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Neuron|December 21, 2005
Loss of the dystonia-associated protein torsinA selectively disrupts the neuronal nuclear envelopeRose E Goodchild, Connie Eunji Kim, William T DauerMovement Disorders : Official Journal of the Movement Disorder Society|July 30, 2013
Emerging common molecular pathways for primary dystoniaMark S Ledoux, William T Dauer, Thomas T WarnerCell Reports|September 23, 2016
Neuronal Nuclear Membrane Budding Occurs during a Developmental Window Modulated by Torsin ParalogsLauren M Tanabe, Chun-Chi Liang, William T DauerHandbook of Clinical Neurology|January 13, 2018
Inherited dystonias: clinical features and molecular pathwaysCorinne E Weisheit, Samuel S Pappas, William T DauerSeminars in Cell & Developmental Biology|February 11, 2014
Lamina-associated polypeptide 1: protein interactions and tissue-selective functionsJi-Yeon Shin, William T Dauer, Howard J WormanJCI Insight|February 22, 2021
CNS critical periods: implications for dystonia and other neurodevelopmental disordersJay Li, Sumin Kim, Samuel S Pappas, et al.Annals of Neurology|December 11, 2008
A critical evaluation of the Braak staging scheme for Parkinson's diseaseRobert E Burke, William T Dauer, Jean Paul G VonsattelDystonia (Lausanne, Switzerland)|March 6, 2023
Genetic evidence of aberrant striatal synaptic maturation and secretory pathway alteration in a dystonia mouse modelDhananjay Yellajoshyula, Sunday Opeyemi, William T Dauer, et al.Nature Reviews. Neurology|October 15, 2009
Primary dystonia: molecules and mechanismsLauren M Tanabe, Connie E Kim, Noga Alagem, et al.Elife|March 24, 2020
TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse modelsJay Li, Chun-Chi Liang, Samuel S Pappas, et al.Pageof 203