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entities exhibit properties from enzymes (transport kinetics), receptors (inhibitor binding) and channels (current properties). Our research is grounded in fundamental molecular pharmacology but has
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. Nygaard et al. 2024, Nat Commun; Schmidt et al. 2022, Nat Commun; Pugh et al. 2022, Cells). Your job The current project concerns the solvation of structures of the human dopamine transporter (hDAT) using
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on understanding charge carrier generation, transport, recombination dynamics, and energy transfer mechanisms. These insights will drive the development of highly efficient materials for advanced biomedical imaging
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