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Links from GEO DataSets

Items: 20

1.

MicroRNA profiling of demyelination and remyelination areas in corpus callosum of cuprizone-treated mice

(Submitter supplied) Mouse cuprizone (CPZ ) model of experimental de- and remyelination was applied to mimic demyelination pathology of multiple sclerosis. In order to identify differentially expressed microRNAs involved in de- and remyelination, the affected areas of corpus callosum were isolated from mice exposed to CPZ and conducted an Agilent microarray analysis. To induce demyelination, CPZ was administrated for four weeks. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL8824
14 Samples
Download data: TXT
Series
Accession:
GSE100662
ID:
200100662
2.

Loss of miR-145 promotes remyelination and functional recovery in a model of chronic centrel demyelination

(Submitter supplied) Strategies for treating progressive multiple sclerosis (MS) remain limited. Here, we found that miR-145-5p is overabundant uniquely in chronic lesion tissues from secondary progressive MS patients. We induced both acute and chronic demyelination in miR-145 knockout mice to determine its contributions to remyelination failure. Following acute demyelination, no advantage to miR-145 loss could be detected. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20084
10 Samples
Download data: TXT
Series
Accession:
GSE268808
ID:
200268808
3.

Gene expression profiles from corpus callosum brain tissue obtained from cuprizone-treated mice

(Submitter supplied) Mouse cuprizone (CPZ ) model of experimental de- and remyelination was applied to mimic demyelination pathology of multiple sclerosis. The aim of the study was to profile whole genome expression to identify differentially expressed genes during the demyelinisation and after discontinuation of cuprizon treatment, during rapid remyelinisation in affected areas of mouse corpus callosum. Control mice were kept on a normal diet. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
16 Samples
Download data: TXT
Series
Accession:
GSE100663
ID:
200100663
4.

MicroRNA expression in the cuprizone-induced demyelination mouse model

(Submitter supplied) Myelin abnormalities, oligodendrocyte damage, and concomitant glia activation are common in demyelinating diseases of the central nervous system (CNS). The neurotoxicant cuprizone (CPZ) has been extensively used to create a mouse model of demyelination. However, the changes of miRNA expression and effects on behavior of cuprizone treatment have not been clearly reported. We have analyzed the behavioral changes of mice given a diet containing 0.2% cuprizone for 6 weeks. more...
Organism:
synthetic construct; Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL21572
2 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE122839
ID:
200122839
5.

Gene expression analysis after miR-125a-3p over-expression in oligodendrocyte precursor cells (OPCs)

(Submitter supplied) MiR-125a-3p over-expression in OPCs impairs their differentiation into fully mature oligodendrocytes. We performed a whole microarray profiling to identify new miR-125a-3p direct targets and altered signaling pathways responsible for its the detrimental effect on oligodendrocyte maturation.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL22740
4 Samples
Download data: TXT
Series
Accession:
GSE143876
ID:
200143876
6.

Bulk RNAseq of AnnexinV+ and AnnexinV- cells from the Mertk-KO corpus callosum at the 4 week cuprizone timepoint

(Submitter supplied) Purpose: Following 4 weeks of 0.2% cuprizone treatment, Mertk-KO mice accumulate dying cells in the corpus callosum (based on cleaved-cas3 staining). These cells are not seen in Mertk-WT animals at the same cuprizone timepoint. The goal of this study is to identify these dying cells in the Mertk-KO corpus callosum Methods: 2 biological replicates (mice) were used. Corpus callosa were dissected from Mertk-KO mice after 4 weeks of 0.2% cuprizone treatment. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: TXT
Series
Accession:
GSE148677
ID:
200148677
7.

scRNAseq of Mertk-WT and Mertk-KO corpus callosum

(Submitter supplied) Purpose: The goal of this study is to characterize the the different CNS cell types in the mouse corpus callosum over three different cuprizone treatment timepoints - (Baseline, 4 weeks, 4 weeks + 3 weeks of recovery) and compare the Mertk-WT vs Mertk-KO response to demyelination. Methods: 3-4 biological replicates (mice) were used for each timepoint/genotype. Tissues were dissociated into single cells for preparation of 10X libraries and sequenced with HiSeq 2500 (Illumina). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
20 Samples
Download data: TXT
Series
Accession:
GSE148676
ID:
200148676
8.

Human brain tissues from healthy controls and multiple sclerosis patients

(Submitter supplied) Multiple sclerosis (MS) is characterized by cell proliferation, migration and damage in various cell types in different CNS regions and causes disabilities related to distinct neurological pathways, such as walking, vision and cognition. Here, region-specific transcriptomic approach was used to determine changes in gene expression in five different CNS regions (hippocampus, frontal cortex, internal capsule, corpus callosum, and parietal cortex) in MS.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21290
50 Samples
Download data: CSV
9.

Gene expression in oligodendrocytes during remyelination reveals cholesterol homeostasis as a therapeutic target in multiple sclerosis.

(Submitter supplied) Regional differences in neurons, astrocytes, oligodendrocytes, and microglia exist in the brain during health, and regional differences in the transcriptome may occur for each cell type during neurodegeneration. Multiple sclerosis (MS) is multifocal, and regional differences in the astrocyte transcriptome occur in experimental autoimmune encephalomyelitis (EAE), an MS model. MS and EAE are characterized by inflammation, demyelination, and axonal damage, with minimal remyelination. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21493
6 Samples
Download data: TXT
Series
Accession:
GSE118451
ID:
200118451
10.

Gene expression profile in the cuprizone-induced demyelination mouse model

(Submitter supplied) Myelin abnormalities, oligodendrocyte damage, and concomitant glia activation are common in demyelinating diseases of the central nervous system (CNS). The neurotoxicant cuprizone (CPZ) has been extensively used to create a mouse model of demyelination. However, the changes of miRNA expression and effects on behavior of cuprizone treatment have not been clearly reported. We have analyzed the behavioral changes of mice given a diet containing 0.2% cuprizone for 6 weeks. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
2 Samples
Download data: CEL, CHP, XLSX
Series
Accession:
GSE129049
ID:
200129049
11.

Spinal cord gene expression profiling of the effect of EHP-101 in EAE model

(Submitter supplied) Spinal cord gene expression profiling of the effect of EHP-101 in EAE model
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
9 Samples
Download data: TXT
Series
Accession:
GSE131854
ID:
200131854
12.

ChIP-sequencing of PRMT1 proficient and deficient microglia

(Submitter supplied) ChIP_sequencing analysis defined a novel role for the PRMT1 in microglia during normal and 0.2% cuprizone diet 5weeks We then performed ChIP analysis using data obtained from ChIP-seq of microglia at two time points
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21103
19 Samples
Download data: XLSX
Series
Accession:
GSE205309
ID:
200205309
13.

RNA-sequencing of PRMT1 proficient and deficient microglia

(Submitter supplied) RNA_sequencing analysis defined a novel role for the PRMT1 in microglia during normal and 0.2% cuprizone diet 5weeks We then performed gene expression profiling analysis using data obtained from RNA-seq of 4 different cells at two time points.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
8 Samples
Download data: XLSX
Series
Accession:
GSE201145
ID:
200201145
14.

scRNAseq from WT and PRMT1-KO microglia

(Submitter supplied) scRNAseq of WT and PRMT1-KO microglia during CPZ diet 5 weeks
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
4 Samples
Download data: MTX, TSV
Series
Accession:
GSE199574
ID:
200199574
15.

Comparative analysis of gene expression profile of pre-defined niches within demyelinated white matter in rats

(Submitter supplied) Microenviromental niche characterization by comparative transcriptome profiling. The hypothesis tested in the present study was that unique properties of the perivascular niche within remyelinating white matter would create microenvironment that favor the alternative differentiation of oligodendrocyte precursor cells.
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL6101
24 Samples
Download data: TXT
Series
Accession:
GSE93645
ID:
200093645
16.

Transcriptomic atlas and interaction networks of brain cells in mouse CNS demyelination and remyelination

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
26 Samples
Download data: H5
Series
Accession:
GSE204770
ID:
200204770
17.

Transcriptomic atlas and interaction networks of brain cells in mouse CNS demyelination and remyelination [Trem2KO]

(Submitter supplied) Demyelination is a hallmark of multiple sclerosis, leukoencephalopathies, cerebral vasculopathies and several neurodegenerative diseases. The cuprizone mouse model is widely used to simulate demyelination occurring in these diseases. Here, we present a high-resolution snRNA-seq analysis of gene expression changes across all brain cells in this model. We define signatures of prototypic responses to demyelination and remyelination for each cell type, including anti-stress, anti-oxidant-, metabolic-, hypoxia-, IFN-, and IL-33-driven responses, and validate them at the protein level and in IL-33R-deficient mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
18 Samples
Download data: H5, TSV
Series
Accession:
GSE204769
ID:
200204769
18.

Transcriptomic atlas and interaction networks of brain cells in mouse CNS demyelination and remyelination [B6]

(Submitter supplied) Demyelination is a hallmark of multiple sclerosis, leukoencephalopathies, cerebral vasculopathies and several neurodegenerative diseases. The cuprizone mouse model is widely used to simulate demyelination occurring in these diseases. Here, we present a high-resolution snRNA-seq analysis of gene expression changes across all brain cells in this model. We define signatures of prototypic responses to demyelination and remyelination for each cell type, including anti-stress, anti-oxidant-, metabolic-, hypoxia-, IFN-, and IL-33-driven responses, and validate them at the protein level and in IL-33R-deficient mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data: H5, TSV
Series
Accession:
GSE204755
ID:
200204755
19.

Oligodendrocyte intrinsic miR-27a controls myelination and remyelination

(Submitter supplied) The goal of this study was to understand miR-27a gene regulation in mouse OPCs
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: CSV
Series
Accession:
GSE135308
ID:
200135308
20.

Temporal transcriptomic profiles of brain regions following acute and chronic demyelinating injury

(Submitter supplied) Purpose: The central nervous system (CNS) possesses intrinsic remyelination capabilities in response to demyelinating injury. However, this remyelination potential is diminished as demyelinating disease such as multiple sclerosis progresses overtime. To better understand myelin repair processes, the goal of this study was to determine temporal transcriptomic changes in cerebral white matter (corpus callosum) and gray matter (cortex and hippocampus) after acute and chronic demyelinating injury. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL17021 GPL24247
47 Samples
Download data: XLSX
Series
Accession:
GSE212147
ID:
200212147
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