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Binding affinities for titrations were all fit to the following equation: Y = Fmax*(A sqrt(A^2-B))/(2*C), where X is the concentration of inhibitor, Fmax is the maximum chemical shift change, A = ([BLVRB] + X + KD), B = 4*[BLVRB]*X, and C = [BLVRB]

107 elaborated on the critical role of skin-on-a-chip in modeling dynamic skin changes, particularly in drug screening and physiological studies

This was accompanied by reduced expression levels of ferritin and IP heme oxygenase 1

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however, the gene numbers in microsomal GSTs are fewer than the cytosolic GSTs (Table 1) [62, 64, 65]