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REBO potential assumes complex multi-body interaction model, that is difficult to represent efficiently in the SIMD or SIMT programming model.
The kinetic response of the proton conductance to its driving force (proton-motive force) can therefore be measured as the relationship between oxygen consumption and mitochondrial membrane potential (assuming no slip reaction in the mitochondrial proton pumps) when the potential is varied with increasing doses of electron transport chain inhibitors [ 21, 25, 38, 39].
If, as we hypothesized, the cone dim flash response originates in coupled rods, while the bright flash response originates in both photoreceptors, they should have a different apparent reversal potential (assuming the actual reversal potential EOS in rods and cones to be the same; EOS ≈ 0 mV; Luo et al., 2008).
It can be inferred that UEGLS ordinarily has the morphology of an inverted action potential; assuming the exploring electrode is the anode, the lead field ∇ Z and elemental surface vector d S ⃑ will typically be oriented in approximately opposite directions in the dominant region of ΘL, so that their dot product ∇ Z ⋅ d S ⃑ is negative.
The numerical solution of this expression for V r was used to evaluate the sodium current at rest, I Na, rest = g N a (V r ) · (E N a − V r ), which defines the sodium-current-based cost of the resting potential (assuming the current is proportional to the activity of the Na- K-ATPase at rest).
On the contrary, antibodies selectively targeting HER4 JM-a, such as the recently introduced monoclonal antibody 1479 [ 60], could have therapeutic potential, assuming that JM-a-specific antibodies are expected not to cause adverse effects in tissues, such as the heart, that exclusively express ErbB4 JM-b.
Classical derivations of pairwise potentials assume statistical independence of all pairs of atoms.
The magnetic potential, its first derivatives, and the electric potential are assumed to be exponentially decaying.
