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Links from GEO DataSets

Items: 13

1.

Antibody-based selective isolation of atrial and ventricular cardiomyocytes by differential expression of integrin α6 (CD49f)

(Submitter supplied) Central questions like cardiomyocyte subtype emergence during cardiogenesis or availability of cardiomyocyte subtypes for cell replacement therapy require selective identification and purification of atrial and ventricular cardiomyocytes. However, characterization and implementation of pure cardiomyocyte subtypes is still challenging due to technical limitations. Our aim was to identify surface markers enabling the selective detection and purification of atrial and ventricular cardiomyocytes from mouse hearts. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
16 Samples
Download data: TXT
Series
Accession:
GSE57131
ID:
200057131
2.

Atrial Identity Is Determined by A COUP-TFII Regulatory Network

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL15103 GPL1261
11 Samples
Download data: CEL, WIG
Series
Accession:
GSE46498
ID:
200046498
3.

Atrial Identity Is Determined by A COUP-TFII Regulatory Network (ChIP-Seq)

(Submitter supplied) Embryonic cardiomyocytes possess the plasticity to choose between atrial and ventricular fates. For a limited window of time, the transcription factor COUP-TFII (Nr2f2) sufficiently and essentially confers the atrial identity through direct and indirect regulation of nearly half of chamber specific genes.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL15103
2 Samples
Download data: WIG
Series
Accession:
GSE46497
ID:
200046497
4.

Atrial Identity Is Determined by A COUP-TFII Regulatory Network (RNA)

(Submitter supplied) Atria and ventricles exhibit distinct molecular profiles that produce structural and functional differences between the two cardiac compartments. However, factors that determine these differences remain largely undefined. Cardiomyocyte-specific COUP- TFII ablation produces ventricularized atria that exhibit ventricle-like action potentials, increased cardiomyocyte size, and development of extensive T-tubules. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
9 Samples
Download data: CEL
Series
Accession:
GSE46496
ID:
200046496
5.

Generation of mature compact ventricular cardiomyocytes from human pluripotent stem cells

(Submitter supplied) Here we established a differentiation strategy  that promotes the specification, proliferation and maturation of a compact cardiomyocyte population from hPSCs. The cardiomyocytes generated under these conditions display the hallmark phenotypic characteristics of post-natal cardiomyocytes.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
3 Samples
Download data: TAR
6.

Comparison of atrial tissue of patients with atrial fibrillation and sinus rhythm with ventricular gene expression

(Submitter supplied) GSE2240 contains two different experimental subsets: 1) Comparison of atrial and ventricular gene expression (atrial tissue of patients with sinus rhythm vs. human left ventricular non-failing myocardium) The purpose of our investigation was to identify the transcriptional basis for ultrastructural and functional specialization of human atria and ventricles. Using exploratory microarray analysis (Affymetrix U133A+B), we detected 11,740 transcripts expressed in human heart, representing the most comprehensive report of the human myocardial transcriptome to date. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS1557 GDS1559
Platforms:
GPL96 GPL97
70 Samples
Download data: CEL
Series
Accession:
GSE2240
ID:
200002240
7.
Full record GDS1559

Permanent atrial fibrillation (HG-U133B)

Analysis of atrium from patients with permanent atrial fibrillation (AF). AF is associated with extensive structural, contractile, and electrophysiological remodeling. Results identify adoption of a ventricular-like genomic signature as a general feature of the fibrillating atrium.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state, 2 tissue sets
Platform:
GPL97
Series:
GSE2240
35 Samples
Download data: CEL
DataSet
Accession:
GDS1559
ID:
1559
8.
Full record GDS1557

Atrial and ventricular myocardium comparison (HG-U133B)

Analysis of right atria and left ventricles of hearts. While both the ventricle and atrium contract, the atrium is also a source and target for neurohumoral signals. Results provide insight into the molecular basis for the ultrastructural and functional differences between the atrium and ventricle.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 tissue sets
Platform:
GPL97
Series:
GSE2240
25 Samples
Download data: CEL
DataSet
Accession:
GDS1557
ID:
1557
9.

Neonatal murine cardiomyocyte transcriptome

(Submitter supplied) Cardiomyocyte poly(A) RNA was sequenced from purified bulk cardiomyocytes collected from one male and female murine heart at postnatal day 2 (P2). Neonatal cardiomyocytes were isolated and purified (96% cardiomyocytes at P2) by Langendorff retrograde perfusion and immunomagnetic cell separation, respectively. We found evidence of sexual dimorphism with 9 differentially expressed genes (FDR<0.05) encoded on XY chromosomes in this RNA-Seq dataset.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data: TXT
Series
Accession:
GSE193137
ID:
200193137
10.

An autofluorescence-based method for the isolation of highly purified ventricular cardiomyocytes

(Submitter supplied) Profiling of the transcriptome of FITChigh/FSCdim and FITCdim/FSChigh sub-populations. Three biological replicates were profiled for each cell type.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
6 Samples
Download data: BW, TXT
Series
Accession:
GSE94413
ID:
200094413
11.

The single-cell atlas of the heart reveals an unexpected erythrocyte-like cardiomyocyte

(Submitter supplied) BACKGROUND: Single-cell RNA sequencing (scRNA-seq) is widely used in cancer research and organ development since its powerful ability to analyze cellular heterogeneity. However, its application in cardiomyocytes is rare mainly because the cardiomyocytes are too large and fragile to withstand traditional single-cell approaches. METHODS: Through designing the isolation procedure of neonatal mouse cardiac cells, we perform scRNA-seq with samples from 27 neonatal mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
4 Samples
Download data: MTX, TSV
Series
Accession:
GSE232466
ID:
200232466
12.

Dissecting cell composition and cell-cell interaction network of human disease heart tissue by single-cell sequencing

(Submitter supplied) We studied the cell compositon of two types of human heart disease (coronary atherosclerotic heart disease and dilated cardiomyopathy) by single-cell sequencing. Distinct subgroups of cardiac muscle, fibroblast cell and endothelial cell were detected. We generated a cell-cell interaction network using specific expressed ligands and receptors of cells. And we also observed the change of interaction and cell transformation with age.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: CSV, TXT
Series
Accession:
GSE121893
ID:
200121893
13.

Dissecting cell composition and cell-cell interaction network of normal human heart tissue by single-cell sequencing

(Submitter supplied) We studied the cell compositon of normal human heart by single-cell sequencing. Distint subgroups of cardiac muscle, fibroblast cell and endothelial cell were detected. We drawed a cell-cell interaction network using specific expressed ligands and receptors of cells. And we also observed the change of interaction and cell transformation with age.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: CSV, TXT
Series
Accession:
GSE109816
ID:
200109816
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