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Low levels of mutant ubiquitin are degraded by the proteasome in vivo

P. van Tijn,M. Verhage,2 Authors,D. Fischer

2010 · DOI: 10.1002/jnr.22396
Journal of Neuroscience Research · 18 Citations

TLDR

It is confirmed that, in healthy brain, UBB+1 is continuously degraded and disease‐related UBB-1 accumulation serves as an endogenous marker for proteasomal dysfunction, and this novel transgenic mouse line can give more insight into the intrinsic properties of U BB+1 and its role in neurodegenerative disease.