From molecule to molecule and cell to cell: Prion-like mechanisms in amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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From molecule to molecule and cell to cell: Prion-like mechanisms in amyotrophic lateral sclerosis

Published:2015-05 Issue: Volume:77 Page:257-265
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Grad Leslie I.,Fernando Sarah M.,Cashman Neil R.

Funder

Webster Foundation

Allen T. Lambert Neural Research Fund

Temerty Family Foundation

PrioNet Canada

Canadian Institutes of Health Research (CIHR)

Biogen-Idec Corp

University of British Columbia

Publisher

Elsevier BV

Subject

Neurology

Reference139 articles.

1. Cell biology: beyond the prion principle;Aguzzi;Nature,2009

2. The transcellular spread of cytosolic amyloids, prions, and prionoids;Aguzzi;Neuron,2009

3. A systematic survey identifies prions and illuminates sequence features of prionogenic proteins;Alberti;Cell,2009

4. ALS Mutation Database,2007

5. Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase;Andersen;Nat. Genet.,1995

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1. The prion-like effect and prion-like protein targeting strategy in amyotrophic lateral sclerosis;Heliyon;2024-08

2. A hydrophobic core stabilizes the residual structure in the RRM2 intermediate state of the ALS-linked protein TDP-43;2024-06-12

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4. N-glycosylation as a eukaryotic protective mechanism against protein aggregation;Science Advances;2024-02-02

5. The pathogenic mechanism of TAR DNA-binding protein 43 (TDP-43) in amyotrophic lateral sclerosis;Neural Regeneration Research;2023-09-04

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