M0+EXO(C) VS M0+EXO(S)

NIAID Data Ecosystem2026-05-01 收录

肝肾疾病分子机制

外泌体介导的免疫调节

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1004757 数据链接链接失效反馈

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资源简介：

mRNA profiles of macrophages with the stimulation of EXO(C) or EXO(S).EXO(C): exosomes derived from HK2 cells without the stimulation of CaOx stones.EXO(S): exosomes derived from HK2 cells with the stimulation of CaOx stones.

创建时间：

2023-08-12

Transcriptomic analyses of the effects of hepatic insulin signaling on hepatic gene expression in the PiZ mouse model of alpha-1-antitrypsin deficiency liver disease

肝肾疾病分子机制

胰岛素信号通路

RNA-Seq data on livers from 4-5 month old male PiZ mice with or without genetic disruption of insulin receptor and FOXO1 hepatic expression Analyses of WT, Z, and ZZ mice, WT v LIRKO v LIRKO-FOXO1-KO

NIAID Data Ecosystem50

Mesenchymal Stromal Cell-Derived Exosomes Attenuate Myocardial Ischemia-Reperfusion Injury through miR-182-Regulated Macrophage Polarization

外泌体介导的免疫调节

心肌缺血再灌注损伤修复

Aims: Mesenchymal stem cells (MSCs) gradually become attractive candidates for cardiac inflammation modulation, yet understanding of the mechanism remains elusive. Strikingly, recent studies indicated

NIAID Data Ecosystem20

Transcriptome profile of liver biopsy tissues from patients with non-alcoholic fatty liver disease. Transcriptome profile of liver biopsy tissues from patients with non-alcoholic fatty liver disease

非酒精性脂肪肝转录组学

肝肾疾病分子机制

This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series

NIAID Data Ecosystem20

A single-nucleus RNA-sequencing pipeline to decipher the molecular anatomy and pathophysiology of human kidneys

肾脏单细胞转录组

肝肾疾病分子机制

Defining cellular and molecular identities within the kidney is necessary to understand its organization and function in health and disease. Here we demonstrate a reproducible method with minimal arti

NIAID Data Ecosystem30

Effect of ApoE in communicating CD4+ T cell activation and proliferation. Effect of ApoE in communicating CD4+ T cell activation and proliferation

细胞信号传导

外泌体介导的免疫调节

While ApoE expression by myeloid cells is recognized to control inflammation, whether such benefits can be communicated via extracellular vesicles including exosomes is not known. Through the study of

NIAID Data Ecosystem20

M0+EXO(C) VS M0+EXO(S)

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