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Adverse events were what you would expect from an incretin-class drug in a supervised trial: nausea in 42.4 percent of 12 mg patients versus 14.8 percent on placebo, diarrhea in 32.0 percent versus 13.5 percent, vomiting in 25.3 percent versus 4.8 percent

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J., Lai, M

However, this relatively new analytical technique has never been applied to arthropod-derived EVs

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