The autophagy/lysosome pathway is impaired in SCA7 patients and SCA7 knock-in mice

VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy

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Overexpression of the autophagic beclin-1 protein clears mutant ataxin-3 and alleviates Machado–Joseph disease

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Altered expression of autophagic genes in the peripheral leukocytes of patients with sporadic Parkinson's disease

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Ataxin-7 associates with microtubules and stabilizes the cytoskeletal network

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Early autophagic response in a novel knock-in model of Huntington disease

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Cargo recognition failure is responsible for inefficient autophagy in Huntington's disease

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Immunohistochemical evidence for macroautophagy in neurones and endothelial cells in Alzheimer's disease

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Selective Molecular Alterations in the Autophagy Pathway in Patients with Lewy Body Disease and in Models of α-Synucleinopathy

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Inhibition of mTOR by Rapamycin Abolishes Cognitive Deficits and Reduces Amyloid-β Levels in a Mouse Model of Alzheimer's Disease

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Integration of Clearance Mechanisms: The Proteasome and Autophagy

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Nucleocytoplasmic Shuttling of p62/SQSTM1 and Its Role in Recruitment of Nuclear Polyubiquitinated Proteins to Promyelocytic Leukemia Bodies

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Posttranslational Modification of Ataxin-7 at Lysine 257 Prevents Autophagy-Mediated Turnover of an N-Terminal Caspase-7 Cleavage Fragment

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Beclin 1 Gene Transfer Activates Autophagy and Ameliorates the Neurodegenerative Pathology in  -Synuclein Models of Parkinson's and Lewy Body Diseases

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Polyglutamine-expanded ataxin-7 causes cerebellar dysfunction by inducing transcriptional dysregulation

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Structural Basis for Sorting Mechanism of p62 in Selective Autophagy

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The N-terminus and Phe52 residue of LC3 recruit p62/SQSTM1 into autophagosomes

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