Modeling sporadic ALS in iPSC-derived motor neurons identifies a potential therapeutic agent-Reference-Cited by-同舟云学术

Modeling sporadic ALS in iPSC-derived motor neurons identifies a potential therapeutic agent

Published:2018-08-20 Issue:10 Volume:24 Page:1579-1589
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Fujimori Koki,Ishikawa Mitsuru,Otomo Asako,Atsuta Naoki,Nakamura Ryoichi,Akiyama Tetsuya,Hadano Shinji,Aoki Masashi,Saya Hideyuki^ORCID,Sobue Gen,Okano Hideyuki

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/s41591-018-0140-5.pdf

Reference58 articles.

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4. 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).

5. Neumann, M. et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314, 130–133 (2006).

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