In terms of trends, we find that as the complexity of the complex increases, the mean dN/dS ratio of human genes of associated constituent proteins tends to decrease suggesting that complex complexity negatively correlates with purifying selective pressure on genes.
ASARM-peptide disruption of this complex increases FGF23 expression.
The stability of the ribose-boron complex increases with increasing pH.
The Zn2·bisDPA complex increases the interaction of peptides with anionic model membranes, while decreasing interactions with zwitterionic model membranes.
Unfortunately, the weir is too high, and the water level within the lacustrine complex increases alarmingly during floods.
As adsorption density increases, the zeta potential of the shale polyacrylamide complex increases and then levels off when the adsorption density approaches capacity (Menon and Wasan 1987a).
Increasing substitution across the phosphinato complex, increases the activation barrier of the phenyl group, which are significantly greater than the isopropyl analogue.
The addition of 50 wt.% propylene carbonate to the polymer-salt complex increases its conductivity by three orders of magnitude, without degradation of its other physical properties.
For instance, as initial C Fe molar ratio increases from 0.23 to 3.1, the proportion of FeO in the resulting DOM goethite complex increases from 10% (w/w) to 18% (w/w) (Additional file 1: Table S4).
The decrease in global hardness and the gap energy proves that the stability of the nanotube/CO complex decreases significantly from original values and the reactivity of the complex increases.
It is thought that as the side chain length increases from C1 for PAA to C4 for PLL, the hydrophobicity of polyelectolyte complex increases, indicating that much more dehydration occurs around PNIPAAm.
