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Inter-domain tagging implicates caveolin-1 in insulin receptor trafficking and Erk signaling bias in pancreatic beta-cells

机译：域间标记涉及胰岛素受体运输中的caveolin-1和胰腺β细胞中的Erk信号传导偏差

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Tobias Boothe; Gareth E. Lim; Haoning Cen; Søs Skovsø; Micah Piske; Shu Nan Li; Ivan R. Nabi; Patrick Gilon; James D. Johnson;
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1. Inter-domain tagging implicates caveolin-1 in insulin receptor trafficking and Erk signaling bias in pancreatic beta-cells [J] . Tobias Boothe, Gareth E. Lim, Haoning Cen, Molecular Metabolism . 2016,第5期

机译：域间标记暗示小窝蛋白1参与胰岛β细胞的胰岛素受体运输和Erk信号偏向
2. Mutation in Insulin Receptor Attenuates Oxidative Stress and Apoptosis in Pancreatic Beta-Cells Induced by Nutrition Excess: Reduced Insulin Signaling and ROS [J] . Tachibana K., Sakurai K., Yokoh H., Hormone and Metabolic Research . 2015,第3期

机译：胰岛素受体突变可减轻营养过剩引起的胰腺β细胞的氧化应激和凋亡：降低胰岛素信号和ROS
3. A Targeted RNAi Screen Identifies Endocytic Trafficking Factors That Control GLP-1 Receptor Signaling in Pancreatic beta-Cells [J] . Buenaventura Teresa, Kanda Nisha, Douzenis Phoebe C., Fortschritte der Physik . 2018,第3期

机译：靶向RNAi筛网识别在胰腺β细胞中控制GLP-1受体信号传导的内吞贩运因子
4. OPTOGENETIC MODULATION OF INSULIN FUNCTION IN PANCREATIC BETA-CELLS [C] . Emmanuel Tzanakakis, Sameer Sonkusale, Fan Zhang Conference on biochemical and molecular engineering . 2019

机译：胰β-细胞中胰岛素功能的光遗传调控
5. Effect of Aryl-hydrocarbon Receptor Activity on Lipid Accumulation, Insulin Content and Secretion from Clonal Pancreatic Beta-cells [D] . Baghdasarian, Siyouneh. 2018

机译：芳基烃受体活性对克隆胰腺β细胞脂质积累，胰岛素含量和分泌的影响。
6. Inter-domain tagging implicates caveolin-1 in insulin receptor trafficking and Erk signaling bias in pancreatic beta-cells [O] . Tobias Boothe, Gareth E. Lim, Haoning Cen, 2016

机译：域间标记暗示小窝蛋白1参与胰岛β细胞的胰岛素受体运输和Erk信号偏向
7. Inter-domain tagging implicates caveolin-1 in insulin receptor trafficking and Erk signaling bias in pancreatic beta-cells [O] . Boothe, Tobias, Lim, Gareth E, Cen, Haoning, 2016

机译：域间标记暗示小窝蛋白1参与胰岛β细胞的胰岛素受体运输和Erk信号偏向

Inter-domain tagging implicates caveolin-1 in insulin receptor trafficking and Erk signaling bias in pancreatic beta-cells

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