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A functional corollary of sarcopenia in humans is the presence of decreased force and power.
Our data provide an in vivo functional corollary of the established increased pHi and upregulation of H+ efflux mechanisms in cancer cells.
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This has two interesting functional corollaries; first, the articulating half-rings of the mentioned taxa seem to be narrow axial projections of the tergites, while they are well formed devices set off by articulating furrows in the trilobites.
A novel Lyapunov-Krasovskii functional in Corollary 1 is constructed, which includes the Lyapunov-Krasovskii functional term (V_{4} k)=sum_{s=-tau_{1}+1}^{0}sum_{j=s}^{0}sum_{u=k+j}^{k}y^{T} u) times Q_{3}y u)).
and P i : B ¯ → ( a, b ), i = 1, …, p, are continuous functionals from Corollary 9.
Here P i : B ¯ → ( a, b ), i = 1, …, p, are continuous functionals from Corollary 9.
In this article, we will prove the existence and uniqueness of a solution for a class of functional equations using Corollary 2.3.
Now, we study the existence and uniqueness of the bounded solution of a functional equation using again Corollary 2.2.
As a corollary, the functional significance of a particular PDE subtype is not solely determined by its expression level in a given cell or tissue, and PDE subtypes that represent a minor fraction of total PDE activity might have important roles by acting locally in critical microdomains of cAMP signaling.
We prove some results for convex combination of nonnegative functionals, and some corollaries are established.
As a corollary of the functional equivalence derived here, a formula in the literature for the number of unate cascade functions provides such a formula for the number of nested canalyzing functions.
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