I also demonstrate another technique that calls for tying the herbs up in a piece of cheesecloth to make a sachet.
I also demonstrate the use of these indices for institutions.
I also demonstrate large and erratic effects of counting bias on the original h-index, and show how the harmonic version of the h-index provides unbiased bibliometric ranking of scientific merit while retaining the original's essential simplicity, transparency and intended fairness.
Furthermore, I also demonstrate increased power and mapping resolution for MANTRA over random-effects meta-analysis when the pattern of allelic effects between populations is well captured by the Bayesian partition model.
I have also demonstrated that the net social benefits of a sustainable equilibrium are between those of a market equilibrium and a socially optimal equilibrium.
I have also demonstrated empirically that all model-based methods engendered in the software SCRalyze, developed by myself with colleagues, are more sensitive than conventional peak-scoring approaches (Bach, Daunizeau, et al., 2010; Bach, Daunizeau, et al., 2011; Bach, Friston, & Dolan, 2013).
Similarly, Annexin V/PI staining also demonstrated significant induction of early (Annexin V) and late (PI) apoptosis after 24 h A β42O (1 μM) treatment, which was nearly completely blocked by SSH1 siRNA knockdown, indicating that SSH1-dependent Cofilin activation is required for A β42O-induced apoptosis.
Figure 14 shows that the PSFC I-Beam also demonstrated superior flexure-shear performance when compared with the traditional PC I-Beams.
Replicons in which replication and translation activities were uncoupled (GBneoD-I-IIGB/II-IIIHC, GBneoD-I-IIGB/II-IVHC, GBneoD-I-IIIGB/II-IVHC) also demonstrated translational competence, although with decreased efficiency compared to chimeras in which domains II-III were swapped, in particular for GBneoD-I-IIGB/II-IIIHC (Fig. 2A).
