Transcription profiling of mouse developing T lymphocytes as a model system for discovery of Egr-dependent target genes

ChEBI2008-06-13 更新2026-07-21 收录

Th2细胞转录组学

Egr靶基因发现

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https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-5587 数据链接链接失效反馈

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Transcription profiling of mouse developing T lymphocytes as a model system for discovery of Egr-dependent target genes

创建时间：

2008-06-13

Analysis of difference in transcriptome of Th2 cells derived from Gata3(fl/fl) and Klrg1Cre Gata3(fl/fl) mice. Analysis of difference in transcriptome of Th2 cells derived from Gata3(fl/fl) and Klrg1Cre Gata3(fl/fl) mice

Th2细胞转录组学

条件性基因敲除模型

Purpose: To analyze the transcriptome difference of Th2 cells derived from Gata3(fl/fl) and Klrg1Cre Gata3(fl/fl) mice Method: Lung Th2 cells were used from mice chronically challenged with papain (40

NIAID Data Ecosystem70

RNA seq of vhlfl/fl cd4 cre, hif1afl/fl vhlfl/fl cd4 cre and WT CD4 T cells before and after anti-CD3/CD28 stimulation. RNA seq of vhlfl/fl cd4 cre, hif1afl/fl vhlfl/fl cd4 cre and WT CD4 T cells before and after anti-CD3/CD28 stimulation

Th2细胞转录组学

基因敲除T细胞转录组

Purpose: We compared the transcriptomes of murine CD4 T cells lacking either the vhl gene ( vhlfl/fl cd4 cre (vhl cKO) ) or both vhl and hif1a (hif1afl/fl vhlfl/fl cd4 cre (dcKO)) with WT controls bef

NIAID Data Ecosystem40

Low-input bulk RNA sequencing of thymic, mediastinal adipose tissue, and aortic arch CD4+CD8+ (DP) cells

Th2细胞转录组学

组织驻留免疫细胞分析

Purpose: To establish if and how mediastinal and adipose tissue and aortic arch CD4+CD8+TCRb- cells (DPs) would differ from thymic DPs, we sorted DPs from all three regions by flow cytometry and subje

NIAID Data Ecosystem20

MOESM2 of New insights into the heterogeneity of Th17 subsets contributing to HIV-1 persistence during antiretroviral therapy

HIV潜伏感染

Th2细胞转录组学

Additional file 2. Genome-wide transcriptional profiling of the newly identified CCR6+DN and CCR6+DP subsets relative to the previously characterized Th17/CCR4+CCR6+ cells. See attached document.

Figshare2016-12-14 更新50

RNAseq in NMe wild type and NMe GATA site 1 and 2 homozygous mutant DN3 thymocytes. RNAseq in NMe wild type and NMe GATA site 1 and 2 homozygous mutant DN3 thymocytes

Th2细胞转录组学

急性淋巴细胞白血病

The NOTCH1-driven MYC enhancer (NMe) is essential for T cell development, transformation and the development of acute lymphoblastic leukemia. Here we analyze by RNAseq the gene expression profile of D

NIAID Data Ecosystem40

Transcription profiling of mouse developing T lymphocytes as a model system for discovery of Egr-dependent target genes

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