טוען...

Disrupted glucose homeostasis and skeletal-muscle-specific glucose uptake in an exocyst knockout mouse model

Skeletal muscle is responsible for the majority of glucose disposal following meals, and this is achieved by insulin-mediated trafficking of glucose transporter type 4 (GLUT4) to the cell membrane. The eight-protein exocyst trafficking complex facilitates targeted docking of membrane-bound vesicles,...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
הוצא לאור ב:J Biol Chem
Main Authors: Fujimoto, Brent A., Young, Madison, Nakamura, Nicole, Ha, Herena, Carter, Lamar, Pitts, Matthew W., Torres, Daniel, Noh, Hye-Lim, Suk, Sujin, Kim, Jason K., Polgar, Noemi
פורמט: Artigo
שפה:Inglês
יצא לאור: American Society for Biochemistry and Molecular Biology 2021
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC8027262/
https://ncbi.nlm.nih.gov/pubmed/33647317
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jbc.2021.100482
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