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Links from GEO DataSets

Items: 20

1.

Gene regulation and priming by Topoisomerase IIα in embryonic stem cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array; Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13161 GPL13112
7 Samples
Download data: PAIR
Series
Accession:
GSE46070
ID:
200046070
2.

Gene regulation and priming by Topoisomerase IIα in embryonic stem cells [FAIRE-Seq]

(Submitter supplied) Topoisomerases are essential for resolving topological problems in the genome, while their function in gene regulation, especially during cellular differentiation, remains unknown. We reveal that the expression of two Topo II isoforms, Top2a and Top2ß, is characteristic of dividing and postmitotic tissues, respectively. In embryonic stem cells, Top2a preferentially binds to promoters embedded in an active chromatin environment. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
3 Samples
Download data: BED
Series
Accession:
GSE49141
ID:
200049141
3.

Gene regulation and priming by Topoisomerase IIα in embryonic stem cells [RNA-Seq]

(Submitter supplied) Topoisomerases are essential for resolving topological problems in the genome, while their function in gene regulation, especially during cellular differentiation, remains unknown. We reveal that the expression of two Topo II isoforms, Top2a and Top2ß, is characteristic of dividing and postmitotic tissues, respectively. In embryonic stem cells, Top2a preferentially binds to promoters embedded in an active chromatin environment. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: TXT
Series
Accession:
GSE46066
ID:
200046066
4.

Gene regulation and priming by Topoisomerase IIα in embryonic stem cells [ChIP-chip]

(Submitter supplied) Topoisomerases are essential for resolving topological problems in the genome, while their function in gene regulation, especially during cellular differentiation, remains elusive/unknown. We reveal that the expression of two Topo II isoforms, Top2α and Top2β, is characteristic of dividing and postmitotic tissues, respectively. In embryonic stem cells, Top2α preferentially binds to promoters embedded in an active chromatin environment. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL13161
2 Samples
Download data: PAIR
Series
Accession:
GSE45890
ID:
200045890
5.

Topoisomerase IIbeta occupies H3K4 methylated sites and regulates neuronal survival via repression of the neurotrophin receptor p75

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL6246 GPL13161
30 Samples
Download data: CEL, PAIR
Series
Accession:
GSE27247
ID:
200027247
6.

Top2β ChIP-chip

(Submitter supplied) Chromatin IP was performed with Top2β antibodies in WT neurons and hybridized to custom designed tiling array.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL13161
2 Samples
Download data: PAIR
Series
Accession:
GSE27246
ID:
200027246
7.

Expression data from Top2β KO cells as well ICRF-193 treatment of in vitro derived neurons and cortical glutamatergic neurons

(Submitter supplied) Expression profiling of from Top2β knokout and ICRF-193 treated neurons reveals a significant number of genes that are transcriptionally deregulated
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
28 Samples
Download data: CEL
Series
Accession:
GSE27245
ID:
200027245
8.

A chromatin-modifying function of JNK during embryonic stem cell differentiation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9250 GPL6246
43 Samples
Download data: CEL, WIG
Series
Accession:
GSE25533
ID:
200025533
9.

A chromatin-modifying function of JNK during stem cell differentiation

(Submitter supplied) Signaling mediates cellular responses to extracellular stimuli. The c-Jun NH2-terminal kinase (JNK) pathway exemplifies one sub-group of Mitogen-activated protein (MAP) kinases, which besides established functions in stress response, also contributes to developmental processes by an unknown mechanism 1-4. Here we show by genome-wide location analysis that JNK binds directly to a large set of active promoters during differentiation of stem cells to neurons. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9250
33 Samples
Download data: WIG
Series
Accession:
GSE25532
ID:
200025532
10.

Expression data from DMSO and SP600125 treated neurons

(Submitter supplied) Expression profiling of from DMSO and SP600125 treated glutamatergic neurons reveals JNK target genes that are transcriptionally regulated by JNK signaling. SP600125 is a known JNK signaling inhibitor and therefore, we used this to test whether the expression of JNK bound genes is affected upon inhibition of JNK kinase activity.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
10 Samples
Download data: CEL
Series
Accession:
GSE25529
ID:
200025529
11.

Role of DNA Topoisomerase IIbeta in Gene Expression

(Submitter supplied) Mice lacking topoisomerase IIβ (Top IIβ) are known to exhibit a perinatal death phenotype. In the current study, transcription profiles of the brains of wild type and top2β knockout mouse embryos were generated. Surprisingly, only a small number (1-4%) of genes were affected in top2β knockout embryos. However, the expression of nearly 30% of developmentally regulated genes was either up- or down-regulated. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2702
Platform:
GPL81
6 Samples
Download data: CEL
Series
Accession:
GSE5458
ID:
200005458
12.
Full record GDS2702

Topoisomerase IIbeta deficiency effect on the developing embryonic brain

Anlaysis of brains from topoisomerase IIbeta (TopIIbeta) deficient embryos at various ages up to embryonic day 18.5. TopIIbeta null animals exhibit a perinatal death phenotype. Results provide insight into the role of TopIIbeta at the late stages of neuronal differentiation.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 age, 2 genotype/variation sets
Platform:
GPL81
Series:
GSE5458
6 Samples
Download data: CEL
13.

Control of RNA polymerase II promoter-proximal pausing by DNA supercoiling

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL11154 GPL18573
26 Samples
Download data: BIGWIG, TXT
Series
Accession:
GSE141800
ID:
200141800
14.

Control of RNA polymerase II promoter-proximal pausing by DNA supercoiling [RNA-seq]

(Submitter supplied) During transcription, DNA supercoiling generated by the advance of RNA polymerase II (Pol II) is resolved by DNA topoisomerases, enzymes that bind chromatin and produce transient breaks to relax DNA. Recently, this idea of mere facilitators of transcription progression is changing, as topoisomerases are being assigned new functions in regulating the expression of specific genes. In fact, mammalian type II topoisomerases, both the [Symbol] (TOP2A) and [Symbol] (TOP2B) paralogs, are enriched at promoter regions, where they have been proposed to trigger transcription through the generation of DNA double-strand breaks (DSBs). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL11154
10 Samples
Download data: BIGWIG, TXT
15.

Control of RNA polymerase II promoter-proximal pausing by DNA supercoiling [ChIP-seq]

(Submitter supplied) During transcription, DNA supercoiling generated by the advance of RNA polymerase II (Pol II) is resolved by DNA topoisomerases, enzymes that bind chromatin and produce transient breaks to relax DNA. Recently, this idea of mere facilitators of transcription progression is changing, as topoisomerases are being assigned new functions in regulating the expression of specific genes. In fact, mammalian type II topoisomerases, both the [Symbol] (TOP2A) and [Symbol] (TOP2B) paralogs, are enriched at promoter regions, where they have been proposed to trigger transcription through the generation of DNA double-strand breaks (DSBs). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
16 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE141798
ID:
200141798
16.

GRO analysis of topoisomerase mutants

(Submitter supplied) Genomic Run-on analysis of topoisomerase mutants (top1-delta/top2ts or top2ts) has been conducted at reference temperature for wt strain and at non-permissive temperature for wt and mutant strains. Keywords: Genomic Run On
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL7871
13 Samples
Download data
Series
Accession:
GSE16673
ID:
200016673
17.

Expression data from human pluripotent stem cells treated with PluriSIn#2

(Submitter supplied) Pluripotent-specific inhibitors (PluriSIns) make a powerful tool for studying the mechanisms that control the survival of human pluripotent stem cells (hPSCs). Here we characterize PluriSIn#2 as a novel selective indirect inhibitor of topoisomerase II alpha (TOP2A). We find that TOP2A is uniquely expressed in undifferentiated hPSCs, and that its inhibition results in their rapid cell death. These findings reveal a dependency of hPSCs on the activity of TOP2A, which can be harnessed for their selective elimination from culture.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
3 Samples
Download data: CEL
Series
Accession:
GSE57909
ID:
200057909
18.

DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
16 Samples
Download data
Series
Accession:
GSE89893
ID:
200089893
19.

DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes [FAIRE-Seq]

(Submitter supplied) The Autoimmune Regulator (AIRE) protein is the key factor in thymic negative selection of autoreactive T-cells by promoting the ectopic expression of tissue-specific genes in thymic medullary epithelium. Mutations in AIRE cause a monogenic autoimmune disease called autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). AIRE has been shown to promote DNA breaks via its interaction with topoisomerase 2 (TOP2). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
8 Samples
Download data: TXT
Series
Accession:
GSE89892
ID:
200089892
20.

DNA breaks and chromatin structural changes enhance the transcription of Autoimmune Regulator target genes [RNA-Seq]

(Submitter supplied) The Autoimmune Regulator (AIRE) protein is the key factor in thymic negative selection of autoreactive T-cells by promoting the ectopic expression of tissue-specific genes in thymic medullary epithelium. Mutations in AIRE cause a monogenic autoimmune disease called autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). AIRE has been shown to promote DNA breaks via its interaction with topoisomerase 2 (TOP2). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
8 Samples
Download data: CSV
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