Inherited Isolated Dystonia: Clinical Genetics and Gene Function

Por Dauer, William
Publicado no Neurotherapeutics (2014)

Neurogenetic Disease: Genes, Mechanisms, and Future Promise

Por Dauer, William T.
Publicado no Neurotherapeutics (2014)

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

Por Goodchild, Rose E., Dauer, William T.
Publicado em 2004

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

Por Goodchild, Rose E., Dauer, William T.
Publicado em 2005

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

Por Kett, Lauren R., Dauer, William T.
Publicado em 2012

The Nuclear Envelope: An Intriguing Focal Point for Neurogenetic Disease

Por Worman, Howard J., Dauer, William T.
Publicado no Neurotherapeutics (2014)

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

Por Weisheit, Corinne E., Dauer, William T.
Publicado no Hum Mol Genet (2015)

Endolysosomal Dysfunction in Parkinson Disease: Recent Developments and Future Challenges

Por Kett, Lauren R., Dauer, William T.
Publicado no Mov Disord (2016)

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

Por Tanabe, Lauren M., Martin, Caitlin, Dauer, William T.
Publicado em 2012

Emerging Common Molecular Pathways for Primary Dystonia

Por LeDoux, Mark S, Dauer, William T, Warner, Thomas T
Publicado em 2013

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

Por Shin, Ji-Yeon, Dauer, William T., Worman, Howard J.
Publicado em 2014

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

Por Tanabe, Lauren M., Liang, Chun-Chi, Dauer, William T.
Publicado no Cell Rep (2016)

CNS critical periods: implications for dystonia and other neurodevelopmental disorders

Por Li, Jay, Kim, Sumin, Pappas, Samuel S., Dauer, William T.
Publicado no JCI Insight (2021)

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

Por Burke, Robert E., Dauer, William T., Vonsattel, Jean Paul G.
Publicado em 2008

TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models

Por Li, Jay, Liang, Chun-Chi, Pappas, Samuel S, Dauer, William T
Publicado no eLife (2020)

Primary dystonia: molecules and mechanisms

Por Tanabe, Lauren M., Kim, Connie E., Alagem, Noga, Dauer, William T.
Publicado em 2009

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

Por Pappas, Samuel S., Leventhal, Daniel K., Albin, Roger L., Dauer, William T.
Publicado no Curr Top Dev Biol (2014)

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

Por Li, Jay, Levin, Daniel S., Kim, Audrey J., Pappas, Samuel S., Dauer, William T.
Publicado no J Clin Invest (2021)

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

Por Kim, Connie E., Perez, Alex, Perkins, Guy, Ellisman, Mark H., Dauer, William T.
Publicado em 2010

TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration

Por Liang, Chun-Chi, Tanabe, Lauren M., Jou, Stephanie, Chi, Frank, Dauer, William T.
Publicado em 2014