Review: Prion-like mechanisms of transactive response DNA binding protein of 43 kDa (TDP-43) in amyotrophic lateral sclerosis (ALS)-Reference-Cited by-同舟云学术

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Review: Prion-like mechanisms of transactive response DNA binding protein of 43 kDa (TDP-43) in amyotrophic lateral sclerosis (ALS)

Published:2015-04-20 Issue:5 Volume:41 Page:578-597
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Smethurst Phillip¹,Sidle Katie Claire Louise¹,Hardy John¹

Affiliation:

1. Department of Molecular Neuroscience; UCL Institute of Neurology; Queen Square House; London UK

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Reference194 articles.

1. Amyotrophic lateral sclerosis;Wijesekera;Orphanet J Rare Dis,2009

2. The seeds of neurodegeneration: prion-like spreading in ALS;Polymenidou;Cell,2011

3. ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration;Ravits;Neurology,2009

4. Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis;Chia;PLoS ONE,2010

5. Intracellular seeded aggregation of mutant Cu,Zn-superoxide dismutase associated with amyotrophic lateral sclerosis;Furukawa;FEBS Lett,2013

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