The developmental pattern of error processing was similar to one component of task switching (switch cost of the response-repetition condition), indicating that inhibition could be a common mechanism underlying both the processes.
Atomic structural information is now available for all components of the switch complex, including the full-length or fragmented FliG, FliM, FliN fragments, and the complex of FliG/FliM fragments.
To design new proteins that can switch conformation, protein designers have focused on the two key components of protein switches: the amino acid sequence must be compatible with the multiple target states and there must be a mechanism for perturbing the relative stability of these states.
Such crystals might serve as components of optical switches which would, among other things, fulfill the role played by transistors in conventional electronics.In order to make a photonic crystal, though, the materials have to be organised into structures no more than a wavelength of light apart.
This review focuses on recent advances from Drosophila in analysis of the functional components of transcriptional switches, including basal promoters, enhancers, boundary elements, and maintenance elements.
Whether neural activation in these regions is dissociable and associated with separable cognitive components of task switching has been a matter of recent debate.
where ξ i ( k ), i ∈ I [ 1 N ] are the components of the switching function given in (2.3), μ i l ( k ), l ∈ I [ 1 N l ] and λ i q ( k ), q ∈ I [ 1 N q ] are unknown polytopic uncertain parameters given in (2.4) and (2.5) for each i ∈ I [ 1 N ].
where x ( k ) is the state vector of components x p ( k ), p = 1, …, n. ξ i ( k ), i ∈ I [ 1 N ] are the components of the switching function given in (2.3), μ i l ( k ), l ∈ I [ 1 N l ] and λ i q ( k ), q ∈ I [ 1 N q ] are unknown polytopic uncertain parameters given in (2.4) and (2.5) for each i ∈ I [ 1 N ].
Different components of task switching can be investigated by manipulating the delay between consecutive trials, or between the task cue and the target trials.
Modulation of pH-driven conformational transitions by selective manipulation of the electrostatic component of the switch is an extremely difficult undertaking.
The mce1 locus appears to be a component of the switch to slow growth rate, which is consistent with the proposed role in virulence of M. tuberculosis.
