The phrase "a corresponding one for" is correct and usable in written English.
It can be used when referring to something that matches or relates to another item or concept in a similar way.
Example: "For every action, there is a corresponding one for every reaction in the physical world."
Alternatives: "a matching one for" or "an equivalent one for".
Choose a corresponding one then wait for a little while for the source be totally loaded.
By computing the "closeness" of each attachment protein in P R to all the possible protein-complex cores, we can get a best corresponding one for each attachment.
This theory, however, is very far from as much advanced a theory as the corresponding one for single-valued nonexpansive mappings.
That is why it naturally comes under what additional conditions on the module structure this type of results hold for every n ∈ N. To achieve this goal we state the following new concept, which is a generalization of the corresponding one for Σ -module.
In particular, the stability analysis shows that for a given value of the stride (Δt 1, there is an optimum value of the small time step for which the computational speed is the fastest (N is a minimum), being this speed significantly larger than the corresponding one for an explicit method using (Δt c only.
However, we are more interested in how to establish new inequalities for two-parameter trigonometric means from these ones derived by using Propositions 3.1-5.2 3.1-5.2asning an inequality fobtainingane mans from the correspondinequalityr hyperbolic forctions (see [22–24, 30]).
Rule (S-Res) is slightly more general than the corresponding one for CCS, as it requires that no action in (sigma ) can be a or (overline{a}).
The above homotopy result includes the corresponding one for the class of Kannan maps, and in the following theorem we show that an analogous result is true for the wider class of weakly Kannan maps.
At higher excitation levels I 0>I t, the efficiencies of photodarkening effect for the Ce doped crystals are similar and exceed the corresponding one for the nominally pure hosts by up to 5%.
