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Jiou Wang et al.
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Misfolded proteins partition between two distinct quality control compartments
Daniel Kaganovich et al.
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Ehud Cohen et al.
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Peter M. Douglas et al.
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David J. Gifondorwa et al.
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Maria A. Rujano et al.
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Opposing activities protect against age-onset proteotoxicity
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G Matsumoto et al.
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G Matsumoto et al.
JOURNAL OF CELL BIOLOGY (2005)
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AJ McClellan et al.
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AJ McClellan et al.
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J Shorter et al.
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M Arrasate et al.
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T Kobayashi et al.
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Decreased metallation and activity in subsets of mutant superoxide dismutases associated with familial amyotrophic lateral sclerosis
LJ Hayward et al.
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The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Aβ protofibril formation
C Nilsberth et al.
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Aggresomes, inclusion bodies and protein aggregation
RR Kopito
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