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Links from GEO DataSets

Items: 10

1.

Expression data from hearts of wild-type C57BL/6 mice infected with T. cruzi and controls (uninfected)

(Submitter supplied) An efficient innate immune recognition of the intracellular parasite T. cruzi is crucial for host protection against development of Chagas disease, which often leads to multiple organ damage, particularly the heart leading to cardiomyopathy. Mechanisms modulated by MyD88 have been shown to be necessary for resistance against T, cruzi infection. Recently, Nod-like receptors have been shown to play an important role as innate immune sensors, particularly as they relate to inflammasome function, caspase activation, and inflammatory cytokine production. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5112
Platform:
GPL8321
6 Samples
Download data: CEL, CHP, XLS
Series
Accession:
GSE41089
ID:
200041089
2.
Full record GDS5112

Heart response to Trypanosoma cruzi infection

Analysis of hearts of C57BL/6 animals infected with the intracellular parasite Trypanosoma cruzi. T. cruzi causes Chagas disease which can lead to cardiomyopathy. Results provide insight into the molecular mechanisms underlying the innate immune response in the heart to T. cruzi infections.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 infection sets
Platform:
GPL8321
Series:
GSE41089
6 Samples
Download data: CEL, CHP
DataSet
Accession:
GDS5112
ID:
5112
3.

Lung gene expression analysis of WT, Nlrp3-, Asc-deficient mice in Streptococcus pneumoniae D39 and ATCC6303 infection

(Submitter supplied) Streptococcus (S.) pneumoniae is the most frequently isolated causative pathogen community-acquired pneumonia, a leading cause of mortality worldwide. We investigated the role of the inflammasome sensor NLRP3 and the inflammasome adapter ASC during S. pneumoniae pneumonia. Detailed analysis of the early inflammatory response in the lung by whole genome transcriptional profiling, we identified several mediators that were differentially expressed between Nlrp3-/- and Asc-/ - mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
64 Samples
Download data: TXT
Series
Accession:
GSE42464
ID:
200042464
4.

Chromatin interaction analysis of transcription factors and NLRP3 in CD4+ T cells differentiated from wild-type and NLRP3KO mice

(Submitter supplied) We report that the NLRP3 protein is able to interact with chromatin during Th2 differentiation
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16417
12 Samples
Download data: BED
Series
Accession:
GSE64749
ID:
200064749
5.

Transcriptome analysis of Th2 CD4+ T cells differentiated from wild-type and NLRP3KO mice

(Submitter supplied) We report that the Th2 differentiation program is altered in absence of NRLP3 protein
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16417
6 Samples
Download data: TXT
Series
Accession:
GSE54561
ID:
200054561
6.

A comprehensive analysis of gene expression patterns in wild-type and Batf2-/- bone marrow-derived macrophages (BMMφ)

(Submitter supplied) We previously identified TLR-independent expression of 4933430F08Rik, encoding Batf2, in T. cruzi-infected bone marrow-derived dendritic cells (BMDCs) (Kayama et al., 2009). To determine the functions of Batf2 in innate immune responses, we performed a comprehensive gene expression analysis in wild-type and Batf2-/- bone marrow-derived macrophages (BMMφ). RNA-seq analysis showed that 98 genes are upregulated in Batf2-/- BMMφ stimulated with LPS following IFN-γ treatment, when compared with that in wild-type cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT
Series
Accession:
GSE81724
ID:
200081724
7.

Genomic profiling of human Leishmania braziliensis lesions identifies transcriptional modules associated with cutaneous immunopathology

(Submitter supplied) The host immune response plays a critical role not only in protection from human leishmaniasis, but also in promoting disease severity. Although candidate gene approaches in mouse models of leishmaniasis have been extremely informative, a global understanding of the immune pathways active in lesions from human patients is lacking. To address this issue, genome-wide transcriptional profiling of Leishmania braziliensis-infected cutaneous lesions and normal skin controls was carried out. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
35 Samples
Download data: TXT
Series
Accession:
GSE55664
ID:
200055664
8.

Cytosolic immunity against Moraxella catarrhalis requires innate immune signalling pillars converging on inflammasome activation

(Submitter supplied) RNA-sequencing of uninfected and Moraxella catarrhalis-infected bone marrow-derived macrophages (BMDMs) isolated from Ifnar1 knockout and wild-type mice.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL28457
12 Samples
Download data: TXT
Series
Accession:
GSE196164
ID:
200196164
9.

T cell-intrinsic MyD88 signaling in cognate immune response to intracellular parasite infection: crucial role for IL-18R

(Submitter supplied) We compared gene expression between WT CD4+ (CD45.1) and Myd88-/- CD4+ (CD45.2) T cells from the spleen of infected mix bone marrow chimeras at day 14 of T. cruzi infection. The hypothesis studied in this experiment was that MyD88-/- CD4+ cells have suppressed Th1 differentiation potencial when compared to WT CD4+ T cells. The results indicate that CD4+ T cell-intrinsic MyD88 signaling is necessary for sustaining a more robust Th1 differentiation program and increased expansion among WT CD4+ T cells, resultant of relative higher proliferation and lower apoptosis
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
4 Samples
Download data: TXT
Series
Accession:
GSE57738
ID:
200057738
10.

Immediate/Early Response to Trypanosoma cruzi Infection Involves Minimal Modulation of Host Cell Transcription

(Submitter supplied) Host cell infection by the intracellular pathogen, Trypanosoma cruzi, involves activation of signaling pathways, cytoskeletal reorganization, and targeted recruitment of host cell lysosomes. To determine the consequences of T. cruzi invasion on host cell gene expression, high density microarrays consisting of approximately 27,000 human cDNAs were hybridized with fluorescent probes generated from T. cruzi-infected human fibroblasts (HFF) at early time points following infection (2-24 h). Surprisingly, no genes were induced > or =2-fold in HFF between 2 and 6 h post-infection (hpi) in repeated experiments while immediate repression of six host cell transcripts was observed. A significant increase in transcript abundance for 106 host cell genes was observed at 24 hpi. Among the most highly induced is a set of interferon-stimulated genes, indicative of a type I interferon (IFN) response to T. cruzi. In support of this, T. cruzi-infected fibroblasts begin to secrete IFNbeta at 18 hpi following the induction of IFNbeta transcripts. As compared with global transcriptional responses evoked by other intracellular pathogens, T. cruzi is a stealth parasite that elicits few changes in host cell transcription during the initiation of infection. Set of arrays organized by shared biological context, such as organism, tumors types, processes, etc. Keywords: Logical Set
Organism:
Homo sapiens
Type:
Expression profiling by array
4 related Platforms
22 Samples
Download data
Series
Accession:
GSE3476
ID:
200003476
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