O. Volpina, D. Koroev, T. D. Volkova, A. Kamynina, M. Serebryakova, N. Bobkova
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Abstract
It was shown the correlation between the resistance to proteolysis of (60-76) RAGE fragment and its protected analogue, formation of their fragments and revealed biological activity. We assumed that protected RAGE fragment is a promising for development of anti-AD therapy.
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