doi: 10.1038/33308
Fumagalli L, Nazlie Mohebiany A, Premereur J, Polanco Miquel P, Bijnens B, Van de Walle P et al
In this context, using a previously reported -helical peptide as a template sequence (Behera et al., 2022), this study discusses the rational computational design and in silico evaluation of an -helical peptide (SR18: 18 aa) as a potent agonist of GLP-1R, with native GLP-1 and Semaglutide serving as references
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serum BUN was determined using the Bioassay systems assay (DIUR-100) according to the manufacturers directions
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