Emerging Therapies and Novel Targets for TDP-43 Proteinopathy in ALS/FTD-Reference-Cited by-同舟云学术

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Emerging Therapies and Novel Targets for TDP-43 Proteinopathy in ALS/FTD

Published:2022-07 Issue:4 Volume:19 Page:1061-1084
ISSN:1933-7213
Container-title:Neurotherapeutics
language:en
Short-container-title:Neurotherapeutics

Author:

Hayes Lindsey R.^ORCID,Kalab Petr

Funder

National Institute of Neurological Disorders and Stroke

Robert Packard Center for ALS Research, Johns Hopkins University

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Neurology (clinical),Pharmacology

Link

https://link.springer.com/content/pdf/10.1007/s13311-022-01260-5.pdf

Reference241 articles.

1. Prasad A, Bharathi V, Sivalingam V, Girdhar A, Patel BK. Molecular mechanisms of TDP-43 misfolding and pathology in amyotrophic lateral sclerosis. Front Mol Neurosci. 2019;12:25.

2. François-Moutal L, Perez-Miller S, Scott DD, Miranda VG, Mollasalehi N, Khanna M. Structural insights Into TDP-43 and effects of post-translational modifications. Front Mol Neurosci. 2019;12:1199.

3. Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science. 2006;314:130–3.

4. Arai T, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, Mori H, et al. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Bioph Res Co. 2006;351:602–11.

5. Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, Velde CV, et al. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat Genet. 2008;40:572–4.

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