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The cells were differentiated with PC-conditioned medium and cARLA (48 h) and the confluent monolayers were incubated with nanocarriers (100 g/ml) diluted in hEC culture medium at 37 C for 24 h in a CO 2 incubator
B., ob TMAO die Schaumzellbildung (Schlsselprozess der Atherogenese) frdert
Muzykewicz, D
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Witko-SarsatVFriedlanderMCapeillre-BlandinCNguyen-KhoaTNguyenAZingraffJet alAdvanced oxidation protein products as a novel marker of oxidative stress in uremia
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