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M Hersch

Showing results (81-90 of 129) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|May 26, 2011
A tale of two factors: what determines the rate of progression in Huntington's disease? A longitudinal MRI studyH Diana Rosas, Martin Reuter, Gheorghe Doros, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 1, 1995
The dopamine transporter: immunochemical characterization and localization in brainB J Ciliax, C Heilman, L L Demchyshyn, et al.
Annals of Neurology|December 10, 1999
Huntington aggregates may not predict neuronal death in Huntington's diseaseS Kuemmerle, C A Gutekunst, A M Klein, et al.
Cell|October 20, 1998
Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic miceI A Klement, P J Skinner, M D Kaytor, et al.
Brain : a Journal of Neurology|March 14, 2008
Cerebral cortex and the clinical expression of Huntington's disease: complexity and heterogeneityH Diana Rosas, David H Salat, Stephanie Y Lee, et al.
The Journal of Comparative Neurology|August 30, 2005
Chronology of behavioral symptoms and neuropathological sequela in R6/2 Huntington's disease transgenic miceEdward C Stack, James K Kubilus, Karen Smith, et al.
Archives of Neurology|March 7, 2012
Alterations in brain transition metals in Huntington disease: an evolving and intricate storyH Diana Rosas, Y Iris Chen, Gheorghe Doros, et al.
Human Molecular Genetics|July 28, 2011
The Sirtuin 2 microtubule deacetylase is an abundant neuronal protein that accumulates in the aging CNSMichele M Maxwell, Elizabeth M Tomkinson, Johnathan Nobles, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2005
Genome-wide expression profiling of human blood reveals biomarkers for Huntington's diseaseF Borovecki, L Lovrecic, J Zhou, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 14, 2000
Neuroprotective effects of creatine in a transgenic mouse model of Huntington's diseaseR J Ferrante, O A Andreassen, B G Jenkins, et al.
Pageof 13

Showing results (81-90 of 129) with videos related to

Sort By:
Pageof 13
Movement Disorders : Official Journal of the Movement Disorder Society|May 26, 2011
A tale of two factors: what determines the rate of progression in Huntington's disease? A longitudinal MRI studyH Diana Rosas, Martin Reuter, Gheorghe Doros, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 1, 1995
The dopamine transporter: immunochemical characterization and localization in brainB J Ciliax, C Heilman, L L Demchyshyn, et al.
Annals of Neurology|December 10, 1999
Huntington aggregates may not predict neuronal death in Huntington's diseaseS Kuemmerle, C A Gutekunst, A M Klein, et al.
Cell|October 20, 1998
Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic miceI A Klement, P J Skinner, M D Kaytor, et al.
Brain : a Journal of Neurology|March 14, 2008
Cerebral cortex and the clinical expression of Huntington's disease: complexity and heterogeneityH Diana Rosas, David H Salat, Stephanie Y Lee, et al.
The Journal of Comparative Neurology|August 30, 2005
Chronology of behavioral symptoms and neuropathological sequela in R6/2 Huntington's disease transgenic miceEdward C Stack, James K Kubilus, Karen Smith, et al.
Archives of Neurology|March 7, 2012
Alterations in brain transition metals in Huntington disease: an evolving and intricate storyH Diana Rosas, Y Iris Chen, Gheorghe Doros, et al.
Human Molecular Genetics|July 28, 2011
The Sirtuin 2 microtubule deacetylase is an abundant neuronal protein that accumulates in the aging CNSMichele M Maxwell, Elizabeth M Tomkinson, Johnathan Nobles, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2005
Genome-wide expression profiling of human blood reveals biomarkers for Huntington's diseaseF Borovecki, L Lovrecic, J Zhou, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 14, 2000
Neuroprotective effects of creatine in a transgenic mouse model of Huntington's diseaseR J Ferrante, O A Andreassen, B G Jenkins, et al.
Pageof 13