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RNA-Seq analysis to profile the transcriptome of Bone Marrow Dendritic Cells exposed to different antigen delivery systems

ChEBI2015-03-01 更新2026-07-21 收录

免疫细胞转录组学

抗原递送

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-60231 数据链接链接失效反馈

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资源简介：

RNA-Seq analysis to profile the transcriptome of Bone Marrow Dendritic Cells exposed to different antigen delivery systems

应用场景：

创建时间：

2015-03-01

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

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Gene expression profiling of small intestine (SI) NKp46+RORgt+ and NKp46+RORgt- Innate Lymphoid Cells (ILCs). Mus musculus

免疫细胞转录组学

细胞功能分析

The aim of this study was to analyze the global transcriptional profiles of small intestine (SI) Innate Lymphoid Cells (ILCs) expressing the NK cell marker NKp46. Based on differential expression of t

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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 (

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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

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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

RNA-Seq analysis to profile the transcriptome of Bone Marrow Dendritic Cells exposed to different antigen delivery systems

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