共 55 条
[1]
Orr HT(2007)Trinucleotide repeat disorders Annu Rev Neurosci 39 575-621
[2]
Zoghbi HY(1980)A family with hereditary ataxia: HLA typing Neurology 30 12-20
[3]
Nino HE(2010)Mechanisms underlying inflammation in neurodegeneration Cell 140 918-34
[4]
Glass CK(1997)Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate Neuron 16 675-48
[5]
Dykes-Hoberg M(1995)SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeat Cell 82 937-35
[6]
Pardo CA(2010)SCA1-like disease in mice expressing wild-type ataxin-1 with a serine to aspartic acid replacement at residue 776 Neuron 67 929-20
[7]
Bristol LA(2013)Purkinje cell ataxin-1 modulates climbing fiber synaptic input in developing and adult mouse cerebellum J Neurosci 33 5806-7
[8]
Jin L(2011)Vascular endothelial growth factor ameliorates the ataxic phenotype in a mouse model of spinocerebellar ataxia type 1 Nat Med 17 1445-70
[9]
Kuncl RW(2006)Glutamate transporters GLAST and EAAT4 regulate postischemic Purkinje cell death: an in vivo study using a cardiac arrest model in mice lacking GLAST or EAAT4 Neurosci Res 55 264-43
[10]
Kanai Y(2004)Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice Hum Mol Genet 13 2535-95