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Links from GEO DataSets

Items: 14

1.

Genetic dissection of a super enhancer controlling the Nppa-Nppb cluster in the heart of RE3 mutants

(Submitter supplied) High-resolution chromosome conformation capture-sequencing of RE3 homozygous mutants
Organism:
Mus musculus
Type:
Other
Platform:
GPL16417
12 Samples
Download data: WIG
Series
Accession:
GSE155140
ID:
200155140
2.

Genetic dissection of a super enhancer controlling the Nppa-Nppb cluster in the heart

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Other
Platform:
GPL16417
21 Samples
Download data: WIG
Series
Accession:
GSE158735
ID:
200158735
3.

Genetic dissection of a super enhancer controlling the Nppa-Nppb cluster in the heart after cardiac stress

(Submitter supplied) High-resolution chromosome conformation capture-sequencing of wildtype mice left ventricle after cardiac stress (i.e. hypertrophy and myocardial infarction)
Organism:
Mus musculus
Type:
Other
Platform:
GPL16417
9 Samples
Download data: WIG
Series
Accession:
GSE158708
ID:
200158708
4.

Genetic dissection of a super enhancer controlling the Nppa-Nppb locus in the heart (CUT&RUN)

(Submitter supplied) CUT&RUN H3K27ac PCM-1 sorted left ventricle of Nppa-Nppb double-knockout
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE146734
ID:
200146734
5.

Genetic dissection of a super enhancer controlling the Nppa-Nppb locus in the heart (RNA-Seq)

(Submitter supplied) Whole transcriptome expression analysis of RE1-deficient mice
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
8 Samples
Download data: XLSX
Series
Accession:
GSE146732
ID:
200146732
6.

Identification of a regulatory domain controlling the Nppa-Nppb gene cluster during heart development and stress

(Submitter supplied) The paralogous genes Nppa and Nppb are organized in an evolutionary conserved cluster and are a valuable model to study coregulation and regulatory landscape organization during heart development and disease. Here, we analyzed the chromatin conformation, epigenetic status and enhancer potential of sequences of the Nppa-Nppb cluster in vivo. Our data indicate that the regulatory landscape of the cluster is present within a 60 kbp domain centered around Nppb. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL13112
13 Samples
Download data: WIG
Series
Accession:
GSE81057
ID:
200081057
7.

Transcriptional characterization of LV of Nppb KO

(Submitter supplied) Expression analysis of LV in Nppb KO
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
8 Samples
Download data: XLSX
Series
Accession:
GSE128196
ID:
200128196
8.

Transcriptional characterization of the myocardial infarct border zone

(Submitter supplied) Expression analysis of cardiomyocytes in the border and remote myocarium
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
5 Samples
Download data: XLSX
Series
Accession:
GSE128034
ID:
200128034
9.

Spatiotemporal pattern of the transcriptional regulatory landscape of the mouse ventricle after myocardial infarction

(Submitter supplied) Stress-response gene activity replaces cardiomyocyte lineage-specific program in a transcriptionally discrete infarct border zone
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19057 GPL17021
36 Samples
Download data: BED, XLSX
Series
Accession:
GSE110209
ID:
200110209
10.

Gene expression profiling of hypertrophic and failing cardiomyocytes identifies new players in heart failure

(Submitter supplied) Aim - Pathological cardiac remodeling is characterized by cardiomyocyte hypertrophy and fibroblast activation, which can ultimately lead to heart failure (HF). Genome-wide expression analysis on heart tissue has been instrumental for the identification of molecular mechanisms at play. However, these data were based on signals derived from all cardiac cell types. Here we aimed for a more detailed view on molecular changes driving cardiomyocyte hypertrophy and failure to aid in the development of therapies to reverse maladaptive remodeling. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
1 Sample
Download data: TSV, TXT
Series
Accession:
GSE138299
ID:
200138299
11.

Natriuretic Peptide Receptor 3 (NPR3) is regulated by microRNA-100

(Submitter supplied) The cardiac natriuretic peptide (NPs) plays an important role in the regulation of cardiovascular and renal function. We examined the miRNAs that could be regulating NPs by subjecting the cardiomyocytes, HCMa cells, to hypoxia.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL18331
2 Samples
Download data: TXT
Series
Accession:
GSE55387
ID:
200055387
12.

Transcriptomes of the hybrid mouse diversity panel subjected to Isoproterenol challenge

(Submitter supplied) Transcriptomes performed on left ventricular heart samples from mice of the hybrid mouse diversity panel, a set of over a hundred inbred strains of mice. In this project, the strains were challenged with Isoproterenol, a beta-adrenergic agonist to induce cardiac hypertrophy and failure. Results are useful for the analysis of heart-related traits in mice
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
208 Samples
Download data: TXT
Series
Accession:
GSE48760
ID:
200048760
13.

The Role of Endothelial Autocrine NRG1/ERBB4 Signaling in Cardiac Remodeling

(Submitter supplied) Neuregulin-1 (NRG1) is a paracrine growth factor, secreted by cardiac endothelial cells (Ecs) in conditions of cardiac overload/injury. The current concept is that the cardiac effects of NRG1 are mediated by activation of ERBB4/ERBB2 receptors on cardiomyocytes. However, recent studies have shown that paracrine effects of NRG1 on fibroblasts and macrophages are equally important. Here, we hypothesize that NRG1 autocrine signaling plays a role in cardiac remodeling. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
24 Samples
Download data: TSV
Series
Accession:
GSE150619
ID:
200150619
14.

Altered Enhancer and Promoter Usage Leads to Differential Gene Expression in the Normal and Failed Human Heart

(Submitter supplied) The failed heart is characterized by re-expression of a fetal gene program, which contributes to adaptation and maladaptation in heart failure. To define genomewide enhancer and promoter use in heart failure, Cap Analysis of Gene Expression (CAGE-seq) was applied to healthy and failed human left ventricles to define short RNAs associated with both promoters and enhancers. Integration of CAGE-seq data with RNA sequencing identified a combined ~17,000 promoters and ~1,500 enhancers active in healthy and failed human left ventricles. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL20301 GPL18573
14 Samples
Download data: TXT
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