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Here, we expressed the human GPR17 long isoform (hGPR17L) in GLUTag cells, a murine EEC line, and we used the GPR17 synthetic agonist MDL29,951 together with pharmacological probes and genetic approaches to quantitatively assess the contribution of GPR17 signaling to GLP-1 secretion
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Diese therapeutischen Fortschritte stellen eine Revolution in der Behandlung von Stoffwechselerkrankungen und Fettleibigkeit dar
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