A Point Mutation in the Ubiquitin Ligase RNF170 That Causes Autosomal Dominant Sensory Ataxia Destabilizes the Protein and Impairs Inositol 1,4,5-Trisphosphate Receptor-mediated Ca2+ Signaling.

Autor: Wright, Forrest A.1, Lu, Justine P.1, Sliter, Danielle A.2, Dupré, Nicolas3, Rouleau, Guy A.4, Wojcikiewicz, Richard J. H.1 wojcikir@upstate.edu
Zdroj: Journal of Biological Chemistry. 5/29/2015, Vol. 290 Issue 22, p13948-13957. 10p.
Databáze: Academic Search Ultimate