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Therapeutic effect of Berberine on Huntington's Disease Transgenic Mouse Model
1 di 10
Differential Proteolysis of Mutant Huntingtin in Astrocytes and
Neurons
2 di 10
Ubiquitin Targeting and Differential Accumulation of Mutant Huntingtin
3 di 10
The Role of Oligodendrocyte Dysfunction in Huntington's Disease
4 di 10
Age-dependent, region-specific mechanisms contribute to Spinocerebellar Ataxia 17 pathogenesis.
5 di 10
The role of Huntingtin-associated protein 1 (Hap1) in postnatal development
6 di 10
Cell Type-Dependent Activities of the Ubiquitin-Proteasome Systemand Selective Neurodegeneration
7 di 10
Transcriptional dysregulation of TrkA associates withneurodegeneration in Spinocerebellar Ataxia 17
8 di 10
Mutant Huntingtin Impairs Astrocytic Secretion
9 di 10
The role of glia in Huntington's disease pathology
10 di 10