Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis - Munich Cluster for Systems Neurology - LMU Munich
FUS (fused in sarcoma) is a component of the cellular response to topoisomerase I–induced DNA breakage and transcriptional stress | Life Science Alliance
FUS Transgenic Rats Develop the Phenotypes of Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration | PLOS Genetics
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation | Nature Communications
IJMS | Free Full-Text | Wild-Type and Mutant FUS Expression Reduce Proliferation and Neuronal Differentiation Properties of Neural Stem Progenitor Cells
Frontiers | Aberrant Phase Separation of FUS Leads to Lysosome Sequestering and Acidification
Figure E1: FUS-ALS separation from control WT by marker set. a, FUS-ALS... | Download Scientific Diagram
Addgene: RP1B FUS 1-163 S12xQ
FUS is Phosphorylated by DNA-PK and Accumulates in the Cytoplasm after DNA Damage | Journal of Neuroscience
Expression of Fused in sarcoma mutations in mice recapitulates the neuropathology of FUS proteinopathies and provides insight into disease pathogenesis | Molecular Neurodegeneration | Full Text
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Increased FUS levels in astrocytes leads to astrocyte and microglia activation and neuronal death | Scientific Reports
Identification of a novel interaction of FUS and syntaphilin may explain synaptic and mitochondrial abnormalities caused by ALS mutations | Scientific Reports
RNA-binding protein FUS - Wikipedia
FUS-B-208 Path Marker Boho
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The FUS gene is dual‐coding with both proteins contributing to FUS‐mediated toxicity | EMBO reports
The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response | BMC Molecular and Cell Biology | Full Text
Mutant FUS and ELAVL4 (HuD) Aberrant Crosstalk in Amyotrophic Lateral Sclerosis - ScienceDirect
Addgene: RP1B FUS 1-163 QQ4xSS #1
A scalable screening platform for phenotypic subtyping of ALS patient-derived fibroblasts | bioRxiv
Aberrant axon branching via Fos-B dysregulation in FUS-ALS motor neurons - eBioMedicine
Punctuate staining with SG marker eIF3e was commonly found adjacent to or surrounding FUS-GFP SGs.
