p62 Plays a Protective Role in the Autophagic Degradation of Polyglutamine Protein Oligomers in Polyglutamine Disease Model Flies

Autophagy in Huntington disease and huntingtin in autophagy

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Calpain inhibition mediates autophagy-dependent protection against polyglutamine toxicity

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Differential roles of the ubiquitin proteasome system and autophagy in the clearance of soluble and aggregated TDP-43 species

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p62/SQSTM1 Differentially Removes the Toxic Mutant Androgen Receptor via Autophagy and Inclusion Formation in a Spinal and Bulbar Muscular Atrophy Mouse Model

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Selective autophagy mediated by autophagic adapter proteins

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Serine 403 Phosphorylation of p62/SQSTM1 Regulates Selective Autophagic Clearance of Ubiquitinated Proteins

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Mutant Huntingtin Fragments Form Oligomers in a Polyglutamine Length-dependent Mannerin Vitroandin Vivo

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Regulation of TDP-43 aggregation by phosphorylation andp62/SQSTM1

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The Selective Macroautophagic Degradation of Aggregated Proteins Requires the PI3P-Binding Protein Alfy

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Autophagy Inhibition Compromises Degradation of Ubiquitin-Proteasome Pathway Substrates

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Structural Basis for Sorting Mechanism of p62 in Selective Autophagy

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Use of p62/SQSTM1 antibodies for neuropathological diagnosis

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