A hypomorphic Mpi mutation unlocks an in vivo tool for studying global N-glycosylation deficiency.
Mpi 功能减弱突变为研究全身 N-糖基化缺陷提供了一种体内工具
期刊:JCI Insight
影响因子:6.1
doi:10.1172/jci.insight.180752
Lin Elisa B, Meregini Steve, Zhang Zhao, Roy Avishek, Argula Tandav, Mitchell James M, Israelsen William J, Ludwig Sara, Russell Jamie, Quan Jiexia, Hildebrand Sara, Nair-Gill Evan, Beutler Bruce, SoRelle Jeffrey A
