Furthermore, both i f1 and i f2 increased with an increase in H d and D crw, whereas i f1 increased with an increase in β, and i f2 decreased as β increased.
Similarly, i f1 increased with an increase in β, whereas i f2 decreased with an increase in β (Fig. 14 in Appendix 1).
At low void ratios, i f1 decreased with an increase in antecedent moisture content, whereas i f2 increased as antecedent moisture content increased through the dams.
I-80 transcripts were still detectable at P0 and were found at a very low level also in adult mice brains whereas I-86 transcripts vanished completely [13].
In contrast, Szabo et al. investigated brains using semiquantitative RT-PCR analyses and showed a prevalence of I-86 at earlier developmental stages (E10.5 E11.5) whereas I-80 was found to be more abundant at later embryonic stages (E12.5 E15.5) [13].
We found that overexpression of Id-1 in LNCaP cells reduced their ability to stimulate osteoblast mineralisation and enhanced their ability to promote osteoclast differentiation, whereas Id-1 knockdown in PC3 cells reduced their ability to stimulate osteoclast differentiation.
In recent, 3 subtypes of imidazoline receptors have been proposed; activation of I-1 receptors regulates the blood pressure through central nervous system [ 4], whereas I-3 receptors participate in insulin release [ 5] and activation of I-2 receptors (I-2R) increases glucose uptake into muscle cells [ 6, 7].
After the characterization of agmatine as the endogenous ligand of this receptor, 3 subtypes of imidazoline receptors have been proposed; activation of I-1 receptors regulates blood pressure [ 11], whereas I-3 receptors participate in insulin release [ 12] and activation of I-2 receptors (I-2R) increases glucose uptake into muscle cells [ 13, 14].
In general, I (>50%) shows that heterogeneity among studies produce some impact, whereas I (<50%) shows that homogeneity is good for the reliability of meta-analysis.
AL-09 was extracted from inclusion bodies using 6 M urea, whereas κI O18/O8 and AL-12 were extracted from periplasmic fractions.
The Q statistic indicates whether heterogeneity is statistically significant whereas the I 2 statistic quantifies the extent of heterogeneity.
