In vitro prion-like behaviour of TDP-43 in ALS-Reference-Cited by-同舟云学术

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In vitro prion-like behaviour of TDP-43 in ALS

Published:2016-12 Issue: Volume:96 Page:236-247
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Smethurst Phillip,Newcombe Jia,Troakes Claire,Simone Roberto,Chen Yun-Ru,Patani Rickie,Sidle Katie

Funder

Leasing Foundation

National Institute for Health Research University College London Hospitals Biomedical Research Centre

Wellcome trust

Publisher

Elsevier BV

Subject

Neurology

Reference70 articles.

1. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis;Arai;Biochem. Biophys. Res. Commun.,2006

2. Structural determinants of the cellular localization and shuttling of TDP-43;Ayala;J. Cell Sci.,2008

3. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration;Benajiba;Ann. Neurol.,2009

4. Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease;Borroni;Hum. Mutat.,2009

5. Structural and functional characterization of two alpha-synuclein strains;Bousset;Nat. Commun.,2013

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