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Links from GEO DataSets

Items: 17

1.

Myocardial gene expression in response to pressure overload

(Submitter supplied) Myocardial deletion of klf4 sensitizes mouse to pressure overload. In order to gain a better understanding of molecular mechanisms of such alterations, we profiled gene expression before and after 3-day of pressure overload (induced by transverse aortic constriction -TAC) in the hearts from MHC-cre (Cre) control and MHC-cre-klf4-deficient (KO) mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
15 Samples
Download data: TXT
Series
Accession:
GSE61177
ID:
200061177
2.

Microarray of cardiac biventricle from PGC-1a-/-bf/f/MerCre mice

(Submitter supplied) The following abstract from the submitted manuscript describes the major findings of this work. The metabolic development of high energy-utilizing organs such as the heart involves mitochondrial proliferation at birth followed by a maturation process during the postnatal period. Conditional gene targeting was used in mice to explore the role of the PPARgamma coactivator 1 (PGC-1) coactivators during postnatal development and in adult heart. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4776
Platform:
GPL6246
10 Samples
Download data: CEL
Series
Accession:
GSE43798
ID:
200043798
3.
Full record GDS4776

Peroxisome Proliferator-Activated Receptor γ Coactivator-1 deficiency effect on adult cardiac biventricle

Analysis of heart from adults deficient for peroxisome proliferator-activated receptor γ coactivator-1 (PGC-1) α and PGC-1β. Adult PGC-1α/β deficient heart did not exhibit abnormal mitochondrial dynamics or heart failure. Results provide insight into role of PGC-1 coactivators in adult heart.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL6246
Series:
GSE43798
10 Samples
Download data: CEL
4.

Med1 is Necessary for Cardiac Function

(Submitter supplied) Analysis of ventricular derived mRNA from Med1fl/fl and Med1fl/fl cardiac knockout mice. Results provide insight into the molecual rmechanisms underlying dilated cardiomyopathy.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: TXT
Series
Accession:
GSE84160
ID:
200084160
5.

RNA-Seq transcriptome profiling of postnatal age 35 days or P35 ventricles of cardiac-specific estrogen-related receptor alpha and gamma (ERRa/g) knock down (KD) mouse generated by AAV-cTnT-Cre injection and its control AAV-Luc injection.

(Submitter supplied) Transcriptional regulatory circuits that drive cardiomyocyte maturation during the developmental process are poorly understood. Estrogen-related receptor alpha and gamma (ERRa/g) have been shown to be involved in all aspects of mitochondrial energy production. However, the function of ERR during the postnatal cardiac developmental process is unclear. To examine the role of (ERRa/g) during postnatal cardiac maturation, we generated inducible cardiac-specific ERRa/g knockdown (KD) mice with adeno-associated virus serotype 9 (AAV9) expressing Cre. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
8 Samples
Download data: XLSX
Series
Accession:
GSE135347
ID:
200135347
6.

Estrogen-related Receptor Signaling Coordinately Controls Cardiac Energy Metabolic and Structural Maturation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16791 GPL17021 GPL21103
22 Samples
Download data: BW
Series
Accession:
GSE113784
ID:
200113784
7.

RNA-Seq transcriptome profiling of embryonic age 17.5 or E17.5 ventricles of cardiac specific-estrogen-related receptor alpha and gamma (ERRa/g) knock out (KO) mouse generated by Nkx2.5-Cre driver and its control wild type.

(Submitter supplied) Transcriptional regulatory circuits that drive cardiomyocyte maturation during the developmental process are poorly understood. Estrogen-related receptor alpha and gamma (ERRa/g) have been shown to be involved in all aspects of mitochondrial energy production. However, the function of ERR during the cardiac developmental process is not understood well. To examine the role of (ERRa/g), we generated cardiac-specific ERRa/g knockout (KO) mice and found that the KO mice died within 24 hours post-birth. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: XLSX
Series
Accession:
GSE113761
ID:
200113761
8.

Genome-wide estrogen-related receptor gamma (ERRg) occupancy in human iPS cell-derived cardiomyocytes (hiPSC-CMs)

(Submitter supplied) Estrogen-related receptor gamma (ERRg) has been shown to control gene expression involved in a broad range of mitochondrial energy metabolism including oxidative phosphorylation, TCA cycle, and fatty acid oxidation. However, ERRg direct targets were not identified in cardiomyocytes. With ERRg ChIP-seq, we found ERRg peaks on the promoter regions of mitochondrial energy metabolic genes as expected. Besides, ERRg extensively distributed the promoter regions of cardiac contractile, ion channels and Ca2+ handling protein genes. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
8 Samples
Download data: BW
Series
Accession:
GSE113760
ID:
200113760
9.

mTOR pathway controls mitochondrial gene expression and respiration through the YY1/PGC-1alpha transcriptional complex

(Submitter supplied) Mitochondrial oxidative function is tightly controlled to maintain energy homeostasis in response to nutrient and hormonal signals. An important cellular component in the energy sensing response is the target of rapamycin (TOR) kinase pathway; however whether and how mTOR controls mitochondrial oxidative activity is unknown. Here, we show that mTOR kinase activity stimulates mitochondrial gene expression and oxidative function. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE5332
ID:
200005332
10.

Cardiac mRNA profiling in mice treated with lipopolysaccharide

(Submitter supplied) To identify the messenger RNA (mRNA) profile in the hearts of mice that were treated with lipopolysaccharide (LPS) and identify potential changes in the expression of genes that may account for inhibition of cardiac Ppara that has been observed in LPS-treated mice, 8 mouse samples were analyzed with whole genome microarrays.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19507
8 Samples
Download data: TXT
Series
Accession:
GSE63920
ID:
200063920
11.

Effect of cardiomyocyte KLF5 deletion in cardiac gene expression profile

(Submitter supplied) Kruppel-like factor 5 gene was deleted (Cre-lox) system specifically in cardiomyocytes (aMHC-promoter-driven expression of Cre) and RNA was purified from total hearts (TRIZOL method) following perfusion of the heart with PBS. Basal levels cardiac RNA was analyzed with whole genome microarray chips.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL15691
8 Samples
Download data: TXT
Series
Accession:
GSE63839
ID:
200063839
12.

Expression data from 18h-fasted WT versus KLF15-null mice: heart

(Submitter supplied) We used microarray analysis to identify differences in gene expression levels in heart following an 18h (overnight) fast in WT control and KLF15-null mice
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4780
Platform:
GPL8321
7 Samples
Download data: CEL
Series
Accession:
GSE53231
ID:
200053231
13.
Full record GDS4780

KLF14-deficient hearts during fasting

Analysis of Kruppel-like factor 15 (KLF15)-deficient and wild-type hearts following an 18 hour overnight fast. KLF15-deficient hearts exhibit reduced fatty acid oxidation and increased glucose oxidation. Results provide insight into the role of KLF14 in cardiac lipid metabolism.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL8321
Series:
GSE53231
7 Samples
Download data: CEL
14.

MOF acetyl transferase regulates transcription and respiration in mitochondria

(Submitter supplied) Histone acetylation is sensitive to metabolic cues, however interplay between histone acetyl transferases and cellular metabolism remains poorly understood. Here we report the localization of a classical nuclear HAT- MOF and members of Non-Specific Lethal complex in mitochondria. MOF regulates expression of oxidative phosphorylation (OXPHOS) genes, residing in both nuclear and mitochondrial genomes, selectively in aerobically respiring cells. more...
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL17021 GPL16791
19 Samples
Download data: TSV
Series
Accession:
GSE77784
ID:
200077784
15.

heart/muscle-specific MnSOD-deficient mouse

(Submitter supplied) To investigate the pathological significance of excess oxidative stress in the heart, we generated heart/muscle-specific manganese superoxide dismutase (MnSOD) -deficient mice on a C57BL/6 background using the Cre-loxP system uder the control of the muscle reatin kinase (MCK) promoter. The mutant mice developed progressive congestive heart failure with dilated cardiomyopathy and physical disability and died with a median survival rate of 15.4 ± 4.0 weeks. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS1080
Platform:
GPL1261
4 Samples
Download data
Series
Accession:
GSE2236
ID:
200002236
16.
Full record GDS1080

Manganese superoxide dismutase deficiency effect on hearts

Analysis of hearts from C57BL/6 mutants lacking manganese superoxide dismutase (MnSOD). MnSOD deficiency confined to heart and muscle. Mutants developed progressive congestive heart failure with dilated cardiomyopathy. Results provide insight into the effect of excess oxidative stress on the heart.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE2236
4 Samples
Download data
DataSet
Accession:
GDS1080
ID:
1080
17.

The effect of Tmem135 overexpression on the mouse heart

(Submitter supplied) Transgenic mice overexpressing a novel regulator of mitochondrial dynamics, transmembrane protein 135 (Tmem135) have age-related heart phenotypes. Here we report the gene expression profiles of 6 mo old WT and Tg whole hearts. RNAseq was conducted on Illumina HiSeq 2000 platform.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: DIFF
Series
Accession:
GSE99522
ID:
200099522
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