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Links from GEO DataSets

Items: 7

1.
Full record GDS5356

RAW264.7 macrophage cell line response to murine norovirus infection

Analysis of RAW264.7 macrophage cells infected with murine norovirus (MNV-1). MNV-1 is used a model for human norovirus infection. Results provide insight into the molecular nature of the immune response to norovirus infection.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 infection sets
Platform:
GPL1261
Series:
GSE50093
4 Samples
Download data: CEL
DataSet
Accession:
GDS5356
ID:
5356
2.

Characterization of the chemokine response of RAW264.7 cells to infection by murine norovirus

(Submitter supplied) RAW264.7 macrophages infected with MNV-1 and mock infected gene expression measured by microarray. To be published in Waugh, E. Chen, A. Baird, M. Fleming, S. Brown, C.M. and V K. Ward (2014) Characterization of the chemokine response of RAW264.7 cells to infection by murine norovirus. Virus Genes
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5356
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE50093
ID:
200050093
3.

Differential expression profile between MNV-1 infected and mock-infected RAW 264.7 cells.

(Submitter supplied) Noroviruses have been widely recognized for their importance as causative agents of non-bacterial gastroenteritis. Mouse norovirus is the only representative of the norovirus genus, family Caliciviridae, able to grow in cell culture. The aim of this study is to describe the differences in the expression profiles of MNV-1 and mock-infected macrophages (RAW 264.7 cells), in order to better understand the response of the host cell to norovirus infection. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3549
Platform:
GPL1261
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE12518
ID:
200012518
4.
Full record GDS3549

Norovirus infection effect on macrophage cell line

Analysis of macrophage RAW264.7 cells infected with murine norovirus type 1. Noroviruses cause non-bacterial gastroenteritis in humans. Results provide insight into the molecular pathogenesis of norovirus infections.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 infection sets
Platform:
GPL1261
Series:
GSE12518
6 Samples
Download data: CEL, CHP
5.

Murine Norovirus Effect on Cells

(Submitter supplied) Changes in gene expression on MNV infection of RAW264.7 cells
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
4 Samples
Download data: CEL
Series
Accession:
GSE61562
ID:
200061562
6.

RNA-sequencing of murine norovirus (MNV) infection and loxoribine (Lox) stimulation in RAW264.7 macrophages

(Submitter supplied) This study aimed to generate a comprehensive analysis of changes in the transcriptome following MNV infection. Furthermore, we aimed to perform a differential gene expression analysis between MNV infection and loxoribine (tlr7 agonist) treatment to delineate features of the host modified directly by the MNV as opposed to indirect changes induced through IFN signalling.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
12 Samples
Download data: TXT
Series
Accession:
GSE94843
ID:
200094843
7.

RNA-sequencing of longitudinal murine norovirus (MNV) infection in RAW264.7 mouse macrophages

(Submitter supplied) The transcriptome has an abundance of information about the function of individual cells, tissues and an organism in general. Characterising the transcriptome of virus infected cells can illuminate features of the viral-host relationship that are important for pathogenesis. This study broadly aimed to quantify the host gene expression changes that occur following MNV infection. Furthermore, we aimed to identify alterations in specific biological pathways by identifying alterations in transcript abundance that increase or decrease in intensity with MNV infection over time.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
6 Samples
Download data: TXT
Series
Accession:
GSE94821
ID:
200094821
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