FUS/TLS forms cytoplasmic aggregates, inhibits cell growth and interacts with TDP-43 in a yeast model of amyotrophic lateral sclerosis

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Amyotrophic Lateral Sclerosis-associated Proteins TDP-43 and FUS/TLS Function in a Common Biochemical Complex to Co-regulate HDAC6 mRNA

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Nuclear localization sequence of FUS and induction of stress granules by ALS mutants

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A Systematic Survey Identifies Prions and Illuminates Sequence Features of Prionogenic Proteins

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Bridging high-throughput genetic and transcriptional data reveals cellular responses to alpha-synuclein toxicity

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Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

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Misfolded proteins partition between two distinct quality control compartments

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A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity

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TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

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