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Links from GEO DataSets

Items: 18

1.

Kinetic analysis of T cell anergy induction

(Submitter supplied) T cell receptor(TCR) engagement in the absence of costimulation leads to a state of T cell tolerance known as anergy. Anergy induction requires new protein synthesis since it is inhibited by cycloheximide. In this experiment, we tried to figure out kinetic properties of the gene expression in anergy induction phase and the subsequent anergy maintenance phase.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL83 GPL81 GPL82
15 Samples
Download data: CEL
Series
Accession:
GSE72731
ID:
200072731
2.

Role of EGR2 transcription factor in T cell anergy

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by array
Platforms:
GPL9185 GPL1261
15 Samples
Download data: BED, CEL, CHP
Series
Accession:
GSE46243
ID:
200046243
3.

Egr2-dependent expression in T cell anergy

(Submitter supplied) T cell anergy is one of the mechanisms contributing to peripheral tolerance, particularly in the context of progressively growing tumors and in tolerogenic treatments promoting allograft acceptance. We recently reported that early growth response gene 2 (Egr2) is a critical transcription factor for the induction of anergy in vitro and in vivo, which was identified based on its ability to regulate the expression of inhibitory signaling molecules diacylglycerol kinase (DGK)-a and -z. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE46242
ID:
200046242
4.

Genome-wide maps of EGR2 transcription factor binding sites in T cell anergy

(Submitter supplied) We report the application of sequencing technology for mapping the EGR2 transcriptional program in T cell anergy
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9185
3 Samples
Download data: BED
Series
Accession:
GSE46241
ID:
200046241
5.

Anergy Induction

(Submitter supplied) pooled mRNA (2, 4, 6 hrs) from A.E7 T cells under conditions which promote or inhibit anergy induction Keywords: ordered
Organism:
Mus musculus
Type:
Expression profiling by array
Datasets:
GDS1336 GDS1338 GDS1339
Platforms:
GPL82 GPL83 GPL81
15 Samples
Download data
Series
Accession:
GSE2323
ID:
200002323
6.
Full record GDS1339

T cell anergy induction regulation by Egr-2 and Egr-3 (MG-U74C)

Analysis of pooled mRNA (2, 4, 6 hours) from A.E7 T cell clones activated in conditions that promote (anti-TCR) or inhibit (anti-TCR + CsA or PKCi or Combo) anergy induction. Results identify the early growth response gene 2 (Egr-2) and Egr-3 as key positive regulators of T cell anergy induction.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 5 agent, 3 protocol sets
Platform:
GPL83
Series:
GSE2323
5 Samples
Download data
DataSet
Accession:
GDS1339
ID:
1339
7.
Full record GDS1338

T cell anergy induction regulation by Egr-2 and Egr-3 (MG-U74B)

Analysis of pooled mRNA (2, 4, 6 hours) from A.E7 T cell clones activated in conditions that promote (anti-TCR) or inhibit (anti-TCR + CsA or PKCi or Combo) anergy induction. Results identify the early growth response gene 2 (Egr-2) and Egr-3 as key positive regulators of T cell anergy induction.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 5 agent, 3 protocol sets
Platform:
GPL82
Series:
GSE2323
5 Samples
Download data
DataSet
Accession:
GDS1338
ID:
1338
8.
Full record GDS1336

T cell anergy induction regulation by Egr-2 and Egr-3 (MG-U74A)

Analysis of pooled mRNA (2, 4, 6 hours) from A.E7 T cell clones activated in conditions that promote (anti-TCR) or inhibit (anti-TCR + CsA or PKCi or Combo) anergy induction. Results identify the early growth response gene 2 (Egr-2) and Egr-3 as key positive regulators of T cell anergy induction.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 5 agent, 3 protocol sets
Platform:
GPL81
Series:
GSE2323
5 Samples
Download data
DataSet
Accession:
GDS1336
ID:
1336
9.

Antigen-driven EGR2 expression is required for exhausted CD8+ T cell stability and maintenance [scRNAseq]

(Submitter supplied) In this study, we examined the role of the transcriptional regulator EGR2 in CD8+ T cell exhaustion during chronic viral infection. We conducted scRNAseq analysis on sorted virus-specific tetramer+ CD8+ T cells isolated at day 20 post-infection with chronic LCMV-Cl13 from either littermate control or EGR2 T cell conditional knock-out mice. Cells were labelled with hashtags and mixed prior to multiplexed analysis. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24247 GPL19057
2 Samples
Download data: H5
Series
Accession:
GSE154143
ID:
200154143
10.

Antigen-driven EGR2 expression is required for exhausted CD8+ T cell stability and maintenance [ATACseq]

(Submitter supplied) In this study, we examined the role of the transcriptional regulator EGR2 in CD8+ T cell exhaustion during chronic viral infection. Flow cytometric and scRNAseq analysis indicated that EGR2 deficient CD8+ T cells had an abnormal effector-like phenotype. To examine whether this was due to epigenetic alterations, we conducted ATACseq analysis on sorted virus-specific tetramer+ CD8+ T cells isolated at day 20 post-infection with chronic LCMV-Cl13 from either littermate control or EGR2 T cell conditional knock-out mice. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: BW
Series
Accession:
GSE153136
ID:
200153136
11.

Antigen-driven EGR2 expression is required for exhausted CD8+ T cell stability and maintenance [RNA-seq II]

(Submitter supplied) In this study, we examined the role of the transcriptional regulator EGR2 in CD8+ T cell exhaustion during chronic viral infection. Flow cytometric analysis indicated that EGR2 is expressed selectively within the progenitor exhausted subset, however a subpopulation of progenitor exhausted cells did not express in EGR2. To define the differences between the EGR2+ and EGR2- progenitor exhausted cells, GFP+ and GFP- polyclonal progenitor exhausted (ie. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: TXT
Series
Accession:
GSE152849
ID:
200152849
12.

Antigen-driven EGR2 expression is required for exhausted CD8+ T cell stability and maintenance

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL19057 GPL24247
16 Samples
Download data: BW, H5, NARROWPEAK
Series
Accession:
GSE134710
ID:
200134710
13.

Antigen-driven EGR2 expression is required for exhausted CD8+ T cell stability and maintenance [CHIP-seq]

(Submitter supplied) In this study, we examined the role of the transcriptional regulator EGR2 in CD8+ T cell exhaustion during chronic viral infection. Flow cytometric and RNAseq analysis indicated that EGR2 deficient CD8+ T cells had a block in differentiation and failed to undergo terminal exhaustion. To examine the direct gene targets of EGR2 during exhaustion, we conducted ChIPseq analysis on enriched bulk splenic CD8+ T cells isolated at day 20 post-infection with chronic LCMV-Cl13 from C57BL/6J mice. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
2 Samples
Download data: NARROWPEAK
Series
Accession:
GSE134708
ID:
200134708
14.

Antigen-driven EGR2 expression is required for exhausted CD8+ T cell stability and maintenance [RNA-seq I]

(Submitter supplied) In this study, we examined the role of the transcriptional regulator EGR2 in CD8+ T cell exhaustion during chronic viral infection. Flow cytometric analysis indicated that EGR2 deficient CD8+ T cells had a block in differentiation and failed to undergo terminal exhaustion. To confirm this at a whole transcriptome level, we conducted RNAseq analysis on sorted splenic virus-specific tetramer+ CD8+ T cells isolated at day 20 post-infection with chronic LCMV-Cl13 from either littermate control or EGR2 T cell conditional knock-out mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: CSV
Series
Accession:
GSE134689
ID:
200134689
15.

Profiling and Rewiring Dysfunctional NK cells to Restore Anti-Tumor Activity

(Submitter supplied) Unraveling the molecular mechanisms of NK cell dysfunction and implications for anti-tumor immunotherapy.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: TXT
Series
Accession:
GSE248228
ID:
200248228
16.

Differential expression of mRNAs in naïve, effector, and memory CD8 T cells of mir-150 KO and wild-type mice

(Submitter supplied) microRNA-150 (miR-150) is mainly expressed in the lymph nodes and spleen and is highly up-regulated during the development of mature T and B cells. To understand the signal-transduction network for 'effector or memory T cells' and 'mir-150' in naïve, effector, or memory CD8 T cells of mir-150 knockout and wild-type mice, we analyzed gene expression profiles by microarray. The genetic background of the cells used in this study is CD8 T cells from spleen of the 8 week-old male C57BL/6J mice (for female: WT-memory_2 & KO-memory_2). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
8 Samples
Download data: TXT
Series
Accession:
GSE62262
ID:
200062262
17.

BATF represses BIM to sustain tolerant T cells in the periphery (RNA-Seq)

(Submitter supplied) T cells that encounter self-antigens after exiting the thymus avert autoimmunity through peripheral tolerance. Pathways for this include an unresponsive state known as anergy, clonal deletion, and T regulatory (Treg) cell induction. The transcription factor cues and kinetics that guide distinct peripheral tolerance outcomes remain unclear. Here, we found that anergic T cells are epigenetically primed for regulation by the non-classical AP-1 family member BATF. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
12 Samples
Download data: BIGWIG, TXT
Series
Accession:
GSE244278
ID:
200244278
18.

BATF represses BIM to sustain tolerant T cells in the periphery (ATAC-Seq)

(Submitter supplied) T cells that encounter self-antigens after exiting the thymus avert autoimmunity through peripheral tolerance. Pathways for this include an unresponsive state known as anergy, clonal deletion, and T regulatory (Treg) cell induction. The transcription factor cues and kinetics that guide distinct peripheral tolerance outcomes remain unclear. Here, we found that anergic T cells are epigenetically primed for regulation by the non-classical AP-1 family member BATF. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
11 Samples
Download data: BIGWIG, TXT
Series
Accession:
GSE244276
ID:
200244276
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