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Links from GEO DataSets

Items: 20

1.

Transcriptional basis of CD4 T cel help for memory CD8 T cell formation

(Submitter supplied) CD4+ T-cell help is required for the generation of CD8+ cytotoxic T lymphocyte (CTL) memory. We here reveal how “help” signals delivered during priming impact memory differentiation of CTLs, as informed by genome-wide analyses. “Help” signals promoted the IL-15-dependent maintenance of central memory (TCM) cells. However, they had a much larger impact on the generation of effector memory (TEM) cells and their gene expression program . more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: XLSX
Series
Accession:
GSE135141
ID:
200135141
2.

CD4+ T-cell help creates effector memory CTLs with innate and help-independent recall capacities

(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
Platform:
GPL17021
30 Samples
Download data: BROADPEAK, NARROWPEAK
Series
Accession:
GSE118160
ID:
200118160
3.

Epigenetic basis of CD4 T cel help for memory CD8 T cell formation

(Submitter supplied) We report here the effects of CD4 T cell help during priming on the acquistion of specific epigenetic program by memory CD8 T cells.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
18 Samples
Download data: BROADPEAK, NARROWPEAK
Series
Accession:
GSE118159
ID:
200118159
4.

Precursors of human CD4+ cytotoxic T lymphocytes identified by single-cell transcriptome analysis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL15520 GPL16791
2396 Samples
Download data
Series
Accession:
GSE106544
ID:
200106544
5.

Precursors of human CD4+ cytotoxic T lymphocytes identified by single-cell transcriptome analysis [10X genomics]

(Submitter supplied) CD4+ cytotoxic T lymphocytes (CD4-CTLs) have been reported to play a protective role in several viral infections. However, little is known in humans about the biology of CD4-CTL generation, their functional properties, heterogeneity and clonal diversity, especially in relation to other well-described CD4+ memory T cell subsets. We performed single-cell RNA-seq in over 9000 cells to unravel CD4-CTL heterogeneity, transcriptional profile and clonality in humans. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
2 Samples
Download data: TXT
Series
Accession:
GSE106543
ID:
200106543
6.

Precursors of human CD4+ cytotoxic T lymphocytes identified by single-cell transcriptome analysis [bulk RNA-seq]

(Submitter supplied) CD4+ cytotoxic T lymphocytes (CD4-CTLs) have been reported to play a protective role in several viral infections. However, little is known in humans about the biology of CD4-CTL generation, their functional properties, heterogeneity and clonal diversity, especially in relation to other well-described CD4+ memory T cell subsets. We performed single-cell RNA-seq in over 9000 cells to unravel CD4-CTL heterogeneity, transcriptional profile and clonality in humans. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
40 Samples
Download data: TXT
Series
Accession:
GSE106542
ID:
200106542
7.

Precursors of human CD4+ cytotoxic T lymphocytes identified by single-cell transcriptome analysis [TCRseq]

(Submitter supplied) CD4+ cytotoxic T lymphocytes (CD4-CTLs) have been reported to play a protective role in several viral infections. However, little is known in humans about the biology of CD4-CTL generation, their functional properties, heterogeneity and clonal diversity, especially in relation to other well-described CD4+ memory T cell subsets. We performed single-cell RNA-seq in over 9000 cells to unravel CD4-CTL heterogeneity, transcriptional profile and clonality in humans. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL15520
110 Samples
Download data: TXT
Series
Accession:
GSE106541
ID:
200106541
8.

Precursors of human CD4+ cytotoxic T lymphocytes identified by single-cell transcriptome analysis [scRNA-seq]

(Submitter supplied) CD4+ cytotoxic T lymphocytes (CD4-CTLs) have been reported to play a protective role in several viral infections. However, little is known in humans about the biology of CD4-CTL generation, their functional properties, heterogeneity and clonal diversity, especially in relation to other well-described CD4+ memory T cell subsets. We performed single-cell RNA-seq in over 9000 cells to unravel CD4-CTL heterogeneity, transcriptional profile and clonality in humans. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
2244 Samples
Download data: TXT
Series
Accession:
GSE106540
ID:
200106540
9.

Expression data from LCMV-infected P14 and Akt transgenic P14 CD8 T cells

(Submitter supplied) The PI3K/Akt signaling pathway impacts various aspects of CD8 T cell homeostasis, such as effect versus memory cell differentiation, during viral infection. We used microarrays to determine which downstream molecules were affected and what other signaling pathways were interconnected with the Akt pathway by constitutive activation of Akt in LCMV-infected CD8 T cells.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4554
Platform:
GPL6246
5 Samples
Download data: CEL
Series
Accession:
GSE36168
ID:
200036168
10.
Full record GDS4554

Akt transgenic response to lymphocytic choriomeningitis virus (LCMV) infection: CD8 T cell types

Analysis of naïve CD8 T cells, short-lived effector or memory precursor effector cells from LCMV-infected P14/WT or P14/Akt transgenic females. Results provide insight into the role of Akt in effector and memory CD8 T cell differentiation during viral infection.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 3 cell type, 2 genotype/variation, 2 infection sets
Platform:
GPL6246
Series:
GSE36168
5 Samples
Download data: CEL
11.

Analysis of transcriptomes of healthy donor and CD46 deficient CD8 T cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below. We analyze the transcriptomes of healthy donor and CD46 deficieint patients with and without in vitro activation by microarray and RNA-seq
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by high throughput sequencing
Platforms:
GPL21290 GPL10558
21 Samples
Download data: IDAT
Series
Accession:
GSE119919
ID:
200119919
12.

Transcriptome analysis of CD8+ T cells from healthy controls and patients wth CD46 deficiency

(Submitter supplied) RNA-seq data from CD8+ T cells of healthy controls and patients with CD46-deficiency activated, or not, in vitro
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21290
15 Samples
Download data
13.

Gene expression in T cells from CD46-deficient patients and matcherd healthy controls

(Submitter supplied) Recent data indicate that intracellularly activated and autocrine-functioning complement activation fragments - in conjunction with an NLRP3 inflammasome - is critical for normal human Th1 induction and contraction. More specifically, engagement of of the C3aR and CD46 by autocrine generated C3a and C3b, respectively, drives the metabolic reprogramming needed for IFN-gamma secrtion by human CD4+ T cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
6 Samples
Download data: IDAT, TXT
Series
Accession:
GSE119913
ID:
200119913
14.

The impact of Tbet and/or Runx3 deficiency on Tle3 binding pattern in early effector CD8 T cells

(Submitter supplied) The goal of this study is to determine if central memory (Tcm) and effector memory (Tem) CD8 T cells can be reprogrammed to change their fate. We demonstrate that genetic ablation of Tle3 can promote generation of Tcm cells at the expense of Tem cells, and this can occur during the effector phase of the immune response.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21273
15 Samples
Download data: BW, NARROWPEAK
Series
Accession:
GSE241534
ID:
200241534
15.

Impact of Tle3 induced deletion on chromatin accessibility profile of effector memory CD8 cells

(Submitter supplied) The goal of this study is to determine if central memory (Tcm) and effector memory (Tem) CD8 T cells can be reprogrammed to change their fate. We demonstrate that genetic ablation of Tle3 can promote generation of Tcm cells at the expense of Tem cells, and this can occur during the effector phase of the immune response.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21273
5 Samples
Download data: BW, NARROWPEAK
Series
Accession:
GSE241533
ID:
200241533
16.

Impact of Tle3 induced deletion on transcriptomes of effector memory CD8 cells

(Submitter supplied) The goal of this study is to determine if central memory (Tcm) and effector memory (Tem) CD8 T cells can be reprogrammed to change their fate. We demonstrate that genetic ablation of Tle3 can promote generation of Tcm cells at the expense of Tem cells, and this can occur during the effector phase of the immune response.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
6 Samples
Download data: COUNTS
Series
Accession:
GSE241532
ID:
200241532
17.

Reprogramming fate of central memory CD8+T cells by targetig the transcriptional coregulator Tle3 [scRNA-seq]

(Submitter supplied) The goal of this study is to determine if central memory (Tcm) and effector memory (Tem) CD8 T cells can be reprogrammed to change their fate. We demonstrate that genetic ablation of Tle3 can promote generation of Tcm cells at the expense of Tem cells, and this can occur during the effector phase of the immune response.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
2 Samples
Download data: TXT
Series
Accession:
GSE216633
ID:
200216633
18.

Reprogramming fate of central memory CD8+T cells by targetig the transcriptional coregulator Tle3

(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
Platform:
GPL21273
59 Samples
Download data: BW, COUNTS, TXT
Series
Accession:
GSE213041
ID:
200213041
19.

Impact of Tle3 deficiency on memory T cell transcriptome

(Submitter supplied) The goal of this study is to determine if central memory (Tcm) and effector memory (Tem) CD8 T cells can be reprogrammed to change their fate. We demonstrate that genetic ablation of Tle3 can promote generation of Tcm cells at the expense of Tem cells, and this can occur during the effector phase of the immune response.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
12 Samples
Download data: TXT
Series
Accession:
GSE213037
ID:
200213037
20.

Mapping dynamic Tle3 distribution during CD8 T cell responses

(Submitter supplied) The goal of this study is to determine if central memory (Tcm) and effector memory (Tem) CD8 T cells can be reprogrammed to change their fate. We demonstrate that genetic ablation of Tle3 can promote generation of Tcm cells at the expense of Tem cells, and this can occur during the effector phase of the immune response.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21273
9 Samples
Download data: BW
Series
Accession:
GSE213036
ID:
200213036
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