Pages that link to "Q35097613"
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The following pages link to Are Huntington's and polyglutamine-based ataxias proteasome storage diseases? (Q35097613):
Displaying 12 items.
- The ubiquitin-proteasome reporter GFPu does not accumulate in neurons of the R6/2 transgenic mouse model of Huntington's disease (Q33427852) (← links)
- Comparative analysis of REG{gamma} expression in mouse and human tissues (Q34042286) (← links)
- The ubiquitin proteasome system in neurodegenerative diseases: sometimes the chicken, sometimes the egg. (Q35558459) (← links)
- Recent advances in hereditary spinocerebellar ataxias (Q36085900) (← links)
- Proteasomes cleave at multiple sites within polyglutamine tracts: activation by PA28gamma(K188E). (Q36741580) (← links)
- Molecular pathogenesis of spinocerebellar ataxia type 6. (Q36774733) (← links)
- Screening of therapeutic strategies for Huntington's disease in YAC128 transgenic mice. (Q37866383) (← links)
- Eukaryotic proteasomes cannot digest polyglutamine sequences and release them during degradation of polyglutamine-containing proteins (Q44833524) (← links)
- Enhanced striatal NR2B-containing N-methyl-D-aspartate receptor-mediated synaptic currents in a mouse model of Huntington disease (Q44968954) (← links)
- Sharing of polyglutamine localization by the neuronal nucleus and cytoplasm in CAG-repeat diseases (Q45148750) (← links)
- Huntington's Disease (Q83728053) (← links)
- Pioglitazone, extract of compound Danshen dripping pill, and quercetin ameliorate diabetic nephropathy in diabetic rats (Q85610593) (← links)