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Her idea hinged on the fact that Bell's paper showed 'the predicted sequence of GLP- 1 flanked by enzymatic cleavage sites known to release biologically active peptides from prohormones.' As she explains, 'It predicted the sequence of a 37- amino acid-long version of GLP- 1 and compared it with the sequence of glucagon and other peptides in the same family

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it sheds light on the physiological significance of these variations in infants as well as the effects of the environmental light/dark cycle on neonates

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