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Links from GEO DataSets

Items: 7

1.
Full record GDS4842

SARM-deficient brain response to vesicular stomatitis virus infection

Analysis of brains from SARM-deficient animals infected with the vesicular stomatitis virus (VSV). SARM is a member of the Toll/IL-1R domain-containing adaptor family. VSV is used to study the response to neurotropic viral infections. Results provide insight into the role of SARM in innate immunity.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation, 2 infection sets
Platform:
GPL1261
Series:
GSE44331
12 Samples
Download data: CEL, CHP
2.

Expression data from C57BL/6J and C57BL6/J Sarm-deficient mice uninfected or infected with vesicular stomatitis virus (VSV)

(Submitter supplied) Sarm-deficient mice are protected from VSV encephalitis and death. Microarray was done to examine genes contributing to this phenotype
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4842
Platform:
GPL1261
12 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE44331
ID:
200044331
3.

RNAseq of C57BL/6J and C57BL6/J Sarm1-deficient mice to determine if genes surrounding the knockout locus are B6 or 129 sequence

(Submitter supplied) The Toll/IL-1R domain-containing adaptor protein SARM1 is expressed primarily in the brain, where it mediates axonal degeneration. Additional roles for SARM1 in a number of other processes including TLR-signaling, viral infection, chemokine expression, and XAF1 expression have also been described. Here we report defects in the induction of Ccl3, Ccl4, and Ccl5 in Sarm1-/- macrophages, for which we were unable to find mechanistic support. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: BAM, TXT
Series
Accession:
GSE136284
ID:
200136284
4.

Differential gene expression in the brainstem of uninfected and West Nile Virus infected C57BL6/J and Sarm1-em3AGS mice

(Submitter supplied) The Toll/IL-1R domain-containing adaptor protein SARM1 is expressed primarily in the brain, where it mediates axonal degeneration. Additional roles for SARM1 in a number of other processes including TLR-signaling, viral infection, chemokine expression, and XAF1 expression have also been described. Here we report defects in the induction of Ccl3, Ccl4, and Ccl5 in Sarm1-/- macrophages, for which we were unable to find mechanistic support. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
48 Samples
Download data: TXT
Series
Accession:
GSE136221
ID:
200136221
5.

Next Generation Sequencing Facilitates Quantitative Analysis of peritoneal macrophages Transcriptomes of Dnmt3a macrophage conditional knockout mouse

(Submitter supplied) Purpose:The purpose of this study is to measure the gene expression profile in Dnmt3a conditional knockout macrophages. Methods:Dnmt3a conditional knockout macrophages mRNA profiles were generated by deep sequencing,using Illumina. Results: We mapped about 20 million sequence reads per sample to the mouse genome, identified hundreds of genes with significant mRNA variation during Dnmt3a conditional knockout in macrophages.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: TXT
Series
Accession:
GSE74750
ID:
200074750
6.

Microarray analysis of gene expression in Dnmt3a-knockdown macrophages.

(Submitter supplied) To measure the gene expression profile in Dnmt3a-knockdown macrophages
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
2 Samples
Download data: TXT
Series
Accession:
GSE70631
ID:
200070631
7.

Next Generation Sequencing Facilitates Quantitative Analysis of dendritic cell Transcriptomes during LPS response

(Submitter supplied) Purpose:The purpose of this study is to detect activated or silenced genes during LPS-induced dendritic cell. Gene expression differences between two samples could be found using transcriptome profiling (RNA-seq) analysis. Methods:Mouse dendritic cells were generated from bone marrow cells in RPMI-1640 medium with recombinant mouse GM-CSF and IL-4, immature DCs were obtained before or after LPS stimulation. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: TXT
Series
Accession:
GSE69256
ID:
200069256
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Supplemental Content

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