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However, it is important to note that, due to potential underreporting by the informants, there were also instances of unknown indications ( n = 2,281, 27.68%)
[123] to reduce intraplaque inflammation and increase plaque stability
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In order to test this possibility, we engineered a murinized version of the anti-IGF-1R mAb, L2-C (L2-Cmu), in order to reduce effector function and enable chronic administration in mice
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