Thus, the interaction of the depressing effect of propofol on CBF combined with SCH23390's nearly irreversible kinetics leads to (1) significantly lower receptor binding in high receptor density regions for propofol compared to isoflurane anesthesia and (2) significant differences in the tracer influx in all regions, regardless of receptor density (Table 4).
However, in Musa, we found that CNGC 1, CNGC 5 and CNGC 6 changed after PAMP perception, which suggested that there is a fundamental difference in the Ca2+ influx mechanism between banana and Arabidopsis.
Previous studies showed a dynamic and transient disruption of the blood brain barrier (BBB) during epileptogenesis and the chronic epileptic state [25, 34], which may cause tracer perfusion differences in the KASE model and therefore differences in tracer influx (k1), as well as tracer efflux (k2).
To determine the nitrogen percentage of the biomass the difference between the nitrogen concentrations in the influx and efflux medium in g · L-1 was divided by the C x.
However, there were no significant differences in the mean values of Ca2+ influx onset time (approximately 65 sec; supplementary material Fig. S7B), maximum Ca2+ concentration (supplementary material Fig. S7C), and slope (Ca2+ increase rate; supplementary material Fig. S7D) between the genotypes.
In line with renal function and histology, there were also no differences in granulocyte influx between MyD88−/− and TRIF-mutant mice compared with their wild types one day after I/R injury (figure 8d).
These data suggest that the parameter values in Table 2 give a good description of the parameter settings underlying fast calcium dynamics in spines and dendrites with most likely no or small differences in calcium influx and extrusion parameters between spines and small dendrites.
Moreover, no differences in Ca2+ influx were observed between Nck1- or Nck2 knockdown cells following stimulation at limiting concentration of the stimulating antibody (data not shown).
There were no differences in neutrophil influx between rm-APC and buffer control treated mice after 48 or 96 hours, as evidenced by equal percentages of positivity in Ly-6G stainings.
There were no differences in neutrophil influx between WT, heterozygous and homozygous FVL mice as evidenced by equal percentages of positivity in Ly-6G stainings both at 24 hours and 48 hours after infection.
