Inherited Isolated Dystonia: Clinical Genetics and Gene Function

Autor Dauer, William
Vydáno v Neurotherapeutics (2014)

Neurogenetic Disease: Genes, Mechanisms, and Future Promise

Autor Dauer, William T.
Vydáno v Neurotherapeutics (2014)

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

Autor Goodchild, Rose E., Dauer, William T.
Vydáno 2004

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

Autor Goodchild, Rose E., Dauer, William T.
Vydáno 2005

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

Autor Kett, Lauren R., Dauer, William T.
Vydáno 2012

The Nuclear Envelope: An Intriguing Focal Point for Neurogenetic Disease

Autor Worman, Howard J., Dauer, William T.
Vydáno v Neurotherapeutics (2014)

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

Autor Weisheit, Corinne E., Dauer, William T.
Vydáno v Hum Mol Genet (2015)

Endolysosomal Dysfunction in Parkinson Disease: Recent Developments and Future Challenges

Autor Kett, Lauren R., Dauer, William T.
Vydáno v Mov Disord (2016)

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

Autor Tanabe, Lauren M., Martin, Caitlin, Dauer, William T.
Vydáno 2012

Emerging Common Molecular Pathways for Primary Dystonia

Autor LeDoux, Mark S, Dauer, William T, Warner, Thomas T
Vydáno 2013

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

Autor Shin, Ji-Yeon, Dauer, William T., Worman, Howard J.
Vydáno 2014

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

Autor Tanabe, Lauren M., Liang, Chun-Chi, Dauer, William T.
Vydáno v Cell Rep (2016)

CNS critical periods: implications for dystonia and other neurodevelopmental disorders

Autor Li, Jay, Kim, Sumin, Pappas, Samuel S., Dauer, William T.
Vydáno v JCI Insight (2021)

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

Autor Burke, Robert E., Dauer, William T., Vonsattel, Jean Paul G.
Vydáno 2008

TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models

Autor Li, Jay, Liang, Chun-Chi, Pappas, Samuel S, Dauer, William T
Vydáno v eLife (2020)

Primary dystonia: molecules and mechanisms

Autor Tanabe, Lauren M., Kim, Connie E., Alagem, Noga, Dauer, William T.
Vydáno 2009

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

Autor Pappas, Samuel S., Leventhal, Daniel K., Albin, Roger L., Dauer, William T.
Vydáno v Curr Top Dev Biol (2014)

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

Autor Li, Jay, Levin, Daniel S., Kim, Audrey J., Pappas, Samuel S., Dauer, William T.
Vydáno v J Clin Invest (2021)

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

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

TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration

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