TDP-43 and Cytoskeletal Proteins in ALS-Reference-Cited by-同舟云学术

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TDP-43 and Cytoskeletal Proteins in ALS

Published:2017-05-02 Issue:4 Volume:55 Page:3143-3151
ISSN:0893-7648
Container-title:Molecular Neurobiology
language:en
Short-container-title:Mol Neurobiol

Author:

Oberstadt Moritz,Claßen Joseph,Arendt Thomas,Holzer Max

Funder

EU funds (EFRE; SAB)

Deutsche Gesellschaft für Muskelkranke

Publisher

Springer Science and Business Media LLC

Subject

Neuroscience (miscellaneous),Cellular and Molecular Neuroscience,Neurology

Link

http://link.springer.com/article/10.1007/s12035-017-0543-1/fulltext.html

Reference101 articles.

1. Morgan S, Orrell RW (2016) Pathogenesis of amyotrophic lateral sclerosis. Br Med Bull. doi: 10.1093/bmb/ldw026

2. Brettschneider J, Arai K, Del Tredici K, Toledo JB, Robinson JL, Lee EB, Kuwabara S, Shibuya K et al (2014) TDP-43 pathology and neuronal loss in amyotrophic lateral sclerosis spinal cord. Acta Neuropathol 128(3):423–437. doi: 10.1007/s00401-014-1299-6

3. Feiler MS, Strobel B, Freischmidt A, Helferich AM, Kappel J, Brewer BM, Li D, Thal DR et al (2015) TDP-43 is intercellularly transmitted across axon terminals. J Cell Biol 211(4):897–911. doi: 10.1083/jcb.201504057

4. Spiller KJ, Cheung CJ, Restrepo CR, Kwong LK, Stieber AM, Trojanowski JQ, Lee VM (2016) Selective motor neuron resistance and recovery in a new inducible mouse model of TDP-43 proteinopathy. J Neurosci 36(29):7707–7717. doi: 10.1523/JNEUROSCI.1457-16.2016

5. Gershoni-Emek N, Chein M, Gluska S, Perlson E (2015) Amyotrophic lateral sclerosis as a spatiotemporal mislocalization disease: location, location, location. Int Rev Cell Mol Biol 315:23–71. doi: 10.1016/bs.ircmb.2014.11.003

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