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Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis - Munich Cluster for Systems Neurology - LMU Munich
Addgene: RP1B FUS 1-163 S12xQ
FUS regulates autophagy by mediating the transcription of genes critical to the autophagosome formation - Arenas - 2021 - Journal of Neurochemistry - Wiley Online Library
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Increased FUS levels in astrocytes leads to astrocyte and microglia activation and neuronal death | Scientific Reports
Frontiers | Aberrant Phase Separation of FUS Leads to Lysosome Sequestering and Acidification
FUS (fused in sarcoma) is a component of the cellular response to topoisomerase I–induced DNA breakage and transcriptional stress | Life Science Alliance
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Punctuate staining with SG marker eIF3e was commonly found adjacent to or surrounding FUS-GFP SGs.
Model of FUS distribution in relationship to synaptic markers in... | Download Scientific Diagram
Addgene: RP1B FUS 1-163 QQ4xSS #1
Identification of a novel interaction of FUS and syntaphilin may explain synaptic and mitochondrial abnormalities caused by ALS mutations | Scientific Reports
FUS Transgenic Rats Develop the Phenotypes of Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration | PLOS Genetics
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
The FUS gene is dual‐coding with both proteins contributing to FUS‐mediated toxicity | EMBO reports
FUS is Phosphorylated by DNA-PK and Accumulates in the Cytoplasm after DNA Damage | Journal of Neuroscience
Characterization of the Fus-Mid-GFP marker. (A) Schematic... | Download Scientific Diagram
Synaptic FUS accumulation triggers early misregulation of synaptic RNAs in a mouse model of ALS | Nature Communications
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A scalable screening platform for phenotypic subtyping of ALS patient-derived fibroblasts | bioRxiv
The long non-coding RNA nuclear-enriched abundant transcript 1_2 induces paraspeckle formation in the motor neuron during the early phase of amyotrophic lateral sclerosis | Molecular Brain | Full Text
IJMS | Free Full-Text | Stress-Specific Spatiotemporal Responses of RNA-Binding Proteins in Human Stem Cell-Derived Motor Neurons
RNA-binding protein FUS - Wikipedia
TDP‐43 and FUS/TLS: cellular functions and implications for neurodegeneration - Fiesel - 2011 - The FEBS Journal - Wiley Online Library
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation | Nature Communications
Mutant FUS and ELAVL4 (HuD) Aberrant Crosstalk in Amyotrophic Lateral Sclerosis - ScienceDirect
Mutant Human FUS Is Ubiquitously Mislocalized and Generates Persistent Stress Granules in Primary Cultured Transgenic Zebrafish Cells | PLOS ONE