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Links from GEO DataSets

Items: 7

1.

TRANSCRIPTOMIC PROFILING OF ASTROCYTES TREATED WITH THE RHO KINASE INHIBITOR FASUDIL REVEALS CYTOSKELETAL AND PRO-SURVIVAL RESPONSESTRANSFORMATION INDUCED BY THE RHO KINASE INHIBITOR FASUDIL.

(Submitter supplied) Analysis of genome wide gene expression changes over a time course of 24 hours induced by the Rho kinase inhibitor Fasudil in primary mouse astrocyte cultures.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3944
Platform:
GPL6885
32 Samples
Download data: TXT
Series
Accession:
GSE25829
ID:
200025829
2.
Full record GDS3944

Rho kinase inhibitor fasudil effect on forebrain astrocyte culture: time course

Analysis of astrocytes treated with Rho kinase (ROCK) inhibitor fasudil for up to 24 hrs. ROCK inhibitors inhibit glial scarring, a reactive process involving astrogliosis that occurs after injury to CNS. Results provide mechanistic insights into beneficial action of fasudil during brain injury.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 4 time sets
Platform:
GPL6885
Series:
GSE25829
32 Samples
Download data
DataSet
Accession:
GDS3944
ID:
3944
3.

Transcriptional profiling of the cellular transformation induced by Rho subfamily GTPases

(Submitter supplied) We have used microarray technology to identify the transcriptional targets of Rho subfamily GTPases. This analysis indicated that murine fibroblasts transformed by these proteins show similar transcriptomal profiles. Functional annotation of the regulated genes indicate that Rho subfamily GTPases target a wide spectrum of biological functions, although loci encoding proteins linked to proliferation and DNA synthesis/transcription are up-regulated preferentially. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL81
37 Samples
Download data: CEL, EXP
Series
Accession:
GSE5913
ID:
200005913
4.

RNAi profiling of primary human AML cells identifies ROCK1 as a therapeutic target and nominates Fasudil as an anti-leukemic drug.

(Submitter supplied) Acute myeloid leukemia (AML) is characterized by a marked genetic heterogeneity, which complicates the development of novel therapeutics. The delineation of pathways essential within the patient-individual mutational background might overcome this limitation and facilitate personalized treatment. We report the results of a large-scale lentiviral loss-offunction RNA-interference-(RNAi)-screen in primary leukemic cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome variation profiling by high throughput sequencing; Other
Platform:
GPL11154
10 Samples
Download data: TXT, VCF
Series
Accession:
GSE68925
ID:
200068925
5.

Single cell transcriptome profiling of the human alcohol-dependent brain samples.

(Submitter supplied) Over 16,000 nuclei were isolated from human postmartum brain frozen prefrontal cortex samples of alcoholic and control individuals. Libraries were prepared with 10X Genomics platform and sequenced using NovaSeq 6000.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
8 Samples
Download data: MTX, TSV
Series
Accession:
GSE141552
ID:
200141552
6.

Transcriptome analysis of oxdative-stress induced senescence in human astrocytes

(Submitter supplied) Purpose: Cellular senescence is a cell stress response resulting in permanent growth arrest and the production of an altered pro-inflammatory secretory profile known as the senescecnce-associated secretory phenotype (SASP). The induction of senescence in astrocytes, a cell type responsible for maintaining homeostasis within the central nervous system (CNS) and responding to CNS insults, has been implicated in neurodegenerative disease. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: CSV
7.

Conservation and divergence of vulnerability and responses to stressors between human and mouse astrocytes

(Submitter supplied) Astrocytes were purified from mouse cortices and human cortex tissue by immunopanning with HepaCAM. All treatments were proceeded on 3DIV in serum-free medium. Astrocytes were treated by TNFα for 48hr, by Poly I:C for 72hr, or by hypoxia for 72hr. Acutely purified atrocytes RNA was harvest immediately after HepaCAM immunopanning. Serum selected astrocytes RNA was collected after 4-6 days culturing in serum medium. more...
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by high throughput sequencing
4 related Platforms
77 Samples
Download data: XLSX
Series
Accession:
GSE147870
ID:
200147870
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