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Links from GEO DataSets

Items: 17

1.
Full record GDS5499

Pulmonary hypertensions: PBMCs

Analysis of PBMCs from patients with idiopathic pulmonary arterial hypertension (IPAH), systemic sclerosis (SSc), SSc associated PAH (SSc-PAH), and SSc complicated by interstitial lung disease and PH (SSc-PH-ILD). Results provide insight into the molecular basis of the various disease groups.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 5 disease state sets
Platform:
GPL6947
Series:
GSE33463
140 Samples
Download data
2.

Erythroid-Specific Transcriptional Changes in PBMCs from Pulmonary Hypertension Patients

(Submitter supplied) The hypothesis tested in this study was that chronic exposure of PBMCs to a hypertensive environment in remodeled pulmonary vessels would be reflected by specific transcriptional changes in these cells. The transcript profiles of PBMCs from 30 idiopathic pulmonary arterial hypertension patients (IPAH), 19 patients with systemic sclerosis without pulmonary hypertension (SSc), 42 scleroderma-associated PAH patients (SSc-PAH), and 8 patients with SSc complicated by interstitial lung disease and PH (SSC-PH-ILD) were compared to the gene expression profiles of PBMCs from 41 healthy individuals.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5499
Platform:
GPL6947
140 Samples
Download data: TXT
Series
Accession:
GSE33463
ID:
200033463
3.

Multi-tissue functional genomic study of systemic sclerosis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
7 related Platforms
577 Samples
Download data: CEL, GPR, TXT
Series
Accession:
GSE76809
ID:
200076809
4.

Lung tissues in systemic sclerosis have gene expression patterns unique to pulmonary fibrosis and pulmonary hypertension

(Submitter supplied) Objective: Pulmonary complications in systemic sclerosis (SSc), including pulmonary fibrosis (PF) and pulmonary arterial hypertension (PAH), are the leading cause of mortality. We compared the molecular fingerprint of SSc lung tissues and matching primary lung fibroblasts to those of normal donors, and patients with idiopathic pulmonary fibrosis (IPF) and idiopathic pulmonary arterial hypertension (IPAH). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16221
53 Samples
Download data: XLS
Series
Accession:
GSE48149
ID:
200048149
5.

Gene expression in limited cutaneous SSc skin

(Submitter supplied) Systemic sclerosis (SSc) is an autoimmune disease characterized by clinical heterogeneity, multi-organ involvement, and complex genetic risk. Here, we report the first multi-tissue meta-analysis of ten independent SSc gene expression datasets. We identify a common immune-fibrotic expression axis across all tissues that is associated with the most severe disease phenotypes. The coexpression patterns conserved across tissues and phenotypes were used to query functional genomic networks, which allowed us to identify common and tissue-specific disease drivers. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
15 Samples
Download data: TXT
Series
Accession:
GSE76807
ID:
200076807
6.

Gene expression in limited cutaneous systemic sclerosis skin

(Submitter supplied) Systemic sclerosis (SSc) is an autoimmune disease characterized by clinical heterogeneity, multi-organ involvement, and complex genetic risk. Here, we report the first multi-tissue meta-analysis of ten independent SSc gene expression datasets. We identify a common immune-fibrotic expression axis across all tissues that is associated with the most severe disease phenotypes. The coexpression patterns conserved across tissues and phenotypes were used to query functional genomic networks, which allowed us to identify common and tissue-specific disease drivers. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL14550
24 Samples
Download data: TXT
Series
Accession:
GSE76806
ID:
200076806
7.

Changes in Gene Expression Profiles in Patients with Pulmonary Arterial Hypertension Associated with Scleroderma Treated with Tadalafil

(Submitter supplied) The study looked at changes in gene expression profiles in subjects with Pulmonary Arterial Hypertension and Scleroderma (PAH-SSc) before and after treatment with Tadalafil. A total of ten subjects were enrolled and various clinical assessments including 6-minute walk tes, cardiac MRI and right heart catheterization were done in addition to gene expression study.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15034
20 Samples
Download data: CEL
Series
Accession:
GSE75173
ID:
200075173
8.

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
9.
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
10.

Immature cell populations and an erythropoiesis gene expression signature in systemic juvenile idiopathic arthritis: Implications for pathogenesis

(Submitter supplied) Objective. Previous observations suggest that active systemic juvenile idiopathic arthritis (sJIA) is associated with a prominent erythropoiesis gene expression signature. The aim of this study was to determine the association of this signature with peripheral blood mononuclear cell (PBMC) subpopulations and its specificity for sJIA as compared to related conditions. 125 patients with JIA (18 sJIA and 107 non-sJIA) and 29 controls were studied. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4267
Platform:
GPL570
154 Samples
Download data: CEL
Series
Accession:
GSE21521
ID:
200021521
11.
Full record GDS4267

Systemic juvenile idiopathic arthritis and non-systemic JIA subtypes: peripheral blood mononuclear cells

Analysis of PBMCs from patients with systemic juvenile idiopathic arthritis (sJIA) or non-sJIA. sJIA patients have significantly increased expansion of immature PBMC subpopulations, including CD34+ cells. Results provide insight into molecular mechanisms underlying sJIA pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 disease state, 8 other sets
Platform:
GPL570
Series:
GSE21521
154 Samples
Download data: CEL
12.

Limited systemic sclerosis patients with PAH show biomarkers of inflammation and vascular injury

(Submitter supplied) Limited systemic sclerosis patients with pulmonary arterial hypertension show biomarkers of inflammation and vascular injury Forty-nine PBMC samples were obtained from 21 lSSc subjects without PAH (lSSc-noPAH), 15 lSSc subjects with PAH (lSSc-PAH), and 10 healthy controls; three subjects provided PBMCs one year later. Genome-wide gene expression was measured for each sample. Gene expression clearly distinguished lSSc samples from healthy controls, and separated lSSc-PAH from lSSc-NoPAH patients. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
54 Samples
Download data: GPR
Series
Accession:
GSE19617
ID:
200019617
13.

Gene expression profiling in blood of patients with chronic respiratory failure

(Submitter supplied) Genes dysregulated in cystic fibrosis (CF) and primary pulmonary arterial hypertension (PAH) at a late stage of pulmonary failure are still largely unknown. Blood samples taken in the frame of the French cohort of lung transplantation COLT offers the opportunity to identify in blood specific gene signatures of each disease and a common gene signature for both pathologies. A microarray analysis was performed with homogeneous groups of CF patients (n=23), PAH (n=13) patients and healthy volunteers (n=28). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13607
64 Samples
Download data: TXT
Series
Accession:
GSE38267
ID:
200038267
14.

Meta-analysis of Blood Genome-Wide Expression Profiling Studies in Pulmonary Arterial Hypertension

(Submitter supplied) Aberrantly remodeled vasculature in pulmonary arterial hypertension (PAH) features a prominent inflammatory cell infiltrate suggesting that immune effector cells may contribute to disease progression. Global expression studies of peripheral blood mononuclear cells (PBMCs) and whole blood have attempted to better define this inflammatory component of PAH pathobiology.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
20 Samples
Download data: CEL
Series
Accession:
GSE131793
ID:
200131793
15.

Transcriptome analysis of peripheral blood mononuclear cells in pulmonary sarcoidosis

(Submitter supplied) Purpose: This study aimed to explore the pathobiological markers of sarcoidosis in PBMCs by comparing the transcriptional signature of PBMCs from patients with pulmonary sarcoidosis and those of healthy controls by RNA sequencing. Methods:PBMC samples were collected from subjects with pulmonary sarcoidosis with no steroid/immunosuppressant drugs (n = 8) and healthy controls (n = 11) from August 2020 to April 2021, and RNA sequencing was performed with the PBMC samples. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
19 Samples
Download data: TXT
Series
Accession:
GSE192829
ID:
200192829
16.

Comparative Analysis of Methods to Reduce Activation Signature Gene Expression in PBMCs

(Submitter supplied) Preserving the in vivo cell transcriptome is essential for accurate profiling, yet factors during cell isolation including time ex vivo and temperature induce artifactual gene expression, particularly in stress-responsive immune cells. In this study, we investigated two methods to mitigate ex vivo activation signature gene (ASG) expression in peripheral blood mononuclear cells (PBMCs): transcription and translation inhibitors (TTis) and cold temperatures during isolation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
25 Samples
Download data: TXT
Series
Accession:
GSE236732
ID:
200236732
17.

Systems Analysis of the Human Pulmonary Arterial Hypertension Lung Transcriptome

(Submitter supplied) Rationale: Pulmonary arterial hypertension (PAH) is characterized by increased pulmonary artery pressure and vascular resistance, typically leading to right heart failure and death. Current therapies improve quality of life of the patients but have a modest effect on long-term survival. A detailed transcriptomics and systems biology view of the PAH lung is expected to provide new testable hypotheses for exploring novel treatments. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
83 Samples
Download data: CEL
Series
Accession:
GSE117261
ID:
200117261
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