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Enrichment of Mammalian Tissues and Xenopus Oocytes with Cholesterol
Published on: March 25, 2020
Niemann-Pick NPC1: sterols to the rescue and beyond
1Department of Medicine and Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada.
Abstract:
In Niemann-Pick type C disease, the most prevalent I1061T mutation inhibits folding and trafficking of the NPC1 protein to the endosomes/lysosomes. In this issue of Chemistry & Biology, Ohgane and colleagues used pharmacological chaperones to repair the defect and identify a second sterol-binding site.
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