Back to search

Article

Droplets of amyotrophic lateral sclerosis-associated p62/SQSTM1 mutants show slower inner fluidity

2021-06-07

Abstract excerpt

<h4>Summary</h4> A series of amyotrophic lateral sclerosis (ALS)-related proteins such as FUS, TDP-43 and hnRNPA1 has an ability to be liquid-liquid phase separation, and their disease-related mutations cause the transition of their responsible liquid droplets to aggregates. Missense mutations in SQSTM1/p62 , which have been identified throughout the gene, are associated with ALS, frontotemporal degeneration (FT...

Topics

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

Identifiers and source

Literature Corpus work
13d3d05f-c17f-5348-b9e2-2e5937287ebc
DOI
10.1101/2021.06.07.447422
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.
Droplets of amyotrophic lateral sclerosis-associated p62/SQSTM1 mutants show slower inner fluidityDOI 10.1101/2021.06.07.447422
Select a neighboring publication to make it the new centre.