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This structural modification also reduces its binding affinity to IGF binding proteins, allowing it to remain bioactive in circulation significantly longer than endogenous IGF-1

Pan J, Hittelman WN, Wu TT, Bresalier R, Swisher S , Correa AM, Ajani J, Izzo JG

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Die Nennmenge beschreibt die ausgewiesene Produktvariante, ersetzt jedoch keine methodenspezifische Bestimmung

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