Elimination of TDP-43 inclusions linked to amyotrophic lateral sclerosis by a misfolding-specific intrabody with dual proteolytic signals-Reference-Cited by-同舟云学术

Elimination of TDP-43 inclusions linked to amyotrophic lateral sclerosis by a misfolding-specific intrabody with dual proteolytic signals

Published:2018-04-16 Issue:1 Volume:8 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Tamaki Yoshitaka,Shodai Akemi,Morimura Toshifumi,Hikiami Ryota,Minamiyama Sumio,Ayaki Takashi,Tooyama Ikuo^ORCID,Furukawa Yoshiaki,Takahashi Ryosuke,Urushitani Makoto^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-018-24463-3.pdf

Reference58 articles.

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2. Brown, R. H. & Al-Chalabi, A. Amyotrophic Lateral Sclerosis. N Engl. J. Med. 377, 162–172 (2017).

3. Philips, T. & Rothstein, J. D. Glial cells in amyotrophic lateral sclerosis. Exp. Neurol. 262, 111–120 (2014).

4. Taylor, J. P., Brown, R. H. Jr. & Cleveland, D. W. Decoding ALS: from genes to mechanism. Nature 539, 197–206 (2016).

5. Arai, T. et al. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem. Biophys. Res. Commun. 351, 602–611 (2006).

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