ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repair-Reference-Cited by-同舟云学术

ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repair

Published:2019-01-14 Issue:2 Volume:22 Page:167-179
ISSN:1097-6256
Container-title:Nature Neuroscience
language:en
Short-container-title:Nat Neurosci

Author:

Klim Joseph R.^ORCID,Williams Luis A.,Limone Francesco,Guerra San Juan Irune,Davis-Dusenbery Brandi N.,Mordes Daniel A.,Burberry Aaron,Steinbaugh Michael J.,Gamage Kanchana K.,Kirchner Rory,Moccia Rob,Cassel Seth H.,Chen Kuchuan,Wainger Brian J.,Woolf Clifford J.^ORCID,Eggan Kevin^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Neuroscience

Link

http://www.nature.com/articles/s41593-018-0300-4.pdf

Reference61 articles.

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3. Miller, R. G., Mitchell, J. D. & Moore, D. H. Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND). Cochrane Database Syst. Rev. 3, CD001447 (2012).

4. Ling, S.-C., Polymenidou, M. & Cleveland, D. W. Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis. Neuron 79, 416–438 (2013).

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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