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Links from GEO DataSets

Items: 20

1.

RNA-seq, ChIP-seq and ATAC-seq analysis of MKL1 blocked cells during reprogramming

(Submitter supplied) Actins and regulators of actin dynamics generate contractile forces providing major mechanical and structural support for the cell. Whether and how they actively participate in cell fate control is not clear. Here, we report the actin responsive transcription factor complex MKL1/SRF, the major transcriptional regulator of large numbers of actin cytoskeletal genes, as an important regulator of genomic accessibility and cell fate outcome. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13112 GPL17021
44 Samples
Download data: BIGWIG, BW, CSV, XLSX
Series
Accession:
GSE120399
ID:
200120399
2.

Comparative transcriptome analysis of DFAT cells after the treatment with Y-27632 and the transfection of Mkl1 siRNA

(Submitter supplied) Cellular differentiation is regulated through activation and repression of defined transcription factors. A hallmark of differentiation is a pronounced change in cell shape, which is determined by dynamics of the actin cytoskeleton. In de-differentiated fat (DFAT) cells and 3T3-L1 cells, we showed that treatment with the ROCK inhibitor Y-27632, by inducing remodeling of the actin cytoskelton, causes adipocyte differentiation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE52334
ID:
200052334
3.

MKL1 deficiency results in a severe neutrophil motility defect due to impaired actin polymerization

(Submitter supplied) Megakaryoblastic leukemia 1 (MKL1) promotes the regulation of essential cell processes, including actin cytoskeletal dynamics by co-activating serum response factor. Recently, the first human case with MKL1 deficiency, leading to a novel primary immunodeficiency, was identified. We report a second family with two siblings with a homozygous frameshift mutation in MKL1. The index case deceased as an infant from progressive and severe pneumonia by Pseudomonas aeruginosa and poor wound healing. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23934
10 Samples
Download data: XLSX
Series
Accession:
GSE134644
ID:
200134644
4.

The interactome of Pou5f1 enhancer in mouse embryonic stem cells

(Submitter supplied) We report the application of enyzme-based 4C-Seq technique for exploring Pou5f1 enhancer interactome in mouse ES cells.
Organism:
Mus musculus
Type:
Other
Platform:
GPL13112
2 Samples
Download data: BED
Series
Accession:
GSE45418
ID:
200045418
5.

Transition of breast cancer cells from luminal to basal-like phenotype engages a shift from genomic to non-genomic activities of ERα activity

(Submitter supplied) Estrogen receptor (ERα) is central in driving the development of hormone-dependent breast cancers. A major challenge in treating these cancers is to understand and struggle endocrine resistance. We have previously shown that the Megakaryoblastic Leukemia 1 (MKL1) protein, a master regulator of actin dynamic and cellular motile functions, directs down-regulation of ERα and hormonal escape of estrogen-responsive breast cancer cell lines. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16699
16 Samples
Download data: TXT
Series
Accession:
GSE107924
ID:
200107924
6.

Transition of breast cancer cells from luminal to basal-like phenotype engages a shift from genomic to non-genomic activities of estrogen receptor-alpha activity

(Submitter supplied) Estrogen receptor (ERα) is central in driving the development of hormone-dependent breast cancers. A major challenge in treating these cancers is to understand and struggle endocrine resistance. We have previously shown that the Megakaryoblastic Leukemia 1 (MKL1) protein, a master regulator of actin dynamic and cellular motile functions, directs down-regulation of ERα and hormonal escape of estrogen-responsive breast cancer cell lines. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: WIG
Series
Accession:
GSE107476
ID:
200107476
7.

Differential regulation of gene expression by two isoforms of the human transcriptional coactivator MKL1

(Submitter supplied) We identified two isoforms of human MKL1 that differ in their N-terminal domains. Since MKL1 is a transcriptional coactivator of SRF and regulates many SRF target genes, we wanted to analyze if transcription is differentially regulated by the two isoforms upon stimulation of the Rho-actin-MKL1-SRF pathway.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
9 Samples
Download data: CEL
Series
Accession:
GSE47209
ID:
200047209
8.

Chromatin and signaling pathways in reprogramming

(Submitter supplied) Reprogramming intermediates (pre-iPSCs) were subjected to control DMSO, ascorbic acid (AA), 2i ( MAP kinase inhibitor + GSKinhibitor) or AA+2i conditions to assess conversion to the iinduced pluripotent stem cell state (iPSC) after 10days.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: TXT
Series
Accession:
GSE58836
ID:
200058836
9.

Srf destabilizes cell identity (ChIP-seq)

(Submitter supplied) Multicellular organisms consist of multiple cell types, whose identities are maintained appropriately at locations where they are reside. The identity of each cell type is primarily maintained by cell-type-specific gene expression programs, but mechanisms that suppress these programs are poorly defined. Here we show that serum response factor (Srf), a transcription factor that is activated by various extracellular stimuli, can repress cell-type-specific genes and promote cellular reprogramming to pluripotency. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL17021 GPL19057
16 Samples
Download data: BW
Series
Accession:
GSE106319
ID:
200106319
10.

Srf destabilizes cell identity (ATAC-seq)

(Submitter supplied) Multicellular organisms consist of multiple cell types, whose identities are maintained appropriately at locations where they are reside. The identity of each cell type is primarily maintained by cell-type-specific gene expression programs, but mechanisms that suppress these programs are poorly defined. Here we show that serum response factor (Srf), a transcription factor that is activated by various extracellular stimuli, can repress cell-type-specific genes and promote cellular reprogramming to pluripotency. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: BW
Series
Accession:
GSE106318
ID:
200106318
11.

Srf destabilizes cell identity (RNA-seq)

(Submitter supplied) Multicellular organisms consist of multiple cell types, whose identities are maintained appropriately at locations where they are reside. The identity of each cell type is primarily maintained by cell-type-specific gene expression programs, but mechanisms that suppress these programs are poorly defined. Here we show that serum response factor (Srf), a transcription factor that is activated by various extracellular stimuli, can repress cell-type-specific genes and promote cellular reprogramming to pluripotency. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: TXT
Series
Accession:
GSE106315
ID:
200106315
12.

Srf destabilizes cell identity

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing; Other
4 related Platforms
41 Samples
Download data: BEDGRAPH, BW, CEL, TXT
Series
Accession:
GSE90034
ID:
200090034
13.

Srf destabilizes cell identity (Hi-C-seq)

(Submitter supplied) Multicellular organisms consist of multiple cell types, whose identities are maintained by the locations in which they reside. The identity of a cell is primarily maintained by cell-type-specific gene expression programs, but mechanisms that suppress these programs are poorly defined. Here we show that serum response factor (Srf), a transcription factor that is activated by various extracellular stimuli, can repress cell-type-specific genes and promote cellular reprogramming to pluripotency. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL17021
8 Samples
Download data: BEDGRAPH
Series
Accession:
GSE90033
ID:
200090033
14.

Srf destabilizes cell identity (Microarray_affymetrix)

(Submitter supplied) Multicellular organisms consist of multiple cell types, whose identities are maintained appropriately at locations where they are reside. The identity of each cell type is primarily maintained by cell-type-specific gene expression programs, but mechanisms that suppress these programs are poorly defined. Here we show that serum response factor (Srf), a transcription factor that is activated by various extracellular stimuli, can repress cell-type-specific genes and promote cellular reprogramming to pluripotency. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
2 Samples
Download data: CEL
Series
Accession:
GSE90032
ID:
200090032
15.

Srf destabilizes cell identity (Microarray_Agilent Technologies)

(Submitter supplied) Multicellular organisms consist of multiple cell types, whose identities are maintained appropriately at locations where they are reside. The identity of each cell type is primarily maintained by cell-type-specific gene expression programs, but mechanisms that suppress these programs are poorly defined. Here we show that serum response factor (Srf), a transcription factor that is activated by various extracellular stimuli, can repress cell-type-specific genes and promote cellular reprogramming to pluripotency. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
12 Samples
Download data: TXT
Series
Accession:
GSE89427
ID:
200089427
16.

Fine-tuning Mybl2 levels are required for proper MET process during somatic reprogramming [ChIP-Seq]

(Submitter supplied) Genome wide data investigating the role of Mybl2 in reprogramming
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
1 Sample
Download data: BEDGRAPH
Series
Accession:
GSE109952
ID:
200109952
17.

Fine-tuning Mybl2 levels are required for proper MET process during somatic reprogramming

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19057 GPL17021
17 Samples
Download data: BEDGRAPH
Series
Accession:
GSE107579
ID:
200107579
18.

Fine-tuning Mybl2 levels are required for proper MET process during somatic reprogramming [RNA-seq]

(Submitter supplied) Genome wide data investigating the role of Mybl2 in reprogramming
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: DIFF
Series
Accession:
GSE107578
ID:
200107578
19.

Fine-tuning Mybl2 levels are required for proper MET process during somatic reprogramming [ATAC-Seq]

(Submitter supplied) Genome wide data investigating the role of Mybl2 in reprogramming
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
12 Samples
Download data: BEDGRAPH
Series
Accession:
GSE107577
ID:
200107577
20.

Comprehensive role of Zfp217 in m6A methylation [ChIP-seq]

(Submitter supplied) Many transcriptional and epigenetic networks must be integrated to maintain self-renewal and pluripotency in embryonic stem cells (ESCs) and to enable induced pluripotent stem cell (iPSC) reprogramming. Here, we explore the role of Zfp217 as a key transcriptional factor in maintaining ES cell self-renewal by permorming genome-wide ChIP-Seq analyses.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9185
2 Samples
Download data: BED
Series
Accession:
GSE65730
ID:
200065730
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