Inherited Isolated Dystonia: Clinical Genetics and Gene Function

door Dauer, William
Gepubliceerd in Neurotherapeutics (2014)

Neurogenetic Disease: Genes, Mechanisms, and Future Promise

door Dauer, William T.
Gepubliceerd in Neurotherapeutics (2014)

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

door Goodchild, Rose E., Dauer, William T.
Gepubliceerd in 2004

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

door Goodchild, Rose E., Dauer, William T.
Gepubliceerd in 2005

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

door Kett, Lauren R., Dauer, William T.
Gepubliceerd in 2012

The Nuclear Envelope: An Intriguing Focal Point for Neurogenetic Disease

door Worman, Howard J., Dauer, William T.
Gepubliceerd in Neurotherapeutics (2014)

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

door Weisheit, Corinne E., Dauer, William T.
Gepubliceerd in Hum Mol Genet (2015)

Endolysosomal Dysfunction in Parkinson Disease: Recent Developments and Future Challenges

door Kett, Lauren R., Dauer, William T.
Gepubliceerd in Mov Disord (2016)

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

door Tanabe, Lauren M., Martin, Caitlin, Dauer, William T.
Gepubliceerd in 2012

Emerging Common Molecular Pathways for Primary Dystonia

door LeDoux, Mark S, Dauer, William T, Warner, Thomas T
Gepubliceerd in 2013

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

door Shin, Ji-Yeon, Dauer, William T., Worman, Howard J.
Gepubliceerd in 2014

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

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

CNS critical periods: implications for dystonia and other neurodevelopmental disorders

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

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

door Burke, Robert E., Dauer, William T., Vonsattel, Jean Paul G.
Gepubliceerd in 2008

TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models

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

Primary dystonia: molecules and mechanisms

door Tanabe, Lauren M., Kim, Connie E., Alagem, Noga, Dauer, William T.
Gepubliceerd in 2009

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

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

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

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

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

door Kim, Connie E., Perez, Alex, Perkins, Guy, Ellisman, Mark H., Dauer, William T.
Gepubliceerd in 2010

TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration

door Liang, Chun-Chi, Tanabe, Lauren M., Jou, Stephanie, Chi, Frank, Dauer, William T.
Gepubliceerd in 2014