Human PSEN1 Mutant Glia Improve Spatial Learning and Memory in Aged Mice
The <i>PSEN1</i> ΔE9 mutation causes a familial form of Alzheimer’s disease (AD) by shifting the processing of amyloid precursor protein (APP) towards the generation of highly amyloidogenic Aβ42 peptide. We have previously shown that the <i>PSEN1</i> ΔE9 mutation in human-ind...
Main Authors: | Henna Jäntti, Minna Oksanen, Pinja Kettunen, Stella Manta, Lionel Mouledous, Hennariikka Koivisto, Johanna Ruuth, Kalevi Trontti, Hiramani Dhungana, Meike Keuters, Isabelle Weert, Marja Koskuvi, Iiris Hovatta, Anni-Maija Linden, Claire Rampon, Tarja Malm, Heikki Tanila, Jari Koistinaho, Taisia Rolova |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-12-01
|
Series: | Cells |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4409/11/24/4116 |
Similar Items
-
UNVEIL PERICYTE INVOLVEMENT IN VASCULAR DYSFUNCTION IN ALZHEIMER'S DISEASE USING AN IPSC-DERIVED MODEL
by: Ying Chieh Wu, et al.
Published: (2023-10-01) -
A pedigree study on early ⁃ onset Alzheimer's disease associated with PSEN2 V214L mutation
by: Hong⁃qian CAI, et al.
Published: (2023-04-01) -
Early⁃onset Alzheimer's disease caused by PSEN1 gene mutation: two cases reports and literature review
by: ZHANG Yuan, et al.
Published: (2021-11-01) -
Spastic paraplegia preceding PSEN1‐related familial Alzheimer's disease
by: Viorica Chelban, et al.
Published: (2021-01-01) -
Genetics, Functions, and Clinical Impact of Presenilin-1 (PSEN1) Gene
by: Jaya Bagaria, et al.
Published: (2022-09-01)