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They result from the body adjusting to the medication's effects on gastrointestinal function and appetite regulation

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Transcobalamin deficiency is a rare autosomal recessive disorder arising from mutations in the transcobalamin ( TCN2 ) gene (35)

Cardiac myocyte miR-29 promotes pathological remodeling of the heart by activating Wnt signaling

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Despite the robust body of evidence showing the cardiovascular benefits of GLP-1 RAs, their origins as diabetes/glucose medications and the mode of administration of all but one by subcutaneous injection have posed barriers for cardiologists to adopt them as a routine part of clinical practice