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Links from GEO DataSets

Items: 20

1.

Transcriptional profile of isoproterenol-induced cardiomyopathy and comparison to exercise-induced cardiac hypertrophy

(Submitter supplied) We performed microarray analyses on RNA from mice with isoproterenol-induced cardiac hypertrophy and mice with exercise-induced physiological hypertrophy and identified 865 and 2,534 genes that were significantly altered in pathological and physiological cardiac hypertrophy models, respectively.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3596
Platform:
GPL1261
9 Samples
Download data: CEL
Series
Accession:
GSE18801
ID:
200018801
2.
Full record GDS3596

Isoproterenol-induced cardiomyopathy and exercise-induced cardiac hypertrophy

Comparison of hearts of C57BL/6 males with isoproterenol-induced cardiomyopathy to those with exercise-induced cardiac hypertrophy. Results provide insight into the molecular differences between pathological and physiological cardiac hypertrophy models.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 3 protocol sets
Platform:
GPL1261
Series:
GSE18801
9 Samples
Download data: CEL
3.

Analysis of Akt1 activation in transgenic mouse hearts show expression profiles associated with hypertrophy and failure

(Submitter supplied) To investigate molecular mechanisms involved in the development of cardiac hypertrophy and heart failure, a tetracycline-regulated transgenic system to conditionally switch a constitutively-active form of the Akt1 protein kinase on or off in the adult heart was developed. Short-term activation (2 weeks) of Akt1 resulted in completely reversible hypertrophy with maintained contractility. In contrast, chronic Akt1 activation (6 weeks) induced extensive cardiac hypertrophy, severe contractile dysfunction, and massive interstitial fibrosis. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS2304 GDS2308
Platforms:
GPL339 GPL340
36 Samples
Download data
Series
Accession:
GSE3383
ID:
200003383
4.
Full record GDS2308

Akt1 serine-threonine protein kinase activation effect on the heart (MG-430B)

Analysis of hearts after acute or chronic induction of a transgenic Akt1 kinase. Acute activation results in reversible hypertrophy, while chronic activation induces transition to failure. Results provide insight into the mechanisms involved in the development of cardiac hypertrophy and failure.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 5 protocol sets
Platform:
GPL340
Series:
GSE3383
18 Samples
Download data
DataSet
Accession:
GDS2308
ID:
2308
5.
Full record GDS2304

Akt1 serine-threonine protein kinase activation effect on the heart (MG-430A)

Analysis of hearts after acute or chronic induction of a transgenic Akt1 kinase. Acute activation results in reversible hypertrophy, while chronic activation induces transition to failure. Results provide insight into the mechanisms involved in the development of cardiac hypertrophy and failure.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 5 protocol sets
Platform:
GPL339
Series:
GSE3383
18 Samples
Download data
DataSet
Accession:
GDS2304
ID:
2304
6.

Analysis of cardiac gene expression in response to isoproterenol-induced heart failure (part 2)

(Submitter supplied) Myoglobin knockout mice (myo-/-) adapt to the loss of myoglobin by the activation of a variety of compensatory mechanisms on the structural and functional level. In order to analyze to what extent myo-/- mice would tolerate cardiac stress we used the model of chronic isoproterenol application to induce cardiac hypertrophy in myo-/- mice and wild type (WT) controls. After 14 d of isoproterenol infusion cardiac hypertrophy in WT and myo-/- mice reached a similar level. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8600
16 Samples
Download data: GPR
Series
Accession:
GSE16246
ID:
200016246
7.

Analysis of cardiac gene expression in response to isoproterenol-induced heart failure (part 1)

(Submitter supplied) Myoglobin knockout mice (myo-/-) adapt to the loss of myoglobin by the activation of a variety of compensatory mechanisms on the structural and functional level. In order to analyze to what extent myo-/- mice would tolerate cardiac stress we used the model of chronic isoproterenol application to induce cardiac hypertrophy in myo-/- mice and wild type (WT) controls. After 14 d of isoproterenol infusion cardiac hypertrophy in WT and myo-/- mice reached a similar level. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8599
16 Samples
Download data: GPR
Series
Accession:
GSE16243
ID:
200016243
8.

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
9.

Expression data from Bama minipig hearts - high-fat, high-sucrose diet

(Submitter supplied) In order to study the heart disorder that the long term, high energy diet caused, Bama miniature pigs were fed a high-fat, high-sucrose diet for 23 months. These pigs developed symptoms of metabolic syndrome and showed cardiac steatosis and hypertrophy with a greatly increased heart weight (1.82-fold, P<0.05) and heart volume (1.60-fold, P<0.05) compared with the control pigs. To understand the molecular mechanisms of cardiac steatosis and hypertrophy, nine pig heart cRNA samples were hybridized to porcine GeneChips.
Organism:
Sus scrofa
Type:
Expression profiling by array
Platform:
GPL3533
9 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE67890
ID:
200067890
10.

Loss of mouse P2Y6 nucleotide receptor is associated with physiological macrocardia and amplified pathological cardiac hypertrophy

(Submitter supplied) The study of the mechanisms leading to cardiac hypertrophy is essential to better understand cardiac development and regeneration. Pathological conditions such as ischemia or pressure overload can induce a release of extracellular nucleotides within the heart. We recently investigated the potential role of nucleotide P2Y receptors in cardiac development. We showed that adult P2Y4-null mice displayed microcardia resulting from defective cardiac angiogenesis. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18480
4 Samples
Download data: CSV
Series
Accession:
GSE76215
ID:
200076215
11.

Gene and exon expression change in cardiac hypertrophy with pressure overload

(Submitter supplied) Pathological cardiac hypertrophy was induced by pressure overload on the heart. We performed genome-wide exon array experiments with left ventricles of mice with 1 week and 4 week of transverse aortic constriction (TAC). The exon level analysis revealed widespread regulation of alternative splicing and alternative polyadenylation during hypertrophy.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6096
6 Samples
Download data: CEL
Series
Accession:
GSE24242
ID:
200024242
12.

Whole-transcriptome analysis identifies re-expression of fetal splice variants in cardiac hypertrophy

(Submitter supplied) Cardiac hypertrophy has been well-characterized at the level of transcription. During cardiac hypertrophy, genes normally expressed primarily during fetal heart development are re-expressed, and this fetal gene program is believed to be a critical component of the hypertrophic process. Recently, alternative splicing of mRNA transcripts has been shown to be temporally regulated during heart development, leading us to consider whether fetal patterns of splicing also reappear during hypertrophy.We hypothesized that patterns of alternative splicing occurring during heart development are recapitulated during cardiac hypertrophy. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10669
9 Samples
Download data: TXT
Series
Accession:
GSE42411
ID:
200042411
13.

Transcriptome profiling of cardiomyocytes treated with antiretroviral drugs

(Submitter supplied) The use of antiretroviral therapy (ART) improved the life expectancy of HIV patients through the suppression of HIV propagation in host. However, recent studies suggest that long-term use of ART induces comorbid conditions and heart failure in surviving HIV patients. The mechanism associated with the antiretroviral drugs (ARVs) induced cardiotoxicity and heart failure is not clear. In this study, we performed an RNA sequencing with ARV drugs-treated neonatal rat ventricular cardiomyocytes to explore drugs-induced cardiotoxicity. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18694
6 Samples
Download data: XLS
Series
Accession:
GSE188210
ID:
200188210
14.

Remodeling of the m6A landscape in the heart reveals conserved post-transcriptional events underlying cardiomyocyte hypertrophy

(Submitter supplied) Regulation of gene expression plays a fundamental role in cardiac stress-responses. Modification of coding transcripts by adenosine methylation (m6A) has recently emerged as a critical post-transcriptional mechanism underlying heart disease. Thousands of mammalian mRNAs are known to be m6A-modified, suggesting that remodeling of the m6A landscape may play an important role in cardiac pathophysiology. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
20 Samples
Download data: BED, CSV, TXT
15.

Expression data from WT and VAChT KDHOM ventricles

(Submitter supplied) VAChT KDHOM mice have a 70% decrease in the vesicular acetylcholine transporter (VAChT) and this leads to a systemic decrease in ACh release and cardiac dysfunction. We used this microarray to determine whether there were transcriptional alterations in the hearts of mutant mice as a result of this long-term decrease in cholinergic tone.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4325
Platform:
GPL6246
6 Samples
Download data: CEL
Series
Accession:
GSE37458
ID:
200037458
16.
Full record GDS4325

Vesicular acetylcholine transporter knockdown effect on heart

Analysis of heart from vesicular acetylcholine transporter (VAChT)-deficient C57BL/6 males. The VAChT KD animals have a systemic decrease in ACh release and cardiac dysfunction. Results provide insight into potential molecular changes in the heart induced by decreased cholinergic neurotransmission.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL6246
Series:
GSE37458
6 Samples
Download data: CEL
17.

Comparison of exercise and pregnancy-induced cardiac hypertrophy

(Submitter supplied) Comparative analysis of mouse cardiac left ventricle gene expression: voluntary wheel exercise and pregnancy-induced cardiac hypertrophy
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
18 Samples
Download data: CEL
Series
Accession:
GSE36330
ID:
200036330
18.

Small RNA sequencing of hearts from female mice on high fat diet, from 85 strains

(Submitter supplied) We used small RNA-Seq to characterize heart non-coding RNAs in 85 inbred strains of mice from the Hybrid Mouse Diversity Panel (HMDP), a reference resource population for cardiovascular and metabolic traits.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL21493
85 Samples
Download data: CSV
Series
Accession:
GSE207142
ID:
200207142
19.

Transcriptional changes during Isoproterenol induced cardiac fibrosis in mice

(Submitter supplied) Introduction: β-adrenergic stimulation using β-agonists such as isoproterenol has been routinely used to induce cardiac fibrosis in experimental in animal models. While transcriptome changes in surgical models of cardiac fibrosis such as Transverse aortic constriction (TAC), and coronary artery ligation (CAL) are well-studied, transcriptional changes during isoproterenol induced cardiac fibrosis is not well explored. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
15 Samples
Download data: RESULTS
Series
Accession:
GSE239653
ID:
200239653
20.

Post-mortem cardiac tissue maintains gene expression profile even after late harvesting.

(Submitter supplied) Gene expression studies are used to help identify disease-associated genes, by comparing the levels of expressed transcripts between cases and controls, and to identify functional genetic variants known as expression quantitative loci (eQTLs). While many of these studies are performed in blood or lymphoblastoid cell lines due to tissue accessibility, the relevance of expression differences in tissues that are not the primary site of disease is unclear. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
29 Samples
Download data: CEL
Series
Accession:
GSE32519
ID:
200032519
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