TDP-43 pathology: From noxious assembly to therapeutic removal
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference382 articles.
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4. Impaired nucleoporins are present in sporadic amyotrophic lateral sclerosis motor neurons that exhibit mislocalization of the 43-kDa TAR DNA-binding protein;Aizawa;J. Clin. Neurol.,2019
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1. TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis: From pathomechanisms to therapeutic strategies;Ageing Research Reviews;2024-09
2. Inactivation of cGAS signaling pathway mediated by TDP-43 deficiency protects microglia from hypoxia/reoxygenation induced injury;Brain Research;2024-09
3. hnRNPs: roles in neurodevelopment and implication for brain disorders;Frontiers in Molecular Neuroscience;2024-07-17
4. Dissecting the effect of ALS mutation S375G on the conformational properties and aggregation dynamics of TDP-43370-375 fragment;Biophysical Chemistry;2024-07
5. Electrostatics Choreographs the Aggregation Dynamics of Full-Length TDP-43 via a Monomeric Amyloid Precursor;Biochemistry;2024-05-31
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