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This enables fully coupled acousto-elastic calculations to be made for complex geometries.
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All of this is making for complex calculations on both sides.
A similar argument can be made for clonal complex 4 isolates and for each of the singletons scattered across the country.
A similar abstraction can also be made for the RNAP-cofactor complexes.
Similar observations can be made for the strains in the ST-354 complex (μ = 83 ± 15 vs. μ = 35 ± 15).
A similar case for a complex interaction can be made for the lifespan QTL identified on chromosome IV (Table 2), a QTL also found by Doroszuk et al. (2009).
Exemplification is made for the complex case of the oxidation of D-glucose (DG) to 2-keto-d-glucose (kDG) in the presence of P2Ox (Pyranose oxidase, EC 1.1.3.10) and catalase, continuously operated in a three-phase mechanically agitated semibatch reactor (MASCR) with co-immobilized enzymes on alginate beads.
Similar observations have been made for lanceolate complexes of hair follicles from facial skin or ear hairy skin in mouse, rat, and humans (Yamamoto, 1966; Cauna, 1969; Hashimoto, 1972; Kaidoh and Inoue, 2000), although the sensory neuron subtype under investigation in those studies was not known.
A comparison has been made for a given complex input between the outputs of the MATLAB complex FIR filter code with the fixed point assembly code and are shown in Figure14 (Magnitude plot) and Figure13 (Phase plot).
Spectroscopic studies have been made for an intermediate complex formation between N-haloamine and Pt(IV).
Also a proposition is made for another target complex showing even more promise regarding the catalytic fixation of nitrogen.
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