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The rate dependence on NAD(P)+ concentration is complex and is probably only partly explained by negative binding cooperativity.
Modelling a multiphase stirred tank at a high solids concentration is complex owing to particle particle and particle wall interactions which are generally neglected at low concentrations.
The dependence of the emission spectrum of PMP-GSAM on potassium iodide concentration is complex.
Biologically, this means that a high OLP environment will select for networks whose response to a linear gradient of concentration is complex.
The explicit dependence of the reaction velocity on substrate concentration is complex and generally requires the solution of the cubic polynomial encapsulated by Eqs.
In critically ill patients, particularly those with sepsis, the relationship between COP and the albumin concentration is complex, being influenced by altered permeability and increased transcapillary escape rates [ 14, 15].
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The relationship between tumor and plasma concentration was complex, indicating multiple determinants.
The molecular mechanisms by which plants respond and acclimate to changes in the nutritional Pi concentration are complex but of great importance and could be useful in developing strategies for elucidating the gene networks involved in plant response to various kinds of abiotic stress.
The dependence of ROS concentration on plasma power density is complex [24], [34].
Even with the relatively simple layering, patterns of flow and resulting concentrations are complex.
The distribution of the pairwise Spearman correlations of the chemical concentrations was complex (see Supplemental Material, Figure S1), with pairwise correlations ranging from slightly negative (r = –0.15) to nearly perfect correlation (r = 0.99 for cis- and trans-permethrin).
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