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A transcriptional signature of fatigue derived from patients with primary SjÃ¶gren's Syndrome

ChEBI2015-12-31 更新2026-07-12 收录

自身免疫性疾病转录组学

疲劳生物标志物发现

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-66795 数据链接链接失效反馈

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资源简介：

A transcriptional signature of fatigue derived from patients with primary SjÃ¶gren's Syndrome

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创建时间：

2015-12-31

基因表达量化

自身免疫性疾病转录组学

Data relevant to a 2021 study of SSc transcriptomes. This file contains counts of all sequencing reads that overlap at least a single base with the start and end of a known gene on the correct strand.

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Whole Blood Transcriptome Profiling in Juvenile Idiopathic Arthritis and Inflammatory Bowel Disease. Whole Blood Transcriptome Profiling in Juvenile Idiopathic Arthritis and Inflammatory Bowel Disease

自身免疫性疾病转录组学

疾病亚型基因表达差异

We report whole blood gene expression of 12 healthy controls and 190 patients with either oligoarticular (n=43), polyarticular (n=46), or systemic JIA (n=26), or Crohn's disease (n=60) and ulcerative

NIAID Data Ecosystem60

Healthy control samples for Juvenile Sjogrens Syndrome (JSS) Transcriptome Study

自身免疫性疾病转录组学

单细胞RNA测序

To investigate the inflammatory signature and transcriptomical changes in CD14 positive monocytes, we have isolated and purified monocytes cells from whole blood. Bulk RNA-seq were conducted with an I

NIAID Data Ecosystem40

Transcriptome analysis of CD14+ monocytes from SSc patients

自身免疫性疾病转录组学

单核细胞病理

Purpose: To compare transcriptome profile of CD14+ blood monocytes from systemic sclerosis (SSc) patients and healthy controls. Methods: CD14+ monocytes were isolated from peripheral blood of lcSSc (n

NIAID Data Ecosystem70

RNA-sequencing of ILC3 during murine EAE. RNA-sequencing of ILC3 during murine EAE

自身免疫性疾病转录组学

固有淋巴细胞功能

To determine the unique gene expression profile of central nervous system (CNS)-associated ILC3, we performed RNA-sequencing on sort-purified ILC3 from the CNS, cervical lymph nodes (cLN) and small in

NIAID Data Ecosystem50

A transcriptional signature of fatigue derived from patients with primary SjÃ¶gren's Syndrome

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