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Links from GEO DataSets

Items: 19

1.
Full record GDS2741

TCR-alpha/beta CD8-alpha/alpha intestinal intraepithelial lymphocytes

Analysis of TCR-alpha/beta CD8-alpha/alpha intestinal intraepithelial lymphocytes (IELs). Results provide insight into the function of TCR-alpha/beta CD8-alpha/alpha IELs in the mucosal immune system.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 cell type sets
Platform:
GPL81
Series:
GSE5355
6 Samples
Download data
DataSet
Accession:
GDS2741
ID:
2741
2.

Microarray Analysis of Murine IEL Subsets

(Submitter supplied) Mouse small intestine intraepithelial lymphocytes (IEL) that express a ab TCR and CD8aa homodimers are an enigmatic T cell subset, as their specificity and in vivo function remain to be defined. To gain insight into the nature of these cells, we performed global gene expression profiling using microarray analysis, combined with PCR and flow cytometry to determine the level of expression of selected genes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2741
Platform:
GPL81
6 Samples
Download data
Series
Accession:
GSE5355
ID:
200005355
3.

Global expression profiling of peripheral Qa-1 class Ib-restricted CD8aa+TCRab+ regulatory T Cells reveals innate-like features: implications for immune regulatory repertoire

(Submitter supplied) To better understand the function of CD8aa Tregs, we have recently characterized several CD8aa+TCRab+ T cell clones and lines that are physiologically primed and are involved in recovery and protection from EAE (REF). In this report, we present a comparison of global gene expression patterns in CD8aa Tregs versus OT-1 CD8aa+TCRab+ T cells. The results of microarray data analysis are confirmed by real-time PCR and flow cytometry for better accuracy and phenotype expression. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE22985
ID:
200022985
4.

Gene expressions of TCRαβ+ CD8αα+ intraepithelial lymphocyte (IELs) in the small intestine with or without Rbpj gene

(Submitter supplied) cDNA microarray data of TCRαβ+ CD8αα+ IELs in the small intestine with or without Rbpj gene
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
2 Samples
Download data: TXT
Series
Accession:
GSE117122
ID:
200117122
5.

Genome-wide maps of chromatin state in mouse small intestinal intraepithelial lymphocytes.

(Submitter supplied) We performed CUT&Tag-Seq against histone H3K27me3 in mouse small intestinal TCRβ+CD8αα+ intraepithelial lymphocytes (IELs) of wild-type mice to analyze epigenetic modifications.
Organism:
Mus musculus
Type:
Other
Platform:
GPL24247
1 Sample
Download data: BIGWIG
Series
Accession:
GSE185798
ID:
200185798
6.

Kdm6b is required for the maturation and function of intestinal TCRβ+CD8αα+ intraepithelial lymphocytes

(Submitter supplied) To under the role of Kdm6b in the regulation of intestinal TCRβ+CD8αα+ intraepithelial lymphocytes (IELs), Kdm6b was conditionally deleted in mouse T cells. Small intestinal TCRβ+CD8αα+ IELs were sorted by flow cytometry and RNA-seq was conducted to identify the differentially expressed genes.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: TXT
Series
Accession:
GSE154444
ID:
200154444
7.

Single-cell ATAC of WT thymic IEL precursors (IELp)

(Submitter supplied) To examine the chromatin accessibility of IELp, single cell epigenomic analysis of IELp from control mice (Cd4 Cre–Lrffl/fl) were determined by scATACseq
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL30172
2 Samples
Download data: CSV, H5, TBI, TSV
Series
Accession:
GSE186291
ID:
200186291
8.

Single-cell Gene expression of WT CD8aa IEL and LRF-deficient CD8aa splenocytes

(Submitter supplied) To examine how the cluster composition of CD8aa IEL and their transcriptomic signatures were affected by LRF disruption, single-cell gene expression of CD8aa IEL from control (Cd4 Cre–Lrffl/fl) and CD8aa splenocytes from LRF KO (Cd4 Cre+Lrffl/fl ) mice were determined by scRNAseq.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21626
4 Samples
Download data: H5
Series
Accession:
GSE186164
ID:
200186164
9.

LRF genome-wide occupancy in CD4+ T cells

(Submitter supplied) To examine whether LRF protein could bind cis-regulatory elements in the genes that LRF regulates. We performed Chromatin immunoprecipitation followed by deep-sequencing (ChIPseq) on activated T cells using an in vivo biotinylation and streptavidin pull-down approach.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
6 Samples
Download data: BW
Series
Accession:
GSE149993
ID:
200149993
10.

Single-cell Gene expression of WT and LRF-deficient thymic IEL precusors (IELp)

(Submitter supplied) To examine how the cluster composition of IELp and their transcriptomic signatures were affected by LRF disruption, single-cell gene expression of IELp from control (Cd4 Cre–Lrffl/fl) and LRF KO(Cd4 Cre+Lrffl/fl )mice were determined by scRNAseq
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: H5, MTX, TSV
Series
Accession:
GSE149985
ID:
200149985
11.

Gene expression in WT and LRF-deficient thymic IEL precusors (IELp) and their progeny CD8aa IEL

(Submitter supplied) Gene expression of IELp and CD8aa IEL was determined by RNAseq
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
12 Samples
Download data: CSV
Series
Accession:
GSE149943
ID:
200149943
12.

HNF4A regulation of transcription profiles in the mouse intestinal epithelial cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30172
22 Samples
Download data
Series
Accession:
GSE199417
ID:
200199417
13.

HNF4A regulation of transcription profiles in the mouse ileal and colonic epithelial cells

(Submitter supplied) Purpose: HNF4A is a highly conserved nuclear receptor that has been associated with inflammatory bowel diseases. The goal of this study is to determine and compare transcriptional regulation by HNF4A in the small intestine and large intestine in mice. Methods: Intestinal epithelial cells (IECs) were flow sorted from the ileum and colon of WT and HNF4A IEC-specific KO mice at 21~22 days old and sequenced for transcriptome. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30172
16 Samples
Download data: CSV
Series
Accession:
GSE199416
ID:
200199416
14.

HNF4A regulation of transcription profiles in the mouse cecal epithelial cells

(Submitter supplied) Purpose: HNF4A is a highly conserved nuclear receptor that has been associated with inflammatory bowel diseases. The goal of this study is to determine transcriptional regulation by HNF4A in the cecal IECs.. Methods: Intestinal epithelial cells (IECs) were sorted from the ceca of young adult WT and HNF4A IEC-specific KO mice and sequenced for transcriptome. Differentially expressed genes comparing the WT and HNF4A IEC-KO were determined. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30172
6 Samples
Download data: CSV
Series
Accession:
GSE199415
ID:
200199415
15.

Single cell analysis revealed that two distinct, unique CD4+ T cell subsets were increased in the small intestinal intraepithelial lymphocytes of aged mice

(Submitter supplied) Recent advances in research suggest that aging has a controllable chronic inflammatory disease aspect. Aging systemic T cells, which secrete pro-inflammatory factors, affect surrounding somatic cells, and accelerate the aging process through chronic inflammation, have attracted attention as potential therapeutic targets in aging. On the other hand, there are few reports on the aging of the intestinal immune system, which differs from the systemic immune system in many ways. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL24247
7 Samples
Download data: CSV, MTX, TSV, TXT
Series
Accession:
GSE252360
ID:
200252360
16.

Single cell analysis revealed that two distinct, unique CD4+ T cell subsets were increased in the small intestinal intraepithelial lymphocytes of aged mice

(Submitter supplied) Recent advances in research suggest that aging has a controllable chronic inflammatory disease aspect. Aging systemic T cells, which secrete pro-inflammatory factors, affect surrounding somatic cells, and accelerate the aging process through chronic inflammation, have attracted attention as potential therapeutic targets in aging. On the other hand, there are few reports on the aging of the intestinal immune system, which differs from the systemic immune system in many ways. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL22438
6 Samples
Download data: TXT
Series
Accession:
GSE249501
ID:
200249501
17.

Human MAIT and CD8++ cell development

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
17 Samples
Download data: CEL
Series
Accession:
GSE33425
ID:
200033425
18.

Expression data from human cord blood CD161++/CD161+/CD161- CD8+ T cell subsets

(Submitter supplied) We used microarray to compare gene expression between CD161++/CD161+/CD161-CD8+ T cells from human cord blood.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
9 Samples
Download data: CEL
Series
Accession:
GSE33424
ID:
200033424
19.

Expression data from healthy human CD161++CD8aa and CD161++CD8ab T cells

(Submitter supplied) We used microarrays to compare gene expression between healthy human CD161++CD8aa and CD161++CD8ab T cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE33374
ID:
200033374
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