Asian Association for the Study of Diabetes 18^th Scientific Sessions: Human Cell Design presents its latest research on GLP1-R KD EndoC-βH5®

Scientists from Human Cell Design participated in the AASD2026 of the Japan Diabetes Society (JDS), in Osaka (Japan). During the event, our team shared our latest results on the 𝗠𝗲𝗰𝗵𝗮𝗻𝗶𝘀𝘁𝗶𝗰 𝗗𝗶𝘀𝘀𝗲𝗰𝘁𝗶𝗼𝗻 𝗼𝗳 𝗧𝗶𝗿𝘇𝗲𝗽𝗮𝘁𝗶𝗱𝗲 𝗦𝗶𝗴𝗻𝗮𝗹𝗶𝗻𝗴 𝗶𝗻 𝗛𝘂𝗺𝗮𝗻 𝗘𝗻𝗱𝗼𝗖-𝗕𝗛𝟱 𝗖𝗲𝗹𝗹𝘀: 𝗜𝘀 𝗶𝘁 𝘁𝗿𝘂𝗹𝘆 𝗮 𝗯𝗶𝗮𝘀𝗲𝗱 𝗱𝘂𝗮𝗹 𝗮𝗴𝗼𝗻𝗶𝘀𝘁? Our experts exposed how GLP1-R KD EndoC-ßH5® derived model can help enhance research on Obesity:

✔️ 𝗢𝘃𝗲𝗿𝗰𝗼𝗺𝗲𝘀 𝗢𝗯𝗲𝘀𝗶𝘁𝘆 𝗥𝗲𝘀𝗲𝗮𝗿𝗰𝗵 𝗖𝗼𝗻𝘀𝘁𝗿𝗮𝗶𝗻𝘁𝘀: The ultimate translational tool.
✔️ 𝗧𝗮𝗶𝗹𝗼𝗿𝘀 𝗕𝗶𝗮𝘀𝗲𝗱 𝗔𝗴𝗼𝗻𝗶𝘀𝗺 𝗦𝘁𝗿𝗮𝘁𝗲𝗴𝗶𝗲𝘀: Deep insights into β-arrestin and cAMP signaling pathways.
✔️ 𝗘𝗹𝗶𝗺𝗶𝗻𝗮𝘁𝗲𝘀 𝗙𝗮𝗹𝘀𝗲 𝗣𝗼𝘀𝗶𝘁𝗶𝘃𝗲𝘀: Leveraging physiological receptor density for superior accuracy.
✔️ 𝗥𝗮𝗻𝗸𝘀 𝗖𝗮𝗻𝗱𝗶𝗱𝗮𝘁𝗲 𝗠𝗼𝗹𝗲𝗰𝘂𝗹𝗲𝘀: Precision screening for twincretins and triagonists.
✔️ 𝗜𝗱𝗲𝗻𝘁𝗶𝗳𝗶𝗲𝘀 𝗜𝗻𝗰𝗿𝗲𝘁𝗶𝗻-𝗗𝗿𝗶𝘃𝗲𝗻 𝗜𝗻𝘁𝗲𝗿𝗻𝗮𝗹𝗶𝘇𝗮𝘁𝗶𝗼𝗻: Mapping the mechanisms of receptor trafficking and desensitization.

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