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Links from GEO DataSets

Items: 14

1.

SHAE004: SARS-CoV, SARS-dORF6 and SARS-BatSRBD infection of HAE cultures.

(Submitter supplied) HAE cultures were infected with SARS-CoV, SARS-dORF6 or SARS-BatSRBD and were directly compared to A/CA/04/2009 H1N1 influenza-infected cultures. Cell samples were collected at various hours post-infection for analysis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
134 Samples
Download data: TXT
Series
Accession:
GSE47962
ID:
200047962
2.

SARS-CoV, SARS-dORF6 and SARS-BatSRBD infection of HAE cultures.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
438 Samples
Download data: TXT
Series
Accession:
GSE47963
ID:
200047963
3.

SHAE003: SARS-CoV, SARS-dORF6 and SARS-BatSRBD infection of HAE cultures.

(Submitter supplied) HAE cultures were infected with SARS-CoV, SARS-ddORF6 or SARS-BatSRBD and were directly compared to A/CA/04/2009 H1N1 influenza-infected cultures. Cell samples were collected at various hours post-infection for analysis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
141 Samples
Download data: TXT
Series
Accession:
GSE47961
ID:
200047961
4.

SHAE002: SARS-CoV, SARS-dORF6 and SARS-BatSRBD infection of HAE cultures.

(Submitter supplied) HAE cultures were infected with SARS-CoV, SARS-dORF6 or SARS-BatSRBD and were directly compared to A/CA/04/2009 H1N1 influenza-infected cultures. Cell samples were collected at various hours post-infection for analysis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
163 Samples
Download data: TXT
Series
Accession:
GSE47960
ID:
200047960
5.

SM001: SARS CoV MA15 infection of C57Bl/6 mouse model – Data from 4 viral doses at 1, 2, 4 and 7 days post infection.

(Submitter supplied) Purpose of experiment was to perform transcriptomic analysis on C57Bl/6 mice infected with different doses of SARS CoV MA15 at 4 different days post infection.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
92 Samples
Download data: TXT
Series
Accession:
GSE33266
ID:
200033266
6.

Cell host-response to infection with novel human coronavirus EMC predict potential antivirals and important differences with SARS-coronavirus.

(Submitter supplied) Differential expression was determined in Calu-3 cells between mock infected and infection with either Human coronavirus EMC and SARS coronavirus at different times post infection.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
32 Samples
Download data: TXT
Series
Accession:
GSE45042
ID:
200045042
7.

Host response in the lung to influenza infection with PR8, VN or X31 strains at 12, 16 and 24 hours

(Submitter supplied) Array analysis of total lung RNA obtained from mice 12,16,24 h post infection with influenza. Strains used were Mock, PR8, X31, VN62 (1x10^5pfu)
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
30 Samples
Download data: TXT
Series
Accession:
GSE42285
ID:
200042285
8.

Integrative deep sequencing of the mouse lung transcriptome reveals differential expression of diverse classes of small RNAs in response to respiratory virus infection.

(Submitter supplied) We previously reported widespread differential expression of long non-protein-coding RNAs (ncRNAs) in response to virus infection. Here, we expanded the study through small RNA transcriptome sequencing analysis of the host response to both severe acute respiratory syndrome coronavirus (SARS-CoV) and influenza virus infections across four founder mouse strains of the Collaborative Cross, a recombinant inbred mouse resource for mapping complex traits. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL11002
20 Samples
Download data: TXT
Series
Accession:
GSE36971
ID:
200036971
9.

Host responses contributing to the attenuation of severe acute respiratory syndrome coronaviruses missing E protein domains

(Submitter supplied) Severe acute respiratory syndrome coronavirus (SARS-CoV) causes a respiratory disease leading to death in 10% of the infected people. A mouse adapted SARS-CoV lacking the envelope (E) protein (rSARS-CoV-MA15-ΔE) is attenuated in vivo. To identify E protein domains and host responses that contribute to rSARS-CoV-MA15-ΔE attenuation, several mutants (rSARS-CoV-MA15-E*) containing point mutations or deletions in the amino-terminal or the carboxy-terminal regions of E protein, respectively, were generated. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
15 Samples
Download data: TXT
Series
Accession:
GSE59185
ID:
200059185
10.

Expression data from well-differentiated human bronchial epithelial cells infected with H1N1 Influenza isolates

(Submitter supplied) We used microarrays to compare the gene expression profiles of different H1N1 isolates (seasonal and pandemic) in lung epithelial cells in vitro.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4855
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE48466
ID:
200048466
11.
Full record GDS4855

Pandemic and seasonal H1N1 influenza virus infections of bronchial epithelial cells in vitro

Analysis of well-differentiated primary lung bronchial epithelial cells 36 hs after infection with various H1N1 influenza isolates: seasonal H1N1 BN/59, pandemic H1N1 KY/136 and KY/180. Results provide insight into the molecular basis of host responses to different H1N1 Influenza isolates.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 4 infection sets
Platform:
GPL570
Series:
GSE48466
12 Samples
Download data: CEL
12.

Transcriptome analysis of influenza infected GFP+ AEC compared to bystander GFP- AEC

(Submitter supplied) A GFP-expressing recombinant A/Puerto Rico/8/1934 influenza virus was used to infect C57BL/6 wild type mice and on day 3 post infection, lung alveolar epithelial cells (AEC) were isolated and sorted based on GFP expression. GFP+ AEC represent the infected AEC and GFP- AEC represent the bystander AEC. AEC were also sorted from uninfected mice to serve as controls.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
13 Samples
Download data: TXT
Series
Accession:
GSE119123
ID:
200119123
13.

The 1918 PB2 protein, not HA, enhances the virulence of an avian influenza virus closely related to the 1918 pandemic virus through the inhibition of wnt signaling.

(Submitter supplied) The purpose of this experiment was to understand the pathogenic role of individual 1918 genes on the host response to the 1918 pandemic influenza virus. We examined reassortant avian viruses nearly identical to the pandemic 1918 virus (1918-like avian virus) carrying either the 1918 HA or PB2 gene. Both genes enhanced 1918-like avian virus replication, but only the mammalian host adaptation of the 1918-like avian virus through reassortment of the 1918 PB2 led to increased lethality in mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
66 Samples
Download data: TXT
Series
Accession:
GSE70502
ID:
200070502
14.

Primary Human Airway Epithelial Cultures infected with SARS-CoV-2

(Submitter supplied) We performed RNAseq analysis on primary human airway epithelial cultures either mock infected (PBS) or infected with SARS-CoV-2. Transcriptional profiling studies found that infected pHAE cells had a molecular signature dominated by pro-inflammatory cytokines and chemokine induction, including IL-6, TNFα, CXCL8, and identified NF-κB and ATF4 as key drivers of this pro-inflammatory cytokine response. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
6 Samples
Download data: TXT
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