Lauren M. Tanabe, Ph.D.

neurology

William T. Dauer	grad student	2010	Columbia
(Modeling Aspects of DYT1 Dystonia at the Cellular and Systems Levels: Implications for TorsinA in Neural Development.)

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Tanabe LM, List K. (2016) The Role of Type II Transmembrane Serine Protease Mediated Signaling in Cancer. The Febs Journal
Tanabe LM, Liang CC, Dauer WT. (2016) Neuronal Nuclear Membrane Budding Occurs during a Developmental Window Modulated by Torsin Paralogs. Cell Reports. 16: 3322-33
Liang CC, Tanabe LM, Jou S, et al. (2014) TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration. The Journal of Clinical Investigation. 124: 3080-92
Tanabe LM, Martin C, Dauer WT. (2012) Genetic background modulates the phenotype of a mouse model of DYT1 dystonia. Plos One. 7: e32245
UluÄŸ AM, Vo A, Argyelan M, et al. (2011) Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice. Proceedings of the National Academy of Sciences of the United States of America. 108: 6638-43
Tanabe LM, Kim CE, Alagem N, et al. (2009) Primary dystonia: molecules and mechanisms. Nature Reviews. Neurology. 5: 598-609
Akman HO, Dorado B, LÃ³pez LC, et al. (2008) Thymidine kinase 2 (H126N) knockin mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance. Human Molecular Genetics. 17: 2433-40