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Structural studies reveal that full-length human RAGE has three domains (Figure 4): an extracellular part responsible for ligand binding, a hydrophobic transmembrane spanning region, and a highly charged cytoplasmic tail, which is essential for RAGE ligand-mediated signal transduction (83, 87)

Induction of glutathione S-transferase by phenobarbital in rat hepatocyte culture

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Finally, for the application proposed, the efficiency of these SPIONs for T 2 -weighted MRI applications was also evaluated from relaxation Nuclear Magnetic Resonance (NMR) experiments