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Links from GEO DataSets

Items: 20

1.

RNA-seq analysis of miR-324-5p overexpression upon H5N1 infection in A549 cells

(Submitter supplied) The goals of this study are to compare NGS-derived whole transcriptome profiles (RNA-seq) of H5N1 infected A549 cells overexpressing either negative control mimic or miR-324-5p mimic
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
3 Samples
Download data: TXT
2.

MicroRNA profiling in HEK293T cells after NDV infection

(Submitter supplied) Mammals have highly evolved receptors for sensing invading viral pathogens. RLRs comprise of one such family of receptors involved in sensing RNA viruses. The antiviral signaling cascade is tightly regulatedd by various post transcriptional modifications however the post transcriptional regulation by microRNAs is not well understood. We performed miRNA profiling to identify miRNAs induced by virus infections with potential role in regulating RLR signaling cascade.
Organism:
synthetic construct; Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL19117
4 Samples
Download data: CEL
Series
Accession:
GSE65694
ID:
200065694
3.

microRNA (miRNA) expression profiling of A549 with H5N1 Influenza A Virus (hm/06)infection

(Submitter supplied) To study miRNA expression profiles during highly pathogenic avian influenza virus infection, we conducted global miRNA expression profiling in human lung epithelial cells (A549) with or without H5N1 IAV infection. .
Organism:
Homo sapiens; Human alphaherpesvirus 1; Human betaherpesvirus 5; Betapolyomavirus macacae; Lymphocryptovirus; Human immunodeficiency virus 1
Type:
Non-coding RNA profiling by array
Platform:
GPL19221
6 Samples
Download data: TXT
Series
Accession:
GSE61701
ID:
200061701
4.

Viral determinants in H5N1 influenza A virus enable productive infection of HeLa cells

(Submitter supplied) Influenza A virus (IAV) is a human respiratory pathogen that causes yearly global epidemics, and sporadic pandemics due to human adaptation of pathogenic strains. Efficient replication of IAV in different species is, in part, dictated by its ability to exploit the genetic environment of the host cell. To investigate IAV tropism in human cells, we evaluated the replication of IAV strains in a diverse subset of epithelial cell lines. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
8 Samples
Download data: TXT
5.

Differential miRNA expression profiling of A549 cells infected with influenza A virus

(Submitter supplied) To further understand the roles of miRNA during influenza A virus infection, we performed miRNA profiling in human alveolar adenocarcinoma cell lines, A549 cells, infected with influenza A virus A/Beijing/501/2009(H1N1) and A/goose/Jilin/hb/2003(H5N1).
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL16770
18 Samples
Download data: TXT
Series
Accession:
GSE96857
ID:
200096857
6.

Microarray analysis of microRNAs expression in A549 cells during influenza A virus infection

(Submitter supplied) To investigate whether influenza A virus (IAV) infection alters cellular miRNA profiles, A549 cells were either mock-infected or infected with two different subtypes of IAV, A/Beijing/501/2009 (H1N1; MOI=5) and A/Vietnam/1194/2004 (H5N1; MOI=2), for 24 or 48 h. Total RNA was purified from cell samples, and microarray analysis of miRNAs was performed. The expression of selected miRNAs was further confirmed by quantitative real-time PCR.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL8179
6 Samples
Download data: IDAT, TXT
Series
Accession:
GSE107186
ID:
200107186
7.

Expression data of mRNA from wild-type A549 cells and microRNA-203 knockout A549 cells during H5N1 infections

(Submitter supplied) MicroRNA-203 was up-regulated markedly upon H5N1 virus infection. To identify the potential target genes of miR-203, we constructed a miR-203 knockout A549 cell line. Then wild-type and miR-203 knockout A549 cells were mock-infected or infected with H5N1 virus for 48h. The Agilent Whole Human Genome Oligo Microarray was performed to analyze the mRNA expression profiling. Meanwhile, the online tool TargetScanHuman (http://www.targetscan.org/vert_71/) was used to predict biological targets of miR-203. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13497
6 Samples
Download data: TXT
Series
Accession:
GSE107089
ID:
200107089
8.

Expression data of lungs from chickens infected with different H5N1 Avian Influenza Viruses

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Gallus gallus
Type:
Expression profiling by array
Platform:
GPL3213
18 Samples
Download data: CEL
Series
Accession:
GSE53932
ID:
200053932
9.

Expression data of lungs from chickens infected with different H5N1 Avian Influenza Viruses [24 hours post infection]

(Submitter supplied) Recently, a novel protein in the influenza virus segment 3 has been identified, namely PA-X. This small protein has been reported to play a role in modulating host response of the 1918 H1N1 pandemic virus-infected mice. However, poteinal role of this protein in the pathogenicity and regulating host response of the highly pathogenic H5N1 virus in a chicken animal model is completely unknown. We used microarray analysis to evaluate the global transcriptional response in the lungs of the chickens infected with the parental strain (CK10) and PA-X deficiency mutant strain (CK-PAX3).
Organism:
Gallus gallus
Type:
Expression profiling by array
Platform:
GPL3213
9 Samples
Download data: CEL
Series
Accession:
GSE53931
ID:
200053931
10.

Expression data of lungs from chickens infected with different H5N1 Avian Influenza Viruses [12 hours post infection]

(Submitter supplied) Recently, a novel protein in the influenza virus segment 3 has been identified, namely PA-X. This small protein has been reported to play a role in modulating host response of the 1918 H1N1 pandemic virus-infected mice. However, poteinal role of this protein in the pathogenicity and regulating host response of the highly pathogenic H5N1 virus in a chicken animal model is completely unknown. We used microarray analysis to evaluate the global transcriptional response in the lungs of the chickens infected with the parental strain (CK10) and PA-X deficiency mutant strain (CK-PAX3).
Organism:
Gallus gallus
Type:
Expression profiling by array
Platform:
GPL3213
9 Samples
Download data: CEL
Series
Accession:
GSE53930
ID:
200053930
11.

Study of PB1-F2 functions in avian host.

(Submitter supplied) Highly pathogenic avian influenza virus (HPAIV) is a permanent threat due to its capacity to cross species barriers and generate severe infections and high mortality in humans. Recent findings have highlighted the potential role of PB1-F2, a small accessory influenza protein, in the pathogenesis process mediated by HPAIV in mammals. In this study, using a recombinant H5N1 HPAIV (wt) and its PB1-F2-deleted mutant (ΔF2), we studied the effects of PB1-F2 in a chicken model. more...
Organism:
Gallus gallus
Type:
Expression profiling by array
Platform:
GPL13790
10 Samples
Download data: TXT
Series
Accession:
GSE56506
ID:
200056506
12.

Deep sequencing analysis of differences in miRNA expression between IBDV-infected and Mock-infected DF-1 cells

(Submitter supplied) To evaluate the change of miRNA expression profile in DF-1 cells in respond to Infectious bursal disease virus (IBDV) infection, Deep sequencing was performed by LC Sciences (Hangzhou, China) on DF-1 cells infected with mock or IBDV Lx strain at an MOI of 1 for 24 h.
Organism:
Gallus gallus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL19005
2 Samples
Download data: XLS
Series
Accession:
GSE90095
ID:
200090095
13.

An H5N1 virus-encoded atypical microRNA is a major contributor to cytokine storm and mortality

(Submitter supplied) An H5N1 virus-encoded microRNA directly targets mammalian poly(rC) binding protein 2 and is a major contributor to H5N1-associated ‘cytokine storm’ and mortality.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL10999
1 Sample
Download data: TXT
Series
Accession:
GSE67222
ID:
200067222
14.

Analysis of Expression Profiles of long noncoding RNAs in A549 cells infected by H1N1 [lncRNA-seq]

(Submitter supplied) Although accumulating evidence has shown that long non-coding RNAs (lncRNAs) are involved in multiple biological processes, considerably less is known regarding their functions in influenza A virus (IAV) replication. Here, lncRNA expression profiles were determined by RNA sequencing in three pairs of influenza virus A/Puerto Rico/8/34 (H1N1)-infected or uninfected A549 cells.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL21290
6 Samples
Download data: FA, GTF, TXT
Series
Accession:
GSE208546
ID:
200208546
15.

Plant microRNA profiling of Honeysuckle and Honeysuckle Decoction

(Submitter supplied) Influenza A viruses (IAVs), particularly H1N1, H5N1 and H7N9, pose a substantial threat to public health worldwide. Here, we report that MIR2911, a honeysuckle (HS)-encoded atypical microRNA, directly targets IAVs with a broad spectrum. MIR2911 is highly stable in HS decoction, and continuous drinking or gavage feeding of HS decoction leads to a significant elevation of the MIR2911 level in mouse peripheral blood and lung. more...
Organism:
Lonicera japonica
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18317
2 Samples
Download data: TXT
Series
Accession:
GSE55268
ID:
200055268
16.

Disease severity is associated with differential gene expression at the early and late phases of infection in non-human primates infected with different H5N1 highly pathogenic avian influenza viruses

(Submitter supplied) Occasional transmission of highly pathogenic avian H5N1 influenza viruses to humans causes severe pneumonia with high mortality. To better understand the mechanisms via which H5N1 viruses induce severe disease in humans, we infected cynomolgus macaques with six different H5N1 strains isolated from human patients and compared their pathogenicity and the global host responses to the virus infection. Although all H5N1 viruses replicated in the respiratory tract, there was substantial heterogeneity in their replicative ability and in the disease severity induced, which ranged from asymptomatic to fatal. more...
Organism:
Macaca mulatta
Type:
Expression profiling by array
Platform:
GPL14569
45 Samples
Download data: TXT
Series
Accession:
GSE57970
ID:
200057970
17.

Whole transcriptome analysis of human macrophages infected with H5N1 and H1N1 influenza viruses reveals the significant up-regulation of RIG-I-like receptor signaling pathway

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL9115
18 Samples
Download data: TXT
Series
Accession:
GSE99079
ID:
200099079
18.

Whole transcriptome analysis of human macrophages infected with H5N1 and H1N1 influenza viruses reveals the significant up-regulation of RIG-I-like receptor signaling pathway [miRNA-seq]

(Submitter supplied) For the small RNA portion in the whole transcriptome, a total of 105,842,096 filtered high-quality sequencing reads, representing 2,854,995 unique miRNA species, were generated for miRNAs for H1N1- or H5N1- infected macrophage cell populations at 1-, 3-, and 6-hr post-infection. A total of 361 mature miRNAs and 113 mature star miRNAs were identified from the samples. We calculated the miRNA expression fold change in influenza A viruses infected cells compared to mock-infected control cells andassessed the significance of the differential expression for each miRNA using Z-statistics. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL9115
9 Samples
Download data: XLS
Series
Accession:
GSE99054
ID:
200099054
19.

Whole transcriptome analysis of human macrophages infected with H5N1 and H1N1 influenza viruses reveals the significant up-regulation of RIG-I-like receptor signaling pathway [mRNA]

(Submitter supplied) We generated an average of 868 million nucleotides and 30 folds coverage per sample. More than 76% of the sequencing reads were mapped to the human genome, and 45.5% of the annotated reference genes were mapped by at least 10 reads. Differential expression quantification showed that H5N1 virus elicits greater changes in host gene expression than the H1N1 virus at nearly all three time points with 1198,273,and 620 up-regulated in H5N1, and 426,285, and 523 in H1N1 compared with mock control (fold-change >= 2.0, and p-value <= 0.05). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9115
9 Samples
Download data: TXT, XLS
Series
Accession:
GSE98665
ID:
200098665
20.

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
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