Assessing recovery from neurodegeneration in spinocerebellar ataxia 1: Comparison of in vivo magnetic resonance spectroscopy with motor testing, gene expression and histology

Suppression of transgene expression in a conditional transgenic mouse model of spinocerebellar ataxia 1 (SCA1) reverses the Purkinje cell pathology and motor dysfunction that are hallmarks of SCA1. We previously showed that cerebellar neurochemical levels measured by magnetic resonance spectroscopy...

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Bibliographic Details
Main Authors: Gülin Öz, Emily Kittelson, Döne Demirgöz, Orion Rainwater, Lynn E. Eberly, Harry T. Orr, H. Brent Clark
Format: Article
Language:English
Published: Elsevier 2015-02-01
Series:Neurobiology of Disease
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Online Access:http://www.sciencedirect.com/science/article/pii/S0969996114003568