Another point of controversy is that, as mentioned above, the violation of abstract rules or complex inter-stimulus relationships can also elicit an MMN.
In more complex paradigms an abstract rule is broken, such as inter-stimulus relationships (Tervaniemi et al., 1994; Paavilainen et al., 2001; Vuust et al., 2005) or phoneme regularity (Näätänen et al., 1997).
Interestingly, our inverse transient post-stimulus relationship between fun and GSR was the opposite of that found for baseline enjoyment by Mandryk and Inkpen.
We initially constructed stimulus response relationships for monochromatic stimuli at 458 and 580 nm.
Indeed, there is debate in the cerebellum literature as to whether the cerebellar cortex is responsible for storing memory traces of temporal 54 or conditioned unconditioned stimulus 55 relationships.
No significant differences were present in the VEP amplitude-stimulus intensity relationships, and the latency-stimulus intensity relationship of the ChR2V+/− rats was also identical to that of the ChR2−/− rats (Fig. 6C).
Our deterministic model offers insight into stimulus-response relationships between Epo and several downstream effectors.
The stimulus-response relationships for extracellular field excitatory postsynaptic potentials (fEPSPs) obtained from UCB exposure and control slices were compared.
However, no significant differences in stimulus-response relationships were found between SAL- and DEX-treated rats in Group B (p>0.05) (Figure 3B).
Excitatory postsynaptic currents (EPSCs) at parallel fibre synapses showed similar rise times, decay times, and stimulus-response relationships in cells from both strains (Figure 1A and B).
No significant differences in stimulus-response relationships were found between SAL- and DEX-treated rats of both Group A and Group B (Figure S4A and S4B).
