TDP-43 in ALS: Stay on Target…Almost There
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference12 articles.
1. Axonal Transport of TDP-43 mRNA Granules Is Impaired by ALS-Causing Mutations
2. TAR DNA-binding protein 43 in neurodegenerative disease
3. Global Analysis of TDP-43 Interacting Proteins Reveals Strong Association with RNA Splicing and Translation Machinery
4. TDP-43 Is Intrinsically Aggregation-prone, and Amyotrophic Lateral Sclerosis-linked Mutations Accelerate Aggregation and Increase Toxicity
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1. SBT-272 improves TDP-43 pathology in ALS upper motor neurons by modulating mitochondrial integrity, motility, and function;Neurobiology of Disease;2023-03
2. SBT-272 improves TDP-43 pathology in the ALS motor cortex by modulating mitochondrial integrity, motility, and function;2022-10-07
3. Concomitant gain and loss of function pathomechanisms in C9ORF72 amyotrophic lateral sclerosis;Life Science Alliance;2021-02-22
4. High content live profiling reveals concomitant gain and loss of function pathomechanisms in C9ORF72 amyotrophic lateral sclerosis;2020-04-17
5. TDP-43 Regulates Coupled Dendritic mRNA Transport-Translation Processes in Co-operation with FMRP and Staufen1;Cell Reports;2019-12
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