Back to search

Article

Tryptophan residues in TDP-43 and SOD1 mediate the cross-seeding and toxicity of SOD1

2020-07-28

Abstract excerpt

<h4>ABSTRACT</h4> Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease of motor neurons. Neuronal superoxide dismutase-1 (SOD1) inclusion bodies are characteristic of familial ALS with SOD1 mutations, while a hallmark of sporadic ALS is inclusions containing aggregated wild-type TAR DNA-binding protein 43 (TDP-43). Co-expression of mutant or wild-type TDP-43 with SOD1 leads to misfolding of en...

Topics

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

Identifiers and source

Literature Corpus work
eea77144-8d38-54bc-96e2-08fe44a51b6f
DOI
10.1101/2020.07.27.224188
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.
Tryptophan residues in TDP-43 and SOD1 mediate the cross-seeding and toxicity of SOD1DOI 10.1101/2020.07.27.224188
Select a neighboring publication to make it the new centre.