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Links from GEO DataSets

Items: 20

1.
Full record GDS3613

Luteolin effect on pro-inflammatory challenged microglial cell line

Analysis of lipopolysaccharide-activated microglial BV-2 cells treated with luteolin, a plant derived flavonoid. Luteolin possesses the ability to scavenge oxygen and nitrogen species, and exhibits anti-inflammatory activities. Results provide insight into the immuno-modulatory effects of luteolin.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 agent sets
Platform:
GPL1261
Series:
GSE18740
12 Samples
Download data: CEL
2.

Luteolin has anti-inflammatory and neurotrophic effects on microglia

(Submitter supplied) Our aim was to identify genes that were differentially expressed in microglia stimulated with Lipopolysaccharide, Luteolin, or both. Affymetrix microarrays were used to analyze RNA samples
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3613
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE18740
ID:
200018740
3.

Minocycline counter regulates the global pro-inflammatory response in microglia and protects from retinal degeneration

(Submitter supplied) Minocycline is a potent modulator of retinal microglia
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15103
6 Samples
Download data: TXT
Series
Accession:
GSE71025
ID:
200071025
4.

Integrated expression profiles of mRNA and miRNA in polarized primary murine microglia

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
synthetic construct; Mus musculus
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL14613 GPL11078
18 Samples
Download data: CEL
Series
Accession:
GSE49331
ID:
200049331
5.

Integrated expression profiles of mRNA and miRNA in polarized primary murine microglia (miRNA)

(Submitter supplied) The aim of this study was to determine the role that miRNAs have on influencing murine microgial phenotypes under M1(LPS) and M2a (IL-4) stimulating conditions. This Series includes expression data obtained from miRNA gene expression microarrays; mRNA expression profiles obtained from the same RNA samples were deposited as a separate Series.
Organism:
synthetic construct; Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL14613
9 Samples
Download data: CEL
Series
Accession:
GSE49330
ID:
200049330
6.

Integrated expression profiles of mRNA and miRNA in polarized primary murine microglia (mRNA)

(Submitter supplied) The aim of this study was to determine the role that miRNAs have on influencing murine microgial phenotypes under M1(LPS) and M2a (IL-4) stimulating conditions. This Series includes expression data obtained from mRNA gene expression microarrays; miRNA expression profiles obtained from the same RNA samples were deposited as a separate Series.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11078
9 Samples
Download data: CEL
Series
Accession:
GSE49329
ID:
200049329
7.

Microarray and Pathway Analysis Reveal Distinct Mechanisms Underlying Cannabinoid-Mediated Modulation of LPS-Induced Activation of BV-2 Microglial Cells

(Submitter supplied) Cannabinoids are known to exert immunosuppressive activities. However, the mechanisms which contribute to these effects are unknown. Using lipopolysaccharide (LPS) to activate BV-2 microglial cells, we examined how Δ9-tetrahydrocannabinol (THC), the major psychoactive component of marijuana, and cannabidiol (CBD) the non-psychoactive component, modulate the inflammatory response.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7868
24 Samples
Download data: TXT
Series
Accession:
GSE70689
ID:
200070689
8.

Expression data from amoeboid and ramified microglia isolated from the corpus callosum of 5-day and 4-week old rat brain

(Submitter supplied) Microglia, the resident immune cells of the central nervous system (CNS), have two distinct phenotypes in the developing brain: amoeboid form, known to be amoeboid microglial cells (AMC) and ramified form, known to be ramified microglial cells (RMC) alongside several intermediate forms. The AMC are characterized by being proliferative, phagocytic and migratory whereas the RMC are quiescent and exhibit a slow turnover rate. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL1355
6 Samples
Download data: CEL, TXT
Series
Accession:
GSE29885
ID:
200029885
9.

IFN-gamma activation of cultured neonatal rat microglia

(Submitter supplied) IFN-gamma is a classical microglial stimulant. We used microarrays to investigate the microglial gene regulatory network activated by interferon-gamma. Keywords: Microglia activation
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL85
10 Samples
Download data: CEL
Series
Accession:
GSE6353
ID:
200006353
10.

The microglial transcriptome of age-associated deep subcortical white matter lesions suggests a neuroprotective response to blood-brain barrier dysfunction (microarray)

(Submitter supplied) Age-associated deep-subcortical white matter lesions (DSCL) are an independent risk factor for dementia, displaying high levels of CD68+ microglia. This study aimed to characterise the transcriptomic profile of microglia in DSCL and surrounding radiologically normal-appearing white matter (NAWM) compared to non-lesional control white matter. CD68+ microglia were isolated from white matter groups (n=4 cases per group) from the Cognitive Function and Ageing Study neuropathology cohort by immuno-laser capture microdissection. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL23159
12 Samples
Download data: CEL
Series
Accession:
GSE260815
ID:
200260815
11.

The microglial transcriptome of age-associated deep subcortical white matter lesions suggests a neuroprotective response to blood-brain barrier dysfunction

(Submitter supplied) Age-associated deep-subcortical white matter lesions (DSCL) are an independent risk factor for dementia, displaying high levels of CD68+ microglia. This study aimed to characterise the transcriptomic profile of microglia in DSCL and surrounding radiologically normal-appearing white matter (NAWM) compared to non-lesional control white matter. CD68+ microglia were isolated from white matter groups (n=4 cases per group) from the Cognitive Function and Ageing Study neuropathology cohort by immuno-laser capture microdissection. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: XLSX
Series
Accession:
GSE260619
ID:
200260619
12.

Global transcriptomic profiling of nitric oxide-mediated neuronal death

(Submitter supplied) Nitric oxide (NO) is implicated in the pathogenesis of various neuropathologies characterised by oxidative stress. NO has been reported to be involved in the exacerbation of oxidative stress by various mechanisms, including protein modification, genotoxic damage and elevated production of reactive oxygen species resulting in deregulation and disruption of cellular homeostasis. Although multiple roles for NO has been reported in neuronal death signaling, existent data fail to provide a holistic description of how nitrergic pathobiology elicits neuronal injury. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4408
Platform:
GPL1261
14 Samples
Download data: CEL
Series
Accession:
GSE22087
ID:
200022087
13.
Full record GDS4408

Nitric oxide generator DETA-NONOate effect on in vitro neuronal injury model: time course

Analysis of primary cortical neurons treated with nitric oxide (NO) generator DETA-NONOate for up to 24 hrs. High doses of NO, often observed in neurodegenerative disease pathogenesis, cause neuronal death. Results provide insight into molecular events contributing to NO-induced neuronal injury.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 4 time sets
Platform:
GPL1261
Series:
GSE22087
14 Samples
Download data: CEL
14.

LPS inflammation model and thalidomide effect using PBMC cells

(Submitter supplied) In this research, we use DNA microarray analysis to clarify the gene expression responses from thalidomide in PBMC cells after lipopolysaccharide (LPS) treatment.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13422
9 Samples
Download data: TXT
Series
Accession:
GSE28708
ID:
200028708
15.

Expression data from the Neural Stem Cells (NSCs) of LPS induced depression mice model treated with Luteolin

(Submitter supplied) Gene expression profiling reveals a potential role of Luteolin in LPS induced depression model LPS depression induced mice were orally treated with luteolin (10 mg/kg body weight) once per day during 8 consecutive days. Microarray gene expression was conducted for isolated mice Neural Stem Cells (NSCs) . Two mice brain were used for each expermient. The Microarray gene expression was conducted on NSCs and hipocampus from LPS depression induced depression mice (LPS group), LPS depression induced depression mice treated with luteolin(LPS+L group), Normal mice (PBS group) and Normal mice treated with luteolin (PBS+L).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
7 Samples
Download data: CEL, CHP, XLS
Series
Accession:
GSE181522
ID:
200181522
16.

Expression data from the hippocampus of LPS induced depression mice model treated with Luteolin

(Submitter supplied) Gene expression profiling reveals a potential role of Luteolin in LPS induced depression model LPS depression induced mice were orally treated with luteolin (10 mg/kg body weight) once per day during 8 consecutive days. Microarray gene expression was conducted on mice hippocampal tissues. Two mice brains were used for each expermient . The Microarray gene expression was conducted on hipocampus from LPS depression induced mice model(LPS group), LPS depression induced mice model treated with luteolin(LPS+L group), Normal mice (PBS group) and Normal mice treated with luteolin (PBS+L).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
16 Samples
Download data: CEL, CHP, XLSX
Series
Accession:
GSE181285
ID:
200181285
17.

Expression data from Luteolin-treated human Neural Stem Cells (hNSCs)

(Submitter supplied) Gene expression profiling reveals a potential role of Luteolin in human neuronal stem cells (hNSCs) differentiation . hNSCs purchased from Gibco were treated with 1 μM verbenalin for 24 hours. Microarray gene expression profiling was conducted for biological replicates of hNSCs cultured in differentiation cell culture medium supplemented with Luteolin for 24 hours and untreated control cells cultured in differentiation cell cultured medium .
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13667
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE148160
ID:
200148160
18.

Mesenchymal signature of post-pneumonectomy lung regeneration in adult mice

(Submitter supplied) The adult human lung has a very limited capacity to regenerate functional alveoli. In contrast, adult mice have a remarkable capacity for neoalveolarization following either lung resection or injury. The molecular basis for this unique capability to regenerate lung tissue in mice is largely unknown. We examined the transcriptomic responses to single lung pneumonectomy in adult mice in order to elucidate prospective molecular signaling used in this species during lung regeneration. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
8 Samples
Download data: CEL
Series
Accession:
GSE15999
ID:
200015999
19.

Early-life thermal stress mediates long-term alterations in hypothalamic microglia

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Gallus gallus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL26853 GPL27748
19 Samples
Download data
Series
Accession:
GSE189567
ID:
200189567
20.

Early-life thermal stress mediates long-term alterations in hypothalamic microglia [RNA-Seq]

(Submitter supplied) We identified the microglial population in the chick anterior hypothalamus (AH) and showed that early-life thermal stress (on day 3 post-hatch) influences the inflammatory process in the AH, altering microglial transcriptomic signature in response to LPS treatment (on day 10 post-hatch).
Organism:
Gallus gallus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26853
12 Samples
Download data: XLSX
Series
Accession:
GSE189566
ID:
200189566
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