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Links from GEO DataSets

Items: 20

1.
Full record GDS3481

NOR1 gene and EWS/NOR1 fusion gene overexpression

Analysis of cells overexpressing NOR1 or the EWS/NOR1 fusion gene. NOR1 encodes an orphan nuclear receptor. The EWS gene is involved in various malignancies by way of chromosomal translocations, and the EWS/NOR1 gene fusion is implicated in the pathogenesis of extraskeletal myxoid chondrosarcomas.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 4 protocol sets
Platform:
GPL570
Series:
GSE11185
4 Samples
Download data: CEL
DataSet
Accession:
GDS3481
ID:
3481
2.

Differences between NOR1 and EWS/NOR1

(Submitter supplied) To examine the differences between NOR1 and its fusion gene product EWS/NOR1, we compared the gene expression profiles of NOR1- and EWS/NOR1-overexpressing 293 cells. Keywords: gene comparison
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3481
Platform:
GPL570
4 Samples
Download data: CEL
Series
Accession:
GSE11185
ID:
200011185
3.

Genome-wide ChIP-seq analysis of Nr4a1 binding sites in regulatory T (Treg) cells

(Submitter supplied) We have revealed that Nr4a family nuclear orphan receptors broadly regulate a transcriptional program in Treg cells. In this study, to give an insight into Nr4a-mediated regulation of the transcriptional program in Treg cells, we performed ChIP-seq experiment using anti-Nr4a1 antibodies and a chromatin lysate from Treg cells.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11002
1 Sample
Download data: TXT
Series
Accession:
GSE70417
ID:
200070417
4.

Comparison of mRNA expression pattern between wild-type regulatory T (Treg) cells and Nr4a-deficient Treg cells

(Submitter supplied) Regulatory T (Treg) cells, as central mediators of immune suppression, play crucial roles in many aspects of immune system physiology and pathophysiology. Treg cells are characterized by a distinct pattern of gene expression, including upregulation of immune-suppressive genes and silencing of inflammatory cytokine genes. However, the molecular mechanisms that establish and/or maintain such gene regulation in Treg cells remain largely unknown. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11202
2 Samples
Download data: TXT
Series
Accession:
GSE70306
ID:
200070306
5.

Nr4a transcription factors limit CAR-T cell function in solid tumors

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL17021
138 Samples
Download data
Series
Accession:
GSE123739
ID:
200123739
6.

Nr4a transcription factors limit CAR-T cell function in solid tumors [RNA-Seq]

(Submitter supplied) Chromatin accessibility with ATAC-seq and gene expression with RNA-seq for CD8 T cells expressing chimeric antigen receptors in solid tumors or after in vitro culture.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
47 Samples
Download data: TSV
Series
Accession:
GSE123738
ID:
200123738
7.

Nr4a transcription factors limit CAR-T cell function in solid tumors [ATAC-Seq]

(Submitter supplied) Chromatin accessibility with ATAC-seq and gene expression with RNA-seq for CD8 T cells expressing chimeric antigen receptors in solid tumors or after in vitro culture.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
91 Samples
Download data: TSV
Series
Accession:
GSE123629
ID:
200123629
8.

Transcriptional profiling of monocytes deficient in Nuclear Orphan Receptors NR4A2 and NR4A3 reveals distinct signalling roles related to antigen presentation and viral response.

(Submitter supplied) Using RNA-sequencing and strategic bioinformatic analysis we investigated the down-stream effects of NR4A2 and NR4A3 in monocytes and dissected their common and distinct signalling roles.NR4A2 selective genes were most associated with antigen presentation, NR4A3 selective genes were most associated with interferon/viral reponse and NR4A2/3 co-regulated genes were most associated with clasical innate immure response signaling e.g. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
18 Samples
Download data: TXT
9.

Schizophrenia: postmortem dorsal lateral prefrontal cortex (DLPFC)

(Submitter supplied) RNA-Seq analysis of post-mortem tissue from DLPFC of 19 schizophrenia patients and 19 controls.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13393
38 Samples
Download data: TXT
10.

EWS and FUS Bind a Subset of Transcribed Genes Encoding Proteins Enriched in RNA Regulatory Functions

(Submitter supplied) Background FUS (TLS) and EWS (EWSR1) belong to the FET-protein family of RNA and DNA binding proteins. FUS and EWS are structurally and functionally related and participate in transcriptional regulation and RNA splicing. FUS and EWS are identified in translocation generated cancer fusion proteins and involved in the human neurological diseases amyotrophic lateral sclerosis and fronto-temporal lobar degeneration. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9052
5 Samples
Download data: BED, TAR, XLS
Series
Accession:
GSE73492
ID:
200073492
11.

NR4A2 and NR4A3 selectively modulate elements of the monocyte response to buffered hypercapnia

(Submitter supplied) In wild type, NR4A2-deficient, and NR4A3-deficient monocytes we used RNA-sequencing to investigate the effect of 4hrs of exposure to buffered hypercapnia (10% CO2) compared to normocapnia (5% CO2) with and without the pro-inflammatory stimulus LPS (2.5ug/ml) for the final 2hrs. Buffered hypercapnia causes transcriptional changes associated with altered metabolic function in both the basal and stimulated states.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
36 Samples
Download data: TXT
Series
Accession:
GSE251925
ID:
200251925
12.

Buffered hypercapnia alters the transcriptional profile in monocytes.

(Submitter supplied) In monocytes we used RNA-sequencing to investigate the effect of 4hrs of exposure to buffered hypercapnia (10% CO2) compared to normocapnia (5% CO2) with and without the pro-inflammatory stimulus LPS (2.5ug/ml) for the final 2hrs. Buffered hypercapnia causes transcriptional changes associated with altered metabolic function in both the basal and stimulated states.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
12 Samples
Download data: TXT
Series
Accession:
GSE206333
ID:
200206333
13.

Regulation of Ag-activated B cells by Nur77/Nr4a1

(Submitter supplied) We identify differentially expressed inducible genes in activated B cells harvested from mice lacking expression of the orphan nuclear hormone receptor Nr4a1.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
10 Samples
Download data: TXT
Series
Accession:
GSE146747
ID:
200146747
14.

KLF15 dependent REV-ERBa binding in the heart

(Submitter supplied) By comparing the ChIPseq signal of REV_ERBa in control (Flox) and cardiomyocytic KLF15 knockout (cKO), we identified the KLF15 dependent REV-ERBa binding and repression in the heart. We further compared the differential binding sites to KLF15 binding site, using a FLAG tagged cardiomyocytic transgenic (cTG1) mice.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: BEDGRAPH
Series
Accession:
GSE73741
ID:
200073741
15.

KLF15 Establishes the Landscape of Circadian Expression in the Heart

(Submitter supplied) In the heart, KLF15 directs a biphasic circadian rhythm, while preventing extraneous oscillation at the transcriptomic level.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
36 Samples
Download data: TXT
Series
Accession:
GSE63243
ID:
200063243
16.

Differential binding of PARP-1 domains

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25244
24 Samples
Download data
Series
Accession:
GSE222877
ID:
200222877
17.

Differential binding of PARP-1 domains (AW-YFP ChIP-seq)

(Submitter supplied) We interrogated the differential binding of PARP-1 domains (ZnI, ZnII, AD-WGR) and a ZnI mutant in Drosophila via ChIP-seq of third-instar larvae.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25244
6 Samples
Download data: BIGWIG
Series
Accession:
GSE222876
ID:
200222876
18.

Differential binding of PARP-1 domains (ZNII-YFP ChIP-seq)

(Submitter supplied) We interrogated the differential binding of PARP-1 domains (ZnI, ZnII, AD-WGR) and a ZnI mutant in Drosophila via ChIP-seq of third-instar larvae.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25244
6 Samples
Download data: BIGWIG
Series
Accession:
GSE222875
ID:
200222875
19.

Differential binding of PARP-1 domains (ZNI-YFP ChIP-seq)

(Submitter supplied) We interrogated the differential binding of PARP-1 domains (ZnI, ZnII, AD-WGR) and a ZnI mutant in Drosophila via ChIP-seq of third-instar larvae.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25244
6 Samples
Download data: BIGWIG
Series
Accession:
GSE222873
ID:
200222873
20.

Differential binding of PARP-1 domains (DZNI-YFP ChIP-seq)

(Submitter supplied) We interrogated the differential binding of PARP-1 domains (ZnI, ZnII, AD-WGR) and a ZnI mutant in Drosophila via ChIP-seq of third-instar larvae.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25244
6 Samples
Download data: BIGWIG
Series
Accession:
GSE222865
ID:
200222865
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