Stathmin-2: adding another piece to the puzzle of TDP-43 proteinopathies and neurodegeneration
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://www.jci.org/articles/view/142854/files/pdf
Reference28 articles.
1. TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease
2. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
3. TDP-43 Is Intrinsically Aggregation-prone, and Amyotrophic Lateral Sclerosis-linked Mutations Accelerate Aggregation and Increase Toxicity
4. Pharmacological promotion of inclusion formation: A therapeutic approach for Huntington's and Parkinson's diseases
5. Cellular toxicity of mutant SOD1 protein is linked to an easily soluble, non-aggregated form in vitro
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3. Genetic ablation of Sarm1 attenuates expression and mislocalization of phosphorylated TDP-43 after mouse repetitive traumatic brain injury;Acta Neuropathologica Communications;2023-12-20
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