Back to search

Article

Proteomic Analysis of Huntington’s Disease Medium Spiny Neurons Identifies Alterations in Lipid Droplets

2022-05-11

Abstract excerpt

<h4>ABSTRACT</h4> Huntington’s disease (HD) is a neurodegenerative disease caused by a CAG repeat expansion in the Huntingtin ( HTT ) gene. The resulting polyglutamine (polyQ) tract alters the function of the HTT protein. Although HTT is expressed in different tissues, the medium spiny projection neurons (MSNs) in the striatum are particularly vulnerable in HD. Thus, we sought to define the proteome of human HD...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
c4a0a131-ab65-5158-b33c-be52c62574e4
DOI
10.1101/2022.05.11.491152
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Proteomic Analysis of Huntington’s Disease Medium Spiny Neurons Identifies Alterations in Lipid DropletsDOI 10.1101/2022.05.11.491152
Select a neighboring publication to make it the new centre.