Analysis of gene expression in CD8+ T cells activated in vitro or in vivo

ChEBI2014-07-13 更新2026-07-21 收录

免疫细胞转录组学

细胞激活机制

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-58081 数据链接链接失效反馈

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Analysis of gene expression in CD8+ T cells activated in vitro or in vivo

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2014-07-13

Transcriptome data of WT and Ddb1-KO activated CD4+ T cells

免疫细胞转录组学

基因敲除效应

The goals of this study are to compare the transcriptome profiling (RNA-seq) of wild type and Ddb1-knock out activated CD4+ T cells We sorted Ddb1-KO and WT SMARTA cells in adoptive transfer experimen

NIAID Data Ecosystem60

RNA expression in CCL19-treated CD4+ T cells

免疫细胞转录组学

趋化因子信号通路

Transcriptome analysis of mouse naÃ¯ve CD4+ T cells with or witout chemokine CCL19 treatment. Overall design: Purified naÃ¯ve CD4+ T cells (1 million) were cultured in 200 microlitter complete RPMI164

NIAID Data Ecosystem40

Salt augments macrophage-driven host defense in the skin. Salt augments macrophage-driven host defense in the skin

皮肤抗菌免疫

细胞激活机制

Immune cells regulate a hypertonic microenvironment in the skin; however, possible functions of increased skin Na+ concentrations are unknown. We found that Na+ accumulated at the site of bacterial sk

NIAID Data Ecosystem30

Table_1_Modifications of the Transcriptomic Profile of Autoreactive B Cells From Pemphigus Patients After Treatment With Rituximab or a Standard Corticosteroid Regimen.docx

自身免疫病精准治疗

免疫细胞转录组学

Pemphigus Vulgaris is an autoimmune disease of the skin and mucous membranes, which is due to the production of pathogenic autoantibodies targeting desmoglein (DSG) 1 and 3, which are adhesion protein

NIAID Data Ecosystem50

Bulk RNA-seq of murine ?dT17 and ?dT1 cells from the lamina propria and peripheral lymph nodes of wild-type mice

免疫细胞转录组学

黏膜免疫

This experiment was designed to explore the transcriptional programs of ?dT17 and ?dT1 cells isolated from the lamina propria and peripheral lymph nodes. For this purpose, we sorted intestinal ?dT17 (

NIAID Data Ecosystem30

Analysis of gene expression in CD8+ T cells activated in vitro or in vivo

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