TY  - GEN
AU  - Furrer,Stephanie A
AU  - Mohanachandran,Mathini S
AU  - Waldherr,Sarah M
AU  - Chang,Christopher
AU  - Damian,Vincent A
AU  - Sopher,Bryce L
AU  - Garden,Gwenn A
AU  - La Spada,Albert R
TI  - 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
SN  - 1529-2401
PY  - 2012///0104
KW  - Analysis of Variance
KW  - Animals
KW  - Ataxin-7
KW  - Disease Models, Animal
KW  - Gene Expression Regulation
KW  - genetics
KW  - Humans
KW  - Mice
KW  - Mice, Inbred C57BL
KW  - Mice, Transgenic
KW  - Motor Activity
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - Neuroglia
KW  - pathology
KW  - Neurons
KW  - Peptides
KW  - Phenotype
KW  - Prions
KW  - RNA, Messenger
KW  - metabolism
KW  - Rotarod Performance Test
KW  - Spinocerebellar Ataxias
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural
UR  - https://doi.org/10.1523/JNEUROSCI.4000-11.2011
ER  -