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Cerebellum (London, England)|April 18, 2008
Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegenerationGwenn A Garden, Albert R La SpadaDrug Discovery Today|March 18, 2014
The many faces of autophagy dysfunction in Huntington's disease: from mechanism to therapyConstanza J Cortes, Albert R La SpadaDiscovery Medicine|March 1, 2015
Unwinding the role of senataxin in neurodegenerationCraig L Bennett, Albert R La SpadaEMBO Molecular Medicine|August 24, 2010
Déjà vu with a twist: transglutaminases in bioenergetics and transcriptional dysfunction in Huntington's diseaseParsa Kazemi-Esfarjani, Albert R La SpadaMolecular and Cellular Neurosciences|March 16, 2015
Autophagy in polyglutamine disease: Imposing order on disorder or contributing to the chaos?Constanza J Cortes, Albert R La SpadaRare Diseases (Austin, Tex.)|March 5, 2016
Motor neuron degeneration in spinal and Bulbar Muscular Atrophy is a skeletal muscle-driven process: Relevance to therapy development and implications for related motor neuron diseasesConstanza J Cortes, Albert R La SpadaNeuron|December 13, 2005
Silencing polyglutamine degeneration with RNAiNancy M Bonini, Albert R La SpadaNeuron|March 9, 2004
Androgen receptor YAC transgenic mice recapitulate SBMA motor neuronopathy and implicate VEGF164 in the motor neuron degenerationBryce L Sopher, Patrick S Thomas, Michelle A LaFevre-Bernt, et al.Nature Neuroscience|August 11, 2014
Polyglutamine-expanded androgen receptor interferes with TFEB to elicit autophagy defects in SBMAConstanza J Cortes, Helen C Miranda, Harald Frankowski, et al.Cell Reports|December 1, 2021
Altered H3 histone acetylation impairs high-fidelity DNA repair to promote cerebellar degeneration in spinocerebellar ataxia type 7Pawel M Switonski, Joe R Delaney, Luke C Bartelt, et al.Pageof 16