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Links from GEO DataSets

Items: 14

1.
Full record GDS5626

pH1N1 influenza virus infection of interferon regulatory factor 7-deficient peripheral blood mononuclear cells: time course

Analysis of PBMCs isolated from an IRF7-deficient patient and infected with influenza A/CA/4/2009 for up to 16 hrs. Transcription factor IRF7 amplifies type I and III interferon response to viruses. Results provide insight into the role of IRF7 in antiviral immunity.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 6 individual, 2 infection, 3 time sets
Platform:
GPL10558
Series:
GSE66486
18 Samples
Download data
2.

Response of IRF7-deficient peripheral blood mononuclear cells to pH1N1 influenza virus infection

(Submitter supplied) IRF7 plays a critical role in the production and amplification of the antiviral type I and III interferon response. Autosomal recessive IRF7-deficiency resulted in life-threatening influenza disease in a 3-year-old child. We studied the impact of IRF7-deficiency in non-hematopoietic tissues (fibroblasts and lung epithelial cells) as well in hematopoietic cells (peripheral blood mononuclear cells (PBMCs)). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5626
Platform:
GPL10558
18 Samples
Download data: TXT
Series
Accession:
GSE66486
ID:
200066486
3.

Type I and type III interferons drive redundant amplification loops to induce a transcriptional signature in influenza-infected airway epithelia

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
62 Samples
Download data: CEL
Series
Accession:
GSE43710
ID:
200043710
4.

Expression data from Influenza A infected mouse primary tracheal epithelial cell cultures (MTEC), from both wild-type and MAVS-/- mice

(Submitter supplied) We used microarrays to detail the global programme of gene expression in response to Influenza A (PR8) infection
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL, TXT
Series
Accession:
GSE43709
ID:
200043709
5.

Expression data from Influenza A infected mouse primary tracheal epithelial cell cultures (MTEC), from wild-type, IFNAR1-/-, IL28Ra-/- and IFNAR1-/- IL28Ra-/- double ko

(Submitter supplied) We used microarrays to detail the global programme of gene expression in response to Influenza A (PR8) infection
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
40 Samples
Download data: CEL, TXT
Series
Accession:
GSE43708
ID:
200043708
6.

Expression data from Influenza A infected mouse primary tracheal epithelial cell cultures (MTEC)

(Submitter supplied) We used microarrays to detail the global programme of gene expression in response to Influenza A (PR8) infection
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
10 Samples
Download data: CEL, TXT
Series
Accession:
GSE43707
ID:
200043707
7.

Differential Responses of Plasmacytoid Dendritic Cells to Influenza and Distinct Viral Pathogens

(Submitter supplied) Plasmacytoid dendritic cells (pDCs) are key components of the innate immune response that are capable of synthesizing and rapidly releasing vast amounts of type I interferons (IFNs), particularly IFN-alpha. Here we investigated whether pDCs, often regarded as a mere source of IFN, discriminate between various functionally discrete stimuli and to what extent this reflects differences in pDC responses other than IFN-alpha release. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL7088
95 Samples
Download data: TXT
Series
Accession:
GSE59837
ID:
200059837
8.

Transcriptional repression of IRF7 by MYC is critical for antiviral immune response in human pDC [GEN2.2]

(Submitter supplied) Type I interferons (IFN) are crucial mediators of human innate and adaptive immunity and are massively produced from plasmacytoid dendritic cells (pDC). IRF7 is a critical regulator of type I IFN production when pathogens are detected by TLR7/9 in pDC. However, hyperactivation of pDC can cause life-threatening autoimmune diseases. To avoid the deleterious effects of aberrant pDC activation, tight regulation of IRF7 is required. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
21 Samples
Download data: TXT
Series
Accession:
GSE70276
ID:
200070276
9.

Transcriptional repression of IRF7 by MYC is critical for antiviral immune response in human pDC [ChIP-seq]

(Submitter supplied) Type I interferons (IFN) are crucial mediators of human innate and adaptive immunity and are massively produced from plasmacytoid dendritic cells (pDC). IRF7 is a critical regulator of type I IFN production when pathogens are detected by TLR7/9 in pDC. However, hyperactivation of pDC can cause life-threatening autoimmune diseases. To avoid the deleterious effects of aberrant pDC activation, tight regulation of IRF7 is required. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
2 Samples
Download data: TXT
Series
Accession:
GSE70275
ID:
200070275
10.

Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency

(Submitter supplied) Life-threatening pulmonary influenza can be caused by inborn errors of type I and III IFN immunity. We report a 5 year-old child with severe pulmonary influenza at 2 years. She is homozygous for a loss-of-function IRF9 allele. Her cells activate gamma-activated factor (GAF) STAT1 homodimers but not interferon-stimulated gene factor 3 (ISGF3) trimers (STAT1/STAT2/IRF9) in response to IFN-α2b. The transcriptome induced by IFN-α2b in the patient’s cells is much narrower than that of control cells; however, induction of a subset of interferon-stimulated gene transcripts remains detectable. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
36 Samples
Download data: XLS
11.

Alignment of different types of resting or murine cytomegalovirus-activated mononuclear phagocytes across different datasets

(Submitter supplied) The goal of this experiment was to use global gene expression profiling to assess the global genetic reprogramming of different types of splenic mononuclear phagocytes early after MCMV infection in vivo. This study includes new samples (GSM3178486-GSM3178497; available below) profiling splenic CD11b+ conventional dendritic cells (cDC2), classical monocytes (cMo) and red pulp macrophages (RPM) from untreated or day 1.5 MCMV-infected mice together with re-analysis of previously published data in order to examine the similarities in the pDC gene expression profiles across datasets. more...
Organism:
Mus musculus
Type:
Expression profiling by array; Third-party reanalysis
Platform:
GPL6246
12 Samples
Download data: CEL, TXT
Series
Accession:
GSE115450
ID:
200115450
12.

Dissecting cell-intrinsic roles of MyD88 and IFN-I signalling in pDC responses to a viral infection in vivo

(Submitter supplied) Plasmacytoid dendritic cells (pDC) are the major source of type I interferons (IFN-I) during viral infections, in response to triggering of endosomal Toll Like Receptors (TLR) 7 or 9 by viral single-stranded RNA or unmethylated CpG DNA, respectively. IFN-I production in pDC occurs in specialized endosomes encompassing preformed signaling complexes of TLR7 or 9 with their adaptor molecule MyD88 and the transcription factor interferon regulatory factor 7 (IRF7). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
36 Samples
Download data: CEL
Series
Accession:
GSE107876
ID:
200107876
13.

Irf3 phenotyping

(Submitter supplied) The interferon regulatory factors IRF3 and IRF7 are key players in the regulation of type I and III IFN genes. In this study, we analyzed the role of IRF3 and IRF7 for the host response to influenza A virus infections in Irf3-/-, Irf7-/- and Irf3-/-Irf7-/- knock-out mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11202
24 Samples
Download data: TXT
Series
Accession:
GSE77600
ID:
200077600
14.

Unique transcriptional architecture in airway epithelial cells and macrophages shapes distinct responses following influenza virus infection ex vivo.

(Submitter supplied) Airway epithelial cells and macrophages differ markedly in their responses to influenza A virus (IAV) infection. To investigate transcriptional responses underlying these differences, purified subsets of type II airway epithelial cells (ATII) and alveolar macrophages (AM) recovered from the lungs of mock- or IAV-infected mice were subjected to RNA sequencing. In the absence of infection, AM predominantly expressed genes related to immunity whereas ATII expressed genes consistent with their physiological roles in the lung. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
96 Samples
Download data: TXT
Series
Accession:
GSE115904
ID:
200115904
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