Extracellular vesicles derived from postmortem human brain tissue contain seed‐competent C‐terminal tau fragments, and provide proteomic clues to the identity of selectively vulnerable cell populations in human tauopathies
Stephanie L. Fowler(University of Oxford), Karen Duff(UK Dementia Research Institute), Sumi Bez(UK Dementia Research Institute), Nancy E. Hernandez Villegas, Efrat Levy(Nathan Kline Institute for Psychiatric Research), Ari W. Schaler(Columbia University Irving Medical Center), Pallavi Gaur(Columbia University Irving Medical Center), Emir Turkes(UK Dementia Research Institute), Chelsea Miller(Nathan Kline Institute for Psychiatric Research), Rocío Pérez‐González(Nathan Kline Institute for Psychiatric Research)
Cited by 1
Related Papers
Inhibition of glycogen synthase kinase-3 by lithium correlates with reduced tauopathy and degeneration<i>in vivo</i>
|Proceedings of the National Academy of Sciences|2005|693
Anesthesia Leads to Tau Hyperphosphorylation through Inhibition of Phosphatase Activity by Hypothermia
|Journal of Neuroscience|2007|389
Genetic dissection of Alzheimer's disease and related dementias: amyloid and its relationship to tau
|Nature Neuroscience|1998|344
5′ Splice Site Mutations in tau Associated with the Inherited Dementia FTDP-17 Affect a Stem-Loop Structure That Regulates Alternative Splicing of Exon 10
|Journal of Biological Chemistry|1999|299