TRE-Htt-N853 Huntington's Disease in vitro model
收藏Alliance of Genome Resources2026-08-01 收录
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Keywords: gene expression study
关键词：基因表达（gene expression）研究
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Additional file 9 of Common disease signatures from gene expression analysis in Huntingtonâs disease human blood and brain
Synapse signature. In this file we include detailed information about the synapse signature, including the annotations and gene identifiers of each module that participates in this signature. (XLS 12.
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Additional file 5: Table S4. of Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntingtonâs disease are not reflected in mutant Huntingtin inclusion prevalence
Over-representation analysis of the 2557 genes nominally significantly differentially expressed between YAC128 and WT striata (XLS 61 kb)
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DataSheet8_A Systematic Review of Transcriptional Dysregulation in Huntington’s Disease Studied by RNA Sequencing.XLSX
Huntington’s disease (HD) is a chronic neurodegenerative disorder caused by an expansion of polyglutamine repeats in exon 1 of the Huntingtin gene. Transcriptional dysregulation accompanied by epigene
NIAID Data Ecosystem30
Additional file 9 of Common disease signatures from gene expression analysis in Huntingtonâs disease human blood and brain
Synapse signature. In this file we include detailed information about the synapse signature, including the annotations and gene identifiers of each module that participates in this signature. (XLS 12.
Figshare2016-12-14 更新50
Striatal gene expression profile of the YAC 128 mouse
The Yeast Artificial Chomosome (YAC) 128 model of Huntington's disease shows substantial deficits in motor, learning and memory tasks and alterations in its transcriptional profile. We examined the ch
NIAID Data Ecosystem40
