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TTP binding site atlas in the macrophage transcriptome reveals a switch for inflammation resolution

ChEBI2016-05-17 更新2026-07-12 收录

炎症转录调控

巨噬细胞功能

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-63468 数据链接链接失效反馈

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资源简介：

TTP binding site atlas in the macrophage transcriptome reveals a switch for inflammation resolution

应用场景：

创建时间：

2016-05-17

巨噬细胞功能

核糖体RNA加工调控

The goal of this study is to compare NGS-derived wild-type Raw264.7 transcriptome profiling (RNA-seq) to NGS-derived Fibrillarin knockdown (Fbl+/-) Raw264.7 RNA-seq. The mRNA profiles of wild-type Raw

NIAID Data Ecosystem50

Genome-wide maps of chromatin accessibility changes in bone marrow derived macrophages (BMDMs) isolated from Baf60a KO or WT mice

染色质可及性

巨噬细胞功能

Bone marrow cells from Baf60a KO or WT mice were differentiated into BMDMs and treated with or without oxLDL for 48h. Quantification of chromatin accessibility and transcription factor footprints in

NIAID Data Ecosystem40

Immune Clearance of Periodontal Pathogens Depends on Autophagy in Macrophages

牙周病免疫机制

巨噬细胞功能

Autophagy is known to eliminate intracellular microorganisms or damaged organelles, control inflammation and suppress adaptive immunity. Although some evidence suggests a relationship between Porphyro

NIAID Data Ecosystem30

PMACS-107

心肌梗死免疫调节

巨噬细胞功能

Project title : PMACS-107 Grant Information: AHA Grant 9TPA34910007, Regulatory role of pericardial macrophages in myocardial infarction Project Description: · Animal Model: Myocardia

DataCite Commons2025-03-11 更新50

H3K27me3 occupancy in primary human peripheral blood derived- macrophages. H3K27me3 occupancy in primary human peripheral blood derived- macrophages

表观遗传学

巨噬细胞功能

H3K27me3 in Primary Human Peripheral blood-derived macrophages Overall design: Fresh human peripheral blood derived macrophages from healthy donors

NIAID Data Ecosystem40