about
Spinocerebellar ataxia type 1--modeling the pathogenesis of a polyglutamine neurodegenerative disorder in transgenic mice.Mediation of Af4 protein function in the cerebellum by Siah proteinsNeuroprotective effects of granulocyte-colony stimulating factor in a novel transgenic mouse model of SCA17.Short-term succinic acid treatment mitigates cerebellar mitochondrial OXPHOS dysfunction, neurodegeneration and ataxia in a Purkinje-specific spinocerebellar ataxia type 1 (SCA1) mouse model.A phenotypic-genetic study of a group of Polish patients with spinal and bulbar muscular atrophy.
P2860
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Mouse models of human CAG repeat disorders.
@en
type
label
Mouse models of human CAG repeat disorders.
@en
prefLabel
Mouse models of human CAG repeat disorders.
@en
P2093
P2860
P1433
P1476
Mouse models of human CAG repeat disorders.
@en
P2093
P2860
P304
P356
10.1111/J.1750-3639.1997.TB00896.X
P577
1997-07-01T00:00:00Z