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Links from GEO DataSets

Items: 14

1.

Gene Expression Analysis of Host Immune Responses in CD11b positive cells isolated from lungs of the UV inactivated SARS-CoV-immunized mice following Lethal SARS-CoV Infection

(Submitter supplied) To better understand the biological pathways by which UV inactivated SARS-CoV-induced pulmonary eosinophilia occurs, we examined global transcriptional changes in macrophages from the lungs of mouse.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
24 Samples
Download data: TXT
Series
Accession:
GSE50855
ID:
200050855
2.

Gene Expression Analysis of Host Immune Responses in the UV inactivated SARS-CoV-immunized mice following Lethal SARS-CoV Infection

(Submitter supplied) To better understand the biological pathways by which UV inactivated SARS-CoV-induced pulmonary eosinophilia occurs, we examined global transcriptional changes in mouse lungs.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
24 Samples
Download data: TXT
Series
Accession:
GSE44274
ID:
200044274
3.

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
4.

Mouse lung tissue transcriptome response to a mouse-adapted strain of SARS-CoV in wild type C57BL6/NJ mice and TLR3-/- mice

(Submitter supplied) The purpose is to determine the role of TLR3-/- on the regulation of the host immune response during lethal SARS-CoV infection
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
52 Samples
Download data: TXT
Series
Accession:
GSE68820
ID:
200068820
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.

Absence of host innate immune responses in SARS-CoV-infected ferrets upon subsequent challenge

(Submitter supplied) To further investigate the underlying mechanisms of severe acute respiratory syndrome (SARS) pathogenesis and evaluate the therapeutic efficacy of potential drugs and vaccines it is necessary to use an animal model that is highly representative of the human condition in terms of respiratory anatomy, physiology and clinical sequelae. The ferret, Mustela putorius furo, supports SARS-CoV replication and displays many of the symptoms and pathological features seen in SARS-CoV-infected humans. more...
Organism:
Mustela putorius furo; Canis lupus familiaris
Type:
Expression profiling by array
Platform:
GPL3738
38 Samples
Download data: CEL
Series
Accession:
GSE11704
ID:
200011704
7.

SM014 - SARS MA15 wild type, and SARS nsp16 mutant virus infections of C57BL6 mice - A time course

(Submitter supplied) This purpose of this experiment was to investigate the transcriptional differences between mice infected with SARS MA15 or SARS nsp16 mutant viruses.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
40 Samples
Download data: TXT
Series
Accession:
GSE49263
ID:
200049263
8.

Transcriptomic analysis of host response to mouse-adapted SARS virus in wild type, STAT1 -/-, and IFNAR1 -/- mouse genetic backgrounds

(Submitter supplied) The mechanisms by which pulmonary lesions and fibrosis are generated during SARS-CoV infection are not known. Using high-throughput mRNA profiling, we examined the transcriptional response of wild-type (WT), type I interferon receptor knockout (IFNAR1−/−), and STAT1 knockout (STAT1−/−) mice infected with a recombinant mouse-adapted SARS-CoV (rMA15) to better understand the contribution of specific gene expression changes to disease progression.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
36 Samples
Download data: TXT
Series
Accession:
GSE36016
ID:
200036016
9.

Transcriptional atlas of the cytokine drivers and cellular contributors mediating enhanced SARS-CoV-2 lung pathology in hamsters after non-protective immunization

(Submitter supplied) Since December 2019, the novel human Coronavirus SARS-CoV-2 has spread globally, causing millions of deaths. Unprecedented efforts have enabled development and authorization of a range of vaccines, which reduce transmission rates and confer protection against the associated disease COVID-19. These vaccines are conceptually diverse, including e.g. classical adjuvanted whole-inactivated virus, viral vectors, and mRNA vaccines. more...
Organism:
Mesocricetus auratus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29592
16 Samples
Download data: CSV
Series
Accession:
GSE195939
ID:
200195939
10.

SARS-CoV-Encoded Small RNAs Contribute to Infection-Associated Lung Pathology

(Submitter supplied) Severe acute respiratory syndrome coronavirus (SARS-CoV) causes lethal disease in humans, which is characterized by exacerbated inflammatory response and extensive lung pathology. To address the relevance of small non-coding RNAs in SARS-CoV pathology, we deep sequenced RNAs from the lungs of infected mice and discovered three 18–22 nt small viral RNAs (svRNAs). The three svRNAs were derived from the nsp3 (svRNA-nsp3.1 and -nsp3.2) and N (svRNA-N) genomic regions of SARS-CoV. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15103
16 Samples
Download data: TXT
Series
Accession:
GSE90624
ID:
200090624
11.

Early gene expression events in ferrets in response to SARS coronavirus infection versus direct interferon-alpha2b stimulation

(Submitter supplied) Background: Type I interferons (IFNs) are essential to the clearance of viral diseases, in part by initiating upregulation of IFN regulated genes (IRGs). A clear distinction between genes upregulated directly by virus and genes upregulated by secondary IFN production has not been made. Here we investigated the genes regulated by IFN-a2b compared to the genes regulated by SARS-CoV infection in ferrets. more...
Organism:
Canis lupus familiaris; Mustela putorius furo
Type:
Expression profiling by array
Platform:
GPL3738
43 Samples
Download data: CEL
Series
Accession:
GSE22581
ID:
200022581
12.

SARS-CoV-2 infection causes heightened disease severity and mortality in a mouse model of Down syndrome

(Submitter supplied) Recent epidemiological studies suggest that individuals with Down syndrome are more susceptible to SARS-CoV-2 infection and have higher rates of hospitalization and mortality than the general population. However, the main drivers behind these disparate health outcomes remain unknown. Herein we performed experimental infections with SARS-CoV-2 in a well-established mouse model of Down syndrome, Dp(16)1Yey/+;Tg(K18-ACE2)2Prlmn/+ (abbreviated as Dp16;ACE2). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
18 Samples
Download data: XLS
Series
Accession:
GSE260583
ID:
200260583
13.

Gene expression in mouse lung homogenates treated with synthetic TLR ligands to induce resistance

(Submitter supplied) Infectious pneumonias exact an unacceptable mortality burden worldwide. Efforts to protect populations from pneumonia have historically focused on antibiotic development and vaccine-enhanced adaptive immunity. However, we have recently reported that the lungs’ innate defenses can be therapeutically induced by inhalation of a combination of synthetic TLR ligands that synergize to protect mice against otherwise lethal pneumonia. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
32 Samples
Download data: TXT
Series
Accession:
GSE28994
ID:
200028994
14.

Gene expression in mouse lung epithelial cells treated with synthetic TLR ligands to induce resistance

(Submitter supplied) Infectious pneumonias exact an unacceptable mortality burden worldwide. Efforts to protect populations from pneumonia have historically focused on antibiotic development and vaccine-enhanced adaptive immunity. However, we have recently reported that the lungs’ innate defenses can be therapeutically induced by inhalation of a bacterial lysate that protects mice against otherwise lethal pneumonia. Here, we tested in mice the hypothesis that Toll-like receptors (TLRs) are required for this antimicrobial phenomenon, and found that resistance could not be induced in the absence of the TLR signaling adaptor protein MyD88. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
22 Samples
Download data: TXT
Series
Accession:
GSE26864
ID:
200026864
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