Not surprisingly, conventional QTL mapping alone, being a function of only the flanking markers, failed to accurately predict the precise regulating gene, but the QTL interval was typically identified with reasonable success in our simulation.
Variables are separable if the differential equation can be expressed as f(x dx + g y dy = 0, where f(x) is a function of x alone, and g y) is a function of y alone.
Substituting r1(T), r2(T), and r3(T) into TC1 r,T), TC2 r,T), and TC3 r,T), respectively, each TC i (r,T) becomes a function of T alone rather than a function of r and T, since r is a function of T. Solving the equations d TC i dT = 0, i = 1, 2, 3, we get the optimal solutions T1*, T2*, and T3*.
Since a dependency on two factors is difficult to visualize, the actual values for AMPK used in the term k 2 AMPK in Equation 2 are expressed by a glycemia-dependent term derived from a linear approximate relation between AMPK activation and glycemia, which allows to express glucose uptake as a function of glycemia alone.
Recently, a number of algorithms have been proposed to solve Equation 1 with α = 2, Open image in new window f x, y = f y, Open image in new window a function of y alone and g x = 0 Open image in new window.
Nearly 5,500 genes had expression differences as a function of passage alone.
Similarly, we estimated the parameter γ in models of the form – that is, forcing β = 1 and modelling conversion as a function of X alone.
Considering t as a function of y alone, mean cortical thickness was reduced in ASD in the vicinity of, and somewhat anterior to, the anterior commissure (AC).
So far it was never reported a function of LacZ alone in cognition and we consider quite unlikely that this is the case in our mice.
It is important to note that the switch-like transition from apoptosis competent to resistant is not a function of XIAP alone but rather emanates from the interplay of multiple network components.
