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Adult and neonatal astrocytes exhibit diverse gene expression profiles during exposure to beta amyloid ex vivo

ChEBI2012-07-13 更新2026-07-21 收录

反应性星形胶质细胞

阿尔茨海默病病理学

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-29317 数据链接链接失效反馈

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Adult and neonatal astrocytes exhibit diverse gene expression profiles during exposure to beta amyloid ex vivo

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2012-07-13

蛋白质聚集机制

阿尔茨海默病病理学

Despite the importance of Aβ aggregation in Alzheimer’s disease etiology, our understanding of the sequence determinants of aggregation is sparse and largely derived from in vitro studies. For example

NIAID Data Ecosystem100

Table1.csv

阿尔茨海默病病理学

脑组织分析

This table contains the histological quantitative data measured in the 3D reconstructed AD brain.

DataCite Commons2025-08-13 更新60

Dynamics of reactive astrocytes fosters tissue regeneration after cuprizone-induced demyelination. Dynamics of reactive astrocytes fosters tissue regeneration after cuprizone-induced demyelination

脱髓鞘疾病模型

反应性星形胶质细胞

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

NIAID Data Ecosystem50

Cell-type specific profiling of human entorhinal cortex at the onset of Alzheimer’s disease neuropathology [scRNA-seq]. Cell-type specific profiling of human entorhinal cortex at the onset of Alzheimer’s disease neuropathology [scRNA-seq]

阿尔茨海默病病理学

单细胞RNA测序

Neurons located in the layer II of the entorhinal cortex (ECII) are the primary site of pathological tau accumulation and neurodegeneration at preclinical stages of Alzheimer's disease (AD). Exploring

NIAID Data Ecosystem60

Additional file 3: of Multiscale network modeling of oligodendrocytes reveals molecular components of myelin dysregulation in Alzheimer’s disease

阿尔茨海默病病理学

少突胶质前体细胞转录组学

Differentially expressed proteins in the MSBB proteomics data set between AD cases and controls in the OL-enriched module (which has been randomly assigned the color name “Yellow”). (TSV 9 kb)

Figshare2017-11-07 更新50

Adult and neonatal astrocytes exhibit diverse gene expression profiles during exposure to beta amyloid ex vivo

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