Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7

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Human Molecular Genetics, Vol. 22, Iss. 5, 2013-03 ,pp. : 890-903

Oxford University Press

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Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions

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SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7

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Similarities between spinocerebellar ataxia type 7 (SCA7) cell models and human brain: proteins recruited in inclusions and activation of caspase-3

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Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions

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