Inherited Isolated Dystonia: Clinical Genetics and Gene Function

by Dauer, William
Published in Neurotherapeutics (2014)

Neurogenetic Disease: Genes, Mechanisms, and Future Promise

by Dauer, William T.
Published in Neurotherapeutics (2014)

Mislocalization to the nuclear envelope: An effect of the dystonia-causing torsinA mutation

by Goodchild, Rose E., Dauer, William T.
Published 2004

The AAA+ protein torsinA interacts with a conserved domain present in LAP1 and a novel ER protein

by Goodchild, Rose E., Dauer, William T.
Published 2005

Leucine-Rich Repeat Kinase 2 for Beginners: Six Key Questions

by Kett, Lauren R., Dauer, William T.
Published 2012

The Nuclear Envelope: An Intriguing Focal Point for Neurogenetic Disease

by Worman, Howard J., Dauer, William T.
Published in Neurotherapeutics (2014)

A novel conditional knock-in approach defines molecular and circuit effects of the DYT1 dystonia mutation

by Weisheit, Corinne E., Dauer, William T.
Published in Hum Mol Genet (2015)

Endolysosomal Dysfunction in Parkinson Disease: Recent Developments and Future Challenges

by Kett, Lauren R., Dauer, William T.
Published in Mov Disord (2016)

Genetic Background Modulates the Phenotype of a Mouse Model of DYT1 Dystonia

by Tanabe, Lauren M., Martin, Caitlin, Dauer, William T.
Published 2012

Emerging Common Molecular Pathways for Primary Dystonia

by LeDoux, Mark S, Dauer, William T, Warner, Thomas T
Published 2013

Lamina-associated Polypeptide 1: Protein Interactions and Tissue-selective Functions

by Shin, Ji-Yeon, Dauer, William T., Worman, Howard J.
Published 2014

Neuronal Nuclear Membrane Budding Occurs During a Developmental Window Modulated by Torsin Paralogs

by Tanabe, Lauren M., Liang, Chun-Chi, Dauer, William T.
Published in Cell Rep (2016)

CNS critical periods: implications for dystonia and other neurodevelopmental disorders

by Li, Jay, Kim, Sumin, Pappas, Samuel S., Dauer, William T.
Published in JCI Insight (2021)

A Critical Evaluation of The Braak Staging Scheme for Parkinson’s Disease

by Burke, Robert E., Dauer, William T., Vonsattel, Jean Paul G.
Published 2008

TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models

by Li, Jay, Liang, Chun-Chi, Pappas, Samuel S, Dauer, William T
Published in eLife (2020)

Primary dystonia: molecules and mechanisms

by Tanabe, Lauren M., Kim, Connie E., Alagem, Noga, Dauer, William T.
Published 2009

Mouse Models of Neurodevelopmental Disease of the Basal Ganglia and Associated Circuits

by Pappas, Samuel S., Leventhal, Daniel K., Albin, Roger L., Dauer, William T.
Published in Curr Top Dev Biol (2014)

TorsinA restoration in a mouse model identifies a critical therapeutic window for DYT1 dystonia

by Li, Jay, Levin, Daniel S., Kim, Audrey J., Pappas, Samuel S., Dauer, William T.
Published in J Clin Invest (2021)

A molecular mechanism underlying the neural-specific defect in torsinA mutant mice

by Kim, Connie E., Perez, Alex, Perkins, Guy, Ellisman, Mark H., Dauer, William T.
Published 2010

TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration

by Liang, Chun-Chi, Tanabe, Lauren M., Jou, Stephanie, Chi, Frank, Dauer, William T.
Published 2014