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Autophagy|January 18, 2023
Effects of STAU1/staufen1 on autophagy in neurodegenerative diseasesStefan M Pulst, Daniel R Scoles, Sharan PaulNeuron|January 21, 2021
Splicing Control of Pontocerebellar DevelopmentSharan Paul, Daniel R Scoles, Stefan M PulstThe Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 3, 2006
Proteasome inhibition triggers activity-dependent increase in the size of the recycling vesicle pool in cultured hippocampal neuronsKristen Willeumier, Stefan M Pulst, Felix E SchweizerThe Journal of Physiology|May 21, 2016
Cellular and circuit mechanisms underlying spinocerebellar ataxiasPratap Meera, Stefan M Pulst, Thomas S OtisHuman Molecular Genetics|October 11, 2017
Potassium channel dysfunction underlies Purkinje neuron spiking abnormalities in spinocerebellar ataxia type 2James M Dell'Orco, Stefan M Pulst, Vikram G ShakkottaiNeurology. Genetics|May 24, 2019
Antisense oligonucleotides: A primerDaniel R Scoles, Eric V Minikel, Stefan M PulstArchives of Neurology|December 14, 2005
Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literatureRoongroj Bhidayasiri, Susan L Perlman, Stefan-M Pulst, et al.Human Molecular Genetics|August 20, 2003
The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XIDuong P Huynh, Daniel R Scoles, Dung Nguyen, et al.Human Molecular Genetics|October 23, 2012
Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2Stephen T Hansen, Pratap Meera, Thomas S Otis, et al.JAMA Neurology|October 7, 2014
Amyotrophic lateral sclerosis risk for spinocerebellar ataxia type 2 ATXN2 CAG repeat alleles: a meta-analysisAnnalese G Neuenschwander, Khanh K Thai, Karla P Figueroa, et al.Pageof 15