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Human CD14+CD16- and CD16+ monocyte-derived macrophages primed by GM-CSF or M-CSF

ChEBI2015-04-21 更新2026-07-21 收录

巨噬细胞极化

单核细胞亚群功能

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-68061 数据链接链接失效反馈

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资源简介：

Human CD14+CD16- and CD16+ monocyte-derived macrophages primed by GM-CSF or M-CSF

应用场景：

创建时间：

2015-04-21

巨噬细胞极化

转录组分析

Alveolar macrophages (AMs), the tissue dwelling monocytes of the lungs, are the first to encounter the menagerie of items that pass the mechanical barriers of the nose and throat. AMs must be able to

NIAID Data Ecosystem60

Tumor-associated macrophages (TAMs) with or without HRS knockdown (KD)

巨噬细胞极化

肿瘤微环境

To study the mechanism by which HRS regulates macrophage polarization, we performed bulk RNA sequencing on TAMs with or without HRS KD. Overall design: Enriched human monocytes were obtained from heal

NIAID Data Ecosystem20

Homo sapiens Raw sequence reads. Homo sapiens

RNA测序分析

巨噬细胞极化

RNA-Seq read of human THP-1 knockdown of MNDA after induction into M2 macrophages

NIAID Data Ecosystem10

Herpesvirus-encoded microRNA dysregulate M1 and M2 macrophage miRNA profiles. Herpesvirus-encoded microRNA dysregulate M1 and M2 macrophage miRNA profiles

病毒miRNA调控

巨噬细胞极化

Primary human M1 and M2 macrophages were transfected with different human herpesvirus-derived viral miRNA and the impact on the cellular microRNAs was profiled using microarray. Viral miRNA-mediated i

NIAID Data Ecosystem40

DataSheet5_Three-Dimensionally Printed Ti2448 With Low Stiffness Enhanced Angiogenesis and Osteogenesis by Regulating Macrophage Polarization via Piezo1/YAP Signaling Axis.zip

YAP信号通路

巨噬细胞极化

Previous studies have found that the novel low-elastic-modulus Ti2448 alloy can significantly reduce stress shielding and contribute to better bone repair than the conventional Ti6Al4V alloy. In this

NIAID Data Ecosystem20

Human CD14+CD16- and CD16+ monocyte-derived macrophages primed by GM-CSF or M-CSF

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