GSM5201416[Accession] - GEO DataSets - NCBI

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Items: 4

Select item 2001693861.

Transcriptional profiling of brain tissues from a Q130 Long Evans Knock-in rat model of Huntington’s disease at 10-, 19- and 24-months of age

(Submitter supplied) Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder that is characterized by motor, cognitive, and psychiatric alterations. The mutation responsible for this disease is an abnormally expanded and unstable CAG repeat within the coding region of the gene encoding huntingtin (Htt). A collaboration between the CHDI Foundation and Dr. H.P. Nguyen (huu.nguyen-r7w@ruhr-uni-bochum.de) at Universitat Bochum focused on generating a knock-in rat model of HD that contains expanded CAG repeats inserted within the rat huntingtin gene (Hdh) in order to provide a genetic reconstruction of the human causative mutation within the rat model. more...

Organism:: Rattus norvegicus

Type:: Expression profiling by high throughput sequencing

Platform:: GPL25947
145 Samples

Download data: TXT

Series

Accession:: GSE169386

ID:: 200169386

SRA Run Selector

Select item 2001693882.

Transcriptional profiling of brain tissues from a Q130 Long Evans Knock-in rat model of Huntington’s disease at 2-, 6-, 10-, 12-, 19- and 24-months of age

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.

Organism:: Rattus norvegicus

Type:: Expression profiling by high throughput sequencing

Platforms:: GPL25947 GPL14844
397 Samples

Series

Accession:: GSE169388

ID:: 200169388

Select item 1000259473.

Illumina NovaSeq 6000 (Rattus norvegicus)

Organism:: Rattus norvegicus

602 Series
12522 Samples

Platform

Accession:: GPL25947

ID:: 100025947

Select item 3052014164.

WT Cortex 10 months male mRNA rep1 [10_19_24_mo]

Organism:: Rattus norvegicus

Source name:: Cortex

Platform:: GPL25947
Series:: GSE169386 GSE169388

Sample

Accession:: GSM5201416

ID:: 305201416

SRA Run Selector

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GSM5201416[Accession] (4)
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