Furrer, Stephanie A <br/><br/>
Spinocerebellar ataxia type 7 cerebellar disease requires the coordinated action of mutant ataxin-7 in neurons and glia, and displays non-cell-autonomous bergmann glia degeneration.  [electronic resource] 

 -  The Journal of neuroscience : the official journal of the Society for Neuroscience  Nov 2011 
 - 16269-78 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1529-2401 
<br/><br/><label>Standard No.: </label>10.1523/JNEUROSCI.4000-11.2011  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Analysis of Variance<br/>Animals<br/>Ataxin-7<br/>Disease Models, Animal<br/>Gene Expression Regulation--genetics<br/>Humans<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Transgenic<br/>Motor Activity--genetics<br/>Mutation--genetics<br/>Nerve Tissue Proteins--genetics<br/>Neuroglia--pathology<br/>Neurons--pathology<br/>Peptides--genetics<br/>Phenotype<br/>Prions--genetics<br/>RNA, Messenger--metabolism<br/>Rotarod Performance Test<br/>Spinocerebellar Ataxias--genetics