Article
Microglia produce the amyloidogenic ABri peptide in familial British dementia
2023-06-28
Abstract excerpt
Mutations in ITM2B cause familial British, Danish, Chinese and Korean dementias. In familial British dementia (FBD) a mutation in the stop codon of the ITM2B gene (also known as BRI2 ) causes a C-terminal cleavage fragment of the ITM2B/BRI2 protein to be extended by 11 amino acids. This fragment, termed amyloid-Bri (ABri), is highly insoluble and forms extracellular plaques in the brain. ABri plaques are accomp...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 916ea599-f68a-54b0-9e2b-52c051c5e2e2
- DOI
- 10.1101/2023.06.27.546552
