwarf chickens and normal-type chickens. Skeletal muscle tissues of Dwarf recessive White Rock chickens and normal recessive White Rock chickens were used to make the microarray assay. more...
Organism:
Gallus gallus
Type:
Non-coding RNA profiling by array
Platform:
GPL15455
3 Samples
Download data: TXT
Series
Accession:
GSE37367
ID:
200037367
7.

Let-7b regulates skeletal muscle growth, development and fat deposition in deletion-type dwarf chickens (14-day-old embryos)

(Submitter supplied) A deletion mutation in the growth hormone receptor (GHR) gene results in the inhibition of skeletal muscle growth and fat deposition in dwarf chickens. In this study, microarray techniques were used to detect the miRNA and mRNA expression profiles of 14-day-old embryo and 7-week-old chicken skeletal muscle of deletion-type dwarf chickens and normal-type chickens. Skeletal muscle tissues of Dwarf recessive White Rock chickens and normal recessive White Rock chickens were used to make the microarray assay. more...
Organism:
Gallus gallus
Type:
Non-coding RNA profiling by array
Platform:
GPL15455
3 Samples
Download data: TXT
Series
Accession:
GSE37360
ID:
200037360
8.

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
9.
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
10.

Circulating miR-let7a levels predict future development of chronic thromboembolic pulmonary hypertension

(Submitter supplied) RNA was isolated from plasma of 20 healthy patients and 20 patients with acute pulmonary embolism. Dysregulated microRNA patterns were screened in these samples
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL33921
40 Samples
Download data: TXT
Series
Accession:
GSE247365
ID:
200247365
11.

MicroRNA expression of fetal pulmonary hypertension in an ovine model

(Submitter supplied) Persistent pulmonary hypertension of the newborn (PPHN) occurs when pulmonary vascular resistance (PVR) fails to decrease at birth. Decreased angiogenesis in the lung contributes to the persistence of high PVR at birth. MicroRNAs (miRNAs) regulate gene expression through transcript binding and degradation. They were implicated in dysregulated angiogenesis in cancer and cardiovascular disease. We investigated whether altered miRNA levels contribute to impaired angiogenesis in PPHN. more...
Organism:
Ovis aries
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL24916
12 Samples
Download data: XLSX
Series
Accession:
GSE211867
ID:
200211867
12.

Single-cell mRNAseq human pulmonary arterial endothelial cells in healthy and pulmonary arterial hypertension

(Submitter supplied) We report the single cell transcriptomic profiles of isolated and cultured human pulmonary arterial endothelial cells. Details were published in Scientifc Reports | (2021) 11:14714
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: MTX, TSV
Series
Accession:
GSE185479
ID:
200185479
13.

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
14.

Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension [ChIA-PET]

(Submitter supplied) Pulmonary Arterial Hypertension (PAH) is a cardiovascular disease characterized by progressively increasing blood pressure as a result of obliteration and loss of pulmonary arteries. We have extracted pulmonary arterial endothelial cells from lungs of a cohort of PAH patients (n=10) and controls (n=9), cultured the cells for 3-5 passages, and performed chromatin (H3K27ac, H3K4me1, and H3K4me3 ChIP-Seq), expression (RNA-Seq) and chromatin interaction profiling (ChIA-PET). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: BED
Series
Accession:
GSE139234
ID:
200139234
15.

Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension

(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
Platforms:
GPL11154 GPL20301
73 Samples
Download data: BEDGRAPH, TAB
Series
Accession:
GSE126325
ID:
200126325
16.

Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension [ChIP-seq]

(Submitter supplied) Pulmonary Arterial Hypertension (PAH) is a cardiovascular disease characterized by progressively increasing blood pressure as a result of obliteration and loss of pulmonary arteries. We have extracted pulmonary arterial endothelial cells from lungs of a cohort of PAH patients (n=10) and controls (n=9), cultured the cells for 3-5 passages, and performed chromatin (H3K27ac, H3K4me1, and H3K4me3 ChIP-Seq), expression (RNA-Seq) and chromatin interaction profiling (ChIA-PET). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
55 Samples
Download data: BEDGRAPH
Series
Accession:
GSE126322
ID:
200126322
17.

Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension [RNA-seq]

(Submitter supplied) Pulmonary Arterial Hypertension (PAH) is a cardiovascular disease characterized by progressively increasing blood pressure as a result of obliteration and loss of pulmonary arteries. We have extracted pulmonary arterial endothelial cells from lungs of a cohort of PAH patients (n=10) and controls (n=9), cultured the cells for 3-5 passages, and performed chromatin (H3K27ac, H3K4me1, and H3K4me3 ChIP-Seq), expression (RNA-Seq) and chromatin interaction profiling (ChIA-PET). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
18 Samples
Download data: TAB
18.

RNA-seq transcriptome profiling of human pulmonary artery endothelial cells and brain microvascular endothelal cells in response to hypoxia

(Submitter supplied) In this study, we analzyed differences in the effect of hypoxia on the transcriptomic profile of cultured human pulmonary artery endothelial cells (HPAECs) vs. human brain microvascular endothelial cells (HBMVECs). To determine which hypoxia-regulated genes were dependent on hypoxia inducible factor 1-alpha (HIF-1alpha), some cells were transfected with an siRNA against HIF-1alpha prior to treatment with hypoxia. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
18 Samples
Download data: TXT
19.

MicroRNA sequencing of BIBINS HIE dried blood spot

(Submitter supplied) Able to seqence microRNA from 2 x 6 mm dired blood spot chads from the BIBINS study. Samples are from newborns with moderate-severe HIE undergoing therapeutic hypothermia at around 16-24 h post insult, mild HIE without therapeutic hypothermia, and umbilical cord blodd from normal pregnancies.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15520
32 Samples
Download data: TXT
20.

Peripheral blood gene expression as a novel genomic biomarker in complicated sarcoidosis

(Submitter supplied) Sarcoidosis, a systemic granulomatous syndrome invariably affecting the lung, typically spontaneously remits but in ~20% of cases progresses with severe lung dysfunction or cardiac and neurologic involvement (complicated sarcoidosis). Unfortunately, current biomarkers fail to distinguish patients with remitting (uncomplicated) sarcoidosis from other fibrotic lung disorders, and fail to identify individuals at risk for complicated sarcoidosis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
74 Samples
Download data: CEL
Series
Accession:
GSE37912
ID:
200037912
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