SFX by Ex Libris Inc.

Title:	alpha-Synuclein strains cause distinct synucleinopathies after local and systemic administration
Source:	Nature [0028-0836] Peelaerts, W yr:2015

Basic

Full text

Full text available via Nature

Year:

Volume:

Issue:

Start Page:

Document delivery

Request document via Library/Bibliothek

Users interested in this article also expressed an interest in the following:
description	1.	Nonaka, T. "Prion-like Properties of Pathological TDP-43 Aggregates from Diseased Brains." Cell Reports 4.1 (2013): 124-134.
description	2.	Peelaerts, W. "α-Synuclein strains cause distinct synucleinopathies after local and systemic administration." Nature 522.7556 (2015): 340-4.
description	3.	Brettschneider, J. "Stages of pTDP-43 pathology in amyotrophic lateral sclerosis." Annals of neurology 74.1 (2013): 20-38.
description	4.	Jucker, A. "Aβ seeds resist inactivation by formaldehyde." Acta neuropathologica 128.4 (2014): 477-84.
description	5.	Masuda Suzukake, M. "Prion-like spreading of pathological Î±-synuclein in brain." Brain 136.4 (2013): 1128-1138.
description	6.	Sidle, Katie Claire Louise C. "Review: Prion-like mechanisms of transactive response DNA binding protein of 43 kDa (TDP-43) in amyotrophic lateral sclerosis (ALS)." Neuropathology & applied neurobiology 41.5 (2015): 578-597.
description	7.	Heilbronner, G. "Seeded strain-like transmission of β-amyloid morphotypes in APP transgenic mice." EMBO reports 14.11 (2013): 1017-1022.
description	8.	Morales, R. "De novo induction of amyloid-[beta] deposition in vivo." Molecular Psychiatry Publish Ahead of Print.12 (2011): 266-266.
description	9.	Mougenot, Simon L. "Prion-like acceleration of a synucleinopathy in a transgenic mouse model." Neurobiology of Aging 33.9 (2011): 7-10.
description	10.	Ravits, John M. "ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration." Neurology 73.10 (2009): 805-11.
description	11.	Wakabayashi, K. "Parkinson's disease: the presence of Lewy bodies in Auerbach's and Meissner's plexuses." Acta neuropathologica 76.3 (1988): 217-221.
description	12.	Wichterle, H.. "Directed differentiation of embryonic stem cells into motor neurons." Cell 110.3 (2002): 385-397.
description	13.	Wernig, M. "Neurons derived from reprogrammed fibroblasts functionally integrate into the fetal brain and improve symptoms of rats with Parkinson's disease." Proceedings of the National Academy of Sciences of the United States of America 105.15 (2008): 5856-61.
description	14.	Watts, Joel C. "Transmission of multiple system atrophy prions to transgenic mice." Proceedings of the National Academy of Sciences of the United States of America 110.48 (2013): 19555-19560.
description	15.	Bolmont, T. "Induction of Tau Pathology by Intracerebral Infusion of Amyloid- -Containing Brain Extract and by Amyloid- Deposition in APP x Tau Transgenic Mice." The American journal of pathology 171.6 (2008): 2012-20.
description	16.	Luk, Kelvin C. "Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in mice." The Journal of experimental medicine just published on line.5 (2012): 975-986.
description	17.	Giasson, Benoit I I. "Initiation and synergistic fibrillization of tau and alpha-synuclein." Science 300.5619 (2003): 636-640.
description	18.	Volpicelli Daley, Laura A. "Exogenous α-synuclein fibrils induce Lewy body pathology leading to synaptic dysfunction and neuron death." Neuron 72.1 (2011): 57-71.
description	19.	Clavaguera, F. "Transmission and spreading of tauopathy in transgenic mouse brain." Nature Cell Biology 11.7 (2009): 909-13.
description	20.	Ayers, Jacob I. "Prion-like propagation of mutant SOD1 misfolding and motor neuron disease spread along neuroanatomical pathways." Acta Neuropathologica 131.1 (2016): 103-14.