Aircraft noise, rail and road traffic noise caused similar after-effects but physiological sleep parameters were most severely affected by rail noise.
When placing the magnet over the somatosensory cortex, a similar inhibitory after effect could be observed as well.
Similar hyperactivation effects after high temperature incubation have been described for other thermophilic proteins also likely due to conformational reordering of particular regions of the protein missfolded during expression at low temperatures [ 48- 50].
The illustrated values are again based on the average settings for the five observers tested, who each showed a similar pattern of after-effects on contrast sensitivity.
Similar to the effects observed after the suppression of Arfrp1 (Fig. 2E), the cellular triglyceride content was significantly elevated, whereas the release at the basal site was markedly reduced after depleting the mRNA of Arl1 (Fig. 7A), Golgin-245 (Fig. 7B) or Rab2 (Fig. 7C).
Similar contrasting effects were observed after lateral ventricle versus cisternal administration of lysine-vasopressin [ 269, 270].
Similar protective effects were observed after use of ERK1/2 siRNA or DN-MEK1 to downregulate the ERK1/2 signaling pathway.
Similar parallel effects are maintained after 24 h, when cell adhesion and cell motion seems induced by both EGF and RA.
The increased sweet preference seen after exposure to PBDE-99 in adult male offspring is similar to effects seen after treatment with a PCB mixture reconstituted according to the congener pattern found in human milk (Hany et al. 1999; Kaya et al. 2002).
These effects remained similar after adjustment for potential confounding effects of education on immediate recall T2 (Radjusted = 0.12, P = 0.017) and T3 (Radjusted = 0.1, P = 0.029) (LS model age, education adjusted).
Similar effects were reported after knockdown of CEP135 through RNA interference; we could provoke them also by ectopic overexpression of the mutant protein.
