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Items: 1 to 20 of 41

1.

Osteopontin drives neuroinflammation and cell loss in MAPT-N279K frontotemporal dementia patient neurons

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by high throughput sequencing
Platforms:
GPL24676 GPL17930
61 Samples
Download data: CEL, TXT
Series
Accession:
GSE230520
ID:
200230520
2.

Osteopontin drives neuroinflammation and cell loss in MAPT-N279K frontotemporal dementia patient neurons

(Submitter supplied) Frontotemporal dementia (FTD) is an incurable group of early-onset dementias that can be caused by deposition of hyperphosphorylated tau in patient brains. However, the mechanisms leading to neurodegeneration remain largely unknown. Here, we combined single-cell analyses of FTD patient brains with a stem cell culture and transplantation model of FTD. We identified disease phenotypes in FTD neurons carrying the MAPT-N279K mutation, which were related to oxidative stress, oxidative phosphorylation and neuroinflammation with an upregulation of the inflammation-associated protein osteopontin (OPN). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
18 Samples
Download data: CEL
Series
Accession:
GSE230447
ID:
200230447
3.

Microarray expression data of E7386-treated HSC3 cells

(Submitter supplied) E7386 inhibits interaction between B-catenin and CREB-binding protein (CBP), which drives oncogenic gene expression and aggressive cancer phenotypes in oral squamous cell carcinomas (OSCC). We use microarrays to profile the effects of E7386 treatment on gene expression of HSC3 human OSCC cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
6 Samples
Download data: CEL
Series
Accession:
GSE190377
ID:
200190377
4.

Expression data from MCF10A cells treated with TGFβ for multiple time points

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
synthetic construct; Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array; Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL19117 GPL17930
28 Samples
Download data: CEL
Series
Accession:
GSE194019
ID:
200194019
5.

Expression data from MCF10A cells treated with TGFβ for multiple time points [HuGene-2_0]

(Submitter supplied) We combine state-of-the-art data acquisition platforms and bioinformatics tools to devise PAMAF, a workflow that simultaneously examines twelve omics modalities, i.e., protein abundance from whole-cells, nucleus, exosomes, secretome and membrane; N-glycosylation, phosphorylation; metabolites; mRNA, miRNA; and, in parallel, single-cell transcriptomes. Here we apply PAMAF in an established in vitro model of TGFβ-induced epithelial to mesenchymal transition (EMT) to quantify >61,000 molecules from 12 omics and 10 timepoints over 12 days. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
10 Samples
Download data: CEL
Series
Accession:
GSE193985
ID:
200193985
6.

RAB38 Facilitates Energy Metabolism and Counteracts Cell Death in Glioblastoma Model Systems

(Submitter supplied) Glioblastoma is a high-grade glial neoplasm with a patient survival of 12-18 months. Therefore, there is an urgent need for identification of novel therapeutic targets. RAB38 is a member of a family of small GTPase proteins and has been implicated in regulating cell proliferation and survival in tumors. The role of RAB38 in glioblastoma is unexplored. Here, we used human glioblastoma cell lines to test the hypothesis that RAB38 regulates glioblastoma growth. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
4 Samples
Download data: CEL
Series
Accession:
GSE162444
ID:
200162444
7.

AURKA Inhibition Reprograms Metabolism dependent on PGC1α to Drive Synthetic Lethality with Fatty Acid Oxidation Inhibition in Glioblastoma

(Submitter supplied) We described the metabolic alterations in glioblastoma model systems elicited by AURKA inhibition. By utilizing proteomic and transcriptomic analyses coupled with untargeted polar and nonpolar metabolite analysis by LC/MC, we found that AURKA inhibition leads to a profound reprogramming of tumor metabolism, which suppresses c-Myc protein levels and increases pro-survival PGC1α which in concert mediate a suppression of glycolysis and a concomitant activation of oxidative phosphorylation (OXPHOS) that is fueled by enhanced fatty acid oxidation (FAO). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
4 Samples
Download data: CEL
Series
Accession:
GSE152612
ID:
200152612
8.

Expression data of glioblastoma cells with Crizotinib acute and chronic treatment vs its own vehicle control

(Submitter supplied) Gene expression of chronically or acutely Crizotinib treated glioblastoma cells vs vehicle controls
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
4 Samples
Download data: CEL
Series
Accession:
GSE113961
ID:
200113961
9.

MITF Expression Predicts Therapeutic Vulnerability to p300 Inhibition in Human Melanoma

(Submitter supplied) Histone modifications, largely regulated by histone acetyltransferases (HATs) and histone deacetylases (HDACs) have been recognized as major regulatory mechanisms governing human diseases including cancer. Despite significant effort and recent advances, the mechanism by which the p300 transcriptional coactivator mediates tumorigenesis remains unclear. Here, we use a genetic and chemical approach to identify the Microphthalmia-associated transcription factor (MITF) as a critical downstream target of p300 driving human melanoma growth. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
8 Samples
Download data: CEL
Series
Accession:
GSE128737
ID:
200128737
10.

Skeletal Muscle Fibrosis in Pancreatic Cancer Patients with Respect to Survival

(Submitter supplied) Skeletal muscle wasting is a devastating consequence of cancer that may be responsible for nearly 30% of cancer-related deaths. In addition to muscle atrophy, we have identified significant muscle fiber damage and replacement of muscle with fibrotic tissue in rectus abdominis muscle biopsies from cachectic pancreatic ductal adenocarcinoma (PDAC) patients that associates with poor survival. Transcriptional profiling of muscle harvested from these same patients supported these findings by identifying gene clusters related to wounding, inflammation and cellular response to TGF-B upregulated in cachectic PDAC patients compared with non-cancer controls. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
46 Samples
Download data: CEL
Series
Accession:
GSE130563
ID:
200130563
11.

Combination effect of G-TPP and LXR623 on stem cell like glioma cells

(Submitter supplied) We performed microarray analysis in order to evaluate the combination effect of the mitochondrial matrix chaperone inhibitor gamitrinib-triphenylphosphonium (G-TPP) and Liver X receptor agonist LXR623 on gene expression in stem cell like glioma cells (NCH644).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
8 Samples
Download data: CEL
Series
Accession:
GSE104272
ID:
200104272
12.

Effect of TIC10/ONC201 on glioma cells

(Submitter supplied) We performed microarray analysis in order to evaluate the effect of ONC201 on gene expression in glioma cells (U87).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
2 Samples
Download data: CEL
Series
Accession:
GSE103963
ID:
200103963
13.

Comparison of stem cell like glioma cells (NCH644 and NCH690) and their differentiated cells

(Submitter supplied) Microarray analysis was performed to compare gene expression between stem cell like glioma cells and their differentiated cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
4 Samples
Download data: CEL
Series
Accession:
GSE103962
ID:
200103962
14.

Expression data of U87 MG glioblastoma cells with vehicle or with 30nM Panobinostat treatment for 3 weeks

(Submitter supplied) Low dose of HDAC inhibitor (Panobinostat) treatment causes U87 cells to become resistant to the drug. Gene expression of the resistant cell line is altered comparing to the vehicle control.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
2 Samples
Download data: CEL
Series
Accession:
GSE103961
ID:
200103961
15.

Global gene expression of human iPSC directed differentation towards smooth muscle cells using an Acta2eGFP human iPSC reporter line

(Submitter supplied) Here, we generated and differentiated a human induced pluripotent stem cell line with an ACTA2eGFP reporter towards a smooth muscle-like cell that can be purified and expresses characteristic markers of smooth muscle cells. We performed microarray analysis of day 30 ACTA2eGFP+ and ACTA2eGFP- sorted populations, and the transcriptomic profile of the ACTA2eGFP+ cells is reminiscent of an immature or a synthetic smooth muscle cell phenotype.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
6 Samples
Download data: CEL
Series
Accession:
GSE132454
ID:
200132454
16.

Novel Upstream Regulators of YAP/TAZ Activation

(Submitter supplied) The goal of this study was to determine if loss of STK25 or gain of miR-24-3p resulted in YAP/TAZ activation.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
9 Samples
Download data: CEL
Series
Accession:
GSE119503
ID:
200119503
17.

Constitutively Active YAP/TAZ Target Genes

(Submitter supplied) The goal of this study was to identify an active YAP/TAZ signature in the hTERT-RPE-1 cell line.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
8 Samples
Download data: CEL
Series
Accession:
GSE119502
ID:
200119502
18.

Effect of LXR623, liver X receptor agonist, on glioma cells

(Submitter supplied) We performed micro array analysis in order to evaluate the effect of LXR623 on gene expression in glioma cancer cells (U87).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
2 Samples
Download data: CEL
Series
Accession:
GSE110152
ID:
200110152
19.

Effect of LXR623, liver X receptor agonist, on colon cancer cells

(Submitter supplied) We performed micro array analysis in order to evaluate the effect of LXR623 on gene expression in colon cancer cells (HCT116).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
2 Samples
Download data: CEL
Series
Accession:
GSE110151
ID:
200110151
20.

Expression data from stem like glioblastoma cells treated with vehicle, or BRD protein inhibitor, or HDAC inhibitor or the combination

(Submitter supplied) Inhibition of BRD proteins by OTX015, and inhibition of HDAC by Panobinostat and the combination alters the gene expression of the glioblastoma cells. To compare the drug effect and find out the resonal of the synergisty of the bombination, we performed microarray experiments.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
8 Samples
Download data: CEL
Series
Accession:
GSE108958
ID:
200108958
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