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Links from GEO DataSets

Items: 19

1.

Gene expression analysis of CBFbeta knockdown PPC1 cells

(Submitter supplied) Whole genome array expression analysis was performed to identify changes in gene expression associated with the downregulation of the Core Binding Factor subunit CBFbeta.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
6 Samples
Download data: TXT
Series
Accession:
GSE21561
ID:
200021561
2.

Microarray analysis of Cbfb-deficient regulatory T cells

(Submitter supplied) Gene expression profiles of Cbfb-deficient and control Treg cells were compared. Abstract: Naturally arising regulatory T (Treg) cells express the transcription factor FoxP3, which critically controls the development and function of Treg cells. FoxP3 interacts with another transcription factor Runx1 (also known as AML1). Here we showed that Treg cell-specific deficiency of Cbfβ, a cofactor for all Runx proteins, or that of Runx1, but not Runx3, induced lymphoproliferation, autoimmune disease, and hyper-production of IgE. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3577
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE18148
ID:
200018148
3.
Full record GDS3577

Cbfbeta deficiency effect on regulatory T cells

Analysis of regulatory T cells lacking Cbfbeta. Cbfbeta is a cofactor for the Runx family of transcription factors. Results provide insight into the role of the Runx1-Cbfbeta transcription complex in regulatory T cell function.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE18148
6 Samples
Download data: CEL
DataSet
Accession:
GDS3577
ID:
3577
4.

caArray_green-00001: Alterations in Gene Expression Profiles during Prostate Cancer Progression

(Submitter supplied) To identify molecular changes that occur during prostate tumor progression, we have characterized a series of prostate cancer cell lines isolated at different stages of tumorigenesis from C3(1)/Tag transgenic mice.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platform:
GPL20562
19 Samples
Download data: GPR
Series
Accession:
GSE69892
ID:
200069892
5.

Gene expression of human soft tissue sarcoma

(Submitter supplied) Gene expression profiles of 39 human sarcoma samples (GSM 52571-GSM52609) and 15 control samples (GSM52556-GSM52570) were assessed using Affymetrix HG U133A oligonucleotide arrays. Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1209
Platform:
GPL96
54 Samples
Download data
Series
Accession:
GSE2719
ID:
200002719
6.
Full record GDS1209

Sarcoma and hypoxia

Expression profiling of soft tissue sarcoma samples. Hypoxic regions often develop in tumors as they increase in size. Results provide insight into the expression of hypoxia-related genes in sarcomas.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state, 23 tissue sets
Platform:
GPL96
Series:
GSE2719
54 Samples
Download data
DataSet
Accession:
GDS1209
ID:
1209
7.

Gene expression in Ewing tumor cell lines after STEAP1 silencing

(Submitter supplied) Goal: identification of differentially expressed genes after STEAP1 silencing. Ewing tumors (ET) are characterized by oncogenic EWS/ETS translocations and early metastasis. STEAP1 is a membrane-bound channel protein of unkown function. While overexpressed in many cancers, STEAP1 expression is strongly restricted to mesenchymal stem cells, prostate and urothelium among benign tissues. Here we show that STEAP1 is a direct transcriptional target of EWS/FLI1 and critical for ET malignancy. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
6 Samples
Download data: CEL
Series
Accession:
GSE26422
ID:
200026422
8.

Affymetrix SNP array data for ovarian cancer cells OVCAR-3 and FU-OV-1

(Submitter supplied) A subset of ovarian cancer are characterized by 19q12 amplification. To perform funtional studies of this amplicon the profile has been determined by SNP analysis.
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array
Platform:
GPL6801
2 Samples
Download data: CEL, CNCHP
Series
Accession:
GSE26301
ID:
200026301
9.

CBFβ promotes colorectal tumor growth and metastasis in a RUNX2-dependent manner

(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
Platforms:
GPL11154 GPL10999
6 Samples
Download data: BW
Series
Accession:
GSE154876
ID:
200154876
10.

CBFβ promotes colorectal tumor growth and metastasis in a RUNX2-dependent manner (ChIP-seq)

(Submitter supplied) Transcriptional regulation is critically involved in colorectal cancer (CRC) pathogenesis, the mechanism of which remains incompletely understood. Here, we report that core-binding factor β (CBFβ) is commonly upregulated in human colorectal cancer and is associated with the survival rate of CRC patients. Immunohistochemistry (IHC) analysis of RUNX1-3 expression in CRC patients and other in vitro data revealed that CBFβ promotes cell proliferation and liver metastasis in a RUNX2-dependent way. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL10999
2 Samples
Download data: BW, TXT
Series
Accession:
GSE153682
ID:
200153682
11.

CBFβ promotes colorectal tumor growth and metastasis in a RUNX2-dependent manner (RNA-seq)

(Submitter supplied) Transcriptional regulation is critically involved in colorectal cancer (CRC) pathogenesis, the mechanism of which remains incompletely understood. Here, we report that core-binding factor β (CBFβ) is commonly upregulated in human colorectal cancer and is associated with the survival rate of CRC patients. Immunohistochemistry (IHC) analysis of RUNX1-3 expression in CRC patients and other in vitro data revealed that CBFβ promotes cell proliferation and liver metastasis in a RUNX2-dependent way. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: TXT
12.

Expression data from human osteosarcoma cells treated with CDK11 siRNA

(Submitter supplied) The U-2OS and KHOS osteosarcoma cell lines where seeded onto the 100mm cell culture plate, then treated with CDK11 siRNA (40nM) or nonspecificsiRNA (40nM). Change with regular medium 24 hour later. Total RNA was collected from these cells using TRIzol® Reagent (GIBCO Grand Island, NY) according to the manufacturer’s instructions. To account for and eliminate biologic noise, RNA was isolated from three distinct flasks of each cell line and pooled together. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE73422
ID:
200073422
13.

Core Binding Factor β Is Required For Group-2 Innate Lymphoid Cell Activation

(Submitter supplied) Group-2 innate lymphoid cells (ILC2) are tissue-resident, long-lived innate effector cells implicated in allergy and asthma. Upon activation, mature ILC2 rapidly secret large amounts of type-2 cytokines and other effector molecules. The molecular pathways that drive ILC2 activation are not well understood. Here we report that the transcriptional controller Core-binding factor β (CBFβ) is required for ILC2 activation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17791
6 Samples
Download data: CEL
Series
Accession:
GSE116062
ID:
200116062
14.

siRNA knockdown of ribosomal protein gene RPL19 abrogates the aggressive phenotype of human prostate cancer

(Submitter supplied) Ribosomal protein RPL19 is an integral component of eukaryotic ribosomes and universally involved in protein synthesis. Although consistently stable  in normal cells, RPL19 transcription is relatively elevated in prostate cancer. Using siRNA, we inhibited RPL19 transcription and demonstrated the gene to be functionally involved in promoting the malignant phenotype. Reducing RPL19 modulates a subset of genes rather than globally down-regulating protein synthesis, as evidenced by Western blotting and maintenance of cell proliferation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
10 Samples
Download data: TXT
Series
Accession:
GSE26774
ID:
200026774
15.

Genomic binding of RUNX1 in MCF10A cells

(Submitter supplied) The overall goal of this study is to identify the genomic binding of RUNX1 in MCF10A cells. We used ChIPseq (chromatin immunoprecipitation assay followed by deep sequencing) to identify the binding sites of RUNX1 in MCF10A cells. We performed ChIPseq of RUNX1 using parental MCF10A cells and did not identify high confident binding sites. To overcome this hurdle, we first generated a RUNX1 deleted MCF10A cell line using CRISPR-Cas9. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
2 Samples
Download data: TXT
Series
Accession:
GSE129314
ID:
200129314
16.

Identifying transcripts that are transcriptinoally regulated by CBFB and RUNX1 using RNAseq

(Submitter supplied) Using RNAseq to identify differentially expressed transcripts between CBFB wild type (WT) and knockout (KO) or between RUNX1 wild type (WT) and knockout (KO) MCF10A cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
18 Samples
Download data: CSV, XLSX
17.

RNA binding of CBFB and hnRNPK

(Submitter supplied) RNA immunoprecipitation assay followed by next generation sequencing (RIPseq) to identify RNAs bound by CBFB and hnRNPK in breast cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
5 Samples
Download data: TXT
18.

RNAseq of ribosomal fractionation to assess the effect of CBFB on translation regulation

(Submitter supplied) Five million wild type (WT) and CBFB knockout (CBFB_KO) MCF10A cells were subject to ribosomal fractination. Total RNA from each fraction was extracted using Trizol followed by Qiagen RNAeasy kit. Polyribosomal fractions were polled as one sample. RNAs in the free, mono- (mono) and polyribosomal (poly) fractions were used for RNAseq.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: TXT
19.

Maintenance of mammary epithelial phenotype by AML1/RUNX1 through mitotic gene bookmarking

(Submitter supplied) Genetic and epigenetic changes in mammary epithelial cells facilitate epithelial-to-mesenchymal transition (EMT) which leads to invasion and metastasis. RUNX1 is a phenotypic transcription factor pivotal for maintenance of mammary epithelial phenotype, whose loss leads to EMT. However, the mechanisms by which RUNX1 maintains mammary epithelial phenotype are not known. Here, we report RUNX1-mediated mitotic gene bookmarking as a key epigenetic mechanism through which RUNX1 stabilizes mammary epithelial phenotype by conveying regulatory information for cell proliferation, growth, and identity through successive cell divisions. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18460
6 Samples
Download data: BED, BW
Series
Accession:
GSE121370
ID:
200121370
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