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Description
Conclusions Complexes (1,2) are expected to be isostructural due to similarity of the N.N-chelating ligands used, but due to the difference in supramolecular architectures no similar unit cells were observed
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The time-resolved data obtained by single-cell confocal microscopy of green fluorescent protein (GFP) reporters and qPCR of the Nrf2 pathway components complemented with siRNA knock down experiments, is accurately described by the calibrated mathematical model

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