首页/数据集/Transcription profiling of mouse striatum from 3- and 18-month-old Q92 vs. control animals

Transcription profiling of mouse striatum from 3- and 18-month-old Q92 vs. control animals

ChEBI2008-06-15 更新2026-07-21 收录

亨廷顿病模型

年龄相关转录组

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-7958 数据链接链接失效反馈

官方服务：

资源简介：

Transcription profiling of mouse striatum from 3- and 18-month-old Q92 vs. control animals

应用场景：

创建时间：

2008-06-15

亨廷顿病模型

神经类器官

Striato nigral circuit is composed of medium spiny neuronal projections that were mainly sent from striatum to midbrain substantial nigra (SN), which is essential for regulating motor behaviors. Dysfu

NIAID Data Ecosystem110

Huntingtin’s Function in Axonal Transport Is Conserved in Drosophila melanogaster

亨廷顿病模型

轴突运输研究

Huntington’s disease (HD) is a devastating dominantly inherited neurodegenerative disorder caused by an abnormal polyglutamine expansion in the N-terminal part of the huntingtin (HTT) protein. HTT is

NIAID Data Ecosystem40

Autophagy gene expression in rAAV-htt853 injected mice.

自噬基因表达

亨廷顿病模型

Selected autophagy markers were analyzed by qRT-PCR in hypothalamic tissue from mice injected with rAAV5-htt853-79Q or rAAV5-htt853-18Q and uninjected controls, 8 weeks post injection (n = 7/group). T

Figshare2015-12-02 更新10

Euploid HD iPSC lines (e.g. lines with a normal karyotype when first generated) accumulate abnormalities at the same rate as euploid control lines.

干细胞遗传稳定性

亨廷顿病模型

Euploid HD iPSC lines (e.g. lines with a normal karyotype when first generated) accumulate abnormalities at the same rate as euploid control lines.

NIAID Data Ecosystem40

Transcription profiling of mouse model of Huntingdons disease embryonic stem cells with expanded CAG repeats

亨廷顿病模型

干细胞转录组学

Transcription profiling of mouse model of Huntingdons disease embryonic stem cells with expanded CAG repeats

ChEBI2008-06-16 更新20