ALS-linked TDP-43 mutations interfere with the recruitment of RNA recognition motifs to G-quadruplex RNA | Scientific Reports
Domain structures and assembly of TDP-43 proteins. (A) TDP-43 has two... | Download Scientific Diagram
TDP-43 functions and pathogenic mechanisms implicated in TDP-43 proteinopathies: Trends in Molecular Medicine
Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis | The EMBO Journal
Connecting TDP-43 Pathology with Neuropathy: Trends in Neurosciences
IJMS | Free Full-Text | TDP-43 and Inflammation: Implications for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
Frontiers | Structural Insights Into TDP-43 and Effects of Post-translational Modifications
Multi-phaseted problems of TDP-43 in selective neuronal vulnerability in ALS | SpringerLink
A. Schematic representation of the primary structural architecture of... | Download Scientific Diagram
RNA Binding Antagonizes Neurotoxic Phase Transitions of TDP-43 - ScienceDirect
Addgene: pLVX-Puro-TDP-43-A315T
IJMS | Free Full-Text | The Different Faces of the TDP-43 Low-Complexity Domain: The Formation of Liquid Droplets and Amyloid Fibrils
TAR DNA Binding Protein - an overview | ScienceDirect Topics
TAR DNA-binding protein 43 - Wikipedia
TAR DNA-binding protein 43 - Wikipedia
Regulation of TDP-43 phosphorylation in aging and disease | SpringerLink
Frontiers | Molecular Mechanisms of TDP-43 Misfolding and Pathology in Amyotrophic Lateral Sclerosis
Representation of the protein domain structure of TDP-43 and FUS. The... | Download Scientific Diagram
Templated Aggregation of TAR DNA-binding Protein of 43 kDa (TDP-43) by Seeding with TDP-43 Peptide Fibrils* - Journal of Biological Chemistry
TDP-43 functions and pathogenic mechanisms implicated in TDP-43 proteinopathies. | Semantic Scholar
Structure of TDP-43 including functional domains and identified... | Download Scientific Diagram
The N-terminal dimerization is required for TDP-43 splicing activity | Scientific Reports
Pathogenic Mutation of TDP-43 Impairs RNA Processing in a Cell Type-Specific Manner: Implications for the Pathogenesis of ALS/FTLD | eNeuro
Frontiers | A C-Terminally Truncated TDP-43 Splice Isoform Exhibits Neuronal Specific Cytoplasmic Aggregation and Contributes to TDP-43 Pathology in ALS
The role of TDP-43 mislocalization in amyotrophic lateral sclerosis | Molecular Neurodegeneration | Full Text
Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis | The EMBO Journal
Structural analysis of disease-related TDP-43 D169G mutation: linking enhanced stability and caspase cleavage efficiency to protein accumulation | Scientific Reports
TDP-43-mediated neurodegeneration: towards a loss-of-function hypothesis?: Trends in Molecular Medicine
Why TDP-43? Why Not? Mechanisms of Metabolic Dysfunction in Amyotrophic Lateral Sclerosis - Mara-Luciana Floare, Scott P. Allen, 2020
