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Links from GEO DataSets

Items: 20

1.

Expression profiles of mouse glioma-initiating cells.

(Submitter supplied) To identify factors involved in glioma-initiating cells (GICs), we compared gene expressions between GIC-like cells and non-GICs.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE28091
ID:
200028091
2.

Expression profiles of mouse glioma-initiating cell-like subclones

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
8 Samples
Download data: CEL
Series
Accession:
GSE17101
ID:
200017101
3.

Expression profiling of sox11-expressing glioma-initiating cell-like cells

(Submitter supplied) To identify factors involved in tumorigenicity of glioma-initiating cells (GICs), we compared gene expression in GIC-like cells with and without sox11 expression.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE17076
ID:
200017076
4.

Expression profiling of mouse glioma-initiating cell-like cells (GICs) and non-GICs

(Submitter supplied) To identify factors involved in glioma-initiating cells (GICs), we compared gene expression between GIC-like cells and non-GICs.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE17062
ID:
200017062
5.

Microarray analysis of differentiation of human glioblastoma stem cells

(Submitter supplied) Glioblastoma multiforme is one of the most devastating cancers and presents unique challenges to therapy due to its aggressive behaviour. Cancer stem cells have been described to be the only cell population with tumorogenic capacity in glioblastoma. Therefore, effective therapeutic strategies targeting these cells may be beneficial. We have established different cultures of glioblastoma stem cells (GSCs) derived from surgical specimens and found that, after induction of differentiation, NFκB was activated, which allows intermediate tumor precursor cells to remain cycling. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4535
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE20736
ID:
200020736
6.
Full record GDS4535

Differentiating glioblastoma-initiating cells

Analysis of cultures of progenitor and 4-day differentiated glioblastoma cells (GICs) derived from surgical specimens. Following induction of differentiation, NFκB is activated in GICs. Results provide insight into molecular mechanisms underlying the control of differentiation of GICs.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 cell type, 3 specimen sets
Platform:
GPL570
Series:
GSE20736
6 Samples
Download data: CEL
DataSet
Accession:
GDS4535
ID:
4535
7.

Transformation of quiescent adult oligodendrocyte precursor cells into malignant glioma through a multi-step reactivation process

(Submitter supplied) How malignant gliomas arise in a mature brain remains a mystery, hindering the development of preventive and therapeutic interventions. We previously showed that oligodendrocyte precursor cells (OPCs) can be transformed into glioma when mutations are introduced perinatally. However, adult OPCs rarely proliferate compared to their perinatal counterparts. Whether these relatively quiescent cells have the potential to transform is unknown, which is a critical question considering the late onset of human glioma. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19163
14 Samples
Download data: GPR
Series
Accession:
GSE61282
ID:
200061282
8.

Mosaic Analysis with Double Markers Reveals Tumor Cell of Origin in Glioma

(Submitter supplied) Cancer results from molecular mutations occurring in specific cell types, thus determining the cell-of-origin is critical for effective cancer treatment. Inferring such information from terminal tumors can be misleading because malignant tumor cells tend to acquire aberrant properties. Animal models are widely used because one can initiate mutations in specific cell types. However, cell-of-mutation that harbors initial molecular changes may not directly transform, rather merely passes along mutations to its progeny cell lineage, which then serves as cell-of-origin and finally transforms into malignancy. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11531
11 Samples
Download data: GPR
Series
Accession:
GSE26676
ID:
200026676
9.

Gene expression profiling of human gliomas and human glioblastoma cell lines

(Submitter supplied) To identify signaling pathways that are differentially regulated in human gliomas, a microarray analysis on 30 brain tumor samples (12 primary glioblastomas (GBM), 3 secondary glioblastomas (GBM-2), 8 astrocytomas (Astro) and 7 oligodendrogliomas (Oligo)) and on 5 glioblastoma cell lines (LN018, LN215, LN229, LN319 and BS149) was performed. Normal brain tissue (NB) and normal human astrocytes (NHA) were used as a control. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS4467 GDS4468
Platform:
GPL570
45 Samples
Download data: CEL
Series
Accession:
GSE15824
ID:
200015824
10.
Full record GDS4468

Glioblastoma cell lines: LN018, LN215, LN229, LN319 and BS149

Analysis of 5 glioblastoma cell lines (LN018, LN215, LN229, LN319 and BS149). Results provide insight into molecular mechanisms underlying glioblastoma multiforme and other aggressive brain cancers.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 5 cell line sets
Platform:
GPL570
Series:
GSE15824
10 Samples
Download data: CEL
DataSet
Accession:
GDS4468
ID:
4468
11.
Full record GDS4467

Primary and secondary brain tumors: glioblastomas, astrocytomas and oligodendrogliomas

Analysis of primary glioblastomas (GBM), astrocytomas, oligodendrogliomas and secondary GBM brain tumors. MNK1 kinase upregulation observed in primary GBM brain tumors. Results identifiy signaling pathways differentially regulated in gliomas.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 5 cell type, 8 other, 3 tissue sets
Platform:
GPL570
Series:
GSE15824
35 Samples
Download data: CEL
DataSet
Accession:
GDS4467
ID:
4467
12.

Targeting PBK/TOPK decreases growth and survival of glioblastoma stem cells in vitro and attenuates tumor growth in vivo

(Submitter supplied) Gene knockdown of PBK led to decreased proliferation and sphere formation in the GSC cultures. Treatment of cells with different concentrations of HI-TOPK-032 almost completely abolished growth and proliferation and elicited a large increase in apoptosis
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
36 Samples
Download data: TXT
Series
Accession:
GSE53800
ID:
200053800
13.

Comparison study of glioma stem cells and adult human neural stem cells

(Submitter supplied) Glioblastoma, the most common and malignant brain tumor, harbors stem-like cells that self-renew and propagate upon serial transplantation. Although they share functional, morphological and developmental similarities to adult brain neural stem cells, stem cell characteristic pathways contributing to glioblastoma stem-like cells have not been consistently determined. Towards this goal we have provided an internally coherent molecular reference that compares adult neural and glioblastoma stem cells cultivated under identical conditions. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL2986
14 Samples
Download data: TXT
Series
Accession:
GSE31262
ID:
200031262
14.

Candidate pathways for promoting differentiation and quiescence of oligodendrocyte progenitor-like cells in glioblastoma

(Submitter supplied) The mature CNS contains PDGFRA+ ‘oligodendrocyte progenitor cells’ (OPC) which may remain quiescent, proliferate, or differentiate into oligodendrocytes. In human gliomas, rapidly proliferating Olig2+ cells resembling OPCs are frequently observed. We sought to identify, in vivo, candidate pathways uniquely required for OPC differentiation or quiescence. Using the bacTRAP methodology, we generated and analyzed mouse lines for translational profiling the major cells types (including OPCs), in the normal mouse brain. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL9746
38 Samples
Download data: CEL
Series
Accession:
GSE30626
ID:
200030626
15.

Olig1/2-expressing intermediate lineage progenitors are predisposed to PTEN/p53-loss-induced gliomagenesis and harbor specific therapeutic vulnerabilities

(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; Other
4 related Platforms
30 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE200892
ID:
200200892
16.

Transit-amplifying lineage states convey the susceptibility of PTEN and P53 loss to gliomagenesis [CUT&RUN]

(Submitter supplied) To investigate the glioma mouse model by knocking out Pten and Trp53 in embryonal Olig2 and Olig1 positive cells in glioma pathogenesis. Chromatin immunoprecipitation DNA-sequencing (ChIP-seq) for H3K27Ac in PPO1 and PPO2 mouse glioma cell lines and compare the active enhancers with oligodendrocyte progenitor cells.
Organism:
Mus musculus
Type:
Other
Platform:
GPL24247
4 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE200891
ID:
200200891
17.

Transit-amplifying lineage states convey the susceptibility of PTEN and P53 loss to gliomagenesis [ATAC-seq]

(Submitter supplied) To investigate the glioma mouse model by knocking out Pten and Trp53 in embryonal Olig2 and Olig1 positive cells in glioma pathogenesis. ATAC-seq
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE200890
ID:
200200890
18.

Transit-amplifying lineage states convey the susceptibility of PTEN and P53 loss to gliomagenesis [PPO1_and PPO1_Cells_RNA-seq]

(Submitter supplied) To investigate the glioma mouse model by knocking out Pten and Trp53 in embryonal Olig2 and Olig1 positive cells in glioma pathogenesis. We then performed gene expression profiling analysis using data obtained from RNA-seq of 4 PPO2, 4 PPO1 and 2 OPN cell lines.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
10 Samples
Download data: TXT
Series
Accession:
GSE200889
ID:
200200889
19.

Transit-amplifying lineage states convey the susceptibility of PTEN and P53 loss to gliomagenesis [PPO2_Bulk_RNA-seq]

(Submitter supplied) To investigate the glioma mouse model by knocking out Pten and Trp53 in embryonal Olig2 positive cells in glioma pathogenesis. We then performed gene expression profiling analysis using data obtained from RNA-seq of 4 PPO2 tumor tissue with 2 Control cortex tissue.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
6 Samples
Download data: TXT
Series
Accession:
GSE200888
ID:
200200888
20.

Transit-amplifying lineage states convey the susceptibility of PTEN and P53 loss to gliomagenesis [PPO1_Bulk_RNA-seq]

(Submitter supplied) To investigate the glioma mouse model by knocking out Pten and Trp53 in embryonal Olig1 positive cells in glioma pathogenesis and track its evolution over multiple time-points. We then performed gene expression profiling analysis using data obtained from RNA-seq of 5 PPO1 tumor tissue with 3 Control cortex tissue.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: TXT
Series
Accession:
GSE200887
ID:
200200887
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