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Links from GEO DataSets

Items: 20

1.

Glucocorticoid receptor (GR) target genes in C2C12 myotubes

(Submitter supplied) Analysis of C2C12 myotubes treated with dexamethasone (Dex) for 6 or 24 hours. Dex is a synthetic glucorticoid receptor agonist. Results provide insight to the effect of glucocorticoids on myotubes.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
18 Samples
Download data
Series
Accession:
GSE28840
ID:
200028840
2.

Glucocorticoid target genes in 3T3-L1 adipocytes

(Submitter supplied) Analysis of 3T3-L1 adipocytes treeated with dexamethasone (Dex) for 6 hours. Dex is a synthetic glucorticoid (GC) receptor agonist. Results provide insight into the effect of glucocorticoids on adipocytes.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
6 Samples
Download data: TXT
Series
Accession:
GSE24105
ID:
200024105
3.

Histone deacetylase 5 regulates Interleukin 6 secretion and insulin action in skeletal muscle

(Submitter supplied) Physical exercise training is associated with increased glucose uptake in skeletal muscle and improved glycemic control. Histone Deacetylases (HDACs) are divided into three structurally defined subclasses and are critical for transcriptional regulation, cell cycle progression, and developmental events. HDAC5, a class IIa histone deacetylase regulates transcription of the insulin-responsive glucose transporter GLUT4 in cultured muscle cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
8 Samples
Download data: CEL, CHP
Series
Accession:
GSE150485
ID:
200150485
4.

Genome-wide analysis of LY294002 effect on the glucocorticoid receptor function in human keratinocytes

(Submitter supplied) LY294002 increased negative effect of glucocorticoid fluocinolone acetonide (FA) on gene expression and blunted activation of some GR-target genes by glucocorticoid FA.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
12 Samples
Download data: TXT
Series
Accession:
GSE120991
ID:
200120991
5.

Effects of dexamethasone and KLF15 on genome-wide occupancy of the glucocorticoid receptor (NR3C1) and RNA polymerase II (RNAPII) in human airway smooth muscle

(Submitter supplied) The objective of this study was to determine how dexamethasone and KLF15 modify GR and RNAPII occupancy in human airway smooth muscle on a genome-wide basis.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
20 Samples
Download data: NARROWPEAK
Series
Accession:
GSE95632
ID:
200095632
6.

Genome-wide transcriptional targets of KLF15 in human airway smooth muscle

(Submitter supplied) We previously demonstrated that the transcription factor, KLF15, is a glucocorticoid-regulated gene that represses primary human airway smooth muscle (ASM) proliferation. Here, we show that KLF15 also represses ASM hypertrophy. To uncover the mechanistic basis for these effects, we integrated transcriptome data from KLF15 over-expression with genome-wide analysis of RNA Polymerase II (RNAPII) and glucocorticoid receptor (GR) occupancy (i.e. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17303
8 Samples
Download data: TXT
7.

mRNA profiling of human Multipotent Adipose-Derived Stem (hMADS) cells transfected with miR-29a and subjected to adipocyte differentiation

(Submitter supplied) The human microRNA hsa-miR-29a is a member of the miR-29 family of microRNAs, which is expressed in the adipogenic lineage. To identify putative direct target mRNAs of the miR-29 family, and to get an idea about potential functions of the miR-29 family in adipocyte development, we transfected human Multipotent Adipose-Derived Stem (hMADS) cells with miR-29a mimics (leading to elevation of intracellular levels of mature miR-29a). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL19627
7 Samples
Download data: GPR
Series
Accession:
GSE65704
ID:
200065704
8.

Distinct genome-wide, gene-specific selectivity patterns of four glucocorticoid receptor coregulators

(Submitter supplied) Glucocorticoids are a class of steroid hormones that bind to and activate the Glucocorticoid Receptor, which then positively or negatively regulates transcription of many genes that govern multiple important physiological pathways such as inflammation and metabolism of glucose, fat and bone. Previous studies focusing on single coregulators demonstrated that each coregulator is required for regulation of only a subset of all the genes regulated by a steroid hormone. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
40 Samples
Download data: TXT
Series
Accession:
GSE58715
ID:
200058715
9.

Genome-wide identification of glucocorticoid receptor binding sites in the whole hippocampus of adrenalectomised male rats given corticosterone infusion and stressed or non-stressed.

(Submitter supplied) We have applied next-generation sequencing technology to obtain high through-put profiling of glucocorticoid receptor (GR) DNA binding in whole hippocampus from male rat brain. By obtaining sequence from immunoprecipitated, sonicated chromatin, we have generated genome-wide binding maps for GR in two contexts, testing whether chromatin is primed for GR binding according to the animal's acute experience. more...
Organism:
Rattus norvegicus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL10669
8 Samples
Download data: BEDGRAPH, CSV
Series
Accession:
GSE94008
ID:
200094008
10.

Expression data from dexamethasone treated mouse embryonic neural progenitor/stem cells isolated from wild type C57Bl/6 or caveolin-1 knockout mice

(Submitter supplied) Neurosphere cultures prepared from E14.5 mouse cerebral cortex at passage 3 were treated for 4 hours with 100 nM dexamethasone We used microarrays to detail the global program of dexamethasone regulated gene expression in embryonic neural progenitor/stem cells
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5256
Platform:
GPL8321
20 Samples
Download data: CEL
Series
Accession:
GSE49804
ID:
200049804
11.
Full record GDS5256

Caveolin-1 deficiency effect on dexamethasone treatment: embryonic day E14.5 cerebral cortex

Analysis of E14.5 cerebral cortex, Caveolin-1 (Cav-1) deficient, cultured neurospheres treated with glucocorticoid (GC) dexamethasone (100nM, 4h). Cav-1 involved in GC signaling in neural stem cells. Results provide insight into role of Cav-1 in GC treatment and impact fetal brain development.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 2 genotype/variation sets
Platform:
GPL8321
Series:
GSE49804
20 Samples
Download data: CEL
12.

The Signature of Glucocorticoid Receptor -Dependent Hypertrophic Transcriptome in Cardiomyocytes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL20084
6 Samples
Download data: BW
Series
Accession:
GSE114767
ID:
200114767
13.

The Signature of Glucocorticoid Receptor -Dependent Hypertrophic Transcriptome in Cardiomyocytes [RNA-Seq]

(Submitter supplied) We examined Glucocorticoid receptor binding sites in isolated neonatal cardiomyocytes treated with Dexamethasone (100nM) for 1hr or Ethanol using GR-ChIP-Seq. In addition to determine the change in the resulting transcriptional status of genes we performed RNAseq in cardiomyocytes treated with Dexamethasone (100nM) or Ethanol for 1hr or 24hrs.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20084
3 Samples
Download data: PDF, XLSX
Series
Accession:
GSE114766
ID:
200114766
14.

The Signature of Glucocorticoid Receptor -Dependent Hypertrophic Transcriptome in Cardiomyocytes [ChIP-Seq]

(Submitter supplied) We examined Glucocorticoid receptor binding sites in isolated neonatal cardiomyocytes treated with Dexamethasone (100nM) for 1hr or Ethanol using GR-ChIP-Seq.
Organism:
Rattus norvegicus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20084
3 Samples
Download data: BW, PDF, XLSX
Series
Accession:
GSE114616
ID:
200114616
15.

Global changes of enhancer and chromatin accessibility due to microgravity in C2C12 myotubes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18480
6 Samples
Download data: BEDGRAPH
Series
Accession:
GSE184911
ID:
200184911
16.

Analysis of accessible chromatin regions in response to microgravity in C2C12 mouse myotubes

(Submitter supplied) We analyzed the accessible chromatin regions globally in response to microgravity in C2C12 mouse myotubes.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18480
4 Samples
Download data: BEDGRAPH
Series
Accession:
GSE184907
ID:
200184907
17.

Comparison of gene expression profiles for hormone induction in the presence and absence of AP1 binding.

(Submitter supplied) Gene expression array analysis component. Ligand-dependent transcription by the nuclear receptor glucocorticoid receptor (GR) is mediated by interactions with co-regulators. The role of these interactions in determining selective binding of GR to regulatory elements remains unclear. Recent findings indicate a large fraction of genomic GR binding coincides with chromatin that is accessible prior to hormone treatment, suggesting that receptor binding is dictated by proteins that maintain chromatin in an open state. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
8 Samples
Download data: CEL
Series
Accession:
GSE29983
ID:
200029983
18.

Genome-wide Binding Potential and Regulatory Activity of the Glucocorticoid Receptor’s Monomeric and Dimeric Forms

(Submitter supplied) A widely regarded model for glucocorticoid receptor (GR) action postulates that dimeric binding to DNA regulates unfavorable metabolic pathways while monomeric receptor binding promotes repressive gene responses related to its anti-inflammatory effects. This model has been built upon the characterization of the GRdim mutant, reported to be incapable of DNA binding and dimerization. Although quantitative live-cell imaging data shows GRdim as mostly dimeric, genomic studies, on the basis of recovery of enriched half-site response elements, suggest monomeric engagement on DNA. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19057 GPL17021 GPL21103
44 Samples
Download data: BEDGRAPH
Series
Accession:
GSE117661
ID:
200117661
19.

Gas lean obob GRf/fGRmKO

(Submitter supplied) Muscle glucocorticoid receptor (GR) signaling regulates gene expressions in skeletal muscle. To reveal the roles of muscle GR in systemic metabolism in obesity, ob/ob background muscle-specific GR knockout (ob/ob GRmKO) mice were generated.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28457
4 Samples
Download data: TXT
Series
Accession:
GSE198536
ID:
200198536
20.

GasLiverWAT GRf/fGRmKO vehicleCORT

(Submitter supplied) Muscle glucocorticoid receptor (GR) signaling regulates gene expressions in skeletal muscle and promotes protein catabolism. To reveal the roles of muscle GR in systemic metabolism, corticosterone was chronically administered to GR-floxed (GRf/f) or muscle-specific GR knockout (GRmKO) mice, and metabolic changes were analyzed.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28457
12 Samples
Download data: TXT
Series
Accession:
GSE198535
ID:
200198535
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