U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.

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
2.

Global murine pulmonary response to highly and less virulent influenza A (H3N2) virus infections at 12, 48 and 96 h post-infection

(Submitter supplied) Array analysis of total lung RNAs from female BALB/c mice collected at 12, 48 and 96 h post-infection with highly and less virulent influenza A (H3N2) viruses. Viruses (designated as LVI and HVI) were derived from influenza strain virus A/Aichi/2/68 (Aichi68). LVI is Aichi68 propagated in eggs, and HVI is mouse adapted Aichi68.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5159
Platform:
GPL6103
18 Samples
Download data: TXT
Series
Accession:
GSE55994
ID:
200055994
3.
Full record GDS5159

Lung response to highly virulent or low virulent influenza A H3N2 virus infection: time course

Analysis of total lung from BALB/c females infected with highly virulent influenza A (HVI) or low virulent influenza A (LVI), up to 96 hrs following infection. Results provide insight into the molecular mechanisms underlying the host pulmonary responses to HVI and LVI infections.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 3 infection, 3 time sets
Platform:
GPL6103
Series:
GSE55994
18 Samples
Download data
DataSet
Accession:
GDS5159
ID:
5159
4.

RNA-seq influenza infected B6 & D2 mice

(Submitter supplied) The host response to influenza A infections is strongly influenced by host genetic factors. Animal models of genetically diverse mouse strains are well suitable to identify host genes involved in severe pathology, viral replication and immune responses. Here, we have utilizing a dual RNAseq approach that allowed us to investigate both viral and host gene expression in the same individual from a single expression assay after H1N1 infection. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16790
36 Samples
Download data: TXT
Series
Accession:
GSE66040
ID:
200066040
5.

Transcriptome analysis of lungs from six different mouse strains after infection with highly pathogenic H5N1 influenza A virus

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8833
104 Samples
Download data
Series
Accession:
GSE64800
ID:
200064800
6.

Transcriptome analysis of lungs from six different mouse strains after infection with highly pathogenic H5N1 influenza A virus [set 2]

(Submitter supplied) Susceptible (DBA/2J, 129/SvImJ, A/J) and Resistant (SM/J, C57BL/6J, Balb/cJ) mouse strain were inoculated with a highly pathogenic H5N1 influenza A virus (A/Hong Kong/213/2003) for 72 hours or not infected (control animals). Differences in expression were analyzed and used to identify candidate genes and pathways that contributed to the difference in H5N1 pathogenesis in these two groups of mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8833
35 Samples
Download data: TXT
Series
Accession:
GSE64799
ID:
200064799
7.

Transcriptome analysis of lungs from six different mouse strains after infection with highly pathogenic H5N1 influenza A virus [set 1]

(Submitter supplied) Susceptible (DBA/2J, 129/SvImJ, A/J) and Resistant (SM/J, C57BL/6J, Balb/cJ) mouse strain were inoculated with a highly pathogenic H5N1 influenza A virus (A/Hong Kong/213/2003) for 24 and 168 hours. Uninfected control animals were included. Differences in expression were analyzed and used to identify candidate genes and pathways that contributed to the difference in H5N1 pathogenesis in these two groups of mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL8833
69 Samples
Download data: TXT
Series
Accession:
GSE64798
ID:
200064798
8.

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
9.

Response of swine lung to H1N1 swine influenza virus infection revealed by transcription analysis

(Submitter supplied) As a mild, highly contagious, respiratory disease, swine influenza always damages the innate immune systems, and increases susceptibility to secondary infections which results in considerable morbidity and mortality in pigs. Nevertheless, the systematical host response of pigs to swine influenza virus infection remains largely unknown. To explore these, a time-course gene expression profiling was performed to detect comprehensive analysis of the global host response induced by H1N1 swine influenza virus in pigs.
Organism:
Sus scrofa
Type:
Expression profiling by array
Platform:
GPL10162
12 Samples
Download data: TXT
Series
Accession:
GSE28871
ID:
200028871
10.

Highly Pathogenic Avian Influenza Viruses Avoid Effective Inflammatory Response of Human Macrophages

(Submitter supplied) Macrophages were infected with low (PR8) and high pathogenic influenza viruses (FPV and H5N1). To our surprise a genome-wide comparative systems biology approach revealed that in contrast PR8 infections with HPAIV H5N1 and FPV result in a reduced immune response of human macrophages contradicting a primary role of this cell type for the cytokine storm. Our data point to a viral strategy of HPAIV to bypass a major amplifier of the initial local inflammatory response thereby hampering antiviral effector mechanisms and facilitating virus spreading and systemic disease.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE27702
ID:
200027702
11.

Expression data of lungs of mice infected with two highly pathogenic avian influenza viruses

(Submitter supplied) We isolated two highly pathogenic H5N1 avian influenza viruses (AIVs) (CK10 and GS10) with similar genetic background but greatly differ in pathogencity in mice. CK10 is highly pathogenic in mice, whereas GS10 is nonpathogenic. However, the host mechanism of this differecne in pathogenicity is unclear. We used microarray analysis to evaluate the global transcriptional response in the lung of mice infected with CK10 or GS10.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
9 Samples
Download data: TXT
Series
Accession:
GSE41126
ID:
200041126
12.

Glycosylation of the HA protein of H5N1 virus increases its virulence in mice by exacerbating the host immune response

(Submitter supplied) The highly pathogenic avian influenza (HPAI) H5N1 viruses continue to circulate in nature and threaten public health. Although several viral determinants and host factors that influence the virulence of HPAI H5N1 viruses in mammals have been identified, the detailed molecular mechanism remains poorly defined and requires further clarification. In our previous studies, we characterized two naturally isolated HPAI H5N1 viruses that had similar viral genomes but differed substantially in their lethality in mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
9 Samples
Download data: TXT
Series
Accession:
GSE89246
ID:
200089246
13.

Influenza H3N2 infection of the Collaborative Cross founder strains reveals highly divergent host responses and identifies a unique phenotype in CAST/EiJ mice

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11202
93 Samples
Download data: TXT
Series
Accession:
GSE74077
ID:
200074077
14.

Influenza H3N2 infection of the Collaborative Cross founder strains reveals highly divergent host responses and identifies a unique phenotype in CAST/EiJ mice (lung)

(Submitter supplied) To determine if genetic background can modulate severity of an infection, we studied the host responses to influenza infections in the eight genetically highly diverse Collaborative Cross (CC) founder mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11202
43 Samples
Download data: TXT
Series
Accession:
GSE74074
ID:
200074074
15.

Influenza H3N2 infection of the Collaborative Cross founder strains reveals highly divergent host responses and identifies a unique phenotype in CAST/EiJ mice (blood)

(Submitter supplied) To determine if genetic background can modulate severity of an infection, we studied the host responses to influenza infections in the eight genetically highly diverse Collaborative Cross (CC) founder mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11202
50 Samples
Download data: TXT
Series
Accession:
GSE74073
ID:
200074073
16.

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
17.

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
18.

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
19.

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
20.

Comparative transcriptional profiling of the lung discriminates S. pneumoniae and Influenza A Virus infections

(Submitter supplied) Peumonia is the most common cause of death due to infectious diseases in the western hemisphere. The molecular events associated with pulmonary infections caused by Streptococcus pneumoniae and Influenza A virus are incompletely understood. Pathophysiological and protective processes are initiated by immune receptors specifically recognizing pathogenic structures serving to elicit a qualitatively and quantitatively adequate immune response. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2165
Platform:
GPL1868
7 Samples
Download data
Series
Accession:
GSE5289
ID:
200005289
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=4|blobid=MCID_674e1da78c9ed417fb09d464|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center