UMB Dataset
Single-Nucleus RNA-Seq Reveals Dysregulation of Striatal Cell Identity Due to Huntington’s Disease Mutations
UID: 204
- Description
- The involvement of specific medium spiny neuro (MSN) subtype and of other striatal cell types remains poorly understood. To gain insight into cell type-specific disease processes, researchers studied the nuclear transcriptomes of 4524 cells from the striatum of a genetically precise knock-in mouse model of the Huntington's Disease (HD) mutation, HttQ175/1. Three 14-month-old and one 15-month-old male mice were used to generate the primary dataset.
- Timeframe
- 2020
- Geographic Coverage
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Ethiopia
Access
- Restrictions
-
Unrestricted access
- Instructions
- Access data via article and the Gene Expression Analysis Resources
BioPulverizer
MoxiGo cytometer
Observational
- Grant Support
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R24 MH114815/BRAIN Initiative