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Links from GEO DataSets

Items: 13

1.

Comparative analysis of ependymal cells from the lateral ventricular wall and the spinal cord of adult mice

(Submitter supplied) In contrast to ependymal cells in the lateral ventricle wall (LVW), spinal cord (SC) ependymal cells possess certain neural stem cell characteristics. Isolated CD133+/CD24+/CD45-/CD34- ependymal cells from the SC displayed in vitro self renewal and differentiation capacity, whereas those from the LVW did not. The molecular basis of this difference is unknown. In this study, antibodies against multiple surface markers were applied to isolate SC and LVW ependymal cells which allowed a direct comparison of their in vitro behavior and gene expression profile.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6105
12 Samples
Download data: TXT
Series
Accession:
GSE18528
ID:
200018528
2.

Single-cell transcriptome analyses reveal signals to activate dormant neural stem cells.

(Submitter supplied) Through single cell transcriptome analysis, we uncovered molecular signatures of CD133+/GFAP- ependymal (E) cells, CD133+/GFAP+ neural stem (B) cells, Dlx2+ neuroblasts (A cells), and Sox10+ oligodendrocyte progenitors (O cells) in the adult mouse forebrain neurogenic zone. prominent hub genes of the gene network unique to ependymal CD133+/GFAP- quiescent cells are enriched for receptors of angiogenic factors and immune-responsive genes. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL13112 GPL19179
32 Samples
Download data: TXT
Series
Accession:
GSE61288
ID:
200061288
3.

Single-Cell Transcriptomics and Fate Mapping of Ependymal Cells Reveals an Absence of Neural Stem Cell Function

(Submitter supplied) Ependymal cells are multi-ciliated cells that form the brain’s ventricular epithelium and a niche for neural stem cells (NSCs) in the ventricular-subventricular zone (V-SVZ). In addition, ependymal cells are suggested to be latent NSCs with a capacity to acquire neurogenic function. This remains highly controversial due to a lack of prospective in vivo labeling techniques that can effectively distinguish ependymal cells from neighboring V-SVZ NSCs. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
3 Samples
Download data: MTX, TSV
Series
Accession:
GSE100320
ID:
200100320
4.

Direct contact with mesenchymal stromal cells impacts CD133+ hematopoietic stem cells during ex-vivo expansion

(Submitter supplied) Direct contact with mesenchymal stromal impacts on migratory behavior and gene expression profile of CD133+ hematopoietic stem cells during ex-vivo expansion Objective: To investigate the impact of direct contact between mesenchymal stromal cells (MSCs) and CD133+ hematopoietic stem cells (HSCs) in terms of expansion potential differentiation, migratory capacity and gene expression profile. Methods: CD133+ purified HSCs were cultured for 7 days on subconfluent MSCs supplemented with growth factor containing medium. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
1 Sample
Download data: TXT
Series
Accession:
GSE13566
ID:
200013566
5.

Knockdown of CD133 in melanoma cells

(Submitter supplied) CD133 (Prominin-1) is considered the most important cancer stem cell (CSC)-associated marker identified so far, with increased expression in the CSC fraction of a large variety of human malignancies, including melanoma. Here we investigated the effects of CD133 down-regulation in vitro and in vivo in human metastatic melanoma. The average number of CD133 molecules on the cell surface of FEMX-I melanoma cells was decreased by 8.7-fold and 1.8-fold using two different short hairpin RNAs. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3489
Platform:
GPL7430
4 Samples
Download data: GPR
Series
Accession:
GSE13144
ID:
200013144
6.
Full record GDS3489

CD133 depletion effect on metastatic melanoma cell line

Analysis of metastatic melanoma FEMX-I cells depleted for CD133. CD133 is a cancer stem cell-associated antigen expressed in many malignancies such as melanoma. Results provide insight into the role of CD133 in cancer progression.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 protocol sets
Platform:
GPL7430
Series:
GSE13144
4 Samples
Download data: GPR
7.

Identification of genes enriched in putative stem/progenitor cells from mouse embryonic pancreas

(Submitter supplied) Identification of genes enriched in putative stem/progenitor cells (CD133highPDGFRb- cell population) from the mouse embryonic pancreas that are purified by fluorescence activated cell sorting (FACS). Success in islet transplantation-based therapies for type 1 diabetes mellitus and an extreme shortage of pancreatic islets has motivated efforts to develop renewable sources of islet-replacement tissue. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
1 Sample
Download data: TXT
Series
Accession:
GSE7800
ID:
200007800
8.

Expression data from ependymal layer of wild type and FoxJ1 null postnatal male mice

(Submitter supplied) FoxJ1 dependent gene expression is required for establishment of ependymal cells in the postnatal brain. This data set compares gene expression profiles of wildtype and FoxJ1 null microdissected dissected tissues at multiple postnatal time points. We used microarrays to detail the FoxJ1-dependent programme of gene expression underlying ependymal cell differentiation in the mouse brain.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
6 Samples
Download data: CEL, TXT
Series
Accession:
GSE18678
ID:
200018678
9.

High throughput analysis of the human and mouse spinal cord neural stem cell niche

(Submitter supplied) Anamniotes, rodents and man maintain a pool of adult neural stem cells around the central canal in the spinal cord representing an attractive cellular source for endogenous repair. Cell diversity and genes specific for this niche are still ill-defined in mammals. To identify genes specifically expressed in the niche, we microdissected (with laser) the central canal region and the adjacent tissue in human and mice adult tissues. more...
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL13158 GPL11180
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE118445
ID:
200118445
10.

Gene expression from induced CB-derived neurons at different time of differentiation

(Submitter supplied) Gene expression from cord blood stem cells and respective derived neuronal cells at different times point of differentiation:CD133+ cells; Keywords: Expression Profiling by array
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
13 Samples
Download data: CEL
Series
Accession:
GSE38431
ID:
200038431
11.

Single-cell RNA sequencing of spinal cord CD133+ DNGR-1 traced and CD133+ non-traced cells

(Submitter supplied) Using CD133 as a pan-ependymal cell marker, we wished to understand whether CD133+ DNGR-1 traced cells constituted a distinct subset of ependymal cells by comparing these at the single cell level with CD133+ non-traced cells purified from spinal cords of DNGR-1 lineage tracer mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
2 Samples
Download data: TXT
Series
Accession:
GSE202959
ID:
200202959
12.

Single-cell RNA sequencing analysis of non-haematopoietic DNGR-1 lineage traced cells from murine spinal cord

(Submitter supplied) Stem cells are defined by two cardinal properties: limitless self-renewal and multipotency. We have serendipitously found that non-haematopoietic DNGR-1 lineage traced cells residing in the ependymal cell layer of the central nervous system display the two cardinal properties of stem cells, both in vitro and in vivo. However, whether these properties were a feature of all DNGR-1-traced cells or were confined to a particular subset of these is unclear. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
1 Sample
Download data: TXT
Series
Accession:
GSE146226
ID:
200146226
13.

Bulk transcriptomic comparison between in vitro propagated DNGR-1-lineage traced cells and hippocampus derived neural stem cells

(Submitter supplied) We compared by bulk RNA sequencing the transcriptomic profile of in vitro cultured DNGR-1-traced neural stem cells or their differentiated astrocytic progeny with similar cell fates generated from bonafide neural stem cells derived from the hippocampus.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
18 Samples
Download data: TXT
Series
Accession:
GSE145824
ID:
200145824
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