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Items: 3

1.

Mutant Huntingtin promotes neuronal death through cell autonomous microglial activation via myeloid lineage- determining factors

(Submitter supplied) Huntington's Disease (HD) is a fatal neurodegenerative disorder caused by an extended polyglutamine repeat in the N-terminus of the huntingtin (Htt) protein. Reactive microglia and elevated cytokine levels are observed in the brains of HD patients, but the extent to which neuroinflammation results from extrinsic or cell-autonomous mechanisms is unknown. Furthermore, the impact of microglia activation on the pathogenesis of HD remains to be established. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11002 GPL13112
22 Samples
Download data: BED, TXT
Series
Accession:
GSE54443
ID:
200054443
2.

Illumina Genome Analyzer IIx (Mus musculus)

Platform
Accession:
GPL11002
ID:
100011002
3.

BV2-RNAseq-notx-48h-Nmu

Organism:
Mus musculus
Source name:
BV2 cells
Platform:
GPL11002
Series:
GSE54443
Download data
Sample
Accession:
GSM1315473
ID:
301315473
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db=gds|term=GSM1315473[Accession]|query=1|qty=2|blobid=MCID_67490db143705129cf50eaa5|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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