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The Salk researchers suspect this longer-term presence may explain some of the wonder drug benefits of GLP-1 drugs

These compounds displayed elevated binding affinities, particularly engaging critical residues including Lys66, Thr339, Leu337, Ser177, Thr57, Cys63, Leu338, and Ile198 (Table 1), accompanied by hydrophobic interactions

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The severity of symptoms depends on the extent of the infection and complications

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Table 1 Demographics of study population