Sentence examples for scheme of activation from inspiring English sources

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Given that all of the GCKIII and GCKVI members except YSK1/SOK1 contain a serine/threonine residue +1 to the W(I/S/E)(F/W) motif (and, even in YSK1/SOK1, there is a threonine residue at +3), we suggest that the scheme of activation that we are proposing for MST3 might be more widely applicable to other GCKIII/VI members.

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We base our model of ventricular myocytes of adult mouse on three existing model components: 1) a model of cardiomyocyte electrophysiology by Bondarenko et al. [ 53], 2) a description of the contractile element by Cortassa et al. [ 54] and 3) a biochemical scheme of CaMK activation by Bhalla and Iyengar [ 46].

The employment of pairwise sampling scheme showed maintenance of activation foci shift but decrease in both activation detection sensitivity and specificity compared to the results without pairwise sampling and 10(d)), regardless of PC angle and k-t FOCUSS algorithm.

Figure 4 contains a scheme of the complement activation process in both, classical and alternative pathways and shows the MAC formation by the action of C3 convertases.

For the response associated with the PID control scheme, the activation of the horizontal actuator affects the system's stability and allows the TWRM to move 10 cm away from its original location ((delta_{text{R}}) = −0.1 m, (delta_) = −0.1 m).

The scheme of injections during the activation and differentiation phases is given in Figure 12 (A).

If the concentration of d-serine were to increase, it would decrease the activation effect of l-serine if it was not capable of activation itself (in Scheme 2, b > 1 > a).

B) Scheme of C3 proteolysis during complement activation.

Likewise, we show that the robustness of the acquisition scheme is strongly dependent on the detailed kinetics of activation and bleaching.

Unlike αIIbβ3, CD154 interacts with constitutively inactive α5β1, which is uncommon to the classical scheme of integrin outside-in signaling and activation.

Thus, a thiol-bearing derivative of AmB, 3, was first synthesized as outlined in Scheme 1. Activation of previously reported Fmoc-protected AmB, 4, with N, N, N′, N′-tetramethyl-1,2-dihydrobenzo-1,2,3-triazineuronium tetrafluoroborate (TDBTU) and condensation with 2-pyridyldithioethylamine afforded 5. Subsequent deprotection with piperidine and dithiothreitol (DTT) then afforded 3.

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